During the initial peak of coronavirus disease 2019 (COVID-19) cases, US models suggested hospital bed shortages, hinting at the dire possibility of an overwhelmed healthcare system.^1,2 Such projections invoked widespread uncertainty and fear of massive loss of life secondary to an undersupply of treatment resources. This led many state governments to rush into a series of historically unprecedented interventions, including the rapid deployment of field hospitals. US state governments, in partnership with the Army Corps of Engineers, invested more than $660 million to transform convention halls, university campus buildings, and even abandoned industrial warehouses, into overflow hospitals for the care of COVID-19 patients.¹ Such a national scale of field hospital construction is truly historic, never before having occurred at this speed and on this scale. The only other time field hospitals were deployed nearly as widely in the United States was during the Civil War.³

The use of COVID-19 field hospital resources has been variable, with patient volumes ranging from 0 at many to more than 1,000 at the Javits Center field hospital in New York City.¹ In fact, most field hospitals did not treat any patients because early public health measures, such as stay-at-home orders, helped contain the virus in most states.¹ As of this writing, the United States has seen a dramatic surge in COVID-19 transmission and hospitalizations. This has led many states to re-introduce field hospitals into their COVID emergency response.

Our site, the Baltimore Convention Center Field Hospital (BCCFH), is one of few sites that is still operational and, to our knowledge, is the longest-running US COVID-19 field hospital. We have cared for 543 patients since opening and have had no cardiac arrests or on-site deaths. To safely offload lower-acuity COVID-19 patients from Maryland hospitals, we designed admission criteria and care processes to provide medical care on site until patients are ready for discharge. However, we anticipated that some patients would decompensate and need to return to a higher level of care. Here, we share our experience with identifying, assessing, resuscitating, and transporting unstable patients. We believe that this process has allowed us to treat about 80% of our patients in place with successful discharge to outpatient care. We have safely transferred about 20% to a higher level of care, having learned from our early cases to refine and improve our rapid response process.

Case 1

A 39-year-old man was transferred to the BCCFH on his 9th day of symptoms following a 3-day hospital admission for COVID-19. On BCCFH day 1, he developed an oxygen requirement of 2 L/min and a fever of 39.9 ^oC. Testing revealed worsening hyponatremia and new proteinuria, and a chest radiograph showed increased bilateral interstitial infiltrates. Cefdinir and fluid restriction were initiated. On BCCFH day 2, the patient developed hypotension (88/55 mm Hg), tachycardia (180 bpm), an oxygen requirement of 3 L/min, and a brief syncopal episode while sitting in bed. The charge physician and nurse were directed to the bedside. They instructed staff to bring a stretcher and intravenous (IV) supplies. Unable to locate these supplies in the triage bay, the staff found them in various locations. An IV line was inserted, and fluids administered, after which vital signs improved. Emergency medical services (EMS), which were on standby outside the field hospital, were alerted via radio; they donned personal protective equipment (PPE) and arrived at the triage bay. They were redirected to patient bedside, whence they transported the patient to the hospital.

Case 2

A 64-year-old man with a history of homelessness, myocardial infarctions, cerebrovascular accident, and paroxysmal atrial fibrillation was transferred to the BCCFH on his 6th day of symptoms after a 2-day hospitalization with COVID-19 respiratory illness. On BCCFH day 1, he had a temperature of 39.3 ^oC and atypical chest pain. A laboratory workup was unrevealing. On BCCFH day 2, he had asymptomatic hypotension and a heart rate of 60-85 bpm while receiving his usual metoprolol dose. On BCCFH day 3, he reported dizziness and was found to be hypotensive (83/41 mm Hg) and febrile (38.6 ^oC). The rapid response team (RRT) was called over radio, and they quickly assessed the patient and transported him to the triage bay. EMS, signaled through the RRT radio announcement, arrived at the triage bay and transported the patient to a traditional hospital.

The BCCFH, which opened in April 2020, is a 252-bed facility that’s spread over a single exhibit hall floor and cares for stable adult COVID-19 patients from any hospital or emergency department in Maryland (Appendix A). The site offers basic laboratory tests, radiography, a limited on-site pharmacy, and spot vital sign monitoring without telemetry. Both EMS and a certified registered nurse anesthetist are on standby in the nonclinical area and must don PPE before entering the patient care area when called. The appendices show the patient beds (Appendix B) and triage area (Appendix C) used for patient evaluation and resuscitation. Unlike conventional hospitals, the BCCFH has limited consultant access, and there are frequent changes in clinical teams. In addition to clinicians, our site has physical therapists, occupational therapists, and social work teams to assist in patient care and discharge planning. As of this writing, we have cared for 543 patients, sent to us from one-third of Maryland’s hospitals. Use during the first wave of COVID was variable, with some hospitals sending us just a few patients. One Baltimore hospital sent us 8% of its COVID-19 patients. Because the patients have an average 5-day stay, the BCCFH has offloaded 2,600 bed-days of care from acute hospitals.

COVID-19 field hospitals must be prepared to respond effectively to decompensating patients. In our experience, effective RRTs provide a standard and reproducible approach to patient emergencies. In the conventional hospital setting, these teams consist of clinicians who can be called on by any healthcare worker to quickly assess deteriorating patients and intervene with treatment. The purpose of an RRT is to provide immediate care to a patient before progression to respiratory or cardiac arrest. RRTs proliferated in US hospitals after 2004 when the Institute for Healthcare Improvement in Boston, Massachusetts, recommended such teams for improved quality of care. Though studies report conflicting findings on the impact of RRTs on mortality rates, these studies were performed in traditional hospitals with ample resources, consultants, and clinicians familiar with their patients rather than in resource-limited field hospitals.^4-13 Our field hospital has found RRTs, and the principles behind them, useful in the identification and management of decompensating COVID-19 patients.

An approach to managing decompensating patients in a COVID-19 field hospital can be considered in four phases: identification, assessment, resuscitation, and transport. Referring to these phases, the first case shows opportunities for improvement in resuscitation and transport. Although decompensation was identified, the patient was not transported to the triage bay for resuscitation, and there was confusion when trying to obtain the proper equipment. Additionally, EMS awaited the patient in the triage bay, while he remained in his cubicle, which delayed transport to an acute care hospital. The second case shows opportunities for improvement in identification and assessment. The patient had signs of impending decompensation that were not immediately recognized and treated. However, once decompensation occurred, the RRT was called and the patient was transported quickly to the triage bay, and then to the hospital via EMS.

In our experience at the BCCFH, identification is a key phase in COVID-19 care at a field hospital. Identification involves recognizing impending deterioration, as well as understanding risk factors for decompensation. For COVID-19 specifically, this requires heightened awareness of patients who are in the 2nd to 3rd week of symptoms. Data from Wuhan, China, suggest that decompensation occurs predictably around symptom day 9.^14,15 At the BCCFH, the median symptom duration for patients who decompensated and returned to a hospital was 13 days. In both introductory cases, patients were in the high-risk 2nd week of symptoms when decompensation occurred. Clinicians at the BCCFH now discuss patient symptom day during their handoffs, when rounding, and when making decisions regarding acute care transfer. Our team has also integrated clinical information from our electronic health record to create a dashboard describing those patients requiring acute care transfer to assist in identifying other trends or predictive factors (Appendix D).

Although RRTs are designed to activate when an individual patient decompensates, they should fit within a larger operational framework for patient safety. Our experience with emergencies at the BCCFH has yielded four opportunities for learning relevant to COVID-19 care in nontraditional settings (Table). These lessons include how to update staff on clinical process changes, unify communication systems, create a clinical drilling culture, and review cases to improve performance. They illustrate the importance of standardizing emergency processes, conducting frequent updates and drills, and ensuring continuous improvement. We found that, while caring for patients with an unpredictable, novel disease in a nontraditional setting and while wearing PPE and working with new colleagues during every shift, the best approach to support patients and staff is to anticipate emergencies rather than relying on individual staff to develop on-the-spot solutions.

The COVID-19 era has seen the unprecedented construction and utilization of emergency field hospital facilities. Such facilities can serve to offload some COVID-19 patients from strained healthcare infrastructure and provide essential care to these patients. We share many of the unique physical and logistical considerations specific to a nontraditional site. We optimized our space, our equipment, and our communication system. We learned how to identify, assess, resuscitate, and transport decompensating COVID-19 patients. Ultimately, our field hospital has been well utilized and successful at caring for patients because of its adaptability, accessibility, and safety record. Of the 15% of patients we transferred to a hospital for care, 81% were successfully stabilized and were willing to return to the BCCFH to complete their care. Our design included supportive care such as social work, physical and occupational therapy, and treatment of comorbidities, such as diabetes and substance use disorder. Our model demonstrates an effective nonhospital option for the care of lower-acuity, medically complex COVID-19 patients. If such facilities are used in subsequent COVID-19 outbreaks, we advise structured planning for the care of decompensating patients that takes into account the need for effective communication, drilling, and ongoing process improvement.

During the initial peak of coronavirus disease 2019 (COVID-19) cases, US models suggested hospital bed shortages, hinting at the dire possibility of an overwhelmed healthcare system.^1,2 Such projections invoked widespread uncertainty and fear of massive loss of life secondary to an undersupply of treatment resources. This led many state governments to rush into a series of historically unprecedented interventions, including the rapid deployment of field hospitals. US state governments, in partnership with the Army Corps of Engineers, invested more than $660 million to transform convention halls, university campus buildings, and even abandoned industrial warehouses, into overflow hospitals for the care of COVID-19 patients.¹ Such a national scale of field hospital construction is truly historic, never before having occurred at this speed and on this scale. The only other time field hospitals were deployed nearly as widely in the United States was during the Civil War.³

The use of COVID-19 field hospital resources has been variable, with patient volumes ranging from 0 at many to more than 1,000 at the Javits Center field hospital in New York City.¹ In fact, most field hospitals did not treat any patients because early public health measures, such as stay-at-home orders, helped contain the virus in most states.¹ As of this writing, the United States has seen a dramatic surge in COVID-19 transmission and hospitalizations. This has led many states to re-introduce field hospitals into their COVID emergency response.

Our site, the Baltimore Convention Center Field Hospital (BCCFH), is one of few sites that is still operational and, to our knowledge, is the longest-running US COVID-19 field hospital. We have cared for 543 patients since opening and have had no cardiac arrests or on-site deaths. To safely offload lower-acuity COVID-19 patients from Maryland hospitals, we designed admission criteria and care processes to provide medical care on site until patients are ready for discharge. However, we anticipated that some patients would decompensate and need to return to a higher level of care. Here, we share our experience with identifying, assessing, resuscitating, and transporting unstable patients. We believe that this process has allowed us to treat about 80% of our patients in place with successful discharge to outpatient care. We have safely transferred about 20% to a higher level of care, having learned from our early cases to refine and improve our rapid response process.

Case 1

A 39-year-old man was transferred to the BCCFH on his 9th day of symptoms following a 3-day hospital admission for COVID-19. On BCCFH day 1, he developed an oxygen requirement of 2 L/min and a fever of 39.9 ^oC. Testing revealed worsening hyponatremia and new proteinuria, and a chest radiograph showed increased bilateral interstitial infiltrates. Cefdinir and fluid restriction were initiated. On BCCFH day 2, the patient developed hypotension (88/55 mm Hg), tachycardia (180 bpm), an oxygen requirement of 3 L/min, and a brief syncopal episode while sitting in bed. The charge physician and nurse were directed to the bedside. They instructed staff to bring a stretcher and intravenous (IV) supplies. Unable to locate these supplies in the triage bay, the staff found them in various locations. An IV line was inserted, and fluids administered, after which vital signs improved. Emergency medical services (EMS), which were on standby outside the field hospital, were alerted via radio; they donned personal protective equipment (PPE) and arrived at the triage bay. They were redirected to patient bedside, whence they transported the patient to the hospital.

Case 2

A 64-year-old man with a history of homelessness, myocardial infarctions, cerebrovascular accident, and paroxysmal atrial fibrillation was transferred to the BCCFH on his 6th day of symptoms after a 2-day hospitalization with COVID-19 respiratory illness. On BCCFH day 1, he had a temperature of 39.3 ^oC and atypical chest pain. A laboratory workup was unrevealing. On BCCFH day 2, he had asymptomatic hypotension and a heart rate of 60-85 bpm while receiving his usual metoprolol dose. On BCCFH day 3, he reported dizziness and was found to be hypotensive (83/41 mm Hg) and febrile (38.6 ^oC). The rapid response team (RRT) was called over radio, and they quickly assessed the patient and transported him to the triage bay. EMS, signaled through the RRT radio announcement, arrived at the triage bay and transported the patient to a traditional hospital.

The BCCFH, which opened in April 2020, is a 252-bed facility that’s spread over a single exhibit hall floor and cares for stable adult COVID-19 patients from any hospital or emergency department in Maryland (Appendix A). The site offers basic laboratory tests, radiography, a limited on-site pharmacy, and spot vital sign monitoring without telemetry. Both EMS and a certified registered nurse anesthetist are on standby in the nonclinical area and must don PPE before entering the patient care area when called. The appendices show the patient beds (Appendix B) and triage area (Appendix C) used for patient evaluation and resuscitation. Unlike conventional hospitals, the BCCFH has limited consultant access, and there are frequent changes in clinical teams. In addition to clinicians, our site has physical therapists, occupational therapists, and social work teams to assist in patient care and discharge planning. As of this writing, we have cared for 543 patients, sent to us from one-third of Maryland’s hospitals. Use during the first wave of COVID was variable, with some hospitals sending us just a few patients. One Baltimore hospital sent us 8% of its COVID-19 patients. Because the patients have an average 5-day stay, the BCCFH has offloaded 2,600 bed-days of care from acute hospitals.

COVID-19 field hospitals must be prepared to respond effectively to decompensating patients. In our experience, effective RRTs provide a standard and reproducible approach to patient emergencies. In the conventional hospital setting, these teams consist of clinicians who can be called on by any healthcare worker to quickly assess deteriorating patients and intervene with treatment. The purpose of an RRT is to provide immediate care to a patient before progression to respiratory or cardiac arrest. RRTs proliferated in US hospitals after 2004 when the Institute for Healthcare Improvement in Boston, Massachusetts, recommended such teams for improved quality of care. Though studies report conflicting findings on the impact of RRTs on mortality rates, these studies were performed in traditional hospitals with ample resources, consultants, and clinicians familiar with their patients rather than in resource-limited field hospitals.^4-13 Our field hospital has found RRTs, and the principles behind them, useful in the identification and management of decompensating COVID-19 patients.

An approach to managing decompensating patients in a COVID-19 field hospital can be considered in four phases: identification, assessment, resuscitation, and transport. Referring to these phases, the first case shows opportunities for improvement in resuscitation and transport. Although decompensation was identified, the patient was not transported to the triage bay for resuscitation, and there was confusion when trying to obtain the proper equipment. Additionally, EMS awaited the patient in the triage bay, while he remained in his cubicle, which delayed transport to an acute care hospital. The second case shows opportunities for improvement in identification and assessment. The patient had signs of impending decompensation that were not immediately recognized and treated. However, once decompensation occurred, the RRT was called and the patient was transported quickly to the triage bay, and then to the hospital via EMS.

In our experience at the BCCFH, identification is a key phase in COVID-19 care at a field hospital. Identification involves recognizing impending deterioration, as well as understanding risk factors for decompensation. For COVID-19 specifically, this requires heightened awareness of patients who are in the 2nd to 3rd week of symptoms. Data from Wuhan, China, suggest that decompensation occurs predictably around symptom day 9.^14,15 At the BCCFH, the median symptom duration for patients who decompensated and returned to a hospital was 13 days. In both introductory cases, patients were in the high-risk 2nd week of symptoms when decompensation occurred. Clinicians at the BCCFH now discuss patient symptom day during their handoffs, when rounding, and when making decisions regarding acute care transfer. Our team has also integrated clinical information from our electronic health record to create a dashboard describing those patients requiring acute care transfer to assist in identifying other trends or predictive factors (Appendix D).

Although RRTs are designed to activate when an individual patient decompensates, they should fit within a larger operational framework for patient safety. Our experience with emergencies at the BCCFH has yielded four opportunities for learning relevant to COVID-19 care in nontraditional settings (Table). These lessons include how to update staff on clinical process changes, unify communication systems, create a clinical drilling culture, and review cases to improve performance. They illustrate the importance of standardizing emergency processes, conducting frequent updates and drills, and ensuring continuous improvement. We found that, while caring for patients with an unpredictable, novel disease in a nontraditional setting and while wearing PPE and working with new colleagues during every shift, the best approach to support patients and staff is to anticipate emergencies rather than relying on individual staff to develop on-the-spot solutions.

The COVID-19 era has seen the unprecedented construction and utilization of emergency field hospital facilities. Such facilities can serve to offload some COVID-19 patients from strained healthcare infrastructure and provide essential care to these patients. We share many of the unique physical and logistical considerations specific to a nontraditional site. We optimized our space, our equipment, and our communication system. We learned how to identify, assess, resuscitate, and transport decompensating COVID-19 patients. Ultimately, our field hospital has been well utilized and successful at caring for patients because of its adaptability, accessibility, and safety record. Of the 15% of patients we transferred to a hospital for care, 81% were successfully stabilized and were willing to return to the BCCFH to complete their care. Our design included supportive care such as social work, physical and occupational therapy, and treatment of comorbidities, such as diabetes and substance use disorder. Our model demonstrates an effective nonhospital option for the care of lower-acuity, medically complex COVID-19 patients. If such facilities are used in subsequent COVID-19 outbreaks, we advise structured planning for the care of decompensating patients that takes into account the need for effective communication, drilling, and ongoing process improvement.

During the initial peak of coronavirus disease 2019 (COVID-19) cases, US models suggested hospital bed shortages, hinting at the dire possibility of an overwhelmed healthcare system.^1,2 Such projections invoked widespread uncertainty and fear of massive loss of life secondary to an undersupply of treatment resources. This led many state governments to rush into a series of historically unprecedented interventions, including the rapid deployment of field hospitals. US state governments, in partnership with the Army Corps of Engineers, invested more than $660 million to transform convention halls, university campus buildings, and even abandoned industrial warehouses, into overflow hospitals for the care of COVID-19 patients.¹ Such a national scale of field hospital construction is truly historic, never before having occurred at this speed and on this scale. The only other time field hospitals were deployed nearly as widely in the United States was during the Civil War.³

The use of COVID-19 field hospital resources has been variable, with patient volumes ranging from 0 at many to more than 1,000 at the Javits Center field hospital in New York City.¹ In fact, most field hospitals did not treat any patients because early public health measures, such as stay-at-home orders, helped contain the virus in most states.¹ As of this writing, the United States has seen a dramatic surge in COVID-19 transmission and hospitalizations. This has led many states to re-introduce field hospitals into their COVID emergency response.

Our site, the Baltimore Convention Center Field Hospital (BCCFH), is one of few sites that is still operational and, to our knowledge, is the longest-running US COVID-19 field hospital. We have cared for 543 patients since opening and have had no cardiac arrests or on-site deaths. To safely offload lower-acuity COVID-19 patients from Maryland hospitals, we designed admission criteria and care processes to provide medical care on site until patients are ready for discharge. However, we anticipated that some patients would decompensate and need to return to a higher level of care. Here, we share our experience with identifying, assessing, resuscitating, and transporting unstable patients. We believe that this process has allowed us to treat about 80% of our patients in place with successful discharge to outpatient care. We have safely transferred about 20% to a higher level of care, having learned from our early cases to refine and improve our rapid response process.

Case 1

A 39-year-old man was transferred to the BCCFH on his 9th day of symptoms following a 3-day hospital admission for COVID-19. On BCCFH day 1, he developed an oxygen requirement of 2 L/min and a fever of 39.9 ^oC. Testing revealed worsening hyponatremia and new proteinuria, and a chest radiograph showed increased bilateral interstitial infiltrates. Cefdinir and fluid restriction were initiated. On BCCFH day 2, the patient developed hypotension (88/55 mm Hg), tachycardia (180 bpm), an oxygen requirement of 3 L/min, and a brief syncopal episode while sitting in bed. The charge physician and nurse were directed to the bedside. They instructed staff to bring a stretcher and intravenous (IV) supplies. Unable to locate these supplies in the triage bay, the staff found them in various locations. An IV line was inserted, and fluids administered, after which vital signs improved. Emergency medical services (EMS), which were on standby outside the field hospital, were alerted via radio; they donned personal protective equipment (PPE) and arrived at the triage bay. They were redirected to patient bedside, whence they transported the patient to the hospital.

Case 2

A 64-year-old man with a history of homelessness, myocardial infarctions, cerebrovascular accident, and paroxysmal atrial fibrillation was transferred to the BCCFH on his 6th day of symptoms after a 2-day hospitalization with COVID-19 respiratory illness. On BCCFH day 1, he had a temperature of 39.3 ^oC and atypical chest pain. A laboratory workup was unrevealing. On BCCFH day 2, he had asymptomatic hypotension and a heart rate of 60-85 bpm while receiving his usual metoprolol dose. On BCCFH day 3, he reported dizziness and was found to be hypotensive (83/41 mm Hg) and febrile (38.6 ^oC). The rapid response team (RRT) was called over radio, and they quickly assessed the patient and transported him to the triage bay. EMS, signaled through the RRT radio announcement, arrived at the triage bay and transported the patient to a traditional hospital.

The BCCFH, which opened in April 2020, is a 252-bed facility that’s spread over a single exhibit hall floor and cares for stable adult COVID-19 patients from any hospital or emergency department in Maryland (Appendix A). The site offers basic laboratory tests, radiography, a limited on-site pharmacy, and spot vital sign monitoring without telemetry. Both EMS and a certified registered nurse anesthetist are on standby in the nonclinical area and must don PPE before entering the patient care area when called. The appendices show the patient beds (Appendix B) and triage area (Appendix C) used for patient evaluation and resuscitation. Unlike conventional hospitals, the BCCFH has limited consultant access, and there are frequent changes in clinical teams. In addition to clinicians, our site has physical therapists, occupational therapists, and social work teams to assist in patient care and discharge planning. As of this writing, we have cared for 543 patients, sent to us from one-third of Maryland’s hospitals. Use during the first wave of COVID was variable, with some hospitals sending us just a few patients. One Baltimore hospital sent us 8% of its COVID-19 patients. Because the patients have an average 5-day stay, the BCCFH has offloaded 2,600 bed-days of care from acute hospitals.

COVID-19 field hospitals must be prepared to respond effectively to decompensating patients. In our experience, effective RRTs provide a standard and reproducible approach to patient emergencies. In the conventional hospital setting, these teams consist of clinicians who can be called on by any healthcare worker to quickly assess deteriorating patients and intervene with treatment. The purpose of an RRT is to provide immediate care to a patient before progression to respiratory or cardiac arrest. RRTs proliferated in US hospitals after 2004 when the Institute for Healthcare Improvement in Boston, Massachusetts, recommended such teams for improved quality of care. Though studies report conflicting findings on the impact of RRTs on mortality rates, these studies were performed in traditional hospitals with ample resources, consultants, and clinicians familiar with their patients rather than in resource-limited field hospitals.^4-13 Our field hospital has found RRTs, and the principles behind them, useful in the identification and management of decompensating COVID-19 patients.

An approach to managing decompensating patients in a COVID-19 field hospital can be considered in four phases: identification, assessment, resuscitation, and transport. Referring to these phases, the first case shows opportunities for improvement in resuscitation and transport. Although decompensation was identified, the patient was not transported to the triage bay for resuscitation, and there was confusion when trying to obtain the proper equipment. Additionally, EMS awaited the patient in the triage bay, while he remained in his cubicle, which delayed transport to an acute care hospital. The second case shows opportunities for improvement in identification and assessment. The patient had signs of impending decompensation that were not immediately recognized and treated. However, once decompensation occurred, the RRT was called and the patient was transported quickly to the triage bay, and then to the hospital via EMS.

In our experience at the BCCFH, identification is a key phase in COVID-19 care at a field hospital. Identification involves recognizing impending deterioration, as well as understanding risk factors for decompensation. For COVID-19 specifically, this requires heightened awareness of patients who are in the 2nd to 3rd week of symptoms. Data from Wuhan, China, suggest that decompensation occurs predictably around symptom day 9.^14,15 At the BCCFH, the median symptom duration for patients who decompensated and returned to a hospital was 13 days. In both introductory cases, patients were in the high-risk 2nd week of symptoms when decompensation occurred. Clinicians at the BCCFH now discuss patient symptom day during their handoffs, when rounding, and when making decisions regarding acute care transfer. Our team has also integrated clinical information from our electronic health record to create a dashboard describing those patients requiring acute care transfer to assist in identifying other trends or predictive factors (Appendix D).

Although RRTs are designed to activate when an individual patient decompensates, they should fit within a larger operational framework for patient safety. Our experience with emergencies at the BCCFH has yielded four opportunities for learning relevant to COVID-19 care in nontraditional settings (Table). These lessons include how to update staff on clinical process changes, unify communication systems, create a clinical drilling culture, and review cases to improve performance. They illustrate the importance of standardizing emergency processes, conducting frequent updates and drills, and ensuring continuous improvement. We found that, while caring for patients with an unpredictable, novel disease in a nontraditional setting and while wearing PPE and working with new colleagues during every shift, the best approach to support patients and staff is to anticipate emergencies rather than relying on individual staff to develop on-the-spot solutions.

The COVID-19 era has seen the unprecedented construction and utilization of emergency field hospital facilities. Such facilities can serve to offload some COVID-19 patients from strained healthcare infrastructure and provide essential care to these patients. We share many of the unique physical and logistical considerations specific to a nontraditional site. We optimized our space, our equipment, and our communication system. We learned how to identify, assess, resuscitate, and transport decompensating COVID-19 patients. Ultimately, our field hospital has been well utilized and successful at caring for patients because of its adaptability, accessibility, and safety record. Of the 15% of patients we transferred to a hospital for care, 81% were successfully stabilized and were willing to return to the BCCFH to complete their care. Our design included supportive care such as social work, physical and occupational therapy, and treatment of comorbidities, such as diabetes and substance use disorder. Our model demonstrates an effective nonhospital option for the care of lower-acuity, medically complex COVID-19 patients. If such facilities are used in subsequent COVID-19 outbreaks, we advise structured planning for the care of decompensating patients that takes into account the need for effective communication, drilling, and ongoing process improvement.

Isolation in response to COVID-19 pandemic has driven many people to reestablish long forgotten connections between old friends and geographically distant relatives. Fed by the ease in which Zoom and other electronic miracles can bring once familiar voices and faces into our homes, we no longer need to wait until our high school or college reunions to reconnect.

The Class of 1962 at Pleasantville (N.Y.) High School has always attracted an unusually large number of attendees at its reunions, and its exuberant response to pandemic-fueled mini Zoom reunions is not surprising. With each virtual gathering we learn and relearn more about each other. I had always felt that because my birthday was in December that I was among the very youngest in my class. (New York’s school enrollment calendar cutoff is in December.) However, I recently learned that some of my classmates were even younger, having been born in the following spring.

This revelation prompted a discussion among the younger septuagenarians about whether we felt that our relative immaturity, at least as measured by the calendar, affected us. It was generally agreed that for the women, being younger seemed to present little problem. For, the men there were a few for whom immaturity put them at an athletic disadvantage. But, there was uniform agreement that social immaturity made dating an uncomfortable adventure. No one felt that his or her immaturity placed them at an academic disadvantage. Of course, all of these observations are heavily colored by the bias of those who have chosen to maintain contact with classmates.

A recent flurry of papers and commentaries about relative age at school entry and the diagnosis of attention deficit/hyperactivity disorder prompted me to ask my Zoom mates if they could recall anyone whom they would label as having exhibited the behavior we have all come to associate with ADHD (Vuori M et al. Children’s relative age and ADHD medication use: A Finnish population-based study. Pediatrics 2020 Oct. doi: 10.1542/peds.2019-4046, and Butter EM. Keeping relative age effects and ADHD care in context. Pediatrics. 2020;146[4]:e2020022798).

We could all recall classmates who struggled academically and seemed to not be paying attention. However, when one includes the hyperactivity descriptor we couldn’t recall anyone whose in-classroom physical activity drew our attention. Of course, there were many shared anecdotes about note passing, spitball throwing, and out-of-class shenanigans. But, from the perspective of behavior that disrupted the classroom there were very few. And, not surprisingly, given the intervening 6 decades, none of us could make an association between immaturity and the behavior.

While I have very few memories of what happened when I was in grade school, many of my classmates have vivid recollections of events both mundane and dramatic even as far back as first and second grade. Why do none of them recall classmates whose behavior would in current terminology be labeled as ADHD?

Were most of us that age bouncing off the walls and so there were no outliers? Were the teachers more tolerant because they expected that many children, particularly the younger ones, would be more physically active? Or, maybe we arrived at school, even those who were chronologically less mature, having already been settled down by home environments that neither fostered nor tolerated hyperactivity?

If you ask a pediatrician over the age of 70 if he or she recalls being taught anything about ADHD in medical school or seeing any children in his or her first years of practice who would fit the current diagnostic criteria, you will see them simply shrug. ADHD was simply not on our radar in the 1970s and 1980s. And it’s not because radar hadn’t been invented. We pediatricians were paying attention, and I trust in my high school classmates’ observations. I am sure there were isolated cases that could easily have been labeled as ADHD if the term had existed. But, the volume of hyperactive children a pediatrician sees today in the course of a normal office day just didn’t exist.

I have trouble believing that this dramatic increase in frequency is the result of accumulating genetic damage from Teflon cookware or climate change or air pollution. Although I am open to any serious attempt to explain the phenomenon I think we should look first into the home environment in which children are being raised. Sleep schedules, activity, and amusement opportunities as well as discipline styles – just to name a few – are far different now than before the ADHD diagnosis overtook the landscape.
 

Dr. Wilkoff practiced primary care pediatrics in Brunswick, Maine for nearly 40 years. He has authored several books on behavioral pediatrics, including “How to Say No to Your Toddler.” Other than a Littman stethoscope he accepted as a first-year medical student in 1966, Dr. Wilkoff reports having nothing to disclose. Email him at [email protected].

Isolation in response to COVID-19 pandemic has driven many people to reestablish long forgotten connections between old friends and geographically distant relatives. Fed by the ease in which Zoom and other electronic miracles can bring once familiar voices and faces into our homes, we no longer need to wait until our high school or college reunions to reconnect.

The Class of 1962 at Pleasantville (N.Y.) High School has always attracted an unusually large number of attendees at its reunions, and its exuberant response to pandemic-fueled mini Zoom reunions is not surprising. With each virtual gathering we learn and relearn more about each other. I had always felt that because my birthday was in December that I was among the very youngest in my class. (New York’s school enrollment calendar cutoff is in December.) However, I recently learned that some of my classmates were even younger, having been born in the following spring.

This revelation prompted a discussion among the younger septuagenarians about whether we felt that our relative immaturity, at least as measured by the calendar, affected us. It was generally agreed that for the women, being younger seemed to present little problem. For, the men there were a few for whom immaturity put them at an athletic disadvantage. But, there was uniform agreement that social immaturity made dating an uncomfortable adventure. No one felt that his or her immaturity placed them at an academic disadvantage. Of course, all of these observations are heavily colored by the bias of those who have chosen to maintain contact with classmates.

A recent flurry of papers and commentaries about relative age at school entry and the diagnosis of attention deficit/hyperactivity disorder prompted me to ask my Zoom mates if they could recall anyone whom they would label as having exhibited the behavior we have all come to associate with ADHD (Vuori M et al. Children’s relative age and ADHD medication use: A Finnish population-based study. Pediatrics 2020 Oct. doi: 10.1542/peds.2019-4046, and Butter EM. Keeping relative age effects and ADHD care in context. Pediatrics. 2020;146[4]:e2020022798).

We could all recall classmates who struggled academically and seemed to not be paying attention. However, when one includes the hyperactivity descriptor we couldn’t recall anyone whose in-classroom physical activity drew our attention. Of course, there were many shared anecdotes about note passing, spitball throwing, and out-of-class shenanigans. But, from the perspective of behavior that disrupted the classroom there were very few. And, not surprisingly, given the intervening 6 decades, none of us could make an association between immaturity and the behavior.

While I have very few memories of what happened when I was in grade school, many of my classmates have vivid recollections of events both mundane and dramatic even as far back as first and second grade. Why do none of them recall classmates whose behavior would in current terminology be labeled as ADHD?

Were most of us that age bouncing off the walls and so there were no outliers? Were the teachers more tolerant because they expected that many children, particularly the younger ones, would be more physically active? Or, maybe we arrived at school, even those who were chronologically less mature, having already been settled down by home environments that neither fostered nor tolerated hyperactivity?

If you ask a pediatrician over the age of 70 if he or she recalls being taught anything about ADHD in medical school or seeing any children in his or her first years of practice who would fit the current diagnostic criteria, you will see them simply shrug. ADHD was simply not on our radar in the 1970s and 1980s. And it’s not because radar hadn’t been invented. We pediatricians were paying attention, and I trust in my high school classmates’ observations. I am sure there were isolated cases that could easily have been labeled as ADHD if the term had existed. But, the volume of hyperactive children a pediatrician sees today in the course of a normal office day just didn’t exist.

I have trouble believing that this dramatic increase in frequency is the result of accumulating genetic damage from Teflon cookware or climate change or air pollution. Although I am open to any serious attempt to explain the phenomenon I think we should look first into the home environment in which children are being raised. Sleep schedules, activity, and amusement opportunities as well as discipline styles – just to name a few – are far different now than before the ADHD diagnosis overtook the landscape.
 

Dr. Wilkoff practiced primary care pediatrics in Brunswick, Maine for nearly 40 years. He has authored several books on behavioral pediatrics, including “How to Say No to Your Toddler.” Other than a Littman stethoscope he accepted as a first-year medical student in 1966, Dr. Wilkoff reports having nothing to disclose. Email him at [email protected].

Isolation in response to COVID-19 pandemic has driven many people to reestablish long forgotten connections between old friends and geographically distant relatives. Fed by the ease in which Zoom and other electronic miracles can bring once familiar voices and faces into our homes, we no longer need to wait until our high school or college reunions to reconnect.

The Class of 1962 at Pleasantville (N.Y.) High School has always attracted an unusually large number of attendees at its reunions, and its exuberant response to pandemic-fueled mini Zoom reunions is not surprising. With each virtual gathering we learn and relearn more about each other. I had always felt that because my birthday was in December that I was among the very youngest in my class. (New York’s school enrollment calendar cutoff is in December.) However, I recently learned that some of my classmates were even younger, having been born in the following spring.

This revelation prompted a discussion among the younger septuagenarians about whether we felt that our relative immaturity, at least as measured by the calendar, affected us. It was generally agreed that for the women, being younger seemed to present little problem. For, the men there were a few for whom immaturity put them at an athletic disadvantage. But, there was uniform agreement that social immaturity made dating an uncomfortable adventure. No one felt that his or her immaturity placed them at an academic disadvantage. Of course, all of these observations are heavily colored by the bias of those who have chosen to maintain contact with classmates.

A recent flurry of papers and commentaries about relative age at school entry and the diagnosis of attention deficit/hyperactivity disorder prompted me to ask my Zoom mates if they could recall anyone whom they would label as having exhibited the behavior we have all come to associate with ADHD (Vuori M et al. Children’s relative age and ADHD medication use: A Finnish population-based study. Pediatrics 2020 Oct. doi: 10.1542/peds.2019-4046, and Butter EM. Keeping relative age effects and ADHD care in context. Pediatrics. 2020;146[4]:e2020022798).

We could all recall classmates who struggled academically and seemed to not be paying attention. However, when one includes the hyperactivity descriptor we couldn’t recall anyone whose in-classroom physical activity drew our attention. Of course, there were many shared anecdotes about note passing, spitball throwing, and out-of-class shenanigans. But, from the perspective of behavior that disrupted the classroom there were very few. And, not surprisingly, given the intervening 6 decades, none of us could make an association between immaturity and the behavior.

While I have very few memories of what happened when I was in grade school, many of my classmates have vivid recollections of events both mundane and dramatic even as far back as first and second grade. Why do none of them recall classmates whose behavior would in current terminology be labeled as ADHD?

Were most of us that age bouncing off the walls and so there were no outliers? Were the teachers more tolerant because they expected that many children, particularly the younger ones, would be more physically active? Or, maybe we arrived at school, even those who were chronologically less mature, having already been settled down by home environments that neither fostered nor tolerated hyperactivity?

If you ask a pediatrician over the age of 70 if he or she recalls being taught anything about ADHD in medical school or seeing any children in his or her first years of practice who would fit the current diagnostic criteria, you will see them simply shrug. ADHD was simply not on our radar in the 1970s and 1980s. And it’s not because radar hadn’t been invented. We pediatricians were paying attention, and I trust in my high school classmates’ observations. I am sure there were isolated cases that could easily have been labeled as ADHD if the term had existed. But, the volume of hyperactive children a pediatrician sees today in the course of a normal office day just didn’t exist.

I have trouble believing that this dramatic increase in frequency is the result of accumulating genetic damage from Teflon cookware or climate change or air pollution. Although I am open to any serious attempt to explain the phenomenon I think we should look first into the home environment in which children are being raised. Sleep schedules, activity, and amusement opportunities as well as discipline styles – just to name a few – are far different now than before the ADHD diagnosis overtook the landscape.
 

Dr. Wilkoff practiced primary care pediatrics in Brunswick, Maine for nearly 40 years. He has authored several books on behavioral pediatrics, including “How to Say No to Your Toddler.” Other than a Littman stethoscope he accepted as a first-year medical student in 1966, Dr. Wilkoff reports having nothing to disclose. Email him at [email protected].

The rates of osteopenia and osteoporosis among individuals with psoriatic arthritis are comparable to those seen in the general population, research suggests.

The cohort study, published in Arthritis Care & Research, also found that clinicians are likely to refer patients for bone mineral density (BMD) testing based on osteoporosis risk factors or psoriatic arthritis disease severity markers.

Timothy S.H. Kwok, MD, of the University of Toronto, and coauthors wrote that previous research suggested a possible link between psoriatic arthritis and osteoporosis or osteopenia. However, no cohort studies appear to have examined this association.

The study involved 201 individuals with psoriatic arthritis attending a single specialist clinic, who were enrolled in a longitudinal study of psoriatic arthritis (PsA) and who were also referred for BMD testing with dual-energy x-ray absorptiometry.

Of these participants, 13% had a BMD in the osteoporotic range, 45% were in the osteopenic range, and 42% were in the normal range for BMD. The prevalence of osteoporosis observed in the general population aged 50 or above, observed in an earlier large prospective study, ranged from 7% to 16%, and osteopenia ranged from 27% to 46%.

“Our study suggests that patients with PsA have similar BMDs compared to the general population,” the authors wrote.

Researchers did note the suggestion that patients with polyarthritis had lower BMDs over time. Because of the small number of events, this did not achieve statistical significance, but “this relationship warrants further research, given that multiple cohort studies have independently demonstrated polyarticular onset of disease predicting clinical deformities and erosive disease in PsA,” they wrote.

They also saw that patients with increased body mass index had a significant 21% lower odds of having a BMD in the osteoporotic range, while those using biologics had a significant 83% lower odds.

Among participants with BMD scores in the osteopenic or osteoporotic range, these scores were seen in the lumbar spine in 63% of measurements, the femoral neck in 88%, and the total hip in 39%. Mean T-scores for the lumbar spine were –0.30±0.32, and for the femoral neck were –1.10±1.04 and the total hip, –0.45±0.42.

The study also examined what factors were associated with referral for BMD testing. They found that increasing age, menopause, elevated acute phase reactants, or use of biologics, methotrexate, and systemic glucocorticoids were associated with a higher likelihood of undergoing BMD testing.

Noting that the latest Canadian clinical practice guidelines on BMD testing advise that age, menopause, and use of systemic glucocorticoids use are risk factors that should prompt testing, the authors suggested clinicians were using a combination of traditional osteoporosis risk factors and markers of psoriatic disease severity to underpin their decision to refer.

However, they commented that none of the factors associated with a higher likelihood of having a BMD test were actually associated with lower BMD scores.

“This suggests that clinicians may be over-screening patients with PsA for osteopenia/osteoporosis, as they do not appear to be at baseline higher risk for lower BMD scores than the general population,” they wrote. “This is of importance, as there are currently no formal recommendations with regards to the optimal interval or time to commence BMD testing within the recent major PsA guidelines.”

The study was supported by a grant from the Krembil Foundation. No conflicts of interest were declared.

SOURCE: Kwok TSH et al. Arthritis Care Res. 2020 Dec 16. doi: 10.1002/acr.24538.

The rates of osteopenia and osteoporosis among individuals with psoriatic arthritis are comparable to those seen in the general population, research suggests.

The cohort study, published in Arthritis Care & Research, also found that clinicians are likely to refer patients for bone mineral density (BMD) testing based on osteoporosis risk factors or psoriatic arthritis disease severity markers.

Timothy S.H. Kwok, MD, of the University of Toronto, and coauthors wrote that previous research suggested a possible link between psoriatic arthritis and osteoporosis or osteopenia. However, no cohort studies appear to have examined this association.

The study involved 201 individuals with psoriatic arthritis attending a single specialist clinic, who were enrolled in a longitudinal study of psoriatic arthritis (PsA) and who were also referred for BMD testing with dual-energy x-ray absorptiometry.

Of these participants, 13% had a BMD in the osteoporotic range, 45% were in the osteopenic range, and 42% were in the normal range for BMD. The prevalence of osteoporosis observed in the general population aged 50 or above, observed in an earlier large prospective study, ranged from 7% to 16%, and osteopenia ranged from 27% to 46%.

“Our study suggests that patients with PsA have similar BMDs compared to the general population,” the authors wrote.

Researchers did note the suggestion that patients with polyarthritis had lower BMDs over time. Because of the small number of events, this did not achieve statistical significance, but “this relationship warrants further research, given that multiple cohort studies have independently demonstrated polyarticular onset of disease predicting clinical deformities and erosive disease in PsA,” they wrote.

They also saw that patients with increased body mass index had a significant 21% lower odds of having a BMD in the osteoporotic range, while those using biologics had a significant 83% lower odds.

Among participants with BMD scores in the osteopenic or osteoporotic range, these scores were seen in the lumbar spine in 63% of measurements, the femoral neck in 88%, and the total hip in 39%. Mean T-scores for the lumbar spine were –0.30±0.32, and for the femoral neck were –1.10±1.04 and the total hip, –0.45±0.42.

The study also examined what factors were associated with referral for BMD testing. They found that increasing age, menopause, elevated acute phase reactants, or use of biologics, methotrexate, and systemic glucocorticoids were associated with a higher likelihood of undergoing BMD testing.

Noting that the latest Canadian clinical practice guidelines on BMD testing advise that age, menopause, and use of systemic glucocorticoids use are risk factors that should prompt testing, the authors suggested clinicians were using a combination of traditional osteoporosis risk factors and markers of psoriatic disease severity to underpin their decision to refer.

However, they commented that none of the factors associated with a higher likelihood of having a BMD test were actually associated with lower BMD scores.

“This suggests that clinicians may be over-screening patients with PsA for osteopenia/osteoporosis, as they do not appear to be at baseline higher risk for lower BMD scores than the general population,” they wrote. “This is of importance, as there are currently no formal recommendations with regards to the optimal interval or time to commence BMD testing within the recent major PsA guidelines.”

The study was supported by a grant from the Krembil Foundation. No conflicts of interest were declared.

SOURCE: Kwok TSH et al. Arthritis Care Res. 2020 Dec 16. doi: 10.1002/acr.24538.

The rates of osteopenia and osteoporosis among individuals with psoriatic arthritis are comparable to those seen in the general population, research suggests.

The cohort study, published in Arthritis Care & Research, also found that clinicians are likely to refer patients for bone mineral density (BMD) testing based on osteoporosis risk factors or psoriatic arthritis disease severity markers.

Timothy S.H. Kwok, MD, of the University of Toronto, and coauthors wrote that previous research suggested a possible link between psoriatic arthritis and osteoporosis or osteopenia. However, no cohort studies appear to have examined this association.

The study involved 201 individuals with psoriatic arthritis attending a single specialist clinic, who were enrolled in a longitudinal study of psoriatic arthritis (PsA) and who were also referred for BMD testing with dual-energy x-ray absorptiometry.

Of these participants, 13% had a BMD in the osteoporotic range, 45% were in the osteopenic range, and 42% were in the normal range for BMD. The prevalence of osteoporosis observed in the general population aged 50 or above, observed in an earlier large prospective study, ranged from 7% to 16%, and osteopenia ranged from 27% to 46%.

“Our study suggests that patients with PsA have similar BMDs compared to the general population,” the authors wrote.

Researchers did note the suggestion that patients with polyarthritis had lower BMDs over time. Because of the small number of events, this did not achieve statistical significance, but “this relationship warrants further research, given that multiple cohort studies have independently demonstrated polyarticular onset of disease predicting clinical deformities and erosive disease in PsA,” they wrote.

They also saw that patients with increased body mass index had a significant 21% lower odds of having a BMD in the osteoporotic range, while those using biologics had a significant 83% lower odds.

Among participants with BMD scores in the osteopenic or osteoporotic range, these scores were seen in the lumbar spine in 63% of measurements, the femoral neck in 88%, and the total hip in 39%. Mean T-scores for the lumbar spine were –0.30±0.32, and for the femoral neck were –1.10±1.04 and the total hip, –0.45±0.42.

The study also examined what factors were associated with referral for BMD testing. They found that increasing age, menopause, elevated acute phase reactants, or use of biologics, methotrexate, and systemic glucocorticoids were associated with a higher likelihood of undergoing BMD testing.

Noting that the latest Canadian clinical practice guidelines on BMD testing advise that age, menopause, and use of systemic glucocorticoids use are risk factors that should prompt testing, the authors suggested clinicians were using a combination of traditional osteoporosis risk factors and markers of psoriatic disease severity to underpin their decision to refer.

However, they commented that none of the factors associated with a higher likelihood of having a BMD test were actually associated with lower BMD scores.

“This suggests that clinicians may be over-screening patients with PsA for osteopenia/osteoporosis, as they do not appear to be at baseline higher risk for lower BMD scores than the general population,” they wrote. “This is of importance, as there are currently no formal recommendations with regards to the optimal interval or time to commence BMD testing within the recent major PsA guidelines.”

The study was supported by a grant from the Krembil Foundation. No conflicts of interest were declared.

SOURCE: Kwok TSH et al. Arthritis Care Res. 2020 Dec 16. doi: 10.1002/acr.24538.

CASE Unidentified ectopic pregnancy leads to rupture*

A 33-year-old woman (G1 P0010) with 2 positive home pregnancy tests presents to the emergency department (ED) reporting intermittent vaginal bleeding for 3 days. Her last menstrual period was 10 weeks ago, but she reports that her menses are always irregular. She has a history of asymptomatic chlamydia, as well as spontaneous abortion 2 years prior. At present, she denies abdominal pain or vaginal discharge.

Upon examination her vital signs are: temperature, 98.3 °F; pulse, 112 bpm, with a resting rate of 16 bpm; blood pressure (BP), 142/91 mm Hg; pulse O2, 99%; height, 4’ 3”; weight, 115 lb. Her labs are: hemoglobin, 12.1 g/dL; hematocrit, 38%; serum human chorionic gonadotropin (hCG) 236 mIU/mL. Upon pelvic examination, no active bleeding is noted. She agrees to be followed up by her gynecologist and is given a prescription for serum hCG in 2 days. She is instructed to return to the ED should she have pain or increased vaginal bleeding.

Three days later, the patient follows up with her gynecologist reporting mild cramping. She notes having had an episode of heavy vaginal bleeding and a “weakly positive” home pregnancy test. Transvaginal ultrasonography notes endometrial thickness 0.59 mm and unremarkable adnexa. A urine pregnancy test performed in the office is positive; urinalysis is positive for nitrites. With the bleeding slowed, the gynecologist’s overall impression is that the patient has undergone complete spontaneous abortion. She prescribes Macrobid for the urinary tract infection. She does not obtain the ED-prescribed serum HCG levels, as she feels, since complete spontaneous abortion has occurred there is no need to obtain a follow-up serum HCG.

Five days later, the patient returns to the ED reporting abdominal pain after eating. Fever and productive cough of 2 days are noted. The patient states that she had a recent miscarriage. The overall impression of the patient’s condition is bronchitis, and it is noted on the patient’s record, “unlikely ectopic pregnancy and pregnancy test may be false positive,” hence a pregnancy test is not ordered. Examination reveals mild suprapubic tenderness with no rebound; no pelvic exam is performed. The patient is instructed to follow up with a health care clinic within a week, and to return to the ED with severe abdominal pain, higher fever, or any new concerning symptoms. A Zithromax Z-pak is prescribed.

Four days later, the patient is brought by ambulance to the ED of the local major medical center with severe abdominal pain involving the right lower quadrant. She states that she had a miscarriage 3 weeks prior and was recently treated for bronchitis. She has dizziness when standing. Her vital signs are: temperature, 97.8 °F; heart rate, 95 bpm; BP, 72/48 mm Hg; pulse O2, 100%. She reports her abdominal pain to be 6/10.

The patient is given a Lactated Ringer’s bolus of 1,000 mL for a hypotensive episode. Computed tomography is obtained and notes, “low attenuation in the left adnexa with a dilated fallopian tube.” A large heterogeneous collection of fluid in the pelvis is noted with active extravasation, consistent with an “acute bleed.”

The patient is brought to the operating room with a diagnosis of probable ruptured ectopic pregnancy. Intraoperatively she is noted to have a right ruptured ectopic and left tubo-ovarian abscess. The surgeon proceeds with right salpingectomy and left salpingo-oophorectomy. Three liters of hemoperitoneum is found.

She is followed postoperatively with serum hCG until levels are negative. Her postoperative course is uneventful. Her only future option for pregnancy is through assisted reproductive technology (ART) with in vitro fertilization (IVF). The patient sues the gynecologist and second ED physician for presumed inappropriate assessment for ectopic pregnancy.

*The “facts” of this case are a composite, drawn from several cases to illustrate medical and legal issues. The statement of facts should be considered hypothetical.

Continue to: WHAT’S THE VERDICT?...

WHAT’S THE VERDICT?

A defense verdict is returned.

Medical considerations

The incidence of ectopic pregnancy is 2% of all pregnancies, with a higher incidence (about 4%) among infertility patients.¹ Up to 10% of ectopic pregnancies have no symptoms.²

Clinical presentations. Classic signs of ectopic pregnancy include:

• abdominal pain
• vaginal bleeding
• late menses (often noted).

A recent case of ectopic pregnancy presenting with chest pain was reported.³ Clinicians must never lose site of the fact that ectopic pregnancy is the most common cause of maternal mortality in the first trimester, with an incidence of 1% to 10% of all first-trimester deaths.⁴

Risk factors include pelvic inflammatory disease, as demonstrated in the opening case. “The silent epidemic of chlamydia” comes to mind, and tobacco smoking can adversely affect tubal cilia, as can pelvic adhesions and/or prior tubal surgery. All of these factors can predispose a patient to ectopic pregnancy; in addition, intrauterine devices, endometriosis, tubal ligation (or ligation reversal), all can set the stage for an ectopic pregnancy.⁵ Appropriate serum hCG monitoring during early pregnancy can assist in sorting out pregnancies of unknown location (PUL; FIGURE). First trimester ultrasonography, at 5 weeks gestation, usually identifies early intrauterine gestation.

Heterotopic pregnancy includes an intrauterine gestation and an ectopic pregnancy. This presentation includes the presence of a “pseudosac” in the endometrial cavity plus an extrauterine gestation. Heterotopic pregnancies have become somewhat more common as ART/IVF has unfolded, especially prior to the predominance of single embryo transfer.

Managing ectopic pregnancy

For cases of early pregnancy complicated by intermittent bleeding and/or pain, monitoring with serum hCG levels at 48-hour intervals to distinguish a viable IUP from an abnormal IUP or an ectopic is appropriate. The “discriminatory zone” collates serum hCG levels with findings on ultrasonography. Specific lower limits of serum hCG levels are not clear cut, with recommendations of 3,500 mIU/mL to provide sonographic evidence of an intrauterine gestation “to avoid misdiagnosis and possible interruption of intrauterine pregnancy,” as conveyed in the American College of Obstetricians and Gynecologists 2018 practice bulletin.⁸ Serum progesterone levels also have been suggested to complement hCG levels; a progesterone level of <20 nmol/L is consistent with an abnormal pregnancy, whereas levels >25 nmol/L are suggestive of a viable pregnancy.² Inhibin A levels also have been suggested to be helpful, but they are not an ideal monitoring tool.

While most ectopic pregnancies are located in the fallopian tube, other locations also can be abdominal or ovarian. In addition, cesarean scar ectopic pregnancy can occur and often is associated with delay in diagnosis and greater morbidity due to such delay.⁹ With regard to ovarian ectopic, Spiegelberg criteria are established for diagnosis (TABLE 1).¹⁰

Appropriate management of an ectopic pregnancy is dependent upon the gestational age, serum hCG levels, and imaging findings, as well as the patient’s symptoms and exam findings. Treatment is established in large part on a case-by-case basis and includes, for early pregnancy, expectant management and use of methotrexate (TABLE 2).¹¹ Dilation and curettage may be used to identify the pregnancy’s location when the serum hCG level is below 2,000 mIU/mL and there is no evidence of an IUP on ultrasound. Surgical treatment can include minimally invasive salpingostomy or salpingectomy and, depending on circumstance, laparotomy may be indicated.

Continue to: Legal perspective...

Legal perspective

Lawsuits related to ectopic pregnancy are not a new phenomenon. In fact, in 1897, a physician in Ohio who misdiagnosed an “extrauterine pregnancy” as appendicitis was the center of a malpractice lawsuit.¹³ Unrecognized or mishandled ectopic pregnancy can result in serious injuries—in the range of 1% to 10% (see above) of maternal deaths are related to ectopic pregnancy.¹⁴ Ectopic pregnancy cases, therefore, have been the subject of substantial litigation over the years. An informal, noncomprehensive review of malpractice lawsuits brought from 2000 to 2019, found more than 300 ectopic pregnancy cases. Given the large number of malpractice claims against ObGyns,¹⁵ ectopic pregnancy cases are only a small portion of all ObGyn malpractice cases.¹⁶

A common claim: negligent diagnosis or treatment

The most common basis for lawsuits in cases of ectopic pregnancy is the clinician’s negligent failure to properly diagnose the ectopic nature of the pregnancy. There are also a number of cases claiming negligent treatment of an identified ectopic pregnancy. Not every missed diagnosis, or unsuccessful treatment, leads to liability, of course. It is only when a diagnosis or treatment fails to meet the standard of care within the profession that there should be liability. That standard of care is generally defined by what a reasonably prudent physician would do under the circumstances. Expert witnesses, who are familiar with the standard of practice within the specialty, are usually necessary to establish what that practice is. Both the plaintiff and the defense obtain experts, the former to prove what the standard of care is and that the standard was not met in the case at hand. The defense experts are usually arguing that the standard of care was met.¹⁷ Inadequate diagnosis of ectopic pregnancy or other condition may arise from a failure to take a sufficient history, conduct an appropriately thorough physical examination, recognize any of the symptoms that would suggest it is present, use and conduct ultrasound correctly, or follow-up appropriately with additional testing.¹⁸

A malpractice claim of negligent treatment can involve any the following circumstances¹⁹:

• failure to establish an appropriate treatment plan
• prescribing inappropriate medications for the patient (eg, methotrexate, when it is contraindicated)
• delivering the wrong medication or the wrong amount of the right medication
• performing a procedure badly
• undertaking a new treatment without adequate instruction and preparation.

Given the nature and risks of ectopic pregnancy, ongoing, frequent contact with the patient is essential from the point at which the condition is suspected. The greater the risk of harm (probability or consequence), the more careful any professional ought to be. Because ectopic pregnancy is not an uncommon occurrence, and because it can have devastating effects, including death, a reasonably prudent practitioner would be especially aware of the clinical presentations discussed above.²⁰ In the opening case, the treatment plan was not well documented.

Negligence must lead to patient harm. In addition to negligence (proving that the physician did not act in accordance with the standard of care), to prevail in a malpractice case, the plaintiff-patient must prove that the negligence caused the injury, or worsened it. If the failure to make a diagnosis would not have made any difference in a harm the patient suffered, there are no damages and no liability. Suppose, for example, that a physician negligently failed to diagnose ectopic pregnancy, but performed surgery expecting to find the misdiagnosed condition. In the course of the surgery, however, the surgeon discovered and appropriately treated the ectopic pregnancy. (A version of this happened in the old 19th century case mentioned above.) The negligence of the physician did not cause harm, so there are no damages and no liability.

Continue to: Informed consent is vital...

Informed consent is vital

A part of malpractice is informed consent (or the absence of it)—issues that can arise in any medical care.²¹ It is wise to pay particular attention in cases where the nature of the illness is unknown, and where there are significant uncertainties and the nature of testing and treatment may change substantially over a period of a few days or few weeks. As always, informed consent should include a discussion of what process or procedure is proposed, its risks and benefits, alternative approaches that might be available, and the risk of doing nothing. Frequently, the uncertainty of ectopic pregnancy complicates the informed consent process.²²

Because communication with the patient is an essential function of informed consent, the consent process should productively be used in PUL and similar cases to inform the patient about the uncertainty, and the testing and (nonsurgical) treatment that will occur. This is an opportunity to reinforce the message that the patient must maintain ongoing communication with the physician’s office about changes in her condition, and appear for each appointment scheduled. If more invasive procedures—notably surgery—become required, a separate consent process should be completed, because the risks and considerations are now meaningfully different than when treatment began. As a general matter, any possible treatment that may result in infertility or reduced reproductive capacity should specifically be included in the consent process.

In the hypothetical case, the gynecologist failed to obtain a follow-up serum hCG level. In addition, the record did not reflect ectopic pregnancy in the differential diagnosis. As noted above, the patient had predisposing factors for an ectopic pregnancy. The physician should have acknowledged the history of sexually transmitted disease predisposing her to an ectopic pregnancy. Monitoring of serum hCG levels until they are negative is appropriate with ectopic, or presumed ectopic, pregnancy management. Appropriate monitoring did not occur in this case. Each of these errors (following up on serum hCG levels and the inadequacy of notations about the possibility of ectopic pregnancy) seem inconsistent with the usual standard of care. Furthermore, as a result of the outcome, the only future option for the patient to pursue pregnancy was IVF.

Other legal issues

There are a number of other legal issues that are associated with the topic of ectopic pregnancy. There is evidence, for example, that Catholic and non-Catholic hospitals treat ectopic pregnancies differently,²³ which may reflect different views on taking a life or the use of methotrexate and its association with abortion.²⁴ In addition, the possibility of an increase in future ectopic pregnancies is one of the “risks” of abortion that pro-life organizations have pushed to see included in abortion informed consent.²⁵ This has led some commentators to conclude that some Catholic hospitals violate federal law in managing ectopic pregnancy. There is also evidence of “overwhelming rates of medical misinformation on pregnancy center websites, including a link between abortion and ectopic pregnancy.”²⁶

The fact that cesarean deliveries are related to an increased risk for ectopic pregnancy (because of the risk of cesarean scar ectopic pregnancy) also has been cited as information that should play a role in the consent process for cesarean delivery.²⁷ In terms of liability, failed tubal ligation leads to a 33% risk of ectopic pregnancy.²⁸ The risk of ectopic pregnancy is also commonly included in surrogacy contracts.²⁹

Why the outcome was for the defense

The opening hypothetical case illustrates some of the uncertainties of medical malpractice cases. As noted, there appeared a deviation from the usual standard of care, particularly the failure to follow up on the serum hCG level. The weakness in the medical record, failing to note the possibility of ectopic pregnancy, also was probably an error but, apparently, the court felt that this did not result in any harm to the patient.

The question arises of how there would be a defense verdict in light of the failure to track consecutive serum hCG levels. A speculative explanation is that there are many uncertainties in most lawsuits. Procedural problems may result in a case being limited, expert witnesses are essential to both the plaintiff and defense, with the quality of their review and testimony possibly uneven. Judges and juries may rely on one expert witness rather than another, juries vary, and the quality of advocacy differs. Any of these situations can contribute to the unpredictability of the outcome of a case. In the case above, the liability was somewhat uncertain, and the various other factors tipped in favor of a defense verdict. ●

CASE Unidentified ectopic pregnancy leads to rupture*

A 33-year-old woman (G1 P0010) with 2 positive home pregnancy tests presents to the emergency department (ED) reporting intermittent vaginal bleeding for 3 days. Her last menstrual period was 10 weeks ago, but she reports that her menses are always irregular. She has a history of asymptomatic chlamydia, as well as spontaneous abortion 2 years prior. At present, she denies abdominal pain or vaginal discharge.

Upon examination her vital signs are: temperature, 98.3 °F; pulse, 112 bpm, with a resting rate of 16 bpm; blood pressure (BP), 142/91 mm Hg; pulse O2, 99%; height, 4’ 3”; weight, 115 lb. Her labs are: hemoglobin, 12.1 g/dL; hematocrit, 38%; serum human chorionic gonadotropin (hCG) 236 mIU/mL. Upon pelvic examination, no active bleeding is noted. She agrees to be followed up by her gynecologist and is given a prescription for serum hCG in 2 days. She is instructed to return to the ED should she have pain or increased vaginal bleeding.

Three days later, the patient follows up with her gynecologist reporting mild cramping. She notes having had an episode of heavy vaginal bleeding and a “weakly positive” home pregnancy test. Transvaginal ultrasonography notes endometrial thickness 0.59 mm and unremarkable adnexa. A urine pregnancy test performed in the office is positive; urinalysis is positive for nitrites. With the bleeding slowed, the gynecologist’s overall impression is that the patient has undergone complete spontaneous abortion. She prescribes Macrobid for the urinary tract infection. She does not obtain the ED-prescribed serum HCG levels, as she feels, since complete spontaneous abortion has occurred there is no need to obtain a follow-up serum HCG.

Five days later, the patient returns to the ED reporting abdominal pain after eating. Fever and productive cough of 2 days are noted. The patient states that she had a recent miscarriage. The overall impression of the patient’s condition is bronchitis, and it is noted on the patient’s record, “unlikely ectopic pregnancy and pregnancy test may be false positive,” hence a pregnancy test is not ordered. Examination reveals mild suprapubic tenderness with no rebound; no pelvic exam is performed. The patient is instructed to follow up with a health care clinic within a week, and to return to the ED with severe abdominal pain, higher fever, or any new concerning symptoms. A Zithromax Z-pak is prescribed.

Four days later, the patient is brought by ambulance to the ED of the local major medical center with severe abdominal pain involving the right lower quadrant. She states that she had a miscarriage 3 weeks prior and was recently treated for bronchitis. She has dizziness when standing. Her vital signs are: temperature, 97.8 °F; heart rate, 95 bpm; BP, 72/48 mm Hg; pulse O2, 100%. She reports her abdominal pain to be 6/10.

The patient is given a Lactated Ringer’s bolus of 1,000 mL for a hypotensive episode. Computed tomography is obtained and notes, “low attenuation in the left adnexa with a dilated fallopian tube.” A large heterogeneous collection of fluid in the pelvis is noted with active extravasation, consistent with an “acute bleed.”

The patient is brought to the operating room with a diagnosis of probable ruptured ectopic pregnancy. Intraoperatively she is noted to have a right ruptured ectopic and left tubo-ovarian abscess. The surgeon proceeds with right salpingectomy and left salpingo-oophorectomy. Three liters of hemoperitoneum is found.

She is followed postoperatively with serum hCG until levels are negative. Her postoperative course is uneventful. Her only future option for pregnancy is through assisted reproductive technology (ART) with in vitro fertilization (IVF). The patient sues the gynecologist and second ED physician for presumed inappropriate assessment for ectopic pregnancy.

*The “facts” of this case are a composite, drawn from several cases to illustrate medical and legal issues. The statement of facts should be considered hypothetical.

Continue to: WHAT’S THE VERDICT?...

WHAT’S THE VERDICT?

A defense verdict is returned.

Medical considerations

The incidence of ectopic pregnancy is 2% of all pregnancies, with a higher incidence (about 4%) among infertility patients.¹ Up to 10% of ectopic pregnancies have no symptoms.²

Clinical presentations. Classic signs of ectopic pregnancy include:

• abdominal pain
• vaginal bleeding
• late menses (often noted).

A recent case of ectopic pregnancy presenting with chest pain was reported.³ Clinicians must never lose site of the fact that ectopic pregnancy is the most common cause of maternal mortality in the first trimester, with an incidence of 1% to 10% of all first-trimester deaths.⁴

Risk factors include pelvic inflammatory disease, as demonstrated in the opening case. “The silent epidemic of chlamydia” comes to mind, and tobacco smoking can adversely affect tubal cilia, as can pelvic adhesions and/or prior tubal surgery. All of these factors can predispose a patient to ectopic pregnancy; in addition, intrauterine devices, endometriosis, tubal ligation (or ligation reversal), all can set the stage for an ectopic pregnancy.⁵ Appropriate serum hCG monitoring during early pregnancy can assist in sorting out pregnancies of unknown location (PUL; FIGURE). First trimester ultrasonography, at 5 weeks gestation, usually identifies early intrauterine gestation.

Heterotopic pregnancy includes an intrauterine gestation and an ectopic pregnancy. This presentation includes the presence of a “pseudosac” in the endometrial cavity plus an extrauterine gestation. Heterotopic pregnancies have become somewhat more common as ART/IVF has unfolded, especially prior to the predominance of single embryo transfer.

Managing ectopic pregnancy

For cases of early pregnancy complicated by intermittent bleeding and/or pain, monitoring with serum hCG levels at 48-hour intervals to distinguish a viable IUP from an abnormal IUP or an ectopic is appropriate. The “discriminatory zone” collates serum hCG levels with findings on ultrasonography. Specific lower limits of serum hCG levels are not clear cut, with recommendations of 3,500 mIU/mL to provide sonographic evidence of an intrauterine gestation “to avoid misdiagnosis and possible interruption of intrauterine pregnancy,” as conveyed in the American College of Obstetricians and Gynecologists 2018 practice bulletin.⁸ Serum progesterone levels also have been suggested to complement hCG levels; a progesterone level of <20 nmol/L is consistent with an abnormal pregnancy, whereas levels >25 nmol/L are suggestive of a viable pregnancy.² Inhibin A levels also have been suggested to be helpful, but they are not an ideal monitoring tool.

While most ectopic pregnancies are located in the fallopian tube, other locations also can be abdominal or ovarian. In addition, cesarean scar ectopic pregnancy can occur and often is associated with delay in diagnosis and greater morbidity due to such delay.⁹ With regard to ovarian ectopic, Spiegelberg criteria are established for diagnosis (TABLE 1).¹⁰

Appropriate management of an ectopic pregnancy is dependent upon the gestational age, serum hCG levels, and imaging findings, as well as the patient’s symptoms and exam findings. Treatment is established in large part on a case-by-case basis and includes, for early pregnancy, expectant management and use of methotrexate (TABLE 2).¹¹ Dilation and curettage may be used to identify the pregnancy’s location when the serum hCG level is below 2,000 mIU/mL and there is no evidence of an IUP on ultrasound. Surgical treatment can include minimally invasive salpingostomy or salpingectomy and, depending on circumstance, laparotomy may be indicated.

Continue to: Legal perspective...

Legal perspective

Lawsuits related to ectopic pregnancy are not a new phenomenon. In fact, in 1897, a physician in Ohio who misdiagnosed an “extrauterine pregnancy” as appendicitis was the center of a malpractice lawsuit.¹³ Unrecognized or mishandled ectopic pregnancy can result in serious injuries—in the range of 1% to 10% (see above) of maternal deaths are related to ectopic pregnancy.¹⁴ Ectopic pregnancy cases, therefore, have been the subject of substantial litigation over the years. An informal, noncomprehensive review of malpractice lawsuits brought from 2000 to 2019, found more than 300 ectopic pregnancy cases. Given the large number of malpractice claims against ObGyns,¹⁵ ectopic pregnancy cases are only a small portion of all ObGyn malpractice cases.¹⁶

A common claim: negligent diagnosis or treatment

The most common basis for lawsuits in cases of ectopic pregnancy is the clinician’s negligent failure to properly diagnose the ectopic nature of the pregnancy. There are also a number of cases claiming negligent treatment of an identified ectopic pregnancy. Not every missed diagnosis, or unsuccessful treatment, leads to liability, of course. It is only when a diagnosis or treatment fails to meet the standard of care within the profession that there should be liability. That standard of care is generally defined by what a reasonably prudent physician would do under the circumstances. Expert witnesses, who are familiar with the standard of practice within the specialty, are usually necessary to establish what that practice is. Both the plaintiff and the defense obtain experts, the former to prove what the standard of care is and that the standard was not met in the case at hand. The defense experts are usually arguing that the standard of care was met.¹⁷ Inadequate diagnosis of ectopic pregnancy or other condition may arise from a failure to take a sufficient history, conduct an appropriately thorough physical examination, recognize any of the symptoms that would suggest it is present, use and conduct ultrasound correctly, or follow-up appropriately with additional testing.¹⁸

A malpractice claim of negligent treatment can involve any the following circumstances¹⁹:

• failure to establish an appropriate treatment plan
• prescribing inappropriate medications for the patient (eg, methotrexate, when it is contraindicated)
• delivering the wrong medication or the wrong amount of the right medication
• performing a procedure badly
• undertaking a new treatment without adequate instruction and preparation.

Given the nature and risks of ectopic pregnancy, ongoing, frequent contact with the patient is essential from the point at which the condition is suspected. The greater the risk of harm (probability or consequence), the more careful any professional ought to be. Because ectopic pregnancy is not an uncommon occurrence, and because it can have devastating effects, including death, a reasonably prudent practitioner would be especially aware of the clinical presentations discussed above.²⁰ In the opening case, the treatment plan was not well documented.

Negligence must lead to patient harm. In addition to negligence (proving that the physician did not act in accordance with the standard of care), to prevail in a malpractice case, the plaintiff-patient must prove that the negligence caused the injury, or worsened it. If the failure to make a diagnosis would not have made any difference in a harm the patient suffered, there are no damages and no liability. Suppose, for example, that a physician negligently failed to diagnose ectopic pregnancy, but performed surgery expecting to find the misdiagnosed condition. In the course of the surgery, however, the surgeon discovered and appropriately treated the ectopic pregnancy. (A version of this happened in the old 19th century case mentioned above.) The negligence of the physician did not cause harm, so there are no damages and no liability.

Continue to: Informed consent is vital...

Informed consent is vital

A part of malpractice is informed consent (or the absence of it)—issues that can arise in any medical care.²¹ It is wise to pay particular attention in cases where the nature of the illness is unknown, and where there are significant uncertainties and the nature of testing and treatment may change substantially over a period of a few days or few weeks. As always, informed consent should include a discussion of what process or procedure is proposed, its risks and benefits, alternative approaches that might be available, and the risk of doing nothing. Frequently, the uncertainty of ectopic pregnancy complicates the informed consent process.²²

Because communication with the patient is an essential function of informed consent, the consent process should productively be used in PUL and similar cases to inform the patient about the uncertainty, and the testing and (nonsurgical) treatment that will occur. This is an opportunity to reinforce the message that the patient must maintain ongoing communication with the physician’s office about changes in her condition, and appear for each appointment scheduled. If more invasive procedures—notably surgery—become required, a separate consent process should be completed, because the risks and considerations are now meaningfully different than when treatment began. As a general matter, any possible treatment that may result in infertility or reduced reproductive capacity should specifically be included in the consent process.

In the hypothetical case, the gynecologist failed to obtain a follow-up serum hCG level. In addition, the record did not reflect ectopic pregnancy in the differential diagnosis. As noted above, the patient had predisposing factors for an ectopic pregnancy. The physician should have acknowledged the history of sexually transmitted disease predisposing her to an ectopic pregnancy. Monitoring of serum hCG levels until they are negative is appropriate with ectopic, or presumed ectopic, pregnancy management. Appropriate monitoring did not occur in this case. Each of these errors (following up on serum hCG levels and the inadequacy of notations about the possibility of ectopic pregnancy) seem inconsistent with the usual standard of care. Furthermore, as a result of the outcome, the only future option for the patient to pursue pregnancy was IVF.

Other legal issues

There are a number of other legal issues that are associated with the topic of ectopic pregnancy. There is evidence, for example, that Catholic and non-Catholic hospitals treat ectopic pregnancies differently,²³ which may reflect different views on taking a life or the use of methotrexate and its association with abortion.²⁴ In addition, the possibility of an increase in future ectopic pregnancies is one of the “risks” of abortion that pro-life organizations have pushed to see included in abortion informed consent.²⁵ This has led some commentators to conclude that some Catholic hospitals violate federal law in managing ectopic pregnancy. There is also evidence of “overwhelming rates of medical misinformation on pregnancy center websites, including a link between abortion and ectopic pregnancy.”²⁶

The fact that cesarean deliveries are related to an increased risk for ectopic pregnancy (because of the risk of cesarean scar ectopic pregnancy) also has been cited as information that should play a role in the consent process for cesarean delivery.²⁷ In terms of liability, failed tubal ligation leads to a 33% risk of ectopic pregnancy.²⁸ The risk of ectopic pregnancy is also commonly included in surrogacy contracts.²⁹

Why the outcome was for the defense

The opening hypothetical case illustrates some of the uncertainties of medical malpractice cases. As noted, there appeared a deviation from the usual standard of care, particularly the failure to follow up on the serum hCG level. The weakness in the medical record, failing to note the possibility of ectopic pregnancy, also was probably an error but, apparently, the court felt that this did not result in any harm to the patient.

The question arises of how there would be a defense verdict in light of the failure to track consecutive serum hCG levels. A speculative explanation is that there are many uncertainties in most lawsuits. Procedural problems may result in a case being limited, expert witnesses are essential to both the plaintiff and defense, with the quality of their review and testimony possibly uneven. Judges and juries may rely on one expert witness rather than another, juries vary, and the quality of advocacy differs. Any of these situations can contribute to the unpredictability of the outcome of a case. In the case above, the liability was somewhat uncertain, and the various other factors tipped in favor of a defense verdict. ●

CASE Unidentified ectopic pregnancy leads to rupture*

A 33-year-old woman (G1 P0010) with 2 positive home pregnancy tests presents to the emergency department (ED) reporting intermittent vaginal bleeding for 3 days. Her last menstrual period was 10 weeks ago, but she reports that her menses are always irregular. She has a history of asymptomatic chlamydia, as well as spontaneous abortion 2 years prior. At present, she denies abdominal pain or vaginal discharge.

Upon examination her vital signs are: temperature, 98.3 °F; pulse, 112 bpm, with a resting rate of 16 bpm; blood pressure (BP), 142/91 mm Hg; pulse O2, 99%; height, 4’ 3”; weight, 115 lb. Her labs are: hemoglobin, 12.1 g/dL; hematocrit, 38%; serum human chorionic gonadotropin (hCG) 236 mIU/mL. Upon pelvic examination, no active bleeding is noted. She agrees to be followed up by her gynecologist and is given a prescription for serum hCG in 2 days. She is instructed to return to the ED should she have pain or increased vaginal bleeding.

Three days later, the patient follows up with her gynecologist reporting mild cramping. She notes having had an episode of heavy vaginal bleeding and a “weakly positive” home pregnancy test. Transvaginal ultrasonography notes endometrial thickness 0.59 mm and unremarkable adnexa. A urine pregnancy test performed in the office is positive; urinalysis is positive for nitrites. With the bleeding slowed, the gynecologist’s overall impression is that the patient has undergone complete spontaneous abortion. She prescribes Macrobid for the urinary tract infection. She does not obtain the ED-prescribed serum HCG levels, as she feels, since complete spontaneous abortion has occurred there is no need to obtain a follow-up serum HCG.

Five days later, the patient returns to the ED reporting abdominal pain after eating. Fever and productive cough of 2 days are noted. The patient states that she had a recent miscarriage. The overall impression of the patient’s condition is bronchitis, and it is noted on the patient’s record, “unlikely ectopic pregnancy and pregnancy test may be false positive,” hence a pregnancy test is not ordered. Examination reveals mild suprapubic tenderness with no rebound; no pelvic exam is performed. The patient is instructed to follow up with a health care clinic within a week, and to return to the ED with severe abdominal pain, higher fever, or any new concerning symptoms. A Zithromax Z-pak is prescribed.

Four days later, the patient is brought by ambulance to the ED of the local major medical center with severe abdominal pain involving the right lower quadrant. She states that she had a miscarriage 3 weeks prior and was recently treated for bronchitis. She has dizziness when standing. Her vital signs are: temperature, 97.8 °F; heart rate, 95 bpm; BP, 72/48 mm Hg; pulse O2, 100%. She reports her abdominal pain to be 6/10.

The patient is given a Lactated Ringer’s bolus of 1,000 mL for a hypotensive episode. Computed tomography is obtained and notes, “low attenuation in the left adnexa with a dilated fallopian tube.” A large heterogeneous collection of fluid in the pelvis is noted with active extravasation, consistent with an “acute bleed.”

The patient is brought to the operating room with a diagnosis of probable ruptured ectopic pregnancy. Intraoperatively she is noted to have a right ruptured ectopic and left tubo-ovarian abscess. The surgeon proceeds with right salpingectomy and left salpingo-oophorectomy. Three liters of hemoperitoneum is found.

She is followed postoperatively with serum hCG until levels are negative. Her postoperative course is uneventful. Her only future option for pregnancy is through assisted reproductive technology (ART) with in vitro fertilization (IVF). The patient sues the gynecologist and second ED physician for presumed inappropriate assessment for ectopic pregnancy.

*The “facts” of this case are a composite, drawn from several cases to illustrate medical and legal issues. The statement of facts should be considered hypothetical.

Continue to: WHAT’S THE VERDICT?...

WHAT’S THE VERDICT?

A defense verdict is returned.

Medical considerations

The incidence of ectopic pregnancy is 2% of all pregnancies, with a higher incidence (about 4%) among infertility patients.¹ Up to 10% of ectopic pregnancies have no symptoms.²

Clinical presentations. Classic signs of ectopic pregnancy include:

• abdominal pain
• vaginal bleeding
• late menses (often noted).

A recent case of ectopic pregnancy presenting with chest pain was reported.³ Clinicians must never lose site of the fact that ectopic pregnancy is the most common cause of maternal mortality in the first trimester, with an incidence of 1% to 10% of all first-trimester deaths.⁴

Risk factors include pelvic inflammatory disease, as demonstrated in the opening case. “The silent epidemic of chlamydia” comes to mind, and tobacco smoking can adversely affect tubal cilia, as can pelvic adhesions and/or prior tubal surgery. All of these factors can predispose a patient to ectopic pregnancy; in addition, intrauterine devices, endometriosis, tubal ligation (or ligation reversal), all can set the stage for an ectopic pregnancy.⁵ Appropriate serum hCG monitoring during early pregnancy can assist in sorting out pregnancies of unknown location (PUL; FIGURE). First trimester ultrasonography, at 5 weeks gestation, usually identifies early intrauterine gestation.

Heterotopic pregnancy includes an intrauterine gestation and an ectopic pregnancy. This presentation includes the presence of a “pseudosac” in the endometrial cavity plus an extrauterine gestation. Heterotopic pregnancies have become somewhat more common as ART/IVF has unfolded, especially prior to the predominance of single embryo transfer.

Managing ectopic pregnancy

For cases of early pregnancy complicated by intermittent bleeding and/or pain, monitoring with serum hCG levels at 48-hour intervals to distinguish a viable IUP from an abnormal IUP or an ectopic is appropriate. The “discriminatory zone” collates serum hCG levels with findings on ultrasonography. Specific lower limits of serum hCG levels are not clear cut, with recommendations of 3,500 mIU/mL to provide sonographic evidence of an intrauterine gestation “to avoid misdiagnosis and possible interruption of intrauterine pregnancy,” as conveyed in the American College of Obstetricians and Gynecologists 2018 practice bulletin.⁸ Serum progesterone levels also have been suggested to complement hCG levels; a progesterone level of <20 nmol/L is consistent with an abnormal pregnancy, whereas levels >25 nmol/L are suggestive of a viable pregnancy.² Inhibin A levels also have been suggested to be helpful, but they are not an ideal monitoring tool.

While most ectopic pregnancies are located in the fallopian tube, other locations also can be abdominal or ovarian. In addition, cesarean scar ectopic pregnancy can occur and often is associated with delay in diagnosis and greater morbidity due to such delay.⁹ With regard to ovarian ectopic, Spiegelberg criteria are established for diagnosis (TABLE 1).¹⁰

Appropriate management of an ectopic pregnancy is dependent upon the gestational age, serum hCG levels, and imaging findings, as well as the patient’s symptoms and exam findings. Treatment is established in large part on a case-by-case basis and includes, for early pregnancy, expectant management and use of methotrexate (TABLE 2).¹¹ Dilation and curettage may be used to identify the pregnancy’s location when the serum hCG level is below 2,000 mIU/mL and there is no evidence of an IUP on ultrasound. Surgical treatment can include minimally invasive salpingostomy or salpingectomy and, depending on circumstance, laparotomy may be indicated.

Continue to: Legal perspective...

Legal perspective

Lawsuits related to ectopic pregnancy are not a new phenomenon. In fact, in 1897, a physician in Ohio who misdiagnosed an “extrauterine pregnancy” as appendicitis was the center of a malpractice lawsuit.¹³ Unrecognized or mishandled ectopic pregnancy can result in serious injuries—in the range of 1% to 10% (see above) of maternal deaths are related to ectopic pregnancy.¹⁴ Ectopic pregnancy cases, therefore, have been the subject of substantial litigation over the years. An informal, noncomprehensive review of malpractice lawsuits brought from 2000 to 2019, found more than 300 ectopic pregnancy cases. Given the large number of malpractice claims against ObGyns,¹⁵ ectopic pregnancy cases are only a small portion of all ObGyn malpractice cases.¹⁶

A common claim: negligent diagnosis or treatment

The most common basis for lawsuits in cases of ectopic pregnancy is the clinician’s negligent failure to properly diagnose the ectopic nature of the pregnancy. There are also a number of cases claiming negligent treatment of an identified ectopic pregnancy. Not every missed diagnosis, or unsuccessful treatment, leads to liability, of course. It is only when a diagnosis or treatment fails to meet the standard of care within the profession that there should be liability. That standard of care is generally defined by what a reasonably prudent physician would do under the circumstances. Expert witnesses, who are familiar with the standard of practice within the specialty, are usually necessary to establish what that practice is. Both the plaintiff and the defense obtain experts, the former to prove what the standard of care is and that the standard was not met in the case at hand. The defense experts are usually arguing that the standard of care was met.¹⁷ Inadequate diagnosis of ectopic pregnancy or other condition may arise from a failure to take a sufficient history, conduct an appropriately thorough physical examination, recognize any of the symptoms that would suggest it is present, use and conduct ultrasound correctly, or follow-up appropriately with additional testing.¹⁸

A malpractice claim of negligent treatment can involve any the following circumstances¹⁹:

• failure to establish an appropriate treatment plan
• prescribing inappropriate medications for the patient (eg, methotrexate, when it is contraindicated)
• delivering the wrong medication or the wrong amount of the right medication
• performing a procedure badly
• undertaking a new treatment without adequate instruction and preparation.

Given the nature and risks of ectopic pregnancy, ongoing, frequent contact with the patient is essential from the point at which the condition is suspected. The greater the risk of harm (probability or consequence), the more careful any professional ought to be. Because ectopic pregnancy is not an uncommon occurrence, and because it can have devastating effects, including death, a reasonably prudent practitioner would be especially aware of the clinical presentations discussed above.²⁰ In the opening case, the treatment plan was not well documented.

Negligence must lead to patient harm. In addition to negligence (proving that the physician did not act in accordance with the standard of care), to prevail in a malpractice case, the plaintiff-patient must prove that the negligence caused the injury, or worsened it. If the failure to make a diagnosis would not have made any difference in a harm the patient suffered, there are no damages and no liability. Suppose, for example, that a physician negligently failed to diagnose ectopic pregnancy, but performed surgery expecting to find the misdiagnosed condition. In the course of the surgery, however, the surgeon discovered and appropriately treated the ectopic pregnancy. (A version of this happened in the old 19th century case mentioned above.) The negligence of the physician did not cause harm, so there are no damages and no liability.

Continue to: Informed consent is vital...

Informed consent is vital

A part of malpractice is informed consent (or the absence of it)—issues that can arise in any medical care.²¹ It is wise to pay particular attention in cases where the nature of the illness is unknown, and where there are significant uncertainties and the nature of testing and treatment may change substantially over a period of a few days or few weeks. As always, informed consent should include a discussion of what process or procedure is proposed, its risks and benefits, alternative approaches that might be available, and the risk of doing nothing. Frequently, the uncertainty of ectopic pregnancy complicates the informed consent process.²²

Because communication with the patient is an essential function of informed consent, the consent process should productively be used in PUL and similar cases to inform the patient about the uncertainty, and the testing and (nonsurgical) treatment that will occur. This is an opportunity to reinforce the message that the patient must maintain ongoing communication with the physician’s office about changes in her condition, and appear for each appointment scheduled. If more invasive procedures—notably surgery—become required, a separate consent process should be completed, because the risks and considerations are now meaningfully different than when treatment began. As a general matter, any possible treatment that may result in infertility or reduced reproductive capacity should specifically be included in the consent process.

In the hypothetical case, the gynecologist failed to obtain a follow-up serum hCG level. In addition, the record did not reflect ectopic pregnancy in the differential diagnosis. As noted above, the patient had predisposing factors for an ectopic pregnancy. The physician should have acknowledged the history of sexually transmitted disease predisposing her to an ectopic pregnancy. Monitoring of serum hCG levels until they are negative is appropriate with ectopic, or presumed ectopic, pregnancy management. Appropriate monitoring did not occur in this case. Each of these errors (following up on serum hCG levels and the inadequacy of notations about the possibility of ectopic pregnancy) seem inconsistent with the usual standard of care. Furthermore, as a result of the outcome, the only future option for the patient to pursue pregnancy was IVF.

Other legal issues

There are a number of other legal issues that are associated with the topic of ectopic pregnancy. There is evidence, for example, that Catholic and non-Catholic hospitals treat ectopic pregnancies differently,²³ which may reflect different views on taking a life or the use of methotrexate and its association with abortion.²⁴ In addition, the possibility of an increase in future ectopic pregnancies is one of the “risks” of abortion that pro-life organizations have pushed to see included in abortion informed consent.²⁵ This has led some commentators to conclude that some Catholic hospitals violate federal law in managing ectopic pregnancy. There is also evidence of “overwhelming rates of medical misinformation on pregnancy center websites, including a link between abortion and ectopic pregnancy.”²⁶

The fact that cesarean deliveries are related to an increased risk for ectopic pregnancy (because of the risk of cesarean scar ectopic pregnancy) also has been cited as information that should play a role in the consent process for cesarean delivery.²⁷ In terms of liability, failed tubal ligation leads to a 33% risk of ectopic pregnancy.²⁸ The risk of ectopic pregnancy is also commonly included in surrogacy contracts.²⁹

Why the outcome was for the defense

The opening hypothetical case illustrates some of the uncertainties of medical malpractice cases. As noted, there appeared a deviation from the usual standard of care, particularly the failure to follow up on the serum hCG level. The weakness in the medical record, failing to note the possibility of ectopic pregnancy, also was probably an error but, apparently, the court felt that this did not result in any harm to the patient.

The question arises of how there would be a defense verdict in light of the failure to track consecutive serum hCG levels. A speculative explanation is that there are many uncertainties in most lawsuits. Procedural problems may result in a case being limited, expert witnesses are essential to both the plaintiff and defense, with the quality of their review and testimony possibly uneven. Judges and juries may rely on one expert witness rather than another, juries vary, and the quality of advocacy differs. Any of these situations can contribute to the unpredictability of the outcome of a case. In the case above, the liability was somewhat uncertain, and the various other factors tipped in favor of a defense verdict. ●

While 2020 was a challenge to say the least, obstetrician-gynecologists remained on the frontline caring for women through it all. Life continued despite the COVID-19 pandemic: prenatal care was delivered, albeit at times in different ways; babies were born; and our role in improving outcomes for women and their children became even more important. This year’s Update focuses on clinical guidelines centered on safety and optimal outcomes for women and children.

ACOG and SMFM update guidance on FGR management

American College of Obstetricians and Gynecologists. Practice advisory: Updated guidance regarding fetal growth restriction. September 2020. https://www.acog.org/clinical/clinical-guidance/practice-advisory/articles/2020/09/updated-guidance-regarding-fetal-growth-restriction. Accessed December 18, 2020.

Fetal growth restriction (FGR) affects up to 10% of pregnancies and is a leading cause of infant morbidity and mortality. Suboptimal fetal growth can have lasting negative effects on development into early childhood and, some hypothesize, even into adulthood.^1,2 Antenatal detection of fetuses with FGR is critical so that antenatal testing can be implemented in an attempt to deliver improved clinical outcomes. FGR is defined by several different diagnostic criteria, and many studies have been conducted to determine how best to diagnose this condition.

In September 2020, the American College of Obstetricians and Gynecologists (ACOG) released a Practice Advisory regarding guidance on FGR in an effort to align the ACOG Practice Bulletin No. 204, ACOG Committee Opinion No. 764, and SMFM (Society for Maternal-Fetal Medicine) Consult Series No. 52.^3-5 This guidance updates and replaces prior guidelines, with an emphasis on 3 notable changes.

FGR definition, workup have changed

While the original definition of FGR was an estimated fetal weight (EFW) of less than the 10th percentile for gestational age, a similar level of accuracy in prediction of subsequent small for gestational age (SGA) at birth has been shown when this or an abdominal circumference (AC) of less than the 10th percentile is used. Based on these findings, SMFM now recommends that FGR be defined as an EFW or AC of less than the 10th percentile for gestational age.

Recent studies have done head-to-head comparisons of different methods of estimating fetal weight to determine the best detection and pregnancy outcome improvement in FGR. In all instances, the Hadlock formula has continued to more accurately estimate fetal weight, prediction of SGA, and composite neonatal morbidity. As such, new guidelines recommend that population-based fetal growth references (that is, the Hadlock formula) should be used to determine ultrasonography-derived fetal weight percentiles.

The new guidance also suggests classification of FGR based on gestational age at onset, with early FGR at less than 32 weeks and late FGR at 32 or more weeks. The definition of severe FGR is reserved for fetuses with an EFW of less than the 3rd percentile. A diagnosis of FGR should prompt the recommendation for a detailed obstetric ultrasonography. Diagnostic genetic testing should be offered in cases of early-onset FGR, concomitant sonographic abnormalities, and/or polyhydramnios. Routine serum screening for toxoplasmosis, rubella, herpes, or cytomegalovirus (CMV) should not be done unless there are risk factors for infection. If amniocentesis is performed for genetic diagnostic testing, consideration can be made for polymerase chain reaction for CMV in the amniotic fluid.

Continue to: Timing of delivery in isolated FGR...

Timing of delivery in isolated FGR

A complicating factor in diagnosing FGR is distinguishing between the pathologically growth-restricted fetus and the constitutionally small fetus. Antenatal testing and serial umbilical artery Doppler assessment should be done following diagnosis of FGR to monitor for evidence of fetal compromise until delivery is planned.

The current ACOG Practice Bulletin No. 204 and Committee Opinion No. 764 recommend delivery between 38 0/7 and 39 6/7 weeks in the setting of isolated FGR with reassuring fetal testing and umbilical artery Doppler assessment.To further refine this, the new recommendations use the growth percentiles. In cases of isolated FGR with EFW between the 3rd and 10th percentile in the setting of normal umbilical artery Doppler, delivery is recommended between 38 and 39 weeks’ gestation. In cases of isolated FGR with EFW of less than the 3rd percentile (severe FGR) in the setting of normal umbilical artery Doppler, delivery is recommended at 37 weeks.

Timing of delivery in complicated FGR

A normal umbilical artery Doppler reflects the low impedance that is necessary for continuous forward flow of blood to the fetus. Abnormal umbilical artery Doppler signifies aberrations of this low-pressure system that affect the amount of continuous forward flow during diastole of the cardiac cycle. With continued compromise, there is progression to absent end-diastolic velocity (AEDV) and, most concerning, reversed end-diastolic velocity (REDV).

Serial umbilical artery Doppler assessment should be done following diagnosis of FGR to monitor for progression that is associated with perinatal mortality, since intervention can be initiated in the form of delivery. Delivery at 37 weeks is recommended for FGR with elevated umbilical artery Doppler of greater than the 95th percentile for gestational age. For FGR with AEDV, delivery is recommended between 33 and 34 weeks of gestation and for FGR with REDV between 30 and 32 weeks, as the neonatal morbidity and mortality associated with continuing the pregnancy outweighs the risks of prematurity in this setting. Because of the abnormal placental-fetal circulation in FGR complicated by AEDV/REDV, there may be a higher likelihood of fetal intolerance of labor and cesarean delivery (CD) may be considered.

Continue to: New recommendations for PROM management...

New recommendations for PROM management

American College of Obstetricians and Gynecologists Committee on Practice Bulletins–Obstetrics. ACOG practice bulletin no. 217: Prelabor rupture of membranes. Obstet Gynecol. 2020;135:e80-e97.

Rupture of membranes prior to the onset of labor occurs at term in 8% of pregnancies and in the preterm period in 2% to 3% of pregnancies.⁶ Accurate diagnosis, gestational age, evidence of infection, and discussion of the risks and benefits to the mother and fetus/neonate are necessary to optimize outcomes. In the absence of other indications for delivery, a gestational age of 34 or more weeks traditionally has been the cutoff to proceed with delivery, although this has not been globally agreed on and/or practiced.

ACOG has published a comprehensive update that incorporates the results of the PPROMT trial and other recommendations for the diagnosis and management of both term and preterm prelabor rupture of membranes (PROM).^6,7

Making the diagnosis

Diagnosis of PROM usually can be made clinically via history and the classic triad of physical exam findings—pooling of fluid, basic pH, and ferning; some institutions also use commercially available tests that detect placental-derived proteins. Both ACOG and the US Food and Drug Administration caution against using these tests alone without clinical evaluation due to concern for false-positives and false-negatives that lead to adverse maternal and fetal/neonatal outcomes. For equivocal cases, ultrasonography for amniotic fluid evaluation and ultrasonography-guided dye tests can be used to assist in accurate diagnosis, especially in the preterm period in which there are significant implications for pregnancy management.

PROM management depends on gestational age

All management recommendations require reassuring fetal testing, evaluation for infection, and no other contraindications to expectant management. Once these are established, the most important determinant of PROM management then becomes gestational age.

Previable PROM

Previable PROM (usually defined as less than 23–24 weeks) has high risks of both maternal and fetal/neonatal morbidity and mortality from infection, hemorrhage, pulmonary hypoplasia, and extreme prematurity. These very difficult cases benefit from a multidisciplinary approach to patient counseling regarding expectant management versus immediate delivery.

If expectant management is chosen, outpatient management with close monitoring for signs of maternal infection may be done until an agreed on gestational age of viability. Then inpatient management with fetal monitoring, corticosteroids, tocolysis, magnesium for neuroprotection, and group B streptococcus (GBS) prophylaxis may be considered as appropriate.

Preterm PROM at less than 34 weeks

If the mother and fetus are otherwise stable, PROM at less than 34 weeks warrants inpatient expectant management with close maternal and fetal monitoring for signs of infection and labor. Management includes latency antibiotics, antenatal corticosteroids, magnesium for neuroprotection if less than 32 weeks’ gestation and at risk for imminent delivery, and GBS prophylaxis. While tocolysis may increase latency and help with steroid course completion, it should be used cautiously and avoided in cases of abruption or chorioamnionitis. Although there is no definitive recommendation published, a rescue course of steroids may be considered as appropriate but should not delay an indicated delivery.

Continue to: Late preterm PROM...

Late preterm PROM

The biggest change to clinical management in this ACOG Practice Bulletin is for late preterm (34–36 6/7 weeks) PROM, with the recommendation for either immediate delivery or expectant management up to 37 weeks stemming from the PPROMPT study by Morris and colleagues.⁷

From the neonatal perspective, no difference has been demonstrated between immediate delivery and expectant management for neonatal sepsis or a composite neonatal morbidity and mortality. Expectant management may be preferred from the neonatal point of view as immediate delivery was associated with an increased rate of neonatal respiratory distress, mechanical ventilation, and length of stay in the neonatal intensive care unit. The potential for long-term neurodevelopmental outcomes of delivery at 34 versus 37 weeks also should be considered.

From the maternal perspective, expectant management has an increased risk of antepartum and postpartum hemorrhage, fever, antibiotic use, and maternal length of stay, but a decreased risk of CD.

A late preterm steroid course can be considered if delivery is planned in no less than 24 hours and likely to occur in the next 7 days and if the patient has not already received a course of steroids. A rescue course of steroids is not indicated if the patient received a steroid course prior in the pregnancy. While appropriate GBS prophylaxis is recommended, latency antibiotics and tocolysis are not, and delivery should not be delayed if chorioamnionitis is diagnosed.

Ultimately, preterm PROM management with a stable mother and fetus at or beyond 34 weeks requires comprehensive counseling of the risks and benefits for both mother and fetus/neonate. A multidisciplinary team that together counsels the patient also may help with this shared decision making.

Term PROM

For patients with term PROM, delivery is recommended. Although a short period of expectant management for 12 to 24 hours is reported as “reasonable,” the risk of infection increases with the length of rupture of membranes. Therefore, induction of labor or CD soon after rupture of membranes is recommended for patients who are GBS positive and is preferred for all others.

VTE prophylaxis in pregnancy: Regimen adjustments, CD strategies, and COVID-19 considerations

Birsner ML, Turrentine M, Pettker CM, et al. ACOG practice advisory: Options for peripartum anticoagulation in areas affected by shortage of unfractionated heparin. March 2020. https://www.acog.org/clinical/clinical-guidance/practice-advisory/articles/2020/03/options-for-peripartum-anticoagulation-in-areas-affected-by-shortage-of-unfractionated-heparin. Accessed December 8, 2020.

Pacheco LD, Saade G, Metz TD. Society for Maternal-Fetal Medicine Consult Series No. 51: Thromboembolism prophylaxis for cesarean delivery. Am J Obstet Gynecol. 2020;223:B11-B17

Venous thromboembolism (VTE) prophylaxis is a timely topic for a number of reasons. First, a shortage of unfractionated heparin prompted an ACOG Practice Advisory, endorsed by SMFM and the Society for Obstetric Anesthesia and Perinatology, regarding use of low molecular weight heparin (LMWH) in the peripartum period.⁸ In addition, SMFM released updated recommendations for VTE prophylaxis for CD as part of the SMFM Consult Series.⁹ Finally, there is evidence that COVID-19 infection may increase the risk of coagulopathy, leading to consideration of additional VTE prophylaxis for pregnant and postpartum women with COVID-19.

Candidates for prophylaxis

As recommended by the ACOG Practice Bulletin on thromboembolism in pregnancy, women who may require VTE prophylaxis during pregnancy and/or the postpartum period include those with¹⁰:

• VTE diagnosed during pregnancy
• a history of VTE, including during pregnancy or with use of hormonal contraception
• a history of thrombophilia with or without a personal or family history of VTE.

For these patients, LMWH has many advantages over unfractionated heparin, including ease of use and reliability of dosing. It generally is preferred in pregnancy and postpartum (for both prophylactic and therapeutic anticoagulation) by patients and providers.

The Practice Bulletin references a strategy that describes converting LMWH to unfractionated heparin at around 36 weeks’ gestation in preparation for delivery because unfractionated heparin has the advantage of a shorter half-life and the option for anticoagulation reversal with protamine sulfate. In the Practice Advisory, a global shortage of unfractionated heparin and an argument that the above conversion was less about concern for maternal hemorrhage and more about avoiding spinal and epidural hematomas led to the following recommendations for continued use of LMWH through delivery:

• LMWH heparin can be discontinued in a planned fashion prior to scheduled induction of labor or CD (generally 12 hours for prophylactic dosing and 24 hours for intermediate dosing).
• Patients in spontaneous labor may receive neuraxial anesthesia 12 hours after the last prophylactic dose and 24 hours after the last intermediate dose of LMWH.
• Patients who require anticoagulation during pregnancy should be counseled that if they have vaginal bleeding, leakage of fluid, or regular contractions they should be evaluated prior to taking their next dose of anticoagulant.
• In the absence of other complications, delivery should not be before 39 weeks for the indication of anticoagulation requirement alone.

Continue to: Managing VTE risk in CD...

Managing VTE risk in CD

Recognizing that VTE is a major cause of maternal morbidity and mortality, as well as the variety of the published guidelines for VTE prophylaxis after CD, the SMFM Consult Series provides recommendations to assist clinicians caring for postpartum women after CD. As reviewed in the ACOG Practice Bulletin, there are good data to support pharmacologic prophylaxis during pregnancy and the postpartum period for women with a history of VTE or a thrombophilia. Solid evidence is lacking, however, for what to do for women who have a CD without this history but may have other potential risk factors for VTE, such as obesity, preeclampsia, and transfusion requirement. Universal pharmacologic prophylaxis also is not yet supported by evidence. SMFM supports LMWH as the preferred medication in pregnancy and postpartum and provides these additional recommendations:

• All women who have a CD should have sequential compression devices (SCDs) placed prior to surgery and continued until they are ambulatory.
• Women with a history of VTE or thrombophilia without history of VTE should have SCDs and pharmacologic VTE prophylaxis for 6 weeks postpartum.
• Intermediate dosing of LMWH is recommended for patients with class III obesity.
• Institutions should develop patient safety bundles for VTE prophylaxis to identify additional risk factors that may warrant pharmacologic prophylaxis after CD in select patients.

Our approach to patients with COVID-19 infection

At our institution, we recently incorporated a VTE prophylaxis protocol into our electronic medical record that provides risk stratification for each patient. In addition to the above recommendations, our patients may qualify for short-term in-house or longer postpartum prophylaxis depending on risk factors.

A new risk factor in recent months is COVID-19 infection, which appears to increase the risk of coagulopathy, especially in patients with disease severe enough to warrant hospitalization. Given the potential for additive risk in pregnancy, in consult with our medicine colleagues, we have placed some of our more ill hospitalized pregnant patients on a course of prophylactic LMWH both in the hospital and after discharge independent of delivery status or mode of delivery. ●

While 2020 was a challenge to say the least, obstetrician-gynecologists remained on the frontline caring for women through it all. Life continued despite the COVID-19 pandemic: prenatal care was delivered, albeit at times in different ways; babies were born; and our role in improving outcomes for women and their children became even more important. This year’s Update focuses on clinical guidelines centered on safety and optimal outcomes for women and children.

ACOG and SMFM update guidance on FGR management

American College of Obstetricians and Gynecologists. Practice advisory: Updated guidance regarding fetal growth restriction. September 2020. https://www.acog.org/clinical/clinical-guidance/practice-advisory/articles/2020/09/updated-guidance-regarding-fetal-growth-restriction. Accessed December 18, 2020.

Fetal growth restriction (FGR) affects up to 10% of pregnancies and is a leading cause of infant morbidity and mortality. Suboptimal fetal growth can have lasting negative effects on development into early childhood and, some hypothesize, even into adulthood.^1,2 Antenatal detection of fetuses with FGR is critical so that antenatal testing can be implemented in an attempt to deliver improved clinical outcomes. FGR is defined by several different diagnostic criteria, and many studies have been conducted to determine how best to diagnose this condition.

In September 2020, the American College of Obstetricians and Gynecologists (ACOG) released a Practice Advisory regarding guidance on FGR in an effort to align the ACOG Practice Bulletin No. 204, ACOG Committee Opinion No. 764, and SMFM (Society for Maternal-Fetal Medicine) Consult Series No. 52.^3-5 This guidance updates and replaces prior guidelines, with an emphasis on 3 notable changes.

FGR definition, workup have changed

While the original definition of FGR was an estimated fetal weight (EFW) of less than the 10th percentile for gestational age, a similar level of accuracy in prediction of subsequent small for gestational age (SGA) at birth has been shown when this or an abdominal circumference (AC) of less than the 10th percentile is used. Based on these findings, SMFM now recommends that FGR be defined as an EFW or AC of less than the 10th percentile for gestational age.

Recent studies have done head-to-head comparisons of different methods of estimating fetal weight to determine the best detection and pregnancy outcome improvement in FGR. In all instances, the Hadlock formula has continued to more accurately estimate fetal weight, prediction of SGA, and composite neonatal morbidity. As such, new guidelines recommend that population-based fetal growth references (that is, the Hadlock formula) should be used to determine ultrasonography-derived fetal weight percentiles.

The new guidance also suggests classification of FGR based on gestational age at onset, with early FGR at less than 32 weeks and late FGR at 32 or more weeks. The definition of severe FGR is reserved for fetuses with an EFW of less than the 3rd percentile. A diagnosis of FGR should prompt the recommendation for a detailed obstetric ultrasonography. Diagnostic genetic testing should be offered in cases of early-onset FGR, concomitant sonographic abnormalities, and/or polyhydramnios. Routine serum screening for toxoplasmosis, rubella, herpes, or cytomegalovirus (CMV) should not be done unless there are risk factors for infection. If amniocentesis is performed for genetic diagnostic testing, consideration can be made for polymerase chain reaction for CMV in the amniotic fluid.

Continue to: Timing of delivery in isolated FGR...

Timing of delivery in isolated FGR

A complicating factor in diagnosing FGR is distinguishing between the pathologically growth-restricted fetus and the constitutionally small fetus. Antenatal testing and serial umbilical artery Doppler assessment should be done following diagnosis of FGR to monitor for evidence of fetal compromise until delivery is planned.

The current ACOG Practice Bulletin No. 204 and Committee Opinion No. 764 recommend delivery between 38 0/7 and 39 6/7 weeks in the setting of isolated FGR with reassuring fetal testing and umbilical artery Doppler assessment.To further refine this, the new recommendations use the growth percentiles. In cases of isolated FGR with EFW between the 3rd and 10th percentile in the setting of normal umbilical artery Doppler, delivery is recommended between 38 and 39 weeks’ gestation. In cases of isolated FGR with EFW of less than the 3rd percentile (severe FGR) in the setting of normal umbilical artery Doppler, delivery is recommended at 37 weeks.

Timing of delivery in complicated FGR

A normal umbilical artery Doppler reflects the low impedance that is necessary for continuous forward flow of blood to the fetus. Abnormal umbilical artery Doppler signifies aberrations of this low-pressure system that affect the amount of continuous forward flow during diastole of the cardiac cycle. With continued compromise, there is progression to absent end-diastolic velocity (AEDV) and, most concerning, reversed end-diastolic velocity (REDV).

Serial umbilical artery Doppler assessment should be done following diagnosis of FGR to monitor for progression that is associated with perinatal mortality, since intervention can be initiated in the form of delivery. Delivery at 37 weeks is recommended for FGR with elevated umbilical artery Doppler of greater than the 95th percentile for gestational age. For FGR with AEDV, delivery is recommended between 33 and 34 weeks of gestation and for FGR with REDV between 30 and 32 weeks, as the neonatal morbidity and mortality associated with continuing the pregnancy outweighs the risks of prematurity in this setting. Because of the abnormal placental-fetal circulation in FGR complicated by AEDV/REDV, there may be a higher likelihood of fetal intolerance of labor and cesarean delivery (CD) may be considered.

Continue to: New recommendations for PROM management...

New recommendations for PROM management

American College of Obstetricians and Gynecologists Committee on Practice Bulletins–Obstetrics. ACOG practice bulletin no. 217: Prelabor rupture of membranes. Obstet Gynecol. 2020;135:e80-e97.

Rupture of membranes prior to the onset of labor occurs at term in 8% of pregnancies and in the preterm period in 2% to 3% of pregnancies.⁶ Accurate diagnosis, gestational age, evidence of infection, and discussion of the risks and benefits to the mother and fetus/neonate are necessary to optimize outcomes. In the absence of other indications for delivery, a gestational age of 34 or more weeks traditionally has been the cutoff to proceed with delivery, although this has not been globally agreed on and/or practiced.

ACOG has published a comprehensive update that incorporates the results of the PPROMT trial and other recommendations for the diagnosis and management of both term and preterm prelabor rupture of membranes (PROM).^6,7

Making the diagnosis

Diagnosis of PROM usually can be made clinically via history and the classic triad of physical exam findings—pooling of fluid, basic pH, and ferning; some institutions also use commercially available tests that detect placental-derived proteins. Both ACOG and the US Food and Drug Administration caution against using these tests alone without clinical evaluation due to concern for false-positives and false-negatives that lead to adverse maternal and fetal/neonatal outcomes. For equivocal cases, ultrasonography for amniotic fluid evaluation and ultrasonography-guided dye tests can be used to assist in accurate diagnosis, especially in the preterm period in which there are significant implications for pregnancy management.

PROM management depends on gestational age

All management recommendations require reassuring fetal testing, evaluation for infection, and no other contraindications to expectant management. Once these are established, the most important determinant of PROM management then becomes gestational age.

Previable PROM

Previable PROM (usually defined as less than 23–24 weeks) has high risks of both maternal and fetal/neonatal morbidity and mortality from infection, hemorrhage, pulmonary hypoplasia, and extreme prematurity. These very difficult cases benefit from a multidisciplinary approach to patient counseling regarding expectant management versus immediate delivery.

If expectant management is chosen, outpatient management with close monitoring for signs of maternal infection may be done until an agreed on gestational age of viability. Then inpatient management with fetal monitoring, corticosteroids, tocolysis, magnesium for neuroprotection, and group B streptococcus (GBS) prophylaxis may be considered as appropriate.

Preterm PROM at less than 34 weeks

If the mother and fetus are otherwise stable, PROM at less than 34 weeks warrants inpatient expectant management with close maternal and fetal monitoring for signs of infection and labor. Management includes latency antibiotics, antenatal corticosteroids, magnesium for neuroprotection if less than 32 weeks’ gestation and at risk for imminent delivery, and GBS prophylaxis. While tocolysis may increase latency and help with steroid course completion, it should be used cautiously and avoided in cases of abruption or chorioamnionitis. Although there is no definitive recommendation published, a rescue course of steroids may be considered as appropriate but should not delay an indicated delivery.

Continue to: Late preterm PROM...

Late preterm PROM

The biggest change to clinical management in this ACOG Practice Bulletin is for late preterm (34–36 6/7 weeks) PROM, with the recommendation for either immediate delivery or expectant management up to 37 weeks stemming from the PPROMPT study by Morris and colleagues.⁷

From the neonatal perspective, no difference has been demonstrated between immediate delivery and expectant management for neonatal sepsis or a composite neonatal morbidity and mortality. Expectant management may be preferred from the neonatal point of view as immediate delivery was associated with an increased rate of neonatal respiratory distress, mechanical ventilation, and length of stay in the neonatal intensive care unit. The potential for long-term neurodevelopmental outcomes of delivery at 34 versus 37 weeks also should be considered.

From the maternal perspective, expectant management has an increased risk of antepartum and postpartum hemorrhage, fever, antibiotic use, and maternal length of stay, but a decreased risk of CD.

A late preterm steroid course can be considered if delivery is planned in no less than 24 hours and likely to occur in the next 7 days and if the patient has not already received a course of steroids. A rescue course of steroids is not indicated if the patient received a steroid course prior in the pregnancy. While appropriate GBS prophylaxis is recommended, latency antibiotics and tocolysis are not, and delivery should not be delayed if chorioamnionitis is diagnosed.

Ultimately, preterm PROM management with a stable mother and fetus at or beyond 34 weeks requires comprehensive counseling of the risks and benefits for both mother and fetus/neonate. A multidisciplinary team that together counsels the patient also may help with this shared decision making.

Term PROM

For patients with term PROM, delivery is recommended. Although a short period of expectant management for 12 to 24 hours is reported as “reasonable,” the risk of infection increases with the length of rupture of membranes. Therefore, induction of labor or CD soon after rupture of membranes is recommended for patients who are GBS positive and is preferred for all others.

VTE prophylaxis in pregnancy: Regimen adjustments, CD strategies, and COVID-19 considerations

Birsner ML, Turrentine M, Pettker CM, et al. ACOG practice advisory: Options for peripartum anticoagulation in areas affected by shortage of unfractionated heparin. March 2020. https://www.acog.org/clinical/clinical-guidance/practice-advisory/articles/2020/03/options-for-peripartum-anticoagulation-in-areas-affected-by-shortage-of-unfractionated-heparin. Accessed December 8, 2020.

Pacheco LD, Saade G, Metz TD. Society for Maternal-Fetal Medicine Consult Series No. 51: Thromboembolism prophylaxis for cesarean delivery. Am J Obstet Gynecol. 2020;223:B11-B17

Venous thromboembolism (VTE) prophylaxis is a timely topic for a number of reasons. First, a shortage of unfractionated heparin prompted an ACOG Practice Advisory, endorsed by SMFM and the Society for Obstetric Anesthesia and Perinatology, regarding use of low molecular weight heparin (LMWH) in the peripartum period.⁸ In addition, SMFM released updated recommendations for VTE prophylaxis for CD as part of the SMFM Consult Series.⁹ Finally, there is evidence that COVID-19 infection may increase the risk of coagulopathy, leading to consideration of additional VTE prophylaxis for pregnant and postpartum women with COVID-19.

Candidates for prophylaxis

As recommended by the ACOG Practice Bulletin on thromboembolism in pregnancy, women who may require VTE prophylaxis during pregnancy and/or the postpartum period include those with¹⁰:

• VTE diagnosed during pregnancy
• a history of VTE, including during pregnancy or with use of hormonal contraception
• a history of thrombophilia with or without a personal or family history of VTE.

For these patients, LMWH has many advantages over unfractionated heparin, including ease of use and reliability of dosing. It generally is preferred in pregnancy and postpartum (for both prophylactic and therapeutic anticoagulation) by patients and providers.

The Practice Bulletin references a strategy that describes converting LMWH to unfractionated heparin at around 36 weeks’ gestation in preparation for delivery because unfractionated heparin has the advantage of a shorter half-life and the option for anticoagulation reversal with protamine sulfate. In the Practice Advisory, a global shortage of unfractionated heparin and an argument that the above conversion was less about concern for maternal hemorrhage and more about avoiding spinal and epidural hematomas led to the following recommendations for continued use of LMWH through delivery:

• LMWH heparin can be discontinued in a planned fashion prior to scheduled induction of labor or CD (generally 12 hours for prophylactic dosing and 24 hours for intermediate dosing).
• Patients in spontaneous labor may receive neuraxial anesthesia 12 hours after the last prophylactic dose and 24 hours after the last intermediate dose of LMWH.
• Patients who require anticoagulation during pregnancy should be counseled that if they have vaginal bleeding, leakage of fluid, or regular contractions they should be evaluated prior to taking their next dose of anticoagulant.
• In the absence of other complications, delivery should not be before 39 weeks for the indication of anticoagulation requirement alone.

Continue to: Managing VTE risk in CD...

Managing VTE risk in CD

Recognizing that VTE is a major cause of maternal morbidity and mortality, as well as the variety of the published guidelines for VTE prophylaxis after CD, the SMFM Consult Series provides recommendations to assist clinicians caring for postpartum women after CD. As reviewed in the ACOG Practice Bulletin, there are good data to support pharmacologic prophylaxis during pregnancy and the postpartum period for women with a history of VTE or a thrombophilia. Solid evidence is lacking, however, for what to do for women who have a CD without this history but may have other potential risk factors for VTE, such as obesity, preeclampsia, and transfusion requirement. Universal pharmacologic prophylaxis also is not yet supported by evidence. SMFM supports LMWH as the preferred medication in pregnancy and postpartum and provides these additional recommendations:

• All women who have a CD should have sequential compression devices (SCDs) placed prior to surgery and continued until they are ambulatory.
• Women with a history of VTE or thrombophilia without history of VTE should have SCDs and pharmacologic VTE prophylaxis for 6 weeks postpartum.
• Intermediate dosing of LMWH is recommended for patients with class III obesity.
• Institutions should develop patient safety bundles for VTE prophylaxis to identify additional risk factors that may warrant pharmacologic prophylaxis after CD in select patients.

Our approach to patients with COVID-19 infection

At our institution, we recently incorporated a VTE prophylaxis protocol into our electronic medical record that provides risk stratification for each patient. In addition to the above recommendations, our patients may qualify for short-term in-house or longer postpartum prophylaxis depending on risk factors.

A new risk factor in recent months is COVID-19 infection, which appears to increase the risk of coagulopathy, especially in patients with disease severe enough to warrant hospitalization. Given the potential for additive risk in pregnancy, in consult with our medicine colleagues, we have placed some of our more ill hospitalized pregnant patients on a course of prophylactic LMWH both in the hospital and after discharge independent of delivery status or mode of delivery. ●

While 2020 was a challenge to say the least, obstetrician-gynecologists remained on the frontline caring for women through it all. Life continued despite the COVID-19 pandemic: prenatal care was delivered, albeit at times in different ways; babies were born; and our role in improving outcomes for women and their children became even more important. This year’s Update focuses on clinical guidelines centered on safety and optimal outcomes for women and children.

ACOG and SMFM update guidance on FGR management

American College of Obstetricians and Gynecologists. Practice advisory: Updated guidance regarding fetal growth restriction. September 2020. https://www.acog.org/clinical/clinical-guidance/practice-advisory/articles/2020/09/updated-guidance-regarding-fetal-growth-restriction. Accessed December 18, 2020.

Fetal growth restriction (FGR) affects up to 10% of pregnancies and is a leading cause of infant morbidity and mortality. Suboptimal fetal growth can have lasting negative effects on development into early childhood and, some hypothesize, even into adulthood.^1,2 Antenatal detection of fetuses with FGR is critical so that antenatal testing can be implemented in an attempt to deliver improved clinical outcomes. FGR is defined by several different diagnostic criteria, and many studies have been conducted to determine how best to diagnose this condition.

In September 2020, the American College of Obstetricians and Gynecologists (ACOG) released a Practice Advisory regarding guidance on FGR in an effort to align the ACOG Practice Bulletin No. 204, ACOG Committee Opinion No. 764, and SMFM (Society for Maternal-Fetal Medicine) Consult Series No. 52.^3-5 This guidance updates and replaces prior guidelines, with an emphasis on 3 notable changes.

FGR definition, workup have changed

While the original definition of FGR was an estimated fetal weight (EFW) of less than the 10th percentile for gestational age, a similar level of accuracy in prediction of subsequent small for gestational age (SGA) at birth has been shown when this or an abdominal circumference (AC) of less than the 10th percentile is used. Based on these findings, SMFM now recommends that FGR be defined as an EFW or AC of less than the 10th percentile for gestational age.

Recent studies have done head-to-head comparisons of different methods of estimating fetal weight to determine the best detection and pregnancy outcome improvement in FGR. In all instances, the Hadlock formula has continued to more accurately estimate fetal weight, prediction of SGA, and composite neonatal morbidity. As such, new guidelines recommend that population-based fetal growth references (that is, the Hadlock formula) should be used to determine ultrasonography-derived fetal weight percentiles.

The new guidance also suggests classification of FGR based on gestational age at onset, with early FGR at less than 32 weeks and late FGR at 32 or more weeks. The definition of severe FGR is reserved for fetuses with an EFW of less than the 3rd percentile. A diagnosis of FGR should prompt the recommendation for a detailed obstetric ultrasonography. Diagnostic genetic testing should be offered in cases of early-onset FGR, concomitant sonographic abnormalities, and/or polyhydramnios. Routine serum screening for toxoplasmosis, rubella, herpes, or cytomegalovirus (CMV) should not be done unless there are risk factors for infection. If amniocentesis is performed for genetic diagnostic testing, consideration can be made for polymerase chain reaction for CMV in the amniotic fluid.

Continue to: Timing of delivery in isolated FGR...

Timing of delivery in isolated FGR

A complicating factor in diagnosing FGR is distinguishing between the pathologically growth-restricted fetus and the constitutionally small fetus. Antenatal testing and serial umbilical artery Doppler assessment should be done following diagnosis of FGR to monitor for evidence of fetal compromise until delivery is planned.

The current ACOG Practice Bulletin No. 204 and Committee Opinion No. 764 recommend delivery between 38 0/7 and 39 6/7 weeks in the setting of isolated FGR with reassuring fetal testing and umbilical artery Doppler assessment.To further refine this, the new recommendations use the growth percentiles. In cases of isolated FGR with EFW between the 3rd and 10th percentile in the setting of normal umbilical artery Doppler, delivery is recommended between 38 and 39 weeks’ gestation. In cases of isolated FGR with EFW of less than the 3rd percentile (severe FGR) in the setting of normal umbilical artery Doppler, delivery is recommended at 37 weeks.

Timing of delivery in complicated FGR

A normal umbilical artery Doppler reflects the low impedance that is necessary for continuous forward flow of blood to the fetus. Abnormal umbilical artery Doppler signifies aberrations of this low-pressure system that affect the amount of continuous forward flow during diastole of the cardiac cycle. With continued compromise, there is progression to absent end-diastolic velocity (AEDV) and, most concerning, reversed end-diastolic velocity (REDV).

Serial umbilical artery Doppler assessment should be done following diagnosis of FGR to monitor for progression that is associated with perinatal mortality, since intervention can be initiated in the form of delivery. Delivery at 37 weeks is recommended for FGR with elevated umbilical artery Doppler of greater than the 95th percentile for gestational age. For FGR with AEDV, delivery is recommended between 33 and 34 weeks of gestation and for FGR with REDV between 30 and 32 weeks, as the neonatal morbidity and mortality associated with continuing the pregnancy outweighs the risks of prematurity in this setting. Because of the abnormal placental-fetal circulation in FGR complicated by AEDV/REDV, there may be a higher likelihood of fetal intolerance of labor and cesarean delivery (CD) may be considered.

Continue to: New recommendations for PROM management...

New recommendations for PROM management

American College of Obstetricians and Gynecologists Committee on Practice Bulletins–Obstetrics. ACOG practice bulletin no. 217: Prelabor rupture of membranes. Obstet Gynecol. 2020;135:e80-e97.

Rupture of membranes prior to the onset of labor occurs at term in 8% of pregnancies and in the preterm period in 2% to 3% of pregnancies.⁶ Accurate diagnosis, gestational age, evidence of infection, and discussion of the risks and benefits to the mother and fetus/neonate are necessary to optimize outcomes. In the absence of other indications for delivery, a gestational age of 34 or more weeks traditionally has been the cutoff to proceed with delivery, although this has not been globally agreed on and/or practiced.

ACOG has published a comprehensive update that incorporates the results of the PPROMT trial and other recommendations for the diagnosis and management of both term and preterm prelabor rupture of membranes (PROM).^6,7

Making the diagnosis

Diagnosis of PROM usually can be made clinically via history and the classic triad of physical exam findings—pooling of fluid, basic pH, and ferning; some institutions also use commercially available tests that detect placental-derived proteins. Both ACOG and the US Food and Drug Administration caution against using these tests alone without clinical evaluation due to concern for false-positives and false-negatives that lead to adverse maternal and fetal/neonatal outcomes. For equivocal cases, ultrasonography for amniotic fluid evaluation and ultrasonography-guided dye tests can be used to assist in accurate diagnosis, especially in the preterm period in which there are significant implications for pregnancy management.

PROM management depends on gestational age

All management recommendations require reassuring fetal testing, evaluation for infection, and no other contraindications to expectant management. Once these are established, the most important determinant of PROM management then becomes gestational age.

Previable PROM

Previable PROM (usually defined as less than 23–24 weeks) has high risks of both maternal and fetal/neonatal morbidity and mortality from infection, hemorrhage, pulmonary hypoplasia, and extreme prematurity. These very difficult cases benefit from a multidisciplinary approach to patient counseling regarding expectant management versus immediate delivery.

If expectant management is chosen, outpatient management with close monitoring for signs of maternal infection may be done until an agreed on gestational age of viability. Then inpatient management with fetal monitoring, corticosteroids, tocolysis, magnesium for neuroprotection, and group B streptococcus (GBS) prophylaxis may be considered as appropriate.

Preterm PROM at less than 34 weeks

If the mother and fetus are otherwise stable, PROM at less than 34 weeks warrants inpatient expectant management with close maternal and fetal monitoring for signs of infection and labor. Management includes latency antibiotics, antenatal corticosteroids, magnesium for neuroprotection if less than 32 weeks’ gestation and at risk for imminent delivery, and GBS prophylaxis. While tocolysis may increase latency and help with steroid course completion, it should be used cautiously and avoided in cases of abruption or chorioamnionitis. Although there is no definitive recommendation published, a rescue course of steroids may be considered as appropriate but should not delay an indicated delivery.

Continue to: Late preterm PROM...

Late preterm PROM

The biggest change to clinical management in this ACOG Practice Bulletin is for late preterm (34–36 6/7 weeks) PROM, with the recommendation for either immediate delivery or expectant management up to 37 weeks stemming from the PPROMPT study by Morris and colleagues.⁷

From the neonatal perspective, no difference has been demonstrated between immediate delivery and expectant management for neonatal sepsis or a composite neonatal morbidity and mortality. Expectant management may be preferred from the neonatal point of view as immediate delivery was associated with an increased rate of neonatal respiratory distress, mechanical ventilation, and length of stay in the neonatal intensive care unit. The potential for long-term neurodevelopmental outcomes of delivery at 34 versus 37 weeks also should be considered.

From the maternal perspective, expectant management has an increased risk of antepartum and postpartum hemorrhage, fever, antibiotic use, and maternal length of stay, but a decreased risk of CD.

A late preterm steroid course can be considered if delivery is planned in no less than 24 hours and likely to occur in the next 7 days and if the patient has not already received a course of steroids. A rescue course of steroids is not indicated if the patient received a steroid course prior in the pregnancy. While appropriate GBS prophylaxis is recommended, latency antibiotics and tocolysis are not, and delivery should not be delayed if chorioamnionitis is diagnosed.

Ultimately, preterm PROM management with a stable mother and fetus at or beyond 34 weeks requires comprehensive counseling of the risks and benefits for both mother and fetus/neonate. A multidisciplinary team that together counsels the patient also may help with this shared decision making.

Term PROM

For patients with term PROM, delivery is recommended. Although a short period of expectant management for 12 to 24 hours is reported as “reasonable,” the risk of infection increases with the length of rupture of membranes. Therefore, induction of labor or CD soon after rupture of membranes is recommended for patients who are GBS positive and is preferred for all others.

VTE prophylaxis in pregnancy: Regimen adjustments, CD strategies, and COVID-19 considerations

Birsner ML, Turrentine M, Pettker CM, et al. ACOG practice advisory: Options for peripartum anticoagulation in areas affected by shortage of unfractionated heparin. March 2020. https://www.acog.org/clinical/clinical-guidance/practice-advisory/articles/2020/03/options-for-peripartum-anticoagulation-in-areas-affected-by-shortage-of-unfractionated-heparin. Accessed December 8, 2020.

Pacheco LD, Saade G, Metz TD. Society for Maternal-Fetal Medicine Consult Series No. 51: Thromboembolism prophylaxis for cesarean delivery. Am J Obstet Gynecol. 2020;223:B11-B17

Venous thromboembolism (VTE) prophylaxis is a timely topic for a number of reasons. First, a shortage of unfractionated heparin prompted an ACOG Practice Advisory, endorsed by SMFM and the Society for Obstetric Anesthesia and Perinatology, regarding use of low molecular weight heparin (LMWH) in the peripartum period.⁸ In addition, SMFM released updated recommendations for VTE prophylaxis for CD as part of the SMFM Consult Series.⁹ Finally, there is evidence that COVID-19 infection may increase the risk of coagulopathy, leading to consideration of additional VTE prophylaxis for pregnant and postpartum women with COVID-19.

Candidates for prophylaxis

As recommended by the ACOG Practice Bulletin on thromboembolism in pregnancy, women who may require VTE prophylaxis during pregnancy and/or the postpartum period include those with¹⁰:

• VTE diagnosed during pregnancy
• a history of VTE, including during pregnancy or with use of hormonal contraception
• a history of thrombophilia with or without a personal or family history of VTE.

For these patients, LMWH has many advantages over unfractionated heparin, including ease of use and reliability of dosing. It generally is preferred in pregnancy and postpartum (for both prophylactic and therapeutic anticoagulation) by patients and providers.

The Practice Bulletin references a strategy that describes converting LMWH to unfractionated heparin at around 36 weeks’ gestation in preparation for delivery because unfractionated heparin has the advantage of a shorter half-life and the option for anticoagulation reversal with protamine sulfate. In the Practice Advisory, a global shortage of unfractionated heparin and an argument that the above conversion was less about concern for maternal hemorrhage and more about avoiding spinal and epidural hematomas led to the following recommendations for continued use of LMWH through delivery:

• LMWH heparin can be discontinued in a planned fashion prior to scheduled induction of labor or CD (generally 12 hours for prophylactic dosing and 24 hours for intermediate dosing).
• Patients in spontaneous labor may receive neuraxial anesthesia 12 hours after the last prophylactic dose and 24 hours after the last intermediate dose of LMWH.
• Patients who require anticoagulation during pregnancy should be counseled that if they have vaginal bleeding, leakage of fluid, or regular contractions they should be evaluated prior to taking their next dose of anticoagulant.
• In the absence of other complications, delivery should not be before 39 weeks for the indication of anticoagulation requirement alone.

Continue to: Managing VTE risk in CD...

Managing VTE risk in CD

Recognizing that VTE is a major cause of maternal morbidity and mortality, as well as the variety of the published guidelines for VTE prophylaxis after CD, the SMFM Consult Series provides recommendations to assist clinicians caring for postpartum women after CD. As reviewed in the ACOG Practice Bulletin, there are good data to support pharmacologic prophylaxis during pregnancy and the postpartum period for women with a history of VTE or a thrombophilia. Solid evidence is lacking, however, for what to do for women who have a CD without this history but may have other potential risk factors for VTE, such as obesity, preeclampsia, and transfusion requirement. Universal pharmacologic prophylaxis also is not yet supported by evidence. SMFM supports LMWH as the preferred medication in pregnancy and postpartum and provides these additional recommendations:

• All women who have a CD should have sequential compression devices (SCDs) placed prior to surgery and continued until they are ambulatory.
• Women with a history of VTE or thrombophilia without history of VTE should have SCDs and pharmacologic VTE prophylaxis for 6 weeks postpartum.
• Intermediate dosing of LMWH is recommended for patients with class III obesity.
• Institutions should develop patient safety bundles for VTE prophylaxis to identify additional risk factors that may warrant pharmacologic prophylaxis after CD in select patients.

Our approach to patients with COVID-19 infection

At our institution, we recently incorporated a VTE prophylaxis protocol into our electronic medical record that provides risk stratification for each patient. In addition to the above recommendations, our patients may qualify for short-term in-house or longer postpartum prophylaxis depending on risk factors.

A new risk factor in recent months is COVID-19 infection, which appears to increase the risk of coagulopathy, especially in patients with disease severe enough to warrant hospitalization. Given the potential for additive risk in pregnancy, in consult with our medicine colleagues, we have placed some of our more ill hospitalized pregnant patients on a course of prophylactic LMWH both in the hospital and after discharge independent of delivery status or mode of delivery. ●

CASE Fetal anomalies detected on ultrasonography

A 34-year-old woman (G2P1) at 19 weeks’ gestation presented for fetal anatomy ultrasonography evaluation. Ultrasonography demonstrated fetal demise with fetal size less than dates, oligohydramnios, and what appeared to be a full-thickness herniation of the thoracic and abdominal contents. Due to the positioning of the fetus and the oligohydramnios, the fetus appeared to have ectopia cordis and herniated liver and bowel; the bladder was not visualized. The patient was counseled regarding the findings and the suspected diagnosis of pentalogy of Cantrell. After counseling, the patient expressed desire to bury the fetus intact according to her religious custom. She underwent a successful uterine evacuation with misoprostol administration and delivered a nonviable fetus that had a closed thoracic cage without ectopia cordis. Key findings were a very short 2-vessel umbilical cord without coiling that was tethered to the intra-abdominal organs, “pulling” the internal organs out of the abdomen, and lack of an anterior abdominal wall (FIGURE 1). Given these findings, a final diagnosis of body-stalk anomaly was made.

Fetal abdominal wall defects (AWDs) encompass a wide array of congenital defects, although they all involve herniation of 1 or more intra-abdominal content through a ventral abdominal defect.¹ Overall, the estimated incidence of AWDs is approximately 6 per 10,000 births.¹ Gastroschisis and omphalocele are the most common of these defect types.²

The majority of AWDs can be diagnosed during the first trimester of pregnancy via ultrasonography; however, during the first trimester the physiologic midgut herniation resolves by 12 weeks of gestation. It is therefore important to repeat imaging at a later gestational age to confirm the suspicion. Furthermore, the differential diagnosis should include the relatively benign condition of umbilical hernia.

While many AWDs share similarities, they differ significantly in prognosis and management. Early detection is therefore crucial for fetal surveillance, prenatal testing, perinatal planning, and patient counseling (TABLE). In this article, we outline antenatal surveillance and management of AWDs based on recommendations from the American College of Obstetricians and Gynecologists and the Society for Maternal-Fetal Medicine as well as on our experience and practice.

Gastroschisis is an increasingly prevalent AWD

Gastroschisis is a full-thickness, ventral wall defect that results in bowel evisceration; it typically occurs to the right of the umbilical cord insertion.³ It is one of the most common AWDs and its prevalence has increased in the past few decades, from 2 to 3 cases per 10,000 live births in 1995 to as high as 6 cases per 10,000 live births in 2011.^2,4,5

The cause of gastroschisis remains unclear. The main theory is that there is an ischemic disruption of the closure of the abdominal wall at or near the omphalomesenteric artery or the right umbilical vein.^6,7 In addition, investigators have reported an increased incidence of gastroschisis in mothers exposed to cigarette smoking and certain medications, such as pseudoephedrine, salicylates, ibuprofen, and acetaminophen.^8,9

Continue to: Making the diagnosis...

Prenatal diagnosis using ultrasonography is possible at around 10 weeks of gestation. As previously mentioned, however, physiologic herniation of the midgut must be excluded by performing follow-up imaging at a later gestational age. In our practice, we typically do this at around 16 weeks of gestation.

Ultrasonographic features of gastroschisis include loops of bowel herniating through a small paraumbilical wall defect (usually 2–3 cm) floating in amniotic fluid without a covering membrane⁴ (FIGURE 2). Direct exposure to amniotic fluid causes small bowel inflammation and fibrin deposition, leading to a thickened, echogenic appearance. Polyhydramnios and intra-abdominal bowel dilation have been associated with the presence of intestinal atresia.¹⁰

Management

There is no expert consensus regarding optimal prenatal management of gastroschisis.^11-17 Prenatal care, patient counseling, and delivery planning should be individualized based on the defect and should be determined in a multidisciplinary discussion with specialists in maternal-fetal medicine, neonatology, and pediatric surgery, as necessary. In our practice, if the gastroschisis is isolated and uncomplicated, our generalist obstetricians manage the patient with maternal-fetal medicine consultation, increased fetal surveillance as described below, and delivery at our tertiary care institution.

Our standard practice is to use the initial ultrasonography imaging to evaluate the size and contents of the defect, measure the nuchal translucency, and evaluate for additional abnormalities. Serial ultrasonography monitoring of the fetus is required to assess the size and quality of the herniated intestine, amount of amniotic fluid, and fetal growth.¹⁰

As gastroschisis is a full-thickness defect of the anterior abdominal wall, the abdominal contents are exposed to amniotic fluid. This exposure causes progressive intestinal damage, which can be identified on ultrasonography as bowel thickening and dilation.^12-14 Currently, intestinal thickening and dilation is not considered an indication for delivery as it is assumed that the intestinal damage has already occurred. It is debatable whether delivery around 37 weeks compared with delayed delivery beyond 37 weeks improves outcomes and decreases the stillbirth rate.^11,13 Studies show that neonates delivered prior to 37 weeks have worse outcomes compared with those delivered after 37 weeks.^14,15

Fetal surveillance. As standard practice, we evaluate the fetus at around 16 weeks and then again at around 20 weeks. In the absence of fetal growth restriction, which is associated with 25% of cases,^16,17 our standard practice includes performing serial growth ultrasonography every 3 to 4 weeks starting at 28 weeks and biophysical profiles and nonstress testing weekly starting at 32 weeks. Fetal echocardiography can be offered. However, unlike with omphalocele, which has a high incidence of associated cardiac structural anomalies, gastroschisis has a low incidence of congenital cardiac anomalies, estimated to be between 2.5% and 4%.^18,19

Delivery considerations. Little agreement exists regarding when and how to deliver pregnancies complicated by fetal gastroschisis. While some advocate for induction of labor at 36 to 38 weeks, most infants with gastroschisis can be delivered safely at term via either vaginal or cesarean delivery.^14,15

Delivery timing should consider the clinical picture and incorporate performance on antenatal testing, fetal growth, the size and contents of the gastroschisis, and consultation with maternal-fetal medicine. Fetuses with gastroschisis often have non-reassuring antenatal testing. This can necessitate early delivery, although cesarean delivery should be reserved for obstetric indications, with the caveat that if there is large liver involvement, some pediatric surgeons recommend cesarean delivery due to the risk of hepatic rupture.

Neonate management. The survival rate of gastroschisis is reported to be as high as 91% to 94%.² Morbidity is related to intestinal complications, such as strictures, adhesions, and volvulus.

In the case of simple gastroschisis, when the bowel is in good condition, the treatment method of choice is primary reduction.²⁰ If performed in the operating room, an immediate sutured closure of the defect can be done. The benefits of primary repair include decreased length of stay, fewer intensive care bed days, and less time to achieve full feeds.^20,21 Primary reduction has a reported success rate of 50% to 83%.²² A reduction with a delayed spontaneous closure also can be performed at bedside in the neonatal intensive care unit.²²

For complex gastroschisis, characterized by bowel complications such as inflammation, perforation, ischemia, atresia, necrosis, or volvulus, primary closure may not be possible and reduction may need to be achieved through silo application.^22-25 Additionally, further bowel surgery, such as stoma formation and bowel resection, may be required.²⁵

Continue to: Omphalocele often is associated with abnormal karyotype...

Also known as exomphalos, omphalocele is a relatively common defect, with an estimated prevalence of 2 to 3 cases per 10,000 live births.² In this condition, there is a midline defect in which intra-abdominal contents herniate through the base of the umbilical cord. Omphaloceles are covered by amniotic membranes, making them distinguishable from gastroschisis, which has no covering, and congenital umbilical hernias, which are covered by intact skin and subcutaneous tissue.^26-33

Additionally, in omphalocele the umbilical cord insertion site varies, whereas in gastroschisis the umbilical cord insertion is usually to the right of midline. An omphalocele is often categorized based on whether or not it contains the liver (extracorporeal liver) or only the bowel (intracorporeal liver).

Genetic studies

Approximately 67% to 88% of all pregnancies with omphalocele have an abnormal karyotype and/or associated malformations, including Beckwith-Wiedemann syndrome.³¹ Of the aneuploidies, trisomy 18 is the one most commonly associated with omphalocele, accounting for approximately 62% to 75%, while trisomy 13 accounts for approximately 11% to 24%.^32,33 The presence of other anomalies is strongly associated with poor prognosis, and increased defect size is an independent predictor of neonatal morbidity and mortality, as neonates with large omphaloceles with extracorporeal livers can develop respiratory insufficiency and require more complex surgical repairs. It is interesting, however, that the absence of an extracorporeal liver is associated with a higher risk of aneuploidy than are cases with an intracorporeal liver.³³

We offer chorionic villus sampling or amniocentesis to all patients with omphalocele. If the patient undergoes invasive diagnostic testing, the sample then undergoes karyotyping, chromosomal microarray, and testing for Beckwith-Wiedemann syndrome. If the patient declines diagnostic sampling, we perform a cell-free DNA screening to rule out aneuploidy.

Continue to: Making the diagnosis...

Omphaloceles can be diagnosed via prenatal ultrasonography as early as 11 to 14 weeks’ gestation.²⁶ They are classified based on size, location, and contents of the sac.^26,27 A small omphalocele is defined as a defect less than 5 cm with a sac that may contain a few loops of intestines (FIGURE 3).²⁷ A giant omphalocele is a defect with more than 75% of the liver contained in the sac.²⁹

Location can be epigastric, umbilical, or hypogastric, and both small and giant omphaloceles may have ruptured membranes that will result in exposure of the contained viscera.²⁷ Omphaloceles are associated with such structural anomalies as cardiac, gastrointestinal, genitourinary, diaphragmatic, and neural tube defects. We do not routinely perform magnetic resonance imaging (MRI) for evaluation of omphaloceles, but MRI may be used to help predict postnatal outcomes in the case of giant omphaloceles.²⁶

Management

Our standard practice is to use the initial ultrasonography imaging to evaluate the size and contents of defect, measure the nuchal translucency, and evaluate for additional abnormalities. As in cases of gastroschisis, serial ultrasonography monitoring of the fetus is required to assess the size and quality of the herniated intestine, amount of amniotic fluid, and fetal growth. We typically evaluate the fetus at around 16 weeks and then again at around 20 weeks. In the absence of fetal growth restriction, we recommend serial growth ultrasonography every 3 to 4 weeks starting at 28 weeks and biophysical profiles and nonstress testing weekly starting at 32 weeks. Additionally, we routinely obtain a fetal echocardiogram to rule out cardiac structural abnormalities.

Delivery considerations. Fetuses that do not undergo spontaneous abortion or medical termination of pregnancy often are born at term.²⁶ We recommend expectant management until spontaneous labor, another indication for delivery arises, or at least 39 weeks’ estimated gestational age. There are no evidence-based guidelines for the optimal mode of delivery in fetuses with omphalocele, although we recommend cesarean delivery for fetuses with large defects to avoid postnatal sac rupture and liver damage. Preterm induction of labor is not indicated as infants born preterm have about a 50% mortality rate.^26,27

Children born with isolated omphalocele typically have a good prognosis, with an estimated survival rate of 50% to 90%.^32,33 However, compared to gastroschisis, omphaloceles are often associated with other anomalies.^32,33

Management of omphaloceles depends on the size of the defect. In our institution, our generalist obstetricians manage the standard prenatal care with the addition of increased fetal surveillance and testing, interdisciplinary patient counseling with maternal-fetal medicine, pediatric surgeons, and neonatologists for delivery planning, and delivery is performed at our tertiary care center.

Neonate management. Small omphaloceles are amenable to primary early fascial closure.^26-30 However, attempted primary closure of giant omphaloceles carries significant risks, including abdominal compartment syndrome and postoperative herniation.^29,30 Instead, several options exist for staged surgical closure, in which there are multiple operations prior to final fascial closure, as well as nonoperative delayed closure for management of giant omphaloceles.^29,30

Conservative management of giant omphaloceles has certain benefits, such as earlier first feeds, decreased risk of abdominal compartment syndrome, and lower risk of infection.³⁰ Ruptured omphaloceles can be repaired through primary repair, employment of a synthetic or biologic mesh fascial bridge, or silo placement with delayed closure.²⁸

Body-stalk anomaly: Multiple defects and poor prognosis

Also known as limb body wall complex, body-stalk anomaly is a rare malformation that has a reported prevalence of approximately 0.12 cases per 10,000 births (both live and stillbirths).³⁴ Body-stalk anomaly is characterized by multiple defects, including severe kyphosis or scoliosis, a short or absent umbilical cord, and a large anterior abdominal wall defect.^34-36 This malformation is almost entirely incompatible with life, resulting in abortion or stillbirth.³⁵ Survival is extremely rare and limited to case reports.

While the exact etiology of body-stalk anomaly is unknown, 3 possible causes have been hypothesized: early amnion rupture, vascular compromise, and embryonic dysgenesis.^37-40

Continue to: Making the diagnosis...

Body-stalk anomaly typically can be diagnosed by 10 to 14 weeks’ gestation via ultrasonography.^34-41 We currently follow the diagnostic criteria proposed by Van Allen and colleagues, which requires 2 of the following 3 anomalies³⁴:

• exencephaly/encephalocele with facial clefts
• thoraco- and/or abdominoschisis (midline defect)
• limb defect.

Additional ultrasonographic findings can include the identification of evisceration of the abdominal contents, a short umbilical cord, and increased nuchal thickness.^36,42 During the second and third trimesters, oligohydramnios may be seen.²

Management

Body-stalk anomaly is considered a fatal condition without specific therapeutic interventions. Maternal risks include an increased risk of preterm labor and gestational hypertension.³⁵ Research on body-stalk anomaly has not shown any correlation with patients’ age, fetal sex, or abnormal karyotype, and the reported risk of recurrence for this anomaly is very low.^42,43 Early diagnosis therefore is essential to provide families with information and counseling. Given the poor fetal prognosis, increased maternal risk, and low recurrence rates, mothers can be advised toward elective termination of pregnancy.

Should a patient desire expectant management, care can be provided by generalist obstetricians or care can be transferred to maternal-fetal medicine, with the addition of increased fetal surveillance and testing, interdisciplinary patient counseling with maternal-fetal medicine, pediatric surgeons, and neonatologists for delivery planning; delivery should be performed at a tertiary care center.

Pentalogy of Cantrell: Very rare, with variable prognosis

Pentalogy of Cantrell is characterized by a collection of defects in the midline abdominal wall, lower sternum, anterior diaphragm, diaphragmatic pericardium, and some manifestation of intra-cardiac defect.⁴⁴ It is thought to arise early in gestation due to abnormal differentiation, migration, and fusion of the embryonic mesoderm.⁴⁴ The condition is rare, with an incidence of about 1 in 5.5 million live births.⁴⁵

Making the diagnosis

The diagnosis of pentalogy of Cantrell can be made via prenatal ultrasonography as early as the first trimester, although it is diagnosed more commonly in the second trimester.⁴⁶ Three-dimensional ultrasonography and fetal MRI have been used to confirm the diagnosis.⁴⁷

Management

Typically, corrective operations are performed during the neonatal period, and cases of successful staged and one-stage operations have been reported.⁴⁸ Surgical treatment is determined based on the complexity of the condition and the presence of coexistent heart defects.^49,50 However, very few patients survive surgical repair; mortality rates are estimated at around 50% to 60%, with high postsurgical morbidity risks for those who do survive.⁴⁵

Prognosis varies depending on the type and severity of the associated malformations and intracardiac anomalies.⁴⁶ Patients with partial ectopia cordis and incomplete presentation may have more favorable outcomes, but for patients with severe ectopia cordis, the survival rate is only 5% to 10%.⁴⁷

Depending on the severity of the defects, mothers can be advised toward elective termination of pregnancy. In our institution, prenatal care usually is transferred to the maternal-fetal medicine service, and delivery is planned at our tertiary care institution.

OEIS complex comprises abdominal, pelvic, and spinal defects

Omphalocele-exstrophy-imperforate anus-spinal defects (OEIS) complex is a congenital malformation syndrome characterized by the combination of midline abdominal and pelvic defects (including omphalocele, exstrophy of the cloaca, and imperforate anus) and spinal defects.⁵¹ The condition’s etiology is unknown but is thought to be multifactorial.^51-53 It is a rare condition, with an incidence of around 1 in 200,000 to 400,000 pregnancies.⁵²

Making the diagnosis

Prenatal diagnosis of OEIS complex can be made as early as the first trimester via ultrasonographic identification of an infraumbilical abdominal wall defect with protruding mass, absent bladder, and spinal defects.⁵² When OEIS complex is suspected, fetal MRI can play a critical role in the diagnosis.

Management

As OEIS complex is rare, there are no evidence-based guidelines for optimal mode and timing of delivery. Cases are individualized based on their specific pathology, and we recommend cesarean delivery for fetuses with large defects to avoid postnatal sac rupture and liver damage.

The prognosis for infants with OEIS complex depends on the spectrum and severity of the structural defects.^52,53 The many surgeries involved in the repair of OEIS have potential complications, such as urogenital and gastrointestinal dysfunction.^52,53 Advances in medical and surgical treatment have resulted in improved survival and quality of life, and survival rates for OEIS complex are now close to 100%.⁵³ While many OEIS patients live with a permanent colostomy, improvements in management mean that more patients are now candidates for gastrointestinal pull-through procedures, which allow for natural bowel control and a higher degree of bowel cleanliness.⁵³

Prenatal care, patient counseling, and delivery planning should be individualized based on the defects present and determined in a multidisciplinary discussion with maternal-fetal medicine, neonatology, and pediatric surgery as necessary. In our institution, prenatal care usually is transferred to the maternal-fetal medicine service, and delivery is planned at our tertiary care institution.

Multidisciplinary team strategy is essential

Based on our experience, when faced with an anterior AWD in utero, prenatal imaging, genetic testing, increased fetal surveillance, and a multidisciplinary team approach improves outcomes. We must emphasize that careful patient counseling is paramount in our practice. ●

Acknowledgement: The authors would like to thank Ashley Tran, BS, for her assistance in the literature review and drafting of this article.

CASE Fetal anomalies detected on ultrasonography

A 34-year-old woman (G2P1) at 19 weeks’ gestation presented for fetal anatomy ultrasonography evaluation. Ultrasonography demonstrated fetal demise with fetal size less than dates, oligohydramnios, and what appeared to be a full-thickness herniation of the thoracic and abdominal contents. Due to the positioning of the fetus and the oligohydramnios, the fetus appeared to have ectopia cordis and herniated liver and bowel; the bladder was not visualized. The patient was counseled regarding the findings and the suspected diagnosis of pentalogy of Cantrell. After counseling, the patient expressed desire to bury the fetus intact according to her religious custom. She underwent a successful uterine evacuation with misoprostol administration and delivered a nonviable fetus that had a closed thoracic cage without ectopia cordis. Key findings were a very short 2-vessel umbilical cord without coiling that was tethered to the intra-abdominal organs, “pulling” the internal organs out of the abdomen, and lack of an anterior abdominal wall (FIGURE 1). Given these findings, a final diagnosis of body-stalk anomaly was made.

Fetal abdominal wall defects (AWDs) encompass a wide array of congenital defects, although they all involve herniation of 1 or more intra-abdominal content through a ventral abdominal defect.¹ Overall, the estimated incidence of AWDs is approximately 6 per 10,000 births.¹ Gastroschisis and omphalocele are the most common of these defect types.²

The majority of AWDs can be diagnosed during the first trimester of pregnancy via ultrasonography; however, during the first trimester the physiologic midgut herniation resolves by 12 weeks of gestation. It is therefore important to repeat imaging at a later gestational age to confirm the suspicion. Furthermore, the differential diagnosis should include the relatively benign condition of umbilical hernia.

While many AWDs share similarities, they differ significantly in prognosis and management. Early detection is therefore crucial for fetal surveillance, prenatal testing, perinatal planning, and patient counseling (TABLE). In this article, we outline antenatal surveillance and management of AWDs based on recommendations from the American College of Obstetricians and Gynecologists and the Society for Maternal-Fetal Medicine as well as on our experience and practice.

Gastroschisis is an increasingly prevalent AWD

Gastroschisis is a full-thickness, ventral wall defect that results in bowel evisceration; it typically occurs to the right of the umbilical cord insertion.³ It is one of the most common AWDs and its prevalence has increased in the past few decades, from 2 to 3 cases per 10,000 live births in 1995 to as high as 6 cases per 10,000 live births in 2011.^2,4,5

The cause of gastroschisis remains unclear. The main theory is that there is an ischemic disruption of the closure of the abdominal wall at or near the omphalomesenteric artery or the right umbilical vein.^6,7 In addition, investigators have reported an increased incidence of gastroschisis in mothers exposed to cigarette smoking and certain medications, such as pseudoephedrine, salicylates, ibuprofen, and acetaminophen.^8,9

Continue to: Making the diagnosis...

Prenatal diagnosis using ultrasonography is possible at around 10 weeks of gestation. As previously mentioned, however, physiologic herniation of the midgut must be excluded by performing follow-up imaging at a later gestational age. In our practice, we typically do this at around 16 weeks of gestation.

Ultrasonographic features of gastroschisis include loops of bowel herniating through a small paraumbilical wall defect (usually 2–3 cm) floating in amniotic fluid without a covering membrane⁴ (FIGURE 2). Direct exposure to amniotic fluid causes small bowel inflammation and fibrin deposition, leading to a thickened, echogenic appearance. Polyhydramnios and intra-abdominal bowel dilation have been associated with the presence of intestinal atresia.¹⁰

Management

There is no expert consensus regarding optimal prenatal management of gastroschisis.^11-17 Prenatal care, patient counseling, and delivery planning should be individualized based on the defect and should be determined in a multidisciplinary discussion with specialists in maternal-fetal medicine, neonatology, and pediatric surgery, as necessary. In our practice, if the gastroschisis is isolated and uncomplicated, our generalist obstetricians manage the patient with maternal-fetal medicine consultation, increased fetal surveillance as described below, and delivery at our tertiary care institution.

Our standard practice is to use the initial ultrasonography imaging to evaluate the size and contents of the defect, measure the nuchal translucency, and evaluate for additional abnormalities. Serial ultrasonography monitoring of the fetus is required to assess the size and quality of the herniated intestine, amount of amniotic fluid, and fetal growth.¹⁰

As gastroschisis is a full-thickness defect of the anterior abdominal wall, the abdominal contents are exposed to amniotic fluid. This exposure causes progressive intestinal damage, which can be identified on ultrasonography as bowel thickening and dilation.^12-14 Currently, intestinal thickening and dilation is not considered an indication for delivery as it is assumed that the intestinal damage has already occurred. It is debatable whether delivery around 37 weeks compared with delayed delivery beyond 37 weeks improves outcomes and decreases the stillbirth rate.^11,13 Studies show that neonates delivered prior to 37 weeks have worse outcomes compared with those delivered after 37 weeks.^14,15

Fetal surveillance. As standard practice, we evaluate the fetus at around 16 weeks and then again at around 20 weeks. In the absence of fetal growth restriction, which is associated with 25% of cases,^16,17 our standard practice includes performing serial growth ultrasonography every 3 to 4 weeks starting at 28 weeks and biophysical profiles and nonstress testing weekly starting at 32 weeks. Fetal echocardiography can be offered. However, unlike with omphalocele, which has a high incidence of associated cardiac structural anomalies, gastroschisis has a low incidence of congenital cardiac anomalies, estimated to be between 2.5% and 4%.^18,19

Delivery considerations. Little agreement exists regarding when and how to deliver pregnancies complicated by fetal gastroschisis. While some advocate for induction of labor at 36 to 38 weeks, most infants with gastroschisis can be delivered safely at term via either vaginal or cesarean delivery.^14,15

Delivery timing should consider the clinical picture and incorporate performance on antenatal testing, fetal growth, the size and contents of the gastroschisis, and consultation with maternal-fetal medicine. Fetuses with gastroschisis often have non-reassuring antenatal testing. This can necessitate early delivery, although cesarean delivery should be reserved for obstetric indications, with the caveat that if there is large liver involvement, some pediatric surgeons recommend cesarean delivery due to the risk of hepatic rupture.

Neonate management. The survival rate of gastroschisis is reported to be as high as 91% to 94%.² Morbidity is related to intestinal complications, such as strictures, adhesions, and volvulus.

In the case of simple gastroschisis, when the bowel is in good condition, the treatment method of choice is primary reduction.²⁰ If performed in the operating room, an immediate sutured closure of the defect can be done. The benefits of primary repair include decreased length of stay, fewer intensive care bed days, and less time to achieve full feeds.^20,21 Primary reduction has a reported success rate of 50% to 83%.²² A reduction with a delayed spontaneous closure also can be performed at bedside in the neonatal intensive care unit.²²

For complex gastroschisis, characterized by bowel complications such as inflammation, perforation, ischemia, atresia, necrosis, or volvulus, primary closure may not be possible and reduction may need to be achieved through silo application.^22-25 Additionally, further bowel surgery, such as stoma formation and bowel resection, may be required.²⁵

Continue to: Omphalocele often is associated with abnormal karyotype...

Also known as exomphalos, omphalocele is a relatively common defect, with an estimated prevalence of 2 to 3 cases per 10,000 live births.² In this condition, there is a midline defect in which intra-abdominal contents herniate through the base of the umbilical cord. Omphaloceles are covered by amniotic membranes, making them distinguishable from gastroschisis, which has no covering, and congenital umbilical hernias, which are covered by intact skin and subcutaneous tissue.^26-33

Additionally, in omphalocele the umbilical cord insertion site varies, whereas in gastroschisis the umbilical cord insertion is usually to the right of midline. An omphalocele is often categorized based on whether or not it contains the liver (extracorporeal liver) or only the bowel (intracorporeal liver).

Genetic studies

Approximately 67% to 88% of all pregnancies with omphalocele have an abnormal karyotype and/or associated malformations, including Beckwith-Wiedemann syndrome.³¹ Of the aneuploidies, trisomy 18 is the one most commonly associated with omphalocele, accounting for approximately 62% to 75%, while trisomy 13 accounts for approximately 11% to 24%.^32,33 The presence of other anomalies is strongly associated with poor prognosis, and increased defect size is an independent predictor of neonatal morbidity and mortality, as neonates with large omphaloceles with extracorporeal livers can develop respiratory insufficiency and require more complex surgical repairs. It is interesting, however, that the absence of an extracorporeal liver is associated with a higher risk of aneuploidy than are cases with an intracorporeal liver.³³

We offer chorionic villus sampling or amniocentesis to all patients with omphalocele. If the patient undergoes invasive diagnostic testing, the sample then undergoes karyotyping, chromosomal microarray, and testing for Beckwith-Wiedemann syndrome. If the patient declines diagnostic sampling, we perform a cell-free DNA screening to rule out aneuploidy.

Continue to: Making the diagnosis...

Omphaloceles can be diagnosed via prenatal ultrasonography as early as 11 to 14 weeks’ gestation.²⁶ They are classified based on size, location, and contents of the sac.^26,27 A small omphalocele is defined as a defect less than 5 cm with a sac that may contain a few loops of intestines (FIGURE 3).²⁷ A giant omphalocele is a defect with more than 75% of the liver contained in the sac.²⁹

Location can be epigastric, umbilical, or hypogastric, and both small and giant omphaloceles may have ruptured membranes that will result in exposure of the contained viscera.²⁷ Omphaloceles are associated with such structural anomalies as cardiac, gastrointestinal, genitourinary, diaphragmatic, and neural tube defects. We do not routinely perform magnetic resonance imaging (MRI) for evaluation of omphaloceles, but MRI may be used to help predict postnatal outcomes in the case of giant omphaloceles.²⁶

Management

Our standard practice is to use the initial ultrasonography imaging to evaluate the size and contents of defect, measure the nuchal translucency, and evaluate for additional abnormalities. As in cases of gastroschisis, serial ultrasonography monitoring of the fetus is required to assess the size and quality of the herniated intestine, amount of amniotic fluid, and fetal growth. We typically evaluate the fetus at around 16 weeks and then again at around 20 weeks. In the absence of fetal growth restriction, we recommend serial growth ultrasonography every 3 to 4 weeks starting at 28 weeks and biophysical profiles and nonstress testing weekly starting at 32 weeks. Additionally, we routinely obtain a fetal echocardiogram to rule out cardiac structural abnormalities.

Delivery considerations. Fetuses that do not undergo spontaneous abortion or medical termination of pregnancy often are born at term.²⁶ We recommend expectant management until spontaneous labor, another indication for delivery arises, or at least 39 weeks’ estimated gestational age. There are no evidence-based guidelines for the optimal mode of delivery in fetuses with omphalocele, although we recommend cesarean delivery for fetuses with large defects to avoid postnatal sac rupture and liver damage. Preterm induction of labor is not indicated as infants born preterm have about a 50% mortality rate.^26,27

Children born with isolated omphalocele typically have a good prognosis, with an estimated survival rate of 50% to 90%.^32,33 However, compared to gastroschisis, omphaloceles are often associated with other anomalies.^32,33

Management of omphaloceles depends on the size of the defect. In our institution, our generalist obstetricians manage the standard prenatal care with the addition of increased fetal surveillance and testing, interdisciplinary patient counseling with maternal-fetal medicine, pediatric surgeons, and neonatologists for delivery planning, and delivery is performed at our tertiary care center.

Neonate management. Small omphaloceles are amenable to primary early fascial closure.^26-30 However, attempted primary closure of giant omphaloceles carries significant risks, including abdominal compartment syndrome and postoperative herniation.^29,30 Instead, several options exist for staged surgical closure, in which there are multiple operations prior to final fascial closure, as well as nonoperative delayed closure for management of giant omphaloceles.^29,30

Conservative management of giant omphaloceles has certain benefits, such as earlier first feeds, decreased risk of abdominal compartment syndrome, and lower risk of infection.³⁰ Ruptured omphaloceles can be repaired through primary repair, employment of a synthetic or biologic mesh fascial bridge, or silo placement with delayed closure.²⁸

Body-stalk anomaly: Multiple defects and poor prognosis

Also known as limb body wall complex, body-stalk anomaly is a rare malformation that has a reported prevalence of approximately 0.12 cases per 10,000 births (both live and stillbirths).³⁴ Body-stalk anomaly is characterized by multiple defects, including severe kyphosis or scoliosis, a short or absent umbilical cord, and a large anterior abdominal wall defect.^34-36 This malformation is almost entirely incompatible with life, resulting in abortion or stillbirth.³⁵ Survival is extremely rare and limited to case reports.

While the exact etiology of body-stalk anomaly is unknown, 3 possible causes have been hypothesized: early amnion rupture, vascular compromise, and embryonic dysgenesis.^37-40

Continue to: Making the diagnosis...

Body-stalk anomaly typically can be diagnosed by 10 to 14 weeks’ gestation via ultrasonography.^34-41 We currently follow the diagnostic criteria proposed by Van Allen and colleagues, which requires 2 of the following 3 anomalies³⁴:

• exencephaly/encephalocele with facial clefts
• thoraco- and/or abdominoschisis (midline defect)
• limb defect.

Additional ultrasonographic findings can include the identification of evisceration of the abdominal contents, a short umbilical cord, and increased nuchal thickness.^36,42 During the second and third trimesters, oligohydramnios may be seen.²

Management

Body-stalk anomaly is considered a fatal condition without specific therapeutic interventions. Maternal risks include an increased risk of preterm labor and gestational hypertension.³⁵ Research on body-stalk anomaly has not shown any correlation with patients’ age, fetal sex, or abnormal karyotype, and the reported risk of recurrence for this anomaly is very low.^42,43 Early diagnosis therefore is essential to provide families with information and counseling. Given the poor fetal prognosis, increased maternal risk, and low recurrence rates, mothers can be advised toward elective termination of pregnancy.

Should a patient desire expectant management, care can be provided by generalist obstetricians or care can be transferred to maternal-fetal medicine, with the addition of increased fetal surveillance and testing, interdisciplinary patient counseling with maternal-fetal medicine, pediatric surgeons, and neonatologists for delivery planning; delivery should be performed at a tertiary care center.

Pentalogy of Cantrell: Very rare, with variable prognosis

Pentalogy of Cantrell is characterized by a collection of defects in the midline abdominal wall, lower sternum, anterior diaphragm, diaphragmatic pericardium, and some manifestation of intra-cardiac defect.⁴⁴ It is thought to arise early in gestation due to abnormal differentiation, migration, and fusion of the embryonic mesoderm.⁴⁴ The condition is rare, with an incidence of about 1 in 5.5 million live births.⁴⁵

Making the diagnosis

The diagnosis of pentalogy of Cantrell can be made via prenatal ultrasonography as early as the first trimester, although it is diagnosed more commonly in the second trimester.⁴⁶ Three-dimensional ultrasonography and fetal MRI have been used to confirm the diagnosis.⁴⁷

Management

Typically, corrective operations are performed during the neonatal period, and cases of successful staged and one-stage operations have been reported.⁴⁸ Surgical treatment is determined based on the complexity of the condition and the presence of coexistent heart defects.^49,50 However, very few patients survive surgical repair; mortality rates are estimated at around 50% to 60%, with high postsurgical morbidity risks for those who do survive.⁴⁵

Prognosis varies depending on the type and severity of the associated malformations and intracardiac anomalies.⁴⁶ Patients with partial ectopia cordis and incomplete presentation may have more favorable outcomes, but for patients with severe ectopia cordis, the survival rate is only 5% to 10%.⁴⁷

Depending on the severity of the defects, mothers can be advised toward elective termination of pregnancy. In our institution, prenatal care usually is transferred to the maternal-fetal medicine service, and delivery is planned at our tertiary care institution.

OEIS complex comprises abdominal, pelvic, and spinal defects

Omphalocele-exstrophy-imperforate anus-spinal defects (OEIS) complex is a congenital malformation syndrome characterized by the combination of midline abdominal and pelvic defects (including omphalocele, exstrophy of the cloaca, and imperforate anus) and spinal defects.⁵¹ The condition’s etiology is unknown but is thought to be multifactorial.^51-53 It is a rare condition, with an incidence of around 1 in 200,000 to 400,000 pregnancies.⁵²

Making the diagnosis

Prenatal diagnosis of OEIS complex can be made as early as the first trimester via ultrasonographic identification of an infraumbilical abdominal wall defect with protruding mass, absent bladder, and spinal defects.⁵² When OEIS complex is suspected, fetal MRI can play a critical role in the diagnosis.

Management

As OEIS complex is rare, there are no evidence-based guidelines for optimal mode and timing of delivery. Cases are individualized based on their specific pathology, and we recommend cesarean delivery for fetuses with large defects to avoid postnatal sac rupture and liver damage.

The prognosis for infants with OEIS complex depends on the spectrum and severity of the structural defects.^52,53 The many surgeries involved in the repair of OEIS have potential complications, such as urogenital and gastrointestinal dysfunction.^52,53 Advances in medical and surgical treatment have resulted in improved survival and quality of life, and survival rates for OEIS complex are now close to 100%.⁵³ While many OEIS patients live with a permanent colostomy, improvements in management mean that more patients are now candidates for gastrointestinal pull-through procedures, which allow for natural bowel control and a higher degree of bowel cleanliness.⁵³

Prenatal care, patient counseling, and delivery planning should be individualized based on the defects present and determined in a multidisciplinary discussion with maternal-fetal medicine, neonatology, and pediatric surgery as necessary. In our institution, prenatal care usually is transferred to the maternal-fetal medicine service, and delivery is planned at our tertiary care institution.

Multidisciplinary team strategy is essential

Based on our experience, when faced with an anterior AWD in utero, prenatal imaging, genetic testing, increased fetal surveillance, and a multidisciplinary team approach improves outcomes. We must emphasize that careful patient counseling is paramount in our practice. ●

Acknowledgement: The authors would like to thank Ashley Tran, BS, for her assistance in the literature review and drafting of this article.

CASE Fetal anomalies detected on ultrasonography

A 34-year-old woman (G2P1) at 19 weeks’ gestation presented for fetal anatomy ultrasonography evaluation. Ultrasonography demonstrated fetal demise with fetal size less than dates, oligohydramnios, and what appeared to be a full-thickness herniation of the thoracic and abdominal contents. Due to the positioning of the fetus and the oligohydramnios, the fetus appeared to have ectopia cordis and herniated liver and bowel; the bladder was not visualized. The patient was counseled regarding the findings and the suspected diagnosis of pentalogy of Cantrell. After counseling, the patient expressed desire to bury the fetus intact according to her religious custom. She underwent a successful uterine evacuation with misoprostol administration and delivered a nonviable fetus that had a closed thoracic cage without ectopia cordis. Key findings were a very short 2-vessel umbilical cord without coiling that was tethered to the intra-abdominal organs, “pulling” the internal organs out of the abdomen, and lack of an anterior abdominal wall (FIGURE 1). Given these findings, a final diagnosis of body-stalk anomaly was made.

Fetal abdominal wall defects (AWDs) encompass a wide array of congenital defects, although they all involve herniation of 1 or more intra-abdominal content through a ventral abdominal defect.¹ Overall, the estimated incidence of AWDs is approximately 6 per 10,000 births.¹ Gastroschisis and omphalocele are the most common of these defect types.²

The majority of AWDs can be diagnosed during the first trimester of pregnancy via ultrasonography; however, during the first trimester the physiologic midgut herniation resolves by 12 weeks of gestation. It is therefore important to repeat imaging at a later gestational age to confirm the suspicion. Furthermore, the differential diagnosis should include the relatively benign condition of umbilical hernia.

While many AWDs share similarities, they differ significantly in prognosis and management. Early detection is therefore crucial for fetal surveillance, prenatal testing, perinatal planning, and patient counseling (TABLE). In this article, we outline antenatal surveillance and management of AWDs based on recommendations from the American College of Obstetricians and Gynecologists and the Society for Maternal-Fetal Medicine as well as on our experience and practice.

Gastroschisis is an increasingly prevalent AWD

Gastroschisis is a full-thickness, ventral wall defect that results in bowel evisceration; it typically occurs to the right of the umbilical cord insertion.³ It is one of the most common AWDs and its prevalence has increased in the past few decades, from 2 to 3 cases per 10,000 live births in 1995 to as high as 6 cases per 10,000 live births in 2011.^2,4,5

The cause of gastroschisis remains unclear. The main theory is that there is an ischemic disruption of the closure of the abdominal wall at or near the omphalomesenteric artery or the right umbilical vein.^6,7 In addition, investigators have reported an increased incidence of gastroschisis in mothers exposed to cigarette smoking and certain medications, such as pseudoephedrine, salicylates, ibuprofen, and acetaminophen.^8,9

Continue to: Making the diagnosis...

Prenatal diagnosis using ultrasonography is possible at around 10 weeks of gestation. As previously mentioned, however, physiologic herniation of the midgut must be excluded by performing follow-up imaging at a later gestational age. In our practice, we typically do this at around 16 weeks of gestation.

Ultrasonographic features of gastroschisis include loops of bowel herniating through a small paraumbilical wall defect (usually 2–3 cm) floating in amniotic fluid without a covering membrane⁴ (FIGURE 2). Direct exposure to amniotic fluid causes small bowel inflammation and fibrin deposition, leading to a thickened, echogenic appearance. Polyhydramnios and intra-abdominal bowel dilation have been associated with the presence of intestinal atresia.¹⁰

Management

There is no expert consensus regarding optimal prenatal management of gastroschisis.^11-17 Prenatal care, patient counseling, and delivery planning should be individualized based on the defect and should be determined in a multidisciplinary discussion with specialists in maternal-fetal medicine, neonatology, and pediatric surgery, as necessary. In our practice, if the gastroschisis is isolated and uncomplicated, our generalist obstetricians manage the patient with maternal-fetal medicine consultation, increased fetal surveillance as described below, and delivery at our tertiary care institution.

Our standard practice is to use the initial ultrasonography imaging to evaluate the size and contents of the defect, measure the nuchal translucency, and evaluate for additional abnormalities. Serial ultrasonography monitoring of the fetus is required to assess the size and quality of the herniated intestine, amount of amniotic fluid, and fetal growth.¹⁰

As gastroschisis is a full-thickness defect of the anterior abdominal wall, the abdominal contents are exposed to amniotic fluid. This exposure causes progressive intestinal damage, which can be identified on ultrasonography as bowel thickening and dilation.^12-14 Currently, intestinal thickening and dilation is not considered an indication for delivery as it is assumed that the intestinal damage has already occurred. It is debatable whether delivery around 37 weeks compared with delayed delivery beyond 37 weeks improves outcomes and decreases the stillbirth rate.^11,13 Studies show that neonates delivered prior to 37 weeks have worse outcomes compared with those delivered after 37 weeks.^14,15

Fetal surveillance. As standard practice, we evaluate the fetus at around 16 weeks and then again at around 20 weeks. In the absence of fetal growth restriction, which is associated with 25% of cases,^16,17 our standard practice includes performing serial growth ultrasonography every 3 to 4 weeks starting at 28 weeks and biophysical profiles and nonstress testing weekly starting at 32 weeks. Fetal echocardiography can be offered. However, unlike with omphalocele, which has a high incidence of associated cardiac structural anomalies, gastroschisis has a low incidence of congenital cardiac anomalies, estimated to be between 2.5% and 4%.^18,19

Delivery considerations. Little agreement exists regarding when and how to deliver pregnancies complicated by fetal gastroschisis. While some advocate for induction of labor at 36 to 38 weeks, most infants with gastroschisis can be delivered safely at term via either vaginal or cesarean delivery.^14,15

Delivery timing should consider the clinical picture and incorporate performance on antenatal testing, fetal growth, the size and contents of the gastroschisis, and consultation with maternal-fetal medicine. Fetuses with gastroschisis often have non-reassuring antenatal testing. This can necessitate early delivery, although cesarean delivery should be reserved for obstetric indications, with the caveat that if there is large liver involvement, some pediatric surgeons recommend cesarean delivery due to the risk of hepatic rupture.

Neonate management. The survival rate of gastroschisis is reported to be as high as 91% to 94%.² Morbidity is related to intestinal complications, such as strictures, adhesions, and volvulus.

In the case of simple gastroschisis, when the bowel is in good condition, the treatment method of choice is primary reduction.²⁰ If performed in the operating room, an immediate sutured closure of the defect can be done. The benefits of primary repair include decreased length of stay, fewer intensive care bed days, and less time to achieve full feeds.^20,21 Primary reduction has a reported success rate of 50% to 83%.²² A reduction with a delayed spontaneous closure also can be performed at bedside in the neonatal intensive care unit.²²

For complex gastroschisis, characterized by bowel complications such as inflammation, perforation, ischemia, atresia, necrosis, or volvulus, primary closure may not be possible and reduction may need to be achieved through silo application.^22-25 Additionally, further bowel surgery, such as stoma formation and bowel resection, may be required.²⁵

Continue to: Omphalocele often is associated with abnormal karyotype...

Also known as exomphalos, omphalocele is a relatively common defect, with an estimated prevalence of 2 to 3 cases per 10,000 live births.² In this condition, there is a midline defect in which intra-abdominal contents herniate through the base of the umbilical cord. Omphaloceles are covered by amniotic membranes, making them distinguishable from gastroschisis, which has no covering, and congenital umbilical hernias, which are covered by intact skin and subcutaneous tissue.^26-33

Additionally, in omphalocele the umbilical cord insertion site varies, whereas in gastroschisis the umbilical cord insertion is usually to the right of midline. An omphalocele is often categorized based on whether or not it contains the liver (extracorporeal liver) or only the bowel (intracorporeal liver).

Genetic studies

Approximately 67% to 88% of all pregnancies with omphalocele have an abnormal karyotype and/or associated malformations, including Beckwith-Wiedemann syndrome.³¹ Of the aneuploidies, trisomy 18 is the one most commonly associated with omphalocele, accounting for approximately 62% to 75%, while trisomy 13 accounts for approximately 11% to 24%.^32,33 The presence of other anomalies is strongly associated with poor prognosis, and increased defect size is an independent predictor of neonatal morbidity and mortality, as neonates with large omphaloceles with extracorporeal livers can develop respiratory insufficiency and require more complex surgical repairs. It is interesting, however, that the absence of an extracorporeal liver is associated with a higher risk of aneuploidy than are cases with an intracorporeal liver.³³

We offer chorionic villus sampling or amniocentesis to all patients with omphalocele. If the patient undergoes invasive diagnostic testing, the sample then undergoes karyotyping, chromosomal microarray, and testing for Beckwith-Wiedemann syndrome. If the patient declines diagnostic sampling, we perform a cell-free DNA screening to rule out aneuploidy.

Continue to: Making the diagnosis...

Omphaloceles can be diagnosed via prenatal ultrasonography as early as 11 to 14 weeks’ gestation.²⁶ They are classified based on size, location, and contents of the sac.^26,27 A small omphalocele is defined as a defect less than 5 cm with a sac that may contain a few loops of intestines (FIGURE 3).²⁷ A giant omphalocele is a defect with more than 75% of the liver contained in the sac.²⁹

Location can be epigastric, umbilical, or hypogastric, and both small and giant omphaloceles may have ruptured membranes that will result in exposure of the contained viscera.²⁷ Omphaloceles are associated with such structural anomalies as cardiac, gastrointestinal, genitourinary, diaphragmatic, and neural tube defects. We do not routinely perform magnetic resonance imaging (MRI) for evaluation of omphaloceles, but MRI may be used to help predict postnatal outcomes in the case of giant omphaloceles.²⁶

Management

Our standard practice is to use the initial ultrasonography imaging to evaluate the size and contents of defect, measure the nuchal translucency, and evaluate for additional abnormalities. As in cases of gastroschisis, serial ultrasonography monitoring of the fetus is required to assess the size and quality of the herniated intestine, amount of amniotic fluid, and fetal growth. We typically evaluate the fetus at around 16 weeks and then again at around 20 weeks. In the absence of fetal growth restriction, we recommend serial growth ultrasonography every 3 to 4 weeks starting at 28 weeks and biophysical profiles and nonstress testing weekly starting at 32 weeks. Additionally, we routinely obtain a fetal echocardiogram to rule out cardiac structural abnormalities.

Delivery considerations. Fetuses that do not undergo spontaneous abortion or medical termination of pregnancy often are born at term.²⁶ We recommend expectant management until spontaneous labor, another indication for delivery arises, or at least 39 weeks’ estimated gestational age. There are no evidence-based guidelines for the optimal mode of delivery in fetuses with omphalocele, although we recommend cesarean delivery for fetuses with large defects to avoid postnatal sac rupture and liver damage. Preterm induction of labor is not indicated as infants born preterm have about a 50% mortality rate.^26,27

Children born with isolated omphalocele typically have a good prognosis, with an estimated survival rate of 50% to 90%.^32,33 However, compared to gastroschisis, omphaloceles are often associated with other anomalies.^32,33

Management of omphaloceles depends on the size of the defect. In our institution, our generalist obstetricians manage the standard prenatal care with the addition of increased fetal surveillance and testing, interdisciplinary patient counseling with maternal-fetal medicine, pediatric surgeons, and neonatologists for delivery planning, and delivery is performed at our tertiary care center.

Neonate management. Small omphaloceles are amenable to primary early fascial closure.^26-30 However, attempted primary closure of giant omphaloceles carries significant risks, including abdominal compartment syndrome and postoperative herniation.^29,30 Instead, several options exist for staged surgical closure, in which there are multiple operations prior to final fascial closure, as well as nonoperative delayed closure for management of giant omphaloceles.^29,30

Conservative management of giant omphaloceles has certain benefits, such as earlier first feeds, decreased risk of abdominal compartment syndrome, and lower risk of infection.³⁰ Ruptured omphaloceles can be repaired through primary repair, employment of a synthetic or biologic mesh fascial bridge, or silo placement with delayed closure.²⁸

Body-stalk anomaly: Multiple defects and poor prognosis

Also known as limb body wall complex, body-stalk anomaly is a rare malformation that has a reported prevalence of approximately 0.12 cases per 10,000 births (both live and stillbirths).³⁴ Body-stalk anomaly is characterized by multiple defects, including severe kyphosis or scoliosis, a short or absent umbilical cord, and a large anterior abdominal wall defect.^34-36 This malformation is almost entirely incompatible with life, resulting in abortion or stillbirth.³⁵ Survival is extremely rare and limited to case reports.

While the exact etiology of body-stalk anomaly is unknown, 3 possible causes have been hypothesized: early amnion rupture, vascular compromise, and embryonic dysgenesis.^37-40

Continue to: Making the diagnosis...

Body-stalk anomaly typically can be diagnosed by 10 to 14 weeks’ gestation via ultrasonography.^34-41 We currently follow the diagnostic criteria proposed by Van Allen and colleagues, which requires 2 of the following 3 anomalies³⁴:

• exencephaly/encephalocele with facial clefts
• thoraco- and/or abdominoschisis (midline defect)
• limb defect.

Additional ultrasonographic findings can include the identification of evisceration of the abdominal contents, a short umbilical cord, and increased nuchal thickness.^36,42 During the second and third trimesters, oligohydramnios may be seen.²

Management

Body-stalk anomaly is considered a fatal condition without specific therapeutic interventions. Maternal risks include an increased risk of preterm labor and gestational hypertension.³⁵ Research on body-stalk anomaly has not shown any correlation with patients’ age, fetal sex, or abnormal karyotype, and the reported risk of recurrence for this anomaly is very low.^42,43 Early diagnosis therefore is essential to provide families with information and counseling. Given the poor fetal prognosis, increased maternal risk, and low recurrence rates, mothers can be advised toward elective termination of pregnancy.

Should a patient desire expectant management, care can be provided by generalist obstetricians or care can be transferred to maternal-fetal medicine, with the addition of increased fetal surveillance and testing, interdisciplinary patient counseling with maternal-fetal medicine, pediatric surgeons, and neonatologists for delivery planning; delivery should be performed at a tertiary care center.

Pentalogy of Cantrell: Very rare, with variable prognosis

Pentalogy of Cantrell is characterized by a collection of defects in the midline abdominal wall, lower sternum, anterior diaphragm, diaphragmatic pericardium, and some manifestation of intra-cardiac defect.⁴⁴ It is thought to arise early in gestation due to abnormal differentiation, migration, and fusion of the embryonic mesoderm.⁴⁴ The condition is rare, with an incidence of about 1 in 5.5 million live births.⁴⁵

Making the diagnosis

The diagnosis of pentalogy of Cantrell can be made via prenatal ultrasonography as early as the first trimester, although it is diagnosed more commonly in the second trimester.⁴⁶ Three-dimensional ultrasonography and fetal MRI have been used to confirm the diagnosis.⁴⁷

Management

Typically, corrective operations are performed during the neonatal period, and cases of successful staged and one-stage operations have been reported.⁴⁸ Surgical treatment is determined based on the complexity of the condition and the presence of coexistent heart defects.^49,50 However, very few patients survive surgical repair; mortality rates are estimated at around 50% to 60%, with high postsurgical morbidity risks for those who do survive.⁴⁵

Prognosis varies depending on the type and severity of the associated malformations and intracardiac anomalies.⁴⁶ Patients with partial ectopia cordis and incomplete presentation may have more favorable outcomes, but for patients with severe ectopia cordis, the survival rate is only 5% to 10%.⁴⁷

Depending on the severity of the defects, mothers can be advised toward elective termination of pregnancy. In our institution, prenatal care usually is transferred to the maternal-fetal medicine service, and delivery is planned at our tertiary care institution.

OEIS complex comprises abdominal, pelvic, and spinal defects

Omphalocele-exstrophy-imperforate anus-spinal defects (OEIS) complex is a congenital malformation syndrome characterized by the combination of midline abdominal and pelvic defects (including omphalocele, exstrophy of the cloaca, and imperforate anus) and spinal defects.⁵¹ The condition’s etiology is unknown but is thought to be multifactorial.^51-53 It is a rare condition, with an incidence of around 1 in 200,000 to 400,000 pregnancies.⁵²

Making the diagnosis

Prenatal diagnosis of OEIS complex can be made as early as the first trimester via ultrasonographic identification of an infraumbilical abdominal wall defect with protruding mass, absent bladder, and spinal defects.⁵² When OEIS complex is suspected, fetal MRI can play a critical role in the diagnosis.

Management

As OEIS complex is rare, there are no evidence-based guidelines for optimal mode and timing of delivery. Cases are individualized based on their specific pathology, and we recommend cesarean delivery for fetuses with large defects to avoid postnatal sac rupture and liver damage.

The prognosis for infants with OEIS complex depends on the spectrum and severity of the structural defects.^52,53 The many surgeries involved in the repair of OEIS have potential complications, such as urogenital and gastrointestinal dysfunction.^52,53 Advances in medical and surgical treatment have resulted in improved survival and quality of life, and survival rates for OEIS complex are now close to 100%.⁵³ While many OEIS patients live with a permanent colostomy, improvements in management mean that more patients are now candidates for gastrointestinal pull-through procedures, which allow for natural bowel control and a higher degree of bowel cleanliness.⁵³

Prenatal care, patient counseling, and delivery planning should be individualized based on the defects present and determined in a multidisciplinary discussion with maternal-fetal medicine, neonatology, and pediatric surgery as necessary. In our institution, prenatal care usually is transferred to the maternal-fetal medicine service, and delivery is planned at our tertiary care institution.

Multidisciplinary team strategy is essential

Based on our experience, when faced with an anterior AWD in utero, prenatal imaging, genetic testing, increased fetal surveillance, and a multidisciplinary team approach improves outcomes. We must emphasize that careful patient counseling is paramount in our practice. ●

Acknowledgement: The authors would like to thank Ashley Tran, BS, for her assistance in the literature review and drafting of this article.

REFERENCES

1. Oliver SE, Gargano JW, Marin M; et al. The Advisory Committee on Immunization Practices’ interim recommendation for use of Pfizer-BioNTech COVID-19 vaccine—United States, December 2020. MMWR Morbid Mortal Wkly Rep. 2020;69:1922-1924. Accessed January 13, 2021. www.cdc.gov/mmwr/volumes/69/wr/mm6950e2.htm
2. 2. Oliver SE, Gargano JW, Marin M; et al. The Advisory Committee on Immunization Practices’ interim recommendation for use of Moderna COVID-19 vaccine—United States, December 2020. MMWR Morbid Mortal Wkly Rep. 2021;69:1653-1656. Accessed January 13, 2021. www.cdc.gov/mmwr/volumes/69/wr/mm695152e1.htm
3. CDC. COVID-19 vaccines: update on allergic reactions, contraindications, and precautions [webinar]. December 30, 2020. Accessed January 6, 2021. https://emergency.cdc.gov/coca/calls/2020/callinfo_123020.asp
4. CDC. What clinicians need to know about the Pfizer-BioNTech and Moderna COVID-19 vaccines [webinar]. December 18, 2020. Accessed January 6, 2021. https://emergency.cdc.gov/coca/calls/2020/callinfo_121820.asp
5. CDC COVID-19 Response Team; Food and Drug Administration. Allergic reactions including anaphylaxis after receipt of the first dose of Pfizer-BioNTech COVID-19 vaccine—United States, December 14-23, 2020. MMWR Morb Mortal Wkly Rep. ePub: January 6, 2021. Accessed January 13, 2021. www.cdc.gov/mmwr/volumes/70/wr/mm7002e1.htm

REFERENCES

1. Oliver SE, Gargano JW, Marin M; et al. The Advisory Committee on Immunization Practices’ interim recommendation for use of Pfizer-BioNTech COVID-19 vaccine—United States, December 2020. MMWR Morbid Mortal Wkly Rep. 2020;69:1922-1924. Accessed January 13, 2021. www.cdc.gov/mmwr/volumes/69/wr/mm6950e2.htm
2. 2. Oliver SE, Gargano JW, Marin M; et al. The Advisory Committee on Immunization Practices’ interim recommendation for use of Moderna COVID-19 vaccine—United States, December 2020. MMWR Morbid Mortal Wkly Rep. 2021;69:1653-1656. Accessed January 13, 2021. www.cdc.gov/mmwr/volumes/69/wr/mm695152e1.htm
3. CDC. COVID-19 vaccines: update on allergic reactions, contraindications, and precautions [webinar]. December 30, 2020. Accessed January 6, 2021. https://emergency.cdc.gov/coca/calls/2020/callinfo_123020.asp
4. CDC. What clinicians need to know about the Pfizer-BioNTech and Moderna COVID-19 vaccines [webinar]. December 18, 2020. Accessed January 6, 2021. https://emergency.cdc.gov/coca/calls/2020/callinfo_121820.asp
5. CDC COVID-19 Response Team; Food and Drug Administration. Allergic reactions including anaphylaxis after receipt of the first dose of Pfizer-BioNTech COVID-19 vaccine—United States, December 14-23, 2020. MMWR Morb Mortal Wkly Rep. ePub: January 6, 2021. Accessed January 13, 2021. www.cdc.gov/mmwr/volumes/70/wr/mm7002e1.htm

REFERENCES

1. Oliver SE, Gargano JW, Marin M; et al. The Advisory Committee on Immunization Practices’ interim recommendation for use of Pfizer-BioNTech COVID-19 vaccine—United States, December 2020. MMWR Morbid Mortal Wkly Rep. 2020;69:1922-1924. Accessed January 13, 2021. www.cdc.gov/mmwr/volumes/69/wr/mm6950e2.htm
2. 2. Oliver SE, Gargano JW, Marin M; et al. The Advisory Committee on Immunization Practices’ interim recommendation for use of Moderna COVID-19 vaccine—United States, December 2020. MMWR Morbid Mortal Wkly Rep. 2021;69:1653-1656. Accessed January 13, 2021. www.cdc.gov/mmwr/volumes/69/wr/mm695152e1.htm
3. CDC. COVID-19 vaccines: update on allergic reactions, contraindications, and precautions [webinar]. December 30, 2020. Accessed January 6, 2021. https://emergency.cdc.gov/coca/calls/2020/callinfo_123020.asp
4. CDC. What clinicians need to know about the Pfizer-BioNTech and Moderna COVID-19 vaccines [webinar]. December 18, 2020. Accessed January 6, 2021. https://emergency.cdc.gov/coca/calls/2020/callinfo_121820.asp
5. CDC COVID-19 Response Team; Food and Drug Administration. Allergic reactions including anaphylaxis after receipt of the first dose of Pfizer-BioNTech COVID-19 vaccine—United States, December 14-23, 2020. MMWR Morb Mortal Wkly Rep. ePub: January 6, 2021. Accessed January 13, 2021. www.cdc.gov/mmwr/volumes/70/wr/mm7002e1.htm

Yland JJ, Bresnick KA, Hatch EE, et al. Pregravid contraceptive use and fecundability: prospective cohort study. BMJ. 2020;371:m3966.

EXPERT COMMENTARY

Most US women aged 15 to 49 currently use contraception, with long-acting reversible contraception (LARC)—IUDs and the contraceptive implant—increasing in popularity over the last decade.¹ Oral contraceptive pills, male condoms, and LARC are the most common reversible methods used.¹ While the efficacy and safety of contraception have been established, few studies have examined the effect of recent contraceptive use on fertility.

Fecundability is the probability of pregnancy during a single menstrual cycle for a couple engaging in regular intercourse and not using contraception.² Small studies have found short-term reductions in fecundability after discontinuing combined oral contraceptives and larger reductions after stopping injectable contraceptives, with no long-term differences among methods.^3,4

Data are limited regarding the effects of other forms of contraception on fecundability, particularly LARC methods. A recent study was designed to evaluate the association between the last contraceptive method used and subsequent fecundability.²

Details of the study

Yland and colleagues pooled data from 3 prospective cohort studies of 17,954 women planning pregnancies in Denmark, Canada, and the United States. Participants reported the contraceptive method used most recently before trying to conceive. They completed questionnaires every 2 months for 12 months or until they reported a pregnancy. Women were excluded if they tried to conceive for more than 6 menstrual cycles at study entry.

The authors calculated the fecundability ratio—the average probability of conception per cycle for a specific contraceptive method compared with a reference method—using proportional probability models adjusted for potential confounders. They also calculated pregnancy attempt time using participant-reported menstrual cycle length and date of last menstrual period during follow-up questionnaires.

Continue to: Injectable contraceptives associated with longest delayed fertility return...

After adjusting for personal factors, medical history, lifestyle characteristics, and indicators of underlying fertility, the authors found that injectable contraceptive use was associated with decreased fecundability compared with barrier method use (fecundability ratio [FR], 0.65; 95% confidence interval [CI], 0.47–0.89). Hormonal IUD use was associated with slight increases in fecundability compared with barrier method use (FR, 1.14; 95% CI, 1.07–1.22) and copper IUD use (FR, 1.18; 95% CI, 1.05–1.33). All other contraceptive methods were not significantly different from barrier methods.

LARC method use was associated with the shortest delay in return of normal fertility (2 cycles), followed by oral and ring contraceptives (3 cycles) and patch (4 cycles). Women using injectable contraceptives experienced the longest delay (5–8 menstrual cycles). Lifetime duration of contraceptive use did not impact fecundability in the North American cohort.

Study strengths and limitations

This large, prospective study contributes useful information about fecundability after stopping contraceptive methods. It confirms earlier studies’ findings that showed decreased fecundability after stopping injectable contraceptives. Study participants’ most recent method used was similar to overall US method distribution.¹

Study limitations include online recruitment of self-selecting participants, which introduces selection bias. The study population was overwhelmingly white (92%) and highly educated (70% with college degrees), quite different from the US population. These findings may therefore have limited generalizability. Additionally, injectable contraceptive users had higher body mass index and were more likely to smoke and have diabetes, infertility, or irregular menstrual cycles. IUD users were more likely to be parous and have a history of unplanned pregnancy, indicating possible higher baseline fertility. Even after adjusting, possible unmeasured factors could impact study results. ●

Yland JJ, Bresnick KA, Hatch EE, et al. Pregravid contraceptive use and fecundability: prospective cohort study. BMJ. 2020;371:m3966.

EXPERT COMMENTARY

Most US women aged 15 to 49 currently use contraception, with long-acting reversible contraception (LARC)—IUDs and the contraceptive implant—increasing in popularity over the last decade.¹ Oral contraceptive pills, male condoms, and LARC are the most common reversible methods used.¹ While the efficacy and safety of contraception have been established, few studies have examined the effect of recent contraceptive use on fertility.

Fecundability is the probability of pregnancy during a single menstrual cycle for a couple engaging in regular intercourse and not using contraception.² Small studies have found short-term reductions in fecundability after discontinuing combined oral contraceptives and larger reductions after stopping injectable contraceptives, with no long-term differences among methods.^3,4

Data are limited regarding the effects of other forms of contraception on fecundability, particularly LARC methods. A recent study was designed to evaluate the association between the last contraceptive method used and subsequent fecundability.²

Details of the study

Yland and colleagues pooled data from 3 prospective cohort studies of 17,954 women planning pregnancies in Denmark, Canada, and the United States. Participants reported the contraceptive method used most recently before trying to conceive. They completed questionnaires every 2 months for 12 months or until they reported a pregnancy. Women were excluded if they tried to conceive for more than 6 menstrual cycles at study entry.

The authors calculated the fecundability ratio—the average probability of conception per cycle for a specific contraceptive method compared with a reference method—using proportional probability models adjusted for potential confounders. They also calculated pregnancy attempt time using participant-reported menstrual cycle length and date of last menstrual period during follow-up questionnaires.

Continue to: Injectable contraceptives associated with longest delayed fertility return...

After adjusting for personal factors, medical history, lifestyle characteristics, and indicators of underlying fertility, the authors found that injectable contraceptive use was associated with decreased fecundability compared with barrier method use (fecundability ratio [FR], 0.65; 95% confidence interval [CI], 0.47–0.89). Hormonal IUD use was associated with slight increases in fecundability compared with barrier method use (FR, 1.14; 95% CI, 1.07–1.22) and copper IUD use (FR, 1.18; 95% CI, 1.05–1.33). All other contraceptive methods were not significantly different from barrier methods.

LARC method use was associated with the shortest delay in return of normal fertility (2 cycles), followed by oral and ring contraceptives (3 cycles) and patch (4 cycles). Women using injectable contraceptives experienced the longest delay (5–8 menstrual cycles). Lifetime duration of contraceptive use did not impact fecundability in the North American cohort.

Study strengths and limitations

This large, prospective study contributes useful information about fecundability after stopping contraceptive methods. It confirms earlier studies’ findings that showed decreased fecundability after stopping injectable contraceptives. Study participants’ most recent method used was similar to overall US method distribution.¹

Study limitations include online recruitment of self-selecting participants, which introduces selection bias. The study population was overwhelmingly white (92%) and highly educated (70% with college degrees), quite different from the US population. These findings may therefore have limited generalizability. Additionally, injectable contraceptive users had higher body mass index and were more likely to smoke and have diabetes, infertility, or irregular menstrual cycles. IUD users were more likely to be parous and have a history of unplanned pregnancy, indicating possible higher baseline fertility. Even after adjusting, possible unmeasured factors could impact study results. ●

Yland JJ, Bresnick KA, Hatch EE, et al. Pregravid contraceptive use and fecundability: prospective cohort study. BMJ. 2020;371:m3966.

EXPERT COMMENTARY

Most US women aged 15 to 49 currently use contraception, with long-acting reversible contraception (LARC)—IUDs and the contraceptive implant—increasing in popularity over the last decade.¹ Oral contraceptive pills, male condoms, and LARC are the most common reversible methods used.¹ While the efficacy and safety of contraception have been established, few studies have examined the effect of recent contraceptive use on fertility.

Fecundability is the probability of pregnancy during a single menstrual cycle for a couple engaging in regular intercourse and not using contraception.² Small studies have found short-term reductions in fecundability after discontinuing combined oral contraceptives and larger reductions after stopping injectable contraceptives, with no long-term differences among methods.^3,4

Data are limited regarding the effects of other forms of contraception on fecundability, particularly LARC methods. A recent study was designed to evaluate the association between the last contraceptive method used and subsequent fecundability.²

Details of the study

Yland and colleagues pooled data from 3 prospective cohort studies of 17,954 women planning pregnancies in Denmark, Canada, and the United States. Participants reported the contraceptive method used most recently before trying to conceive. They completed questionnaires every 2 months for 12 months or until they reported a pregnancy. Women were excluded if they tried to conceive for more than 6 menstrual cycles at study entry.

The authors calculated the fecundability ratio—the average probability of conception per cycle for a specific contraceptive method compared with a reference method—using proportional probability models adjusted for potential confounders. They also calculated pregnancy attempt time using participant-reported menstrual cycle length and date of last menstrual period during follow-up questionnaires.

Continue to: Injectable contraceptives associated with longest delayed fertility return...

After adjusting for personal factors, medical history, lifestyle characteristics, and indicators of underlying fertility, the authors found that injectable contraceptive use was associated with decreased fecundability compared with barrier method use (fecundability ratio [FR], 0.65; 95% confidence interval [CI], 0.47–0.89). Hormonal IUD use was associated with slight increases in fecundability compared with barrier method use (FR, 1.14; 95% CI, 1.07–1.22) and copper IUD use (FR, 1.18; 95% CI, 1.05–1.33). All other contraceptive methods were not significantly different from barrier methods.

LARC method use was associated with the shortest delay in return of normal fertility (2 cycles), followed by oral and ring contraceptives (3 cycles) and patch (4 cycles). Women using injectable contraceptives experienced the longest delay (5–8 menstrual cycles). Lifetime duration of contraceptive use did not impact fecundability in the North American cohort.

Study strengths and limitations

This large, prospective study contributes useful information about fecundability after stopping contraceptive methods. It confirms earlier studies’ findings that showed decreased fecundability after stopping injectable contraceptives. Study participants’ most recent method used was similar to overall US method distribution.¹

Study limitations include online recruitment of self-selecting participants, which introduces selection bias. The study population was overwhelmingly white (92%) and highly educated (70% with college degrees), quite different from the US population. These findings may therefore have limited generalizability. Additionally, injectable contraceptive users had higher body mass index and were more likely to smoke and have diabetes, infertility, or irregular menstrual cycles. IUD users were more likely to be parous and have a history of unplanned pregnancy, indicating possible higher baseline fertility. Even after adjusting, possible unmeasured factors could impact study results. ●

Oxytocin is the hormone most commonly administered to women on labor and delivery. It is used for induction of labor, augmentation of labor, and to reduce the risk of postpartum hemorrhage. Licensed independent prescribers, including physicians and nurse midwives, order oxytocin, and licensed professional nurses execute the order by administering the hormone. Optimal management of oxytocin infusion requires effective interprofessional communication and collaboration. During labor it is common for disagreements to arise between the professionals ordering and the professionals administering oxytocin. The disagreements are usually caused by differing perspectives on the appropriate oxytocin dose. Standardized protocols and checklists reduce practice variation and improve patient safety.

Oxytocin hormone

Oxytocin is a cyclic nonapeptide synthesized in the hypothalamus and secreted into the circulation from axonal terminals in the posterior pituitary. In the myometrium, oxytocin activates a membrane G protein-coupled receptor, increasing phospholipase C and intracellular calcium. Following several intracellular chemical cascades, oxytocin stimulation results in myosin and actin filaments sliding over each other initiating shortening of the smooth muscle cell. Myometrial smooth muscle cells are connected by gap junctions, facilitating the coordinated contraction of the uterus.¹

Oxytocin pulse frequency and uterine oxytocin receptor concentration both increase during pregnancy and labor, facilitating the birth process. Oxytocin pulse frequency increases from 2.4 pulses per hour before labor to 13.4 pulses per hour in the second stage.² In addition, uterine oxytocin receptor concentration increases 12-fold from the early second trimester of pregnancy to term.³

Oxytocin has a half-life of approximately 10 to 15 minutes. Many pharmacologists believe that for a given dose of a drug, it takes 4 to 5 half-lives for a stabilized circulating concentration to be achieved. Therefore, during an oxytocin infusion, when the dose is increased it may take 40 to 50 minutes to achieve a new higher, stabile circulating concentration.⁴

Low-dose vs high-dose oxytocin protocols

Oxytocin is often used in a premixed solution of 30 units of oxytocin in 500 mL of lactated Ringer’s solution. With this mixture, an infusion of 1 mL/hour results in the administration of 1 mU of oxytocin per minute (1 mU/min). There is no national consensus on an optimal oxytocin infusion regimen for induction or augmentation of labor. A commonly used low-dose regimen is an initial dose of 1 to 2 mU/min, with a dose increase of 1 to 2 mU/min every 30 to 40 minutes until regular uterine contractions occur every 2 to 3 minutes.⁵ An example of a high-dose oxytocin regimen is an initial dose of 6 mU/min with an increase of 3 to 6 mU/min every 30 to 40 minutes (induction of labor).⁶

A randomized trial reported that, compared with a low-dose oxytocin regimen, a high-dose regimen increased the risk of tachysystole without a significant change in cesarean birth rate.⁷ A Cochrane review concluded that, compared with low-dose regimens, high-dose oxytocin regimens were more likely to be associated with tachysystole.⁸ Based on these reports, I would suggest avoiding the use of a high-dose oxytocin regimen. Experts have reported that an oxytocin dose of approximately 6 mU/min achieves a circulating oxytocin concentration similar to that observed in normal spontaneous labor.⁹

Continue to: Maximum dose of oxytocin infusion...

Maximum dose of oxytocin infusion

There is no national consensus on the maximum safe dose of oxytocin for induction or augmentation of labor. Many labor and delivery units have a protocol where the maximum dose of oxytocin is 20 mU/min for women in the following clinical situations: previous vaginal delivery, prior cesarean delivery, multiple gestation, and nulliparous women in the second stage of labor. A maximum oxytocin dose of 30 mU/min may be appropriate for nulliparous women in the first stage of labor. Some units permit an oxytocin dose of 40 mU/min. Many labor nurses are concerned that an oxytocin dose that high may be associated with an increased frequency of adverse effects.

Management of the oxytocin dose when tachysystole is diagnosed

Tachysystole is defined as more than 5 uterine contractions in 10 minutes averaged over 30 minutes.^5,6 Because uterine contractions cause a reduction in oxygen delivery to the fetus, tachysystole, prolonged uterine contractions, and sustained elevated intrauterine pressure can result in fetal hypoxia and an abnormal fetal heart rate (FHR) pattern. If tachysystole is detected and the FHR pattern is Category 1, the oxytocin dose should be reduced. If tachysystole is detected and the FHR pattern is a concerning Category 2 or Category 3 pattern, the oxytocin infusion should be discontinued until the concerning FHR pattern resolves. If tachysystole is diagnosed, changing the maternal position (ensuring a lateral maternal position) and administering an intravenous bolus of 500 mL of lactated Ringer’s solution may help resolve an abnormal FHR. Terbutaline 0.25 mg, administered by subcutaneous injection, may be given to reduce myometrial contractility. Following resolution of an episode of tachysystole with a concerning FHR tracing, the oxytocin infusion can be restarted at a dose less than the dose that was associated with the tachysystole.

Inadvertent excess oxytocin administration

Oxytocin only should be administered using a computerized medication infusion pump with the oxytocin line piggybacked into a main infusion line.⁵ Occasionally, an excessively large bolus of oxytocin is administered inadvertently because the oxytocin line was mistakenly thought to be the main line or because of an infusion pump failure. These situations usually result in a tetanic contraction that will need to be treated by the immediate discontinuation of the oxytocin infusion, a fluid bolus, and one or more doses of terbutaline.

Reduction in oxytocin dose as labor progresses

Many investigators have reported that once rapid cervical dilation is occurring, or in the second stage of labor, the dose of exogenous oxytocin often can be reduced without stalling the progress of labor. Dilation of the vagina and pelvic floor, which occurs late in the process of labor, is a powerful stimulus for the release of oxytocin from the posterior pituitary.^10,11 The marked increase in endogenous secretion of oxytocin during the second stage of labor may be the reason that the exogenous oxytocin infusion can be reduced or discontinued.

In a systematic review and meta-analysis, discontinuation of oxytocin after 5 cm of cervical dilation was associated with a reduced rate of uterine tachysystole and no increase in cesarean delivery.¹² A Cochrane evidence-based review also concluded that once rapid cervical dilation is occurring, the dose of oxytocin can be reduced with a decrease in the rate of tachysystole with an abnormal FHR and without an increase in the rate of cesarean delivery.¹³

Continue to: Management of the oxytocin dose is a common cause of clinical disagreement...

Management of the oxytocin dose is a common cause of clinical disagreement

As noted in two recent research studies, experienced independent professional labor nurses often feel pressured by obstetricians to increase the dose of oxytocin. One nurse reported that physicians “like the pit pushed and you’d better push it and go, go, go, otherwise they’ll be…really mad if it is not going.” Many obstetricians favor working with a labor nurse who will actively manage labor by aggressively increasing the oxytocin dose. One obstetrician reported, “When I hear I’ve got a nurse who will go up on the pit, I know it’s going to be a good day.”¹⁴

Obstetricians and labor nurses with a good relationship can openly discuss differing perspectives and find a compromise solution. However, if the relationship is not good, the conflict may not be resolved, and the labor nurse may use a passive-aggressive approach to the situation. As one nurse reported, “It actually depends on the doctor and his personality. I know that there were times when I had a doc who would throw a fit if I didn’t up the pitocin, so I would pacify him by agreeing to, but never would.”¹⁵

An oxytocin checklist may help to reduce conflict over the optimal management of oxytocin infusion and improve patient safety.¹⁶ Practice variation among nurses, obstetricians, and nurse midwives may contribute to difficulty in achieving a consensus on how to manage oxytocin. One approach to reducing practice variation is to use checklists to improve collaboration and uniformity on a clinical team. Clark and colleagues describe the beneficial effect of both a pre-oxytocin checklist and an oxytocin in-use checklist.¹⁶ Their in-use checklist, which is completed every 30 minutes by the labor nurse, recommended decreasing the dose of oxytocin unless the FHR is reassuring and no tachysystole has occurred. In one retrospective study, when compared against outcomes prior to the use of a checklist, the use of the checklist resulted in a lower maximum dose of oxytocin (11.4 vs 13.8 mU/min; P = .003), a greater 1-minute Apgar score at birth (7.9 vs 7.6; P = .048), and no increase in time to delivery (8.2 vs 8.5 hours) or cesarean delivery rate (13% vs 15%).¹⁶ When nurses and obstetricians collaborate using an oxytocin in-use checklist, both clinical variation and probability of conflict are reduced.

Consider use of a checklist to reduce conflict

Oxytocin infusion for induction or augmentation of labor is one of the most common and most important interventions on labor and delivery units. Oxytocin infusion practices vary widely among labor and delivery units. In addition to the lack of a consensus national standard, within any one labor unit the perspectives of obstetricians and labor nurses regarding the management of oxytocin infusions often differ, leading to conflict. The use of an oxytocin in-use checklist may help to reduce variability and improve patient outcomes.¹⁷ ●

Oxytocin is the hormone most commonly administered to women on labor and delivery. It is used for induction of labor, augmentation of labor, and to reduce the risk of postpartum hemorrhage. Licensed independent prescribers, including physicians and nurse midwives, order oxytocin, and licensed professional nurses execute the order by administering the hormone. Optimal management of oxytocin infusion requires effective interprofessional communication and collaboration. During labor it is common for disagreements to arise between the professionals ordering and the professionals administering oxytocin. The disagreements are usually caused by differing perspectives on the appropriate oxytocin dose. Standardized protocols and checklists reduce practice variation and improve patient safety.

Oxytocin hormone

Oxytocin is a cyclic nonapeptide synthesized in the hypothalamus and secreted into the circulation from axonal terminals in the posterior pituitary. In the myometrium, oxytocin activates a membrane G protein-coupled receptor, increasing phospholipase C and intracellular calcium. Following several intracellular chemical cascades, oxytocin stimulation results in myosin and actin filaments sliding over each other initiating shortening of the smooth muscle cell. Myometrial smooth muscle cells are connected by gap junctions, facilitating the coordinated contraction of the uterus.¹

Oxytocin pulse frequency and uterine oxytocin receptor concentration both increase during pregnancy and labor, facilitating the birth process. Oxytocin pulse frequency increases from 2.4 pulses per hour before labor to 13.4 pulses per hour in the second stage.² In addition, uterine oxytocin receptor concentration increases 12-fold from the early second trimester of pregnancy to term.³

Oxytocin has a half-life of approximately 10 to 15 minutes. Many pharmacologists believe that for a given dose of a drug, it takes 4 to 5 half-lives for a stabilized circulating concentration to be achieved. Therefore, during an oxytocin infusion, when the dose is increased it may take 40 to 50 minutes to achieve a new higher, stabile circulating concentration.⁴

Low-dose vs high-dose oxytocin protocols

Oxytocin is often used in a premixed solution of 30 units of oxytocin in 500 mL of lactated Ringer’s solution. With this mixture, an infusion of 1 mL/hour results in the administration of 1 mU of oxytocin per minute (1 mU/min). There is no national consensus on an optimal oxytocin infusion regimen for induction or augmentation of labor. A commonly used low-dose regimen is an initial dose of 1 to 2 mU/min, with a dose increase of 1 to 2 mU/min every 30 to 40 minutes until regular uterine contractions occur every 2 to 3 minutes.⁵ An example of a high-dose oxytocin regimen is an initial dose of 6 mU/min with an increase of 3 to 6 mU/min every 30 to 40 minutes (induction of labor).⁶

A randomized trial reported that, compared with a low-dose oxytocin regimen, a high-dose regimen increased the risk of tachysystole without a significant change in cesarean birth rate.⁷ A Cochrane review concluded that, compared with low-dose regimens, high-dose oxytocin regimens were more likely to be associated with tachysystole.⁸ Based on these reports, I would suggest avoiding the use of a high-dose oxytocin regimen. Experts have reported that an oxytocin dose of approximately 6 mU/min achieves a circulating oxytocin concentration similar to that observed in normal spontaneous labor.⁹

Continue to: Maximum dose of oxytocin infusion...

Maximum dose of oxytocin infusion

There is no national consensus on the maximum safe dose of oxytocin for induction or augmentation of labor. Many labor and delivery units have a protocol where the maximum dose of oxytocin is 20 mU/min for women in the following clinical situations: previous vaginal delivery, prior cesarean delivery, multiple gestation, and nulliparous women in the second stage of labor. A maximum oxytocin dose of 30 mU/min may be appropriate for nulliparous women in the first stage of labor. Some units permit an oxytocin dose of 40 mU/min. Many labor nurses are concerned that an oxytocin dose that high may be associated with an increased frequency of adverse effects.

Management of the oxytocin dose when tachysystole is diagnosed

Tachysystole is defined as more than 5 uterine contractions in 10 minutes averaged over 30 minutes.^5,6 Because uterine contractions cause a reduction in oxygen delivery to the fetus, tachysystole, prolonged uterine contractions, and sustained elevated intrauterine pressure can result in fetal hypoxia and an abnormal fetal heart rate (FHR) pattern. If tachysystole is detected and the FHR pattern is Category 1, the oxytocin dose should be reduced. If tachysystole is detected and the FHR pattern is a concerning Category 2 or Category 3 pattern, the oxytocin infusion should be discontinued until the concerning FHR pattern resolves. If tachysystole is diagnosed, changing the maternal position (ensuring a lateral maternal position) and administering an intravenous bolus of 500 mL of lactated Ringer’s solution may help resolve an abnormal FHR. Terbutaline 0.25 mg, administered by subcutaneous injection, may be given to reduce myometrial contractility. Following resolution of an episode of tachysystole with a concerning FHR tracing, the oxytocin infusion can be restarted at a dose less than the dose that was associated with the tachysystole.

Inadvertent excess oxytocin administration

Oxytocin only should be administered using a computerized medication infusion pump with the oxytocin line piggybacked into a main infusion line.⁵ Occasionally, an excessively large bolus of oxytocin is administered inadvertently because the oxytocin line was mistakenly thought to be the main line or because of an infusion pump failure. These situations usually result in a tetanic contraction that will need to be treated by the immediate discontinuation of the oxytocin infusion, a fluid bolus, and one or more doses of terbutaline.

Reduction in oxytocin dose as labor progresses

Many investigators have reported that once rapid cervical dilation is occurring, or in the second stage of labor, the dose of exogenous oxytocin often can be reduced without stalling the progress of labor. Dilation of the vagina and pelvic floor, which occurs late in the process of labor, is a powerful stimulus for the release of oxytocin from the posterior pituitary.^10,11 The marked increase in endogenous secretion of oxytocin during the second stage of labor may be the reason that the exogenous oxytocin infusion can be reduced or discontinued.

In a systematic review and meta-analysis, discontinuation of oxytocin after 5 cm of cervical dilation was associated with a reduced rate of uterine tachysystole and no increase in cesarean delivery.¹² A Cochrane evidence-based review also concluded that once rapid cervical dilation is occurring, the dose of oxytocin can be reduced with a decrease in the rate of tachysystole with an abnormal FHR and without an increase in the rate of cesarean delivery.¹³

Continue to: Management of the oxytocin dose is a common cause of clinical disagreement...

Management of the oxytocin dose is a common cause of clinical disagreement

As noted in two recent research studies, experienced independent professional labor nurses often feel pressured by obstetricians to increase the dose of oxytocin. One nurse reported that physicians “like the pit pushed and you’d better push it and go, go, go, otherwise they’ll be…really mad if it is not going.” Many obstetricians favor working with a labor nurse who will actively manage labor by aggressively increasing the oxytocin dose. One obstetrician reported, “When I hear I’ve got a nurse who will go up on the pit, I know it’s going to be a good day.”¹⁴

Obstetricians and labor nurses with a good relationship can openly discuss differing perspectives and find a compromise solution. However, if the relationship is not good, the conflict may not be resolved, and the labor nurse may use a passive-aggressive approach to the situation. As one nurse reported, “It actually depends on the doctor and his personality. I know that there were times when I had a doc who would throw a fit if I didn’t up the pitocin, so I would pacify him by agreeing to, but never would.”¹⁵

An oxytocin checklist may help to reduce conflict over the optimal management of oxytocin infusion and improve patient safety.¹⁶ Practice variation among nurses, obstetricians, and nurse midwives may contribute to difficulty in achieving a consensus on how to manage oxytocin. One approach to reducing practice variation is to use checklists to improve collaboration and uniformity on a clinical team. Clark and colleagues describe the beneficial effect of both a pre-oxytocin checklist and an oxytocin in-use checklist.¹⁶ Their in-use checklist, which is completed every 30 minutes by the labor nurse, recommended decreasing the dose of oxytocin unless the FHR is reassuring and no tachysystole has occurred. In one retrospective study, when compared against outcomes prior to the use of a checklist, the use of the checklist resulted in a lower maximum dose of oxytocin (11.4 vs 13.8 mU/min; P = .003), a greater 1-minute Apgar score at birth (7.9 vs 7.6; P = .048), and no increase in time to delivery (8.2 vs 8.5 hours) or cesarean delivery rate (13% vs 15%).¹⁶ When nurses and obstetricians collaborate using an oxytocin in-use checklist, both clinical variation and probability of conflict are reduced.

Consider use of a checklist to reduce conflict

Oxytocin infusion for induction or augmentation of labor is one of the most common and most important interventions on labor and delivery units. Oxytocin infusion practices vary widely among labor and delivery units. In addition to the lack of a consensus national standard, within any one labor unit the perspectives of obstetricians and labor nurses regarding the management of oxytocin infusions often differ, leading to conflict. The use of an oxytocin in-use checklist may help to reduce variability and improve patient outcomes.¹⁷ ●

Oxytocin is the hormone most commonly administered to women on labor and delivery. It is used for induction of labor, augmentation of labor, and to reduce the risk of postpartum hemorrhage. Licensed independent prescribers, including physicians and nurse midwives, order oxytocin, and licensed professional nurses execute the order by administering the hormone. Optimal management of oxytocin infusion requires effective interprofessional communication and collaboration. During labor it is common for disagreements to arise between the professionals ordering and the professionals administering oxytocin. The disagreements are usually caused by differing perspectives on the appropriate oxytocin dose. Standardized protocols and checklists reduce practice variation and improve patient safety.

Oxytocin hormone

Oxytocin is a cyclic nonapeptide synthesized in the hypothalamus and secreted into the circulation from axonal terminals in the posterior pituitary. In the myometrium, oxytocin activates a membrane G protein-coupled receptor, increasing phospholipase C and intracellular calcium. Following several intracellular chemical cascades, oxytocin stimulation results in myosin and actin filaments sliding over each other initiating shortening of the smooth muscle cell. Myometrial smooth muscle cells are connected by gap junctions, facilitating the coordinated contraction of the uterus.¹

Oxytocin pulse frequency and uterine oxytocin receptor concentration both increase during pregnancy and labor, facilitating the birth process. Oxytocin pulse frequency increases from 2.4 pulses per hour before labor to 13.4 pulses per hour in the second stage.² In addition, uterine oxytocin receptor concentration increases 12-fold from the early second trimester of pregnancy to term.³

Oxytocin has a half-life of approximately 10 to 15 minutes. Many pharmacologists believe that for a given dose of a drug, it takes 4 to 5 half-lives for a stabilized circulating concentration to be achieved. Therefore, during an oxytocin infusion, when the dose is increased it may take 40 to 50 minutes to achieve a new higher, stabile circulating concentration.⁴

Low-dose vs high-dose oxytocin protocols

Oxytocin is often used in a premixed solution of 30 units of oxytocin in 500 mL of lactated Ringer’s solution. With this mixture, an infusion of 1 mL/hour results in the administration of 1 mU of oxytocin per minute (1 mU/min). There is no national consensus on an optimal oxytocin infusion regimen for induction or augmentation of labor. A commonly used low-dose regimen is an initial dose of 1 to 2 mU/min, with a dose increase of 1 to 2 mU/min every 30 to 40 minutes until regular uterine contractions occur every 2 to 3 minutes.⁵ An example of a high-dose oxytocin regimen is an initial dose of 6 mU/min with an increase of 3 to 6 mU/min every 30 to 40 minutes (induction of labor).⁶

A randomized trial reported that, compared with a low-dose oxytocin regimen, a high-dose regimen increased the risk of tachysystole without a significant change in cesarean birth rate.⁷ A Cochrane review concluded that, compared with low-dose regimens, high-dose oxytocin regimens were more likely to be associated with tachysystole.⁸ Based on these reports, I would suggest avoiding the use of a high-dose oxytocin regimen. Experts have reported that an oxytocin dose of approximately 6 mU/min achieves a circulating oxytocin concentration similar to that observed in normal spontaneous labor.⁹

Continue to: Maximum dose of oxytocin infusion...

Maximum dose of oxytocin infusion

There is no national consensus on the maximum safe dose of oxytocin for induction or augmentation of labor. Many labor and delivery units have a protocol where the maximum dose of oxytocin is 20 mU/min for women in the following clinical situations: previous vaginal delivery, prior cesarean delivery, multiple gestation, and nulliparous women in the second stage of labor. A maximum oxytocin dose of 30 mU/min may be appropriate for nulliparous women in the first stage of labor. Some units permit an oxytocin dose of 40 mU/min. Many labor nurses are concerned that an oxytocin dose that high may be associated with an increased frequency of adverse effects.

Management of the oxytocin dose when tachysystole is diagnosed

Tachysystole is defined as more than 5 uterine contractions in 10 minutes averaged over 30 minutes.^5,6 Because uterine contractions cause a reduction in oxygen delivery to the fetus, tachysystole, prolonged uterine contractions, and sustained elevated intrauterine pressure can result in fetal hypoxia and an abnormal fetal heart rate (FHR) pattern. If tachysystole is detected and the FHR pattern is Category 1, the oxytocin dose should be reduced. If tachysystole is detected and the FHR pattern is a concerning Category 2 or Category 3 pattern, the oxytocin infusion should be discontinued until the concerning FHR pattern resolves. If tachysystole is diagnosed, changing the maternal position (ensuring a lateral maternal position) and administering an intravenous bolus of 500 mL of lactated Ringer’s solution may help resolve an abnormal FHR. Terbutaline 0.25 mg, administered by subcutaneous injection, may be given to reduce myometrial contractility. Following resolution of an episode of tachysystole with a concerning FHR tracing, the oxytocin infusion can be restarted at a dose less than the dose that was associated with the tachysystole.

Inadvertent excess oxytocin administration

Oxytocin only should be administered using a computerized medication infusion pump with the oxytocin line piggybacked into a main infusion line.⁵ Occasionally, an excessively large bolus of oxytocin is administered inadvertently because the oxytocin line was mistakenly thought to be the main line or because of an infusion pump failure. These situations usually result in a tetanic contraction that will need to be treated by the immediate discontinuation of the oxytocin infusion, a fluid bolus, and one or more doses of terbutaline.

Reduction in oxytocin dose as labor progresses

Many investigators have reported that once rapid cervical dilation is occurring, or in the second stage of labor, the dose of exogenous oxytocin often can be reduced without stalling the progress of labor. Dilation of the vagina and pelvic floor, which occurs late in the process of labor, is a powerful stimulus for the release of oxytocin from the posterior pituitary.^10,11 The marked increase in endogenous secretion of oxytocin during the second stage of labor may be the reason that the exogenous oxytocin infusion can be reduced or discontinued.

In a systematic review and meta-analysis, discontinuation of oxytocin after 5 cm of cervical dilation was associated with a reduced rate of uterine tachysystole and no increase in cesarean delivery.¹² A Cochrane evidence-based review also concluded that once rapid cervical dilation is occurring, the dose of oxytocin can be reduced with a decrease in the rate of tachysystole with an abnormal FHR and without an increase in the rate of cesarean delivery.¹³

Continue to: Management of the oxytocin dose is a common cause of clinical disagreement...

Management of the oxytocin dose is a common cause of clinical disagreement

As noted in two recent research studies, experienced independent professional labor nurses often feel pressured by obstetricians to increase the dose of oxytocin. One nurse reported that physicians “like the pit pushed and you’d better push it and go, go, go, otherwise they’ll be…really mad if it is not going.” Many obstetricians favor working with a labor nurse who will actively manage labor by aggressively increasing the oxytocin dose. One obstetrician reported, “When I hear I’ve got a nurse who will go up on the pit, I know it’s going to be a good day.”¹⁴

Obstetricians and labor nurses with a good relationship can openly discuss differing perspectives and find a compromise solution. However, if the relationship is not good, the conflict may not be resolved, and the labor nurse may use a passive-aggressive approach to the situation. As one nurse reported, “It actually depends on the doctor and his personality. I know that there were times when I had a doc who would throw a fit if I didn’t up the pitocin, so I would pacify him by agreeing to, but never would.”¹⁵

An oxytocin checklist may help to reduce conflict over the optimal management of oxytocin infusion and improve patient safety.¹⁶ Practice variation among nurses, obstetricians, and nurse midwives may contribute to difficulty in achieving a consensus on how to manage oxytocin. One approach to reducing practice variation is to use checklists to improve collaboration and uniformity on a clinical team. Clark and colleagues describe the beneficial effect of both a pre-oxytocin checklist and an oxytocin in-use checklist.¹⁶ Their in-use checklist, which is completed every 30 minutes by the labor nurse, recommended decreasing the dose of oxytocin unless the FHR is reassuring and no tachysystole has occurred. In one retrospective study, when compared against outcomes prior to the use of a checklist, the use of the checklist resulted in a lower maximum dose of oxytocin (11.4 vs 13.8 mU/min; P = .003), a greater 1-minute Apgar score at birth (7.9 vs 7.6; P = .048), and no increase in time to delivery (8.2 vs 8.5 hours) or cesarean delivery rate (13% vs 15%).¹⁶ When nurses and obstetricians collaborate using an oxytocin in-use checklist, both clinical variation and probability of conflict are reduced.

Consider use of a checklist to reduce conflict

Oxytocin infusion for induction or augmentation of labor is one of the most common and most important interventions on labor and delivery units. Oxytocin infusion practices vary widely among labor and delivery units. In addition to the lack of a consensus national standard, within any one labor unit the perspectives of obstetricians and labor nurses regarding the management of oxytocin infusions often differ, leading to conflict. The use of an oxytocin in-use checklist may help to reduce variability and improve patient outcomes.¹⁷ ●

Pregnant women, or women considering pregnancy, want to know—is pregnancy safe in the midst of the coronavirus disease 2019 (COVID-19) pandemic? In this article, I tackle common questions facing reproductive-aged or pregnant women and their providers.

1. What are the risks of COVID-19 in pregnancy?

A large, national prospective cohort study of outpatient pregnant and recently postpartum women with the diagnosis of suspected or confirmed COVID-19 demonstrated that many affected women have mild illnesses, with typical symptoms including cough, sore throat, body aches, fever, and headache.¹ Although symptoms were most common within the first 3 weeks of presentation, approximately 25% of women had a protracted course of symptoms (8 or more weeks). As this cohort disproportionately enrolled outpatients, it is important to note that many women had mild illnesses, which is the most likely course of infection in otherwise healthy, young women.

Data on the impact of COVID-19 on rates of miscarriage and birth defects are limited, yet the published reports are reassuring, with no increased risks of miscarriage, and no clear signal for birth defects.²

In a prospective cohort study across 3 New York City institutions when universal severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) testing was recommended upon admission for delivery, approximately 80% of women who were positive were asymptomatic.³ Maternal outcomes generally were reassuring, with no patients experiencing severe or critical illness. There were no differences in preterm delivery rates by SARS-CoV-2 status, but the rate of cesarean delivery was higher among women with COVID-19, for unclear reasons. Most notably, the rate of postpartum complications was 13% among women with COVID-19, versus 2.5% among women without COVID-19. These complications included readmission for worsening COVID-19, postpartum hypoxia, and postpartum fever.

A recent prospective cohort study from 1 institution in Texas similarly demonstrated favorable maternal outcomes with COVID-19, with 95% of women with asymptomatic or mild illness, and no differences in adverse pregnancy outcomes between COVID-19–positive and COVID-19–negative women, including cesarean delivery rate.⁴

Finally, certain characteristics increase the risk of COVID-19 among pregnant women and nonpregnant individuals alike. In a nationwide prospective cohort from the United Kingdom, medical comorbidities including obesity, diabetes (gestational or pregestational), hypertension, as well as Black or other minority ethnicities are associated with COVID-19.⁵ This is particularly notable given universal health insurance in the United Kingdom. Other data have also confirmed that women with comorbidities, women of Black or Hispanic ethnicity, and women with lower socioeconomic status, are at increased risk of COVID-19.^3,6,7

2. Is COVID-19 worse in pregnancy?

Given the well-documented risks of COVID-19 outside of pregnancy, is COVID-19 worse in a pregnant woman than in a nonpregnant woman? The most recent guidance from the Centers for Disease Control and Prevention (CDC) from November 2020 suggests that pregnant women are at increased risk for severe illness.⁸ However, it is important to understand the design of this study in order to appreciate its implications. Laboratory confirmed SARS-CoV-2 in the United States is systematically reported to the CDC. Among women aged 15–44 years with such confirmation, data on pregnancy status were available for 35.5%, almost 90% of whom were symptomatic. Within this cohort of largely symptomatic pregnant women, risks of intensive care unit (ICU) admission, invasive ventilation, and use of extracorporeal membrane oxygenation (ECMO) were approximately 2 to 3 times higher for pregnant women than for nonpregnant women. The absolute risks, however, were low. The risk of ICU admission for symptomatic pregnant women was approximately 1%; the risk of invasive ventilation, 0.3%; and the risk of ECMO, 0.1%.

Moreover, the lack of uniform data capture on pregnancy status for all women ages 15–44 years may skew the population with known pregnancy status to be sicker and, thus, may bias the results toward increased risks. Nevertheless, there is consistency in several publications with different data sources, all of which suggest pregnancy is an independent risk factor for increased severity of COVID-19.^9-11 Additionally, women with medical comorbidities (such as pregestational or gestational diabetes or obesity) are more likely to have severe COVID-19.

Continue to: 3. What are newborn outcomes if COVID-19 is diagnosed during pregnancy?...

Two large cohorts of newborns, disproportionately term infants, from the first wave of the pandemic in New York City, have reassuring news. In one cohort of 101 infants born at 2 New York City institutions to SARS-CoV-2–positive mothers, 2 neonates were diagnosed with SARS-CoV-2 during the immediate postnatal period.¹² Neither infant demonstrated clinical COVID-19. In another cohort of 120 infants born at 3 other New York City institutions to SARS-CoV-2–positive mothers and tested systematically within 24 hours of life, 5–7 days of life, and 14 days of life, there were no neonates who tested positive for SARS-CoV-2 at the initial time point. Among the 79 infants who had testing at 5–7 days of life and the 72 tested at 14 days of life, there were no infants positive for SARS-CoV-2.¹³ It is important to note that case reports and small case series have demonstrated some convincing evidence of vertical transmission. However, the overwhelming evidence suggests this risk is very low.

4. What is a reasonable outpatient setting–approach to managing COVID-19 in a pregnant woman?

Women should be counseled to quarantine for 10 to 14 days from symptom onset or, if asymptomatic, from positive polymerase chain reaction (PCR) test. Warning signs of worsening COVID-19 disease should be reviewed. Serial telemedicine follow-up for 10 to 14 days is recommended to ensure clinical stability and continued management as an outpatient. A home pulse oximeter is also recommended. Women should be advised to check their oxygen saturation daily and to call if oxygen saturation becomes less than 93%. Supportive care is recommended.

If delay in obstetric care may result in adverse pregnancy outcomes (for instance, postponing indicated fetal surveillance), obstetric care should be delivered, with appropriate personal protective equipment for health care workers and minimization of exposure of other pregnant women to the infected patient. Appointments should be scheduled at the end of the day.

During influenza season, women should receive empiric oseltamivir treatment (75 mg twice a day) per CDC guidelines for symptoms that may also be consistent with influenza, regardless of testing.

Prophylactic anticoagulation is not indicated for pregnant antepartum women who do not require inpatient care.

If inpatient care is required, management is individualized.

The approach to prenatal care after resolution of COVID-19 is not evidence-based. At my institution, all patients have a detailed mid-trimester anatomic evaluation, but if this is not routine, a detailed anatomic ultrasound (Current Procedural Terminology code 76811) may be considered. Additionally, for women with COVID-19 we perform one third-trimester growth ultrasound to screen for fetal growth restriction, on the basis of several placental studies demonstrating clots on the fetal or maternal side of the placenta.^3,14 Routine antenatal testing in the absence of growth restriction, or other comorbid conditions for which testing occurs, is not recommended.

Continue to: 5. What if asymptomatic or mild COVID-19 is diagnosed at the time of delivery?...

5. What if asymptomatic or mild COVID-19 is diagnosed at the time of delivery? What is reasonable management?

Asymptomatic or mildly symptomatic COVID-19 should not alter obstetric management, beyond appropriate use of personal protective equipment. Delayed cord clamping is also reasonable, if there are no other contraindications, as there is no documented harm associated with this practice among women with COVID-19.

Women with COVID-19 may be at higher risk for venous thromboembolic events in the postpartum period. At my institution, prophylactic postpartum anticoagulation is recommended for 2 weeks after vaginal delivery, and 6 weeks after cesarean delivery.

During the postpartum hospitalization, given reassuring data about vertical transmission and postnatal horizontal transmission risks, babies may room in with mothers in a single private room, if rooming-in is the current standard of care—as long as the mother and newborn do not require higher levels of care. Mothers should wear a mask and use hand hygiene when in contact with the baby. Skin-to-skin and breastfeeding or infant feeding of breast milk are appropriate practices to continue. There is no evidence to suggest that transmission of COVID-19 can occur via breastmilk; however, given the close contact inherent in breastfeeding, transmission through direct contact or maternal respiratory droplets is possible, and thus maternal use of masks and hand hygiene is recommended. When not feeding, the infant should be 6 feet away, and if possible, in an isolette.

6. When can individuals with COVID-19 discontinue transmission precautions or “home quarantine”?

For women with mildly symptomatic COVID-19 and without immunocompromise, home quarantine can be discontinued 10 days after onset of symptoms as long as there has been symptom improvement and no fever for at least 24 hours without the use of antipyretics. For immunocompetent women with incidentally diagnosed asymptomatic COVID-19, home quarantine can be discontinued 10 days after the positive test was obtained. Pregnancy in and of itself is not an immunocompromising condition.^15,16

For women with severe or critical COVID-19, who were hospitalized due to their clinical status, home quarantine can be discontinued when at least 10 days, and up to 20 days, after onset of symptoms and with symptom improvement and with no fever for at least 24 hours, without the use of antipyretics. Local hospital infection control experts may be able to guide the recommended practice for your site better, based on local information.^15,16

Repeating a PCR test to discontinue home quarantine is not recommended in most circumstances, as individuals may have prolonged shedding of noninfectious particles in their nasopharynx. Immunocompromise may be one exception to this general guidance, but consultation with local hospital infection control experts will help guide management.^15,16

7. Should women get pregnant during the COVID-19 pandemic?

Every pandemic has its own set of implications for the health of the mother, fetus, or both, and COVID-19 is no exception. While there are risks, described above, to mother and fetus, these risks are not so catastrophic as to strongly and directively recommend a patient not become pregnant.¹⁷ Moreover, the last several months of the pandemic have demonstrated that consistent mask usage, social distancing, and hand hygiene, are effective methods of preventing the acquisition of COVID-19. All of these risk-reducing strategies are available to pregnant women. Finally, accessing care during a pandemic in a hospital setting does not also pose a risk for acquisition of SARS-CoV-2.¹⁸

Continue to: 8. Is the COVID-19 vaccine safe for pregnant or postpartum/lactating women?...

8. Is the COVID-19 vaccine safe for pregnant or postpartum/lactating women?

On December 11, 2020, the US Food and Drug Administration (FDA) issued emergency use authorization (EUA) for the Pfizer-BioNtech mRNA vaccine (BNT 162b2) against COVID-19, for individuals aged 16 and older as a 2-dose series given 21 days apart. Among the more than 40,000 individuals in the trial that led to this EUA, vaccine efficacy was 95%.¹⁹ Adverse effects included fatigue and headache most commonly, with 16% of vaccine recipients experiencing fever after the second dose. Follow-up regarding safety is planned for 2 years by the manufacturer, in addition to safety monitoring by pre-existing national systems.

On December 18, 2020, the FDA announced EUA for Moderna’s mRNA-based vaccine, mRNA-1273, in men and women aged 18 and older. This is a 2-dose series given 28 days apart. The vaccine efficacy has been reported at 94.5%, with the most common adverse effects being injection site pain, tiredness, headache, muscle pain, chills, joint pain, swollen lymph nodes in the same arm as the injection, nausea and vomiting, and fever.^20,21 The phase 3 trial is ongoing.

Despite the speed with which these effective vaccines were developed, it is important to note that all regulatory and safety steps mandated for the development of any vaccine were met for these two, as well as for other COVID-19 vaccinations that will similarly receive EUA from the FDA.

In the EUA for BNT 162b2, the specific language regarding pregnant and lactating women recommends that patients and providers have an individualized conversation about vaccination. In the data presented to the FDA for the Pfizer-BioNtech mRNA vaccine, a limited number of pregnant women received either the vaccine (12 women) or placebo (11 women), with no long-term follow-up data available to characterize either maternal or fetal benefits and risks. The mechanism of action of an mRNA vaccine is to induce the cytoplasmic machinery within cells to create the coronavirus spike protein, which then allows the body’s immune system to create antibodies against this protein and confer protection accordingly. While the above mechanism is not theorized to result in different outcomes or different efficacy, the safety for the pregnant woman and fetus are unknown. It is not believed that vaccination during lactation would cause any adverse outcomes to a neonate, and lactating women do not need to interrupt or discontinue breast milk production in order to receive the vaccine.

The American College of Obstetricians and Gynecologists (ACOG) released a Practice Advisory on December 13, 2020, regarding their recommendations.²² ACOG recommends that vaccines against COVID-19 not be withheld from pregnant or lactating women, if they might otherwise meet criteria for and have access to vaccination. Currently, the CDC’s Advisory Committee on Immunization Practices (ACIP) stated that health care workers and long-term care facility residents represent priority groups to vaccinate in the initial phases of vaccination, given limitations in supply.²³ This recommendation is likely to be updated frequently as additional vaccines become available. Shared decision-making between patient and provider may help the patient to make the best decision for herself, but provider input is not required prior to a pregnant woman being vaccinated.

Additional animal data evaluating adverse effects on the reproductive system from developmental and reproductive toxicity (DART) studies for both mRNA vaccines should be available in the coming weeks, which may aid in the counseling of reproductive-aged women.

Vaccine trials to specifically enroll pregnant women are set to begin in early 2021, and more data will certainly inform the conversation between patient and provider regarding risks and benefits.

Conclusions

While the absolute risks of COVID-19 to mothers, fetuses, and neonates is low, pregnancy is a risk factor for severe disease. Many pregnant women with COVID-19 can be safely followed as outpatients via telemedicine, and supportive care is recommended. Inpatient care should be individualized. Pregnancy during the COVID-19 pandemic should be not be absolutely discouraged; instead, a conversation about risk mitigation should be undertaken. The COVID-19 vaccine is available to pregnant and lactating women, and the decision to choose vaccination in pregnancy is in the purview of the patient, in consultation with her physician. ●

Pregnant women, or women considering pregnancy, want to know—is pregnancy safe in the midst of the coronavirus disease 2019 (COVID-19) pandemic? In this article, I tackle common questions facing reproductive-aged or pregnant women and their providers.

1. What are the risks of COVID-19 in pregnancy?

A large, national prospective cohort study of outpatient pregnant and recently postpartum women with the diagnosis of suspected or confirmed COVID-19 demonstrated that many affected women have mild illnesses, with typical symptoms including cough, sore throat, body aches, fever, and headache.¹ Although symptoms were most common within the first 3 weeks of presentation, approximately 25% of women had a protracted course of symptoms (8 or more weeks). As this cohort disproportionately enrolled outpatients, it is important to note that many women had mild illnesses, which is the most likely course of infection in otherwise healthy, young women.

Data on the impact of COVID-19 on rates of miscarriage and birth defects are limited, yet the published reports are reassuring, with no increased risks of miscarriage, and no clear signal for birth defects.²

In a prospective cohort study across 3 New York City institutions when universal severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) testing was recommended upon admission for delivery, approximately 80% of women who were positive were asymptomatic.³ Maternal outcomes generally were reassuring, with no patients experiencing severe or critical illness. There were no differences in preterm delivery rates by SARS-CoV-2 status, but the rate of cesarean delivery was higher among women with COVID-19, for unclear reasons. Most notably, the rate of postpartum complications was 13% among women with COVID-19, versus 2.5% among women without COVID-19. These complications included readmission for worsening COVID-19, postpartum hypoxia, and postpartum fever.

A recent prospective cohort study from 1 institution in Texas similarly demonstrated favorable maternal outcomes with COVID-19, with 95% of women with asymptomatic or mild illness, and no differences in adverse pregnancy outcomes between COVID-19–positive and COVID-19–negative women, including cesarean delivery rate.⁴

Finally, certain characteristics increase the risk of COVID-19 among pregnant women and nonpregnant individuals alike. In a nationwide prospective cohort from the United Kingdom, medical comorbidities including obesity, diabetes (gestational or pregestational), hypertension, as well as Black or other minority ethnicities are associated with COVID-19.⁵ This is particularly notable given universal health insurance in the United Kingdom. Other data have also confirmed that women with comorbidities, women of Black or Hispanic ethnicity, and women with lower socioeconomic status, are at increased risk of COVID-19.^3,6,7

2. Is COVID-19 worse in pregnancy?

Given the well-documented risks of COVID-19 outside of pregnancy, is COVID-19 worse in a pregnant woman than in a nonpregnant woman? The most recent guidance from the Centers for Disease Control and Prevention (CDC) from November 2020 suggests that pregnant women are at increased risk for severe illness.⁸ However, it is important to understand the design of this study in order to appreciate its implications. Laboratory confirmed SARS-CoV-2 in the United States is systematically reported to the CDC. Among women aged 15–44 years with such confirmation, data on pregnancy status were available for 35.5%, almost 90% of whom were symptomatic. Within this cohort of largely symptomatic pregnant women, risks of intensive care unit (ICU) admission, invasive ventilation, and use of extracorporeal membrane oxygenation (ECMO) were approximately 2 to 3 times higher for pregnant women than for nonpregnant women. The absolute risks, however, were low. The risk of ICU admission for symptomatic pregnant women was approximately 1%; the risk of invasive ventilation, 0.3%; and the risk of ECMO, 0.1%.

Moreover, the lack of uniform data capture on pregnancy status for all women ages 15–44 years may skew the population with known pregnancy status to be sicker and, thus, may bias the results toward increased risks. Nevertheless, there is consistency in several publications with different data sources, all of which suggest pregnancy is an independent risk factor for increased severity of COVID-19.^9-11 Additionally, women with medical comorbidities (such as pregestational or gestational diabetes or obesity) are more likely to have severe COVID-19.

Continue to: 3. What are newborn outcomes if COVID-19 is diagnosed during pregnancy?...

Two large cohorts of newborns, disproportionately term infants, from the first wave of the pandemic in New York City, have reassuring news. In one cohort of 101 infants born at 2 New York City institutions to SARS-CoV-2–positive mothers, 2 neonates were diagnosed with SARS-CoV-2 during the immediate postnatal period.¹² Neither infant demonstrated clinical COVID-19. In another cohort of 120 infants born at 3 other New York City institutions to SARS-CoV-2–positive mothers and tested systematically within 24 hours of life, 5–7 days of life, and 14 days of life, there were no neonates who tested positive for SARS-CoV-2 at the initial time point. Among the 79 infants who had testing at 5–7 days of life and the 72 tested at 14 days of life, there were no infants positive for SARS-CoV-2.¹³ It is important to note that case reports and small case series have demonstrated some convincing evidence of vertical transmission. However, the overwhelming evidence suggests this risk is very low.

4. What is a reasonable outpatient setting–approach to managing COVID-19 in a pregnant woman?

Women should be counseled to quarantine for 10 to 14 days from symptom onset or, if asymptomatic, from positive polymerase chain reaction (PCR) test. Warning signs of worsening COVID-19 disease should be reviewed. Serial telemedicine follow-up for 10 to 14 days is recommended to ensure clinical stability and continued management as an outpatient. A home pulse oximeter is also recommended. Women should be advised to check their oxygen saturation daily and to call if oxygen saturation becomes less than 93%. Supportive care is recommended.

If delay in obstetric care may result in adverse pregnancy outcomes (for instance, postponing indicated fetal surveillance), obstetric care should be delivered, with appropriate personal protective equipment for health care workers and minimization of exposure of other pregnant women to the infected patient. Appointments should be scheduled at the end of the day.

During influenza season, women should receive empiric oseltamivir treatment (75 mg twice a day) per CDC guidelines for symptoms that may also be consistent with influenza, regardless of testing.

Prophylactic anticoagulation is not indicated for pregnant antepartum women who do not require inpatient care.

If inpatient care is required, management is individualized.

The approach to prenatal care after resolution of COVID-19 is not evidence-based. At my institution, all patients have a detailed mid-trimester anatomic evaluation, but if this is not routine, a detailed anatomic ultrasound (Current Procedural Terminology code 76811) may be considered. Additionally, for women with COVID-19 we perform one third-trimester growth ultrasound to screen for fetal growth restriction, on the basis of several placental studies demonstrating clots on the fetal or maternal side of the placenta.^3,14 Routine antenatal testing in the absence of growth restriction, or other comorbid conditions for which testing occurs, is not recommended.

Continue to: 5. What if asymptomatic or mild COVID-19 is diagnosed at the time of delivery?...

5. What if asymptomatic or mild COVID-19 is diagnosed at the time of delivery? What is reasonable management?

Asymptomatic or mildly symptomatic COVID-19 should not alter obstetric management, beyond appropriate use of personal protective equipment. Delayed cord clamping is also reasonable, if there are no other contraindications, as there is no documented harm associated with this practice among women with COVID-19.

Women with COVID-19 may be at higher risk for venous thromboembolic events in the postpartum period. At my institution, prophylactic postpartum anticoagulation is recommended for 2 weeks after vaginal delivery, and 6 weeks after cesarean delivery.

During the postpartum hospitalization, given reassuring data about vertical transmission and postnatal horizontal transmission risks, babies may room in with mothers in a single private room, if rooming-in is the current standard of care—as long as the mother and newborn do not require higher levels of care. Mothers should wear a mask and use hand hygiene when in contact with the baby. Skin-to-skin and breastfeeding or infant feeding of breast milk are appropriate practices to continue. There is no evidence to suggest that transmission of COVID-19 can occur via breastmilk; however, given the close contact inherent in breastfeeding, transmission through direct contact or maternal respiratory droplets is possible, and thus maternal use of masks and hand hygiene is recommended. When not feeding, the infant should be 6 feet away, and if possible, in an isolette.

6. When can individuals with COVID-19 discontinue transmission precautions or “home quarantine”?

For women with mildly symptomatic COVID-19 and without immunocompromise, home quarantine can be discontinued 10 days after onset of symptoms as long as there has been symptom improvement and no fever for at least 24 hours without the use of antipyretics. For immunocompetent women with incidentally diagnosed asymptomatic COVID-19, home quarantine can be discontinued 10 days after the positive test was obtained. Pregnancy in and of itself is not an immunocompromising condition.^15,16

For women with severe or critical COVID-19, who were hospitalized due to their clinical status, home quarantine can be discontinued when at least 10 days, and up to 20 days, after onset of symptoms and with symptom improvement and with no fever for at least 24 hours, without the use of antipyretics. Local hospital infection control experts may be able to guide the recommended practice for your site better, based on local information.^15,16

Repeating a PCR test to discontinue home quarantine is not recommended in most circumstances, as individuals may have prolonged shedding of noninfectious particles in their nasopharynx. Immunocompromise may be one exception to this general guidance, but consultation with local hospital infection control experts will help guide management.^15,16

7. Should women get pregnant during the COVID-19 pandemic?

Every pandemic has its own set of implications for the health of the mother, fetus, or both, and COVID-19 is no exception. While there are risks, described above, to mother and fetus, these risks are not so catastrophic as to strongly and directively recommend a patient not become pregnant.¹⁷ Moreover, the last several months of the pandemic have demonstrated that consistent mask usage, social distancing, and hand hygiene, are effective methods of preventing the acquisition of COVID-19. All of these risk-reducing strategies are available to pregnant women. Finally, accessing care during a pandemic in a hospital setting does not also pose a risk for acquisition of SARS-CoV-2.¹⁸

Continue to: 8. Is the COVID-19 vaccine safe for pregnant or postpartum/lactating women?...

8. Is the COVID-19 vaccine safe for pregnant or postpartum/lactating women?

On December 11, 2020, the US Food and Drug Administration (FDA) issued emergency use authorization (EUA) for the Pfizer-BioNtech mRNA vaccine (BNT 162b2) against COVID-19, for individuals aged 16 and older as a 2-dose series given 21 days apart. Among the more than 40,000 individuals in the trial that led to this EUA, vaccine efficacy was 95%.¹⁹ Adverse effects included fatigue and headache most commonly, with 16% of vaccine recipients experiencing fever after the second dose. Follow-up regarding safety is planned for 2 years by the manufacturer, in addition to safety monitoring by pre-existing national systems.

On December 18, 2020, the FDA announced EUA for Moderna’s mRNA-based vaccine, mRNA-1273, in men and women aged 18 and older. This is a 2-dose series given 28 days apart. The vaccine efficacy has been reported at 94.5%, with the most common adverse effects being injection site pain, tiredness, headache, muscle pain, chills, joint pain, swollen lymph nodes in the same arm as the injection, nausea and vomiting, and fever.^20,21 The phase 3 trial is ongoing.

Despite the speed with which these effective vaccines were developed, it is important to note that all regulatory and safety steps mandated for the development of any vaccine were met for these two, as well as for other COVID-19 vaccinations that will similarly receive EUA from the FDA.

In the EUA for BNT 162b2, the specific language regarding pregnant and lactating women recommends that patients and providers have an individualized conversation about vaccination. In the data presented to the FDA for the Pfizer-BioNtech mRNA vaccine, a limited number of pregnant women received either the vaccine (12 women) or placebo (11 women), with no long-term follow-up data available to characterize either maternal or fetal benefits and risks. The mechanism of action of an mRNA vaccine is to induce the cytoplasmic machinery within cells to create the coronavirus spike protein, which then allows the body’s immune system to create antibodies against this protein and confer protection accordingly. While the above mechanism is not theorized to result in different outcomes or different efficacy, the safety for the pregnant woman and fetus are unknown. It is not believed that vaccination during lactation would cause any adverse outcomes to a neonate, and lactating women do not need to interrupt or discontinue breast milk production in order to receive the vaccine.

The American College of Obstetricians and Gynecologists (ACOG) released a Practice Advisory on December 13, 2020, regarding their recommendations.²² ACOG recommends that vaccines against COVID-19 not be withheld from pregnant or lactating women, if they might otherwise meet criteria for and have access to vaccination. Currently, the CDC’s Advisory Committee on Immunization Practices (ACIP) stated that health care workers and long-term care facility residents represent priority groups to vaccinate in the initial phases of vaccination, given limitations in supply.²³ This recommendation is likely to be updated frequently as additional vaccines become available. Shared decision-making between patient and provider may help the patient to make the best decision for herself, but provider input is not required prior to a pregnant woman being vaccinated.

Additional animal data evaluating adverse effects on the reproductive system from developmental and reproductive toxicity (DART) studies for both mRNA vaccines should be available in the coming weeks, which may aid in the counseling of reproductive-aged women.

Vaccine trials to specifically enroll pregnant women are set to begin in early 2021, and more data will certainly inform the conversation between patient and provider regarding risks and benefits.

Conclusions

While the absolute risks of COVID-19 to mothers, fetuses, and neonates is low, pregnancy is a risk factor for severe disease. Many pregnant women with COVID-19 can be safely followed as outpatients via telemedicine, and supportive care is recommended. Inpatient care should be individualized. Pregnancy during the COVID-19 pandemic should be not be absolutely discouraged; instead, a conversation about risk mitigation should be undertaken. The COVID-19 vaccine is available to pregnant and lactating women, and the decision to choose vaccination in pregnancy is in the purview of the patient, in consultation with her physician. ●

Pregnant women, or women considering pregnancy, want to know—is pregnancy safe in the midst of the coronavirus disease 2019 (COVID-19) pandemic? In this article, I tackle common questions facing reproductive-aged or pregnant women and their providers.

1. What are the risks of COVID-19 in pregnancy?

A large, national prospective cohort study of outpatient pregnant and recently postpartum women with the diagnosis of suspected or confirmed COVID-19 demonstrated that many affected women have mild illnesses, with typical symptoms including cough, sore throat, body aches, fever, and headache.¹ Although symptoms were most common within the first 3 weeks of presentation, approximately 25% of women had a protracted course of symptoms (8 or more weeks). As this cohort disproportionately enrolled outpatients, it is important to note that many women had mild illnesses, which is the most likely course of infection in otherwise healthy, young women.

Data on the impact of COVID-19 on rates of miscarriage and birth defects are limited, yet the published reports are reassuring, with no increased risks of miscarriage, and no clear signal for birth defects.²

In a prospective cohort study across 3 New York City institutions when universal severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) testing was recommended upon admission for delivery, approximately 80% of women who were positive were asymptomatic.³ Maternal outcomes generally were reassuring, with no patients experiencing severe or critical illness. There were no differences in preterm delivery rates by SARS-CoV-2 status, but the rate of cesarean delivery was higher among women with COVID-19, for unclear reasons. Most notably, the rate of postpartum complications was 13% among women with COVID-19, versus 2.5% among women without COVID-19. These complications included readmission for worsening COVID-19, postpartum hypoxia, and postpartum fever.

A recent prospective cohort study from 1 institution in Texas similarly demonstrated favorable maternal outcomes with COVID-19, with 95% of women with asymptomatic or mild illness, and no differences in adverse pregnancy outcomes between COVID-19–positive and COVID-19–negative women, including cesarean delivery rate.⁴

Finally, certain characteristics increase the risk of COVID-19 among pregnant women and nonpregnant individuals alike. In a nationwide prospective cohort from the United Kingdom, medical comorbidities including obesity, diabetes (gestational or pregestational), hypertension, as well as Black or other minority ethnicities are associated with COVID-19.⁵ This is particularly notable given universal health insurance in the United Kingdom. Other data have also confirmed that women with comorbidities, women of Black or Hispanic ethnicity, and women with lower socioeconomic status, are at increased risk of COVID-19.^3,6,7

2. Is COVID-19 worse in pregnancy?

Given the well-documented risks of COVID-19 outside of pregnancy, is COVID-19 worse in a pregnant woman than in a nonpregnant woman? The most recent guidance from the Centers for Disease Control and Prevention (CDC) from November 2020 suggests that pregnant women are at increased risk for severe illness.⁸ However, it is important to understand the design of this study in order to appreciate its implications. Laboratory confirmed SARS-CoV-2 in the United States is systematically reported to the CDC. Among women aged 15–44 years with such confirmation, data on pregnancy status were available for 35.5%, almost 90% of whom were symptomatic. Within this cohort of largely symptomatic pregnant women, risks of intensive care unit (ICU) admission, invasive ventilation, and use of extracorporeal membrane oxygenation (ECMO) were approximately 2 to 3 times higher for pregnant women than for nonpregnant women. The absolute risks, however, were low. The risk of ICU admission for symptomatic pregnant women was approximately 1%; the risk of invasive ventilation, 0.3%; and the risk of ECMO, 0.1%.

Moreover, the lack of uniform data capture on pregnancy status for all women ages 15–44 years may skew the population with known pregnancy status to be sicker and, thus, may bias the results toward increased risks. Nevertheless, there is consistency in several publications with different data sources, all of which suggest pregnancy is an independent risk factor for increased severity of COVID-19.^9-11 Additionally, women with medical comorbidities (such as pregestational or gestational diabetes or obesity) are more likely to have severe COVID-19.

Continue to: 3. What are newborn outcomes if COVID-19 is diagnosed during pregnancy?...

Two large cohorts of newborns, disproportionately term infants, from the first wave of the pandemic in New York City, have reassuring news. In one cohort of 101 infants born at 2 New York City institutions to SARS-CoV-2–positive mothers, 2 neonates were diagnosed with SARS-CoV-2 during the immediate postnatal period.¹² Neither infant demonstrated clinical COVID-19. In another cohort of 120 infants born at 3 other New York City institutions to SARS-CoV-2–positive mothers and tested systematically within 24 hours of life, 5–7 days of life, and 14 days of life, there were no neonates who tested positive for SARS-CoV-2 at the initial time point. Among the 79 infants who had testing at 5–7 days of life and the 72 tested at 14 days of life, there were no infants positive for SARS-CoV-2.¹³ It is important to note that case reports and small case series have demonstrated some convincing evidence of vertical transmission. However, the overwhelming evidence suggests this risk is very low.

4. What is a reasonable outpatient setting–approach to managing COVID-19 in a pregnant woman?

Women should be counseled to quarantine for 10 to 14 days from symptom onset or, if asymptomatic, from positive polymerase chain reaction (PCR) test. Warning signs of worsening COVID-19 disease should be reviewed. Serial telemedicine follow-up for 10 to 14 days is recommended to ensure clinical stability and continued management as an outpatient. A home pulse oximeter is also recommended. Women should be advised to check their oxygen saturation daily and to call if oxygen saturation becomes less than 93%. Supportive care is recommended.

If delay in obstetric care may result in adverse pregnancy outcomes (for instance, postponing indicated fetal surveillance), obstetric care should be delivered, with appropriate personal protective equipment for health care workers and minimization of exposure of other pregnant women to the infected patient. Appointments should be scheduled at the end of the day.

During influenza season, women should receive empiric oseltamivir treatment (75 mg twice a day) per CDC guidelines for symptoms that may also be consistent with influenza, regardless of testing.

Prophylactic anticoagulation is not indicated for pregnant antepartum women who do not require inpatient care.

If inpatient care is required, management is individualized.

The approach to prenatal care after resolution of COVID-19 is not evidence-based. At my institution, all patients have a detailed mid-trimester anatomic evaluation, but if this is not routine, a detailed anatomic ultrasound (Current Procedural Terminology code 76811) may be considered. Additionally, for women with COVID-19 we perform one third-trimester growth ultrasound to screen for fetal growth restriction, on the basis of several placental studies demonstrating clots on the fetal or maternal side of the placenta.^3,14 Routine antenatal testing in the absence of growth restriction, or other comorbid conditions for which testing occurs, is not recommended.

Continue to: 5. What if asymptomatic or mild COVID-19 is diagnosed at the time of delivery?...

5. What if asymptomatic or mild COVID-19 is diagnosed at the time of delivery? What is reasonable management?

Asymptomatic or mildly symptomatic COVID-19 should not alter obstetric management, beyond appropriate use of personal protective equipment. Delayed cord clamping is also reasonable, if there are no other contraindications, as there is no documented harm associated with this practice among women with COVID-19.

Women with COVID-19 may be at higher risk for venous thromboembolic events in the postpartum period. At my institution, prophylactic postpartum anticoagulation is recommended for 2 weeks after vaginal delivery, and 6 weeks after cesarean delivery.

During the postpartum hospitalization, given reassuring data about vertical transmission and postnatal horizontal transmission risks, babies may room in with mothers in a single private room, if rooming-in is the current standard of care—as long as the mother and newborn do not require higher levels of care. Mothers should wear a mask and use hand hygiene when in contact with the baby. Skin-to-skin and breastfeeding or infant feeding of breast milk are appropriate practices to continue. There is no evidence to suggest that transmission of COVID-19 can occur via breastmilk; however, given the close contact inherent in breastfeeding, transmission through direct contact or maternal respiratory droplets is possible, and thus maternal use of masks and hand hygiene is recommended. When not feeding, the infant should be 6 feet away, and if possible, in an isolette.

6. When can individuals with COVID-19 discontinue transmission precautions or “home quarantine”?

For women with mildly symptomatic COVID-19 and without immunocompromise, home quarantine can be discontinued 10 days after onset of symptoms as long as there has been symptom improvement and no fever for at least 24 hours without the use of antipyretics. For immunocompetent women with incidentally diagnosed asymptomatic COVID-19, home quarantine can be discontinued 10 days after the positive test was obtained. Pregnancy in and of itself is not an immunocompromising condition.^15,16

For women with severe or critical COVID-19, who were hospitalized due to their clinical status, home quarantine can be discontinued when at least 10 days, and up to 20 days, after onset of symptoms and with symptom improvement and with no fever for at least 24 hours, without the use of antipyretics. Local hospital infection control experts may be able to guide the recommended practice for your site better, based on local information.^15,16

Repeating a PCR test to discontinue home quarantine is not recommended in most circumstances, as individuals may have prolonged shedding of noninfectious particles in their nasopharynx. Immunocompromise may be one exception to this general guidance, but consultation with local hospital infection control experts will help guide management.^15,16

7. Should women get pregnant during the COVID-19 pandemic?

Every pandemic has its own set of implications for the health of the mother, fetus, or both, and COVID-19 is no exception. While there are risks, described above, to mother and fetus, these risks are not so catastrophic as to strongly and directively recommend a patient not become pregnant.¹⁷ Moreover, the last several months of the pandemic have demonstrated that consistent mask usage, social distancing, and hand hygiene, are effective methods of preventing the acquisition of COVID-19. All of these risk-reducing strategies are available to pregnant women. Finally, accessing care during a pandemic in a hospital setting does not also pose a risk for acquisition of SARS-CoV-2.¹⁸

Continue to: 8. Is the COVID-19 vaccine safe for pregnant or postpartum/lactating women?...

8. Is the COVID-19 vaccine safe for pregnant or postpartum/lactating women?

On December 11, 2020, the US Food and Drug Administration (FDA) issued emergency use authorization (EUA) for the Pfizer-BioNtech mRNA vaccine (BNT 162b2) against COVID-19, for individuals aged 16 and older as a 2-dose series given 21 days apart. Among the more than 40,000 individuals in the trial that led to this EUA, vaccine efficacy was 95%.¹⁹ Adverse effects included fatigue and headache most commonly, with 16% of vaccine recipients experiencing fever after the second dose. Follow-up regarding safety is planned for 2 years by the manufacturer, in addition to safety monitoring by pre-existing national systems.

On December 18, 2020, the FDA announced EUA for Moderna’s mRNA-based vaccine, mRNA-1273, in men and women aged 18 and older. This is a 2-dose series given 28 days apart. The vaccine efficacy has been reported at 94.5%, with the most common adverse effects being injection site pain, tiredness, headache, muscle pain, chills, joint pain, swollen lymph nodes in the same arm as the injection, nausea and vomiting, and fever.^20,21 The phase 3 trial is ongoing.

Despite the speed with which these effective vaccines were developed, it is important to note that all regulatory and safety steps mandated for the development of any vaccine were met for these two, as well as for other COVID-19 vaccinations that will similarly receive EUA from the FDA.

In the EUA for BNT 162b2, the specific language regarding pregnant and lactating women recommends that patients and providers have an individualized conversation about vaccination. In the data presented to the FDA for the Pfizer-BioNtech mRNA vaccine, a limited number of pregnant women received either the vaccine (12 women) or placebo (11 women), with no long-term follow-up data available to characterize either maternal or fetal benefits and risks. The mechanism of action of an mRNA vaccine is to induce the cytoplasmic machinery within cells to create the coronavirus spike protein, which then allows the body’s immune system to create antibodies against this protein and confer protection accordingly. While the above mechanism is not theorized to result in different outcomes or different efficacy, the safety for the pregnant woman and fetus are unknown. It is not believed that vaccination during lactation would cause any adverse outcomes to a neonate, and lactating women do not need to interrupt or discontinue breast milk production in order to receive the vaccine.

The American College of Obstetricians and Gynecologists (ACOG) released a Practice Advisory on December 13, 2020, regarding their recommendations.²² ACOG recommends that vaccines against COVID-19 not be withheld from pregnant or lactating women, if they might otherwise meet criteria for and have access to vaccination. Currently, the CDC’s Advisory Committee on Immunization Practices (ACIP) stated that health care workers and long-term care facility residents represent priority groups to vaccinate in the initial phases of vaccination, given limitations in supply.²³ This recommendation is likely to be updated frequently as additional vaccines become available. Shared decision-making between patient and provider may help the patient to make the best decision for herself, but provider input is not required prior to a pregnant woman being vaccinated.

Additional animal data evaluating adverse effects on the reproductive system from developmental and reproductive toxicity (DART) studies for both mRNA vaccines should be available in the coming weeks, which may aid in the counseling of reproductive-aged women.

Vaccine trials to specifically enroll pregnant women are set to begin in early 2021, and more data will certainly inform the conversation between patient and provider regarding risks and benefits.

Conclusions

While the absolute risks of COVID-19 to mothers, fetuses, and neonates is low, pregnancy is a risk factor for severe disease. Many pregnant women with COVID-19 can be safely followed as outpatients via telemedicine, and supportive care is recommended. Inpatient care should be individualized. Pregnancy during the COVID-19 pandemic should be not be absolutely discouraged; instead, a conversation about risk mitigation should be undertaken. The COVID-19 vaccine is available to pregnant and lactating women, and the decision to choose vaccination in pregnancy is in the purview of the patient, in consultation with her physician. ●