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Diagnostic errors top malpractice claims against emergency physicians
BY ALICIA GALLEGOS
FRONTLINE MEDICAL NEWS
More than half of medical malpractice lawsuits against emergency physicians involve allegations of diagnostic errors, according to a study by national medical liability insurer The Doctors Company.
The study analyzed 332 emergency medicine claims in the insurer’s database that were closed from 2007 to 2013. The findings show the importance of strong communication in the emergency department (ED), and how communication breakdowns can be catalysts for legal claims, Darrell Ranum, vice president for patient safety and risk management for The Doctors Company, said.
Mr. Ranum pointed out one claim in which a patient’s vital signs had changed during the course of a visit. The changes were not communicated to the emergency physician, and he inappropriately discharged the patient. In another case, a patient’s history of overdoses was not conveyed during a patient hand-off, which resulted in an overdose that was not treated in a timely manner.
“Sometimes, we find that patients don’t always understand instructions,” Mr. Ranum said. “If patients don’t understand the communication from their providers or if a patient receives inadequate information, such as in situations where you have a language barrier, you can have problems there as well.”
Another key lesson from the study is the importance of a thorough differential diagnosis, Dr David B. Troxel, medical director for The Doctors Company said in an interview.
Of the 332 claims, 57% were diagnosis related; they included allegations of failure to establish a differential diagnosis, failure to order diagnostic tests, failure to address abnormal findings, and failure to consider available clinical information.
View on the News Workflow bottlenecks contribute Dr Roneet Lev is director of ED operations for Scripps Mercy Hospital in San Diego. She made her remarks in an interview. |
“Our hope is that as physicians review the findings of this study, they will scrutinize their own systems and processes and determine whether the weaknesses identified in the study exist in their organization,” Dr Troxel said.
Among the other claims, 13% related to improper management or treatment, 5% claimed improper performance of treatment, and 3% alleged failure to order medication.
Claims could have more than one contributing factor. Problems with patient assessments, such as failure to address abnormal findings, contributed to 52% of claims. Patient factors, such as physical characteristics and noncompliance, were the second-most-frequent contributor at 21%. Other factors were lack of communication among physicians (17%), poor communication between doctors and patients (14%), insufficient or lack of documentation (13%), and workflow/workload issues (12%).
On Twitter @legal_med
ED-initiated buprenorphine ups treatment rates for opioid addiction
BY BIANCA NOGRADY
FROM JAMA
Vitals Key clinical point: Emergency department–initiated buprenorphine treatment increases the likelihood that opioid-dependent patients will seek addiction treatment. Major finding: Significantly more patients in the buprenorphine group sought addiction treatment in the 30 days after randomization, compared to the referral or intervention arms. Data source: Randomized controlled trial of 104 opioid-dependent patients. Disclosures: The National Institute on Drug Abuse funded the study. Reckitt-Benckiser Pharmaceuticals provided the drug. One author reported honoraria from private industry. |
Initiating buprenorphine treatment during an emergency department visit can significantly increase the likelihood that opioid-dependent patients will seek addiction treatment, according to results of a randomized clinical trial published in April 28 in JAMA.
Researchers randomized 104 opioid-dependent patients who had presented to the ED to screening and treatment referral, screening and a brief intervention with referral to a community-based treatment service, or screening with a brief intervention and ED-initiated treatment with buprenorphine/naloxone and referral to primary care.
Significantly more patients in the buprenorphine group sought addiction treatment in the 30 days after randomization compared to the referral or intervention arms (78% vs. 37% vs. 45%, P < .001), and they showed significant reductions in the number of days of illicit opioid use per week.
“Expanded use of ED-initiated buprenorphine with community follow-up should help increase access to treatment options for this chronic and relapsing medical condition that has substantial morbidity and mortality and that affects health care use and costs,” wrote Dr Gail D’Onofrio of Yale School of Medicine, New Haven, Ct., and coauthors (JAMA 2015; 313:1636-1644 [doi:10.1001/jama.2015.3474]).
More than 75% with sickle cell crises don’t get hydroxyurea
BY MARY ANN MOON
FROM JAMA
Vitals Key clinical point: More than 75% of adults with sickle cell anemia who have frequent pain crises fail to get hydroxyurea therapy as recommended. Major finding: Only 15.1% of adults with sickle cell anemia received hydroxyurea within 3 months of their third pain crisis, only 18.2% received the agent within 6 months, and only 22.7% received it within 12 months. Data source: An analysis of information in a large nationwide insurance claims database involving 570 adults with frequent hospitalizations for sickle cell pain crises. Disclosures: This study was funded by the Lewin Group, a health care consulting firm. Dr Stettler and his associates reported having no relevant financial disclosures. |
More than 75% of adults with sickle cell anemia who have frequent pain crises fail to receive hydroxyurea therapy as strongly recommended in National Heart, Lung, and Blood Institute clinical guidelines, according to a Research Letter to the Editor published online April 28 in JAMA.
Despite proven benefits in decreasing pain crises, hospitalizations, blood transfusions, and possibly mortality, hydroxyurea, a “safe and inexpensive drug,” is thought to be underused. To document the actual use of the drug when indicated, investigators analyzed information in a nationwide insurance claims database covering nearly 27 million patients per year. They focused on the records of 570 adults hospitalized or treated in an emergency department for a sickle cell pain crisis at least three times during a 1-year period, said Dr Nicolas Stettler of the Lewin Group, a health care consulting firm in Falls Church, Va., and his associates.
Only 15.1% of these patients received hydroxyurea within 3 months of their third crisis, only 18.2% received the agent within 6 months, and only 22.7% received it within 12 months. These figures likely represent a conservative estimate of the hydroxyurea treatment gap, since the study didn’t include the large uninsured and publicly insured populations who have more limited access to health care, Dr Stettler and his associates noted (JAMA 2015;313:1671-2).
Several barriers to this treatment have been identified in previous research, including fear of adverse events, lack of clinician training, and failure to use shared decision making. “To address this gap, it may be necessary to enhance patient outreach and clinician training and develop health care quality measures aimed at increasing the use of hydroxyurea for all patients who would benefit,” they added.
Recognizing human trafficking victims
BY ALICIA GALLEGOS
AT THE AMWA ANNUAL MEETING
CHICAGO – Emergency physicians encounter nearly 40% of human trafficking victims who come in contact with health providers, according to Dr Holly G. Atkinson.
In a 2014 survey of domestic sex-trafficking victims, 88% said they encountered one or more health professions during the period in which they were being trafficked, yet none was identified as a victim by physicians during the visits. In another 2014 survey of survivors, 39% of victims reported having contact with emergency departments; 29%, with primary care physicians; 17%, with ob.gyns.; 17%, with dentists; and 3%, with pediatricians.
Key indicators for potential victimization include discrepancies between history and clinical presentation, multiple sexually transmitted diseases, and the accompaniment of a controlling third-party who is not a guardian, said Dr Atkinson, director of the human rights program at Arnhold Global Health Institute at the Icahn School of Medicine at Mount Sinai in New York City, said at the annual meeting of the American Medical Women’s Association.
In 2014, the National Human Trafficking Resource Center, operated by the antislavery organization Polaris, received 3,598 reports of sex-trafficking cases inside the United States. The National Center for Missing & Exploited Children estimates that between 100,000 and 300,000 U.S. children are at risk of being sexually trafficked each year.
Physical signs that could denote the possibility of patients being trafficked include visible tattoos with “daddy,” “property of,” or a trafficker’s street name. Perpetrators often brand their victims so that they are easily recognizable and can be returned if they escape, Dr Atkinson explained.
Dehydration, malnutrition, multiple sexually transmitted infections, and multiple pregnancies or abortions could also be clues. The inability to provide an address, confusion about their current location, an appearance younger than the stated age, avoidance of eye contact, and answers that sound scripted are potential signs of human trafficking, as is the presence of a controlling third party who does not let the patient answer questions or who interrupts or corrects the patient.
The Via Christi Health system in Wichita, Kan., recently published guidance for clinicians on how to proceed if they suspect a patient is a victim of human trafficking. Steps include following child abuse or domestic violence protocols; separating the patient from the controlling third party; providing the patient a comfortable, safe area; and ensuring a patient interview is performed by a trauma-informed social worker or nurse.
Some questions physicians may want to ask patients include: Have you ever exchanged sex for money, food, or shelter? Have you been forced to have sex against your will? Have you been asked to have sex with multiple partners? If the patient answers yes, physicians should follow child abuse protocols and mandatory reporting requirements. If the patient is aged 18 or older, doctors should obtain the patient’s permission to call law enforcement or assist the patient in calling 911.
AMWA recently launched Physicians Against the Trafficking of Humans (PATH). The PATH website includes resources for physicians and an online video about trafficking that doctors can share with their practices and colleagues.
On Twitter @legal_med
Indiana HIV outbreak prompts national advisory
BY SHARON WORCESTER
FRONTLINE MEDICAL NEWS
As health officials continue to battle an intravenous drug use–related HIV outbreak in a rural county in Indiana, the Centers for Disease Control and Prevention has issued an official health advisory stressing the need for vigilance at the state and local levels with respect to detecting and controlling similar outbreaks across the United States.
The Indiana outbreak began in November, with 11 new HIV infections diagnosed by January in Scott County, where fewer than 5 infections per year had been identified previously; since January, an unprecedented 135 infections have been confirmed, and 6 others are under investigation, according to Dr Jerome M. Adams, Indiana State Health Commissioner.
“To put this in further perspective, from 2009 through 2013, the county only reported three new cases of HIV,” Dr Adams said in a joint Indiana State Department of Health/CDC teleconference.
The affected community includes only 4,200 people, and 84% of those diagnosed with HIV also tested positive for hepatitis C virus (HCV) infection, Dr Joan Duwve, chief medical consultant, Indiana State Department of Health, said during the teleconference.
According to the CDC advisory, 96% of 108 infected individuals who were interviewed reported injecting dissolved prescription-type oxymorphone, as well as sharing syringes.
“The United States is facing an epidemic of prescription opioid abuse that must be addressed. Opioid poisoning deaths have nearly quadrupled from 1999 through 2011. This epidemic of opioid abuse has already contributed to a severe and growing epidemic of viral hepatitis among people who inject drugs,” said Dr Jonathan Mermin, director of the National Center for HIV/AIDS Viral Hepatitis, STD, and TB Prevention, who also participated in the teleconference.
New CDC data on HCV show a 150% increase in reports of acute HCV infections nationwide between 2010 to 2013.
“The majority of these infections are believed to be attributable to injection drug use, so we must act now to reverse this trend and to prevent this from undoing progress in HIV prevention to date,” he said.
Among the recommendations were routine opt-out of HIV testing as well as HCV testing per current recommendations. Further, health care professionals should report suspected clusters to their local or state health department, ensure that HCV-infected patients are also tested for HIV and vice versa, and ensure that those receiving treatment for either HIV or HCV are adhering to prescribed therapy and are engaged in ongoing care.
Syringe-sharing and sexual partners of those diagnosed with HIV or HCV should be encouraged to undergo testing, and all persons with substance abuse problems should be referred for medication-assisted treatment and counseling. In Indiana, where a public health emergency was declared on March 26 and has been extended until May 24, care includes HIV and HCV treatment, as well as substance abuse counseling and treatment, according to a “Notes From the Field Report” in the Morbidity and Mortality Weekly Report (MMWR 2015 April 24;64:1-2).
Most accidental genital trauma cases manageable in ED
BY SHARON WORCESTER
AT THE NASPAG ANNUAL MEETING
Vitals Key clinical point: With adequate sedation, most girls with AGT requiring treatment can undergo evaluation and repair in the ED. Major finding: 82% of cases reviewed were minor and managed expectantly. Data source: A retrospective medical records review of 359 cases of accidental genital trauma. Disclosures: Dr Dowlut-McElroy reported having no disclosures. One of her coauthors, Dr Julie Strickland, is a Nexplanon trainer for Merck. |
ORLANDO – Most cases of accidental genital trauma in girls are caused by straddle injuries and are isolated to the labia, and most can be managed expectantly or treated in the emergency department, according to findings from a retrospective cohort study.
Penetrating injuries, however, should be considered an indication for management in the operating room, Dr Tazim Dowlut-McElroy reported at the annual meeting of the North American Society for Pediatric and Adolescent Gynecology.
A review of 359 cases showed that the vast majority – 82% – were minor and managed expectantly.
“Only 18% required surgical management. Of those, 37% required general anesthesia in the OR, but 63% were adequately evaluated and treated in the ED,” said Dr Dowlut-McElroy of Children’s Mercy Hospitals and Clinics, Kansas City.
About 64% of the patients presented during the day, and 36% presented at night. The most common presenting complaint was bleeding and pain (89% of cases), followed by voiding issues in 8% of cases. No presenting complaint was recorded in the remaining patient charts.
The most common mechanism of injury was straddle injury (73% of cases), followed by non-straddle blunt trauma in 15% of cases, and penetrating injury in the remaining cases, Dr Dowlut-McElroy said.
Injuries included lacerations in 86% of cases, abrasions or contusions in 7%, and hematomas in 3%.
Pediatric genital injuries comprised 0.2%-8% of reported childhood trauma, and despite public health efforts to reduce injuries, the number of such pediatric injuries continues to rise, Dr Dowlut-McElroy said.
Patients included in the current review were identified by a medical database query from January 2000 to July 2014. They were aged 0-18 years and had been treated in the ED for genital trauma; those with obstetrical injuries were excluded.
EDs pump up pediatric preparedness
BY MARY ANN MOON
FROM JAMA PEDIATRICS
Vitals Key clinical point: Nationally, emergency departments have improved their compliance with guidelines regarding emergency health care for children. Major finding: The overall median weighted pediatric readiness score (WPRS) was 68.9, a solid improvement over the previously reported median WPRS of 55. Data source: A web-based self-reported assessment of pediatric readiness at 4,149 EDs across the country that have approximately 24 million pediatric visits annually. Disclosures: This project was supported by the Emergency Medical Services for Children network and the EMS for Children National Resource Center under the U.S. Department of Health & Human Services. Dr Gausche-Hill and her associates reported having no financial disclosures. |
Pediatric readiness has improved in emergency departments across the country, as measured by EDs’ compliance with 2009 guidelines for emergency care in children, according to a report published online April 13 in JAMA Pediatrics.
In what they described as “the most comprehensive evaluation of pediatric readiness of our nation’s EDs to date,” investigators performed a web-based assessment of 4,137 hospitals’ self-reported compliance with guidelines addressing child-specific emergency care. The overall median weighted pediatric readiness score (WPRS) was 68.9, a solid improvement over the previously reported median WPRS of 55, said Dr Marianne Gausche-Hill of Harbor-UCLA Medical Center, Torrance, Calif., and her associates.
The single most important factor found to enhance pediatric readiness was to designate two people, one of whom is a physician or nurse, as the hospital’s pediatric emergency care coordinator, as recommended by the Institute of Medicine, the researchers wrote. Nearly half (47.5%) of EDs now have a physician coordinator, and 59.3% now have a nurse coordinator, compared with 18% and 12%, respectively, in a previous report. The presence of coordinators quadrupled the chances that a hospital would put important quality-improvement plans in place to address children’s care needs, the investigators said (JAMA Pediatr. 2015 April 13 [doi:10.1001/jamapediatrics.2015.138]).
Other findings included the following:
- Most physicians providing emergency care for children were specifically trained in emergency medicine (88.6%) or pediatric emergency medicine (55.4%) at high-volume hospitals; low-volume hospitals were more likely to have family-medicine-trained physicians doing so (78.9%).
- Mandatory competency evaluations for providing pediatric emergency care were relatively common for nurses (66.6%) but less so for physicians (38.7%) and midlevel staff (18.1%).
- 99.5% of EDs said all staff are trained on the location of pediatric equipment in the ED, including tools to ensure correct sizing of resuscitation equipment and appropriate dosing of medications.
- 83.1% of EDs said they verified the proper location and function of pediatric equipment daily.
- EDs routinely stocked 91% of recommended pediatric equipment. Equipment that was missing in more than 15% of EDs included laryngeal mask airways, umbilical vein catheters, central venous catheters, tracheostomy tubes, size 00 laryngoscope blades, continuous end-tidal carbon dioxide monitoring equipment, pediatric Magill forceps, and infant and child nasopharyngeal airways.
- Only 46.8% of EDs had disaster plans that specifically addressed children, as recommended. Even among high-volume hospitals, which were the most compliant with guidelines, only 67.4% had such disaster plans.
- Approximately one-third of EDs said their providers failed to weigh children and record the weight in kilograms only, as recommended. This safety measure is crucial to preventing drug-dosing errors.
- The most frequently cited barriers to complying with guidelines were the cost of child-specific training (reported by 54.4% of EDs) and a lack of educational resources (reported by 49.0%). Few EDs reported that a lack of interest was a barrier to implementing the guidelines.
Simplified PESI identified low-risk pulmonary embolism
BY AMY KARON
FROM ACADEMIC EMERGENCY MEDICINE
Vitals Key clinical point: The simplified version of the PESI identified low-risk pulmonary embolism patients. Major finding: Patients with scores of 0 or 1 had low rates of major adverse events during the first 30 days, regardless of which treatment they received. Data source: Post hoc analysis of simplified PESI scores and outcomes among 4,831 patients with acute pulmonary embolism who received either rivaroxaban or an enoxaparin–vitamin K antagonist combination. Disclosures:Bayer HealthCare Pharmaceuticals and Janssen Research & Development funded the study. Dr Fermann reported an advisory relationship with Janssen and research funding from Cardiorentis, Trevena, Novartis, Siemens, and Pfizer. Two coauthors reported employment with Bayer, and two other coauthors reported relationships with several other pharmaceutical companies. |
A simplified version of the Pulmonary Embolism Severity Index identified patients with acute pulmonary embolism who were at low risk of adverse events and might be suitable for outpatient care.
“Although guidelines, such as those from the American College of Chest Physicians, recommend outpatient treatment for selected PE patients at low risk of recurrence, existing evidence for the outpatient management of patients with PE is derived from small cohorts of patients from outside the United States,” said Dr Gregory J. Fermann of the University of Cincinnati department of emergency medicine and his associates. “Risk stratification of PE patients may allow a cohort of low-risk patients to be treated in a clinical decision unit or by a closely monitored outpatient strategy. Such an approach might relieve some of the burden placed on the emergency department,” they wrote (Acad. Emerg. Med. 2015;22:299-307).
The simplified PESI includes 6 of the 11 variables measured in PESI, which has been shown to identify patients at increased risk of death and adverse outcome events after acute PE. The six features of the simplified PESI are age greater than 80 years, history of cancer, history of chronic cardiopulmonary disease, heart rate of at least 110 beats per minutes, systolic blood pressure less than 100 mm Hg, and oxygen saturation less than 90%. Each factor is assigned a score of 1.
They carried out a post hoc analysis of simplified PESI scores and outcomes among 4,831 acute PE patients from the EINSTEIN-PE study of rivaroxaban and an enoxaparin–vitamin K antagonist combination (N. Engl. J. Med. 2012;366:1287-97).
Roughly half (53.6%) of the patients had a score of 0, one-third (36.7%) had a score of 1, and 9.7% had a score of 2 or 3, the researchers reported. Higher simplified PESI scores were associated with increased risk of almost all adverse outcomes measured, including recurrent VTE, fatal PE, all-cause mortality, and major bleeding. Patients with scores of 0 or 1 had low rates of major adverse events during the first 30 days of treatment, regardless of which protocol they received. Scores of 2 or 3 were associated with greater risk of recurrent VTE, fatal PE, all-cause mortality, and major bleeding in both treatment groups.
Diagnostic errors top malpractice claims against emergency physicians
BY ALICIA GALLEGOS
FRONTLINE MEDICAL NEWS
More than half of medical malpractice lawsuits against emergency physicians involve allegations of diagnostic errors, according to a study by national medical liability insurer The Doctors Company.
The study analyzed 332 emergency medicine claims in the insurer’s database that were closed from 2007 to 2013. The findings show the importance of strong communication in the emergency department (ED), and how communication breakdowns can be catalysts for legal claims, Darrell Ranum, vice president for patient safety and risk management for The Doctors Company, said.
Mr. Ranum pointed out one claim in which a patient’s vital signs had changed during the course of a visit. The changes were not communicated to the emergency physician, and he inappropriately discharged the patient. In another case, a patient’s history of overdoses was not conveyed during a patient hand-off, which resulted in an overdose that was not treated in a timely manner.
“Sometimes, we find that patients don’t always understand instructions,” Mr. Ranum said. “If patients don’t understand the communication from their providers or if a patient receives inadequate information, such as in situations where you have a language barrier, you can have problems there as well.”
Another key lesson from the study is the importance of a thorough differential diagnosis, Dr David B. Troxel, medical director for The Doctors Company said in an interview.
Of the 332 claims, 57% were diagnosis related; they included allegations of failure to establish a differential diagnosis, failure to order diagnostic tests, failure to address abnormal findings, and failure to consider available clinical information.
View on the News Workflow bottlenecks contribute Dr Roneet Lev is director of ED operations for Scripps Mercy Hospital in San Diego. She made her remarks in an interview. |
“Our hope is that as physicians review the findings of this study, they will scrutinize their own systems and processes and determine whether the weaknesses identified in the study exist in their organization,” Dr Troxel said.
Among the other claims, 13% related to improper management or treatment, 5% claimed improper performance of treatment, and 3% alleged failure to order medication.
Claims could have more than one contributing factor. Problems with patient assessments, such as failure to address abnormal findings, contributed to 52% of claims. Patient factors, such as physical characteristics and noncompliance, were the second-most-frequent contributor at 21%. Other factors were lack of communication among physicians (17%), poor communication between doctors and patients (14%), insufficient or lack of documentation (13%), and workflow/workload issues (12%).
On Twitter @legal_med
ED-initiated buprenorphine ups treatment rates for opioid addiction
BY BIANCA NOGRADY
FROM JAMA
Vitals Key clinical point: Emergency department–initiated buprenorphine treatment increases the likelihood that opioid-dependent patients will seek addiction treatment. Major finding: Significantly more patients in the buprenorphine group sought addiction treatment in the 30 days after randomization, compared to the referral or intervention arms. Data source: Randomized controlled trial of 104 opioid-dependent patients. Disclosures: The National Institute on Drug Abuse funded the study. Reckitt-Benckiser Pharmaceuticals provided the drug. One author reported honoraria from private industry. |
Initiating buprenorphine treatment during an emergency department visit can significantly increase the likelihood that opioid-dependent patients will seek addiction treatment, according to results of a randomized clinical trial published in April 28 in JAMA.
Researchers randomized 104 opioid-dependent patients who had presented to the ED to screening and treatment referral, screening and a brief intervention with referral to a community-based treatment service, or screening with a brief intervention and ED-initiated treatment with buprenorphine/naloxone and referral to primary care.
Significantly more patients in the buprenorphine group sought addiction treatment in the 30 days after randomization compared to the referral or intervention arms (78% vs. 37% vs. 45%, P < .001), and they showed significant reductions in the number of days of illicit opioid use per week.
“Expanded use of ED-initiated buprenorphine with community follow-up should help increase access to treatment options for this chronic and relapsing medical condition that has substantial morbidity and mortality and that affects health care use and costs,” wrote Dr Gail D’Onofrio of Yale School of Medicine, New Haven, Ct., and coauthors (JAMA 2015; 313:1636-1644 [doi:10.1001/jama.2015.3474]).
More than 75% with sickle cell crises don’t get hydroxyurea
BY MARY ANN MOON
FROM JAMA
Vitals Key clinical point: More than 75% of adults with sickle cell anemia who have frequent pain crises fail to get hydroxyurea therapy as recommended. Major finding: Only 15.1% of adults with sickle cell anemia received hydroxyurea within 3 months of their third pain crisis, only 18.2% received the agent within 6 months, and only 22.7% received it within 12 months. Data source: An analysis of information in a large nationwide insurance claims database involving 570 adults with frequent hospitalizations for sickle cell pain crises. Disclosures: This study was funded by the Lewin Group, a health care consulting firm. Dr Stettler and his associates reported having no relevant financial disclosures. |
More than 75% of adults with sickle cell anemia who have frequent pain crises fail to receive hydroxyurea therapy as strongly recommended in National Heart, Lung, and Blood Institute clinical guidelines, according to a Research Letter to the Editor published online April 28 in JAMA.
Despite proven benefits in decreasing pain crises, hospitalizations, blood transfusions, and possibly mortality, hydroxyurea, a “safe and inexpensive drug,” is thought to be underused. To document the actual use of the drug when indicated, investigators analyzed information in a nationwide insurance claims database covering nearly 27 million patients per year. They focused on the records of 570 adults hospitalized or treated in an emergency department for a sickle cell pain crisis at least three times during a 1-year period, said Dr Nicolas Stettler of the Lewin Group, a health care consulting firm in Falls Church, Va., and his associates.
Only 15.1% of these patients received hydroxyurea within 3 months of their third crisis, only 18.2% received the agent within 6 months, and only 22.7% received it within 12 months. These figures likely represent a conservative estimate of the hydroxyurea treatment gap, since the study didn’t include the large uninsured and publicly insured populations who have more limited access to health care, Dr Stettler and his associates noted (JAMA 2015;313:1671-2).
Several barriers to this treatment have been identified in previous research, including fear of adverse events, lack of clinician training, and failure to use shared decision making. “To address this gap, it may be necessary to enhance patient outreach and clinician training and develop health care quality measures aimed at increasing the use of hydroxyurea for all patients who would benefit,” they added.
Recognizing human trafficking victims
BY ALICIA GALLEGOS
AT THE AMWA ANNUAL MEETING
CHICAGO – Emergency physicians encounter nearly 40% of human trafficking victims who come in contact with health providers, according to Dr Holly G. Atkinson.
In a 2014 survey of domestic sex-trafficking victims, 88% said they encountered one or more health professions during the period in which they were being trafficked, yet none was identified as a victim by physicians during the visits. In another 2014 survey of survivors, 39% of victims reported having contact with emergency departments; 29%, with primary care physicians; 17%, with ob.gyns.; 17%, with dentists; and 3%, with pediatricians.
Key indicators for potential victimization include discrepancies between history and clinical presentation, multiple sexually transmitted diseases, and the accompaniment of a controlling third-party who is not a guardian, said Dr Atkinson, director of the human rights program at Arnhold Global Health Institute at the Icahn School of Medicine at Mount Sinai in New York City, said at the annual meeting of the American Medical Women’s Association.
In 2014, the National Human Trafficking Resource Center, operated by the antislavery organization Polaris, received 3,598 reports of sex-trafficking cases inside the United States. The National Center for Missing & Exploited Children estimates that between 100,000 and 300,000 U.S. children are at risk of being sexually trafficked each year.
Physical signs that could denote the possibility of patients being trafficked include visible tattoos with “daddy,” “property of,” or a trafficker’s street name. Perpetrators often brand their victims so that they are easily recognizable and can be returned if they escape, Dr Atkinson explained.
Dehydration, malnutrition, multiple sexually transmitted infections, and multiple pregnancies or abortions could also be clues. The inability to provide an address, confusion about their current location, an appearance younger than the stated age, avoidance of eye contact, and answers that sound scripted are potential signs of human trafficking, as is the presence of a controlling third party who does not let the patient answer questions or who interrupts or corrects the patient.
The Via Christi Health system in Wichita, Kan., recently published guidance for clinicians on how to proceed if they suspect a patient is a victim of human trafficking. Steps include following child abuse or domestic violence protocols; separating the patient from the controlling third party; providing the patient a comfortable, safe area; and ensuring a patient interview is performed by a trauma-informed social worker or nurse.
Some questions physicians may want to ask patients include: Have you ever exchanged sex for money, food, or shelter? Have you been forced to have sex against your will? Have you been asked to have sex with multiple partners? If the patient answers yes, physicians should follow child abuse protocols and mandatory reporting requirements. If the patient is aged 18 or older, doctors should obtain the patient’s permission to call law enforcement or assist the patient in calling 911.
AMWA recently launched Physicians Against the Trafficking of Humans (PATH). The PATH website includes resources for physicians and an online video about trafficking that doctors can share with their practices and colleagues.
On Twitter @legal_med
Indiana HIV outbreak prompts national advisory
BY SHARON WORCESTER
FRONTLINE MEDICAL NEWS
As health officials continue to battle an intravenous drug use–related HIV outbreak in a rural county in Indiana, the Centers for Disease Control and Prevention has issued an official health advisory stressing the need for vigilance at the state and local levels with respect to detecting and controlling similar outbreaks across the United States.
The Indiana outbreak began in November, with 11 new HIV infections diagnosed by January in Scott County, where fewer than 5 infections per year had been identified previously; since January, an unprecedented 135 infections have been confirmed, and 6 others are under investigation, according to Dr Jerome M. Adams, Indiana State Health Commissioner.
“To put this in further perspective, from 2009 through 2013, the county only reported three new cases of HIV,” Dr Adams said in a joint Indiana State Department of Health/CDC teleconference.
The affected community includes only 4,200 people, and 84% of those diagnosed with HIV also tested positive for hepatitis C virus (HCV) infection, Dr Joan Duwve, chief medical consultant, Indiana State Department of Health, said during the teleconference.
According to the CDC advisory, 96% of 108 infected individuals who were interviewed reported injecting dissolved prescription-type oxymorphone, as well as sharing syringes.
“The United States is facing an epidemic of prescription opioid abuse that must be addressed. Opioid poisoning deaths have nearly quadrupled from 1999 through 2011. This epidemic of opioid abuse has already contributed to a severe and growing epidemic of viral hepatitis among people who inject drugs,” said Dr Jonathan Mermin, director of the National Center for HIV/AIDS Viral Hepatitis, STD, and TB Prevention, who also participated in the teleconference.
New CDC data on HCV show a 150% increase in reports of acute HCV infections nationwide between 2010 to 2013.
“The majority of these infections are believed to be attributable to injection drug use, so we must act now to reverse this trend and to prevent this from undoing progress in HIV prevention to date,” he said.
Among the recommendations were routine opt-out of HIV testing as well as HCV testing per current recommendations. Further, health care professionals should report suspected clusters to their local or state health department, ensure that HCV-infected patients are also tested for HIV and vice versa, and ensure that those receiving treatment for either HIV or HCV are adhering to prescribed therapy and are engaged in ongoing care.
Syringe-sharing and sexual partners of those diagnosed with HIV or HCV should be encouraged to undergo testing, and all persons with substance abuse problems should be referred for medication-assisted treatment and counseling. In Indiana, where a public health emergency was declared on March 26 and has been extended until May 24, care includes HIV and HCV treatment, as well as substance abuse counseling and treatment, according to a “Notes From the Field Report” in the Morbidity and Mortality Weekly Report (MMWR 2015 April 24;64:1-2).
Most accidental genital trauma cases manageable in ED
BY SHARON WORCESTER
AT THE NASPAG ANNUAL MEETING
Vitals Key clinical point: With adequate sedation, most girls with AGT requiring treatment can undergo evaluation and repair in the ED. Major finding: 82% of cases reviewed were minor and managed expectantly. Data source: A retrospective medical records review of 359 cases of accidental genital trauma. Disclosures: Dr Dowlut-McElroy reported having no disclosures. One of her coauthors, Dr Julie Strickland, is a Nexplanon trainer for Merck. |
ORLANDO – Most cases of accidental genital trauma in girls are caused by straddle injuries and are isolated to the labia, and most can be managed expectantly or treated in the emergency department, according to findings from a retrospective cohort study.
Penetrating injuries, however, should be considered an indication for management in the operating room, Dr Tazim Dowlut-McElroy reported at the annual meeting of the North American Society for Pediatric and Adolescent Gynecology.
A review of 359 cases showed that the vast majority – 82% – were minor and managed expectantly.
“Only 18% required surgical management. Of those, 37% required general anesthesia in the OR, but 63% were adequately evaluated and treated in the ED,” said Dr Dowlut-McElroy of Children’s Mercy Hospitals and Clinics, Kansas City.
About 64% of the patients presented during the day, and 36% presented at night. The most common presenting complaint was bleeding and pain (89% of cases), followed by voiding issues in 8% of cases. No presenting complaint was recorded in the remaining patient charts.
The most common mechanism of injury was straddle injury (73% of cases), followed by non-straddle blunt trauma in 15% of cases, and penetrating injury in the remaining cases, Dr Dowlut-McElroy said.
Injuries included lacerations in 86% of cases, abrasions or contusions in 7%, and hematomas in 3%.
Pediatric genital injuries comprised 0.2%-8% of reported childhood trauma, and despite public health efforts to reduce injuries, the number of such pediatric injuries continues to rise, Dr Dowlut-McElroy said.
Patients included in the current review were identified by a medical database query from January 2000 to July 2014. They were aged 0-18 years and had been treated in the ED for genital trauma; those with obstetrical injuries were excluded.
EDs pump up pediatric preparedness
BY MARY ANN MOON
FROM JAMA PEDIATRICS
Vitals Key clinical point: Nationally, emergency departments have improved their compliance with guidelines regarding emergency health care for children. Major finding: The overall median weighted pediatric readiness score (WPRS) was 68.9, a solid improvement over the previously reported median WPRS of 55. Data source: A web-based self-reported assessment of pediatric readiness at 4,149 EDs across the country that have approximately 24 million pediatric visits annually. Disclosures: This project was supported by the Emergency Medical Services for Children network and the EMS for Children National Resource Center under the U.S. Department of Health & Human Services. Dr Gausche-Hill and her associates reported having no financial disclosures. |
Pediatric readiness has improved in emergency departments across the country, as measured by EDs’ compliance with 2009 guidelines for emergency care in children, according to a report published online April 13 in JAMA Pediatrics.
In what they described as “the most comprehensive evaluation of pediatric readiness of our nation’s EDs to date,” investigators performed a web-based assessment of 4,137 hospitals’ self-reported compliance with guidelines addressing child-specific emergency care. The overall median weighted pediatric readiness score (WPRS) was 68.9, a solid improvement over the previously reported median WPRS of 55, said Dr Marianne Gausche-Hill of Harbor-UCLA Medical Center, Torrance, Calif., and her associates.
The single most important factor found to enhance pediatric readiness was to designate two people, one of whom is a physician or nurse, as the hospital’s pediatric emergency care coordinator, as recommended by the Institute of Medicine, the researchers wrote. Nearly half (47.5%) of EDs now have a physician coordinator, and 59.3% now have a nurse coordinator, compared with 18% and 12%, respectively, in a previous report. The presence of coordinators quadrupled the chances that a hospital would put important quality-improvement plans in place to address children’s care needs, the investigators said (JAMA Pediatr. 2015 April 13 [doi:10.1001/jamapediatrics.2015.138]).
Other findings included the following:
- Most physicians providing emergency care for children were specifically trained in emergency medicine (88.6%) or pediatric emergency medicine (55.4%) at high-volume hospitals; low-volume hospitals were more likely to have family-medicine-trained physicians doing so (78.9%).
- Mandatory competency evaluations for providing pediatric emergency care were relatively common for nurses (66.6%) but less so for physicians (38.7%) and midlevel staff (18.1%).
- 99.5% of EDs said all staff are trained on the location of pediatric equipment in the ED, including tools to ensure correct sizing of resuscitation equipment and appropriate dosing of medications.
- 83.1% of EDs said they verified the proper location and function of pediatric equipment daily.
- EDs routinely stocked 91% of recommended pediatric equipment. Equipment that was missing in more than 15% of EDs included laryngeal mask airways, umbilical vein catheters, central venous catheters, tracheostomy tubes, size 00 laryngoscope blades, continuous end-tidal carbon dioxide monitoring equipment, pediatric Magill forceps, and infant and child nasopharyngeal airways.
- Only 46.8% of EDs had disaster plans that specifically addressed children, as recommended. Even among high-volume hospitals, which were the most compliant with guidelines, only 67.4% had such disaster plans.
- Approximately one-third of EDs said their providers failed to weigh children and record the weight in kilograms only, as recommended. This safety measure is crucial to preventing drug-dosing errors.
- The most frequently cited barriers to complying with guidelines were the cost of child-specific training (reported by 54.4% of EDs) and a lack of educational resources (reported by 49.0%). Few EDs reported that a lack of interest was a barrier to implementing the guidelines.
Simplified PESI identified low-risk pulmonary embolism
BY AMY KARON
FROM ACADEMIC EMERGENCY MEDICINE
Vitals Key clinical point: The simplified version of the PESI identified low-risk pulmonary embolism patients. Major finding: Patients with scores of 0 or 1 had low rates of major adverse events during the first 30 days, regardless of which treatment they received. Data source: Post hoc analysis of simplified PESI scores and outcomes among 4,831 patients with acute pulmonary embolism who received either rivaroxaban or an enoxaparin–vitamin K antagonist combination. Disclosures:Bayer HealthCare Pharmaceuticals and Janssen Research & Development funded the study. Dr Fermann reported an advisory relationship with Janssen and research funding from Cardiorentis, Trevena, Novartis, Siemens, and Pfizer. Two coauthors reported employment with Bayer, and two other coauthors reported relationships with several other pharmaceutical companies. |
A simplified version of the Pulmonary Embolism Severity Index identified patients with acute pulmonary embolism who were at low risk of adverse events and might be suitable for outpatient care.
“Although guidelines, such as those from the American College of Chest Physicians, recommend outpatient treatment for selected PE patients at low risk of recurrence, existing evidence for the outpatient management of patients with PE is derived from small cohorts of patients from outside the United States,” said Dr Gregory J. Fermann of the University of Cincinnati department of emergency medicine and his associates. “Risk stratification of PE patients may allow a cohort of low-risk patients to be treated in a clinical decision unit or by a closely monitored outpatient strategy. Such an approach might relieve some of the burden placed on the emergency department,” they wrote (Acad. Emerg. Med. 2015;22:299-307).
The simplified PESI includes 6 of the 11 variables measured in PESI, which has been shown to identify patients at increased risk of death and adverse outcome events after acute PE. The six features of the simplified PESI are age greater than 80 years, history of cancer, history of chronic cardiopulmonary disease, heart rate of at least 110 beats per minutes, systolic blood pressure less than 100 mm Hg, and oxygen saturation less than 90%. Each factor is assigned a score of 1.
They carried out a post hoc analysis of simplified PESI scores and outcomes among 4,831 acute PE patients from the EINSTEIN-PE study of rivaroxaban and an enoxaparin–vitamin K antagonist combination (N. Engl. J. Med. 2012;366:1287-97).
Roughly half (53.6%) of the patients had a score of 0, one-third (36.7%) had a score of 1, and 9.7% had a score of 2 or 3, the researchers reported. Higher simplified PESI scores were associated with increased risk of almost all adverse outcomes measured, including recurrent VTE, fatal PE, all-cause mortality, and major bleeding. Patients with scores of 0 or 1 had low rates of major adverse events during the first 30 days of treatment, regardless of which protocol they received. Scores of 2 or 3 were associated with greater risk of recurrent VTE, fatal PE, all-cause mortality, and major bleeding in both treatment groups.
Diagnostic errors top malpractice claims against emergency physicians
BY ALICIA GALLEGOS
FRONTLINE MEDICAL NEWS
More than half of medical malpractice lawsuits against emergency physicians involve allegations of diagnostic errors, according to a study by national medical liability insurer The Doctors Company.
The study analyzed 332 emergency medicine claims in the insurer’s database that were closed from 2007 to 2013. The findings show the importance of strong communication in the emergency department (ED), and how communication breakdowns can be catalysts for legal claims, Darrell Ranum, vice president for patient safety and risk management for The Doctors Company, said.
Mr. Ranum pointed out one claim in which a patient’s vital signs had changed during the course of a visit. The changes were not communicated to the emergency physician, and he inappropriately discharged the patient. In another case, a patient’s history of overdoses was not conveyed during a patient hand-off, which resulted in an overdose that was not treated in a timely manner.
“Sometimes, we find that patients don’t always understand instructions,” Mr. Ranum said. “If patients don’t understand the communication from their providers or if a patient receives inadequate information, such as in situations where you have a language barrier, you can have problems there as well.”
Another key lesson from the study is the importance of a thorough differential diagnosis, Dr David B. Troxel, medical director for The Doctors Company said in an interview.
Of the 332 claims, 57% were diagnosis related; they included allegations of failure to establish a differential diagnosis, failure to order diagnostic tests, failure to address abnormal findings, and failure to consider available clinical information.
View on the News Workflow bottlenecks contribute Dr Roneet Lev is director of ED operations for Scripps Mercy Hospital in San Diego. She made her remarks in an interview. |
“Our hope is that as physicians review the findings of this study, they will scrutinize their own systems and processes and determine whether the weaknesses identified in the study exist in their organization,” Dr Troxel said.
Among the other claims, 13% related to improper management or treatment, 5% claimed improper performance of treatment, and 3% alleged failure to order medication.
Claims could have more than one contributing factor. Problems with patient assessments, such as failure to address abnormal findings, contributed to 52% of claims. Patient factors, such as physical characteristics and noncompliance, were the second-most-frequent contributor at 21%. Other factors were lack of communication among physicians (17%), poor communication between doctors and patients (14%), insufficient or lack of documentation (13%), and workflow/workload issues (12%).
On Twitter @legal_med
ED-initiated buprenorphine ups treatment rates for opioid addiction
BY BIANCA NOGRADY
FROM JAMA
Vitals Key clinical point: Emergency department–initiated buprenorphine treatment increases the likelihood that opioid-dependent patients will seek addiction treatment. Major finding: Significantly more patients in the buprenorphine group sought addiction treatment in the 30 days after randomization, compared to the referral or intervention arms. Data source: Randomized controlled trial of 104 opioid-dependent patients. Disclosures: The National Institute on Drug Abuse funded the study. Reckitt-Benckiser Pharmaceuticals provided the drug. One author reported honoraria from private industry. |
Initiating buprenorphine treatment during an emergency department visit can significantly increase the likelihood that opioid-dependent patients will seek addiction treatment, according to results of a randomized clinical trial published in April 28 in JAMA.
Researchers randomized 104 opioid-dependent patients who had presented to the ED to screening and treatment referral, screening and a brief intervention with referral to a community-based treatment service, or screening with a brief intervention and ED-initiated treatment with buprenorphine/naloxone and referral to primary care.
Significantly more patients in the buprenorphine group sought addiction treatment in the 30 days after randomization compared to the referral or intervention arms (78% vs. 37% vs. 45%, P < .001), and they showed significant reductions in the number of days of illicit opioid use per week.
“Expanded use of ED-initiated buprenorphine with community follow-up should help increase access to treatment options for this chronic and relapsing medical condition that has substantial morbidity and mortality and that affects health care use and costs,” wrote Dr Gail D’Onofrio of Yale School of Medicine, New Haven, Ct., and coauthors (JAMA 2015; 313:1636-1644 [doi:10.1001/jama.2015.3474]).
More than 75% with sickle cell crises don’t get hydroxyurea
BY MARY ANN MOON
FROM JAMA
Vitals Key clinical point: More than 75% of adults with sickle cell anemia who have frequent pain crises fail to get hydroxyurea therapy as recommended. Major finding: Only 15.1% of adults with sickle cell anemia received hydroxyurea within 3 months of their third pain crisis, only 18.2% received the agent within 6 months, and only 22.7% received it within 12 months. Data source: An analysis of information in a large nationwide insurance claims database involving 570 adults with frequent hospitalizations for sickle cell pain crises. Disclosures: This study was funded by the Lewin Group, a health care consulting firm. Dr Stettler and his associates reported having no relevant financial disclosures. |
More than 75% of adults with sickle cell anemia who have frequent pain crises fail to receive hydroxyurea therapy as strongly recommended in National Heart, Lung, and Blood Institute clinical guidelines, according to a Research Letter to the Editor published online April 28 in JAMA.
Despite proven benefits in decreasing pain crises, hospitalizations, blood transfusions, and possibly mortality, hydroxyurea, a “safe and inexpensive drug,” is thought to be underused. To document the actual use of the drug when indicated, investigators analyzed information in a nationwide insurance claims database covering nearly 27 million patients per year. They focused on the records of 570 adults hospitalized or treated in an emergency department for a sickle cell pain crisis at least three times during a 1-year period, said Dr Nicolas Stettler of the Lewin Group, a health care consulting firm in Falls Church, Va., and his associates.
Only 15.1% of these patients received hydroxyurea within 3 months of their third crisis, only 18.2% received the agent within 6 months, and only 22.7% received it within 12 months. These figures likely represent a conservative estimate of the hydroxyurea treatment gap, since the study didn’t include the large uninsured and publicly insured populations who have more limited access to health care, Dr Stettler and his associates noted (JAMA 2015;313:1671-2).
Several barriers to this treatment have been identified in previous research, including fear of adverse events, lack of clinician training, and failure to use shared decision making. “To address this gap, it may be necessary to enhance patient outreach and clinician training and develop health care quality measures aimed at increasing the use of hydroxyurea for all patients who would benefit,” they added.
Recognizing human trafficking victims
BY ALICIA GALLEGOS
AT THE AMWA ANNUAL MEETING
CHICAGO – Emergency physicians encounter nearly 40% of human trafficking victims who come in contact with health providers, according to Dr Holly G. Atkinson.
In a 2014 survey of domestic sex-trafficking victims, 88% said they encountered one or more health professions during the period in which they were being trafficked, yet none was identified as a victim by physicians during the visits. In another 2014 survey of survivors, 39% of victims reported having contact with emergency departments; 29%, with primary care physicians; 17%, with ob.gyns.; 17%, with dentists; and 3%, with pediatricians.
Key indicators for potential victimization include discrepancies between history and clinical presentation, multiple sexually transmitted diseases, and the accompaniment of a controlling third-party who is not a guardian, said Dr Atkinson, director of the human rights program at Arnhold Global Health Institute at the Icahn School of Medicine at Mount Sinai in New York City, said at the annual meeting of the American Medical Women’s Association.
In 2014, the National Human Trafficking Resource Center, operated by the antislavery organization Polaris, received 3,598 reports of sex-trafficking cases inside the United States. The National Center for Missing & Exploited Children estimates that between 100,000 and 300,000 U.S. children are at risk of being sexually trafficked each year.
Physical signs that could denote the possibility of patients being trafficked include visible tattoos with “daddy,” “property of,” or a trafficker’s street name. Perpetrators often brand their victims so that they are easily recognizable and can be returned if they escape, Dr Atkinson explained.
Dehydration, malnutrition, multiple sexually transmitted infections, and multiple pregnancies or abortions could also be clues. The inability to provide an address, confusion about their current location, an appearance younger than the stated age, avoidance of eye contact, and answers that sound scripted are potential signs of human trafficking, as is the presence of a controlling third party who does not let the patient answer questions or who interrupts or corrects the patient.
The Via Christi Health system in Wichita, Kan., recently published guidance for clinicians on how to proceed if they suspect a patient is a victim of human trafficking. Steps include following child abuse or domestic violence protocols; separating the patient from the controlling third party; providing the patient a comfortable, safe area; and ensuring a patient interview is performed by a trauma-informed social worker or nurse.
Some questions physicians may want to ask patients include: Have you ever exchanged sex for money, food, or shelter? Have you been forced to have sex against your will? Have you been asked to have sex with multiple partners? If the patient answers yes, physicians should follow child abuse protocols and mandatory reporting requirements. If the patient is aged 18 or older, doctors should obtain the patient’s permission to call law enforcement or assist the patient in calling 911.
AMWA recently launched Physicians Against the Trafficking of Humans (PATH). The PATH website includes resources for physicians and an online video about trafficking that doctors can share with their practices and colleagues.
On Twitter @legal_med
Indiana HIV outbreak prompts national advisory
BY SHARON WORCESTER
FRONTLINE MEDICAL NEWS
As health officials continue to battle an intravenous drug use–related HIV outbreak in a rural county in Indiana, the Centers for Disease Control and Prevention has issued an official health advisory stressing the need for vigilance at the state and local levels with respect to detecting and controlling similar outbreaks across the United States.
The Indiana outbreak began in November, with 11 new HIV infections diagnosed by January in Scott County, where fewer than 5 infections per year had been identified previously; since January, an unprecedented 135 infections have been confirmed, and 6 others are under investigation, according to Dr Jerome M. Adams, Indiana State Health Commissioner.
“To put this in further perspective, from 2009 through 2013, the county only reported three new cases of HIV,” Dr Adams said in a joint Indiana State Department of Health/CDC teleconference.
The affected community includes only 4,200 people, and 84% of those diagnosed with HIV also tested positive for hepatitis C virus (HCV) infection, Dr Joan Duwve, chief medical consultant, Indiana State Department of Health, said during the teleconference.
According to the CDC advisory, 96% of 108 infected individuals who were interviewed reported injecting dissolved prescription-type oxymorphone, as well as sharing syringes.
“The United States is facing an epidemic of prescription opioid abuse that must be addressed. Opioid poisoning deaths have nearly quadrupled from 1999 through 2011. This epidemic of opioid abuse has already contributed to a severe and growing epidemic of viral hepatitis among people who inject drugs,” said Dr Jonathan Mermin, director of the National Center for HIV/AIDS Viral Hepatitis, STD, and TB Prevention, who also participated in the teleconference.
New CDC data on HCV show a 150% increase in reports of acute HCV infections nationwide between 2010 to 2013.
“The majority of these infections are believed to be attributable to injection drug use, so we must act now to reverse this trend and to prevent this from undoing progress in HIV prevention to date,” he said.
Among the recommendations were routine opt-out of HIV testing as well as HCV testing per current recommendations. Further, health care professionals should report suspected clusters to their local or state health department, ensure that HCV-infected patients are also tested for HIV and vice versa, and ensure that those receiving treatment for either HIV or HCV are adhering to prescribed therapy and are engaged in ongoing care.
Syringe-sharing and sexual partners of those diagnosed with HIV or HCV should be encouraged to undergo testing, and all persons with substance abuse problems should be referred for medication-assisted treatment and counseling. In Indiana, where a public health emergency was declared on March 26 and has been extended until May 24, care includes HIV and HCV treatment, as well as substance abuse counseling and treatment, according to a “Notes From the Field Report” in the Morbidity and Mortality Weekly Report (MMWR 2015 April 24;64:1-2).
Most accidental genital trauma cases manageable in ED
BY SHARON WORCESTER
AT THE NASPAG ANNUAL MEETING
Vitals Key clinical point: With adequate sedation, most girls with AGT requiring treatment can undergo evaluation and repair in the ED. Major finding: 82% of cases reviewed were minor and managed expectantly. Data source: A retrospective medical records review of 359 cases of accidental genital trauma. Disclosures: Dr Dowlut-McElroy reported having no disclosures. One of her coauthors, Dr Julie Strickland, is a Nexplanon trainer for Merck. |
ORLANDO – Most cases of accidental genital trauma in girls are caused by straddle injuries and are isolated to the labia, and most can be managed expectantly or treated in the emergency department, according to findings from a retrospective cohort study.
Penetrating injuries, however, should be considered an indication for management in the operating room, Dr Tazim Dowlut-McElroy reported at the annual meeting of the North American Society for Pediatric and Adolescent Gynecology.
A review of 359 cases showed that the vast majority – 82% – were minor and managed expectantly.
“Only 18% required surgical management. Of those, 37% required general anesthesia in the OR, but 63% were adequately evaluated and treated in the ED,” said Dr Dowlut-McElroy of Children’s Mercy Hospitals and Clinics, Kansas City.
About 64% of the patients presented during the day, and 36% presented at night. The most common presenting complaint was bleeding and pain (89% of cases), followed by voiding issues in 8% of cases. No presenting complaint was recorded in the remaining patient charts.
The most common mechanism of injury was straddle injury (73% of cases), followed by non-straddle blunt trauma in 15% of cases, and penetrating injury in the remaining cases, Dr Dowlut-McElroy said.
Injuries included lacerations in 86% of cases, abrasions or contusions in 7%, and hematomas in 3%.
Pediatric genital injuries comprised 0.2%-8% of reported childhood trauma, and despite public health efforts to reduce injuries, the number of such pediatric injuries continues to rise, Dr Dowlut-McElroy said.
Patients included in the current review were identified by a medical database query from January 2000 to July 2014. They were aged 0-18 years and had been treated in the ED for genital trauma; those with obstetrical injuries were excluded.
EDs pump up pediatric preparedness
BY MARY ANN MOON
FROM JAMA PEDIATRICS
Vitals Key clinical point: Nationally, emergency departments have improved their compliance with guidelines regarding emergency health care for children. Major finding: The overall median weighted pediatric readiness score (WPRS) was 68.9, a solid improvement over the previously reported median WPRS of 55. Data source: A web-based self-reported assessment of pediatric readiness at 4,149 EDs across the country that have approximately 24 million pediatric visits annually. Disclosures: This project was supported by the Emergency Medical Services for Children network and the EMS for Children National Resource Center under the U.S. Department of Health & Human Services. Dr Gausche-Hill and her associates reported having no financial disclosures. |
Pediatric readiness has improved in emergency departments across the country, as measured by EDs’ compliance with 2009 guidelines for emergency care in children, according to a report published online April 13 in JAMA Pediatrics.
In what they described as “the most comprehensive evaluation of pediatric readiness of our nation’s EDs to date,” investigators performed a web-based assessment of 4,137 hospitals’ self-reported compliance with guidelines addressing child-specific emergency care. The overall median weighted pediatric readiness score (WPRS) was 68.9, a solid improvement over the previously reported median WPRS of 55, said Dr Marianne Gausche-Hill of Harbor-UCLA Medical Center, Torrance, Calif., and her associates.
The single most important factor found to enhance pediatric readiness was to designate two people, one of whom is a physician or nurse, as the hospital’s pediatric emergency care coordinator, as recommended by the Institute of Medicine, the researchers wrote. Nearly half (47.5%) of EDs now have a physician coordinator, and 59.3% now have a nurse coordinator, compared with 18% and 12%, respectively, in a previous report. The presence of coordinators quadrupled the chances that a hospital would put important quality-improvement plans in place to address children’s care needs, the investigators said (JAMA Pediatr. 2015 April 13 [doi:10.1001/jamapediatrics.2015.138]).
Other findings included the following:
- Most physicians providing emergency care for children were specifically trained in emergency medicine (88.6%) or pediatric emergency medicine (55.4%) at high-volume hospitals; low-volume hospitals were more likely to have family-medicine-trained physicians doing so (78.9%).
- Mandatory competency evaluations for providing pediatric emergency care were relatively common for nurses (66.6%) but less so for physicians (38.7%) and midlevel staff (18.1%).
- 99.5% of EDs said all staff are trained on the location of pediatric equipment in the ED, including tools to ensure correct sizing of resuscitation equipment and appropriate dosing of medications.
- 83.1% of EDs said they verified the proper location and function of pediatric equipment daily.
- EDs routinely stocked 91% of recommended pediatric equipment. Equipment that was missing in more than 15% of EDs included laryngeal mask airways, umbilical vein catheters, central venous catheters, tracheostomy tubes, size 00 laryngoscope blades, continuous end-tidal carbon dioxide monitoring equipment, pediatric Magill forceps, and infant and child nasopharyngeal airways.
- Only 46.8% of EDs had disaster plans that specifically addressed children, as recommended. Even among high-volume hospitals, which were the most compliant with guidelines, only 67.4% had such disaster plans.
- Approximately one-third of EDs said their providers failed to weigh children and record the weight in kilograms only, as recommended. This safety measure is crucial to preventing drug-dosing errors.
- The most frequently cited barriers to complying with guidelines were the cost of child-specific training (reported by 54.4% of EDs) and a lack of educational resources (reported by 49.0%). Few EDs reported that a lack of interest was a barrier to implementing the guidelines.
Simplified PESI identified low-risk pulmonary embolism
BY AMY KARON
FROM ACADEMIC EMERGENCY MEDICINE
Vitals Key clinical point: The simplified version of the PESI identified low-risk pulmonary embolism patients. Major finding: Patients with scores of 0 or 1 had low rates of major adverse events during the first 30 days, regardless of which treatment they received. Data source: Post hoc analysis of simplified PESI scores and outcomes among 4,831 patients with acute pulmonary embolism who received either rivaroxaban or an enoxaparin–vitamin K antagonist combination. Disclosures:Bayer HealthCare Pharmaceuticals and Janssen Research & Development funded the study. Dr Fermann reported an advisory relationship with Janssen and research funding from Cardiorentis, Trevena, Novartis, Siemens, and Pfizer. Two coauthors reported employment with Bayer, and two other coauthors reported relationships with several other pharmaceutical companies. |
A simplified version of the Pulmonary Embolism Severity Index identified patients with acute pulmonary embolism who were at low risk of adverse events and might be suitable for outpatient care.
“Although guidelines, such as those from the American College of Chest Physicians, recommend outpatient treatment for selected PE patients at low risk of recurrence, existing evidence for the outpatient management of patients with PE is derived from small cohorts of patients from outside the United States,” said Dr Gregory J. Fermann of the University of Cincinnati department of emergency medicine and his associates. “Risk stratification of PE patients may allow a cohort of low-risk patients to be treated in a clinical decision unit or by a closely monitored outpatient strategy. Such an approach might relieve some of the burden placed on the emergency department,” they wrote (Acad. Emerg. Med. 2015;22:299-307).
The simplified PESI includes 6 of the 11 variables measured in PESI, which has been shown to identify patients at increased risk of death and adverse outcome events after acute PE. The six features of the simplified PESI are age greater than 80 years, history of cancer, history of chronic cardiopulmonary disease, heart rate of at least 110 beats per minutes, systolic blood pressure less than 100 mm Hg, and oxygen saturation less than 90%. Each factor is assigned a score of 1.
They carried out a post hoc analysis of simplified PESI scores and outcomes among 4,831 acute PE patients from the EINSTEIN-PE study of rivaroxaban and an enoxaparin–vitamin K antagonist combination (N. Engl. J. Med. 2012;366:1287-97).
Roughly half (53.6%) of the patients had a score of 0, one-third (36.7%) had a score of 1, and 9.7% had a score of 2 or 3, the researchers reported. Higher simplified PESI scores were associated with increased risk of almost all adverse outcomes measured, including recurrent VTE, fatal PE, all-cause mortality, and major bleeding. Patients with scores of 0 or 1 had low rates of major adverse events during the first 30 days of treatment, regardless of which protocol they received. Scores of 2 or 3 were associated with greater risk of recurrent VTE, fatal PE, all-cause mortality, and major bleeding in both treatment groups.