Identification of Inpatient DNR Status / Sehgal and Wachter

Article Type
Changed
Display Headline
Identification of inpatient DNR status: A safety hazard begging for standardization

As modern medicine developed the technological capacity to deliver aggressive life‐sustaining interventionsthrough methods such as cardiopulmonary resuscitation (CPR), intensive care units, and mechanical ventilationthe concept of do‐not‐resuscitate (DNR) orders emerged to allow individual patients to choose to forego selected treatments. To encourage patients to articulate these preferences, Congress passed the Patient Self‐Determination Act in 1991, a measure that required health care facilities to discuss advance directives with patients as they enter their system.1 Although the act has had less of an impact on the quality of DNR discussions than originally hoped for,25 its passage was evidence of the importance our society places on patientclinician discussions regarding goals of care. In addition to this legislative push, many organizations and advocacy groups use a variety of marketing campaigns, accreditation standards,6 and standard instruments and tools79 to promote the use of advance directives

Despite all these efforts, fewer than 30% of Americans (54% older than age 65) have completed advance directives.10 Nevertheless, many patientsparticularly those at highest risk for requiring end‐of‐life caredo express preferences regarding resuscitation at the time of hospital admission. In an ideal world, these preferences would be available for all providers to view, respect, and act on.

Unfortunately, research on patient safety and quality has demonstrated wide gaps between ideal and actual practice.1112 In the context of DNR wishes, despite strong efforts to collect patients' preferences, no current regulation provides or mandates a best practice on making these preferences operational. There are also few data that indicate whether patients' preferences are in fact transmitted to providers at the point of care and in an accurate and reliable manner.

Past research on proper identification of DNR orders is limited, with much of the focus on prehospital protocols.1315 Anecdotally, hospitals seem to employ varying strategies to highlight DNR orders using a combination of paper or electronic documentation and color‐coded patient wristbands. There have been several reports of errors involving this issue, including patients receiving CPR despite stated DNR preferences and a patient having CPR withheld because the wrong chart (of another patient with a DNR order) was mistakenly pulled.1617

The patient safety field emphasizes standardization as a key strategy to prevent errors. Because of problems articulating DNR orders (and other important patient‐related information), several hospitals promote the use of color‐coded wristbands to denote preferences for resuscitation. However, without national regulations or standards, the possibility remains that one safety hazard (advance directives on a paper chart distant from a patient's room) may be traded for another hazard (front‐line providers interpreting a color‐coded wristband incorrectly). In addition to the ethical problems inherent in failing to adhere to patients' resuscitation preferences, errors in following advance directives may also create legal liability.18 With all this in mind, we conducted a national survey to determine practice variations in the identification of DNR orders and the use of color‐coded patient wristbands. We hypothesized that there is considerable variation both in identification practices and in the use of color‐coded wristbands across academic medical centers.

METHODS

The project was approved by the University of California, San Francisco Committee on Human Research. We anonymously surveyed nursing executives who are members of the University HealthSystem Consortium (UHC), an alliance of 97 academic medical centers and their affiliated hospitals representing 90% of the nation's nonprofit academic medical centers.19 The nursing executives are senior nursing leaders at participating UHC institutions and members of a dedicated UHC Chief Nursing Officer Council E‐mail listserv. We designed a brief survey and distributed it via their E‐mail listserv using an online commercial survey administration tool.20 Respondents were asked to complete the survey or have one of their colleagues familiar with local DNR identification practices complete it on their behalf. The online tool also provided summary reports and descriptive findings to meet the study objectives. We provided a 1‐month window (during summer 2006) with 1 interval E‐mail reminder to complete the surveys.

RESULTS

Survey announcements were E‐mailed to 127 nursing executives, 69 of whom completed it (response rate 54%). The respondents represented mostly academic medical centers (87%; another 13% represented affiliated community teaching hospitals), public institutions (89%), and large facilities (60% with more than 400 beds; 40% with 201‐400 beds). More than half the respondents (56%) reported their hospitals use paper chart documentation as the only method of identifying patients with a DNR order, whereas 16% reported their hospitals use only electronic health record (EHR) documentation (Fig. 1). Twenty‐five percent of hospitals (n = 17) use a color‐coded patient wristband in addition to either paper or electronic documentation. Of these 17 hospitals, a total of 8 colors or color schemes were employed to designate DNR status (Table 1).

Figure 1
Current practices for identification of DNR orders.
Reported Colors Used for Wristbands Designating DNR Status and the Number Using Them
Green5
Yellow3
Blue3
White with blue stars versus green stars (full DNR versus limited DNR)1
Red1
Red and white1
Purple1
Gold1
Other (not listed)1

The use of color‐coded wristbands was not limited to identification of DNR status. Fifty‐five percent of hospitals (n = 31) use color‐coded wristbands to indicate another piece of patient‐related data such as an allergy, fall risk, or same last name alert (Table 2). In fact, 12 indications were depicted by various colors, with variations in both the color choice for a given indication (eg, allergy wristbands red at one hospital and yellow at another) and across indications (eg, red for allergy at one hospital and red for bleeding risk at another). Nearly 3 of 4 respondents (n = 48) reported being aware of a case at your institution in which confusion about a DNR order led to problems or confusion in patient care. A few respondents shared a brief anecdote of the event, illustrating the spectrum of clinical scenarios that lead to potential confusion (Table 3). Respondents reporting a case of confusion were not more likely to be from an institution that used color‐coded wristbands.

Other Reported Indications Colors Used for Patient Wristbands
Indication (n)Colors used (n)
Drug/allergy (22)Red (16) Yellow (4) White (1) Orange (1)
Fall risk (18)Orange (5) Green (3) (and lime green [1]) Blue (3) Purple (3) Yellow (2) (and fluorescent yellow [1])
Same name alert (7)Blue (3) Orange (2) Yellow2)
Bleeding risk (3)Red
Patient identification (3)Green Red White
Wandering risk (3)Pink (2) (and hot pink [1])
Contact isolation (2)Green
Latex allergy (2)Purple
No blood draws on this arm (1)Orange
MRSA infection (1)Green
No blood products (1)Red
Sleep apnea (1)Purple
Anecdotes about Confusion around a DNR order
The patient had a DNR order written in the chart but no other identifiers at bedside, so a consult service started CPR while trying to determine code status.
Nurse called a code on a patient who was DNR because she failed to see order in chart.
Resuscitation efforts took place on a patient with a DNR order because the entire chart did not accompany the patient to a diagnostic testing area.
Patient was off the unit for a procedure, and staff in the other department did not know patients code status (DNR) and called a code.
Patient transported off nursing unit to radiology and coded. Patient was a DNR, but the order was buried in thinned chart materials.
Prior to implementing the wristbands, there were delays in care. Once wristbands were implemented with stars only, there was confusion as to what a blue star meant and what a green star meant (limited versus no resuscitation efforts).
We used to place a sticker on the chart. A sticker was left on the chart of a discharged patient when a new patient was admitted. The mistake was caught before an incident occurred.

When asked whether most (greater than 75%) physicians and nurses could properly identify the color associated with a DNR patient wristband, responses differed by discipline. Eight‐five percent of respondents believed that most nurses at their institutions could correctly report the color for DNR, whereas only 15% believed physicians could do the same. Only 22% of respondents anticipated a change in the current system within the next 2 years; all these changes were a transition from paper to electronic documentation systems.

DISCUSSION

Regardless of whether the DNR documentation occurs in paper or electronic form (and our study demonstrates significant practice variation in the documentation method), the risk that a hospitalized patient may suddenly stop breathing or become pulseless is ever present. When such a patient is discovered, providers race to the bedside and initiate care, but immediately ask, Is the patient a full code? In these often‐chaotic moments, accurate and timely information about DNR status is critical to respecting a patient's preferences and avoiding a potentially devastating error. A number of the anecdotes shared by survey respondents and highlighted in Table 3 reinforce this concern. Many of these scenarios occur in the middle of the night or off a patient's primary unit (ie, at a test or procedure area), increasing the need for quick and easy identification of DNR status.

Our study demonstrates that a logical point‐of‐care solutiona color‐coded DNR patient wristbandmay create its own safety hazards, particularly if the color designations are not known by all providers (including floating and traveling nurses or trainees who rotate at different hospitals) and if the colors being employed represent different indications at a given hospital (see accompanying Images Dx, page 445). We found that approximately 1 in 4 surveyed hospitals depict DNR status by a color‐coded wristband. We also discovered remarkable variation in the colors chosen and the degree to which institutions use color‐coded wristbands to signal a panoply of other patient‐related issues. Human factors research demonstrates that even well‐meaning patient safety solutions may cause harm in new ways if they are poorly implemented or if the interface between the technology and human work patterns is not well appreciated. For example, recent studies illustrate unintended consequences from safety‐driven solutions, such as the implementation of computerized order entry,2122 quality measurement,23 adoption of EHRs,24 and bar code medication administration systems.25 Because standardization is a key mechanism for decreasing the opportunities for error, our findings raise serious concerns about current wristband use.

Interestingly, the lack of standardization and its related risk of failing to recall the conditions associated with color‐coded wristbands are complicated by societal trends. In December 2004 the issue of patient wristbands made headlines in Florida, when hospitals using yellow DNR wristbands (as was the case in 3 hospitals in our sample) reported several near‐misses among patients wearing yellow Lance Armstrong Livestrong bracelets.2627 Given recent estimates that nearly 1 in 5 Americans wears these bracelets to support people living with cancer,28 even safety‐minded journals and national newspapers have highlighted the issue.2930 Most hospitals that continue to use yellow DNR wristbands now either remove or cover Livestrong bracelets at the time of hospital admission. Furthermore, many other self‐help organizations now issue wristbands in a variety of colors as well, creating a potential hazard for any person wearing one in the hospital. Although patients do not mind wearing color‐coded wristbands,31 they might feel differently if they knew the potential for confusion.

After these anecdotal reports of identification mistakes surfaced, several states, most notably Arizona and Pennsylvania, launched initiatives to address the problem.3233 Arizona, after discovering 8 colors being used in the state, developed plans for a purple DNR color‐coded wristband. The choice of purple, and the careful decision to avoid blue, occurred because many hospitals call their resuscitative efforts a code blue, creating yet another potential source of confusion if a blue wristband is associated with a DNR order. The Pennsylvania Patient Safety Authority also found tremendous color variations in patient wristbands used in a statewide survey. Both states ultimately promoted standardized colors and indications and provided tool kits and implementation manuals.3233

Although statewide initiatives represent a step forward, we believe that a national standard for color‐coded wristbands would improve patient safety. Precedents for this call to action exist. For many years, anecdotal information circulated about the errors caused by ambiguous use of abbreviations, such as qd instead of daily or U instead of units. Individual hospitals often banned or limited the use of such abbreviations, but no standard list of high‐risk abbreviations guided practice or required adherence, and cross‐hospital variation undoubtedly led to confusion. In 2004 the Joint Commission created a uniform list of high‐risk abbreviations as part of their National Patient Safety Goals, which instantly ended the debate about which abbreviations to ban and mandated compliance with the safety practice.34 A national group of stakeholders should similarly be convened to develop a list of colors and associated conditions that should be widely disseminated and enforced by the Joint Commission or a similar body. The statewide efforts by Arizona and Pennsylvania are instructive in this regard. Despite being guided by the goal of standardization, these 2 states chose different colors for DNR identification (interestingly, Pennsylvania chose blue for DNR, perhaps for the same reason that Arizona avoided itcode blue), further supporting the need for national guidelines (Table 4).

Recommendations from Arizona and Pennsylvania for Color‐Coded Wristbands
IndicationColor (PA)Color (AZ)
DNRBluePurple
AllergyRedRed
Fall riskYellowYellow
Latex allergyGreen 
Restricted extremityPink 
Preregistration in emergency roomYellow 
Admission and identificationClear 

Our study represents the first national sample of DNR identification practices. Although it targeted academic health centers and affiliated institutions, we believe that these practice variations likely exist in all health care settings. Our study limitations included reliance on self‐reported institutional practices rather than direct review of existing policies and limited information about the surveyed population, making it impossible to compare respondents and nonrespondents. However, we have no reason to believe that these groups differed sufficiently to influence the study's main findings.

In the future, better technology may ultimately replace color‐coded wristbands. For instance, the time may come when wireless technologies seamlessly linked to the electronic health record will alert providers to a patient's DNR status when entering the patient's room. However, for today, point‐of‐care solutions using color‐coded wristbands remain a reasonable solution. Creating a nationally enforced standardized methodology, understandable and memorable to providers and free of stigma to patients (eg, a black wristband for DNR or writing DNR on a wristband) should be a patient safety priority. Because simplification is another key characteristic of safe systems, it seems prudent to aim for a national system that involves a maximum of 3‐4 colors.

CONCLUSIONS

Patients and families dedicate tremendous energy to making decisions about their advance directives, and discussions of these issues often create considerable angst and sadness. Health care providers are trained to elicit and advocate for such directives so they can act with patients' wishes in mind. Despite the high stakes, all these efforts can be undermined when the system for making providers aware of a patient's DNR status is flawed. Our data confirm the tremendous variability in the systems used to indicate DNR status (and other types of indications), variability that may place patients at risk from catastrophic errors. Following the lead of a few states, we call for a national mandate to standardize the identification of DNR orders and to make the colors of wristbands for a small set of indications uniform in every hospital across the country.

Acknowledgements

We thank Mark Keroack, MD, MPH, and Cathy Krsek, RN, MSN, MBA, from the University HealthSystem Consortium for their contributions to the survey and assistance with administration. We also thank members of the UHC Chief Nursing Council for participating in the survey study.

Article PDF
Issue
Journal of Hospital Medicine - 2(6)
Page Number
366-371
Legacy Keywords
patient safety, standardization, Do Not Resuscitate orders, patient wristbands
Sections
Article PDF
Article PDF

As modern medicine developed the technological capacity to deliver aggressive life‐sustaining interventionsthrough methods such as cardiopulmonary resuscitation (CPR), intensive care units, and mechanical ventilationthe concept of do‐not‐resuscitate (DNR) orders emerged to allow individual patients to choose to forego selected treatments. To encourage patients to articulate these preferences, Congress passed the Patient Self‐Determination Act in 1991, a measure that required health care facilities to discuss advance directives with patients as they enter their system.1 Although the act has had less of an impact on the quality of DNR discussions than originally hoped for,25 its passage was evidence of the importance our society places on patientclinician discussions regarding goals of care. In addition to this legislative push, many organizations and advocacy groups use a variety of marketing campaigns, accreditation standards,6 and standard instruments and tools79 to promote the use of advance directives

Despite all these efforts, fewer than 30% of Americans (54% older than age 65) have completed advance directives.10 Nevertheless, many patientsparticularly those at highest risk for requiring end‐of‐life caredo express preferences regarding resuscitation at the time of hospital admission. In an ideal world, these preferences would be available for all providers to view, respect, and act on.

Unfortunately, research on patient safety and quality has demonstrated wide gaps between ideal and actual practice.1112 In the context of DNR wishes, despite strong efforts to collect patients' preferences, no current regulation provides or mandates a best practice on making these preferences operational. There are also few data that indicate whether patients' preferences are in fact transmitted to providers at the point of care and in an accurate and reliable manner.

Past research on proper identification of DNR orders is limited, with much of the focus on prehospital protocols.1315 Anecdotally, hospitals seem to employ varying strategies to highlight DNR orders using a combination of paper or electronic documentation and color‐coded patient wristbands. There have been several reports of errors involving this issue, including patients receiving CPR despite stated DNR preferences and a patient having CPR withheld because the wrong chart (of another patient with a DNR order) was mistakenly pulled.1617

The patient safety field emphasizes standardization as a key strategy to prevent errors. Because of problems articulating DNR orders (and other important patient‐related information), several hospitals promote the use of color‐coded wristbands to denote preferences for resuscitation. However, without national regulations or standards, the possibility remains that one safety hazard (advance directives on a paper chart distant from a patient's room) may be traded for another hazard (front‐line providers interpreting a color‐coded wristband incorrectly). In addition to the ethical problems inherent in failing to adhere to patients' resuscitation preferences, errors in following advance directives may also create legal liability.18 With all this in mind, we conducted a national survey to determine practice variations in the identification of DNR orders and the use of color‐coded patient wristbands. We hypothesized that there is considerable variation both in identification practices and in the use of color‐coded wristbands across academic medical centers.

METHODS

The project was approved by the University of California, San Francisco Committee on Human Research. We anonymously surveyed nursing executives who are members of the University HealthSystem Consortium (UHC), an alliance of 97 academic medical centers and their affiliated hospitals representing 90% of the nation's nonprofit academic medical centers.19 The nursing executives are senior nursing leaders at participating UHC institutions and members of a dedicated UHC Chief Nursing Officer Council E‐mail listserv. We designed a brief survey and distributed it via their E‐mail listserv using an online commercial survey administration tool.20 Respondents were asked to complete the survey or have one of their colleagues familiar with local DNR identification practices complete it on their behalf. The online tool also provided summary reports and descriptive findings to meet the study objectives. We provided a 1‐month window (during summer 2006) with 1 interval E‐mail reminder to complete the surveys.

RESULTS

Survey announcements were E‐mailed to 127 nursing executives, 69 of whom completed it (response rate 54%). The respondents represented mostly academic medical centers (87%; another 13% represented affiliated community teaching hospitals), public institutions (89%), and large facilities (60% with more than 400 beds; 40% with 201‐400 beds). More than half the respondents (56%) reported their hospitals use paper chart documentation as the only method of identifying patients with a DNR order, whereas 16% reported their hospitals use only electronic health record (EHR) documentation (Fig. 1). Twenty‐five percent of hospitals (n = 17) use a color‐coded patient wristband in addition to either paper or electronic documentation. Of these 17 hospitals, a total of 8 colors or color schemes were employed to designate DNR status (Table 1).

Figure 1
Current practices for identification of DNR orders.
Reported Colors Used for Wristbands Designating DNR Status and the Number Using Them
Green5
Yellow3
Blue3
White with blue stars versus green stars (full DNR versus limited DNR)1
Red1
Red and white1
Purple1
Gold1
Other (not listed)1

The use of color‐coded wristbands was not limited to identification of DNR status. Fifty‐five percent of hospitals (n = 31) use color‐coded wristbands to indicate another piece of patient‐related data such as an allergy, fall risk, or same last name alert (Table 2). In fact, 12 indications were depicted by various colors, with variations in both the color choice for a given indication (eg, allergy wristbands red at one hospital and yellow at another) and across indications (eg, red for allergy at one hospital and red for bleeding risk at another). Nearly 3 of 4 respondents (n = 48) reported being aware of a case at your institution in which confusion about a DNR order led to problems or confusion in patient care. A few respondents shared a brief anecdote of the event, illustrating the spectrum of clinical scenarios that lead to potential confusion (Table 3). Respondents reporting a case of confusion were not more likely to be from an institution that used color‐coded wristbands.

Other Reported Indications Colors Used for Patient Wristbands
Indication (n)Colors used (n)
Drug/allergy (22)Red (16) Yellow (4) White (1) Orange (1)
Fall risk (18)Orange (5) Green (3) (and lime green [1]) Blue (3) Purple (3) Yellow (2) (and fluorescent yellow [1])
Same name alert (7)Blue (3) Orange (2) Yellow2)
Bleeding risk (3)Red
Patient identification (3)Green Red White
Wandering risk (3)Pink (2) (and hot pink [1])
Contact isolation (2)Green
Latex allergy (2)Purple
No blood draws on this arm (1)Orange
MRSA infection (1)Green
No blood products (1)Red
Sleep apnea (1)Purple
Anecdotes about Confusion around a DNR order
The patient had a DNR order written in the chart but no other identifiers at bedside, so a consult service started CPR while trying to determine code status.
Nurse called a code on a patient who was DNR because she failed to see order in chart.
Resuscitation efforts took place on a patient with a DNR order because the entire chart did not accompany the patient to a diagnostic testing area.
Patient was off the unit for a procedure, and staff in the other department did not know patients code status (DNR) and called a code.
Patient transported off nursing unit to radiology and coded. Patient was a DNR, but the order was buried in thinned chart materials.
Prior to implementing the wristbands, there were delays in care. Once wristbands were implemented with stars only, there was confusion as to what a blue star meant and what a green star meant (limited versus no resuscitation efforts).
We used to place a sticker on the chart. A sticker was left on the chart of a discharged patient when a new patient was admitted. The mistake was caught before an incident occurred.

When asked whether most (greater than 75%) physicians and nurses could properly identify the color associated with a DNR patient wristband, responses differed by discipline. Eight‐five percent of respondents believed that most nurses at their institutions could correctly report the color for DNR, whereas only 15% believed physicians could do the same. Only 22% of respondents anticipated a change in the current system within the next 2 years; all these changes were a transition from paper to electronic documentation systems.

DISCUSSION

Regardless of whether the DNR documentation occurs in paper or electronic form (and our study demonstrates significant practice variation in the documentation method), the risk that a hospitalized patient may suddenly stop breathing or become pulseless is ever present. When such a patient is discovered, providers race to the bedside and initiate care, but immediately ask, Is the patient a full code? In these often‐chaotic moments, accurate and timely information about DNR status is critical to respecting a patient's preferences and avoiding a potentially devastating error. A number of the anecdotes shared by survey respondents and highlighted in Table 3 reinforce this concern. Many of these scenarios occur in the middle of the night or off a patient's primary unit (ie, at a test or procedure area), increasing the need for quick and easy identification of DNR status.

Our study demonstrates that a logical point‐of‐care solutiona color‐coded DNR patient wristbandmay create its own safety hazards, particularly if the color designations are not known by all providers (including floating and traveling nurses or trainees who rotate at different hospitals) and if the colors being employed represent different indications at a given hospital (see accompanying Images Dx, page 445). We found that approximately 1 in 4 surveyed hospitals depict DNR status by a color‐coded wristband. We also discovered remarkable variation in the colors chosen and the degree to which institutions use color‐coded wristbands to signal a panoply of other patient‐related issues. Human factors research demonstrates that even well‐meaning patient safety solutions may cause harm in new ways if they are poorly implemented or if the interface between the technology and human work patterns is not well appreciated. For example, recent studies illustrate unintended consequences from safety‐driven solutions, such as the implementation of computerized order entry,2122 quality measurement,23 adoption of EHRs,24 and bar code medication administration systems.25 Because standardization is a key mechanism for decreasing the opportunities for error, our findings raise serious concerns about current wristband use.

Interestingly, the lack of standardization and its related risk of failing to recall the conditions associated with color‐coded wristbands are complicated by societal trends. In December 2004 the issue of patient wristbands made headlines in Florida, when hospitals using yellow DNR wristbands (as was the case in 3 hospitals in our sample) reported several near‐misses among patients wearing yellow Lance Armstrong Livestrong bracelets.2627 Given recent estimates that nearly 1 in 5 Americans wears these bracelets to support people living with cancer,28 even safety‐minded journals and national newspapers have highlighted the issue.2930 Most hospitals that continue to use yellow DNR wristbands now either remove or cover Livestrong bracelets at the time of hospital admission. Furthermore, many other self‐help organizations now issue wristbands in a variety of colors as well, creating a potential hazard for any person wearing one in the hospital. Although patients do not mind wearing color‐coded wristbands,31 they might feel differently if they knew the potential for confusion.

After these anecdotal reports of identification mistakes surfaced, several states, most notably Arizona and Pennsylvania, launched initiatives to address the problem.3233 Arizona, after discovering 8 colors being used in the state, developed plans for a purple DNR color‐coded wristband. The choice of purple, and the careful decision to avoid blue, occurred because many hospitals call their resuscitative efforts a code blue, creating yet another potential source of confusion if a blue wristband is associated with a DNR order. The Pennsylvania Patient Safety Authority also found tremendous color variations in patient wristbands used in a statewide survey. Both states ultimately promoted standardized colors and indications and provided tool kits and implementation manuals.3233

Although statewide initiatives represent a step forward, we believe that a national standard for color‐coded wristbands would improve patient safety. Precedents for this call to action exist. For many years, anecdotal information circulated about the errors caused by ambiguous use of abbreviations, such as qd instead of daily or U instead of units. Individual hospitals often banned or limited the use of such abbreviations, but no standard list of high‐risk abbreviations guided practice or required adherence, and cross‐hospital variation undoubtedly led to confusion. In 2004 the Joint Commission created a uniform list of high‐risk abbreviations as part of their National Patient Safety Goals, which instantly ended the debate about which abbreviations to ban and mandated compliance with the safety practice.34 A national group of stakeholders should similarly be convened to develop a list of colors and associated conditions that should be widely disseminated and enforced by the Joint Commission or a similar body. The statewide efforts by Arizona and Pennsylvania are instructive in this regard. Despite being guided by the goal of standardization, these 2 states chose different colors for DNR identification (interestingly, Pennsylvania chose blue for DNR, perhaps for the same reason that Arizona avoided itcode blue), further supporting the need for national guidelines (Table 4).

Recommendations from Arizona and Pennsylvania for Color‐Coded Wristbands
IndicationColor (PA)Color (AZ)
DNRBluePurple
AllergyRedRed
Fall riskYellowYellow
Latex allergyGreen 
Restricted extremityPink 
Preregistration in emergency roomYellow 
Admission and identificationClear 

Our study represents the first national sample of DNR identification practices. Although it targeted academic health centers and affiliated institutions, we believe that these practice variations likely exist in all health care settings. Our study limitations included reliance on self‐reported institutional practices rather than direct review of existing policies and limited information about the surveyed population, making it impossible to compare respondents and nonrespondents. However, we have no reason to believe that these groups differed sufficiently to influence the study's main findings.

In the future, better technology may ultimately replace color‐coded wristbands. For instance, the time may come when wireless technologies seamlessly linked to the electronic health record will alert providers to a patient's DNR status when entering the patient's room. However, for today, point‐of‐care solutions using color‐coded wristbands remain a reasonable solution. Creating a nationally enforced standardized methodology, understandable and memorable to providers and free of stigma to patients (eg, a black wristband for DNR or writing DNR on a wristband) should be a patient safety priority. Because simplification is another key characteristic of safe systems, it seems prudent to aim for a national system that involves a maximum of 3‐4 colors.

CONCLUSIONS

Patients and families dedicate tremendous energy to making decisions about their advance directives, and discussions of these issues often create considerable angst and sadness. Health care providers are trained to elicit and advocate for such directives so they can act with patients' wishes in mind. Despite the high stakes, all these efforts can be undermined when the system for making providers aware of a patient's DNR status is flawed. Our data confirm the tremendous variability in the systems used to indicate DNR status (and other types of indications), variability that may place patients at risk from catastrophic errors. Following the lead of a few states, we call for a national mandate to standardize the identification of DNR orders and to make the colors of wristbands for a small set of indications uniform in every hospital across the country.

Acknowledgements

We thank Mark Keroack, MD, MPH, and Cathy Krsek, RN, MSN, MBA, from the University HealthSystem Consortium for their contributions to the survey and assistance with administration. We also thank members of the UHC Chief Nursing Council for participating in the survey study.

As modern medicine developed the technological capacity to deliver aggressive life‐sustaining interventionsthrough methods such as cardiopulmonary resuscitation (CPR), intensive care units, and mechanical ventilationthe concept of do‐not‐resuscitate (DNR) orders emerged to allow individual patients to choose to forego selected treatments. To encourage patients to articulate these preferences, Congress passed the Patient Self‐Determination Act in 1991, a measure that required health care facilities to discuss advance directives with patients as they enter their system.1 Although the act has had less of an impact on the quality of DNR discussions than originally hoped for,25 its passage was evidence of the importance our society places on patientclinician discussions regarding goals of care. In addition to this legislative push, many organizations and advocacy groups use a variety of marketing campaigns, accreditation standards,6 and standard instruments and tools79 to promote the use of advance directives

Despite all these efforts, fewer than 30% of Americans (54% older than age 65) have completed advance directives.10 Nevertheless, many patientsparticularly those at highest risk for requiring end‐of‐life caredo express preferences regarding resuscitation at the time of hospital admission. In an ideal world, these preferences would be available for all providers to view, respect, and act on.

Unfortunately, research on patient safety and quality has demonstrated wide gaps between ideal and actual practice.1112 In the context of DNR wishes, despite strong efforts to collect patients' preferences, no current regulation provides or mandates a best practice on making these preferences operational. There are also few data that indicate whether patients' preferences are in fact transmitted to providers at the point of care and in an accurate and reliable manner.

Past research on proper identification of DNR orders is limited, with much of the focus on prehospital protocols.1315 Anecdotally, hospitals seem to employ varying strategies to highlight DNR orders using a combination of paper or electronic documentation and color‐coded patient wristbands. There have been several reports of errors involving this issue, including patients receiving CPR despite stated DNR preferences and a patient having CPR withheld because the wrong chart (of another patient with a DNR order) was mistakenly pulled.1617

The patient safety field emphasizes standardization as a key strategy to prevent errors. Because of problems articulating DNR orders (and other important patient‐related information), several hospitals promote the use of color‐coded wristbands to denote preferences for resuscitation. However, without national regulations or standards, the possibility remains that one safety hazard (advance directives on a paper chart distant from a patient's room) may be traded for another hazard (front‐line providers interpreting a color‐coded wristband incorrectly). In addition to the ethical problems inherent in failing to adhere to patients' resuscitation preferences, errors in following advance directives may also create legal liability.18 With all this in mind, we conducted a national survey to determine practice variations in the identification of DNR orders and the use of color‐coded patient wristbands. We hypothesized that there is considerable variation both in identification practices and in the use of color‐coded wristbands across academic medical centers.

METHODS

The project was approved by the University of California, San Francisco Committee on Human Research. We anonymously surveyed nursing executives who are members of the University HealthSystem Consortium (UHC), an alliance of 97 academic medical centers and their affiliated hospitals representing 90% of the nation's nonprofit academic medical centers.19 The nursing executives are senior nursing leaders at participating UHC institutions and members of a dedicated UHC Chief Nursing Officer Council E‐mail listserv. We designed a brief survey and distributed it via their E‐mail listserv using an online commercial survey administration tool.20 Respondents were asked to complete the survey or have one of their colleagues familiar with local DNR identification practices complete it on their behalf. The online tool also provided summary reports and descriptive findings to meet the study objectives. We provided a 1‐month window (during summer 2006) with 1 interval E‐mail reminder to complete the surveys.

RESULTS

Survey announcements were E‐mailed to 127 nursing executives, 69 of whom completed it (response rate 54%). The respondents represented mostly academic medical centers (87%; another 13% represented affiliated community teaching hospitals), public institutions (89%), and large facilities (60% with more than 400 beds; 40% with 201‐400 beds). More than half the respondents (56%) reported their hospitals use paper chart documentation as the only method of identifying patients with a DNR order, whereas 16% reported their hospitals use only electronic health record (EHR) documentation (Fig. 1). Twenty‐five percent of hospitals (n = 17) use a color‐coded patient wristband in addition to either paper or electronic documentation. Of these 17 hospitals, a total of 8 colors or color schemes were employed to designate DNR status (Table 1).

Figure 1
Current practices for identification of DNR orders.
Reported Colors Used for Wristbands Designating DNR Status and the Number Using Them
Green5
Yellow3
Blue3
White with blue stars versus green stars (full DNR versus limited DNR)1
Red1
Red and white1
Purple1
Gold1
Other (not listed)1

The use of color‐coded wristbands was not limited to identification of DNR status. Fifty‐five percent of hospitals (n = 31) use color‐coded wristbands to indicate another piece of patient‐related data such as an allergy, fall risk, or same last name alert (Table 2). In fact, 12 indications were depicted by various colors, with variations in both the color choice for a given indication (eg, allergy wristbands red at one hospital and yellow at another) and across indications (eg, red for allergy at one hospital and red for bleeding risk at another). Nearly 3 of 4 respondents (n = 48) reported being aware of a case at your institution in which confusion about a DNR order led to problems or confusion in patient care. A few respondents shared a brief anecdote of the event, illustrating the spectrum of clinical scenarios that lead to potential confusion (Table 3). Respondents reporting a case of confusion were not more likely to be from an institution that used color‐coded wristbands.

Other Reported Indications Colors Used for Patient Wristbands
Indication (n)Colors used (n)
Drug/allergy (22)Red (16) Yellow (4) White (1) Orange (1)
Fall risk (18)Orange (5) Green (3) (and lime green [1]) Blue (3) Purple (3) Yellow (2) (and fluorescent yellow [1])
Same name alert (7)Blue (3) Orange (2) Yellow2)
Bleeding risk (3)Red
Patient identification (3)Green Red White
Wandering risk (3)Pink (2) (and hot pink [1])
Contact isolation (2)Green
Latex allergy (2)Purple
No blood draws on this arm (1)Orange
MRSA infection (1)Green
No blood products (1)Red
Sleep apnea (1)Purple
Anecdotes about Confusion around a DNR order
The patient had a DNR order written in the chart but no other identifiers at bedside, so a consult service started CPR while trying to determine code status.
Nurse called a code on a patient who was DNR because she failed to see order in chart.
Resuscitation efforts took place on a patient with a DNR order because the entire chart did not accompany the patient to a diagnostic testing area.
Patient was off the unit for a procedure, and staff in the other department did not know patients code status (DNR) and called a code.
Patient transported off nursing unit to radiology and coded. Patient was a DNR, but the order was buried in thinned chart materials.
Prior to implementing the wristbands, there were delays in care. Once wristbands were implemented with stars only, there was confusion as to what a blue star meant and what a green star meant (limited versus no resuscitation efforts).
We used to place a sticker on the chart. A sticker was left on the chart of a discharged patient when a new patient was admitted. The mistake was caught before an incident occurred.

When asked whether most (greater than 75%) physicians and nurses could properly identify the color associated with a DNR patient wristband, responses differed by discipline. Eight‐five percent of respondents believed that most nurses at their institutions could correctly report the color for DNR, whereas only 15% believed physicians could do the same. Only 22% of respondents anticipated a change in the current system within the next 2 years; all these changes were a transition from paper to electronic documentation systems.

DISCUSSION

Regardless of whether the DNR documentation occurs in paper or electronic form (and our study demonstrates significant practice variation in the documentation method), the risk that a hospitalized patient may suddenly stop breathing or become pulseless is ever present. When such a patient is discovered, providers race to the bedside and initiate care, but immediately ask, Is the patient a full code? In these often‐chaotic moments, accurate and timely information about DNR status is critical to respecting a patient's preferences and avoiding a potentially devastating error. A number of the anecdotes shared by survey respondents and highlighted in Table 3 reinforce this concern. Many of these scenarios occur in the middle of the night or off a patient's primary unit (ie, at a test or procedure area), increasing the need for quick and easy identification of DNR status.

Our study demonstrates that a logical point‐of‐care solutiona color‐coded DNR patient wristbandmay create its own safety hazards, particularly if the color designations are not known by all providers (including floating and traveling nurses or trainees who rotate at different hospitals) and if the colors being employed represent different indications at a given hospital (see accompanying Images Dx, page 445). We found that approximately 1 in 4 surveyed hospitals depict DNR status by a color‐coded wristband. We also discovered remarkable variation in the colors chosen and the degree to which institutions use color‐coded wristbands to signal a panoply of other patient‐related issues. Human factors research demonstrates that even well‐meaning patient safety solutions may cause harm in new ways if they are poorly implemented or if the interface between the technology and human work patterns is not well appreciated. For example, recent studies illustrate unintended consequences from safety‐driven solutions, such as the implementation of computerized order entry,2122 quality measurement,23 adoption of EHRs,24 and bar code medication administration systems.25 Because standardization is a key mechanism for decreasing the opportunities for error, our findings raise serious concerns about current wristband use.

Interestingly, the lack of standardization and its related risk of failing to recall the conditions associated with color‐coded wristbands are complicated by societal trends. In December 2004 the issue of patient wristbands made headlines in Florida, when hospitals using yellow DNR wristbands (as was the case in 3 hospitals in our sample) reported several near‐misses among patients wearing yellow Lance Armstrong Livestrong bracelets.2627 Given recent estimates that nearly 1 in 5 Americans wears these bracelets to support people living with cancer,28 even safety‐minded journals and national newspapers have highlighted the issue.2930 Most hospitals that continue to use yellow DNR wristbands now either remove or cover Livestrong bracelets at the time of hospital admission. Furthermore, many other self‐help organizations now issue wristbands in a variety of colors as well, creating a potential hazard for any person wearing one in the hospital. Although patients do not mind wearing color‐coded wristbands,31 they might feel differently if they knew the potential for confusion.

After these anecdotal reports of identification mistakes surfaced, several states, most notably Arizona and Pennsylvania, launched initiatives to address the problem.3233 Arizona, after discovering 8 colors being used in the state, developed plans for a purple DNR color‐coded wristband. The choice of purple, and the careful decision to avoid blue, occurred because many hospitals call their resuscitative efforts a code blue, creating yet another potential source of confusion if a blue wristband is associated with a DNR order. The Pennsylvania Patient Safety Authority also found tremendous color variations in patient wristbands used in a statewide survey. Both states ultimately promoted standardized colors and indications and provided tool kits and implementation manuals.3233

Although statewide initiatives represent a step forward, we believe that a national standard for color‐coded wristbands would improve patient safety. Precedents for this call to action exist. For many years, anecdotal information circulated about the errors caused by ambiguous use of abbreviations, such as qd instead of daily or U instead of units. Individual hospitals often banned or limited the use of such abbreviations, but no standard list of high‐risk abbreviations guided practice or required adherence, and cross‐hospital variation undoubtedly led to confusion. In 2004 the Joint Commission created a uniform list of high‐risk abbreviations as part of their National Patient Safety Goals, which instantly ended the debate about which abbreviations to ban and mandated compliance with the safety practice.34 A national group of stakeholders should similarly be convened to develop a list of colors and associated conditions that should be widely disseminated and enforced by the Joint Commission or a similar body. The statewide efforts by Arizona and Pennsylvania are instructive in this regard. Despite being guided by the goal of standardization, these 2 states chose different colors for DNR identification (interestingly, Pennsylvania chose blue for DNR, perhaps for the same reason that Arizona avoided itcode blue), further supporting the need for national guidelines (Table 4).

Recommendations from Arizona and Pennsylvania for Color‐Coded Wristbands
IndicationColor (PA)Color (AZ)
DNRBluePurple
AllergyRedRed
Fall riskYellowYellow
Latex allergyGreen 
Restricted extremityPink 
Preregistration in emergency roomYellow 
Admission and identificationClear 

Our study represents the first national sample of DNR identification practices. Although it targeted academic health centers and affiliated institutions, we believe that these practice variations likely exist in all health care settings. Our study limitations included reliance on self‐reported institutional practices rather than direct review of existing policies and limited information about the surveyed population, making it impossible to compare respondents and nonrespondents. However, we have no reason to believe that these groups differed sufficiently to influence the study's main findings.

In the future, better technology may ultimately replace color‐coded wristbands. For instance, the time may come when wireless technologies seamlessly linked to the electronic health record will alert providers to a patient's DNR status when entering the patient's room. However, for today, point‐of‐care solutions using color‐coded wristbands remain a reasonable solution. Creating a nationally enforced standardized methodology, understandable and memorable to providers and free of stigma to patients (eg, a black wristband for DNR or writing DNR on a wristband) should be a patient safety priority. Because simplification is another key characteristic of safe systems, it seems prudent to aim for a national system that involves a maximum of 3‐4 colors.

CONCLUSIONS

Patients and families dedicate tremendous energy to making decisions about their advance directives, and discussions of these issues often create considerable angst and sadness. Health care providers are trained to elicit and advocate for such directives so they can act with patients' wishes in mind. Despite the high stakes, all these efforts can be undermined when the system for making providers aware of a patient's DNR status is flawed. Our data confirm the tremendous variability in the systems used to indicate DNR status (and other types of indications), variability that may place patients at risk from catastrophic errors. Following the lead of a few states, we call for a national mandate to standardize the identification of DNR orders and to make the colors of wristbands for a small set of indications uniform in every hospital across the country.

Acknowledgements

We thank Mark Keroack, MD, MPH, and Cathy Krsek, RN, MSN, MBA, from the University HealthSystem Consortium for their contributions to the survey and assistance with administration. We also thank members of the UHC Chief Nursing Council for participating in the survey study.

Issue
Journal of Hospital Medicine - 2(6)
Issue
Journal of Hospital Medicine - 2(6)
Page Number
366-371
Page Number
366-371
Article Type
Display Headline
Identification of inpatient DNR status: A safety hazard begging for standardization
Display Headline
Identification of inpatient DNR status: A safety hazard begging for standardization
Legacy Keywords
patient safety, standardization, Do Not Resuscitate orders, patient wristbands
Legacy Keywords
patient safety, standardization, Do Not Resuscitate orders, patient wristbands
Sections
Article Source

Copyright © 2007 Society of Hospital Medicine

Disallow All Ads
Correspondence Location
Division of Hospital Medicine, University of California, San Francisco, 533 Parnassus Avenue, Box 0131, San Francisco, CA 94143; Fax: (415) 514‐2094
Content Gating
No Gating (article Unlocked/Free)
Alternative CME
Article PDF Media

Common Myths in Caring for Patients with Terminal Illness

Article Type
Changed
Display Headline
Common myths about caring for patients with terminal illness: Opportunities to improve care in the hospital setting

Shortcomings in the quality of care of hospitalized patients at the end of life, especially in the final days, are well documented.1, 2 Recent studies have highlighted inadequate pain and symptom control for hospitalized terminally ill patients,24 poor communication about treatment preferences,57 and limited or delayed referral for hospice care.810 Efforts to improve the quality of end‐of‐life care have been diverse, including increased educational programs,1113 development of palliative care units in hospitals,14, 15 and greater exposure to palliative care for physicians during residency training.16 Despite these efforts, studies assessing the attitudes and knowledge of physicians about hospice and palliative care continue to show deficits in knowledge about managing pain17, 18 as well as hospice policies and services.9

Among the interventions aimed at improving hospital care, the hospitalist movement has emerged as a model of care for improving the quality and cost efficiency of hospital care.1922 Because hospitalists spend substantial time on inpatient services,23 they are often involved in the care of patients with terminal illness, with potential to improve the quality of care that these patients receive while hospitalized. However, little is known about what specific knowledge and perspectives hospitalists and residents have about the care of patients with terminal illness. Although many studies have been conducted among physicians in private practice,9, 10, 2426 they have not focused on the knowledge, reported practices, and attitudes of hospitalists and residents concerning key aspects of end‐of‐life care and hospice. Such information can help to identify potential areas for improving knowledge and addressing common barriers highlighted in linking hospital and posthospital hospice care.

METHODS

Study Design and Sample

During 2006 we surveyed hospitalists and medical residents who were on their oncology rotation at a large academic medical center that did not have a hospital‐based palliative care unit in order to examine their knowledge, attitudes, and practices regarding terminally ill patients and hospice referrals. Hospitalists (n = 23) and medical residents (n = 29) made up a convenience sample of 52 physicians. The medical residents were completing their oncology rotation during the spring of 2006. The Institutional Review Board at Yale University School of Medicine approved the research protocol and verbal consent procedures.

Survey

The brief survey instrument (see Appendix) assessed physicians' knowledge and attitudes about and practices in caring for patients with terminal illness. The survey was adapted from previously published instruments8, 24 that have been shown24 to have good test‐retest reliability and construct validity. The survey contained 5 items pertaining to clinical knowledge about palliative care practices, including common symptoms and drug indications, doses, and side effects.27 An additional 2 items pertained to respondents' knowledge about nonclinical issues concerning eligibility rules for hospice,8 such as how a patient becomes eligible for hospice and whether Medicare benefits can be revoked or reinstated after hospice is elected. The survey also included 10 statements24 assessing physician attitudes about caring for patients with terminal illness. Responses, provided using a 5‐point Likert scale, were collapsed for reporting into a 3‐point scale of agree, neutral, and disagree. The instrument also included an open‐ended question asking physicians to specify what from their perspective was needed to ensure timely referral for hospice and palliative care.

Data Analysis

We used standard frequency analysis to describe the distribution of responses to the survey items. Based on an analysis of common erroneous answers to clinical knowledge questions, we identified several common myths prevalent among hospitalists and medicine residents. We also examined whether knowledge, reported practices, and attitudes differed significantly between the hospitalist and the resident samples using ANOVA or chi‐square statistics as appropriate. We used content analysis to summarize the open‐ended responses about potential ways to overcome what respondents perceived was underutilization of hospice.

RESULTS

Overview

The response rate for the survey was 85.2%. Almost half of the respondents (44.2%) were hospitalists (Table 1). The remaining respondents included first‐year (n = 9) and second‐ or third‐year (n = 16) residents or fellows (n = 4). Approximately 54% of the 52 respondents were female, and the majority (83%) had graduated from medical school between 2000 and 2005. Several common myths were apparent and pertained to essential areas of treating patients with terminal illness: pain control, symptom control, and eligibility for hospice (Table 2). Respondents generally had strong beliefs about caring for patients with terminal illness, and most agreed that many patients who would benefit from hospice either do not receive hospice or receive it only late in the course of their illness (Table 3).

Demographic Characteristics of Respondents (n = 52)
Characteristicn%
Sex  
Female2853.9%
Male2446.1%
Years since graduation from medical school  
1‐2 Years2656.5%
3‐5 Years1226.1%
>5 Years817.4%
Missing6 
Physician type  
Hospitalist2344.2%
First‐year resident917.3%
Second‐ or third‐year resident1630.8%
Fellow47.7%
Knowledge about Hospice and Palliative Care Practices and Eligibility for Hospice Care (n = 52)*
Questions about hospice and palliative care practicesResponse (%)
  • Correct answers, that is, facts, are in bold.

The incidence of psychological dependence (addiction) to opioids and analgesics when treating pain from cancer or other medical conditions is: 
Common (1 in 10 patients)17.3
Uncommon (1 in 100 patients)48.1
Very rare (fewer than 1 in 1000 patients)34.6
When a patient with cancer who is receiving opioids for pain complains of increasing pain, it most likely indicates: 
Opioid tolerance69.2
Increasing pathology of the cancer26.9
Patient noncompliance0.0
New onset of a different opioid‐resisting pain3.9
In the pain patient receiving opioids, 30 mg of oral morphine is equipotent to of IV morphine 
1 mg4.0
5 mg40.0
10 mg56.0
20 mg0.0
The 2 classes of drugs most commonly recommended for treating terminal dyspnea are: 
Beta‐blockers and Lasix7.7
Opioids and benzodiazepines82.7
Beta‐blockers and corticosteroids9.6
Beta‐blockers and Singulair (montelukast)0.0
A hospice patient whose agitation is primarily from anxiety should be treated with: 
Chlorpromazine (thorazine)0.0
Haloperidol21.6
Lorazepam (Ativan)76.4
Morphine2.0
Questions about eligibility for hospice careResponse (%)
Under the Medicare program, a physician must certify that the patient is expected to die within a specified time for the patients to be eligible for hospice services. To the best of your knowledge, patients become eligible for inpatient hospice care when they are expected to die in: 
2 Weeks5.8
6 Weeks9.6
2 Months9.6
6 Months69.2
Other1.9
Don't know3.8
To the best of your knowledge, patients become eligible for home hospice care when they are expected to die in: 
2 Weeks0.0
6 Weeks5.8
2 Months7.7
6 Months73.1
Other0.0
Don't know13.4
Physicians' Beliefs about Caring for Patients with Terminal Illness (n = 52)
BeliefsDisagree (%)Neutral (%)Agree (%)
Most patients want me to tell them their life‐expectancy.0.017.482.6
Generally, family caregivers want me to tell them the patient's life expectancy.4.48.786.9
Telling the patient and family members that the patient's illness is incurable is difficult for me.23.013.563.5
I think it is essential to discuss the prognosis with a patient, even if it is very poor.0.04.495.6
Most patients' physical symptoms (eg, pain, shortness of breath, and nausea) are controlled better with hospice than with the care that they would receive in the hospital.0.021.778.3
Most patients' emotional symptoms (eg, depression, anxiety) are controlled better with hospice than with the care they would receive in the hospital.0.08.791.3
Hospice meets the needs of the family better than conventional care does.0.08.791.3
Many patients who should receive hospice care do not receive hospice care.21.813.065.2
Many patients would benefit if hospice care were initiated earlier in the course of their illness.0.09.190.9
I feel knowledgeable enough to discuss palliative and hospice care with patients and families.19.238.542.3

Common Myths in Treating Patients with Terminal Illness

Myth 1. Treating cancer pain with opioids or analgesics causes addiction in 1 in 100 patients. Most physicians thought that addiction in patients treated for cancer pain with opioids or analgesics was much more common than it is. Almost half the respondents (48.1%) thought addiction occurred in 1 in 100 patients, and an additional 17.3% of respondents thought addiction occurred in 1 in 10 patients treated for cancer pain with opioids or analgesics. In contrast, the incidence of addiction in patients treated with opioids or analgesics for cancer pain is fewer than 1 in 1000 patients.28

Myth 2. When patients with cancer already receiving opioids for pain control complain of increasing pain, it most likely indicates opioid tolerance. Nearly 70% of respondents reported that the most likely reason for complaints of increased pain was tolerance to the opioid. However, the most likely reason for increased pain is increasing pathology of the cancer.27

Myth 3. The equipotent to 30 mg of oral morphine is 5 mg intravenous. More than half of respondents were inaccurate in their conversion of oral to intravenous (IV) morphine dosing, a common task of physicians caring for terminally ill patients. Almost half the physicians (44%) erroneously reported that 30 mg of oral morphine was equipotent to 5 mg or less morphine IV. However, in fact, 30 mg of oral morphine is equipotent to 10 mg of morphine IV.27

Myth 4. The most highly recommended drug for treating terminal dyspnea is a beta‐blocker, and the most appropriate drug for agitation due to anxiety is Haldol or morphine. Most respondents were able to identify the correct drugs; however, a sizable proportion of respondents (17.3%) erroneously responded that beta‐blockers and Lasix or beta‐blockers and corticosteroids were the best drugs for treating terminal dyspnea. About one‐fifth of respondents (21.6%) responded that Haldol or morphine was the recommended medication for treating agitation. In fact, opioids and benzodiazepines are the recommended drugs for treating terminal dyspnea,27 and the proper drug for treating agitation is lorazepam (Ativan).27

Myth 5. Patient life expectancy must be 2 months or less to be eligible for hospice. One‐quarter of respondents believed this to be true for inpatient hospice, and nearly 13.5% of respondents believe this to be true for home hospice. In fact, patients are eligible for hospice benefits earlier in the course of their illness. Under Medicare and most insurance policies, patients are eligible for hospice benefits as soon as their life expectancy is 6 months or less, not 2 months or less.27

Physician Beliefs about Caring for Patients with Terminal Illness

The physicians' beliefs about hospice were generally positive; the vast majority of respondents agreed or strongly agreed with the statement that physical and emotional symptoms of patients and family needs are better addressed with hospice than with the hospital care (Table 3). Most respondents also agreed that many patients do not receive hospice as they should and that hospice should be initiated earlier in the course of the illness. In addition, more than 80% of respondents believed patients and their families want their doctors to tell them the patient's life expectancy, and 95.6% of respondents thought it was essential to discuss prognosis, even a poor one, with the patient. Nevertheless, many respondents (65.3%) reported it was difficult to tell patients and their families that an illness was incurable. Furthermore, fewer than half the respondents (42.3%) believed they were knowledgeable enough to discuss hospice and palliative care with patients and their families.

In subgroup analyses comparing responses to knowledge and attitude items reported in Tables 2 and 3, we found no significant differences between hospitalists and any subgroup of residents by year of training or fellows, or between hospitalists and the full sample of residents and fellows. Because of the sample size, the statistical power for evaluating significance was limited in these exploratory subgroup analyses.

Among physicians who provided responses to the open‐ended question (n = 42) about how to enhance hospice referral rates and improve their timeliness, the most commonly reported suggestions were: (1) involve family members, not only patients, in discussions of hospice (38.1%), (2) have discussions about hospice earlier in the course of care with patients (26.2%), and (3) be clear with patients and families about the patient's prognosis (19.0%). Table 4 has a list of all responses provided to this question.

Physicians' Suggestions for Improving the Process of Hospice Referral (n = 42)
Responsen%*
  • Percentages add up to more than 100% because some respondents made more than 1 suggestion.

Involving family members as well as patients in discussions of hospice1638.1
Having earlier discussion with patients1126.2
Being clear with patients and families about patient prognosis819.0
Providing education about hospice to patients and families614.3
Discussions of goals of care with patients and families614.3
Involving social worker in discussions49.5
Providing literature to patients and families about hospice37.1
Having hospice representative available to provide education to patient and families24.8

DISCUSSION

This study demonstrated that, among hospitalists and residents, there are several misconceptions about fundamental aspects of caring for terminally ill patients. Given the potential importance of the role hospitalists play in improving the quality of inpatient care,1922 it is critical to identify and address these misconceptions. Additionally, physicians in this study indicated that more and earlier communication with patients and families about prognosis and about the option of hospice would be beneficial, but they themselves did not feel knowledgeable enough to discuss hospice and palliative care with patients and their families.

The nature of the misconceptions identified in this study shed light on the well‐documented phenomena of inadequate pain control24, 29 and poor symptom management2, 4 at the end of life. Having many of the erroneous beliefs apparent in this study may be consistent with providing less pain medication than needed and appropriate. For instance, many physicians believed that developing addiction to opioids used for cancer pain is more likely to occur than it really is, according to research evidence. It is extremely rare for these patients to become addicted to opioids or other analgesics (fewer than 1 in 1000 patients).28 In addition, most physicians believed that complaints of increased pain among patients receiving opioid therapy for pain control meant tolerance to the medication, a belief consistent with physician reluctance to prescribe more medication because it would lead to tolerance.28 In reality, the increased pain experienced in these situations is typically not a result of tolerance to the pain medication but to the cancer getting worse.27 Additionally, many physicians mistakenly decreased the dose of morphine in converting the route of administration from PO to IV, as is often done in hospitals. Such an error may be a contributing factor to the unintended undertreatment of pain in hospitals. Given the variability of cancer pain4 and the difference in time to peak effect depending on the route of administration,5 it is critical for physicians to understand proper dosing in order to effectively treat cancer pain. Furthermore, many physicians were incorrect about the recommended medications for dyspnea and for agitation, 2 symptoms that are prevalent among patients at the end of life.

The hospitalists and residents reported having very positive views about hospice, as is consistent with the literature.10, 30 However, many respondents indicated that patients who would have benefited from hospice did not receive it at all or only late in their illness. Physicians indicated that better communication with patients and families about hospice, prognosis, and goals of care would enhance appropriate use of hospice. While hospitalists and residents are in a position to initiate such discussions, they reported that these discussions were difficult for them. The challenge is how to promote what is necessary and valuable conversation with patients and families despite their difficulty, so that a realistic plan of care can be designed for all involved. Providing hospitalists and residents with evidence about what approaches are most effective in such discussions would be helpful to better prepare them for their roles in caring for hospitalized patients with terminal illness.

The results of this study have substantiated the need to enhance the education of hospitalists and resident physicians, who can play a vital role in improving the transition from hospital to hospice. Such education could take place as part of the residency experience or be embedded in various continuing medical education requirements that most states now have. The results of a recent national survey of hospitalists31 indicates they consider their palliative care training inadequate and feel ill prepared to care for patients with terminal illness. Our findings are consistent with those of that survey, highlighting information that is poorly understood by both residents and hospitalists. As hospitalists continue to play key roles in linking hospital to posthospital care,21 including hospice, there is greater opportunity to improve end‐of‐life care by expanding hospitalists' understanding of these issues.

Our findings should be interpreted in light of the study's limitations. First, this was an exploratory study, and the sample was modest in size. Nevertheless, the response rate was high: 85.2%. Second, we conducted the study in a single location; results may differ in other geographical areas. Last, we were unable to link reported knowledge and attitudes to patient experiences including quality of care or adequacy of pain control. Inadequate knowledge likely limits the quality of clinical practices, but the magnitude of this effect remains unknown and worthy of future study.

Despite these limitations, this study has contributed to the literature by identifying a set of misunderstandings or myths that may be common among hospitalists and residents who frequently care for hospitalized patients with terminal illness. Many of these misunderstandings were related to pain and symptom management, although some misunderstandings related to logistical issues such as hospice eligibility rules. Previous studies have described interventions to improve physicians' knowledge about palliative and end‐of‐life care practices at the undergraduate, graduate, and postgraduate levels.13 Our findings identified specific gaps in physicians' knowledge. Interventions aimed at closing these gaps might emphasize both specific clinical information about pain management and medication recommendations, and more general information about eligibility for hospice and best practices for communicating early with patients and family is needed to promote more effective care for patients with terminal illness being cared for in acute care settings.

As the use of hospitalists has become a widely accepted model of hospital care,32 ensuring their increased training and education in the care of patients with terminal illness is an important step in improving end‐of‐life care. Larger comparison studies are needed to identify differences in the practices and perspectives of hospitalists and residents and to target educational interventions to meet their particular needs. Further, conducting these studies at additional sites including those with established palliative care programs would be useful for identifying needs among a more diverse set of physicians involved in delivering end‐of‐life care.

APPENDIX

Survey on Hospice and End‐of‐Life Care

Survey ID _________________

Date ______________

  • DEMOGRAPHICS

     

    • What is your gender?

       

      • □ Male

      • □ Female

      • What year did you graduate from medical school? ___________

      • What is your primary specialty or area of practice?

         

        • □ Hospitalist

        • □ Oncology fellow

        • □ Oncology resident

        • □ Physician assistant

        • □ Other: _____________

        • KNOWLEDGE OF HOSPICE AND PALLIATIVE CARE PRACTICES

           

          • The incidence of psychological dependence (addiction) to opioids and analgesics when treating pain from cancer or other medical conditions is:

             

            • Common (1 in 10 patients)

            • Uncommon (1 in 100 patients)

            • Very rare (fewer than 1 in 1000 patients)

            • When a patient with cancer who is receiving opioids for pain complains of increasing pain, it most likely indicates:

               

              • Opioid tolerance

              • Increasing pathology of the cancer

              • Patient noncompliance

              • New onset of a different opioid‐resisting pain

              • In the pain patient receiving opioids, 30 mg of oral morphine is equipotent to _______________ of IV.

                 

                • 1mg

                • 5 mg

                • 10 mg

                • 20 mg

                • The 2 classes of drugs most commonly recommended for treating terminal dyspnea are:

                   

                  • Beta‐blockers and Lasix

                  • Opioids and benzodiazepines

                  • Beta‐blockers and corticosteroids

                  • Beta‐blockers and Singulair (montelukast)

                  • A hospice patient whose agitation is due primarily to anxiety should be treated with:

                     

                    • Chlorpromazine

                    • Haloperidol

                    • Lorazepam

                    • Morphine

                    • ELIGIBILITY FOR HOSPICE CARE

                       

                      • Under the Medicare program, a physician must certify that the patient is expected to die within a specified time for the patients to be eligible for hospice services. To the best of your knowledge, patients become eligible for inpatient hospice care when they are expected to die in:

                         

                        • □ 2 Weeks

                        • □ 6 Weeks

                        • □ 2 Months

                        • □ 6 Months

                        • □ Other: ________________________

                        • □ Don't know

                        • To the best of your knowledge, patients are eligible for home hospice care when they are expected to die in:

                           

                          • □ 2 Weeks

                          • □ 6 Weeks

                          • □ 2 Months

                          • □ 6 Months

                          • □ Other: __________________________

                          • □ Don't know

                          • ATTITUDES ABOUT HOSPICE CARE 0

                           

                          Following is a series of statements. Please state whether you strongly agree, agree, neither agree nor disagree, disagree, or strongly disagree with each statement.
                           Strongly agreeStrongly disagree
                          11) Most patients want me to tell them their life expectancy.1 □2 □3 □4 □5 □
                          12) Generally, family caregivers want me to tell them the patient's life expectancy.1 □2 □3 □4 □5 □
                          13) Telling the patient and family members that the patient's illness is incurable is difficult for me.1 □2 □3 □4 □5 □
                          14) I think it is essential to discuss the prognosis with a patient, even if it is very poor.1 □2 □3 □4 □5 □
                          15) Most patients' physical symptoms (eg, pain, shortness of breath, and nausea) are controlled better with hospice than with the care they would receive in the hospital.1 □2 □3 □4 □5 □
                          16) Most patients' emotional symptoms (eg, depression, anxiety) are controlled better with hospice than with the care they would receive in the hospital.1 □2 □3 □4 □5 □
                          17) Hospice care generally meets the needs of the family better than conventional care does.1 □2 □3 □4 □5 □
                          18) Many terminally ill patients who should receive hospice care do not receive hospice care.1 □2 □3 □4 □5 □
                          19) Many patients would benefit if hospice care were initiated earlier in the course of their illness.1 □2 □3 □4 □5 □
                          20) I feel knowledgeable enough to discuss palliative and hospice care with patients and families.1 □2 □3 □4 □5 □
                          21) What do you see as the primary ways to facilitate earlier initiation of hospice care for patients who are eligible? _____________________________________________________________________________________
                          ___________________________________________________________________________________________
References
  1. Institute of Medicine.Approaching Death.Washington, DC:National Academy Press;1997.
  2. SUPPORT Principle Investigators.A controlled trial to improve care for seriously ill hospitalized patients.JAMA.1995;274:15911598.
  3. Morrison RS,Meier DE,Fischberg D, et al.Improving the management of pain in hospitalized adults.Arch Intern Med.2006;166:10331039.
  4. von Gunten CF.Interventions to manage symptoms at the end of life.J Palliat Med.2005;8(suppl 1):S88S94.
  5. Bradley EH,Hallemeier AG,Fried TR, et al.Documentation of discussions about prognosis with terminally ill patients.Am J Med.2001;111:218223.
  6. Chittenden EH,Clark ST,Pantilat SZ.Discussing resuscitation preferences with patients: challenges and rewards.J Hosp Med.2006;1:231249.
  7. Schulman‐Green D,McCorkle R,Curry L,Cherlin E,Johnson‐Hurzeler R,Bradley E.At the crossroads: making the transition to hospice.Palliat Support Care.2004;2:351360.
  8. Bradley EH,Fried TR,Kasl SV,Cicchetti DV,Johnson‐Hurzeler R,Horwitz SM.Referral of terminally ill patients for hospice: frequency and correlates.J Palliat Care.2000;16(4):2026.
  9. Ogle K,Mavis B,Wang T.Hospice and primary care physicians: attitudes, knowledge, and barriers.Am J Hosp Palliat Care.2003;20(1):4151.
  10. Ogle KS,Mavis B,Wyatt GK.Physicians and hospice care: attitudes, knowledge, and referrals.J Palliat Med.2002;5(1):8592.
  11. Block SD.Medical education in end‐of‐life care: the status of reform.J Palliat Med.2002;5(2):243248.
  12. Meier DE,Morrison RS,Cassel CK.Improving palliative care.Ann Intern Med.1997;127(3):225230.
  13. Weissman DE,Mullan P,Ambuel B,von Gunten CF,Hallenbeck J,Warm E.Improving end‐of‐life care: internal medicine curriculum project—abstracts/progress reports.J Palliat Med.2001;4(1):75102.
  14. Bailey FA,Burgio KL,Woodby LL, et al.Improving processes of hospital care during the last hours of life.Arch Intern Med.2005;165:17221727.
  15. Pan CX,Morrison RS,Meier DE, et al.How prevalent are hospital‐based palliative care programs? Status report and future directions.J Palliat Med.2001;4:315324.
  16. von Gunten CF,Twaddle M,Preodor M,Neely KJ,Martinez J,Lyons J.Evidence of improved knowledge and skills after an elective rotation in a hospice and palliative care program for internal medicine residents.Am J Hosp Palliat Care.2005;22(3):195203.
  17. Clark JM,Lurie JD,Claessens MT,Reed VA,Jernstedt GC,Goodlin SG.Factors associated with palliative care knowledge among internal medicine house staff.J Palliat Care.2003;19:253257.
  18. Fineberg IC,Wenger NS,Brown‐Saltzman K.Unrestricted opiate administration for pain and suffering at the end of life: knowledge and attitudes as barriers to care.J Palliat Med.2006;9:873883.
  19. Coffman J,Rundall TG.The impact of hospitalists on the cost and quality of inpatient care in the United States: a research synthesis.Med Care Res Rev.2005;62:379406.
  20. Meltzer D,Manning WG,Morrison J, et al.Effects of physician experience on costs and outcomes on an academic general medicine service: results of a trial of hospitalists.Ann Intern Med.2002;137:866874.
  21. Muir JC,Arnold RM.Palliative care and the hospitalist: an opportunity for cross‐fertilization.Am J Med.2001;111 (9B):10S14S.
  22. Wachter RM.The evolution of the hospitalist model in the United States.Med Clin North Am.2002;86:687706.
  23. Wachter RM,Goldman L.The emerging role of “hospitalists” in the American health care system.N Engl J Med.1996;335:514517.
  24. Bradley EH,Cicchetti DV,Fried TR, et al.Attitudes about care at the end of life among clinicians: a quick, reliable, and valid assessment instrument.J Palliat Care.2000;16(1):614.
  25. Bradley EH,Cramer LD,Bogardus ST,Kasl SV,Johnson‐Hurzeler R,Horwitz SM.Physicians' ratings of their knowledge, attitudes, and end‐of‐life‐care practices.Acad Med.2002;77:305311.
  26. Weggel JM.Barriers to the physician decision to offer hospice as an option for terminal care.WMJ.1999;98(3):4953.
  27. Doyle D,Hanks G,Cherny N,Calman K, eds.Oxford Textbook of Palliative Medicine.3rd ed.Oxford, UK:Oxford University Press;2004.
  28. Portenoy RK,Coyle N.Controversies in the long‐term management of analgesic therapy in patients with advanced cancer.J Pain Symptom Manage.1990;5:307319.
  29. Moynihan TJ.Use of opioids in the treatment of severe pain in terminally ill patients—dying should not be painful.Mayo Clin Proc.2003;78:13971401.
  30. Iwashyna TJ,Christakis NA.Attitude and self‐reported practice regarding hospice referral in a national sample of internists.J Palliat Med.1998;1:241248.
  31. Plauth WH,Pantilat SZ,Wachter RM,Fenton CL.Hospitalists' perceptions of their residency training needs: results of a national survey.Am J Med.2001;111:247254.
  32. Wachter RM,Goldman L.The hospitalist movement 5 years later.JAMA.2002;287:487494.
Article PDF
Issue
Journal of Hospital Medicine - 2(6)
Page Number
357-365
Legacy Keywords
hospice, hospitalist, end‐of‐life
Sections
Article PDF
Article PDF

Shortcomings in the quality of care of hospitalized patients at the end of life, especially in the final days, are well documented.1, 2 Recent studies have highlighted inadequate pain and symptom control for hospitalized terminally ill patients,24 poor communication about treatment preferences,57 and limited or delayed referral for hospice care.810 Efforts to improve the quality of end‐of‐life care have been diverse, including increased educational programs,1113 development of palliative care units in hospitals,14, 15 and greater exposure to palliative care for physicians during residency training.16 Despite these efforts, studies assessing the attitudes and knowledge of physicians about hospice and palliative care continue to show deficits in knowledge about managing pain17, 18 as well as hospice policies and services.9

Among the interventions aimed at improving hospital care, the hospitalist movement has emerged as a model of care for improving the quality and cost efficiency of hospital care.1922 Because hospitalists spend substantial time on inpatient services,23 they are often involved in the care of patients with terminal illness, with potential to improve the quality of care that these patients receive while hospitalized. However, little is known about what specific knowledge and perspectives hospitalists and residents have about the care of patients with terminal illness. Although many studies have been conducted among physicians in private practice,9, 10, 2426 they have not focused on the knowledge, reported practices, and attitudes of hospitalists and residents concerning key aspects of end‐of‐life care and hospice. Such information can help to identify potential areas for improving knowledge and addressing common barriers highlighted in linking hospital and posthospital hospice care.

METHODS

Study Design and Sample

During 2006 we surveyed hospitalists and medical residents who were on their oncology rotation at a large academic medical center that did not have a hospital‐based palliative care unit in order to examine their knowledge, attitudes, and practices regarding terminally ill patients and hospice referrals. Hospitalists (n = 23) and medical residents (n = 29) made up a convenience sample of 52 physicians. The medical residents were completing their oncology rotation during the spring of 2006. The Institutional Review Board at Yale University School of Medicine approved the research protocol and verbal consent procedures.

Survey

The brief survey instrument (see Appendix) assessed physicians' knowledge and attitudes about and practices in caring for patients with terminal illness. The survey was adapted from previously published instruments8, 24 that have been shown24 to have good test‐retest reliability and construct validity. The survey contained 5 items pertaining to clinical knowledge about palliative care practices, including common symptoms and drug indications, doses, and side effects.27 An additional 2 items pertained to respondents' knowledge about nonclinical issues concerning eligibility rules for hospice,8 such as how a patient becomes eligible for hospice and whether Medicare benefits can be revoked or reinstated after hospice is elected. The survey also included 10 statements24 assessing physician attitudes about caring for patients with terminal illness. Responses, provided using a 5‐point Likert scale, were collapsed for reporting into a 3‐point scale of agree, neutral, and disagree. The instrument also included an open‐ended question asking physicians to specify what from their perspective was needed to ensure timely referral for hospice and palliative care.

Data Analysis

We used standard frequency analysis to describe the distribution of responses to the survey items. Based on an analysis of common erroneous answers to clinical knowledge questions, we identified several common myths prevalent among hospitalists and medicine residents. We also examined whether knowledge, reported practices, and attitudes differed significantly between the hospitalist and the resident samples using ANOVA or chi‐square statistics as appropriate. We used content analysis to summarize the open‐ended responses about potential ways to overcome what respondents perceived was underutilization of hospice.

RESULTS

Overview

The response rate for the survey was 85.2%. Almost half of the respondents (44.2%) were hospitalists (Table 1). The remaining respondents included first‐year (n = 9) and second‐ or third‐year (n = 16) residents or fellows (n = 4). Approximately 54% of the 52 respondents were female, and the majority (83%) had graduated from medical school between 2000 and 2005. Several common myths were apparent and pertained to essential areas of treating patients with terminal illness: pain control, symptom control, and eligibility for hospice (Table 2). Respondents generally had strong beliefs about caring for patients with terminal illness, and most agreed that many patients who would benefit from hospice either do not receive hospice or receive it only late in the course of their illness (Table 3).

Demographic Characteristics of Respondents (n = 52)
Characteristicn%
Sex  
Female2853.9%
Male2446.1%
Years since graduation from medical school  
1‐2 Years2656.5%
3‐5 Years1226.1%
>5 Years817.4%
Missing6 
Physician type  
Hospitalist2344.2%
First‐year resident917.3%
Second‐ or third‐year resident1630.8%
Fellow47.7%
Knowledge about Hospice and Palliative Care Practices and Eligibility for Hospice Care (n = 52)*
Questions about hospice and palliative care practicesResponse (%)
  • Correct answers, that is, facts, are in bold.

The incidence of psychological dependence (addiction) to opioids and analgesics when treating pain from cancer or other medical conditions is: 
Common (1 in 10 patients)17.3
Uncommon (1 in 100 patients)48.1
Very rare (fewer than 1 in 1000 patients)34.6
When a patient with cancer who is receiving opioids for pain complains of increasing pain, it most likely indicates: 
Opioid tolerance69.2
Increasing pathology of the cancer26.9
Patient noncompliance0.0
New onset of a different opioid‐resisting pain3.9
In the pain patient receiving opioids, 30 mg of oral morphine is equipotent to of IV morphine 
1 mg4.0
5 mg40.0
10 mg56.0
20 mg0.0
The 2 classes of drugs most commonly recommended for treating terminal dyspnea are: 
Beta‐blockers and Lasix7.7
Opioids and benzodiazepines82.7
Beta‐blockers and corticosteroids9.6
Beta‐blockers and Singulair (montelukast)0.0
A hospice patient whose agitation is primarily from anxiety should be treated with: 
Chlorpromazine (thorazine)0.0
Haloperidol21.6
Lorazepam (Ativan)76.4
Morphine2.0
Questions about eligibility for hospice careResponse (%)
Under the Medicare program, a physician must certify that the patient is expected to die within a specified time for the patients to be eligible for hospice services. To the best of your knowledge, patients become eligible for inpatient hospice care when they are expected to die in: 
2 Weeks5.8
6 Weeks9.6
2 Months9.6
6 Months69.2
Other1.9
Don't know3.8
To the best of your knowledge, patients become eligible for home hospice care when they are expected to die in: 
2 Weeks0.0
6 Weeks5.8
2 Months7.7
6 Months73.1
Other0.0
Don't know13.4
Physicians' Beliefs about Caring for Patients with Terminal Illness (n = 52)
BeliefsDisagree (%)Neutral (%)Agree (%)
Most patients want me to tell them their life‐expectancy.0.017.482.6
Generally, family caregivers want me to tell them the patient's life expectancy.4.48.786.9
Telling the patient and family members that the patient's illness is incurable is difficult for me.23.013.563.5
I think it is essential to discuss the prognosis with a patient, even if it is very poor.0.04.495.6
Most patients' physical symptoms (eg, pain, shortness of breath, and nausea) are controlled better with hospice than with the care that they would receive in the hospital.0.021.778.3
Most patients' emotional symptoms (eg, depression, anxiety) are controlled better with hospice than with the care they would receive in the hospital.0.08.791.3
Hospice meets the needs of the family better than conventional care does.0.08.791.3
Many patients who should receive hospice care do not receive hospice care.21.813.065.2
Many patients would benefit if hospice care were initiated earlier in the course of their illness.0.09.190.9
I feel knowledgeable enough to discuss palliative and hospice care with patients and families.19.238.542.3

Common Myths in Treating Patients with Terminal Illness

Myth 1. Treating cancer pain with opioids or analgesics causes addiction in 1 in 100 patients. Most physicians thought that addiction in patients treated for cancer pain with opioids or analgesics was much more common than it is. Almost half the respondents (48.1%) thought addiction occurred in 1 in 100 patients, and an additional 17.3% of respondents thought addiction occurred in 1 in 10 patients treated for cancer pain with opioids or analgesics. In contrast, the incidence of addiction in patients treated with opioids or analgesics for cancer pain is fewer than 1 in 1000 patients.28

Myth 2. When patients with cancer already receiving opioids for pain control complain of increasing pain, it most likely indicates opioid tolerance. Nearly 70% of respondents reported that the most likely reason for complaints of increased pain was tolerance to the opioid. However, the most likely reason for increased pain is increasing pathology of the cancer.27

Myth 3. The equipotent to 30 mg of oral morphine is 5 mg intravenous. More than half of respondents were inaccurate in their conversion of oral to intravenous (IV) morphine dosing, a common task of physicians caring for terminally ill patients. Almost half the physicians (44%) erroneously reported that 30 mg of oral morphine was equipotent to 5 mg or less morphine IV. However, in fact, 30 mg of oral morphine is equipotent to 10 mg of morphine IV.27

Myth 4. The most highly recommended drug for treating terminal dyspnea is a beta‐blocker, and the most appropriate drug for agitation due to anxiety is Haldol or morphine. Most respondents were able to identify the correct drugs; however, a sizable proportion of respondents (17.3%) erroneously responded that beta‐blockers and Lasix or beta‐blockers and corticosteroids were the best drugs for treating terminal dyspnea. About one‐fifth of respondents (21.6%) responded that Haldol or morphine was the recommended medication for treating agitation. In fact, opioids and benzodiazepines are the recommended drugs for treating terminal dyspnea,27 and the proper drug for treating agitation is lorazepam (Ativan).27

Myth 5. Patient life expectancy must be 2 months or less to be eligible for hospice. One‐quarter of respondents believed this to be true for inpatient hospice, and nearly 13.5% of respondents believe this to be true for home hospice. In fact, patients are eligible for hospice benefits earlier in the course of their illness. Under Medicare and most insurance policies, patients are eligible for hospice benefits as soon as their life expectancy is 6 months or less, not 2 months or less.27

Physician Beliefs about Caring for Patients with Terminal Illness

The physicians' beliefs about hospice were generally positive; the vast majority of respondents agreed or strongly agreed with the statement that physical and emotional symptoms of patients and family needs are better addressed with hospice than with the hospital care (Table 3). Most respondents also agreed that many patients do not receive hospice as they should and that hospice should be initiated earlier in the course of the illness. In addition, more than 80% of respondents believed patients and their families want their doctors to tell them the patient's life expectancy, and 95.6% of respondents thought it was essential to discuss prognosis, even a poor one, with the patient. Nevertheless, many respondents (65.3%) reported it was difficult to tell patients and their families that an illness was incurable. Furthermore, fewer than half the respondents (42.3%) believed they were knowledgeable enough to discuss hospice and palliative care with patients and their families.

In subgroup analyses comparing responses to knowledge and attitude items reported in Tables 2 and 3, we found no significant differences between hospitalists and any subgroup of residents by year of training or fellows, or between hospitalists and the full sample of residents and fellows. Because of the sample size, the statistical power for evaluating significance was limited in these exploratory subgroup analyses.

Among physicians who provided responses to the open‐ended question (n = 42) about how to enhance hospice referral rates and improve their timeliness, the most commonly reported suggestions were: (1) involve family members, not only patients, in discussions of hospice (38.1%), (2) have discussions about hospice earlier in the course of care with patients (26.2%), and (3) be clear with patients and families about the patient's prognosis (19.0%). Table 4 has a list of all responses provided to this question.

Physicians' Suggestions for Improving the Process of Hospice Referral (n = 42)
Responsen%*
  • Percentages add up to more than 100% because some respondents made more than 1 suggestion.

Involving family members as well as patients in discussions of hospice1638.1
Having earlier discussion with patients1126.2
Being clear with patients and families about patient prognosis819.0
Providing education about hospice to patients and families614.3
Discussions of goals of care with patients and families614.3
Involving social worker in discussions49.5
Providing literature to patients and families about hospice37.1
Having hospice representative available to provide education to patient and families24.8

DISCUSSION

This study demonstrated that, among hospitalists and residents, there are several misconceptions about fundamental aspects of caring for terminally ill patients. Given the potential importance of the role hospitalists play in improving the quality of inpatient care,1922 it is critical to identify and address these misconceptions. Additionally, physicians in this study indicated that more and earlier communication with patients and families about prognosis and about the option of hospice would be beneficial, but they themselves did not feel knowledgeable enough to discuss hospice and palliative care with patients and their families.

The nature of the misconceptions identified in this study shed light on the well‐documented phenomena of inadequate pain control24, 29 and poor symptom management2, 4 at the end of life. Having many of the erroneous beliefs apparent in this study may be consistent with providing less pain medication than needed and appropriate. For instance, many physicians believed that developing addiction to opioids used for cancer pain is more likely to occur than it really is, according to research evidence. It is extremely rare for these patients to become addicted to opioids or other analgesics (fewer than 1 in 1000 patients).28 In addition, most physicians believed that complaints of increased pain among patients receiving opioid therapy for pain control meant tolerance to the medication, a belief consistent with physician reluctance to prescribe more medication because it would lead to tolerance.28 In reality, the increased pain experienced in these situations is typically not a result of tolerance to the pain medication but to the cancer getting worse.27 Additionally, many physicians mistakenly decreased the dose of morphine in converting the route of administration from PO to IV, as is often done in hospitals. Such an error may be a contributing factor to the unintended undertreatment of pain in hospitals. Given the variability of cancer pain4 and the difference in time to peak effect depending on the route of administration,5 it is critical for physicians to understand proper dosing in order to effectively treat cancer pain. Furthermore, many physicians were incorrect about the recommended medications for dyspnea and for agitation, 2 symptoms that are prevalent among patients at the end of life.

The hospitalists and residents reported having very positive views about hospice, as is consistent with the literature.10, 30 However, many respondents indicated that patients who would have benefited from hospice did not receive it at all or only late in their illness. Physicians indicated that better communication with patients and families about hospice, prognosis, and goals of care would enhance appropriate use of hospice. While hospitalists and residents are in a position to initiate such discussions, they reported that these discussions were difficult for them. The challenge is how to promote what is necessary and valuable conversation with patients and families despite their difficulty, so that a realistic plan of care can be designed for all involved. Providing hospitalists and residents with evidence about what approaches are most effective in such discussions would be helpful to better prepare them for their roles in caring for hospitalized patients with terminal illness.

The results of this study have substantiated the need to enhance the education of hospitalists and resident physicians, who can play a vital role in improving the transition from hospital to hospice. Such education could take place as part of the residency experience or be embedded in various continuing medical education requirements that most states now have. The results of a recent national survey of hospitalists31 indicates they consider their palliative care training inadequate and feel ill prepared to care for patients with terminal illness. Our findings are consistent with those of that survey, highlighting information that is poorly understood by both residents and hospitalists. As hospitalists continue to play key roles in linking hospital to posthospital care,21 including hospice, there is greater opportunity to improve end‐of‐life care by expanding hospitalists' understanding of these issues.

Our findings should be interpreted in light of the study's limitations. First, this was an exploratory study, and the sample was modest in size. Nevertheless, the response rate was high: 85.2%. Second, we conducted the study in a single location; results may differ in other geographical areas. Last, we were unable to link reported knowledge and attitudes to patient experiences including quality of care or adequacy of pain control. Inadequate knowledge likely limits the quality of clinical practices, but the magnitude of this effect remains unknown and worthy of future study.

Despite these limitations, this study has contributed to the literature by identifying a set of misunderstandings or myths that may be common among hospitalists and residents who frequently care for hospitalized patients with terminal illness. Many of these misunderstandings were related to pain and symptom management, although some misunderstandings related to logistical issues such as hospice eligibility rules. Previous studies have described interventions to improve physicians' knowledge about palliative and end‐of‐life care practices at the undergraduate, graduate, and postgraduate levels.13 Our findings identified specific gaps in physicians' knowledge. Interventions aimed at closing these gaps might emphasize both specific clinical information about pain management and medication recommendations, and more general information about eligibility for hospice and best practices for communicating early with patients and family is needed to promote more effective care for patients with terminal illness being cared for in acute care settings.

As the use of hospitalists has become a widely accepted model of hospital care,32 ensuring their increased training and education in the care of patients with terminal illness is an important step in improving end‐of‐life care. Larger comparison studies are needed to identify differences in the practices and perspectives of hospitalists and residents and to target educational interventions to meet their particular needs. Further, conducting these studies at additional sites including those with established palliative care programs would be useful for identifying needs among a more diverse set of physicians involved in delivering end‐of‐life care.

APPENDIX

Survey on Hospice and End‐of‐Life Care

Survey ID _________________

Date ______________

  • DEMOGRAPHICS

     

    • What is your gender?

       

      • □ Male

      • □ Female

      • What year did you graduate from medical school? ___________

      • What is your primary specialty or area of practice?

         

        • □ Hospitalist

        • □ Oncology fellow

        • □ Oncology resident

        • □ Physician assistant

        • □ Other: _____________

        • KNOWLEDGE OF HOSPICE AND PALLIATIVE CARE PRACTICES

           

          • The incidence of psychological dependence (addiction) to opioids and analgesics when treating pain from cancer or other medical conditions is:

             

            • Common (1 in 10 patients)

            • Uncommon (1 in 100 patients)

            • Very rare (fewer than 1 in 1000 patients)

            • When a patient with cancer who is receiving opioids for pain complains of increasing pain, it most likely indicates:

               

              • Opioid tolerance

              • Increasing pathology of the cancer

              • Patient noncompliance

              • New onset of a different opioid‐resisting pain

              • In the pain patient receiving opioids, 30 mg of oral morphine is equipotent to _______________ of IV.

                 

                • 1mg

                • 5 mg

                • 10 mg

                • 20 mg

                • The 2 classes of drugs most commonly recommended for treating terminal dyspnea are:

                   

                  • Beta‐blockers and Lasix

                  • Opioids and benzodiazepines

                  • Beta‐blockers and corticosteroids

                  • Beta‐blockers and Singulair (montelukast)

                  • A hospice patient whose agitation is due primarily to anxiety should be treated with:

                     

                    • Chlorpromazine

                    • Haloperidol

                    • Lorazepam

                    • Morphine

                    • ELIGIBILITY FOR HOSPICE CARE

                       

                      • Under the Medicare program, a physician must certify that the patient is expected to die within a specified time for the patients to be eligible for hospice services. To the best of your knowledge, patients become eligible for inpatient hospice care when they are expected to die in:

                         

                        • □ 2 Weeks

                        • □ 6 Weeks

                        • □ 2 Months

                        • □ 6 Months

                        • □ Other: ________________________

                        • □ Don't know

                        • To the best of your knowledge, patients are eligible for home hospice care when they are expected to die in:

                           

                          • □ 2 Weeks

                          • □ 6 Weeks

                          • □ 2 Months

                          • □ 6 Months

                          • □ Other: __________________________

                          • □ Don't know

                          • ATTITUDES ABOUT HOSPICE CARE 0

                           

                          Following is a series of statements. Please state whether you strongly agree, agree, neither agree nor disagree, disagree, or strongly disagree with each statement.
                           Strongly agreeStrongly disagree
                          11) Most patients want me to tell them their life expectancy.1 □2 □3 □4 □5 □
                          12) Generally, family caregivers want me to tell them the patient's life expectancy.1 □2 □3 □4 □5 □
                          13) Telling the patient and family members that the patient's illness is incurable is difficult for me.1 □2 □3 □4 □5 □
                          14) I think it is essential to discuss the prognosis with a patient, even if it is very poor.1 □2 □3 □4 □5 □
                          15) Most patients' physical symptoms (eg, pain, shortness of breath, and nausea) are controlled better with hospice than with the care they would receive in the hospital.1 □2 □3 □4 □5 □
                          16) Most patients' emotional symptoms (eg, depression, anxiety) are controlled better with hospice than with the care they would receive in the hospital.1 □2 □3 □4 □5 □
                          17) Hospice care generally meets the needs of the family better than conventional care does.1 □2 □3 □4 □5 □
                          18) Many terminally ill patients who should receive hospice care do not receive hospice care.1 □2 □3 □4 □5 □
                          19) Many patients would benefit if hospice care were initiated earlier in the course of their illness.1 □2 □3 □4 □5 □
                          20) I feel knowledgeable enough to discuss palliative and hospice care with patients and families.1 □2 □3 □4 □5 □
                          21) What do you see as the primary ways to facilitate earlier initiation of hospice care for patients who are eligible? _____________________________________________________________________________________
                          ___________________________________________________________________________________________

Shortcomings in the quality of care of hospitalized patients at the end of life, especially in the final days, are well documented.1, 2 Recent studies have highlighted inadequate pain and symptom control for hospitalized terminally ill patients,24 poor communication about treatment preferences,57 and limited or delayed referral for hospice care.810 Efforts to improve the quality of end‐of‐life care have been diverse, including increased educational programs,1113 development of palliative care units in hospitals,14, 15 and greater exposure to palliative care for physicians during residency training.16 Despite these efforts, studies assessing the attitudes and knowledge of physicians about hospice and palliative care continue to show deficits in knowledge about managing pain17, 18 as well as hospice policies and services.9

Among the interventions aimed at improving hospital care, the hospitalist movement has emerged as a model of care for improving the quality and cost efficiency of hospital care.1922 Because hospitalists spend substantial time on inpatient services,23 they are often involved in the care of patients with terminal illness, with potential to improve the quality of care that these patients receive while hospitalized. However, little is known about what specific knowledge and perspectives hospitalists and residents have about the care of patients with terminal illness. Although many studies have been conducted among physicians in private practice,9, 10, 2426 they have not focused on the knowledge, reported practices, and attitudes of hospitalists and residents concerning key aspects of end‐of‐life care and hospice. Such information can help to identify potential areas for improving knowledge and addressing common barriers highlighted in linking hospital and posthospital hospice care.

METHODS

Study Design and Sample

During 2006 we surveyed hospitalists and medical residents who were on their oncology rotation at a large academic medical center that did not have a hospital‐based palliative care unit in order to examine their knowledge, attitudes, and practices regarding terminally ill patients and hospice referrals. Hospitalists (n = 23) and medical residents (n = 29) made up a convenience sample of 52 physicians. The medical residents were completing their oncology rotation during the spring of 2006. The Institutional Review Board at Yale University School of Medicine approved the research protocol and verbal consent procedures.

Survey

The brief survey instrument (see Appendix) assessed physicians' knowledge and attitudes about and practices in caring for patients with terminal illness. The survey was adapted from previously published instruments8, 24 that have been shown24 to have good test‐retest reliability and construct validity. The survey contained 5 items pertaining to clinical knowledge about palliative care practices, including common symptoms and drug indications, doses, and side effects.27 An additional 2 items pertained to respondents' knowledge about nonclinical issues concerning eligibility rules for hospice,8 such as how a patient becomes eligible for hospice and whether Medicare benefits can be revoked or reinstated after hospice is elected. The survey also included 10 statements24 assessing physician attitudes about caring for patients with terminal illness. Responses, provided using a 5‐point Likert scale, were collapsed for reporting into a 3‐point scale of agree, neutral, and disagree. The instrument also included an open‐ended question asking physicians to specify what from their perspective was needed to ensure timely referral for hospice and palliative care.

Data Analysis

We used standard frequency analysis to describe the distribution of responses to the survey items. Based on an analysis of common erroneous answers to clinical knowledge questions, we identified several common myths prevalent among hospitalists and medicine residents. We also examined whether knowledge, reported practices, and attitudes differed significantly between the hospitalist and the resident samples using ANOVA or chi‐square statistics as appropriate. We used content analysis to summarize the open‐ended responses about potential ways to overcome what respondents perceived was underutilization of hospice.

RESULTS

Overview

The response rate for the survey was 85.2%. Almost half of the respondents (44.2%) were hospitalists (Table 1). The remaining respondents included first‐year (n = 9) and second‐ or third‐year (n = 16) residents or fellows (n = 4). Approximately 54% of the 52 respondents were female, and the majority (83%) had graduated from medical school between 2000 and 2005. Several common myths were apparent and pertained to essential areas of treating patients with terminal illness: pain control, symptom control, and eligibility for hospice (Table 2). Respondents generally had strong beliefs about caring for patients with terminal illness, and most agreed that many patients who would benefit from hospice either do not receive hospice or receive it only late in the course of their illness (Table 3).

Demographic Characteristics of Respondents (n = 52)
Characteristicn%
Sex  
Female2853.9%
Male2446.1%
Years since graduation from medical school  
1‐2 Years2656.5%
3‐5 Years1226.1%
>5 Years817.4%
Missing6 
Physician type  
Hospitalist2344.2%
First‐year resident917.3%
Second‐ or third‐year resident1630.8%
Fellow47.7%
Knowledge about Hospice and Palliative Care Practices and Eligibility for Hospice Care (n = 52)*
Questions about hospice and palliative care practicesResponse (%)
  • Correct answers, that is, facts, are in bold.

The incidence of psychological dependence (addiction) to opioids and analgesics when treating pain from cancer or other medical conditions is: 
Common (1 in 10 patients)17.3
Uncommon (1 in 100 patients)48.1
Very rare (fewer than 1 in 1000 patients)34.6
When a patient with cancer who is receiving opioids for pain complains of increasing pain, it most likely indicates: 
Opioid tolerance69.2
Increasing pathology of the cancer26.9
Patient noncompliance0.0
New onset of a different opioid‐resisting pain3.9
In the pain patient receiving opioids, 30 mg of oral morphine is equipotent to of IV morphine 
1 mg4.0
5 mg40.0
10 mg56.0
20 mg0.0
The 2 classes of drugs most commonly recommended for treating terminal dyspnea are: 
Beta‐blockers and Lasix7.7
Opioids and benzodiazepines82.7
Beta‐blockers and corticosteroids9.6
Beta‐blockers and Singulair (montelukast)0.0
A hospice patient whose agitation is primarily from anxiety should be treated with: 
Chlorpromazine (thorazine)0.0
Haloperidol21.6
Lorazepam (Ativan)76.4
Morphine2.0
Questions about eligibility for hospice careResponse (%)
Under the Medicare program, a physician must certify that the patient is expected to die within a specified time for the patients to be eligible for hospice services. To the best of your knowledge, patients become eligible for inpatient hospice care when they are expected to die in: 
2 Weeks5.8
6 Weeks9.6
2 Months9.6
6 Months69.2
Other1.9
Don't know3.8
To the best of your knowledge, patients become eligible for home hospice care when they are expected to die in: 
2 Weeks0.0
6 Weeks5.8
2 Months7.7
6 Months73.1
Other0.0
Don't know13.4
Physicians' Beliefs about Caring for Patients with Terminal Illness (n = 52)
BeliefsDisagree (%)Neutral (%)Agree (%)
Most patients want me to tell them their life‐expectancy.0.017.482.6
Generally, family caregivers want me to tell them the patient's life expectancy.4.48.786.9
Telling the patient and family members that the patient's illness is incurable is difficult for me.23.013.563.5
I think it is essential to discuss the prognosis with a patient, even if it is very poor.0.04.495.6
Most patients' physical symptoms (eg, pain, shortness of breath, and nausea) are controlled better with hospice than with the care that they would receive in the hospital.0.021.778.3
Most patients' emotional symptoms (eg, depression, anxiety) are controlled better with hospice than with the care they would receive in the hospital.0.08.791.3
Hospice meets the needs of the family better than conventional care does.0.08.791.3
Many patients who should receive hospice care do not receive hospice care.21.813.065.2
Many patients would benefit if hospice care were initiated earlier in the course of their illness.0.09.190.9
I feel knowledgeable enough to discuss palliative and hospice care with patients and families.19.238.542.3

Common Myths in Treating Patients with Terminal Illness

Myth 1. Treating cancer pain with opioids or analgesics causes addiction in 1 in 100 patients. Most physicians thought that addiction in patients treated for cancer pain with opioids or analgesics was much more common than it is. Almost half the respondents (48.1%) thought addiction occurred in 1 in 100 patients, and an additional 17.3% of respondents thought addiction occurred in 1 in 10 patients treated for cancer pain with opioids or analgesics. In contrast, the incidence of addiction in patients treated with opioids or analgesics for cancer pain is fewer than 1 in 1000 patients.28

Myth 2. When patients with cancer already receiving opioids for pain control complain of increasing pain, it most likely indicates opioid tolerance. Nearly 70% of respondents reported that the most likely reason for complaints of increased pain was tolerance to the opioid. However, the most likely reason for increased pain is increasing pathology of the cancer.27

Myth 3. The equipotent to 30 mg of oral morphine is 5 mg intravenous. More than half of respondents were inaccurate in their conversion of oral to intravenous (IV) morphine dosing, a common task of physicians caring for terminally ill patients. Almost half the physicians (44%) erroneously reported that 30 mg of oral morphine was equipotent to 5 mg or less morphine IV. However, in fact, 30 mg of oral morphine is equipotent to 10 mg of morphine IV.27

Myth 4. The most highly recommended drug for treating terminal dyspnea is a beta‐blocker, and the most appropriate drug for agitation due to anxiety is Haldol or morphine. Most respondents were able to identify the correct drugs; however, a sizable proportion of respondents (17.3%) erroneously responded that beta‐blockers and Lasix or beta‐blockers and corticosteroids were the best drugs for treating terminal dyspnea. About one‐fifth of respondents (21.6%) responded that Haldol or morphine was the recommended medication for treating agitation. In fact, opioids and benzodiazepines are the recommended drugs for treating terminal dyspnea,27 and the proper drug for treating agitation is lorazepam (Ativan).27

Myth 5. Patient life expectancy must be 2 months or less to be eligible for hospice. One‐quarter of respondents believed this to be true for inpatient hospice, and nearly 13.5% of respondents believe this to be true for home hospice. In fact, patients are eligible for hospice benefits earlier in the course of their illness. Under Medicare and most insurance policies, patients are eligible for hospice benefits as soon as their life expectancy is 6 months or less, not 2 months or less.27

Physician Beliefs about Caring for Patients with Terminal Illness

The physicians' beliefs about hospice were generally positive; the vast majority of respondents agreed or strongly agreed with the statement that physical and emotional symptoms of patients and family needs are better addressed with hospice than with the hospital care (Table 3). Most respondents also agreed that many patients do not receive hospice as they should and that hospice should be initiated earlier in the course of the illness. In addition, more than 80% of respondents believed patients and their families want their doctors to tell them the patient's life expectancy, and 95.6% of respondents thought it was essential to discuss prognosis, even a poor one, with the patient. Nevertheless, many respondents (65.3%) reported it was difficult to tell patients and their families that an illness was incurable. Furthermore, fewer than half the respondents (42.3%) believed they were knowledgeable enough to discuss hospice and palliative care with patients and their families.

In subgroup analyses comparing responses to knowledge and attitude items reported in Tables 2 and 3, we found no significant differences between hospitalists and any subgroup of residents by year of training or fellows, or between hospitalists and the full sample of residents and fellows. Because of the sample size, the statistical power for evaluating significance was limited in these exploratory subgroup analyses.

Among physicians who provided responses to the open‐ended question (n = 42) about how to enhance hospice referral rates and improve their timeliness, the most commonly reported suggestions were: (1) involve family members, not only patients, in discussions of hospice (38.1%), (2) have discussions about hospice earlier in the course of care with patients (26.2%), and (3) be clear with patients and families about the patient's prognosis (19.0%). Table 4 has a list of all responses provided to this question.

Physicians' Suggestions for Improving the Process of Hospice Referral (n = 42)
Responsen%*
  • Percentages add up to more than 100% because some respondents made more than 1 suggestion.

Involving family members as well as patients in discussions of hospice1638.1
Having earlier discussion with patients1126.2
Being clear with patients and families about patient prognosis819.0
Providing education about hospice to patients and families614.3
Discussions of goals of care with patients and families614.3
Involving social worker in discussions49.5
Providing literature to patients and families about hospice37.1
Having hospice representative available to provide education to patient and families24.8

DISCUSSION

This study demonstrated that, among hospitalists and residents, there are several misconceptions about fundamental aspects of caring for terminally ill patients. Given the potential importance of the role hospitalists play in improving the quality of inpatient care,1922 it is critical to identify and address these misconceptions. Additionally, physicians in this study indicated that more and earlier communication with patients and families about prognosis and about the option of hospice would be beneficial, but they themselves did not feel knowledgeable enough to discuss hospice and palliative care with patients and their families.

The nature of the misconceptions identified in this study shed light on the well‐documented phenomena of inadequate pain control24, 29 and poor symptom management2, 4 at the end of life. Having many of the erroneous beliefs apparent in this study may be consistent with providing less pain medication than needed and appropriate. For instance, many physicians believed that developing addiction to opioids used for cancer pain is more likely to occur than it really is, according to research evidence. It is extremely rare for these patients to become addicted to opioids or other analgesics (fewer than 1 in 1000 patients).28 In addition, most physicians believed that complaints of increased pain among patients receiving opioid therapy for pain control meant tolerance to the medication, a belief consistent with physician reluctance to prescribe more medication because it would lead to tolerance.28 In reality, the increased pain experienced in these situations is typically not a result of tolerance to the pain medication but to the cancer getting worse.27 Additionally, many physicians mistakenly decreased the dose of morphine in converting the route of administration from PO to IV, as is often done in hospitals. Such an error may be a contributing factor to the unintended undertreatment of pain in hospitals. Given the variability of cancer pain4 and the difference in time to peak effect depending on the route of administration,5 it is critical for physicians to understand proper dosing in order to effectively treat cancer pain. Furthermore, many physicians were incorrect about the recommended medications for dyspnea and for agitation, 2 symptoms that are prevalent among patients at the end of life.

The hospitalists and residents reported having very positive views about hospice, as is consistent with the literature.10, 30 However, many respondents indicated that patients who would have benefited from hospice did not receive it at all or only late in their illness. Physicians indicated that better communication with patients and families about hospice, prognosis, and goals of care would enhance appropriate use of hospice. While hospitalists and residents are in a position to initiate such discussions, they reported that these discussions were difficult for them. The challenge is how to promote what is necessary and valuable conversation with patients and families despite their difficulty, so that a realistic plan of care can be designed for all involved. Providing hospitalists and residents with evidence about what approaches are most effective in such discussions would be helpful to better prepare them for their roles in caring for hospitalized patients with terminal illness.

The results of this study have substantiated the need to enhance the education of hospitalists and resident physicians, who can play a vital role in improving the transition from hospital to hospice. Such education could take place as part of the residency experience or be embedded in various continuing medical education requirements that most states now have. The results of a recent national survey of hospitalists31 indicates they consider their palliative care training inadequate and feel ill prepared to care for patients with terminal illness. Our findings are consistent with those of that survey, highlighting information that is poorly understood by both residents and hospitalists. As hospitalists continue to play key roles in linking hospital to posthospital care,21 including hospice, there is greater opportunity to improve end‐of‐life care by expanding hospitalists' understanding of these issues.

Our findings should be interpreted in light of the study's limitations. First, this was an exploratory study, and the sample was modest in size. Nevertheless, the response rate was high: 85.2%. Second, we conducted the study in a single location; results may differ in other geographical areas. Last, we were unable to link reported knowledge and attitudes to patient experiences including quality of care or adequacy of pain control. Inadequate knowledge likely limits the quality of clinical practices, but the magnitude of this effect remains unknown and worthy of future study.

Despite these limitations, this study has contributed to the literature by identifying a set of misunderstandings or myths that may be common among hospitalists and residents who frequently care for hospitalized patients with terminal illness. Many of these misunderstandings were related to pain and symptom management, although some misunderstandings related to logistical issues such as hospice eligibility rules. Previous studies have described interventions to improve physicians' knowledge about palliative and end‐of‐life care practices at the undergraduate, graduate, and postgraduate levels.13 Our findings identified specific gaps in physicians' knowledge. Interventions aimed at closing these gaps might emphasize both specific clinical information about pain management and medication recommendations, and more general information about eligibility for hospice and best practices for communicating early with patients and family is needed to promote more effective care for patients with terminal illness being cared for in acute care settings.

As the use of hospitalists has become a widely accepted model of hospital care,32 ensuring their increased training and education in the care of patients with terminal illness is an important step in improving end‐of‐life care. Larger comparison studies are needed to identify differences in the practices and perspectives of hospitalists and residents and to target educational interventions to meet their particular needs. Further, conducting these studies at additional sites including those with established palliative care programs would be useful for identifying needs among a more diverse set of physicians involved in delivering end‐of‐life care.

APPENDIX

Survey on Hospice and End‐of‐Life Care

Survey ID _________________

Date ______________

  • DEMOGRAPHICS

     

    • What is your gender?

       

      • □ Male

      • □ Female

      • What year did you graduate from medical school? ___________

      • What is your primary specialty or area of practice?

         

        • □ Hospitalist

        • □ Oncology fellow

        • □ Oncology resident

        • □ Physician assistant

        • □ Other: _____________

        • KNOWLEDGE OF HOSPICE AND PALLIATIVE CARE PRACTICES

           

          • The incidence of psychological dependence (addiction) to opioids and analgesics when treating pain from cancer or other medical conditions is:

             

            • Common (1 in 10 patients)

            • Uncommon (1 in 100 patients)

            • Very rare (fewer than 1 in 1000 patients)

            • When a patient with cancer who is receiving opioids for pain complains of increasing pain, it most likely indicates:

               

              • Opioid tolerance

              • Increasing pathology of the cancer

              • Patient noncompliance

              • New onset of a different opioid‐resisting pain

              • In the pain patient receiving opioids, 30 mg of oral morphine is equipotent to _______________ of IV.

                 

                • 1mg

                • 5 mg

                • 10 mg

                • 20 mg

                • The 2 classes of drugs most commonly recommended for treating terminal dyspnea are:

                   

                  • Beta‐blockers and Lasix

                  • Opioids and benzodiazepines

                  • Beta‐blockers and corticosteroids

                  • Beta‐blockers and Singulair (montelukast)

                  • A hospice patient whose agitation is due primarily to anxiety should be treated with:

                     

                    • Chlorpromazine

                    • Haloperidol

                    • Lorazepam

                    • Morphine

                    • ELIGIBILITY FOR HOSPICE CARE

                       

                      • Under the Medicare program, a physician must certify that the patient is expected to die within a specified time for the patients to be eligible for hospice services. To the best of your knowledge, patients become eligible for inpatient hospice care when they are expected to die in:

                         

                        • □ 2 Weeks

                        • □ 6 Weeks

                        • □ 2 Months

                        • □ 6 Months

                        • □ Other: ________________________

                        • □ Don't know

                        • To the best of your knowledge, patients are eligible for home hospice care when they are expected to die in:

                           

                          • □ 2 Weeks

                          • □ 6 Weeks

                          • □ 2 Months

                          • □ 6 Months

                          • □ Other: __________________________

                          • □ Don't know

                          • ATTITUDES ABOUT HOSPICE CARE 0

                           

                          Following is a series of statements. Please state whether you strongly agree, agree, neither agree nor disagree, disagree, or strongly disagree with each statement.
                           Strongly agreeStrongly disagree
                          11) Most patients want me to tell them their life expectancy.1 □2 □3 □4 □5 □
                          12) Generally, family caregivers want me to tell them the patient's life expectancy.1 □2 □3 □4 □5 □
                          13) Telling the patient and family members that the patient's illness is incurable is difficult for me.1 □2 □3 □4 □5 □
                          14) I think it is essential to discuss the prognosis with a patient, even if it is very poor.1 □2 □3 □4 □5 □
                          15) Most patients' physical symptoms (eg, pain, shortness of breath, and nausea) are controlled better with hospice than with the care they would receive in the hospital.1 □2 □3 □4 □5 □
                          16) Most patients' emotional symptoms (eg, depression, anxiety) are controlled better with hospice than with the care they would receive in the hospital.1 □2 □3 □4 □5 □
                          17) Hospice care generally meets the needs of the family better than conventional care does.1 □2 □3 □4 □5 □
                          18) Many terminally ill patients who should receive hospice care do not receive hospice care.1 □2 □3 □4 □5 □
                          19) Many patients would benefit if hospice care were initiated earlier in the course of their illness.1 □2 □3 □4 □5 □
                          20) I feel knowledgeable enough to discuss palliative and hospice care with patients and families.1 □2 □3 □4 □5 □
                          21) What do you see as the primary ways to facilitate earlier initiation of hospice care for patients who are eligible? _____________________________________________________________________________________
                          ___________________________________________________________________________________________
References
  1. Institute of Medicine.Approaching Death.Washington, DC:National Academy Press;1997.
  2. SUPPORT Principle Investigators.A controlled trial to improve care for seriously ill hospitalized patients.JAMA.1995;274:15911598.
  3. Morrison RS,Meier DE,Fischberg D, et al.Improving the management of pain in hospitalized adults.Arch Intern Med.2006;166:10331039.
  4. von Gunten CF.Interventions to manage symptoms at the end of life.J Palliat Med.2005;8(suppl 1):S88S94.
  5. Bradley EH,Hallemeier AG,Fried TR, et al.Documentation of discussions about prognosis with terminally ill patients.Am J Med.2001;111:218223.
  6. Chittenden EH,Clark ST,Pantilat SZ.Discussing resuscitation preferences with patients: challenges and rewards.J Hosp Med.2006;1:231249.
  7. Schulman‐Green D,McCorkle R,Curry L,Cherlin E,Johnson‐Hurzeler R,Bradley E.At the crossroads: making the transition to hospice.Palliat Support Care.2004;2:351360.
  8. Bradley EH,Fried TR,Kasl SV,Cicchetti DV,Johnson‐Hurzeler R,Horwitz SM.Referral of terminally ill patients for hospice: frequency and correlates.J Palliat Care.2000;16(4):2026.
  9. Ogle K,Mavis B,Wang T.Hospice and primary care physicians: attitudes, knowledge, and barriers.Am J Hosp Palliat Care.2003;20(1):4151.
  10. Ogle KS,Mavis B,Wyatt GK.Physicians and hospice care: attitudes, knowledge, and referrals.J Palliat Med.2002;5(1):8592.
  11. Block SD.Medical education in end‐of‐life care: the status of reform.J Palliat Med.2002;5(2):243248.
  12. Meier DE,Morrison RS,Cassel CK.Improving palliative care.Ann Intern Med.1997;127(3):225230.
  13. Weissman DE,Mullan P,Ambuel B,von Gunten CF,Hallenbeck J,Warm E.Improving end‐of‐life care: internal medicine curriculum project—abstracts/progress reports.J Palliat Med.2001;4(1):75102.
  14. Bailey FA,Burgio KL,Woodby LL, et al.Improving processes of hospital care during the last hours of life.Arch Intern Med.2005;165:17221727.
  15. Pan CX,Morrison RS,Meier DE, et al.How prevalent are hospital‐based palliative care programs? Status report and future directions.J Palliat Med.2001;4:315324.
  16. von Gunten CF,Twaddle M,Preodor M,Neely KJ,Martinez J,Lyons J.Evidence of improved knowledge and skills after an elective rotation in a hospice and palliative care program for internal medicine residents.Am J Hosp Palliat Care.2005;22(3):195203.
  17. Clark JM,Lurie JD,Claessens MT,Reed VA,Jernstedt GC,Goodlin SG.Factors associated with palliative care knowledge among internal medicine house staff.J Palliat Care.2003;19:253257.
  18. Fineberg IC,Wenger NS,Brown‐Saltzman K.Unrestricted opiate administration for pain and suffering at the end of life: knowledge and attitudes as barriers to care.J Palliat Med.2006;9:873883.
  19. Coffman J,Rundall TG.The impact of hospitalists on the cost and quality of inpatient care in the United States: a research synthesis.Med Care Res Rev.2005;62:379406.
  20. Meltzer D,Manning WG,Morrison J, et al.Effects of physician experience on costs and outcomes on an academic general medicine service: results of a trial of hospitalists.Ann Intern Med.2002;137:866874.
  21. Muir JC,Arnold RM.Palliative care and the hospitalist: an opportunity for cross‐fertilization.Am J Med.2001;111 (9B):10S14S.
  22. Wachter RM.The evolution of the hospitalist model in the United States.Med Clin North Am.2002;86:687706.
  23. Wachter RM,Goldman L.The emerging role of “hospitalists” in the American health care system.N Engl J Med.1996;335:514517.
  24. Bradley EH,Cicchetti DV,Fried TR, et al.Attitudes about care at the end of life among clinicians: a quick, reliable, and valid assessment instrument.J Palliat Care.2000;16(1):614.
  25. Bradley EH,Cramer LD,Bogardus ST,Kasl SV,Johnson‐Hurzeler R,Horwitz SM.Physicians' ratings of their knowledge, attitudes, and end‐of‐life‐care practices.Acad Med.2002;77:305311.
  26. Weggel JM.Barriers to the physician decision to offer hospice as an option for terminal care.WMJ.1999;98(3):4953.
  27. Doyle D,Hanks G,Cherny N,Calman K, eds.Oxford Textbook of Palliative Medicine.3rd ed.Oxford, UK:Oxford University Press;2004.
  28. Portenoy RK,Coyle N.Controversies in the long‐term management of analgesic therapy in patients with advanced cancer.J Pain Symptom Manage.1990;5:307319.
  29. Moynihan TJ.Use of opioids in the treatment of severe pain in terminally ill patients—dying should not be painful.Mayo Clin Proc.2003;78:13971401.
  30. Iwashyna TJ,Christakis NA.Attitude and self‐reported practice regarding hospice referral in a national sample of internists.J Palliat Med.1998;1:241248.
  31. Plauth WH,Pantilat SZ,Wachter RM,Fenton CL.Hospitalists' perceptions of their residency training needs: results of a national survey.Am J Med.2001;111:247254.
  32. Wachter RM,Goldman L.The hospitalist movement 5 years later.JAMA.2002;287:487494.
References
  1. Institute of Medicine.Approaching Death.Washington, DC:National Academy Press;1997.
  2. SUPPORT Principle Investigators.A controlled trial to improve care for seriously ill hospitalized patients.JAMA.1995;274:15911598.
  3. Morrison RS,Meier DE,Fischberg D, et al.Improving the management of pain in hospitalized adults.Arch Intern Med.2006;166:10331039.
  4. von Gunten CF.Interventions to manage symptoms at the end of life.J Palliat Med.2005;8(suppl 1):S88S94.
  5. Bradley EH,Hallemeier AG,Fried TR, et al.Documentation of discussions about prognosis with terminally ill patients.Am J Med.2001;111:218223.
  6. Chittenden EH,Clark ST,Pantilat SZ.Discussing resuscitation preferences with patients: challenges and rewards.J Hosp Med.2006;1:231249.
  7. Schulman‐Green D,McCorkle R,Curry L,Cherlin E,Johnson‐Hurzeler R,Bradley E.At the crossroads: making the transition to hospice.Palliat Support Care.2004;2:351360.
  8. Bradley EH,Fried TR,Kasl SV,Cicchetti DV,Johnson‐Hurzeler R,Horwitz SM.Referral of terminally ill patients for hospice: frequency and correlates.J Palliat Care.2000;16(4):2026.
  9. Ogle K,Mavis B,Wang T.Hospice and primary care physicians: attitudes, knowledge, and barriers.Am J Hosp Palliat Care.2003;20(1):4151.
  10. Ogle KS,Mavis B,Wyatt GK.Physicians and hospice care: attitudes, knowledge, and referrals.J Palliat Med.2002;5(1):8592.
  11. Block SD.Medical education in end‐of‐life care: the status of reform.J Palliat Med.2002;5(2):243248.
  12. Meier DE,Morrison RS,Cassel CK.Improving palliative care.Ann Intern Med.1997;127(3):225230.
  13. Weissman DE,Mullan P,Ambuel B,von Gunten CF,Hallenbeck J,Warm E.Improving end‐of‐life care: internal medicine curriculum project—abstracts/progress reports.J Palliat Med.2001;4(1):75102.
  14. Bailey FA,Burgio KL,Woodby LL, et al.Improving processes of hospital care during the last hours of life.Arch Intern Med.2005;165:17221727.
  15. Pan CX,Morrison RS,Meier DE, et al.How prevalent are hospital‐based palliative care programs? Status report and future directions.J Palliat Med.2001;4:315324.
  16. von Gunten CF,Twaddle M,Preodor M,Neely KJ,Martinez J,Lyons J.Evidence of improved knowledge and skills after an elective rotation in a hospice and palliative care program for internal medicine residents.Am J Hosp Palliat Care.2005;22(3):195203.
  17. Clark JM,Lurie JD,Claessens MT,Reed VA,Jernstedt GC,Goodlin SG.Factors associated with palliative care knowledge among internal medicine house staff.J Palliat Care.2003;19:253257.
  18. Fineberg IC,Wenger NS,Brown‐Saltzman K.Unrestricted opiate administration for pain and suffering at the end of life: knowledge and attitudes as barriers to care.J Palliat Med.2006;9:873883.
  19. Coffman J,Rundall TG.The impact of hospitalists on the cost and quality of inpatient care in the United States: a research synthesis.Med Care Res Rev.2005;62:379406.
  20. Meltzer D,Manning WG,Morrison J, et al.Effects of physician experience on costs and outcomes on an academic general medicine service: results of a trial of hospitalists.Ann Intern Med.2002;137:866874.
  21. Muir JC,Arnold RM.Palliative care and the hospitalist: an opportunity for cross‐fertilization.Am J Med.2001;111 (9B):10S14S.
  22. Wachter RM.The evolution of the hospitalist model in the United States.Med Clin North Am.2002;86:687706.
  23. Wachter RM,Goldman L.The emerging role of “hospitalists” in the American health care system.N Engl J Med.1996;335:514517.
  24. Bradley EH,Cicchetti DV,Fried TR, et al.Attitudes about care at the end of life among clinicians: a quick, reliable, and valid assessment instrument.J Palliat Care.2000;16(1):614.
  25. Bradley EH,Cramer LD,Bogardus ST,Kasl SV,Johnson‐Hurzeler R,Horwitz SM.Physicians' ratings of their knowledge, attitudes, and end‐of‐life‐care practices.Acad Med.2002;77:305311.
  26. Weggel JM.Barriers to the physician decision to offer hospice as an option for terminal care.WMJ.1999;98(3):4953.
  27. Doyle D,Hanks G,Cherny N,Calman K, eds.Oxford Textbook of Palliative Medicine.3rd ed.Oxford, UK:Oxford University Press;2004.
  28. Portenoy RK,Coyle N.Controversies in the long‐term management of analgesic therapy in patients with advanced cancer.J Pain Symptom Manage.1990;5:307319.
  29. Moynihan TJ.Use of opioids in the treatment of severe pain in terminally ill patients—dying should not be painful.Mayo Clin Proc.2003;78:13971401.
  30. Iwashyna TJ,Christakis NA.Attitude and self‐reported practice regarding hospice referral in a national sample of internists.J Palliat Med.1998;1:241248.
  31. Plauth WH,Pantilat SZ,Wachter RM,Fenton CL.Hospitalists' perceptions of their residency training needs: results of a national survey.Am J Med.2001;111:247254.
  32. Wachter RM,Goldman L.The hospitalist movement 5 years later.JAMA.2002;287:487494.
Issue
Journal of Hospital Medicine - 2(6)
Issue
Journal of Hospital Medicine - 2(6)
Page Number
357-365
Page Number
357-365
Article Type
Display Headline
Common myths about caring for patients with terminal illness: Opportunities to improve care in the hospital setting
Display Headline
Common myths about caring for patients with terminal illness: Opportunities to improve care in the hospital setting
Legacy Keywords
hospice, hospitalist, end‐of‐life
Legacy Keywords
hospice, hospitalist, end‐of‐life
Sections
Article Source

Copyright © 2007 Society of Hospital Medicine

Disallow All Ads
Correspondence Location
Department of Epidemiology and Public Health, Yale School of Medicine, 60 College Street, New Haven, CT 06520‐8034; Fax: (203) 785‐6287
Content Gating
No Gating (article Unlocked/Free)
Alternative CME
Article PDF Media

Editorial / Kutner

Article Type
Changed
Display Headline
Ensuring safe, quality care for hospitalized people with advanced illness, a core obligation for hospitalists

Communication, palliative care, and patient safety have been identified by the Society of Hospital Medicine as core competencies in hospital medicine. Effective communication is recognized as being central to the role of the hospitalist to promote efficient, safe, and high quality care.1 Hospitalists are increasingly recognized as having a central role in initiatives to improve palliative care for hospitalized patients and their families24 and have a vital role in leading and participating in interventions to mitigate system and process failures that affect patient safety.1 The obligation of the hospitalist to assure safe, quality care for hospitalized people with advanced illness extends from direct patient care to advocacy for systems that facilitate the provision of such care.

Four articles in this issue of the Journal of Hospital Medicine provide complementary perspectives on these crucial roles of the hospitalist. Cherlin and colleagues describe findings from a survey of hospitalists and medical residents regarding their knowledge, attitudes, and practices relative to caring for patients with terminal illness. The article identifies misperceptions related to core components of quality palliative care: pain and symptom control, hospice eligibility, and communication about prognosis and hospice and palliative care.5 Although this study was conducted at only a single academic medical center and certainly deserves to be repeated in an expanded and more representative sample, it clearly identifies deficits in core components of quality care for persons with advanced illness. The article by Minichiello and colleagues provides practical guidance and resources for addressing one of the deficits identified: communicating a poor prognosis, or bad news.6

Pain and symptom management and communication are commonly recognized aspects of quality care for persons with advanced illness. Less often appreciated are the significant threats to patient safety and medical errors that occur in the care of this vulnerable population.79 Potential errors include failure of a planned action to be completed as intended (ie, not following advance directives) and failure to treat symptoms adequately. The original research article and accompanying images discussion by Sehgal and colleagues serve as a call to action to both recognize and address the potentially significant patient safety issue related to the use of color‐coded wristbands, particularly variation in color used by different hospitals to designate do not resuscitate status.10, 11 What is exciting about this sequence of articles is that they describe opportunities for improvement and provide potential solutions. We have to be aware that there is a problem in order to initiate change. Hospitalists are in an a prime position to both identify these potential critical issues and effect the necessary changes to facilitate our ability to provide safe, effective care to our patients with advanced illness.

Palliative care is increasingly being accepted as a means for improving care for persons with advanced illness. The National Consensus Project Clinical Practice Guidelines for Quality Palliative Care, released in 2004, was endorsed by the National Quality Forum and incorporated into its Framework for Hospice and Palliative Care in 2007.12, 13 The Joint Commission (TJC; previously known as JCAHO) is developing a Health Care Services Certification Program for palliative care services modeled on existing programs for diabetes and stroke care, to take effect in 2008.14 Newsweek featured palliative care in its August 2006 issue focused on Fixing America's Hospitals.15 US News and World Report has included hospice and palliative care indicators in its ranking of America's Best Hospitals since 2002.16 There has been significant recent growth in hospital‐based palliative care programs, with 1250 hospitals reporting palliative care programs in 2005, an increase of almost 100% over 2000. Seventy percent of U.S. hospitals with more than 250 beds report having a palliative care program.17

Although hospital‐based palliative care programs are increasing, it is the obligation of all hospitalists who care for an ill, often elderly population to assure that all hospitalized patients with advanced illness receive safe, quality care while hospitalized. This includes avoiding medical errors such as inappropriate resuscitation attempts because of miscommunication of do‐not‐resuscitate orders or advance directives, as well as minimizing distress, maximizing comfort, and addressing informational and psychosocial support needs. As evidenced by the 4 articles in this issue of the Journal of Hospital Medicine, we need to make safe, effective care for people with advanced illness a priority, then implement appropriate training and education and create systems that assure delivery of quality care.

References
  1. Pistoria MJ,Amin AN,Dressler DD,McKean SCW,Budnitz TL.The core competencies in hospital medicine: a framework for curriculum development.J Hosp Med.2006;1:167.
  2. Muir JC,Arnold RM.Palliative care and the hospitalist: an opportunity for cross‐fertilization.Am J Med.2001;111:10S14S.
  3. Pantilat SZ.Palliative care and hospitalists: a partnership for hope.J Hosp Med.2006;1:56.
  4. Meier DE.Palliative Care in Hospitals.J Hosp Med.2006;1:2128.
  5. Cherlin E,Morris V,Morris J,Johnson‐Hurzeler R,Sullivan GM,Bradley EH.Common myths about caring for patients with terminal illness: opportunities to improve care in the hospital setting.J Hosp Med.2007;2:357365.
  6. Minichiello T.,Ling D., andUcci D. K.Breaking bad news: a practical approach for the hospitalist.J Hosp Med.2007;2:415421.
  7. Myers SS,Lynn J.Patients with eventually fatal chronic illness: their importance within a national research agenda on improving patient safety and reducing medical errors.J Palliat Med.2001;4:325332.
  8. Lynn J,Goldstein NE.Advance care planning for fatal chronic illness: avoiding commonplace errors and unwarranted suffering.Ann Intern Med.2003;138:812818.
  9. Holloway RG,Quill TE.Mortality as a measure of quality: implications for palliative and end‐of‐life care.JAMA.2007;298:802804.
  10. Sehgal N,Wachter RM.Color‐coded wristbands: promoting safety or confusion?J Hosp Med.2007;2:445.
  11. Sehgal N,Wachter R.Identification of inpatient DNR status: a safety hazard begging for standardization.J Hosp Med.2007;2:366371.
  12. National Consensus Project for Quality Palliative Care. Clinical Practice Guidelines for Quality Palliative Care. Available at: http://www.nationalconsensusproject.org. Accessed August 26,2007.
  13. National Quality Forum. Available at: Available at: http://www.qualityforum.org. Accessed August 25,2007.
  14. Joint Commission for Accreditation of Health Care Organizations. Available at: http://www.jointcommission.org. Accessed August 26,2007.
  15. Noonan D.Special Care at the End of Life.Newsweek. October 16,2006. Available at: http://www.msnbc.msn.com/id/15175919/site/newsweek/page/0/. Accessed September 22,year="2007"2007.
  16. U.S. News and World Report America's Best Hospitals 2007 Methodology. Available at: http://health.usnews.com/usnews/health/best‐hospitals/methodology_report.pdf. Accessed September 22,2007.
  17. Center to Advance Palliative Care (CAPC). Available at: http://www.capc.org. Accessed August 26,2007.
Article PDF
Issue
Journal of Hospital Medicine - 2(6)
Page Number
355-356
Sections
Article PDF
Article PDF

Communication, palliative care, and patient safety have been identified by the Society of Hospital Medicine as core competencies in hospital medicine. Effective communication is recognized as being central to the role of the hospitalist to promote efficient, safe, and high quality care.1 Hospitalists are increasingly recognized as having a central role in initiatives to improve palliative care for hospitalized patients and their families24 and have a vital role in leading and participating in interventions to mitigate system and process failures that affect patient safety.1 The obligation of the hospitalist to assure safe, quality care for hospitalized people with advanced illness extends from direct patient care to advocacy for systems that facilitate the provision of such care.

Four articles in this issue of the Journal of Hospital Medicine provide complementary perspectives on these crucial roles of the hospitalist. Cherlin and colleagues describe findings from a survey of hospitalists and medical residents regarding their knowledge, attitudes, and practices relative to caring for patients with terminal illness. The article identifies misperceptions related to core components of quality palliative care: pain and symptom control, hospice eligibility, and communication about prognosis and hospice and palliative care.5 Although this study was conducted at only a single academic medical center and certainly deserves to be repeated in an expanded and more representative sample, it clearly identifies deficits in core components of quality care for persons with advanced illness. The article by Minichiello and colleagues provides practical guidance and resources for addressing one of the deficits identified: communicating a poor prognosis, or bad news.6

Pain and symptom management and communication are commonly recognized aspects of quality care for persons with advanced illness. Less often appreciated are the significant threats to patient safety and medical errors that occur in the care of this vulnerable population.79 Potential errors include failure of a planned action to be completed as intended (ie, not following advance directives) and failure to treat symptoms adequately. The original research article and accompanying images discussion by Sehgal and colleagues serve as a call to action to both recognize and address the potentially significant patient safety issue related to the use of color‐coded wristbands, particularly variation in color used by different hospitals to designate do not resuscitate status.10, 11 What is exciting about this sequence of articles is that they describe opportunities for improvement and provide potential solutions. We have to be aware that there is a problem in order to initiate change. Hospitalists are in an a prime position to both identify these potential critical issues and effect the necessary changes to facilitate our ability to provide safe, effective care to our patients with advanced illness.

Palliative care is increasingly being accepted as a means for improving care for persons with advanced illness. The National Consensus Project Clinical Practice Guidelines for Quality Palliative Care, released in 2004, was endorsed by the National Quality Forum and incorporated into its Framework for Hospice and Palliative Care in 2007.12, 13 The Joint Commission (TJC; previously known as JCAHO) is developing a Health Care Services Certification Program for palliative care services modeled on existing programs for diabetes and stroke care, to take effect in 2008.14 Newsweek featured palliative care in its August 2006 issue focused on Fixing America's Hospitals.15 US News and World Report has included hospice and palliative care indicators in its ranking of America's Best Hospitals since 2002.16 There has been significant recent growth in hospital‐based palliative care programs, with 1250 hospitals reporting palliative care programs in 2005, an increase of almost 100% over 2000. Seventy percent of U.S. hospitals with more than 250 beds report having a palliative care program.17

Although hospital‐based palliative care programs are increasing, it is the obligation of all hospitalists who care for an ill, often elderly population to assure that all hospitalized patients with advanced illness receive safe, quality care while hospitalized. This includes avoiding medical errors such as inappropriate resuscitation attempts because of miscommunication of do‐not‐resuscitate orders or advance directives, as well as minimizing distress, maximizing comfort, and addressing informational and psychosocial support needs. As evidenced by the 4 articles in this issue of the Journal of Hospital Medicine, we need to make safe, effective care for people with advanced illness a priority, then implement appropriate training and education and create systems that assure delivery of quality care.

Communication, palliative care, and patient safety have been identified by the Society of Hospital Medicine as core competencies in hospital medicine. Effective communication is recognized as being central to the role of the hospitalist to promote efficient, safe, and high quality care.1 Hospitalists are increasingly recognized as having a central role in initiatives to improve palliative care for hospitalized patients and their families24 and have a vital role in leading and participating in interventions to mitigate system and process failures that affect patient safety.1 The obligation of the hospitalist to assure safe, quality care for hospitalized people with advanced illness extends from direct patient care to advocacy for systems that facilitate the provision of such care.

Four articles in this issue of the Journal of Hospital Medicine provide complementary perspectives on these crucial roles of the hospitalist. Cherlin and colleagues describe findings from a survey of hospitalists and medical residents regarding their knowledge, attitudes, and practices relative to caring for patients with terminal illness. The article identifies misperceptions related to core components of quality palliative care: pain and symptom control, hospice eligibility, and communication about prognosis and hospice and palliative care.5 Although this study was conducted at only a single academic medical center and certainly deserves to be repeated in an expanded and more representative sample, it clearly identifies deficits in core components of quality care for persons with advanced illness. The article by Minichiello and colleagues provides practical guidance and resources for addressing one of the deficits identified: communicating a poor prognosis, or bad news.6

Pain and symptom management and communication are commonly recognized aspects of quality care for persons with advanced illness. Less often appreciated are the significant threats to patient safety and medical errors that occur in the care of this vulnerable population.79 Potential errors include failure of a planned action to be completed as intended (ie, not following advance directives) and failure to treat symptoms adequately. The original research article and accompanying images discussion by Sehgal and colleagues serve as a call to action to both recognize and address the potentially significant patient safety issue related to the use of color‐coded wristbands, particularly variation in color used by different hospitals to designate do not resuscitate status.10, 11 What is exciting about this sequence of articles is that they describe opportunities for improvement and provide potential solutions. We have to be aware that there is a problem in order to initiate change. Hospitalists are in an a prime position to both identify these potential critical issues and effect the necessary changes to facilitate our ability to provide safe, effective care to our patients with advanced illness.

Palliative care is increasingly being accepted as a means for improving care for persons with advanced illness. The National Consensus Project Clinical Practice Guidelines for Quality Palliative Care, released in 2004, was endorsed by the National Quality Forum and incorporated into its Framework for Hospice and Palliative Care in 2007.12, 13 The Joint Commission (TJC; previously known as JCAHO) is developing a Health Care Services Certification Program for palliative care services modeled on existing programs for diabetes and stroke care, to take effect in 2008.14 Newsweek featured palliative care in its August 2006 issue focused on Fixing America's Hospitals.15 US News and World Report has included hospice and palliative care indicators in its ranking of America's Best Hospitals since 2002.16 There has been significant recent growth in hospital‐based palliative care programs, with 1250 hospitals reporting palliative care programs in 2005, an increase of almost 100% over 2000. Seventy percent of U.S. hospitals with more than 250 beds report having a palliative care program.17

Although hospital‐based palliative care programs are increasing, it is the obligation of all hospitalists who care for an ill, often elderly population to assure that all hospitalized patients with advanced illness receive safe, quality care while hospitalized. This includes avoiding medical errors such as inappropriate resuscitation attempts because of miscommunication of do‐not‐resuscitate orders or advance directives, as well as minimizing distress, maximizing comfort, and addressing informational and psychosocial support needs. As evidenced by the 4 articles in this issue of the Journal of Hospital Medicine, we need to make safe, effective care for people with advanced illness a priority, then implement appropriate training and education and create systems that assure delivery of quality care.

References
  1. Pistoria MJ,Amin AN,Dressler DD,McKean SCW,Budnitz TL.The core competencies in hospital medicine: a framework for curriculum development.J Hosp Med.2006;1:167.
  2. Muir JC,Arnold RM.Palliative care and the hospitalist: an opportunity for cross‐fertilization.Am J Med.2001;111:10S14S.
  3. Pantilat SZ.Palliative care and hospitalists: a partnership for hope.J Hosp Med.2006;1:56.
  4. Meier DE.Palliative Care in Hospitals.J Hosp Med.2006;1:2128.
  5. Cherlin E,Morris V,Morris J,Johnson‐Hurzeler R,Sullivan GM,Bradley EH.Common myths about caring for patients with terminal illness: opportunities to improve care in the hospital setting.J Hosp Med.2007;2:357365.
  6. Minichiello T.,Ling D., andUcci D. K.Breaking bad news: a practical approach for the hospitalist.J Hosp Med.2007;2:415421.
  7. Myers SS,Lynn J.Patients with eventually fatal chronic illness: their importance within a national research agenda on improving patient safety and reducing medical errors.J Palliat Med.2001;4:325332.
  8. Lynn J,Goldstein NE.Advance care planning for fatal chronic illness: avoiding commonplace errors and unwarranted suffering.Ann Intern Med.2003;138:812818.
  9. Holloway RG,Quill TE.Mortality as a measure of quality: implications for palliative and end‐of‐life care.JAMA.2007;298:802804.
  10. Sehgal N,Wachter RM.Color‐coded wristbands: promoting safety or confusion?J Hosp Med.2007;2:445.
  11. Sehgal N,Wachter R.Identification of inpatient DNR status: a safety hazard begging for standardization.J Hosp Med.2007;2:366371.
  12. National Consensus Project for Quality Palliative Care. Clinical Practice Guidelines for Quality Palliative Care. Available at: http://www.nationalconsensusproject.org. Accessed August 26,2007.
  13. National Quality Forum. Available at: Available at: http://www.qualityforum.org. Accessed August 25,2007.
  14. Joint Commission for Accreditation of Health Care Organizations. Available at: http://www.jointcommission.org. Accessed August 26,2007.
  15. Noonan D.Special Care at the End of Life.Newsweek. October 16,2006. Available at: http://www.msnbc.msn.com/id/15175919/site/newsweek/page/0/. Accessed September 22,year="2007"2007.
  16. U.S. News and World Report America's Best Hospitals 2007 Methodology. Available at: http://health.usnews.com/usnews/health/best‐hospitals/methodology_report.pdf. Accessed September 22,2007.
  17. Center to Advance Palliative Care (CAPC). Available at: http://www.capc.org. Accessed August 26,2007.
References
  1. Pistoria MJ,Amin AN,Dressler DD,McKean SCW,Budnitz TL.The core competencies in hospital medicine: a framework for curriculum development.J Hosp Med.2006;1:167.
  2. Muir JC,Arnold RM.Palliative care and the hospitalist: an opportunity for cross‐fertilization.Am J Med.2001;111:10S14S.
  3. Pantilat SZ.Palliative care and hospitalists: a partnership for hope.J Hosp Med.2006;1:56.
  4. Meier DE.Palliative Care in Hospitals.J Hosp Med.2006;1:2128.
  5. Cherlin E,Morris V,Morris J,Johnson‐Hurzeler R,Sullivan GM,Bradley EH.Common myths about caring for patients with terminal illness: opportunities to improve care in the hospital setting.J Hosp Med.2007;2:357365.
  6. Minichiello T.,Ling D., andUcci D. K.Breaking bad news: a practical approach for the hospitalist.J Hosp Med.2007;2:415421.
  7. Myers SS,Lynn J.Patients with eventually fatal chronic illness: their importance within a national research agenda on improving patient safety and reducing medical errors.J Palliat Med.2001;4:325332.
  8. Lynn J,Goldstein NE.Advance care planning for fatal chronic illness: avoiding commonplace errors and unwarranted suffering.Ann Intern Med.2003;138:812818.
  9. Holloway RG,Quill TE.Mortality as a measure of quality: implications for palliative and end‐of‐life care.JAMA.2007;298:802804.
  10. Sehgal N,Wachter RM.Color‐coded wristbands: promoting safety or confusion?J Hosp Med.2007;2:445.
  11. Sehgal N,Wachter R.Identification of inpatient DNR status: a safety hazard begging for standardization.J Hosp Med.2007;2:366371.
  12. National Consensus Project for Quality Palliative Care. Clinical Practice Guidelines for Quality Palliative Care. Available at: http://www.nationalconsensusproject.org. Accessed August 26,2007.
  13. National Quality Forum. Available at: Available at: http://www.qualityforum.org. Accessed August 25,2007.
  14. Joint Commission for Accreditation of Health Care Organizations. Available at: http://www.jointcommission.org. Accessed August 26,2007.
  15. Noonan D.Special Care at the End of Life.Newsweek. October 16,2006. Available at: http://www.msnbc.msn.com/id/15175919/site/newsweek/page/0/. Accessed September 22,year="2007"2007.
  16. U.S. News and World Report America's Best Hospitals 2007 Methodology. Available at: http://health.usnews.com/usnews/health/best‐hospitals/methodology_report.pdf. Accessed September 22,2007.
  17. Center to Advance Palliative Care (CAPC). Available at: http://www.capc.org. Accessed August 26,2007.
Issue
Journal of Hospital Medicine - 2(6)
Issue
Journal of Hospital Medicine - 2(6)
Page Number
355-356
Page Number
355-356
Article Type
Display Headline
Ensuring safe, quality care for hospitalized people with advanced illness, a core obligation for hospitalists
Display Headline
Ensuring safe, quality care for hospitalized people with advanced illness, a core obligation for hospitalists
Sections
Article Source
Copyright © 2007 Society of Hospital Medicine
Disallow All Ads
Correspondence Location
Division of General Internal Medicine, B180, University of Colorado Denver School of Medicine, Academic Office 1, P.O. Box 6511, 12631 East 17th Ave., Aurora, CO 80045; Fax: (303) 724‐2270
Content Gating
Gated (full article locked unless allowed per User)
Gating Strategy
First Peek Free
Article PDF Media

Play by the Rules

Article Type
Changed
Display Headline
Play by the Rules

How does your hospitalist group make decisions on important issues? There are many reasonable approaches. The best method will vary significantly depending on the group’s size and whether the doctors own their own private practice or are employees of a hospital or large multisite private hospitalist group.

Because many doctors are drawn to the profession in part seeking autonomy and independence, there is often a tension between their desire to make many decisions about business and practice operations independently and the need to set aside some personal interests in order for the group to function well. This can become apparent when the group reaches an agreement regarding a difficult issue for which there are different points of view.

Consider a hospitalist group made up of internists occasionally asked to admit teenagers younger than 17. There might be a variety of opinions about whether this is appropriate, but it will be best for everyone in the group to follow the same policy. If the majority decision is that it is reasonable to admit patients as long as they’re post-pubertal, everyone in the group should abide by this policy.

But when called by the emergency department about such a patient, a dissenting hospitalist might feel entitled to decline the admission despite the group’s decision. For this doctor, autonomy trumps cohesive group functioning.

The best approach to individual doctors not feeling bound by the group’s decisions is complex and will vary depending on the situation. But it can be mitigated by ensuring that the group has a clear governance structure and method for reaching controversial decisions.

The best approach to individual doctors not feeling bound by the group’s decisions is complex and will vary depending on the situation. But it can be mitigated by ensuring that the group has a clear governance structure and method for reaching controversial decisions.

Group Size Matters

A look at hospitalist groups of varying sizes illustrates the growing complexity of decision-making processes.

Small groups (eight or fewer individuals): Hospitalist groups nearly always start with a small number of doctors (often between one and three at the group’s inception) and find little need for a formal governance structure. They tend to make all important decisions based on consensus.

One risk of making decisions by consensus is that the group may be limited by the lowest common denominator. Even if most doctors in the group want to change something to avoid disadvantaging a doctor with a different point of view, the group may be held back and not make the change. In essence, the group can be ruled by the minority. This may not happen often, and as long as the group keeps this risk in mind it is usually fine to operate on consensus.

Medium-size groups (nine-14): A group this size probably needs to acknowledge that it will be unable to reach consensus on a number of issues and will need a voting system. It can be uncomfortable to jump from a culture of consensus to one of majority rule because the latter means there will be winners and losers. A clear set of rules or bylaws can increase the likelihood that those on the losing end of the issue will comply with the majority.

Large groups (more than 14): A large group usuallys face more complex decisions and has a wider range of opinions. Meetings may drag on as an issue is debated and all members have their say.

For this reason, large groups should consider forming a small executive committee consisting of the group’s leader and several representatives elected by a vote of the whole group. This can be a much more efficient way for the group to reach decisions. The executive committee researches issues and forms recommendations for the whole group. For some issues it might be reasonable for the executive committee’s decisions to be final. For others, the decisions of the executive committee might be presented to the whole group as a recommendation and put to a vote of all members.

 

 

It is important for a group of any size to have a clearly designated leader to oversee its operations and meetings and represent the group to external constituents. It’s critical that all groups have a culture of physician ownership even if they are contractual employees of another entity, such as the hospital.

It is best if the leader is not viewed as a boss others work for. That will lead to an employee—not an owner—mentality on the part of the others. TH

Dr. Nelson has been a practicing hospitalist since 1988 and is co-founder and past president of SHM. He is a principal in Nelson/Flores Associates, a national hospitalist practice management consulting firm. He also on the faculty of SHM’s “Best Practices in Managing a Hospital Medicine Program.” This column represents his views and is not intended to reflect an official position of SHM.

AN EXAMPLE

By laws must be customized for each group; here’s one example of how such rules can look. They establish how the group can decide important issues for which consensus can’t be reached.

In the case of hospitalists employed by a larger entity such as a hospital or multispecialty group, these rules are not meant to suggest the hospitalist practice can make decisions independently. As employees of the hospital, the group must seek approval from the hospital and the practice medical director for all its policies and operations. However, there are many issues for which this approval can be anticipated, and the group will need a mechanism to establish how it will reach important decisions about them.

Regular Meetings

  • The whole hospitalist practice will meet monthly, or as required otherwise, to discuss and reach decisions on the group’s business; and
  • When possible, decisions will be reached by voice vote or consensus, but when these measures fail a vote (roll call or written) will be taken.

Who Can Vote

  • Any physician member of the group who works more than 0.6 of a full-time equivalent position and has been with the group for more than one year; and
  • All members are eligible to participate in discussions and make recommendations, but voting is limited to the above.

Majority Vote

  • A simple majority (more than 50%) represents a majority vote except as noted below; and
  • The medical director will have the authority to decide the outcome in cases of a tie vote that cannot be resolved with further discussion.

Quorum

  • Half of group members eligible to vote represents a quorum at any meeting.

Executive Committee

  • An executive committee made up of the practice medical director and three other voting member of the practice will meet monthly as required to address group issues and develop recommendations for consideration at the monthly meetings of the group as a whole;
  • The term of each executive committee member (other than the practice director) will be two years.

Issue
The Hospitalist - 2007(12)
Publications
Sections

How does your hospitalist group make decisions on important issues? There are many reasonable approaches. The best method will vary significantly depending on the group’s size and whether the doctors own their own private practice or are employees of a hospital or large multisite private hospitalist group.

Because many doctors are drawn to the profession in part seeking autonomy and independence, there is often a tension between their desire to make many decisions about business and practice operations independently and the need to set aside some personal interests in order for the group to function well. This can become apparent when the group reaches an agreement regarding a difficult issue for which there are different points of view.

Consider a hospitalist group made up of internists occasionally asked to admit teenagers younger than 17. There might be a variety of opinions about whether this is appropriate, but it will be best for everyone in the group to follow the same policy. If the majority decision is that it is reasonable to admit patients as long as they’re post-pubertal, everyone in the group should abide by this policy.

But when called by the emergency department about such a patient, a dissenting hospitalist might feel entitled to decline the admission despite the group’s decision. For this doctor, autonomy trumps cohesive group functioning.

The best approach to individual doctors not feeling bound by the group’s decisions is complex and will vary depending on the situation. But it can be mitigated by ensuring that the group has a clear governance structure and method for reaching controversial decisions.

The best approach to individual doctors not feeling bound by the group’s decisions is complex and will vary depending on the situation. But it can be mitigated by ensuring that the group has a clear governance structure and method for reaching controversial decisions.

Group Size Matters

A look at hospitalist groups of varying sizes illustrates the growing complexity of decision-making processes.

Small groups (eight or fewer individuals): Hospitalist groups nearly always start with a small number of doctors (often between one and three at the group’s inception) and find little need for a formal governance structure. They tend to make all important decisions based on consensus.

One risk of making decisions by consensus is that the group may be limited by the lowest common denominator. Even if most doctors in the group want to change something to avoid disadvantaging a doctor with a different point of view, the group may be held back and not make the change. In essence, the group can be ruled by the minority. This may not happen often, and as long as the group keeps this risk in mind it is usually fine to operate on consensus.

Medium-size groups (nine-14): A group this size probably needs to acknowledge that it will be unable to reach consensus on a number of issues and will need a voting system. It can be uncomfortable to jump from a culture of consensus to one of majority rule because the latter means there will be winners and losers. A clear set of rules or bylaws can increase the likelihood that those on the losing end of the issue will comply with the majority.

Large groups (more than 14): A large group usuallys face more complex decisions and has a wider range of opinions. Meetings may drag on as an issue is debated and all members have their say.

For this reason, large groups should consider forming a small executive committee consisting of the group’s leader and several representatives elected by a vote of the whole group. This can be a much more efficient way for the group to reach decisions. The executive committee researches issues and forms recommendations for the whole group. For some issues it might be reasonable for the executive committee’s decisions to be final. For others, the decisions of the executive committee might be presented to the whole group as a recommendation and put to a vote of all members.

 

 

It is important for a group of any size to have a clearly designated leader to oversee its operations and meetings and represent the group to external constituents. It’s critical that all groups have a culture of physician ownership even if they are contractual employees of another entity, such as the hospital.

It is best if the leader is not viewed as a boss others work for. That will lead to an employee—not an owner—mentality on the part of the others. TH

Dr. Nelson has been a practicing hospitalist since 1988 and is co-founder and past president of SHM. He is a principal in Nelson/Flores Associates, a national hospitalist practice management consulting firm. He also on the faculty of SHM’s “Best Practices in Managing a Hospital Medicine Program.” This column represents his views and is not intended to reflect an official position of SHM.

AN EXAMPLE

By laws must be customized for each group; here’s one example of how such rules can look. They establish how the group can decide important issues for which consensus can’t be reached.

In the case of hospitalists employed by a larger entity such as a hospital or multispecialty group, these rules are not meant to suggest the hospitalist practice can make decisions independently. As employees of the hospital, the group must seek approval from the hospital and the practice medical director for all its policies and operations. However, there are many issues for which this approval can be anticipated, and the group will need a mechanism to establish how it will reach important decisions about them.

Regular Meetings

  • The whole hospitalist practice will meet monthly, or as required otherwise, to discuss and reach decisions on the group’s business; and
  • When possible, decisions will be reached by voice vote or consensus, but when these measures fail a vote (roll call or written) will be taken.

Who Can Vote

  • Any physician member of the group who works more than 0.6 of a full-time equivalent position and has been with the group for more than one year; and
  • All members are eligible to participate in discussions and make recommendations, but voting is limited to the above.

Majority Vote

  • A simple majority (more than 50%) represents a majority vote except as noted below; and
  • The medical director will have the authority to decide the outcome in cases of a tie vote that cannot be resolved with further discussion.

Quorum

  • Half of group members eligible to vote represents a quorum at any meeting.

Executive Committee

  • An executive committee made up of the practice medical director and three other voting member of the practice will meet monthly as required to address group issues and develop recommendations for consideration at the monthly meetings of the group as a whole;
  • The term of each executive committee member (other than the practice director) will be two years.

How does your hospitalist group make decisions on important issues? There are many reasonable approaches. The best method will vary significantly depending on the group’s size and whether the doctors own their own private practice or are employees of a hospital or large multisite private hospitalist group.

Because many doctors are drawn to the profession in part seeking autonomy and independence, there is often a tension between their desire to make many decisions about business and practice operations independently and the need to set aside some personal interests in order for the group to function well. This can become apparent when the group reaches an agreement regarding a difficult issue for which there are different points of view.

Consider a hospitalist group made up of internists occasionally asked to admit teenagers younger than 17. There might be a variety of opinions about whether this is appropriate, but it will be best for everyone in the group to follow the same policy. If the majority decision is that it is reasonable to admit patients as long as they’re post-pubertal, everyone in the group should abide by this policy.

But when called by the emergency department about such a patient, a dissenting hospitalist might feel entitled to decline the admission despite the group’s decision. For this doctor, autonomy trumps cohesive group functioning.

The best approach to individual doctors not feeling bound by the group’s decisions is complex and will vary depending on the situation. But it can be mitigated by ensuring that the group has a clear governance structure and method for reaching controversial decisions.

The best approach to individual doctors not feeling bound by the group’s decisions is complex and will vary depending on the situation. But it can be mitigated by ensuring that the group has a clear governance structure and method for reaching controversial decisions.

Group Size Matters

A look at hospitalist groups of varying sizes illustrates the growing complexity of decision-making processes.

Small groups (eight or fewer individuals): Hospitalist groups nearly always start with a small number of doctors (often between one and three at the group’s inception) and find little need for a formal governance structure. They tend to make all important decisions based on consensus.

One risk of making decisions by consensus is that the group may be limited by the lowest common denominator. Even if most doctors in the group want to change something to avoid disadvantaging a doctor with a different point of view, the group may be held back and not make the change. In essence, the group can be ruled by the minority. This may not happen often, and as long as the group keeps this risk in mind it is usually fine to operate on consensus.

Medium-size groups (nine-14): A group this size probably needs to acknowledge that it will be unable to reach consensus on a number of issues and will need a voting system. It can be uncomfortable to jump from a culture of consensus to one of majority rule because the latter means there will be winners and losers. A clear set of rules or bylaws can increase the likelihood that those on the losing end of the issue will comply with the majority.

Large groups (more than 14): A large group usuallys face more complex decisions and has a wider range of opinions. Meetings may drag on as an issue is debated and all members have their say.

For this reason, large groups should consider forming a small executive committee consisting of the group’s leader and several representatives elected by a vote of the whole group. This can be a much more efficient way for the group to reach decisions. The executive committee researches issues and forms recommendations for the whole group. For some issues it might be reasonable for the executive committee’s decisions to be final. For others, the decisions of the executive committee might be presented to the whole group as a recommendation and put to a vote of all members.

 

 

It is important for a group of any size to have a clearly designated leader to oversee its operations and meetings and represent the group to external constituents. It’s critical that all groups have a culture of physician ownership even if they are contractual employees of another entity, such as the hospital.

It is best if the leader is not viewed as a boss others work for. That will lead to an employee—not an owner—mentality on the part of the others. TH

Dr. Nelson has been a practicing hospitalist since 1988 and is co-founder and past president of SHM. He is a principal in Nelson/Flores Associates, a national hospitalist practice management consulting firm. He also on the faculty of SHM’s “Best Practices in Managing a Hospital Medicine Program.” This column represents his views and is not intended to reflect an official position of SHM.

AN EXAMPLE

By laws must be customized for each group; here’s one example of how such rules can look. They establish how the group can decide important issues for which consensus can’t be reached.

In the case of hospitalists employed by a larger entity such as a hospital or multispecialty group, these rules are not meant to suggest the hospitalist practice can make decisions independently. As employees of the hospital, the group must seek approval from the hospital and the practice medical director for all its policies and operations. However, there are many issues for which this approval can be anticipated, and the group will need a mechanism to establish how it will reach important decisions about them.

Regular Meetings

  • The whole hospitalist practice will meet monthly, or as required otherwise, to discuss and reach decisions on the group’s business; and
  • When possible, decisions will be reached by voice vote or consensus, but when these measures fail a vote (roll call or written) will be taken.

Who Can Vote

  • Any physician member of the group who works more than 0.6 of a full-time equivalent position and has been with the group for more than one year; and
  • All members are eligible to participate in discussions and make recommendations, but voting is limited to the above.

Majority Vote

  • A simple majority (more than 50%) represents a majority vote except as noted below; and
  • The medical director will have the authority to decide the outcome in cases of a tie vote that cannot be resolved with further discussion.

Quorum

  • Half of group members eligible to vote represents a quorum at any meeting.

Executive Committee

  • An executive committee made up of the practice medical director and three other voting member of the practice will meet monthly as required to address group issues and develop recommendations for consideration at the monthly meetings of the group as a whole;
  • The term of each executive committee member (other than the practice director) will be two years.

Issue
The Hospitalist - 2007(12)
Issue
The Hospitalist - 2007(12)
Publications
Publications
Article Type
Display Headline
Play by the Rules
Display Headline
Play by the Rules
Sections
Disallow All Ads
Content Gating
No Gating (article Unlocked/Free)

Hours to Expertise

Article Type
Changed
Display Headline
Hours to Expertise

Glass of wine in one hand and the Sept. 30 copy of Wine Spectator in the other, I intended to relax a bit—the future of hospital medicine not necessarily uppermost in my mind. But then I was struck by an article by Matt Kramer titled “10,000 hours.” In it he discusses the implications Daniel Levitin’s new book This Is Your Brain on Music: The Science of a Human Obsession (Dutton) may have for the field of wine tasting.

Levitin notes that “ten thousand hours of practice is required to achieve the level of mastery associated with being a world-class expert—in anything.” It turns out it doesn’t matter what you are trying to master.

“In study after study of composers, basketball players, fiction writers, ice skaters, concert pianists, chess players, master criminals, and what have you, this number comes up again and again,” he says. “No one has yet found a case in which true world-class expertise was accomplished in less time.” This is consistent with how we learn. “Learning requires the assimilation and consolidation of information in neural tissue,” writes Levitin. “The more experiences we have with something the stronger the memory/learning trace for the experience becomes.”

Ten thousand hours. Are you an expert in hospital medicine? Have you compiled the requisite 10,000 hours? The average hospitalist working approximately 200 shifts a year of 10 to 12 hours each would take four to five years to master the practice of hospital medicine. On the other hand, a provider spending 10 hours a week in the hospital would require 20 years to achieve the numeric equivalent of expert status.

While Levitin was discussing the impact of this calculation on music and Kramer on wine expertise, it struck me as applicable to one of the great debates surrounding hospital medicine. Early in the days of the hospitalist movement, many inside and outside the field opined as to whether hospitals should be the domain of hospitalists and clinics the domain of primary care doctors, without overlap. SHM and I proclaimed hospitals should be open to all providers, regardless of primary practice site.

Over time the argument has died down as the threat of a hospitalist takeover has given way to the realization that many primary care doctors prefer a practice without inpatient obligations.

Recently the American Board of Internal Medicine (ABIM) has decided to move forward with a Recognition of Focused Practice in hospital medicine (RFP-HM) certification. This designation will utilize the structure of the ABIM Maintenance of Certification (MOC) program. It will be available to those who have practiced hospital medicine at least three years, meet inpatient volume requirements, and successfully complete hospital medicine-specific Self-Evaluation Process (SEP) modules, Practice Improvement Modules (PIM) and a secure exam.

In a healthcare system at best strained and by most evidence severely fractured, we can no longer accept competence as the determinant of a capable provider. Rather, we should use proficiency moving toward expertise as the measuring stick for caring for increasingly more complex patients.

This has again raised concerns about the growth and direction of hospital medicine and the implications for internal medicine. Would this confer specialty status to hospitalists while leaving primary care doctors as the remaining generalists? Would this further fracture the field of internal medicine? Would this allow hospital-credentialing boards to preferentially allow only those with RFP-HM to practice within their walls, effectively outlawing the primary care doctor?

Having been a member of the task force that worked on RFP-HM, I can say emphatically that it is not intended to confer specialty status to hospitalists or exalt them above other general internists. Rather, it is meant to recognize that a practitioner has focused his or her practice in a manner that demonstrates greater proficiency in the practice of hospital medicine. While this denotes a presumably higher level of proficiency by RFP-HM providers, it does not mean those without it are not capable providers.

 

 

How then should we define who is a capable provider in the hospital setting? According to the Dreyfus Model of Skills Acquisition, as learners develop along the continuum from novice to beginner to competent to proficient to expert, their skills become more developed, letting them tackle more complex issues and tasks more efficiently.

For example, the novice knows that a patient with dyspnea might have pneumonia and orders a chest X-ray but little more. The competent provider realizes many other disease states can cause dyspnea and would assess for those as well, often getting bogged down in extraneous details. The proficient provider immediately focuses on the important details and determines pneumonia as the cause of the dyspnea, applying the proper treatment algorithms with a level of efficiency beyond that of the competent peer.

The expert intuitively diagnoses the pneumonia and prescribes the proper diagnostic and therapeutic evaluation. He does so while considering the patient’s immune status, the impact of the hospital’s antimicrobial resistance patterns, and the potential risks and benefits of short-course antimicrobial therapy—all through the prism of quality core measures, cost, and throughput.

In a healthcare system at best strained and by most evidence severely fractured, we can no longer accept competence as the determinant of a capable provider. Rather, we should use proficiency moving toward expertise as the measuring stick for caring for increasingly more complex patients.

The designation “hospitalist” or even RFP-HM should not determine if one is proficient to practice hospital medicine, just as the designation of primary care provider should not exclude one from practicing in the hospital. Certainly, there are practitioners able to seamlessly cross the inpatient/outpatient boundary without losing a step. However, I suspect the more likely scenario is expertise in one and at best proficiency in the other.

Levitin’s 10,000-hour threshold supports this assumption, as it would take at least 10 years to amass 10,000 hours in each practice setting. Most likely, development of expertise in one arena means mere competence in another. As exhibit A, I tremble at the thought of the mischief I would cause if I took my stethoscope to the primary care clinic.

Instead, the ethical standards of our profession should dictate that each provider determines if they meet this pursuit-of-expertise standard. Employers and credentialing boards need to raise the bar toward expertise, ensuring these thresholds are met.

In the end, hospital or clinic sites should be the domain of capable providers, regardless of their primary practice site. However, we need to recalibrate how we define a capable provider who is moving away from competence toward proficiency verging on expertise. Experience as a surrogate for expertise, more than primary practice setting or RFP-HM status, should be the major determinant for who cares for hospitalized patients. TH

Dr. Glasheen is associate professor of medicine at the University of Colorado at Denver, where he serves as director of the Hospital Medicine Program and the Hospitalist Training Program, and as associate program director of the Internal Medicine Residency Program.

Issue
The Hospitalist - 2007(12)
Publications
Sections

Glass of wine in one hand and the Sept. 30 copy of Wine Spectator in the other, I intended to relax a bit—the future of hospital medicine not necessarily uppermost in my mind. But then I was struck by an article by Matt Kramer titled “10,000 hours.” In it he discusses the implications Daniel Levitin’s new book This Is Your Brain on Music: The Science of a Human Obsession (Dutton) may have for the field of wine tasting.

Levitin notes that “ten thousand hours of practice is required to achieve the level of mastery associated with being a world-class expert—in anything.” It turns out it doesn’t matter what you are trying to master.

“In study after study of composers, basketball players, fiction writers, ice skaters, concert pianists, chess players, master criminals, and what have you, this number comes up again and again,” he says. “No one has yet found a case in which true world-class expertise was accomplished in less time.” This is consistent with how we learn. “Learning requires the assimilation and consolidation of information in neural tissue,” writes Levitin. “The more experiences we have with something the stronger the memory/learning trace for the experience becomes.”

Ten thousand hours. Are you an expert in hospital medicine? Have you compiled the requisite 10,000 hours? The average hospitalist working approximately 200 shifts a year of 10 to 12 hours each would take four to five years to master the practice of hospital medicine. On the other hand, a provider spending 10 hours a week in the hospital would require 20 years to achieve the numeric equivalent of expert status.

While Levitin was discussing the impact of this calculation on music and Kramer on wine expertise, it struck me as applicable to one of the great debates surrounding hospital medicine. Early in the days of the hospitalist movement, many inside and outside the field opined as to whether hospitals should be the domain of hospitalists and clinics the domain of primary care doctors, without overlap. SHM and I proclaimed hospitals should be open to all providers, regardless of primary practice site.

Over time the argument has died down as the threat of a hospitalist takeover has given way to the realization that many primary care doctors prefer a practice without inpatient obligations.

Recently the American Board of Internal Medicine (ABIM) has decided to move forward with a Recognition of Focused Practice in hospital medicine (RFP-HM) certification. This designation will utilize the structure of the ABIM Maintenance of Certification (MOC) program. It will be available to those who have practiced hospital medicine at least three years, meet inpatient volume requirements, and successfully complete hospital medicine-specific Self-Evaluation Process (SEP) modules, Practice Improvement Modules (PIM) and a secure exam.

In a healthcare system at best strained and by most evidence severely fractured, we can no longer accept competence as the determinant of a capable provider. Rather, we should use proficiency moving toward expertise as the measuring stick for caring for increasingly more complex patients.

This has again raised concerns about the growth and direction of hospital medicine and the implications for internal medicine. Would this confer specialty status to hospitalists while leaving primary care doctors as the remaining generalists? Would this further fracture the field of internal medicine? Would this allow hospital-credentialing boards to preferentially allow only those with RFP-HM to practice within their walls, effectively outlawing the primary care doctor?

Having been a member of the task force that worked on RFP-HM, I can say emphatically that it is not intended to confer specialty status to hospitalists or exalt them above other general internists. Rather, it is meant to recognize that a practitioner has focused his or her practice in a manner that demonstrates greater proficiency in the practice of hospital medicine. While this denotes a presumably higher level of proficiency by RFP-HM providers, it does not mean those without it are not capable providers.

 

 

How then should we define who is a capable provider in the hospital setting? According to the Dreyfus Model of Skills Acquisition, as learners develop along the continuum from novice to beginner to competent to proficient to expert, their skills become more developed, letting them tackle more complex issues and tasks more efficiently.

For example, the novice knows that a patient with dyspnea might have pneumonia and orders a chest X-ray but little more. The competent provider realizes many other disease states can cause dyspnea and would assess for those as well, often getting bogged down in extraneous details. The proficient provider immediately focuses on the important details and determines pneumonia as the cause of the dyspnea, applying the proper treatment algorithms with a level of efficiency beyond that of the competent peer.

The expert intuitively diagnoses the pneumonia and prescribes the proper diagnostic and therapeutic evaluation. He does so while considering the patient’s immune status, the impact of the hospital’s antimicrobial resistance patterns, and the potential risks and benefits of short-course antimicrobial therapy—all through the prism of quality core measures, cost, and throughput.

In a healthcare system at best strained and by most evidence severely fractured, we can no longer accept competence as the determinant of a capable provider. Rather, we should use proficiency moving toward expertise as the measuring stick for caring for increasingly more complex patients.

The designation “hospitalist” or even RFP-HM should not determine if one is proficient to practice hospital medicine, just as the designation of primary care provider should not exclude one from practicing in the hospital. Certainly, there are practitioners able to seamlessly cross the inpatient/outpatient boundary without losing a step. However, I suspect the more likely scenario is expertise in one and at best proficiency in the other.

Levitin’s 10,000-hour threshold supports this assumption, as it would take at least 10 years to amass 10,000 hours in each practice setting. Most likely, development of expertise in one arena means mere competence in another. As exhibit A, I tremble at the thought of the mischief I would cause if I took my stethoscope to the primary care clinic.

Instead, the ethical standards of our profession should dictate that each provider determines if they meet this pursuit-of-expertise standard. Employers and credentialing boards need to raise the bar toward expertise, ensuring these thresholds are met.

In the end, hospital or clinic sites should be the domain of capable providers, regardless of their primary practice site. However, we need to recalibrate how we define a capable provider who is moving away from competence toward proficiency verging on expertise. Experience as a surrogate for expertise, more than primary practice setting or RFP-HM status, should be the major determinant for who cares for hospitalized patients. TH

Dr. Glasheen is associate professor of medicine at the University of Colorado at Denver, where he serves as director of the Hospital Medicine Program and the Hospitalist Training Program, and as associate program director of the Internal Medicine Residency Program.

Glass of wine in one hand and the Sept. 30 copy of Wine Spectator in the other, I intended to relax a bit—the future of hospital medicine not necessarily uppermost in my mind. But then I was struck by an article by Matt Kramer titled “10,000 hours.” In it he discusses the implications Daniel Levitin’s new book This Is Your Brain on Music: The Science of a Human Obsession (Dutton) may have for the field of wine tasting.

Levitin notes that “ten thousand hours of practice is required to achieve the level of mastery associated with being a world-class expert—in anything.” It turns out it doesn’t matter what you are trying to master.

“In study after study of composers, basketball players, fiction writers, ice skaters, concert pianists, chess players, master criminals, and what have you, this number comes up again and again,” he says. “No one has yet found a case in which true world-class expertise was accomplished in less time.” This is consistent with how we learn. “Learning requires the assimilation and consolidation of information in neural tissue,” writes Levitin. “The more experiences we have with something the stronger the memory/learning trace for the experience becomes.”

Ten thousand hours. Are you an expert in hospital medicine? Have you compiled the requisite 10,000 hours? The average hospitalist working approximately 200 shifts a year of 10 to 12 hours each would take four to five years to master the practice of hospital medicine. On the other hand, a provider spending 10 hours a week in the hospital would require 20 years to achieve the numeric equivalent of expert status.

While Levitin was discussing the impact of this calculation on music and Kramer on wine expertise, it struck me as applicable to one of the great debates surrounding hospital medicine. Early in the days of the hospitalist movement, many inside and outside the field opined as to whether hospitals should be the domain of hospitalists and clinics the domain of primary care doctors, without overlap. SHM and I proclaimed hospitals should be open to all providers, regardless of primary practice site.

Over time the argument has died down as the threat of a hospitalist takeover has given way to the realization that many primary care doctors prefer a practice without inpatient obligations.

Recently the American Board of Internal Medicine (ABIM) has decided to move forward with a Recognition of Focused Practice in hospital medicine (RFP-HM) certification. This designation will utilize the structure of the ABIM Maintenance of Certification (MOC) program. It will be available to those who have practiced hospital medicine at least three years, meet inpatient volume requirements, and successfully complete hospital medicine-specific Self-Evaluation Process (SEP) modules, Practice Improvement Modules (PIM) and a secure exam.

In a healthcare system at best strained and by most evidence severely fractured, we can no longer accept competence as the determinant of a capable provider. Rather, we should use proficiency moving toward expertise as the measuring stick for caring for increasingly more complex patients.

This has again raised concerns about the growth and direction of hospital medicine and the implications for internal medicine. Would this confer specialty status to hospitalists while leaving primary care doctors as the remaining generalists? Would this further fracture the field of internal medicine? Would this allow hospital-credentialing boards to preferentially allow only those with RFP-HM to practice within their walls, effectively outlawing the primary care doctor?

Having been a member of the task force that worked on RFP-HM, I can say emphatically that it is not intended to confer specialty status to hospitalists or exalt them above other general internists. Rather, it is meant to recognize that a practitioner has focused his or her practice in a manner that demonstrates greater proficiency in the practice of hospital medicine. While this denotes a presumably higher level of proficiency by RFP-HM providers, it does not mean those without it are not capable providers.

 

 

How then should we define who is a capable provider in the hospital setting? According to the Dreyfus Model of Skills Acquisition, as learners develop along the continuum from novice to beginner to competent to proficient to expert, their skills become more developed, letting them tackle more complex issues and tasks more efficiently.

For example, the novice knows that a patient with dyspnea might have pneumonia and orders a chest X-ray but little more. The competent provider realizes many other disease states can cause dyspnea and would assess for those as well, often getting bogged down in extraneous details. The proficient provider immediately focuses on the important details and determines pneumonia as the cause of the dyspnea, applying the proper treatment algorithms with a level of efficiency beyond that of the competent peer.

The expert intuitively diagnoses the pneumonia and prescribes the proper diagnostic and therapeutic evaluation. He does so while considering the patient’s immune status, the impact of the hospital’s antimicrobial resistance patterns, and the potential risks and benefits of short-course antimicrobial therapy—all through the prism of quality core measures, cost, and throughput.

In a healthcare system at best strained and by most evidence severely fractured, we can no longer accept competence as the determinant of a capable provider. Rather, we should use proficiency moving toward expertise as the measuring stick for caring for increasingly more complex patients.

The designation “hospitalist” or even RFP-HM should not determine if one is proficient to practice hospital medicine, just as the designation of primary care provider should not exclude one from practicing in the hospital. Certainly, there are practitioners able to seamlessly cross the inpatient/outpatient boundary without losing a step. However, I suspect the more likely scenario is expertise in one and at best proficiency in the other.

Levitin’s 10,000-hour threshold supports this assumption, as it would take at least 10 years to amass 10,000 hours in each practice setting. Most likely, development of expertise in one arena means mere competence in another. As exhibit A, I tremble at the thought of the mischief I would cause if I took my stethoscope to the primary care clinic.

Instead, the ethical standards of our profession should dictate that each provider determines if they meet this pursuit-of-expertise standard. Employers and credentialing boards need to raise the bar toward expertise, ensuring these thresholds are met.

In the end, hospital or clinic sites should be the domain of capable providers, regardless of their primary practice site. However, we need to recalibrate how we define a capable provider who is moving away from competence toward proficiency verging on expertise. Experience as a surrogate for expertise, more than primary practice setting or RFP-HM status, should be the major determinant for who cares for hospitalized patients. TH

Dr. Glasheen is associate professor of medicine at the University of Colorado at Denver, where he serves as director of the Hospital Medicine Program and the Hospitalist Training Program, and as associate program director of the Internal Medicine Residency Program.

Issue
The Hospitalist - 2007(12)
Issue
The Hospitalist - 2007(12)
Publications
Publications
Article Type
Display Headline
Hours to Expertise
Display Headline
Hours to Expertise
Sections
Disallow All Ads
Content Gating
No Gating (article Unlocked/Free)

A Year of Progress

Article Type
Changed
Display Headline
A Year of Progress

It’s hard to believe eight years have gone by since I came to SHM. More than that, it is strange to think of a world without hospitalists. Hospital medicine is part of the fabric of healthcare; there’s no longer a debate over whether hospitalists are good or bad. Now, the talk is about how hospitalists can help solve so many of the ills that vex our healthcare system.

This year has been an extraordinary year even by SHM standards. Witness our progress in the following areas.

ABIM Progress

In a landmark and revolutionary decision, the American Board of Internal Medicine (ABIM) recommended proceeding with a recognition of focused practice (RFP) in hospital medicine as an option in its maintenance of certification (MOC).

This is the culmination of a strategy SHM laid out three years ago. SHM is working with ABIM to continue to make the MOC process meaningful to hospitalists as the ABIM recommendations wend their way through the American Board of Medical Specialties. SHM continues to reach out to the pediatric and family medicine boards so the RFP can be available to all hospitalists.

JHM Listed

In its first year of publication, the Journal of Hospital Medicine (JHM) has been included in PubMed, the National Institutes of Health online archive of life science journals. JHM now resides among other established journals, fielding a marked increased in submissions for publication.

In a landmark and revolutionary decision, the American Board of Internal Medicine recommended proceeding with a recognition of focused practice in hospital medicine as an option in its maintenance of certification. This is the culmination of a strategy SHM laid out three years ago.

Quality

SHM received its third consecutive grant from the John A. Hartford Foundation, this one for $1.4 million over three years to develop interventions to improve care transitions for older adults at discharge.

As part of our work to improve quality for our nation’s seniors, SHM is developing discharge-planning tools and implementation strategies to limit the voltage drop in care at discharge. Hartford’s support means funders see that hospitalists, with SHM support, improve quality at their hospitals. SHM has become a leader in discharge planning tools and is helping set standards for transitions of care.

To help give hospitalists tools and resources to effect change on the front lines, SHM continues to develop online resource rooms and unique strategies such as mentored implementation.

We also have several hospitalist leaders on key panels at the National Quality Forum (NQF). The American Medical Association’s Physician Consortium on Practice Improvement has asked SHM to take the lead in forming a coalition for setting transitions-of-care measurements.

When the Institute for Healthcare Improvement needed a physician group to join the announcement of its 5 Million Lives Campaign, it reached out to SHM. President Rusty Holman took the stage to support the initiative, which intends to protect 5 million patients from incidents of medical harm over the next two years.

Further, the Joint Commission on Accreditation of Healthcare Organ­izations asked SHM to co-sponsor its medication reconciliation workgroup. Lastly, SHM continues to get significant visibility for hospitalists with our leadership of the deep-vein thrombosis awareness coalition of more than 35 organizations.

Annual Meeting

In May, SHM took over the Gaylord Texan in Dallas with professional meeting staging that rivaled older, larger organizations. With banners, Jumbotrons, and devices projecting the SHM logo, we transformed the Gaylord into a “hospitalist city.” We treated the nearly 1,200 attendees to three superlative speakers:

  • David Brailer, MD, national coordinator for health information technology, United States Department of Health and Human Services;
  • Jonathan Perlin, MD, former undersecretary for health at the Veterans Health Administration and now chief medical officer and senior vice president of quality for Hospital Corporation of America in Nashville; and
  • Bob Wachter, MD, professor and chief of the division of hospital medicine at the University of California, San Francisco.
 

 

And, we had our largest poster session ever, with more than 200 submissions, and our largest exhibit hall. We plan to take it up a notch in San Diego in April.

Advocacy and Policy

Our presence in Washington, D.C., allows us to be active in Medicare payment reform. SHM leadership has met with senior staff at MedPAC, the organization that makes recommendations to the Centers for Medicare and Medicaid Services and Congress. MedPAC is interested in working with SHM as Medicare attempts to move away from paying for just visits and procedures and toward reimbursement strategies that drive performance and efficiency.

Current, Future Initiatives

In June, SHM forged a partnership with the Society of General Internal Medicine (SGIM) and the Association of Chiefs of General Internal Medicine to hold an academic summit to develop strategies for academic hospitalists to have a strong and sustainable career in teaching, training, and research in hospital medicine. When the Alliance for Academic Internal Medicine developed its proposal to redesign internal medicine training, SHM took the lead in crafting the hospitalist response.

In July, we joined the SGIM and American College of Physicians to hold a consensus conference on transitions of care. This coalition of more than 25 organizations produced a statement as the basis for future standards and measurements. Also in July, SHM worked with key leaders in emergency medicine and others to redefine the management and opportunities in observation units.

We held a multidisciplinary workforce summit in November to examine the challenges and solutions in growing hospital medicine from 20,000 to 40,000 or more physicians.

Diversity

While at times we may seem to focus more on internal-medicine-trained hospitalists, who make up more than 80% of the field, SHM continues to include hospitalists in family medicine and pediatrics, among other specialties. We also are home to nonphysician providers and physician assistants. We are working to support academic hospitalists, small groups, and multistate companies. In our toughest tightrope walk, SHM continues to be relevant and supportive of labor and management in hospital medicine.

Looking to 2008

The growth and influence of hospital medicine is relentless. Maybe 2008 is the year we will see hospitalists practicing in more than 3,000 hospitals or see the specialty grow to more than 25,000 hospitalists. One thing is for sure: SHM, with your suggestions, ideas, and energy, will be on the front lines with you, supporting and advocating a better healthcare system. TH

Dr. Wellikson is CEO of SHM.

Issue
The Hospitalist - 2007(12)
Publications
Sections

It’s hard to believe eight years have gone by since I came to SHM. More than that, it is strange to think of a world without hospitalists. Hospital medicine is part of the fabric of healthcare; there’s no longer a debate over whether hospitalists are good or bad. Now, the talk is about how hospitalists can help solve so many of the ills that vex our healthcare system.

This year has been an extraordinary year even by SHM standards. Witness our progress in the following areas.

ABIM Progress

In a landmark and revolutionary decision, the American Board of Internal Medicine (ABIM) recommended proceeding with a recognition of focused practice (RFP) in hospital medicine as an option in its maintenance of certification (MOC).

This is the culmination of a strategy SHM laid out three years ago. SHM is working with ABIM to continue to make the MOC process meaningful to hospitalists as the ABIM recommendations wend their way through the American Board of Medical Specialties. SHM continues to reach out to the pediatric and family medicine boards so the RFP can be available to all hospitalists.

JHM Listed

In its first year of publication, the Journal of Hospital Medicine (JHM) has been included in PubMed, the National Institutes of Health online archive of life science journals. JHM now resides among other established journals, fielding a marked increased in submissions for publication.

In a landmark and revolutionary decision, the American Board of Internal Medicine recommended proceeding with a recognition of focused practice in hospital medicine as an option in its maintenance of certification. This is the culmination of a strategy SHM laid out three years ago.

Quality

SHM received its third consecutive grant from the John A. Hartford Foundation, this one for $1.4 million over three years to develop interventions to improve care transitions for older adults at discharge.

As part of our work to improve quality for our nation’s seniors, SHM is developing discharge-planning tools and implementation strategies to limit the voltage drop in care at discharge. Hartford’s support means funders see that hospitalists, with SHM support, improve quality at their hospitals. SHM has become a leader in discharge planning tools and is helping set standards for transitions of care.

To help give hospitalists tools and resources to effect change on the front lines, SHM continues to develop online resource rooms and unique strategies such as mentored implementation.

We also have several hospitalist leaders on key panels at the National Quality Forum (NQF). The American Medical Association’s Physician Consortium on Practice Improvement has asked SHM to take the lead in forming a coalition for setting transitions-of-care measurements.

When the Institute for Healthcare Improvement needed a physician group to join the announcement of its 5 Million Lives Campaign, it reached out to SHM. President Rusty Holman took the stage to support the initiative, which intends to protect 5 million patients from incidents of medical harm over the next two years.

Further, the Joint Commission on Accreditation of Healthcare Organ­izations asked SHM to co-sponsor its medication reconciliation workgroup. Lastly, SHM continues to get significant visibility for hospitalists with our leadership of the deep-vein thrombosis awareness coalition of more than 35 organizations.

Annual Meeting

In May, SHM took over the Gaylord Texan in Dallas with professional meeting staging that rivaled older, larger organizations. With banners, Jumbotrons, and devices projecting the SHM logo, we transformed the Gaylord into a “hospitalist city.” We treated the nearly 1,200 attendees to three superlative speakers:

  • David Brailer, MD, national coordinator for health information technology, United States Department of Health and Human Services;
  • Jonathan Perlin, MD, former undersecretary for health at the Veterans Health Administration and now chief medical officer and senior vice president of quality for Hospital Corporation of America in Nashville; and
  • Bob Wachter, MD, professor and chief of the division of hospital medicine at the University of California, San Francisco.
 

 

And, we had our largest poster session ever, with more than 200 submissions, and our largest exhibit hall. We plan to take it up a notch in San Diego in April.

Advocacy and Policy

Our presence in Washington, D.C., allows us to be active in Medicare payment reform. SHM leadership has met with senior staff at MedPAC, the organization that makes recommendations to the Centers for Medicare and Medicaid Services and Congress. MedPAC is interested in working with SHM as Medicare attempts to move away from paying for just visits and procedures and toward reimbursement strategies that drive performance and efficiency.

Current, Future Initiatives

In June, SHM forged a partnership with the Society of General Internal Medicine (SGIM) and the Association of Chiefs of General Internal Medicine to hold an academic summit to develop strategies for academic hospitalists to have a strong and sustainable career in teaching, training, and research in hospital medicine. When the Alliance for Academic Internal Medicine developed its proposal to redesign internal medicine training, SHM took the lead in crafting the hospitalist response.

In July, we joined the SGIM and American College of Physicians to hold a consensus conference on transitions of care. This coalition of more than 25 organizations produced a statement as the basis for future standards and measurements. Also in July, SHM worked with key leaders in emergency medicine and others to redefine the management and opportunities in observation units.

We held a multidisciplinary workforce summit in November to examine the challenges and solutions in growing hospital medicine from 20,000 to 40,000 or more physicians.

Diversity

While at times we may seem to focus more on internal-medicine-trained hospitalists, who make up more than 80% of the field, SHM continues to include hospitalists in family medicine and pediatrics, among other specialties. We also are home to nonphysician providers and physician assistants. We are working to support academic hospitalists, small groups, and multistate companies. In our toughest tightrope walk, SHM continues to be relevant and supportive of labor and management in hospital medicine.

Looking to 2008

The growth and influence of hospital medicine is relentless. Maybe 2008 is the year we will see hospitalists practicing in more than 3,000 hospitals or see the specialty grow to more than 25,000 hospitalists. One thing is for sure: SHM, with your suggestions, ideas, and energy, will be on the front lines with you, supporting and advocating a better healthcare system. TH

Dr. Wellikson is CEO of SHM.

It’s hard to believe eight years have gone by since I came to SHM. More than that, it is strange to think of a world without hospitalists. Hospital medicine is part of the fabric of healthcare; there’s no longer a debate over whether hospitalists are good or bad. Now, the talk is about how hospitalists can help solve so many of the ills that vex our healthcare system.

This year has been an extraordinary year even by SHM standards. Witness our progress in the following areas.

ABIM Progress

In a landmark and revolutionary decision, the American Board of Internal Medicine (ABIM) recommended proceeding with a recognition of focused practice (RFP) in hospital medicine as an option in its maintenance of certification (MOC).

This is the culmination of a strategy SHM laid out three years ago. SHM is working with ABIM to continue to make the MOC process meaningful to hospitalists as the ABIM recommendations wend their way through the American Board of Medical Specialties. SHM continues to reach out to the pediatric and family medicine boards so the RFP can be available to all hospitalists.

JHM Listed

In its first year of publication, the Journal of Hospital Medicine (JHM) has been included in PubMed, the National Institutes of Health online archive of life science journals. JHM now resides among other established journals, fielding a marked increased in submissions for publication.

In a landmark and revolutionary decision, the American Board of Internal Medicine recommended proceeding with a recognition of focused practice in hospital medicine as an option in its maintenance of certification. This is the culmination of a strategy SHM laid out three years ago.

Quality

SHM received its third consecutive grant from the John A. Hartford Foundation, this one for $1.4 million over three years to develop interventions to improve care transitions for older adults at discharge.

As part of our work to improve quality for our nation’s seniors, SHM is developing discharge-planning tools and implementation strategies to limit the voltage drop in care at discharge. Hartford’s support means funders see that hospitalists, with SHM support, improve quality at their hospitals. SHM has become a leader in discharge planning tools and is helping set standards for transitions of care.

To help give hospitalists tools and resources to effect change on the front lines, SHM continues to develop online resource rooms and unique strategies such as mentored implementation.

We also have several hospitalist leaders on key panels at the National Quality Forum (NQF). The American Medical Association’s Physician Consortium on Practice Improvement has asked SHM to take the lead in forming a coalition for setting transitions-of-care measurements.

When the Institute for Healthcare Improvement needed a physician group to join the announcement of its 5 Million Lives Campaign, it reached out to SHM. President Rusty Holman took the stage to support the initiative, which intends to protect 5 million patients from incidents of medical harm over the next two years.

Further, the Joint Commission on Accreditation of Healthcare Organ­izations asked SHM to co-sponsor its medication reconciliation workgroup. Lastly, SHM continues to get significant visibility for hospitalists with our leadership of the deep-vein thrombosis awareness coalition of more than 35 organizations.

Annual Meeting

In May, SHM took over the Gaylord Texan in Dallas with professional meeting staging that rivaled older, larger organizations. With banners, Jumbotrons, and devices projecting the SHM logo, we transformed the Gaylord into a “hospitalist city.” We treated the nearly 1,200 attendees to three superlative speakers:

  • David Brailer, MD, national coordinator for health information technology, United States Department of Health and Human Services;
  • Jonathan Perlin, MD, former undersecretary for health at the Veterans Health Administration and now chief medical officer and senior vice president of quality for Hospital Corporation of America in Nashville; and
  • Bob Wachter, MD, professor and chief of the division of hospital medicine at the University of California, San Francisco.
 

 

And, we had our largest poster session ever, with more than 200 submissions, and our largest exhibit hall. We plan to take it up a notch in San Diego in April.

Advocacy and Policy

Our presence in Washington, D.C., allows us to be active in Medicare payment reform. SHM leadership has met with senior staff at MedPAC, the organization that makes recommendations to the Centers for Medicare and Medicaid Services and Congress. MedPAC is interested in working with SHM as Medicare attempts to move away from paying for just visits and procedures and toward reimbursement strategies that drive performance and efficiency.

Current, Future Initiatives

In June, SHM forged a partnership with the Society of General Internal Medicine (SGIM) and the Association of Chiefs of General Internal Medicine to hold an academic summit to develop strategies for academic hospitalists to have a strong and sustainable career in teaching, training, and research in hospital medicine. When the Alliance for Academic Internal Medicine developed its proposal to redesign internal medicine training, SHM took the lead in crafting the hospitalist response.

In July, we joined the SGIM and American College of Physicians to hold a consensus conference on transitions of care. This coalition of more than 25 organizations produced a statement as the basis for future standards and measurements. Also in July, SHM worked with key leaders in emergency medicine and others to redefine the management and opportunities in observation units.

We held a multidisciplinary workforce summit in November to examine the challenges and solutions in growing hospital medicine from 20,000 to 40,000 or more physicians.

Diversity

While at times we may seem to focus more on internal-medicine-trained hospitalists, who make up more than 80% of the field, SHM continues to include hospitalists in family medicine and pediatrics, among other specialties. We also are home to nonphysician providers and physician assistants. We are working to support academic hospitalists, small groups, and multistate companies. In our toughest tightrope walk, SHM continues to be relevant and supportive of labor and management in hospital medicine.

Looking to 2008

The growth and influence of hospital medicine is relentless. Maybe 2008 is the year we will see hospitalists practicing in more than 3,000 hospitals or see the specialty grow to more than 25,000 hospitalists. One thing is for sure: SHM, with your suggestions, ideas, and energy, will be on the front lines with you, supporting and advocating a better healthcare system. TH

Dr. Wellikson is CEO of SHM.

Issue
The Hospitalist - 2007(12)
Issue
The Hospitalist - 2007(12)
Publications
Publications
Article Type
Display Headline
A Year of Progress
Display Headline
A Year of Progress
Sections
Disallow All Ads
Content Gating
No Gating (article Unlocked/Free)

Care & Prayer

Article Type
Changed
Display Headline
Care & Prayer

Charles Petit, MD, like many healthcare professionals, spends a good deal of time addressing the needs of the underprivileged. Since 2004, he has taken up the cause of the indigenous Miskito Indians of Puerto Lempira, Honduras. He is putting his own money into developing a modern clinic and international medicine program there.

But medicine isn’t his only mission. Dr. Petit, 56, a hospitalist at Palmetto Health Care’s Richland Memorial Hospital in Columbia, S.C., is also an Episcopal priest.

He joined Palmetto Health Senior Care as its first medical director in 1988 and reconnected with the group in 2004—not in his previous role as an office-based physician but as a hospitalist. In between those stints he pursued his ordination and medical missionary work in Africa and Latin America.

As a physician, Dr. Petit says he feels God’s presence at each patient’s bedside. Years ago he wondered how to handle that.

To deepen his connection between medicine and spirituality, he lived in a Christian intentional community in Indiana, Pa., from 1981 to 1988. Gradually, his views on medicine and spirituality crystallized.

“How does God do what he does?” Dr. Petit wondered. “Can medicine put Him to the test? I have seen that prayer works, including a patient miraculously healed of metastatic ovarian cancer. But God isn’t a vending machine. You don’t drop in a prayer and get a healing back.”

Charles Petit, MD, a hospitalist at Palmetto Health Care’s Richland Memorial Hospital in Columbia, S.C., earned a master’s in divinity in 2003.

The Second Calling

Recognizing he needed something more to integrate medicine and spirituality, Dr. Petit sought a firmer grounding in religious studies.

He moved to Simpsonville, S.C., in 1995 and entered the Episcopal seminary, working as an emergency department doctor to pay the bills. Later, he earned a master’s of divinity from the University of the South in Sewanee, Tenn., in 2003.

His spiritual “internship” was a transitional deaconship from 2003 to 2005, under the Rev. Michael Flanagan, rector at Simpsonville’s Holy Cross Episcopal Church. Both had dual vocations—Flanagan was an engineer who sold electrical equipment for 10 years before ordination. Prior to meeting Dr. Petit, Flanagan was leery of the doctor’s ability to balance pastoral and medical duties.

“Would he be a doctor/priest?” Flanagan wondered. “A priest/doctor? His desire was to meld both and he did. Medicine and spirituality are both in his blood. He sees both as calls from God and connects medicine with spirituality into a holistic view of each person.” He says Dr. Petit “seems to know everything and sucks up knowledge, which he wants to share. He loves being the doctor and having the knowledge to fix the patient’s problem.”

While Dr. Petit keeps his hospitalist and priest roles mostly separate, working with elderly patients sometimes requires the skills of both disciplines. At Richland he wears a clerical collar on pastoral rounds. If a family or patient asks him to pray with them or discuss life’s ending, he does. He has conducted funerals for his own and colleagues’ patients.

“It’s a very powerful experience being both a priest and a doctor,” he says. “I grow so close to the patients and their families that it is natural for me to serve in both roles.”

Dr. Petit is developing a modern clinic with his own money in Puerto Lempira, Honduras, to address the dire medical needs of the Miskito Indians.

Honduras Mission

As a seminarian, Dr. Petit took medical mission trips and briefly supported an African orphanage, looking for a cause to call his own. Until his first trip to Puerto Lempira, a village on the Miskito Coast of the Atlantic Ocean.

 

 

The abject poverty and medical needs of the Miskito Indians there pulled at him. Early on he enlisted the help of Ennis Whiddon, a builder and Holy Cross parishioner. Whiddon, who usually accompanies Dr. Petit to Puerto Lempira, says of his friend: “I knew him as [an emergency department] doctor first. Then I realized his extraordinary spiritual commitment. I went to Puerto Lempira on his first mission trip and I asked myself why anyone would want to be there, but I knew Chuck couldn’t bear not to be there. I also knew he wasn’t just going to give people two aspirins, come home and pray for them.”

Dr. Petit returns to Puerto Lempira three or four times a year with a team of doctors, seeing several hundred patients a day. During one two-week stint he dispensed $200,000 worth of medication he cadged from drug companies for $600 out of his pocket to rid the town’s youngsters of debilitating parasites.

Dr. Petit works with a Miskito nurse who runs their rudimentary clinic in his absence. He also uses hyperbaric medicine to treat divers whose crippling injuries result from diving deeply using pressurized oxygen tanks and rising too quickly to the surface.

“You wouldn’t believe the indescribably poor facilities we found there,” Whiddon says of the town’s clinic. “You wouldn’t have your dog treated there if you loved your dog.”

Last year Dr. Petit ratcheted up his commitment to Puerto Lempira, dreaming of building a permanent clinic there.

He decided to use his money to buy land to build a clinic, but got stonewalled by a stubborn local bureaucracy.

Then Andres Leone, a like-minded younger doctor who was part of the mission trip, stepped in with handy language and cultural skills. Leone who had attended medical school in Ecuador, is a Lutheran seminarian, and is completing a geriatric hospitalist fellowship at Palmetto Healthcare.

“We were in Puerto Lempira for two weeks and visited the mayor several times to buy land,” Dr. Leone explains. “He said the price was $600,000, which was ridiculous. In the town I overheard some conversations, which led to us meeting the 77-year-old daughter of missionaries. She sold us some of her land and even donated money to help build the clinic, which will be dedicated in her name.”

Thinking big, Dr. Petit is adding an apartment complete with air conditioning and a modern bathroom to the clinic’s blueprint, to attract residents in a to-be-formed international medicine program. As an assistant professor of family medicine at the University of South Carolina’s (USC) School of Medicine, he intends to oversee those residents.

Just back from Puerto Lempira, Dr. Petit finalized the clinic’s design, lined up local workers to figure out how to make concrete building blocks with native materials, and met with Anglican bishop the Right Rev. Lloyd E. Allen, bolstering support for the new clinic and the possibility of HIV outreach. Side by side with Honduran and Cuban doctors, Dr. Petit treated hundreds of Puerto Lempira’s villagers every day.

Back in the Hospital

Dr. Petit always wanted to be a doctor. Although his father suggested he become a hospital orderly, Dr. Petit knew being a physician was his calling, graduating from the University of West Virginia School of Medicine (Morgantown) family medicine program in 1978.

He enjoys hospital medicine as a holistic approach to caring for patients, consistent with his work early in his career.

An earlier 10-year stint as a hospitalist at HealthSouth Rehabilitation Hospital, also at USC, involved teaching residents and students rotating through the hospital, as well as a consultative service for neurosurgical patients at Richland. At Wheeling Hospital early in his career he became comfortable as a generalist, covering intensive care, assisting in surgery, and delivering many babies.

 

 

Being a hospitalist keeps that spirit alive. “It gives me the gift of time to spend with patients,” he says. “I try not to tie frail elderly patients down with IVs, Foley catheters, EKG monitors, worries that eating a leafy green vegetable will react badly with their Coumadin [warfarin], and polypharmacy.”

He discusses advanced directives, palliative care, and how the elderly in fragile condition can maintain as much freedom as possible. The hospital medicine group’s accommodating scheduling allows time for his parish duties and medical mission trips.

The group’s medical director, Victor Hirth, MD, describes Dr. Petit as a borderline workaholic who’s always looking for ways to make things better for the practice and patients. “The patients absolutely love him because he takes time to sit and talk to them,” says Dr. Hirth.

Dr. Petit also embraces new technologies. “Our [electronic medical record] makes working with my outpatient colleagues smooth and straightforward.” He relies on a personal digital device assistant for updates on clinical guidelines and optimal drug doses for elderly patients. Integrating a healer’s touch with new technology he says: “While medicine is a science, it’s still an art, a ministry, and a gift.”

What’s Next?

Back in South Carolina, Dr. Petit has picked up his hospitalist and pastoral responsibilities without missing a beat. He looks forward to building the palliative care consulting service and intends to launch a nonprofit corporation to receive donations to support the Puerto Lempira clinic’s construction.

He is planning more mission trips. He thrives on the work. Infused with boundless energy, he’s always looking for more to do.

“I love what I do,” he concludes. “If I felt much better they’d charge me an amusement tax.” TH

Marlene Piturro is a medical writer based in New York.

Issue
The Hospitalist - 2007(12)
Publications
Sections

Charles Petit, MD, like many healthcare professionals, spends a good deal of time addressing the needs of the underprivileged. Since 2004, he has taken up the cause of the indigenous Miskito Indians of Puerto Lempira, Honduras. He is putting his own money into developing a modern clinic and international medicine program there.

But medicine isn’t his only mission. Dr. Petit, 56, a hospitalist at Palmetto Health Care’s Richland Memorial Hospital in Columbia, S.C., is also an Episcopal priest.

He joined Palmetto Health Senior Care as its first medical director in 1988 and reconnected with the group in 2004—not in his previous role as an office-based physician but as a hospitalist. In between those stints he pursued his ordination and medical missionary work in Africa and Latin America.

As a physician, Dr. Petit says he feels God’s presence at each patient’s bedside. Years ago he wondered how to handle that.

To deepen his connection between medicine and spirituality, he lived in a Christian intentional community in Indiana, Pa., from 1981 to 1988. Gradually, his views on medicine and spirituality crystallized.

“How does God do what he does?” Dr. Petit wondered. “Can medicine put Him to the test? I have seen that prayer works, including a patient miraculously healed of metastatic ovarian cancer. But God isn’t a vending machine. You don’t drop in a prayer and get a healing back.”

Charles Petit, MD, a hospitalist at Palmetto Health Care’s Richland Memorial Hospital in Columbia, S.C., earned a master’s in divinity in 2003.

The Second Calling

Recognizing he needed something more to integrate medicine and spirituality, Dr. Petit sought a firmer grounding in religious studies.

He moved to Simpsonville, S.C., in 1995 and entered the Episcopal seminary, working as an emergency department doctor to pay the bills. Later, he earned a master’s of divinity from the University of the South in Sewanee, Tenn., in 2003.

His spiritual “internship” was a transitional deaconship from 2003 to 2005, under the Rev. Michael Flanagan, rector at Simpsonville’s Holy Cross Episcopal Church. Both had dual vocations—Flanagan was an engineer who sold electrical equipment for 10 years before ordination. Prior to meeting Dr. Petit, Flanagan was leery of the doctor’s ability to balance pastoral and medical duties.

“Would he be a doctor/priest?” Flanagan wondered. “A priest/doctor? His desire was to meld both and he did. Medicine and spirituality are both in his blood. He sees both as calls from God and connects medicine with spirituality into a holistic view of each person.” He says Dr. Petit “seems to know everything and sucks up knowledge, which he wants to share. He loves being the doctor and having the knowledge to fix the patient’s problem.”

While Dr. Petit keeps his hospitalist and priest roles mostly separate, working with elderly patients sometimes requires the skills of both disciplines. At Richland he wears a clerical collar on pastoral rounds. If a family or patient asks him to pray with them or discuss life’s ending, he does. He has conducted funerals for his own and colleagues’ patients.

“It’s a very powerful experience being both a priest and a doctor,” he says. “I grow so close to the patients and their families that it is natural for me to serve in both roles.”

Dr. Petit is developing a modern clinic with his own money in Puerto Lempira, Honduras, to address the dire medical needs of the Miskito Indians.

Honduras Mission

As a seminarian, Dr. Petit took medical mission trips and briefly supported an African orphanage, looking for a cause to call his own. Until his first trip to Puerto Lempira, a village on the Miskito Coast of the Atlantic Ocean.

 

 

The abject poverty and medical needs of the Miskito Indians there pulled at him. Early on he enlisted the help of Ennis Whiddon, a builder and Holy Cross parishioner. Whiddon, who usually accompanies Dr. Petit to Puerto Lempira, says of his friend: “I knew him as [an emergency department] doctor first. Then I realized his extraordinary spiritual commitment. I went to Puerto Lempira on his first mission trip and I asked myself why anyone would want to be there, but I knew Chuck couldn’t bear not to be there. I also knew he wasn’t just going to give people two aspirins, come home and pray for them.”

Dr. Petit returns to Puerto Lempira three or four times a year with a team of doctors, seeing several hundred patients a day. During one two-week stint he dispensed $200,000 worth of medication he cadged from drug companies for $600 out of his pocket to rid the town’s youngsters of debilitating parasites.

Dr. Petit works with a Miskito nurse who runs their rudimentary clinic in his absence. He also uses hyperbaric medicine to treat divers whose crippling injuries result from diving deeply using pressurized oxygen tanks and rising too quickly to the surface.

“You wouldn’t believe the indescribably poor facilities we found there,” Whiddon says of the town’s clinic. “You wouldn’t have your dog treated there if you loved your dog.”

Last year Dr. Petit ratcheted up his commitment to Puerto Lempira, dreaming of building a permanent clinic there.

He decided to use his money to buy land to build a clinic, but got stonewalled by a stubborn local bureaucracy.

Then Andres Leone, a like-minded younger doctor who was part of the mission trip, stepped in with handy language and cultural skills. Leone who had attended medical school in Ecuador, is a Lutheran seminarian, and is completing a geriatric hospitalist fellowship at Palmetto Healthcare.

“We were in Puerto Lempira for two weeks and visited the mayor several times to buy land,” Dr. Leone explains. “He said the price was $600,000, which was ridiculous. In the town I overheard some conversations, which led to us meeting the 77-year-old daughter of missionaries. She sold us some of her land and even donated money to help build the clinic, which will be dedicated in her name.”

Thinking big, Dr. Petit is adding an apartment complete with air conditioning and a modern bathroom to the clinic’s blueprint, to attract residents in a to-be-formed international medicine program. As an assistant professor of family medicine at the University of South Carolina’s (USC) School of Medicine, he intends to oversee those residents.

Just back from Puerto Lempira, Dr. Petit finalized the clinic’s design, lined up local workers to figure out how to make concrete building blocks with native materials, and met with Anglican bishop the Right Rev. Lloyd E. Allen, bolstering support for the new clinic and the possibility of HIV outreach. Side by side with Honduran and Cuban doctors, Dr. Petit treated hundreds of Puerto Lempira’s villagers every day.

Back in the Hospital

Dr. Petit always wanted to be a doctor. Although his father suggested he become a hospital orderly, Dr. Petit knew being a physician was his calling, graduating from the University of West Virginia School of Medicine (Morgantown) family medicine program in 1978.

He enjoys hospital medicine as a holistic approach to caring for patients, consistent with his work early in his career.

An earlier 10-year stint as a hospitalist at HealthSouth Rehabilitation Hospital, also at USC, involved teaching residents and students rotating through the hospital, as well as a consultative service for neurosurgical patients at Richland. At Wheeling Hospital early in his career he became comfortable as a generalist, covering intensive care, assisting in surgery, and delivering many babies.

 

 

Being a hospitalist keeps that spirit alive. “It gives me the gift of time to spend with patients,” he says. “I try not to tie frail elderly patients down with IVs, Foley catheters, EKG monitors, worries that eating a leafy green vegetable will react badly with their Coumadin [warfarin], and polypharmacy.”

He discusses advanced directives, palliative care, and how the elderly in fragile condition can maintain as much freedom as possible. The hospital medicine group’s accommodating scheduling allows time for his parish duties and medical mission trips.

The group’s medical director, Victor Hirth, MD, describes Dr. Petit as a borderline workaholic who’s always looking for ways to make things better for the practice and patients. “The patients absolutely love him because he takes time to sit and talk to them,” says Dr. Hirth.

Dr. Petit also embraces new technologies. “Our [electronic medical record] makes working with my outpatient colleagues smooth and straightforward.” He relies on a personal digital device assistant for updates on clinical guidelines and optimal drug doses for elderly patients. Integrating a healer’s touch with new technology he says: “While medicine is a science, it’s still an art, a ministry, and a gift.”

What’s Next?

Back in South Carolina, Dr. Petit has picked up his hospitalist and pastoral responsibilities without missing a beat. He looks forward to building the palliative care consulting service and intends to launch a nonprofit corporation to receive donations to support the Puerto Lempira clinic’s construction.

He is planning more mission trips. He thrives on the work. Infused with boundless energy, he’s always looking for more to do.

“I love what I do,” he concludes. “If I felt much better they’d charge me an amusement tax.” TH

Marlene Piturro is a medical writer based in New York.

Charles Petit, MD, like many healthcare professionals, spends a good deal of time addressing the needs of the underprivileged. Since 2004, he has taken up the cause of the indigenous Miskito Indians of Puerto Lempira, Honduras. He is putting his own money into developing a modern clinic and international medicine program there.

But medicine isn’t his only mission. Dr. Petit, 56, a hospitalist at Palmetto Health Care’s Richland Memorial Hospital in Columbia, S.C., is also an Episcopal priest.

He joined Palmetto Health Senior Care as its first medical director in 1988 and reconnected with the group in 2004—not in his previous role as an office-based physician but as a hospitalist. In between those stints he pursued his ordination and medical missionary work in Africa and Latin America.

As a physician, Dr. Petit says he feels God’s presence at each patient’s bedside. Years ago he wondered how to handle that.

To deepen his connection between medicine and spirituality, he lived in a Christian intentional community in Indiana, Pa., from 1981 to 1988. Gradually, his views on medicine and spirituality crystallized.

“How does God do what he does?” Dr. Petit wondered. “Can medicine put Him to the test? I have seen that prayer works, including a patient miraculously healed of metastatic ovarian cancer. But God isn’t a vending machine. You don’t drop in a prayer and get a healing back.”

Charles Petit, MD, a hospitalist at Palmetto Health Care’s Richland Memorial Hospital in Columbia, S.C., earned a master’s in divinity in 2003.

The Second Calling

Recognizing he needed something more to integrate medicine and spirituality, Dr. Petit sought a firmer grounding in religious studies.

He moved to Simpsonville, S.C., in 1995 and entered the Episcopal seminary, working as an emergency department doctor to pay the bills. Later, he earned a master’s of divinity from the University of the South in Sewanee, Tenn., in 2003.

His spiritual “internship” was a transitional deaconship from 2003 to 2005, under the Rev. Michael Flanagan, rector at Simpsonville’s Holy Cross Episcopal Church. Both had dual vocations—Flanagan was an engineer who sold electrical equipment for 10 years before ordination. Prior to meeting Dr. Petit, Flanagan was leery of the doctor’s ability to balance pastoral and medical duties.

“Would he be a doctor/priest?” Flanagan wondered. “A priest/doctor? His desire was to meld both and he did. Medicine and spirituality are both in his blood. He sees both as calls from God and connects medicine with spirituality into a holistic view of each person.” He says Dr. Petit “seems to know everything and sucks up knowledge, which he wants to share. He loves being the doctor and having the knowledge to fix the patient’s problem.”

While Dr. Petit keeps his hospitalist and priest roles mostly separate, working with elderly patients sometimes requires the skills of both disciplines. At Richland he wears a clerical collar on pastoral rounds. If a family or patient asks him to pray with them or discuss life’s ending, he does. He has conducted funerals for his own and colleagues’ patients.

“It’s a very powerful experience being both a priest and a doctor,” he says. “I grow so close to the patients and their families that it is natural for me to serve in both roles.”

Dr. Petit is developing a modern clinic with his own money in Puerto Lempira, Honduras, to address the dire medical needs of the Miskito Indians.

Honduras Mission

As a seminarian, Dr. Petit took medical mission trips and briefly supported an African orphanage, looking for a cause to call his own. Until his first trip to Puerto Lempira, a village on the Miskito Coast of the Atlantic Ocean.

 

 

The abject poverty and medical needs of the Miskito Indians there pulled at him. Early on he enlisted the help of Ennis Whiddon, a builder and Holy Cross parishioner. Whiddon, who usually accompanies Dr. Petit to Puerto Lempira, says of his friend: “I knew him as [an emergency department] doctor first. Then I realized his extraordinary spiritual commitment. I went to Puerto Lempira on his first mission trip and I asked myself why anyone would want to be there, but I knew Chuck couldn’t bear not to be there. I also knew he wasn’t just going to give people two aspirins, come home and pray for them.”

Dr. Petit returns to Puerto Lempira three or four times a year with a team of doctors, seeing several hundred patients a day. During one two-week stint he dispensed $200,000 worth of medication he cadged from drug companies for $600 out of his pocket to rid the town’s youngsters of debilitating parasites.

Dr. Petit works with a Miskito nurse who runs their rudimentary clinic in his absence. He also uses hyperbaric medicine to treat divers whose crippling injuries result from diving deeply using pressurized oxygen tanks and rising too quickly to the surface.

“You wouldn’t believe the indescribably poor facilities we found there,” Whiddon says of the town’s clinic. “You wouldn’t have your dog treated there if you loved your dog.”

Last year Dr. Petit ratcheted up his commitment to Puerto Lempira, dreaming of building a permanent clinic there.

He decided to use his money to buy land to build a clinic, but got stonewalled by a stubborn local bureaucracy.

Then Andres Leone, a like-minded younger doctor who was part of the mission trip, stepped in with handy language and cultural skills. Leone who had attended medical school in Ecuador, is a Lutheran seminarian, and is completing a geriatric hospitalist fellowship at Palmetto Healthcare.

“We were in Puerto Lempira for two weeks and visited the mayor several times to buy land,” Dr. Leone explains. “He said the price was $600,000, which was ridiculous. In the town I overheard some conversations, which led to us meeting the 77-year-old daughter of missionaries. She sold us some of her land and even donated money to help build the clinic, which will be dedicated in her name.”

Thinking big, Dr. Petit is adding an apartment complete with air conditioning and a modern bathroom to the clinic’s blueprint, to attract residents in a to-be-formed international medicine program. As an assistant professor of family medicine at the University of South Carolina’s (USC) School of Medicine, he intends to oversee those residents.

Just back from Puerto Lempira, Dr. Petit finalized the clinic’s design, lined up local workers to figure out how to make concrete building blocks with native materials, and met with Anglican bishop the Right Rev. Lloyd E. Allen, bolstering support for the new clinic and the possibility of HIV outreach. Side by side with Honduran and Cuban doctors, Dr. Petit treated hundreds of Puerto Lempira’s villagers every day.

Back in the Hospital

Dr. Petit always wanted to be a doctor. Although his father suggested he become a hospital orderly, Dr. Petit knew being a physician was his calling, graduating from the University of West Virginia School of Medicine (Morgantown) family medicine program in 1978.

He enjoys hospital medicine as a holistic approach to caring for patients, consistent with his work early in his career.

An earlier 10-year stint as a hospitalist at HealthSouth Rehabilitation Hospital, also at USC, involved teaching residents and students rotating through the hospital, as well as a consultative service for neurosurgical patients at Richland. At Wheeling Hospital early in his career he became comfortable as a generalist, covering intensive care, assisting in surgery, and delivering many babies.

 

 

Being a hospitalist keeps that spirit alive. “It gives me the gift of time to spend with patients,” he says. “I try not to tie frail elderly patients down with IVs, Foley catheters, EKG monitors, worries that eating a leafy green vegetable will react badly with their Coumadin [warfarin], and polypharmacy.”

He discusses advanced directives, palliative care, and how the elderly in fragile condition can maintain as much freedom as possible. The hospital medicine group’s accommodating scheduling allows time for his parish duties and medical mission trips.

The group’s medical director, Victor Hirth, MD, describes Dr. Petit as a borderline workaholic who’s always looking for ways to make things better for the practice and patients. “The patients absolutely love him because he takes time to sit and talk to them,” says Dr. Hirth.

Dr. Petit also embraces new technologies. “Our [electronic medical record] makes working with my outpatient colleagues smooth and straightforward.” He relies on a personal digital device assistant for updates on clinical guidelines and optimal drug doses for elderly patients. Integrating a healer’s touch with new technology he says: “While medicine is a science, it’s still an art, a ministry, and a gift.”

What’s Next?

Back in South Carolina, Dr. Petit has picked up his hospitalist and pastoral responsibilities without missing a beat. He looks forward to building the palliative care consulting service and intends to launch a nonprofit corporation to receive donations to support the Puerto Lempira clinic’s construction.

He is planning more mission trips. He thrives on the work. Infused with boundless energy, he’s always looking for more to do.

“I love what I do,” he concludes. “If I felt much better they’d charge me an amusement tax.” TH

Marlene Piturro is a medical writer based in New York.

Issue
The Hospitalist - 2007(12)
Issue
The Hospitalist - 2007(12)
Publications
Publications
Article Type
Display Headline
Care & Prayer
Display Headline
Care & Prayer
Sections
Disallow All Ads
Content Gating
No Gating (article Unlocked/Free)

Do feeding tubes improve outcomes in patients with dementia?

Article Type
Changed
Display Headline
Do feeding tubes improve outcomes in patients with dementia?

Case

A 68-year-old cachectic female with a history of Alzheimer’s dementia presents with a slowly progressive decline in functional status. She is bed bound, minimally verbal, and has lost interest in eating.

Her problems with decreased oral intake started when her diet was changed to nectar-thickened liquids. This change was made after the patient was hospitalized multiple times for aspiration pneumonia and she underwent a fluoroscopic swallowing evaluation that revealed aspiration of thin liquids. The patient’s husband requests that a feeding tube be placed so his wife doesn’t “die of pneumonia or starve to death.”

Key Points

  1. PEG tube placement is associated with significant short- and long-term risks.
  2. There is no decrease in risk of aspiration pneumonia with placement of gastric or post-pyloric feeding tube and there might be increased risk.
  3. There is no evidence enteric nutrition by feeding tube improves nutritional markers or decreases the risk for pressure ulcer formation or improves healing of ulcers in a demented patient.
  4. PEG tubes do not appear to contribute to comfort at the end of life.

The Bottom Line

There is no clear evidence feeding tubes improve aspiration risk, decubitus ulcer formation, or nutritional outcomes in patients with dementia. Using these tubes might harm the patient without improving length or quality of life.

Additional Reading

  • Cervo FA, Bryan L, Farber S. To PEG or not to PEG: A review of evidence for placing feeding tubes in advanced dementia and the decision making process. Geriatrics. 2006;61(6):30-35.
  • Funicane TE, Christmas C, Travis K. Tube feeding in patients with advanced dementia: a review of the evidence. JAMA. 1999;282(14):1365-1370.
  • Vollman J. Rethinking the role of tube feeding in patients with advanced dementia. N Engl J Med. 2000;342(23):206-210.

Overview

As the U.S. population ages, hospitalists are seeing a steady increase in the average patient age and the prevalence of dementia. Alzheimer’s dementia affects an estimated 4 million to 5 million Americans; this number expected to triple by the year 2050.1

As patients with dementia near the end of life, they often fail to thrive, with less oral intake and more swallowing disorders leading to aspiration. This is when physicians and patient family members must decide whether a feeding tube should be placed.

Placement of a nasogastric or percutaneous endogastric gastrostomy (PEG) feeding tube has become a relatively common medical intervention instituted to maintain or improve a patient’s nutritional status. Prior to 1980, permanent gastric or postpyloric feeding tubes were placed surgically by laparotomy, but the advent of endoscopy and computed tomography (CT) guided procedures offers a simplified procedure requiring only mild sedation and local anesthesia.2

Many patients who suffer multiple bouts of aspiration pneumonia and fail a swallowing evaluation because of an irreversible process are offered a percutaneous feeding tube to maintain nutrition. A feeding tube is also seen as a way to supply nutrition at the end of life in patients no longer able or willing to take food orally.

Although it seems logical that a feeding tube might improve the outcomes of these clinical scenarios, limited literature exists on the topic because of the legal, ethical, emotional, and religious implications a large, randomized, placebo-controlled trial would entail.

Review of the Data

Placement of a PEG has become accepted as a relatively benign procedure, although it is associated with significant morbidity and mortality. Minor complications including pain, abdominal wall ulcers, wound infections, peristomal leakage, and tube displacement occur in approximately 10% of cases.3 Major complications including hemorrhage, bowel or liver perforation, or aspiration occur in 3% of cases.4

 

 

These numbers do not account for long-term complications including peristomal infections, leakage problems, or the use of physical restraints to avoid self-extubation.

click for large version
click for large version

Aspiration Risk

A common indication for PEG placement is aspiration risk. PEG tubes are often placed in patients who fail swallowing evaluations in order to decrease their risk of aspiration and aspiration pneumonia.

True aspiration pneumonia is thought to originate from an inoculum of oral cavity or nasopharynx bacteria, which placement of a PEG tube would not prevent. Leibovitz, et al., showed that elderly patients with nasogastric or percutaneous feeding tubes are associated with colonization of the oropharynx with more pathogenic bacteria when compared with orally fed patients.5 Thus, the use of PEG tubes might put them at higher risk for pathogenic inoculation.

Aspiration pneumonia occurs in up to 50% of patients with feeding tubes. Studies have shown PEG tube placement decreases lower esophageal sphincter tone, potentially increasing regurgitation risk.6 It has also been shown that aspiration of gastric contents produces a pneumonitis with the resultant inflammatory response allowing for establishment of infection by smaller inoculums of or less virulent organisms.7

Small, randomized trials have shown no decrease in aspiration risk with post-pyloric versus gastric feeding tubes, nasogastric versus percutaneous feeding tubes, or continuous versus intermittent tube feeds.8 There have been no sizable randomized prospective trials to determine if feeding tube placement versus hand feeding patients with end-stage dementia alters aspiration pneumonia risk.

Pressure Ulcers

Patients with end-stage dementia often become bed bound as their disease progresses, and they commonly suffer from pressure ulcers. Pressure ulcers often coexist in patients with malnutrition, and it is well established that patients with biochemical markers of malnutrition are at higher risk for pressure ulcer formation.

Still, no studies show that improved nutrition prevents pressure ulcer formation. In a nursing home population of patients with dementia, a two-year follow-up study showed no significant improvement in pressure ulcer healing or decreased ulcer formation with nutrition by feeding tube.9 These studies are adjusted for independent risk factors for mortality and indication for PEG placement, but we can assume there are confounders that go into the decision for feeding tube placement that are not necessarily identifiable.

click for large version
click for large version

Nutritional Status

Family members are often concerned that if the patient is unable to take food by mouth and no feeding tube is placed, then the patient will suffer from the discomfort of starvation and dehydration.

As a patient with a severe dementing illness enters the end stage of his/her clinical course, practitioners frequently make a plan with families to change the goals of care toward keeping the patient comfortable. Comfort is a difficult clinical parameter to measure, but studies in the hospice population of patients with end-stage cancer and AIDS report that the hunger and thirst are transient and improve with ice chips and mouth swabs.10

Despite the lack of evidence of PEG tubes prolonging survival in patients with dementia who are no longer able or willing to take in food orally, it is logical that withholding all hydration or nutritional support will hasten death despite the risks associated with feeding tubes. This is where the ethical argument arises regarding prolonging life of decreasing quality.

In certain medical and legal sectors, artificial nutrition, and hydration are considered a medical intervention. Therefore, the ideals of patient autonomy dictate that the patient’s proxy should decide whether or not the patient would have wanted the intervention after weighing the risks and benefits.

If hospitalists view artificial nutrition as a medical intervention, our moral obligation is to instruct patients and their families about these risks and benefits.

 

 

Often, the patient will not clinically improve with artificial nutrition. But we can maintain physiologic processes or at least slow their decline.

Emerging research indicates the standard of care in how we present this information is changing to include presentation of data instead of only using a patient’s suspected beliefs about quality of life.

A useful algorithm proposed by Rabeneck, et al., provides comprehensive guidelines for PEG placement in all patient populations based on the reason for PEG consideration.11

Back to the Case

Our patient is likely nearing the end of her life because of end-stage dementia. There is no evidence to suggest placement of a feeding tube would extend her life more than hand feeding.

We know feeding-tube placement could increase aspiration pneumonia risk and significant short- and long-term morbidity and mortality. We can keep her comfortable with small amounts of water, wetting her lips with swabs. If a feeding tube is placed, its use should be evaluated based on the patient’s clinical course. TH

Dr. Pell is an instructor of medicine in the Section of Hospital Medicine at the University of Colorado, Denver.

References

  1. Gauderer MW, Ponsky JL, Izant RJ Jr. Gastrostomy without laparotomy: a percutaneous endoscopic technique. J Pediatr Surg. 1980;15(6):872-875.
  2. Hebert LE, Beckett LA, Scherr PA, and Evans DA. Annual incidence of Alzheimer disease in the United States projected to the years 2000 through 2050. Alzheimer Dis Assoc Disord. 2001;15:169-173.
  3. Grant MD, Rudberg MA, Brody JA. Gastrostomy placement and mortality among hospitalized Medicare beneficiaries. JAMA. 1998;279:1973-1976.
  4. Finocchiaro C, Galletti R, Rovera G, et al. Percutaneous endoscopic gastrostomy: a long-term follow-up. Nutrition. 1997;13(6):520-523.
  5. Leibovitz A, Plotnikov G, Habot B, et al. Pathogenic colonization of oral flora in frail elderly patients fed by nasogastric tube or percutaneous enterogastric tube. J Gerontol A Biol Sci Med. 2003;58(1):52-55.
  6. McCann R. Lack of evidence about tube feeding: food for thought. JAMA. 1999;282(14):1380-1381.
  7. Cameron JL, Caldini P, Toung J-K, et al. Aspiration pneumonia: physiologic data following experimental Aspiration. Surgery. 1972;72:238.
  8. Loeb MB, Becker M, Eady A, et al. Interventions to prevent aspiration pneumonia in older adults: a systematic review. JAGS. 2003;51(7):1018-1022.
  9. Mitchell SL, Kiely DK, Lipsitz LA. The risk factors and impact on survival of feeding tube placement in nursing home residents with severe cognitive impairment. Arch Intern Med. 1997;157:327-332.
  10. McCann RM, Hall WJ, Groth-Junker A. Comfort care for terminally ill patients: the appropriate use of nutrition and hydration. JAMA. 1994;272:1263-1266.
  11. Rabeneck L, McCullough LB. Ethically justified, clinically comprehensive guidelines for percutaneous endoscopic gastrostomy tube placement. Lancet. 1997;349(9050):496-498.
Issue
The Hospitalist - 2007(12)
Publications
Sections

Case

A 68-year-old cachectic female with a history of Alzheimer’s dementia presents with a slowly progressive decline in functional status. She is bed bound, minimally verbal, and has lost interest in eating.

Her problems with decreased oral intake started when her diet was changed to nectar-thickened liquids. This change was made after the patient was hospitalized multiple times for aspiration pneumonia and she underwent a fluoroscopic swallowing evaluation that revealed aspiration of thin liquids. The patient’s husband requests that a feeding tube be placed so his wife doesn’t “die of pneumonia or starve to death.”

Key Points

  1. PEG tube placement is associated with significant short- and long-term risks.
  2. There is no decrease in risk of aspiration pneumonia with placement of gastric or post-pyloric feeding tube and there might be increased risk.
  3. There is no evidence enteric nutrition by feeding tube improves nutritional markers or decreases the risk for pressure ulcer formation or improves healing of ulcers in a demented patient.
  4. PEG tubes do not appear to contribute to comfort at the end of life.

The Bottom Line

There is no clear evidence feeding tubes improve aspiration risk, decubitus ulcer formation, or nutritional outcomes in patients with dementia. Using these tubes might harm the patient without improving length or quality of life.

Additional Reading

  • Cervo FA, Bryan L, Farber S. To PEG or not to PEG: A review of evidence for placing feeding tubes in advanced dementia and the decision making process. Geriatrics. 2006;61(6):30-35.
  • Funicane TE, Christmas C, Travis K. Tube feeding in patients with advanced dementia: a review of the evidence. JAMA. 1999;282(14):1365-1370.
  • Vollman J. Rethinking the role of tube feeding in patients with advanced dementia. N Engl J Med. 2000;342(23):206-210.

Overview

As the U.S. population ages, hospitalists are seeing a steady increase in the average patient age and the prevalence of dementia. Alzheimer’s dementia affects an estimated 4 million to 5 million Americans; this number expected to triple by the year 2050.1

As patients with dementia near the end of life, they often fail to thrive, with less oral intake and more swallowing disorders leading to aspiration. This is when physicians and patient family members must decide whether a feeding tube should be placed.

Placement of a nasogastric or percutaneous endogastric gastrostomy (PEG) feeding tube has become a relatively common medical intervention instituted to maintain or improve a patient’s nutritional status. Prior to 1980, permanent gastric or postpyloric feeding tubes were placed surgically by laparotomy, but the advent of endoscopy and computed tomography (CT) guided procedures offers a simplified procedure requiring only mild sedation and local anesthesia.2

Many patients who suffer multiple bouts of aspiration pneumonia and fail a swallowing evaluation because of an irreversible process are offered a percutaneous feeding tube to maintain nutrition. A feeding tube is also seen as a way to supply nutrition at the end of life in patients no longer able or willing to take food orally.

Although it seems logical that a feeding tube might improve the outcomes of these clinical scenarios, limited literature exists on the topic because of the legal, ethical, emotional, and religious implications a large, randomized, placebo-controlled trial would entail.

Review of the Data

Placement of a PEG has become accepted as a relatively benign procedure, although it is associated with significant morbidity and mortality. Minor complications including pain, abdominal wall ulcers, wound infections, peristomal leakage, and tube displacement occur in approximately 10% of cases.3 Major complications including hemorrhage, bowel or liver perforation, or aspiration occur in 3% of cases.4

 

 

These numbers do not account for long-term complications including peristomal infections, leakage problems, or the use of physical restraints to avoid self-extubation.

click for large version
click for large version

Aspiration Risk

A common indication for PEG placement is aspiration risk. PEG tubes are often placed in patients who fail swallowing evaluations in order to decrease their risk of aspiration and aspiration pneumonia.

True aspiration pneumonia is thought to originate from an inoculum of oral cavity or nasopharynx bacteria, which placement of a PEG tube would not prevent. Leibovitz, et al., showed that elderly patients with nasogastric or percutaneous feeding tubes are associated with colonization of the oropharynx with more pathogenic bacteria when compared with orally fed patients.5 Thus, the use of PEG tubes might put them at higher risk for pathogenic inoculation.

Aspiration pneumonia occurs in up to 50% of patients with feeding tubes. Studies have shown PEG tube placement decreases lower esophageal sphincter tone, potentially increasing regurgitation risk.6 It has also been shown that aspiration of gastric contents produces a pneumonitis with the resultant inflammatory response allowing for establishment of infection by smaller inoculums of or less virulent organisms.7

Small, randomized trials have shown no decrease in aspiration risk with post-pyloric versus gastric feeding tubes, nasogastric versus percutaneous feeding tubes, or continuous versus intermittent tube feeds.8 There have been no sizable randomized prospective trials to determine if feeding tube placement versus hand feeding patients with end-stage dementia alters aspiration pneumonia risk.

Pressure Ulcers

Patients with end-stage dementia often become bed bound as their disease progresses, and they commonly suffer from pressure ulcers. Pressure ulcers often coexist in patients with malnutrition, and it is well established that patients with biochemical markers of malnutrition are at higher risk for pressure ulcer formation.

Still, no studies show that improved nutrition prevents pressure ulcer formation. In a nursing home population of patients with dementia, a two-year follow-up study showed no significant improvement in pressure ulcer healing or decreased ulcer formation with nutrition by feeding tube.9 These studies are adjusted for independent risk factors for mortality and indication for PEG placement, but we can assume there are confounders that go into the decision for feeding tube placement that are not necessarily identifiable.

click for large version
click for large version

Nutritional Status

Family members are often concerned that if the patient is unable to take food by mouth and no feeding tube is placed, then the patient will suffer from the discomfort of starvation and dehydration.

As a patient with a severe dementing illness enters the end stage of his/her clinical course, practitioners frequently make a plan with families to change the goals of care toward keeping the patient comfortable. Comfort is a difficult clinical parameter to measure, but studies in the hospice population of patients with end-stage cancer and AIDS report that the hunger and thirst are transient and improve with ice chips and mouth swabs.10

Despite the lack of evidence of PEG tubes prolonging survival in patients with dementia who are no longer able or willing to take in food orally, it is logical that withholding all hydration or nutritional support will hasten death despite the risks associated with feeding tubes. This is where the ethical argument arises regarding prolonging life of decreasing quality.

In certain medical and legal sectors, artificial nutrition, and hydration are considered a medical intervention. Therefore, the ideals of patient autonomy dictate that the patient’s proxy should decide whether or not the patient would have wanted the intervention after weighing the risks and benefits.

If hospitalists view artificial nutrition as a medical intervention, our moral obligation is to instruct patients and their families about these risks and benefits.

 

 

Often, the patient will not clinically improve with artificial nutrition. But we can maintain physiologic processes or at least slow their decline.

Emerging research indicates the standard of care in how we present this information is changing to include presentation of data instead of only using a patient’s suspected beliefs about quality of life.

A useful algorithm proposed by Rabeneck, et al., provides comprehensive guidelines for PEG placement in all patient populations based on the reason for PEG consideration.11

Back to the Case

Our patient is likely nearing the end of her life because of end-stage dementia. There is no evidence to suggest placement of a feeding tube would extend her life more than hand feeding.

We know feeding-tube placement could increase aspiration pneumonia risk and significant short- and long-term morbidity and mortality. We can keep her comfortable with small amounts of water, wetting her lips with swabs. If a feeding tube is placed, its use should be evaluated based on the patient’s clinical course. TH

Dr. Pell is an instructor of medicine in the Section of Hospital Medicine at the University of Colorado, Denver.

References

  1. Gauderer MW, Ponsky JL, Izant RJ Jr. Gastrostomy without laparotomy: a percutaneous endoscopic technique. J Pediatr Surg. 1980;15(6):872-875.
  2. Hebert LE, Beckett LA, Scherr PA, and Evans DA. Annual incidence of Alzheimer disease in the United States projected to the years 2000 through 2050. Alzheimer Dis Assoc Disord. 2001;15:169-173.
  3. Grant MD, Rudberg MA, Brody JA. Gastrostomy placement and mortality among hospitalized Medicare beneficiaries. JAMA. 1998;279:1973-1976.
  4. Finocchiaro C, Galletti R, Rovera G, et al. Percutaneous endoscopic gastrostomy: a long-term follow-up. Nutrition. 1997;13(6):520-523.
  5. Leibovitz A, Plotnikov G, Habot B, et al. Pathogenic colonization of oral flora in frail elderly patients fed by nasogastric tube or percutaneous enterogastric tube. J Gerontol A Biol Sci Med. 2003;58(1):52-55.
  6. McCann R. Lack of evidence about tube feeding: food for thought. JAMA. 1999;282(14):1380-1381.
  7. Cameron JL, Caldini P, Toung J-K, et al. Aspiration pneumonia: physiologic data following experimental Aspiration. Surgery. 1972;72:238.
  8. Loeb MB, Becker M, Eady A, et al. Interventions to prevent aspiration pneumonia in older adults: a systematic review. JAGS. 2003;51(7):1018-1022.
  9. Mitchell SL, Kiely DK, Lipsitz LA. The risk factors and impact on survival of feeding tube placement in nursing home residents with severe cognitive impairment. Arch Intern Med. 1997;157:327-332.
  10. McCann RM, Hall WJ, Groth-Junker A. Comfort care for terminally ill patients: the appropriate use of nutrition and hydration. JAMA. 1994;272:1263-1266.
  11. Rabeneck L, McCullough LB. Ethically justified, clinically comprehensive guidelines for percutaneous endoscopic gastrostomy tube placement. Lancet. 1997;349(9050):496-498.

Case

A 68-year-old cachectic female with a history of Alzheimer’s dementia presents with a slowly progressive decline in functional status. She is bed bound, minimally verbal, and has lost interest in eating.

Her problems with decreased oral intake started when her diet was changed to nectar-thickened liquids. This change was made after the patient was hospitalized multiple times for aspiration pneumonia and she underwent a fluoroscopic swallowing evaluation that revealed aspiration of thin liquids. The patient’s husband requests that a feeding tube be placed so his wife doesn’t “die of pneumonia or starve to death.”

Key Points

  1. PEG tube placement is associated with significant short- and long-term risks.
  2. There is no decrease in risk of aspiration pneumonia with placement of gastric or post-pyloric feeding tube and there might be increased risk.
  3. There is no evidence enteric nutrition by feeding tube improves nutritional markers or decreases the risk for pressure ulcer formation or improves healing of ulcers in a demented patient.
  4. PEG tubes do not appear to contribute to comfort at the end of life.

The Bottom Line

There is no clear evidence feeding tubes improve aspiration risk, decubitus ulcer formation, or nutritional outcomes in patients with dementia. Using these tubes might harm the patient without improving length or quality of life.

Additional Reading

  • Cervo FA, Bryan L, Farber S. To PEG or not to PEG: A review of evidence for placing feeding tubes in advanced dementia and the decision making process. Geriatrics. 2006;61(6):30-35.
  • Funicane TE, Christmas C, Travis K. Tube feeding in patients with advanced dementia: a review of the evidence. JAMA. 1999;282(14):1365-1370.
  • Vollman J. Rethinking the role of tube feeding in patients with advanced dementia. N Engl J Med. 2000;342(23):206-210.

Overview

As the U.S. population ages, hospitalists are seeing a steady increase in the average patient age and the prevalence of dementia. Alzheimer’s dementia affects an estimated 4 million to 5 million Americans; this number expected to triple by the year 2050.1

As patients with dementia near the end of life, they often fail to thrive, with less oral intake and more swallowing disorders leading to aspiration. This is when physicians and patient family members must decide whether a feeding tube should be placed.

Placement of a nasogastric or percutaneous endogastric gastrostomy (PEG) feeding tube has become a relatively common medical intervention instituted to maintain or improve a patient’s nutritional status. Prior to 1980, permanent gastric or postpyloric feeding tubes were placed surgically by laparotomy, but the advent of endoscopy and computed tomography (CT) guided procedures offers a simplified procedure requiring only mild sedation and local anesthesia.2

Many patients who suffer multiple bouts of aspiration pneumonia and fail a swallowing evaluation because of an irreversible process are offered a percutaneous feeding tube to maintain nutrition. A feeding tube is also seen as a way to supply nutrition at the end of life in patients no longer able or willing to take food orally.

Although it seems logical that a feeding tube might improve the outcomes of these clinical scenarios, limited literature exists on the topic because of the legal, ethical, emotional, and religious implications a large, randomized, placebo-controlled trial would entail.

Review of the Data

Placement of a PEG has become accepted as a relatively benign procedure, although it is associated with significant morbidity and mortality. Minor complications including pain, abdominal wall ulcers, wound infections, peristomal leakage, and tube displacement occur in approximately 10% of cases.3 Major complications including hemorrhage, bowel or liver perforation, or aspiration occur in 3% of cases.4

 

 

These numbers do not account for long-term complications including peristomal infections, leakage problems, or the use of physical restraints to avoid self-extubation.

click for large version
click for large version

Aspiration Risk

A common indication for PEG placement is aspiration risk. PEG tubes are often placed in patients who fail swallowing evaluations in order to decrease their risk of aspiration and aspiration pneumonia.

True aspiration pneumonia is thought to originate from an inoculum of oral cavity or nasopharynx bacteria, which placement of a PEG tube would not prevent. Leibovitz, et al., showed that elderly patients with nasogastric or percutaneous feeding tubes are associated with colonization of the oropharynx with more pathogenic bacteria when compared with orally fed patients.5 Thus, the use of PEG tubes might put them at higher risk for pathogenic inoculation.

Aspiration pneumonia occurs in up to 50% of patients with feeding tubes. Studies have shown PEG tube placement decreases lower esophageal sphincter tone, potentially increasing regurgitation risk.6 It has also been shown that aspiration of gastric contents produces a pneumonitis with the resultant inflammatory response allowing for establishment of infection by smaller inoculums of or less virulent organisms.7

Small, randomized trials have shown no decrease in aspiration risk with post-pyloric versus gastric feeding tubes, nasogastric versus percutaneous feeding tubes, or continuous versus intermittent tube feeds.8 There have been no sizable randomized prospective trials to determine if feeding tube placement versus hand feeding patients with end-stage dementia alters aspiration pneumonia risk.

Pressure Ulcers

Patients with end-stage dementia often become bed bound as their disease progresses, and they commonly suffer from pressure ulcers. Pressure ulcers often coexist in patients with malnutrition, and it is well established that patients with biochemical markers of malnutrition are at higher risk for pressure ulcer formation.

Still, no studies show that improved nutrition prevents pressure ulcer formation. In a nursing home population of patients with dementia, a two-year follow-up study showed no significant improvement in pressure ulcer healing or decreased ulcer formation with nutrition by feeding tube.9 These studies are adjusted for independent risk factors for mortality and indication for PEG placement, but we can assume there are confounders that go into the decision for feeding tube placement that are not necessarily identifiable.

click for large version
click for large version

Nutritional Status

Family members are often concerned that if the patient is unable to take food by mouth and no feeding tube is placed, then the patient will suffer from the discomfort of starvation and dehydration.

As a patient with a severe dementing illness enters the end stage of his/her clinical course, practitioners frequently make a plan with families to change the goals of care toward keeping the patient comfortable. Comfort is a difficult clinical parameter to measure, but studies in the hospice population of patients with end-stage cancer and AIDS report that the hunger and thirst are transient and improve with ice chips and mouth swabs.10

Despite the lack of evidence of PEG tubes prolonging survival in patients with dementia who are no longer able or willing to take in food orally, it is logical that withholding all hydration or nutritional support will hasten death despite the risks associated with feeding tubes. This is where the ethical argument arises regarding prolonging life of decreasing quality.

In certain medical and legal sectors, artificial nutrition, and hydration are considered a medical intervention. Therefore, the ideals of patient autonomy dictate that the patient’s proxy should decide whether or not the patient would have wanted the intervention after weighing the risks and benefits.

If hospitalists view artificial nutrition as a medical intervention, our moral obligation is to instruct patients and their families about these risks and benefits.

 

 

Often, the patient will not clinically improve with artificial nutrition. But we can maintain physiologic processes or at least slow their decline.

Emerging research indicates the standard of care in how we present this information is changing to include presentation of data instead of only using a patient’s suspected beliefs about quality of life.

A useful algorithm proposed by Rabeneck, et al., provides comprehensive guidelines for PEG placement in all patient populations based on the reason for PEG consideration.11

Back to the Case

Our patient is likely nearing the end of her life because of end-stage dementia. There is no evidence to suggest placement of a feeding tube would extend her life more than hand feeding.

We know feeding-tube placement could increase aspiration pneumonia risk and significant short- and long-term morbidity and mortality. We can keep her comfortable with small amounts of water, wetting her lips with swabs. If a feeding tube is placed, its use should be evaluated based on the patient’s clinical course. TH

Dr. Pell is an instructor of medicine in the Section of Hospital Medicine at the University of Colorado, Denver.

References

  1. Gauderer MW, Ponsky JL, Izant RJ Jr. Gastrostomy without laparotomy: a percutaneous endoscopic technique. J Pediatr Surg. 1980;15(6):872-875.
  2. Hebert LE, Beckett LA, Scherr PA, and Evans DA. Annual incidence of Alzheimer disease in the United States projected to the years 2000 through 2050. Alzheimer Dis Assoc Disord. 2001;15:169-173.
  3. Grant MD, Rudberg MA, Brody JA. Gastrostomy placement and mortality among hospitalized Medicare beneficiaries. JAMA. 1998;279:1973-1976.
  4. Finocchiaro C, Galletti R, Rovera G, et al. Percutaneous endoscopic gastrostomy: a long-term follow-up. Nutrition. 1997;13(6):520-523.
  5. Leibovitz A, Plotnikov G, Habot B, et al. Pathogenic colonization of oral flora in frail elderly patients fed by nasogastric tube or percutaneous enterogastric tube. J Gerontol A Biol Sci Med. 2003;58(1):52-55.
  6. McCann R. Lack of evidence about tube feeding: food for thought. JAMA. 1999;282(14):1380-1381.
  7. Cameron JL, Caldini P, Toung J-K, et al. Aspiration pneumonia: physiologic data following experimental Aspiration. Surgery. 1972;72:238.
  8. Loeb MB, Becker M, Eady A, et al. Interventions to prevent aspiration pneumonia in older adults: a systematic review. JAGS. 2003;51(7):1018-1022.
  9. Mitchell SL, Kiely DK, Lipsitz LA. The risk factors and impact on survival of feeding tube placement in nursing home residents with severe cognitive impairment. Arch Intern Med. 1997;157:327-332.
  10. McCann RM, Hall WJ, Groth-Junker A. Comfort care for terminally ill patients: the appropriate use of nutrition and hydration. JAMA. 1994;272:1263-1266.
  11. Rabeneck L, McCullough LB. Ethically justified, clinically comprehensive guidelines for percutaneous endoscopic gastrostomy tube placement. Lancet. 1997;349(9050):496-498.
Issue
The Hospitalist - 2007(12)
Issue
The Hospitalist - 2007(12)
Publications
Publications
Article Type
Display Headline
Do feeding tubes improve outcomes in patients with dementia?
Display Headline
Do feeding tubes improve outcomes in patients with dementia?
Sections
Disallow All Ads
Content Gating
No Gating (article Unlocked/Free)

Patient Proxies

Article Type
Changed
Display Headline
Patient Proxies

In the best interests of the patient. In accordance with the patient’s wishes. Preserving patient autonomy. These concepts are at the core of modern medical decision-making.

Traditionally medical decisions are made by hospitalists and communicated to patients. This approach has shifted to an emphasis on patient autonomy and input in decision-making.

But what about the patient unable to make decisions or provide input to the medical caregivers? How can the comatose or incompetent patient participate in his or her own care decisions? What happens when half of a team is no longer able to share team functions?

In these instances, hospitalists rely on surrogates. A surrogate is empowered not only to speak for but also to make legal decisions for a patient. The relationship becomes a triad of hospitalist, surrogate, and patient. This triad must include:

  • A hospitalist who brings the same degree of trust, respect, and open communication to the new relationship;
  • A surrogate who is an active participant rather than a passive spokesperson; and
  • A patient whose interests are the primary goal.

SURROGATE STEPS

  • Immediately begin building trust to develop understanding about the patient’s needs and wishes.
  • Maintain continuity and open lines of communication with the surrogate. Try to ensure that the surrogate continues talking with the same staff members.
  • Talk to the surrogate often about medical information. Do not allow the surrogate to make a decision without all the information available.
  • Speak to the surrogate in laymen’s terms. Be sure the surrogate understands the medical information about the patient’s status, what is possible, and what is recommended.
  • Consider the surrogate’s emotions and feelings from the beginning. Provide support and comfort. Ask about the surrogate’s values or viewpoint.
  • Call on multidisciplinary staff to facilitate interaction with surrogates whose cultural mores or language may cause confusion or conflict or whose emotions may be interfering with the task at hand.
  • Be prepared to rethink decision-making in light of surrogate and patient’s cultural values or religious beliefs.
  • Talk to the ethics committee early in the patient’s care; do not wait until you see a problem developing. Work within the internal system to prevent a judicial or legal intervention.
  • Do everything possible to avoid a judicial intervention or court guardianship of the patient. Consider this to be a last resort. It not only adds bureaucratic layers, but it also costs money.—AK

Key Issues

The aging of the population and the increased prevalence of medical conditions causing cognitive impairment point up the need to take a closer look at the hospitalist-surrogate relationship. A study this year outlined four key issues:

  • There are unique challenges for both parties in creating a hospitalist-surrogate relationship;
  • The hospitalist and surrogate are dealing not only with each other but also with the decision-making role each will play in regard to the patient;
  • The surrogate must understand that serving as a surrogate for a loved one is completely different from making decisions for oneself; and
  • There may be more than one surrogate decision maker.1

The first challenge facing hospitalist and surrogate is establishing a foundation of trust, respect, and a treatment plan. Their perspectives play a critical role: The surrogate knows the patient as a lively, engaged, and interesting individual, while the hospitalist has seen the patient only in a nonresponsive, incapacitated state. Opening an immediate line of communication is the best way to assume their respective responsibilities.

 

 

Second, even after the hospitalist and surrogate develop an initial working relationship, they may still need to outline mutually satisfying ways to share decision-making with the patient. Both must balance their concern for the patient, their understanding of the patient’s status, and their perspectives of what the patient would want. With time pressures and the capabilities of modern technology, this mutual decision-making responsibility may seem daunting.

Third, surrogates may discover a conflict between their personal values and their patient’s. They may have to make a decision that reflects their patient’s wishes yet contradicts their own beliefs. Sometimes hospitalists can help the surrogate resolve this dilemma by suggesting consultations with other family members or professionals.

The fourth issue, multiple surrogates, may magnify the challenges but can also be an advantage. In most cases families, even those with members who have differing belief systems, tend to support each other during crises to reach a consensus in the patient’s best interests.

Tom Baudendistel, MD, a hospitalist at California Pacific Medical Center in San Francisco, says that although engaging in a dialogue with the multiple surrogates may reveal a family conflict, mistrust, or other issues, the problem is usually resolved. “One surrogate comes around after we make sure the one disagreeing sees in person what the patient is going through, the low quality of life,” says Dr. Baudendistel.

Howard Epstein, MD, medical director, Care Management and Palliative Care, Regions Hospital, St. Paul, Minn., suggests a different approach. “We ask the surrogate to imagine that if the patient could stand outside his or her body, hearing everything that is being said, what would he or she say?” says Dr. Epstein.

The Process

While these issues affect all hospitalists who work with surrogates, hospitalists often encounter additional circumstances that require special attention. These are not always problems but may be situations unique to the hospital setting or the hospitalist’s job.

The hospitalist’s first contact with a patient is often the patient’s admission to the hospital. The hospitalist is most often starting with a blank page with no background information. Gathering information quickly about an unknown patient is critical.

This duty often falls to hospitalists. Donald Krause, MD, medical director for quality assurance at St. Joseph Hospital in Bangor, Maine, and a hospitalist for 11 years, points out that “hospitalists take care of 90% of medical admissions and as part of this job arrange for surrogates if needed as well as anything else to help the patient.”

Beginning with the admission of a patient, the hospitalist may take on the responsibility of finding a surrogate.

Find a surrogate: When a patient is admitted, the hospitalist questions everyone connected to the patient about the existence of a surrogate or family spokesperson. If there is no information available, many hospitalists turn to other staff experts, such as social workers or chaplains, to seek people who know the patient.

Dr. Baudendistel says his medical center resuscitates “unbefriended” patients admitted to the emergency department to allow time to find a family member or surrogate. “Social workers then search the Internet, call shelters, and contact other hospitals and institutions to learn anything they can about the patient,” he says. If the search is unsuccessful, the hospitalist usually consults the institution’s ethics committee for additional suggestions.

Don C. Postema, PhD, ethics consultant for Regions Hospital, chair of the HealthPartners Ethics Committee, and ethicist-in-residence at Gillette Children’s Specialty HealthCare in St. Paul, Minn., proposes that an ethics committee look beyond the standard candidates in searching for a surrogate. “The legal relationship of a potential surrogate to the patient is secondary to what I consider to be the primary relationship, that is, the person who knows the patient best,” says Dr. Postema. “It could be the patient’s landlord or a neighbor who sees the patient on a regular basis.”

 

 

What about the patient whose family lives too far away to see the patient on a regular basis? Look into hiring a local geriatric case manager, Dr. Epstein advises.

There is one person who should not serve as a patient’s surrogate: the attending physician, whether a hospitalist or the primary caregiver. Erin Egan, MD, JD, assistant professor of hospital medicine, University of Colorado Hospitals, warns that a hospitalist acting as a surrogate has a conflict of interest. “Most states prohibit hospitalists from acting as surrogates,” Dr. Egan warns. “In some cases a doctor can presume consent for a short time before a surrogate is appointed in order to make an immediate medical decision. As a general rule, however, a clinician should never assume the surrogate’s role.”

Look for advance directives: Ideally, every patient’s file would contain an advance directive indicating a surrogate or a note that there is no surrogate.2 In addition, there should be a healthcare advance directive, also known as a healthcare power of attorney, that appoints a surrogate. It is often accompanied by a living will, an instruction sheet stipulating what treatment the patient wants if he or she is unable to speak or communicate. Unfortunately, many hospitalists cannot find these documents when they admit a patient.

In this case, the hospitalist must search. Most hospitals, nursing homes, or home healthcare agencies are required by the federal Patient Self-Determination Act (PSDA) to offer information about advance directives at the time of admission. This information states the patient’s healthcare decision-making rights under state law and the institution’s policy about adhering to advance directives. Contacting these agencies is a starting point.

Make difficult decisions: While some advance directives carry legal power, they often are not helpful to hospitalists or surrogates making end-of-life decisions. Because a medical crisis cannot always be predicted and treatment options change rapidly, a specific directive may not be as helpful as a written description of a patient’s beliefs, religious convictions, and cultural values. Equally valuable are notes about conversations among patients, family members, friends, and caregivers.3 This creates a picture of the patient’s feelings about quality of life, treatment preferences, and end-of-life outcomes.

The hospitalist’s role in this situation is to facilitate such discussions among all family and friends involved. The goal is to develop an accurate picture of the patient to make appropriate decisions. The hospitalist should explore the cultural values and religious beliefs of the patient, surrogate, family, and friends. “Different ethnic groups view medical care differently,” says Richard L. Heinrich, MD, medical director of Hospice of the Lakes, Bloomington, Minn. “Some religions believe that suffering in this life is rewarded in the next life, which makes a difference when making treatment decisions,” he says. “We must honor and work with cultural values unless in our view the individual is suffering needlessly.”

The hospitalist should be alert to the need for an interpreter and anything else that will promote a meaningful discussion. And, the hospitalist and the medical staff should be prepared to share as much medical information as is possible, including individual staff opinions, the rationale behind recommendations, and the pros and cons of each suggestion. The surrogate and family cannot make any meaningful contribution without all the pertinent information.

The goal should be a consensus about the patient’s best interests, how certain medical decisions will provide benefit or burden to the patient, and if the decision is what the patient would want. It’s especially critical to call a family conference to allow everyone the opportunity to discuss the patient’s concept of his or her death.

 

 

“Most people are afraid of getting caught in an end-of-life situation where they lose control,” says Dr. Postema. TH

Ann Kepler is a medical writer based in Chicago.

References

  1. Torke AM, Alexander GC, Lantos J, et al. The physician-surrogate relationship. Arch Intern Med. 2007 Jun 11;167(11):1117-1121.
  2. Wenger NS, Rosenfeld K. Quality indicators for end-of-life care in vulnerable elders. Ann Intern Med. 2001 Oct 16;135(8):677-685.
  3. Bloche MG. Managing conflict at the end of life. N Engl J Med. 2005 Jun 9;352:2371-2373.
Issue
The Hospitalist - 2007(12)
Publications
Sections

In the best interests of the patient. In accordance with the patient’s wishes. Preserving patient autonomy. These concepts are at the core of modern medical decision-making.

Traditionally medical decisions are made by hospitalists and communicated to patients. This approach has shifted to an emphasis on patient autonomy and input in decision-making.

But what about the patient unable to make decisions or provide input to the medical caregivers? How can the comatose or incompetent patient participate in his or her own care decisions? What happens when half of a team is no longer able to share team functions?

In these instances, hospitalists rely on surrogates. A surrogate is empowered not only to speak for but also to make legal decisions for a patient. The relationship becomes a triad of hospitalist, surrogate, and patient. This triad must include:

  • A hospitalist who brings the same degree of trust, respect, and open communication to the new relationship;
  • A surrogate who is an active participant rather than a passive spokesperson; and
  • A patient whose interests are the primary goal.

SURROGATE STEPS

  • Immediately begin building trust to develop understanding about the patient’s needs and wishes.
  • Maintain continuity and open lines of communication with the surrogate. Try to ensure that the surrogate continues talking with the same staff members.
  • Talk to the surrogate often about medical information. Do not allow the surrogate to make a decision without all the information available.
  • Speak to the surrogate in laymen’s terms. Be sure the surrogate understands the medical information about the patient’s status, what is possible, and what is recommended.
  • Consider the surrogate’s emotions and feelings from the beginning. Provide support and comfort. Ask about the surrogate’s values or viewpoint.
  • Call on multidisciplinary staff to facilitate interaction with surrogates whose cultural mores or language may cause confusion or conflict or whose emotions may be interfering with the task at hand.
  • Be prepared to rethink decision-making in light of surrogate and patient’s cultural values or religious beliefs.
  • Talk to the ethics committee early in the patient’s care; do not wait until you see a problem developing. Work within the internal system to prevent a judicial or legal intervention.
  • Do everything possible to avoid a judicial intervention or court guardianship of the patient. Consider this to be a last resort. It not only adds bureaucratic layers, but it also costs money.—AK

Key Issues

The aging of the population and the increased prevalence of medical conditions causing cognitive impairment point up the need to take a closer look at the hospitalist-surrogate relationship. A study this year outlined four key issues:

  • There are unique challenges for both parties in creating a hospitalist-surrogate relationship;
  • The hospitalist and surrogate are dealing not only with each other but also with the decision-making role each will play in regard to the patient;
  • The surrogate must understand that serving as a surrogate for a loved one is completely different from making decisions for oneself; and
  • There may be more than one surrogate decision maker.1

The first challenge facing hospitalist and surrogate is establishing a foundation of trust, respect, and a treatment plan. Their perspectives play a critical role: The surrogate knows the patient as a lively, engaged, and interesting individual, while the hospitalist has seen the patient only in a nonresponsive, incapacitated state. Opening an immediate line of communication is the best way to assume their respective responsibilities.

 

 

Second, even after the hospitalist and surrogate develop an initial working relationship, they may still need to outline mutually satisfying ways to share decision-making with the patient. Both must balance their concern for the patient, their understanding of the patient’s status, and their perspectives of what the patient would want. With time pressures and the capabilities of modern technology, this mutual decision-making responsibility may seem daunting.

Third, surrogates may discover a conflict between their personal values and their patient’s. They may have to make a decision that reflects their patient’s wishes yet contradicts their own beliefs. Sometimes hospitalists can help the surrogate resolve this dilemma by suggesting consultations with other family members or professionals.

The fourth issue, multiple surrogates, may magnify the challenges but can also be an advantage. In most cases families, even those with members who have differing belief systems, tend to support each other during crises to reach a consensus in the patient’s best interests.

Tom Baudendistel, MD, a hospitalist at California Pacific Medical Center in San Francisco, says that although engaging in a dialogue with the multiple surrogates may reveal a family conflict, mistrust, or other issues, the problem is usually resolved. “One surrogate comes around after we make sure the one disagreeing sees in person what the patient is going through, the low quality of life,” says Dr. Baudendistel.

Howard Epstein, MD, medical director, Care Management and Palliative Care, Regions Hospital, St. Paul, Minn., suggests a different approach. “We ask the surrogate to imagine that if the patient could stand outside his or her body, hearing everything that is being said, what would he or she say?” says Dr. Epstein.

The Process

While these issues affect all hospitalists who work with surrogates, hospitalists often encounter additional circumstances that require special attention. These are not always problems but may be situations unique to the hospital setting or the hospitalist’s job.

The hospitalist’s first contact with a patient is often the patient’s admission to the hospital. The hospitalist is most often starting with a blank page with no background information. Gathering information quickly about an unknown patient is critical.

This duty often falls to hospitalists. Donald Krause, MD, medical director for quality assurance at St. Joseph Hospital in Bangor, Maine, and a hospitalist for 11 years, points out that “hospitalists take care of 90% of medical admissions and as part of this job arrange for surrogates if needed as well as anything else to help the patient.”

Beginning with the admission of a patient, the hospitalist may take on the responsibility of finding a surrogate.

Find a surrogate: When a patient is admitted, the hospitalist questions everyone connected to the patient about the existence of a surrogate or family spokesperson. If there is no information available, many hospitalists turn to other staff experts, such as social workers or chaplains, to seek people who know the patient.

Dr. Baudendistel says his medical center resuscitates “unbefriended” patients admitted to the emergency department to allow time to find a family member or surrogate. “Social workers then search the Internet, call shelters, and contact other hospitals and institutions to learn anything they can about the patient,” he says. If the search is unsuccessful, the hospitalist usually consults the institution’s ethics committee for additional suggestions.

Don C. Postema, PhD, ethics consultant for Regions Hospital, chair of the HealthPartners Ethics Committee, and ethicist-in-residence at Gillette Children’s Specialty HealthCare in St. Paul, Minn., proposes that an ethics committee look beyond the standard candidates in searching for a surrogate. “The legal relationship of a potential surrogate to the patient is secondary to what I consider to be the primary relationship, that is, the person who knows the patient best,” says Dr. Postema. “It could be the patient’s landlord or a neighbor who sees the patient on a regular basis.”

 

 

What about the patient whose family lives too far away to see the patient on a regular basis? Look into hiring a local geriatric case manager, Dr. Epstein advises.

There is one person who should not serve as a patient’s surrogate: the attending physician, whether a hospitalist or the primary caregiver. Erin Egan, MD, JD, assistant professor of hospital medicine, University of Colorado Hospitals, warns that a hospitalist acting as a surrogate has a conflict of interest. “Most states prohibit hospitalists from acting as surrogates,” Dr. Egan warns. “In some cases a doctor can presume consent for a short time before a surrogate is appointed in order to make an immediate medical decision. As a general rule, however, a clinician should never assume the surrogate’s role.”

Look for advance directives: Ideally, every patient’s file would contain an advance directive indicating a surrogate or a note that there is no surrogate.2 In addition, there should be a healthcare advance directive, also known as a healthcare power of attorney, that appoints a surrogate. It is often accompanied by a living will, an instruction sheet stipulating what treatment the patient wants if he or she is unable to speak or communicate. Unfortunately, many hospitalists cannot find these documents when they admit a patient.

In this case, the hospitalist must search. Most hospitals, nursing homes, or home healthcare agencies are required by the federal Patient Self-Determination Act (PSDA) to offer information about advance directives at the time of admission. This information states the patient’s healthcare decision-making rights under state law and the institution’s policy about adhering to advance directives. Contacting these agencies is a starting point.

Make difficult decisions: While some advance directives carry legal power, they often are not helpful to hospitalists or surrogates making end-of-life decisions. Because a medical crisis cannot always be predicted and treatment options change rapidly, a specific directive may not be as helpful as a written description of a patient’s beliefs, religious convictions, and cultural values. Equally valuable are notes about conversations among patients, family members, friends, and caregivers.3 This creates a picture of the patient’s feelings about quality of life, treatment preferences, and end-of-life outcomes.

The hospitalist’s role in this situation is to facilitate such discussions among all family and friends involved. The goal is to develop an accurate picture of the patient to make appropriate decisions. The hospitalist should explore the cultural values and religious beliefs of the patient, surrogate, family, and friends. “Different ethnic groups view medical care differently,” says Richard L. Heinrich, MD, medical director of Hospice of the Lakes, Bloomington, Minn. “Some religions believe that suffering in this life is rewarded in the next life, which makes a difference when making treatment decisions,” he says. “We must honor and work with cultural values unless in our view the individual is suffering needlessly.”

The hospitalist should be alert to the need for an interpreter and anything else that will promote a meaningful discussion. And, the hospitalist and the medical staff should be prepared to share as much medical information as is possible, including individual staff opinions, the rationale behind recommendations, and the pros and cons of each suggestion. The surrogate and family cannot make any meaningful contribution without all the pertinent information.

The goal should be a consensus about the patient’s best interests, how certain medical decisions will provide benefit or burden to the patient, and if the decision is what the patient would want. It’s especially critical to call a family conference to allow everyone the opportunity to discuss the patient’s concept of his or her death.

 

 

“Most people are afraid of getting caught in an end-of-life situation where they lose control,” says Dr. Postema. TH

Ann Kepler is a medical writer based in Chicago.

References

  1. Torke AM, Alexander GC, Lantos J, et al. The physician-surrogate relationship. Arch Intern Med. 2007 Jun 11;167(11):1117-1121.
  2. Wenger NS, Rosenfeld K. Quality indicators for end-of-life care in vulnerable elders. Ann Intern Med. 2001 Oct 16;135(8):677-685.
  3. Bloche MG. Managing conflict at the end of life. N Engl J Med. 2005 Jun 9;352:2371-2373.

In the best interests of the patient. In accordance with the patient’s wishes. Preserving patient autonomy. These concepts are at the core of modern medical decision-making.

Traditionally medical decisions are made by hospitalists and communicated to patients. This approach has shifted to an emphasis on patient autonomy and input in decision-making.

But what about the patient unable to make decisions or provide input to the medical caregivers? How can the comatose or incompetent patient participate in his or her own care decisions? What happens when half of a team is no longer able to share team functions?

In these instances, hospitalists rely on surrogates. A surrogate is empowered not only to speak for but also to make legal decisions for a patient. The relationship becomes a triad of hospitalist, surrogate, and patient. This triad must include:

  • A hospitalist who brings the same degree of trust, respect, and open communication to the new relationship;
  • A surrogate who is an active participant rather than a passive spokesperson; and
  • A patient whose interests are the primary goal.

SURROGATE STEPS

  • Immediately begin building trust to develop understanding about the patient’s needs and wishes.
  • Maintain continuity and open lines of communication with the surrogate. Try to ensure that the surrogate continues talking with the same staff members.
  • Talk to the surrogate often about medical information. Do not allow the surrogate to make a decision without all the information available.
  • Speak to the surrogate in laymen’s terms. Be sure the surrogate understands the medical information about the patient’s status, what is possible, and what is recommended.
  • Consider the surrogate’s emotions and feelings from the beginning. Provide support and comfort. Ask about the surrogate’s values or viewpoint.
  • Call on multidisciplinary staff to facilitate interaction with surrogates whose cultural mores or language may cause confusion or conflict or whose emotions may be interfering with the task at hand.
  • Be prepared to rethink decision-making in light of surrogate and patient’s cultural values or religious beliefs.
  • Talk to the ethics committee early in the patient’s care; do not wait until you see a problem developing. Work within the internal system to prevent a judicial or legal intervention.
  • Do everything possible to avoid a judicial intervention or court guardianship of the patient. Consider this to be a last resort. It not only adds bureaucratic layers, but it also costs money.—AK

Key Issues

The aging of the population and the increased prevalence of medical conditions causing cognitive impairment point up the need to take a closer look at the hospitalist-surrogate relationship. A study this year outlined four key issues:

  • There are unique challenges for both parties in creating a hospitalist-surrogate relationship;
  • The hospitalist and surrogate are dealing not only with each other but also with the decision-making role each will play in regard to the patient;
  • The surrogate must understand that serving as a surrogate for a loved one is completely different from making decisions for oneself; and
  • There may be more than one surrogate decision maker.1

The first challenge facing hospitalist and surrogate is establishing a foundation of trust, respect, and a treatment plan. Their perspectives play a critical role: The surrogate knows the patient as a lively, engaged, and interesting individual, while the hospitalist has seen the patient only in a nonresponsive, incapacitated state. Opening an immediate line of communication is the best way to assume their respective responsibilities.

 

 

Second, even after the hospitalist and surrogate develop an initial working relationship, they may still need to outline mutually satisfying ways to share decision-making with the patient. Both must balance their concern for the patient, their understanding of the patient’s status, and their perspectives of what the patient would want. With time pressures and the capabilities of modern technology, this mutual decision-making responsibility may seem daunting.

Third, surrogates may discover a conflict between their personal values and their patient’s. They may have to make a decision that reflects their patient’s wishes yet contradicts their own beliefs. Sometimes hospitalists can help the surrogate resolve this dilemma by suggesting consultations with other family members or professionals.

The fourth issue, multiple surrogates, may magnify the challenges but can also be an advantage. In most cases families, even those with members who have differing belief systems, tend to support each other during crises to reach a consensus in the patient’s best interests.

Tom Baudendistel, MD, a hospitalist at California Pacific Medical Center in San Francisco, says that although engaging in a dialogue with the multiple surrogates may reveal a family conflict, mistrust, or other issues, the problem is usually resolved. “One surrogate comes around after we make sure the one disagreeing sees in person what the patient is going through, the low quality of life,” says Dr. Baudendistel.

Howard Epstein, MD, medical director, Care Management and Palliative Care, Regions Hospital, St. Paul, Minn., suggests a different approach. “We ask the surrogate to imagine that if the patient could stand outside his or her body, hearing everything that is being said, what would he or she say?” says Dr. Epstein.

The Process

While these issues affect all hospitalists who work with surrogates, hospitalists often encounter additional circumstances that require special attention. These are not always problems but may be situations unique to the hospital setting or the hospitalist’s job.

The hospitalist’s first contact with a patient is often the patient’s admission to the hospital. The hospitalist is most often starting with a blank page with no background information. Gathering information quickly about an unknown patient is critical.

This duty often falls to hospitalists. Donald Krause, MD, medical director for quality assurance at St. Joseph Hospital in Bangor, Maine, and a hospitalist for 11 years, points out that “hospitalists take care of 90% of medical admissions and as part of this job arrange for surrogates if needed as well as anything else to help the patient.”

Beginning with the admission of a patient, the hospitalist may take on the responsibility of finding a surrogate.

Find a surrogate: When a patient is admitted, the hospitalist questions everyone connected to the patient about the existence of a surrogate or family spokesperson. If there is no information available, many hospitalists turn to other staff experts, such as social workers or chaplains, to seek people who know the patient.

Dr. Baudendistel says his medical center resuscitates “unbefriended” patients admitted to the emergency department to allow time to find a family member or surrogate. “Social workers then search the Internet, call shelters, and contact other hospitals and institutions to learn anything they can about the patient,” he says. If the search is unsuccessful, the hospitalist usually consults the institution’s ethics committee for additional suggestions.

Don C. Postema, PhD, ethics consultant for Regions Hospital, chair of the HealthPartners Ethics Committee, and ethicist-in-residence at Gillette Children’s Specialty HealthCare in St. Paul, Minn., proposes that an ethics committee look beyond the standard candidates in searching for a surrogate. “The legal relationship of a potential surrogate to the patient is secondary to what I consider to be the primary relationship, that is, the person who knows the patient best,” says Dr. Postema. “It could be the patient’s landlord or a neighbor who sees the patient on a regular basis.”

 

 

What about the patient whose family lives too far away to see the patient on a regular basis? Look into hiring a local geriatric case manager, Dr. Epstein advises.

There is one person who should not serve as a patient’s surrogate: the attending physician, whether a hospitalist or the primary caregiver. Erin Egan, MD, JD, assistant professor of hospital medicine, University of Colorado Hospitals, warns that a hospitalist acting as a surrogate has a conflict of interest. “Most states prohibit hospitalists from acting as surrogates,” Dr. Egan warns. “In some cases a doctor can presume consent for a short time before a surrogate is appointed in order to make an immediate medical decision. As a general rule, however, a clinician should never assume the surrogate’s role.”

Look for advance directives: Ideally, every patient’s file would contain an advance directive indicating a surrogate or a note that there is no surrogate.2 In addition, there should be a healthcare advance directive, also known as a healthcare power of attorney, that appoints a surrogate. It is often accompanied by a living will, an instruction sheet stipulating what treatment the patient wants if he or she is unable to speak or communicate. Unfortunately, many hospitalists cannot find these documents when they admit a patient.

In this case, the hospitalist must search. Most hospitals, nursing homes, or home healthcare agencies are required by the federal Patient Self-Determination Act (PSDA) to offer information about advance directives at the time of admission. This information states the patient’s healthcare decision-making rights under state law and the institution’s policy about adhering to advance directives. Contacting these agencies is a starting point.

Make difficult decisions: While some advance directives carry legal power, they often are not helpful to hospitalists or surrogates making end-of-life decisions. Because a medical crisis cannot always be predicted and treatment options change rapidly, a specific directive may not be as helpful as a written description of a patient’s beliefs, religious convictions, and cultural values. Equally valuable are notes about conversations among patients, family members, friends, and caregivers.3 This creates a picture of the patient’s feelings about quality of life, treatment preferences, and end-of-life outcomes.

The hospitalist’s role in this situation is to facilitate such discussions among all family and friends involved. The goal is to develop an accurate picture of the patient to make appropriate decisions. The hospitalist should explore the cultural values and religious beliefs of the patient, surrogate, family, and friends. “Different ethnic groups view medical care differently,” says Richard L. Heinrich, MD, medical director of Hospice of the Lakes, Bloomington, Minn. “Some religions believe that suffering in this life is rewarded in the next life, which makes a difference when making treatment decisions,” he says. “We must honor and work with cultural values unless in our view the individual is suffering needlessly.”

The hospitalist should be alert to the need for an interpreter and anything else that will promote a meaningful discussion. And, the hospitalist and the medical staff should be prepared to share as much medical information as is possible, including individual staff opinions, the rationale behind recommendations, and the pros and cons of each suggestion. The surrogate and family cannot make any meaningful contribution without all the pertinent information.

The goal should be a consensus about the patient’s best interests, how certain medical decisions will provide benefit or burden to the patient, and if the decision is what the patient would want. It’s especially critical to call a family conference to allow everyone the opportunity to discuss the patient’s concept of his or her death.

 

 

“Most people are afraid of getting caught in an end-of-life situation where they lose control,” says Dr. Postema. TH

Ann Kepler is a medical writer based in Chicago.

References

  1. Torke AM, Alexander GC, Lantos J, et al. The physician-surrogate relationship. Arch Intern Med. 2007 Jun 11;167(11):1117-1121.
  2. Wenger NS, Rosenfeld K. Quality indicators for end-of-life care in vulnerable elders. Ann Intern Med. 2001 Oct 16;135(8):677-685.
  3. Bloche MG. Managing conflict at the end of life. N Engl J Med. 2005 Jun 9;352:2371-2373.
Issue
The Hospitalist - 2007(12)
Issue
The Hospitalist - 2007(12)
Publications
Publications
Article Type
Display Headline
Patient Proxies
Display Headline
Patient Proxies
Sections
Disallow All Ads
Content Gating
No Gating (article Unlocked/Free)

To Serve in America

Article Type
Changed
Display Headline
To Serve in America

In the first part of this two-part series, we examined the implications of international medical graduates (IMGs) in hospital medicine groups (November 2007, p. 1). Part 2 features stories from hospitalist IMGs as they establish themselves as professionals in their communities.

December 2005 was a tough time for Charles Onunkwo, MD, and his wife. He had been working since July 1 as a hospitalist with St. Clare’s Hospital in Wausau, a small town in central Wisconsin, and had just received alarming news. His H1-B visa transfer, filed by his immigration attorney, had been denied.

His wife’s application to change from a visitor visa to an H-4 (dependent of an H1-B visa holder) was also denied. As a result, his wife was considered “unlawfully present” in the country. Dr. Onunkwo was now “out of status,” because the Naturalization and Immigration Service (INS) did not recognize St. Clare’s as exempt from caps on the annual number of H1-B visas granted. The couple was faced with a mandatory return trip to their native Nigeria, and no guarantee that the U.S. Consulate in Lagos would grant them permission to return to the United States to work as physicians.

“It was a bad time for us,” he recalls.

Charles Onunkwo, MD, hospitalist, St. Clare’s Hospital, Wausau, Wis.
I feel the skepticism, but I still treat the [patient or colleague] with the respect that they deserve. Ultimately, I just let my work do the talking.

Barriers and Adjustments

The obstacles faced by IMGs in obtaining visas and eventual permanent employment status have been well documented.1 For the Onunkwos, the story had a good outcome: a new immigration attorney hired by St. Clare’s was able to establish the hospital as a “cap-exempt” organization. Intervention by the staff of Rep. David R. Obey, D-Wis., allowed them to secure new H-1B visas and a return to this country.

Dr. Onunkwo and the other hospitalist IMGs attest that immigration hurdles constitute their biggest challenges.

There can be other barriers as well. Mark Dotson, senior recruiter for Cogent Healthcare in Nashville, Tenn., has encountered resistance toward IMG candidates from hospital administrators in some communities. Concerns usually relate to candidates’ ability to communicate effectively and demonstrate appropriate bedside manner. “There are also some misperceptions about some residency programs that can hinder an international medical graduate,” he says. In addition, some communities “want the doctors to reflect the makeup of the local community.” That means in a community that is 95% Caucasian, hospital administrators may be reluctant to hire a physician of color.

Dotson says attention to communication skills should be the primary goal of IMGs, and that buy-in from hospital administrators or leaders of hospital medicine groups is critical for smooth transitions. “I think some of the best physicians we have out there are doctors who are international medical graduates who see this as their life calling,” he says. “And, I think that even people in the general population understand that IMGs are extremely intelligent, and that they work extremely hard.”

As the following stories affirm, communities in remote or medically underserved areas are often welcoming of physicians who offer much-needed primary care.

Dr. Fajardo and his wife, Beverly

A Long Journey

In 1997, Emmanuel Fajardo, MD, medical director of the hospitalist program at St. Dominic-Jackson Memorial Hospital in Jackson, Miss., found himself “between the devil and the deep blue sea.” He had just been offered a chief residency position at the Meharry Medical College Affiliated Hospitals Internal Medicine residency program and was torn between accepting that job and a J-1 waiver offer in Shubuta, Miss., a federally designated Medically Underserved Area (MUSA).

 

 

He had been waiting a full year for the J-1 visa waiver, which allows IMGs to remain in the U.S. in exchange for five years of service in an MUSA. But, he also liked teaching and was attracted to the opportunity to pass on a legacy to the junior residents and incoming interns. He elected to proceed with the waiver because it offered the opportunity to “stay here in the States and to be able to practice medicine for good.”

Born in the Philippines, Dr. Fajardo says his family was wary about his locating to a remote area in Mississippi—but he wasn’t. “When I make a decision, I go for it 100%,” he says. “In everything I do I always do my best and leave the rest to God. I was very fortunate to find out that the community was very involved in and engaged with my waiver.

“Also, to my surprise, I didn’t feel discriminated against at all. They made me feel like I’m a part of the family. There is a strong sense of community here, indeed. The only problem then was, of course, being in a small town, that whatever you do, everybody knows about it.”

Although Dr. Onunkwo moved to Wausau, Wis., a small town in a predominantly white area, he says it was not difficult for him to adjust to life there. Part of the reason, he says, is that his first overseas experience was in Ireland, where he obtained a diploma in tropical medical at the Royal College of Surgeons in Dublin and practiced in a small village nearby. In addition, he and his wife were together in Wausau. “It was probably easier for both of us because we had each other,” he says.

And then there were their great neighbors, says Dr. Onunkwo. ”They made the transition seamless,” he says. “We have formed lifelong relationships with some of our neighbors in Wausau.” The strength of those relationships became apparent on Christmas Day 2005. “They really don’t know what they have done for us,” Dr. Onunkwo recalls warmly. “When we were going through our travails, they knew something was wrong, but we didn’t tell them exactly what we were going through. They made our day for us, because they just rang our bell and here they had the three-course Christmas dinner for us.”

Dr. Patel

Know Your Visas

To enter a residency program in the U.S., an IMG must pass steps one and two of the U.S. Medical Licensure Examination, then the Clinical Skills Examination. To obtain legal visitor status, most IMGs apply for:

  • J-1 visa: This is administered by the INS and allows an IMG to complete residency training at an Educational Commission for Foreign Medical Graduates-accredited program. If the IMG brings a spouse or other dependents, they usually obtain a J-2 visa. The J-1 visa carries a requirement that an IMG return to his or her native country for two years following completion of residency. Many IMGs want to remain in the country, which is why they often make use of the J-1 visa waiver.
  • J-1 visa waiver: This is a mechanism that allows IMGs to stay in the country and eventually apply for permanent status in exchange for five years of working in a medically underserved area. New post-9/11 restrictions of J-1 visas and attendant waivers have led a trend for IMGs to secure the H1-B visa.
  • H1-B visa: This allows the IMG to remain in the U.S. as long as they are employed full-time by an agency, academic institution or employer (such as a hospital) certified by the INS as exempt from immigrant caps on the annual number of H-1B visas granted. Spouses and other dependents of employed H1-B visa holders, then, obtain the H-4 visa in order to remain in the country.—GH

 

 

Prove Yourself

Dr. Onunkwo has been aware of misperceptions about his professional competency. “Depending on what part of the country you find yourself in, you need to continually prove yourself,” he says. “There is this perception, maybe due to the accent or the way you express yourself. It’s unspoken, but it’s there and you don’t need to be a rocket scientist to observe that. You need to prove that you’re good to be able to survive.”

This is easier for some than others.

“I cannot say I have experienced any barriers in that respect,” reports Gunter Kurrle, MD, lead physician with the WellStar Kennestone Hospitalist Group in Atlanta. “I’m European, like most Americans with European background, so it has not been my personal experience to encounter prejudice.” Dr. Kurrle’s journey to his present post as lead hospitalist is also atypical compared with most IMGs who come to the U.S. He initially took his foreign medical graduate examination in the late 1980s, just before the United States Medical Licensing Examination was initiated. He then returned to Germany for five years of additional training after his residency in this country. He came back to the U.S. for personal reasons (his wife is a U.S. citizen and was starting her residency training here) and found that entering hospital medicine was “a better fit than trying to start a practice on my own.”

Hemant Patel, MD, president of the American Association of Physicians of Indian Origin (AAIP), based in Oak Brook, Ill., believes discrimination toward foreign-born physicians has been greatly reduced since the early 1980s, when he entered the country. AAPI, with membership of 45,000, was founded in 1982 to offer support to IMGs from India. Physicians of Indian origin constitute the largest group of IMGs.2

“At that time, it was very difficult to obtain residency slots due to competition, and we had a lot more physicians to occupy those slots,” says Dr. Patel.

Dr. Fajardo believes the inclination to discriminate is inherent in everyone: “It’s latent, but if you give them the reason to discriminate against you, then it will manifest.” With regards to the physician-patient relationship, Dr. Fajardo reports that initially, on rare occasions, he encountered resistance from patients who were reluctant to trust their care to him because of his name (“I can’t pronounce it—are you a terrorist?”) or his looks (“You look too young to be a doctor—are you sure you can take care of me?”).

“At the end of the day, it’s very fulfilling when you hear them say, ‘Thanks a lot, doc, for getting me better,’’ says Dr. Fajardo. “I believe that it isn’t where you come from that matters; it’s what you can do.” Overall, he says, the realities of the medical profession are that “the outcome of what we do speaks for itself, and that’s what matters most.”

Dr. Onunkwo is philosophical about the initial skepticism he sometimes senses from patients and other colleagues. “I understand that people are wary of the unknown, and I think it’s just natural,” he says. “Usually, what happens in my situation is that I feel the skepticism, but I don’t do anything about it. I still treat the person with the respect that they deserve and ultimately, I just let my work do the talking. Everybody gets the same level of respect and attention that they need and nine times out of 10, before patients are done with their hospital stay, their attitudes toward me have changed.” TH

Gretchen Henkel is a frequent contributor to The Hospitalist.

References

 

 

  1. Leon LR Jr, Villar H, Leon CR, et al. The journey of a foreign-trained physician to a United States residency. J Am Coll Surg. 2007 Mar;204(3):486-494.
  2. Hart LG, Skillman SM, Fordyce M, et al. International medical graduate physicians in the United States: changes since 1981. Health Aff. 2007 Jul/Aug;26(4):1159-1169.
Issue
The Hospitalist - 2007(12)
Publications
Sections

In the first part of this two-part series, we examined the implications of international medical graduates (IMGs) in hospital medicine groups (November 2007, p. 1). Part 2 features stories from hospitalist IMGs as they establish themselves as professionals in their communities.

December 2005 was a tough time for Charles Onunkwo, MD, and his wife. He had been working since July 1 as a hospitalist with St. Clare’s Hospital in Wausau, a small town in central Wisconsin, and had just received alarming news. His H1-B visa transfer, filed by his immigration attorney, had been denied.

His wife’s application to change from a visitor visa to an H-4 (dependent of an H1-B visa holder) was also denied. As a result, his wife was considered “unlawfully present” in the country. Dr. Onunkwo was now “out of status,” because the Naturalization and Immigration Service (INS) did not recognize St. Clare’s as exempt from caps on the annual number of H1-B visas granted. The couple was faced with a mandatory return trip to their native Nigeria, and no guarantee that the U.S. Consulate in Lagos would grant them permission to return to the United States to work as physicians.

“It was a bad time for us,” he recalls.

Charles Onunkwo, MD, hospitalist, St. Clare’s Hospital, Wausau, Wis.
I feel the skepticism, but I still treat the [patient or colleague] with the respect that they deserve. Ultimately, I just let my work do the talking.

Barriers and Adjustments

The obstacles faced by IMGs in obtaining visas and eventual permanent employment status have been well documented.1 For the Onunkwos, the story had a good outcome: a new immigration attorney hired by St. Clare’s was able to establish the hospital as a “cap-exempt” organization. Intervention by the staff of Rep. David R. Obey, D-Wis., allowed them to secure new H-1B visas and a return to this country.

Dr. Onunkwo and the other hospitalist IMGs attest that immigration hurdles constitute their biggest challenges.

There can be other barriers as well. Mark Dotson, senior recruiter for Cogent Healthcare in Nashville, Tenn., has encountered resistance toward IMG candidates from hospital administrators in some communities. Concerns usually relate to candidates’ ability to communicate effectively and demonstrate appropriate bedside manner. “There are also some misperceptions about some residency programs that can hinder an international medical graduate,” he says. In addition, some communities “want the doctors to reflect the makeup of the local community.” That means in a community that is 95% Caucasian, hospital administrators may be reluctant to hire a physician of color.

Dotson says attention to communication skills should be the primary goal of IMGs, and that buy-in from hospital administrators or leaders of hospital medicine groups is critical for smooth transitions. “I think some of the best physicians we have out there are doctors who are international medical graduates who see this as their life calling,” he says. “And, I think that even people in the general population understand that IMGs are extremely intelligent, and that they work extremely hard.”

As the following stories affirm, communities in remote or medically underserved areas are often welcoming of physicians who offer much-needed primary care.

Dr. Fajardo and his wife, Beverly

A Long Journey

In 1997, Emmanuel Fajardo, MD, medical director of the hospitalist program at St. Dominic-Jackson Memorial Hospital in Jackson, Miss., found himself “between the devil and the deep blue sea.” He had just been offered a chief residency position at the Meharry Medical College Affiliated Hospitals Internal Medicine residency program and was torn between accepting that job and a J-1 waiver offer in Shubuta, Miss., a federally designated Medically Underserved Area (MUSA).

 

 

He had been waiting a full year for the J-1 visa waiver, which allows IMGs to remain in the U.S. in exchange for five years of service in an MUSA. But, he also liked teaching and was attracted to the opportunity to pass on a legacy to the junior residents and incoming interns. He elected to proceed with the waiver because it offered the opportunity to “stay here in the States and to be able to practice medicine for good.”

Born in the Philippines, Dr. Fajardo says his family was wary about his locating to a remote area in Mississippi—but he wasn’t. “When I make a decision, I go for it 100%,” he says. “In everything I do I always do my best and leave the rest to God. I was very fortunate to find out that the community was very involved in and engaged with my waiver.

“Also, to my surprise, I didn’t feel discriminated against at all. They made me feel like I’m a part of the family. There is a strong sense of community here, indeed. The only problem then was, of course, being in a small town, that whatever you do, everybody knows about it.”

Although Dr. Onunkwo moved to Wausau, Wis., a small town in a predominantly white area, he says it was not difficult for him to adjust to life there. Part of the reason, he says, is that his first overseas experience was in Ireland, where he obtained a diploma in tropical medical at the Royal College of Surgeons in Dublin and practiced in a small village nearby. In addition, he and his wife were together in Wausau. “It was probably easier for both of us because we had each other,” he says.

And then there were their great neighbors, says Dr. Onunkwo. ”They made the transition seamless,” he says. “We have formed lifelong relationships with some of our neighbors in Wausau.” The strength of those relationships became apparent on Christmas Day 2005. “They really don’t know what they have done for us,” Dr. Onunkwo recalls warmly. “When we were going through our travails, they knew something was wrong, but we didn’t tell them exactly what we were going through. They made our day for us, because they just rang our bell and here they had the three-course Christmas dinner for us.”

Dr. Patel

Know Your Visas

To enter a residency program in the U.S., an IMG must pass steps one and two of the U.S. Medical Licensure Examination, then the Clinical Skills Examination. To obtain legal visitor status, most IMGs apply for:

  • J-1 visa: This is administered by the INS and allows an IMG to complete residency training at an Educational Commission for Foreign Medical Graduates-accredited program. If the IMG brings a spouse or other dependents, they usually obtain a J-2 visa. The J-1 visa carries a requirement that an IMG return to his or her native country for two years following completion of residency. Many IMGs want to remain in the country, which is why they often make use of the J-1 visa waiver.
  • J-1 visa waiver: This is a mechanism that allows IMGs to stay in the country and eventually apply for permanent status in exchange for five years of working in a medically underserved area. New post-9/11 restrictions of J-1 visas and attendant waivers have led a trend for IMGs to secure the H1-B visa.
  • H1-B visa: This allows the IMG to remain in the U.S. as long as they are employed full-time by an agency, academic institution or employer (such as a hospital) certified by the INS as exempt from immigrant caps on the annual number of H-1B visas granted. Spouses and other dependents of employed H1-B visa holders, then, obtain the H-4 visa in order to remain in the country.—GH

 

 

Prove Yourself

Dr. Onunkwo has been aware of misperceptions about his professional competency. “Depending on what part of the country you find yourself in, you need to continually prove yourself,” he says. “There is this perception, maybe due to the accent or the way you express yourself. It’s unspoken, but it’s there and you don’t need to be a rocket scientist to observe that. You need to prove that you’re good to be able to survive.”

This is easier for some than others.

“I cannot say I have experienced any barriers in that respect,” reports Gunter Kurrle, MD, lead physician with the WellStar Kennestone Hospitalist Group in Atlanta. “I’m European, like most Americans with European background, so it has not been my personal experience to encounter prejudice.” Dr. Kurrle’s journey to his present post as lead hospitalist is also atypical compared with most IMGs who come to the U.S. He initially took his foreign medical graduate examination in the late 1980s, just before the United States Medical Licensing Examination was initiated. He then returned to Germany for five years of additional training after his residency in this country. He came back to the U.S. for personal reasons (his wife is a U.S. citizen and was starting her residency training here) and found that entering hospital medicine was “a better fit than trying to start a practice on my own.”

Hemant Patel, MD, president of the American Association of Physicians of Indian Origin (AAIP), based in Oak Brook, Ill., believes discrimination toward foreign-born physicians has been greatly reduced since the early 1980s, when he entered the country. AAPI, with membership of 45,000, was founded in 1982 to offer support to IMGs from India. Physicians of Indian origin constitute the largest group of IMGs.2

“At that time, it was very difficult to obtain residency slots due to competition, and we had a lot more physicians to occupy those slots,” says Dr. Patel.

Dr. Fajardo believes the inclination to discriminate is inherent in everyone: “It’s latent, but if you give them the reason to discriminate against you, then it will manifest.” With regards to the physician-patient relationship, Dr. Fajardo reports that initially, on rare occasions, he encountered resistance from patients who were reluctant to trust their care to him because of his name (“I can’t pronounce it—are you a terrorist?”) or his looks (“You look too young to be a doctor—are you sure you can take care of me?”).

“At the end of the day, it’s very fulfilling when you hear them say, ‘Thanks a lot, doc, for getting me better,’’ says Dr. Fajardo. “I believe that it isn’t where you come from that matters; it’s what you can do.” Overall, he says, the realities of the medical profession are that “the outcome of what we do speaks for itself, and that’s what matters most.”

Dr. Onunkwo is philosophical about the initial skepticism he sometimes senses from patients and other colleagues. “I understand that people are wary of the unknown, and I think it’s just natural,” he says. “Usually, what happens in my situation is that I feel the skepticism, but I don’t do anything about it. I still treat the person with the respect that they deserve and ultimately, I just let my work do the talking. Everybody gets the same level of respect and attention that they need and nine times out of 10, before patients are done with their hospital stay, their attitudes toward me have changed.” TH

Gretchen Henkel is a frequent contributor to The Hospitalist.

References

 

 

  1. Leon LR Jr, Villar H, Leon CR, et al. The journey of a foreign-trained physician to a United States residency. J Am Coll Surg. 2007 Mar;204(3):486-494.
  2. Hart LG, Skillman SM, Fordyce M, et al. International medical graduate physicians in the United States: changes since 1981. Health Aff. 2007 Jul/Aug;26(4):1159-1169.

In the first part of this two-part series, we examined the implications of international medical graduates (IMGs) in hospital medicine groups (November 2007, p. 1). Part 2 features stories from hospitalist IMGs as they establish themselves as professionals in their communities.

December 2005 was a tough time for Charles Onunkwo, MD, and his wife. He had been working since July 1 as a hospitalist with St. Clare’s Hospital in Wausau, a small town in central Wisconsin, and had just received alarming news. His H1-B visa transfer, filed by his immigration attorney, had been denied.

His wife’s application to change from a visitor visa to an H-4 (dependent of an H1-B visa holder) was also denied. As a result, his wife was considered “unlawfully present” in the country. Dr. Onunkwo was now “out of status,” because the Naturalization and Immigration Service (INS) did not recognize St. Clare’s as exempt from caps on the annual number of H1-B visas granted. The couple was faced with a mandatory return trip to their native Nigeria, and no guarantee that the U.S. Consulate in Lagos would grant them permission to return to the United States to work as physicians.

“It was a bad time for us,” he recalls.

Charles Onunkwo, MD, hospitalist, St. Clare’s Hospital, Wausau, Wis.
I feel the skepticism, but I still treat the [patient or colleague] with the respect that they deserve. Ultimately, I just let my work do the talking.

Barriers and Adjustments

The obstacles faced by IMGs in obtaining visas and eventual permanent employment status have been well documented.1 For the Onunkwos, the story had a good outcome: a new immigration attorney hired by St. Clare’s was able to establish the hospital as a “cap-exempt” organization. Intervention by the staff of Rep. David R. Obey, D-Wis., allowed them to secure new H-1B visas and a return to this country.

Dr. Onunkwo and the other hospitalist IMGs attest that immigration hurdles constitute their biggest challenges.

There can be other barriers as well. Mark Dotson, senior recruiter for Cogent Healthcare in Nashville, Tenn., has encountered resistance toward IMG candidates from hospital administrators in some communities. Concerns usually relate to candidates’ ability to communicate effectively and demonstrate appropriate bedside manner. “There are also some misperceptions about some residency programs that can hinder an international medical graduate,” he says. In addition, some communities “want the doctors to reflect the makeup of the local community.” That means in a community that is 95% Caucasian, hospital administrators may be reluctant to hire a physician of color.

Dotson says attention to communication skills should be the primary goal of IMGs, and that buy-in from hospital administrators or leaders of hospital medicine groups is critical for smooth transitions. “I think some of the best physicians we have out there are doctors who are international medical graduates who see this as their life calling,” he says. “And, I think that even people in the general population understand that IMGs are extremely intelligent, and that they work extremely hard.”

As the following stories affirm, communities in remote or medically underserved areas are often welcoming of physicians who offer much-needed primary care.

Dr. Fajardo and his wife, Beverly

A Long Journey

In 1997, Emmanuel Fajardo, MD, medical director of the hospitalist program at St. Dominic-Jackson Memorial Hospital in Jackson, Miss., found himself “between the devil and the deep blue sea.” He had just been offered a chief residency position at the Meharry Medical College Affiliated Hospitals Internal Medicine residency program and was torn between accepting that job and a J-1 waiver offer in Shubuta, Miss., a federally designated Medically Underserved Area (MUSA).

 

 

He had been waiting a full year for the J-1 visa waiver, which allows IMGs to remain in the U.S. in exchange for five years of service in an MUSA. But, he also liked teaching and was attracted to the opportunity to pass on a legacy to the junior residents and incoming interns. He elected to proceed with the waiver because it offered the opportunity to “stay here in the States and to be able to practice medicine for good.”

Born in the Philippines, Dr. Fajardo says his family was wary about his locating to a remote area in Mississippi—but he wasn’t. “When I make a decision, I go for it 100%,” he says. “In everything I do I always do my best and leave the rest to God. I was very fortunate to find out that the community was very involved in and engaged with my waiver.

“Also, to my surprise, I didn’t feel discriminated against at all. They made me feel like I’m a part of the family. There is a strong sense of community here, indeed. The only problem then was, of course, being in a small town, that whatever you do, everybody knows about it.”

Although Dr. Onunkwo moved to Wausau, Wis., a small town in a predominantly white area, he says it was not difficult for him to adjust to life there. Part of the reason, he says, is that his first overseas experience was in Ireland, where he obtained a diploma in tropical medical at the Royal College of Surgeons in Dublin and practiced in a small village nearby. In addition, he and his wife were together in Wausau. “It was probably easier for both of us because we had each other,” he says.

And then there were their great neighbors, says Dr. Onunkwo. ”They made the transition seamless,” he says. “We have formed lifelong relationships with some of our neighbors in Wausau.” The strength of those relationships became apparent on Christmas Day 2005. “They really don’t know what they have done for us,” Dr. Onunkwo recalls warmly. “When we were going through our travails, they knew something was wrong, but we didn’t tell them exactly what we were going through. They made our day for us, because they just rang our bell and here they had the three-course Christmas dinner for us.”

Dr. Patel

Know Your Visas

To enter a residency program in the U.S., an IMG must pass steps one and two of the U.S. Medical Licensure Examination, then the Clinical Skills Examination. To obtain legal visitor status, most IMGs apply for:

  • J-1 visa: This is administered by the INS and allows an IMG to complete residency training at an Educational Commission for Foreign Medical Graduates-accredited program. If the IMG brings a spouse or other dependents, they usually obtain a J-2 visa. The J-1 visa carries a requirement that an IMG return to his or her native country for two years following completion of residency. Many IMGs want to remain in the country, which is why they often make use of the J-1 visa waiver.
  • J-1 visa waiver: This is a mechanism that allows IMGs to stay in the country and eventually apply for permanent status in exchange for five years of working in a medically underserved area. New post-9/11 restrictions of J-1 visas and attendant waivers have led a trend for IMGs to secure the H1-B visa.
  • H1-B visa: This allows the IMG to remain in the U.S. as long as they are employed full-time by an agency, academic institution or employer (such as a hospital) certified by the INS as exempt from immigrant caps on the annual number of H-1B visas granted. Spouses and other dependents of employed H1-B visa holders, then, obtain the H-4 visa in order to remain in the country.—GH

 

 

Prove Yourself

Dr. Onunkwo has been aware of misperceptions about his professional competency. “Depending on what part of the country you find yourself in, you need to continually prove yourself,” he says. “There is this perception, maybe due to the accent or the way you express yourself. It’s unspoken, but it’s there and you don’t need to be a rocket scientist to observe that. You need to prove that you’re good to be able to survive.”

This is easier for some than others.

“I cannot say I have experienced any barriers in that respect,” reports Gunter Kurrle, MD, lead physician with the WellStar Kennestone Hospitalist Group in Atlanta. “I’m European, like most Americans with European background, so it has not been my personal experience to encounter prejudice.” Dr. Kurrle’s journey to his present post as lead hospitalist is also atypical compared with most IMGs who come to the U.S. He initially took his foreign medical graduate examination in the late 1980s, just before the United States Medical Licensing Examination was initiated. He then returned to Germany for five years of additional training after his residency in this country. He came back to the U.S. for personal reasons (his wife is a U.S. citizen and was starting her residency training here) and found that entering hospital medicine was “a better fit than trying to start a practice on my own.”

Hemant Patel, MD, president of the American Association of Physicians of Indian Origin (AAIP), based in Oak Brook, Ill., believes discrimination toward foreign-born physicians has been greatly reduced since the early 1980s, when he entered the country. AAPI, with membership of 45,000, was founded in 1982 to offer support to IMGs from India. Physicians of Indian origin constitute the largest group of IMGs.2

“At that time, it was very difficult to obtain residency slots due to competition, and we had a lot more physicians to occupy those slots,” says Dr. Patel.

Dr. Fajardo believes the inclination to discriminate is inherent in everyone: “It’s latent, but if you give them the reason to discriminate against you, then it will manifest.” With regards to the physician-patient relationship, Dr. Fajardo reports that initially, on rare occasions, he encountered resistance from patients who were reluctant to trust their care to him because of his name (“I can’t pronounce it—are you a terrorist?”) or his looks (“You look too young to be a doctor—are you sure you can take care of me?”).

“At the end of the day, it’s very fulfilling when you hear them say, ‘Thanks a lot, doc, for getting me better,’’ says Dr. Fajardo. “I believe that it isn’t where you come from that matters; it’s what you can do.” Overall, he says, the realities of the medical profession are that “the outcome of what we do speaks for itself, and that’s what matters most.”

Dr. Onunkwo is philosophical about the initial skepticism he sometimes senses from patients and other colleagues. “I understand that people are wary of the unknown, and I think it’s just natural,” he says. “Usually, what happens in my situation is that I feel the skepticism, but I don’t do anything about it. I still treat the person with the respect that they deserve and ultimately, I just let my work do the talking. Everybody gets the same level of respect and attention that they need and nine times out of 10, before patients are done with their hospital stay, their attitudes toward me have changed.” TH

Gretchen Henkel is a frequent contributor to The Hospitalist.

References

 

 

  1. Leon LR Jr, Villar H, Leon CR, et al. The journey of a foreign-trained physician to a United States residency. J Am Coll Surg. 2007 Mar;204(3):486-494.
  2. Hart LG, Skillman SM, Fordyce M, et al. International medical graduate physicians in the United States: changes since 1981. Health Aff. 2007 Jul/Aug;26(4):1159-1169.
Issue
The Hospitalist - 2007(12)
Issue
The Hospitalist - 2007(12)
Publications
Publications
Article Type
Display Headline
To Serve in America
Display Headline
To Serve in America
Sections
Disallow All Ads
Content Gating
No Gating (article Unlocked/Free)