Transporting the high-risk psychiatric patient: Clinical and legal challenges

Article Type
Changed
Thu, 07/07/2022 - 15:17

“I’ve given up, doctor. We gave it our best, but I am at the point where I want to end my life.” You receive this call at 2 a.m., and you’re flooded with a series of emotions and are bewildered – until your training kicks in.

Dr. Lorenzo Norris, editor-in-chief of MDedge Psychiatry, and assistant professor of psychiatry and behavioral sciences at George Washington University, Washington
Dr. Lorenzo Norris

Countless hours of working with patients in emergency department settings while on call as a resident inform your ability to triage the situation. Years of supervision guide your supportive statements as you work collaboratively with your patient to address the emotional and existential distress. As the call proceeds and you realize that your patient will require hospitalization, you are struck by a sobering question: “How am I going to arrange for my patient to go to the nearest hospital in the middle of the night?”

The options for transporting patients with serious mental illness (SMI) typically vary from bad to worse and usually filter down to three possibilities:

1. Get a friend or family member to transport them to the nearest ED.

2. Call emergency medical services (EMS) for transport to the nearest ED.

3. Call the police and request transport to the nearest ED.

Several factors would determine which of those options you would use alone or in combination. Current training paradigms for mental health professionals offer a limited body of literature on evidenced-based strategies for patients with SMI. Transporting high-risk psychiatric patients requires great care and respect, and in-depth knowledge about patients’ vulnerabilities. At best – if not handled properly – these experiences can aggravate patients’ mental health conditions. At worst, they can lead to the loss of our patients. Together, we have more than 40 years’ experience working in complex mental health care systems that run the gamut, from providing direct clinical care to directing mental health care divisions.



Sobering statistics prevail

In 2017, suicide was the 10th leading cause of death in the United States, accounting for more than 47,000 deaths. Suicide was the second-leading cause of death among individuals aged 10-34 and the fourth leading cause of death for individuals aged 35- 54.1 In 2017, more than 70,200 Americans died from a drug overdose, including illicit drugs and prescription opioids.2 Drug overdose deaths nearly quadrupled between 1999 and 2017, from 16,849 deaths to 70,237, respectively.2

Shana Palmieri, JD, a managing partner of Healthcare Legal Education & Consulting Network, and chief clinical officer and cofounder of XFERALL
Shana Palmieri

The life expectancy of an American with SMI is 14-32 years less than that of the average population.3 Those numbers are on par with many sub-Saharan countries, including Sudan and Ethiopia, and surpass the health disparities for most racial and ethnic groups.

The decrease in life expectancy for people with SMI is rarely the result of suicide but rather the effect of medical comorbidities, including heart disease, stroke, pulmonary disease, diabetes, and cancer.3 Individuals with SMI are much more likely to suffer from chronic illnesses that are associated with co-occurring addictions, side effects of psychotropic medications, and social determinants of mental health, such as poverty.

Major depressive disorder among people with SMI presents acute and chronic medical risks. For example, people with major depressive disorder are at a higher risk for stroke and cardiovascular disease.4 There is a threefold increase in cardiac-related deaths for individuals who experience depression after a heart attack.5 In addition, depression increases the risk of cardiac-related death after a heart attack more than any other risk factor, except for congestive heart failure.6

 

 

The transportation challenge

When the complexity of psychiatric conditions is conceptualized to include decreased life expectancy because of medical comorbidities, medical complications that can result from psychotropic medications, and the high incidence of co-occurring substance use disorders (SUDs), it is clear why we are concerned about the type of transport used for patients experiencing a psychiatric emergency.

Mollie Slater, a managing partner of legal education for Healthcare Legal Education & Consulting Network, and a trial attorney at Colley Shroyer & Abraham in Columbus, Ohio
Mollie Slater, JD

A common practice for patients presenting for medical treatment for a mental health condition is for them to be transported by law enforcement in handcuffs, or by private vehicle, because of a lack of medical transport options.

One tragic example occurred on Sept. 18, 2018, when two Horry County, S.C., deputies were providing a hospital-to-hospital transport for two mental health patients. The patients, who had no legal charges and were not under arrest, were locked in a transport cage in the back of a law enforcement vehicle for transport during Hurricane Florence. While the driver tried to move through floodwaters, the car stalled and became submerged. The patients were unable to open the locked cage door, and the deputies responsible for the transport did not have a key to unlock the cage.

The two women died as a result of the incident. Both deputies are facing two counts of involuntary manslaughter – with a potential prison sentence of 5 years each.7

The system that promotes the use of law enforcement to transport medical patients who are not in legal custody perpetuates a high risk to patients. Also at risk are law enforcement professionals who often are not adequately trained to evaluate, intervene, and manage patients in need of medical treatment (for acute medical, SUDs, or mental illness).
 

Recommendations for transporting high-risk patients

The legal and regulatory standards required by the Centers for Medicare & Medicaid Services guidelines8 for behavioral health patients are consistent in saying that law enforcement restraints cannot be used in hospital settings – unless the patient is under law enforcement custody. If the patient is admitted to an inpatient psychiatric unit, law enforcement restraints are never allowed to be used. Despite those guidelines for handling these situations within hospital settings, a similar standard does not exist for interhospital transport of high-risk behavioral health patients.

Kevin Whaley II, director of the safety and security department at George Washington University Hospital, Washington
Kevin Whaley II

Patients often are transported between facilities by law enforcement, and at times, with the use of law enforcement restraints. However, use of law enforcement for interhospital transport of patients not in the custody of law enforcement is both detrimental to and clinically dangerous for the patient. Not only does the scenario put the patient at risk, but it also places law enforcement professionals at risk with the potential for legal liability if the patient medically decompensates during the transport.

Also, using law enforcement to intervene and provide transportation for behavioral health patients in crisis might cause further harm to the patient’s psychological condition and deter the patient from presenting for treatment.

The appropriate level of interfacility transport for a behavioral health patient requiring an inpatient level of care is secure transport with trained medical professionals. If necessary, restraint guidelines should follow the same standard as they do in hospital settings. In situations with high risk for violence or agitation, law enforcement should be requested to accompany EMS during the transport. Handling the situation in this way allows for a collaborative approach to provide adequate medical support, and provide for the physical safety and security of the patient – and of EMS personnel.

Across police and sheriffs’ departments nationwide, law enforcement officers are required to transport mental health patients from one location or hospital to another. Hospitals and outpatient locations, often with no alternative, rely on local law enforcement agencies to provide safe transport between acute and mental health facilities. Departmental policies and the widespread belief that mental health patients automatically pose a substantial danger to themselves or others have led to these patients being handcuffed and put in the back of police cruisers. Essentially, they are treated like criminals who are under arrest.

The CMS has strict criteria for ordering, applying, evaluating, reevaluating, and reporting restraint-associated deaths. Likewise, The Joint Commission, during its accreditation survey, rightly scrutinizes a facility’s use of restraints. Both the CMS and The Joint Commission define restraint by the function of the device and not the type of the device.

According to the CMS, a restraint is any manual method, physical or mechanic device, material, or equipment that immobilizes or reduces the ability of a patient to move his or her arms, legs, body, or head freely. Within a police cruiser, handcuffs on a mental health patient who is not under arrest would fall squarely within this definition of restraint.

A patient’s current behavior or clinical needs – not history or diagnosis – should determine whether a restraint is warranted. A patient experiencing a psychiatric crisis who is not under arrest might very well escalate and become destructive and combative when being placed in handcuffs in the back of a police vehicle. What should police do at that point? Should they arrest the individual? We offer the following five recommendations.
 

 

 

Key recommendations

  • Patients who require interhospital transport for an acute behavioral health crisis should be transported by medical professionals with the training and expertise to manage mental health and medical conditions.
  • Interhospital transport restraint guidelines should be in line with CMS guidelines for hospital restraints. No patient that is not under law enforcement custody should be transported in law enforcement restraints.
  • Patients at high risk for violence/agitation (an underlying condition causing violence/agitation may include dementia, traumatic brain injuries, delirium, SUDs, or psychiatric conditions) should be managed in accordance with medically indicated intervention such as medical restraints or medications.
  • If required, a request should be made for law enforcement officers to accompany EMS to provide support and to ensure the safety of the patient and EMS professionals during the transport.
  • EMS professionals should receive specific training to manage acute psychiatric and SUD conditions, and should be aware of the life-threatening medical complications that can result from SUDs and psychiatric conditions/medications.

We recognize that patients with SMI require clinicians to work collaboratively, perhaps with law enforcement, to safely transport them from one point to another. Only when the rules we have outlined are followed will our patients get transported in such ways that allow them to get the care they need.
 

Dr. Norris is editor-in-chief of MDedge Psychiatry, and assistant professor of psychiatry and behavioral sciences at George Washington University, Washington. He serves as assistant dean of student affairs at the university, and medical director of psychiatric and behavioral sciences at GWU Hospital. Ms. Palmieri is a managing partner of Healthcare Legal Education & Consulting Network (HLECN), and the chief clinical officer and cofounder of XFERALL. HLECN focuses on clinical education and training, and XFERALL is a company that provides a technology platform aimed at improving access to care for behavioral health and medical patients. Ms. Slater is a managing partner of legal education for HLECN, and a trial attorney at Colley Shroyer & Abraham in Columbus, Ohio. Mr. Whaley is director of the safety and security department at GWU Hospital.

References

1. National Institute of Mental Health: Suicide.

2. National Institute on Drug Abuse. Overdose death rates. Revised January 2019.

3. Post by former NIMH Director Thomas Insel: No health without mental health. Sept. 6, 2011.

4. Dhar AK and Barton DA. Depression and the link with cardiovascular disease. Front Psychiatry. 2016 Mar 21;7:33.

5. Lichtman JH et al. Depression and coronary heart disease. Circulation. 2008;118:1768-75.

6. Hare DL et al. Depression and cardiovascular disease: A clinical review. European Heart J. 2014 Jun;35(21):1365-72.

7. “ ‘How many people have to die?’ SC mental health patients endure nightmare transport.” The News & Observer. 2019 May 29.

8. 42 C.F.R. Part 482. Part IV. Department of Health and Human Services. Medicare & Medicaid programs; Hospital conditions of participation; Patients’ rights; Final rule. 2006 Dec 8.

Publications
Topics
Sections

“I’ve given up, doctor. We gave it our best, but I am at the point where I want to end my life.” You receive this call at 2 a.m., and you’re flooded with a series of emotions and are bewildered – until your training kicks in.

Dr. Lorenzo Norris, editor-in-chief of MDedge Psychiatry, and assistant professor of psychiatry and behavioral sciences at George Washington University, Washington
Dr. Lorenzo Norris

Countless hours of working with patients in emergency department settings while on call as a resident inform your ability to triage the situation. Years of supervision guide your supportive statements as you work collaboratively with your patient to address the emotional and existential distress. As the call proceeds and you realize that your patient will require hospitalization, you are struck by a sobering question: “How am I going to arrange for my patient to go to the nearest hospital in the middle of the night?”

The options for transporting patients with serious mental illness (SMI) typically vary from bad to worse and usually filter down to three possibilities:

1. Get a friend or family member to transport them to the nearest ED.

2. Call emergency medical services (EMS) for transport to the nearest ED.

3. Call the police and request transport to the nearest ED.

Several factors would determine which of those options you would use alone or in combination. Current training paradigms for mental health professionals offer a limited body of literature on evidenced-based strategies for patients with SMI. Transporting high-risk psychiatric patients requires great care and respect, and in-depth knowledge about patients’ vulnerabilities. At best – if not handled properly – these experiences can aggravate patients’ mental health conditions. At worst, they can lead to the loss of our patients. Together, we have more than 40 years’ experience working in complex mental health care systems that run the gamut, from providing direct clinical care to directing mental health care divisions.



Sobering statistics prevail

In 2017, suicide was the 10th leading cause of death in the United States, accounting for more than 47,000 deaths. Suicide was the second-leading cause of death among individuals aged 10-34 and the fourth leading cause of death for individuals aged 35- 54.1 In 2017, more than 70,200 Americans died from a drug overdose, including illicit drugs and prescription opioids.2 Drug overdose deaths nearly quadrupled between 1999 and 2017, from 16,849 deaths to 70,237, respectively.2

Shana Palmieri, JD, a managing partner of Healthcare Legal Education & Consulting Network, and chief clinical officer and cofounder of XFERALL
Shana Palmieri

The life expectancy of an American with SMI is 14-32 years less than that of the average population.3 Those numbers are on par with many sub-Saharan countries, including Sudan and Ethiopia, and surpass the health disparities for most racial and ethnic groups.

The decrease in life expectancy for people with SMI is rarely the result of suicide but rather the effect of medical comorbidities, including heart disease, stroke, pulmonary disease, diabetes, and cancer.3 Individuals with SMI are much more likely to suffer from chronic illnesses that are associated with co-occurring addictions, side effects of psychotropic medications, and social determinants of mental health, such as poverty.

Major depressive disorder among people with SMI presents acute and chronic medical risks. For example, people with major depressive disorder are at a higher risk for stroke and cardiovascular disease.4 There is a threefold increase in cardiac-related deaths for individuals who experience depression after a heart attack.5 In addition, depression increases the risk of cardiac-related death after a heart attack more than any other risk factor, except for congestive heart failure.6

 

 

The transportation challenge

When the complexity of psychiatric conditions is conceptualized to include decreased life expectancy because of medical comorbidities, medical complications that can result from psychotropic medications, and the high incidence of co-occurring substance use disorders (SUDs), it is clear why we are concerned about the type of transport used for patients experiencing a psychiatric emergency.

Mollie Slater, a managing partner of legal education for Healthcare Legal Education & Consulting Network, and a trial attorney at Colley Shroyer & Abraham in Columbus, Ohio
Mollie Slater, JD

A common practice for patients presenting for medical treatment for a mental health condition is for them to be transported by law enforcement in handcuffs, or by private vehicle, because of a lack of medical transport options.

One tragic example occurred on Sept. 18, 2018, when two Horry County, S.C., deputies were providing a hospital-to-hospital transport for two mental health patients. The patients, who had no legal charges and were not under arrest, were locked in a transport cage in the back of a law enforcement vehicle for transport during Hurricane Florence. While the driver tried to move through floodwaters, the car stalled and became submerged. The patients were unable to open the locked cage door, and the deputies responsible for the transport did not have a key to unlock the cage.

The two women died as a result of the incident. Both deputies are facing two counts of involuntary manslaughter – with a potential prison sentence of 5 years each.7

The system that promotes the use of law enforcement to transport medical patients who are not in legal custody perpetuates a high risk to patients. Also at risk are law enforcement professionals who often are not adequately trained to evaluate, intervene, and manage patients in need of medical treatment (for acute medical, SUDs, or mental illness).
 

Recommendations for transporting high-risk patients

The legal and regulatory standards required by the Centers for Medicare & Medicaid Services guidelines8 for behavioral health patients are consistent in saying that law enforcement restraints cannot be used in hospital settings – unless the patient is under law enforcement custody. If the patient is admitted to an inpatient psychiatric unit, law enforcement restraints are never allowed to be used. Despite those guidelines for handling these situations within hospital settings, a similar standard does not exist for interhospital transport of high-risk behavioral health patients.

Kevin Whaley II, director of the safety and security department at George Washington University Hospital, Washington
Kevin Whaley II

Patients often are transported between facilities by law enforcement, and at times, with the use of law enforcement restraints. However, use of law enforcement for interhospital transport of patients not in the custody of law enforcement is both detrimental to and clinically dangerous for the patient. Not only does the scenario put the patient at risk, but it also places law enforcement professionals at risk with the potential for legal liability if the patient medically decompensates during the transport.

Also, using law enforcement to intervene and provide transportation for behavioral health patients in crisis might cause further harm to the patient’s psychological condition and deter the patient from presenting for treatment.

The appropriate level of interfacility transport for a behavioral health patient requiring an inpatient level of care is secure transport with trained medical professionals. If necessary, restraint guidelines should follow the same standard as they do in hospital settings. In situations with high risk for violence or agitation, law enforcement should be requested to accompany EMS during the transport. Handling the situation in this way allows for a collaborative approach to provide adequate medical support, and provide for the physical safety and security of the patient – and of EMS personnel.

Across police and sheriffs’ departments nationwide, law enforcement officers are required to transport mental health patients from one location or hospital to another. Hospitals and outpatient locations, often with no alternative, rely on local law enforcement agencies to provide safe transport between acute and mental health facilities. Departmental policies and the widespread belief that mental health patients automatically pose a substantial danger to themselves or others have led to these patients being handcuffed and put in the back of police cruisers. Essentially, they are treated like criminals who are under arrest.

The CMS has strict criteria for ordering, applying, evaluating, reevaluating, and reporting restraint-associated deaths. Likewise, The Joint Commission, during its accreditation survey, rightly scrutinizes a facility’s use of restraints. Both the CMS and The Joint Commission define restraint by the function of the device and not the type of the device.

According to the CMS, a restraint is any manual method, physical or mechanic device, material, or equipment that immobilizes or reduces the ability of a patient to move his or her arms, legs, body, or head freely. Within a police cruiser, handcuffs on a mental health patient who is not under arrest would fall squarely within this definition of restraint.

A patient’s current behavior or clinical needs – not history or diagnosis – should determine whether a restraint is warranted. A patient experiencing a psychiatric crisis who is not under arrest might very well escalate and become destructive and combative when being placed in handcuffs in the back of a police vehicle. What should police do at that point? Should they arrest the individual? We offer the following five recommendations.
 

 

 

Key recommendations

  • Patients who require interhospital transport for an acute behavioral health crisis should be transported by medical professionals with the training and expertise to manage mental health and medical conditions.
  • Interhospital transport restraint guidelines should be in line with CMS guidelines for hospital restraints. No patient that is not under law enforcement custody should be transported in law enforcement restraints.
  • Patients at high risk for violence/agitation (an underlying condition causing violence/agitation may include dementia, traumatic brain injuries, delirium, SUDs, or psychiatric conditions) should be managed in accordance with medically indicated intervention such as medical restraints or medications.
  • If required, a request should be made for law enforcement officers to accompany EMS to provide support and to ensure the safety of the patient and EMS professionals during the transport.
  • EMS professionals should receive specific training to manage acute psychiatric and SUD conditions, and should be aware of the life-threatening medical complications that can result from SUDs and psychiatric conditions/medications.

We recognize that patients with SMI require clinicians to work collaboratively, perhaps with law enforcement, to safely transport them from one point to another. Only when the rules we have outlined are followed will our patients get transported in such ways that allow them to get the care they need.
 

Dr. Norris is editor-in-chief of MDedge Psychiatry, and assistant professor of psychiatry and behavioral sciences at George Washington University, Washington. He serves as assistant dean of student affairs at the university, and medical director of psychiatric and behavioral sciences at GWU Hospital. Ms. Palmieri is a managing partner of Healthcare Legal Education & Consulting Network (HLECN), and the chief clinical officer and cofounder of XFERALL. HLECN focuses on clinical education and training, and XFERALL is a company that provides a technology platform aimed at improving access to care for behavioral health and medical patients. Ms. Slater is a managing partner of legal education for HLECN, and a trial attorney at Colley Shroyer & Abraham in Columbus, Ohio. Mr. Whaley is director of the safety and security department at GWU Hospital.

References

1. National Institute of Mental Health: Suicide.

2. National Institute on Drug Abuse. Overdose death rates. Revised January 2019.

3. Post by former NIMH Director Thomas Insel: No health without mental health. Sept. 6, 2011.

4. Dhar AK and Barton DA. Depression and the link with cardiovascular disease. Front Psychiatry. 2016 Mar 21;7:33.

5. Lichtman JH et al. Depression and coronary heart disease. Circulation. 2008;118:1768-75.

6. Hare DL et al. Depression and cardiovascular disease: A clinical review. European Heart J. 2014 Jun;35(21):1365-72.

7. “ ‘How many people have to die?’ SC mental health patients endure nightmare transport.” The News & Observer. 2019 May 29.

8. 42 C.F.R. Part 482. Part IV. Department of Health and Human Services. Medicare & Medicaid programs; Hospital conditions of participation; Patients’ rights; Final rule. 2006 Dec 8.

“I’ve given up, doctor. We gave it our best, but I am at the point where I want to end my life.” You receive this call at 2 a.m., and you’re flooded with a series of emotions and are bewildered – until your training kicks in.

Dr. Lorenzo Norris, editor-in-chief of MDedge Psychiatry, and assistant professor of psychiatry and behavioral sciences at George Washington University, Washington
Dr. Lorenzo Norris

Countless hours of working with patients in emergency department settings while on call as a resident inform your ability to triage the situation. Years of supervision guide your supportive statements as you work collaboratively with your patient to address the emotional and existential distress. As the call proceeds and you realize that your patient will require hospitalization, you are struck by a sobering question: “How am I going to arrange for my patient to go to the nearest hospital in the middle of the night?”

The options for transporting patients with serious mental illness (SMI) typically vary from bad to worse and usually filter down to three possibilities:

1. Get a friend or family member to transport them to the nearest ED.

2. Call emergency medical services (EMS) for transport to the nearest ED.

3. Call the police and request transport to the nearest ED.

Several factors would determine which of those options you would use alone or in combination. Current training paradigms for mental health professionals offer a limited body of literature on evidenced-based strategies for patients with SMI. Transporting high-risk psychiatric patients requires great care and respect, and in-depth knowledge about patients’ vulnerabilities. At best – if not handled properly – these experiences can aggravate patients’ mental health conditions. At worst, they can lead to the loss of our patients. Together, we have more than 40 years’ experience working in complex mental health care systems that run the gamut, from providing direct clinical care to directing mental health care divisions.



Sobering statistics prevail

In 2017, suicide was the 10th leading cause of death in the United States, accounting for more than 47,000 deaths. Suicide was the second-leading cause of death among individuals aged 10-34 and the fourth leading cause of death for individuals aged 35- 54.1 In 2017, more than 70,200 Americans died from a drug overdose, including illicit drugs and prescription opioids.2 Drug overdose deaths nearly quadrupled between 1999 and 2017, from 16,849 deaths to 70,237, respectively.2

Shana Palmieri, JD, a managing partner of Healthcare Legal Education & Consulting Network, and chief clinical officer and cofounder of XFERALL
Shana Palmieri

The life expectancy of an American with SMI is 14-32 years less than that of the average population.3 Those numbers are on par with many sub-Saharan countries, including Sudan and Ethiopia, and surpass the health disparities for most racial and ethnic groups.

The decrease in life expectancy for people with SMI is rarely the result of suicide but rather the effect of medical comorbidities, including heart disease, stroke, pulmonary disease, diabetes, and cancer.3 Individuals with SMI are much more likely to suffer from chronic illnesses that are associated with co-occurring addictions, side effects of psychotropic medications, and social determinants of mental health, such as poverty.

Major depressive disorder among people with SMI presents acute and chronic medical risks. For example, people with major depressive disorder are at a higher risk for stroke and cardiovascular disease.4 There is a threefold increase in cardiac-related deaths for individuals who experience depression after a heart attack.5 In addition, depression increases the risk of cardiac-related death after a heart attack more than any other risk factor, except for congestive heart failure.6

 

 

The transportation challenge

When the complexity of psychiatric conditions is conceptualized to include decreased life expectancy because of medical comorbidities, medical complications that can result from psychotropic medications, and the high incidence of co-occurring substance use disorders (SUDs), it is clear why we are concerned about the type of transport used for patients experiencing a psychiatric emergency.

Mollie Slater, a managing partner of legal education for Healthcare Legal Education & Consulting Network, and a trial attorney at Colley Shroyer & Abraham in Columbus, Ohio
Mollie Slater, JD

A common practice for patients presenting for medical treatment for a mental health condition is for them to be transported by law enforcement in handcuffs, or by private vehicle, because of a lack of medical transport options.

One tragic example occurred on Sept. 18, 2018, when two Horry County, S.C., deputies were providing a hospital-to-hospital transport for two mental health patients. The patients, who had no legal charges and were not under arrest, were locked in a transport cage in the back of a law enforcement vehicle for transport during Hurricane Florence. While the driver tried to move through floodwaters, the car stalled and became submerged. The patients were unable to open the locked cage door, and the deputies responsible for the transport did not have a key to unlock the cage.

The two women died as a result of the incident. Both deputies are facing two counts of involuntary manslaughter – with a potential prison sentence of 5 years each.7

The system that promotes the use of law enforcement to transport medical patients who are not in legal custody perpetuates a high risk to patients. Also at risk are law enforcement professionals who often are not adequately trained to evaluate, intervene, and manage patients in need of medical treatment (for acute medical, SUDs, or mental illness).
 

Recommendations for transporting high-risk patients

The legal and regulatory standards required by the Centers for Medicare & Medicaid Services guidelines8 for behavioral health patients are consistent in saying that law enforcement restraints cannot be used in hospital settings – unless the patient is under law enforcement custody. If the patient is admitted to an inpatient psychiatric unit, law enforcement restraints are never allowed to be used. Despite those guidelines for handling these situations within hospital settings, a similar standard does not exist for interhospital transport of high-risk behavioral health patients.

Kevin Whaley II, director of the safety and security department at George Washington University Hospital, Washington
Kevin Whaley II

Patients often are transported between facilities by law enforcement, and at times, with the use of law enforcement restraints. However, use of law enforcement for interhospital transport of patients not in the custody of law enforcement is both detrimental to and clinically dangerous for the patient. Not only does the scenario put the patient at risk, but it also places law enforcement professionals at risk with the potential for legal liability if the patient medically decompensates during the transport.

Also, using law enforcement to intervene and provide transportation for behavioral health patients in crisis might cause further harm to the patient’s psychological condition and deter the patient from presenting for treatment.

The appropriate level of interfacility transport for a behavioral health patient requiring an inpatient level of care is secure transport with trained medical professionals. If necessary, restraint guidelines should follow the same standard as they do in hospital settings. In situations with high risk for violence or agitation, law enforcement should be requested to accompany EMS during the transport. Handling the situation in this way allows for a collaborative approach to provide adequate medical support, and provide for the physical safety and security of the patient – and of EMS personnel.

Across police and sheriffs’ departments nationwide, law enforcement officers are required to transport mental health patients from one location or hospital to another. Hospitals and outpatient locations, often with no alternative, rely on local law enforcement agencies to provide safe transport between acute and mental health facilities. Departmental policies and the widespread belief that mental health patients automatically pose a substantial danger to themselves or others have led to these patients being handcuffed and put in the back of police cruisers. Essentially, they are treated like criminals who are under arrest.

The CMS has strict criteria for ordering, applying, evaluating, reevaluating, and reporting restraint-associated deaths. Likewise, The Joint Commission, during its accreditation survey, rightly scrutinizes a facility’s use of restraints. Both the CMS and The Joint Commission define restraint by the function of the device and not the type of the device.

According to the CMS, a restraint is any manual method, physical or mechanic device, material, or equipment that immobilizes or reduces the ability of a patient to move his or her arms, legs, body, or head freely. Within a police cruiser, handcuffs on a mental health patient who is not under arrest would fall squarely within this definition of restraint.

A patient’s current behavior or clinical needs – not history or diagnosis – should determine whether a restraint is warranted. A patient experiencing a psychiatric crisis who is not under arrest might very well escalate and become destructive and combative when being placed in handcuffs in the back of a police vehicle. What should police do at that point? Should they arrest the individual? We offer the following five recommendations.
 

 

 

Key recommendations

  • Patients who require interhospital transport for an acute behavioral health crisis should be transported by medical professionals with the training and expertise to manage mental health and medical conditions.
  • Interhospital transport restraint guidelines should be in line with CMS guidelines for hospital restraints. No patient that is not under law enforcement custody should be transported in law enforcement restraints.
  • Patients at high risk for violence/agitation (an underlying condition causing violence/agitation may include dementia, traumatic brain injuries, delirium, SUDs, or psychiatric conditions) should be managed in accordance with medically indicated intervention such as medical restraints or medications.
  • If required, a request should be made for law enforcement officers to accompany EMS to provide support and to ensure the safety of the patient and EMS professionals during the transport.
  • EMS professionals should receive specific training to manage acute psychiatric and SUD conditions, and should be aware of the life-threatening medical complications that can result from SUDs and psychiatric conditions/medications.

We recognize that patients with SMI require clinicians to work collaboratively, perhaps with law enforcement, to safely transport them from one point to another. Only when the rules we have outlined are followed will our patients get transported in such ways that allow them to get the care they need.
 

Dr. Norris is editor-in-chief of MDedge Psychiatry, and assistant professor of psychiatry and behavioral sciences at George Washington University, Washington. He serves as assistant dean of student affairs at the university, and medical director of psychiatric and behavioral sciences at GWU Hospital. Ms. Palmieri is a managing partner of Healthcare Legal Education & Consulting Network (HLECN), and the chief clinical officer and cofounder of XFERALL. HLECN focuses on clinical education and training, and XFERALL is a company that provides a technology platform aimed at improving access to care for behavioral health and medical patients. Ms. Slater is a managing partner of legal education for HLECN, and a trial attorney at Colley Shroyer & Abraham in Columbus, Ohio. Mr. Whaley is director of the safety and security department at GWU Hospital.

References

1. National Institute of Mental Health: Suicide.

2. National Institute on Drug Abuse. Overdose death rates. Revised January 2019.

3. Post by former NIMH Director Thomas Insel: No health without mental health. Sept. 6, 2011.

4. Dhar AK and Barton DA. Depression and the link with cardiovascular disease. Front Psychiatry. 2016 Mar 21;7:33.

5. Lichtman JH et al. Depression and coronary heart disease. Circulation. 2008;118:1768-75.

6. Hare DL et al. Depression and cardiovascular disease: A clinical review. European Heart J. 2014 Jun;35(21):1365-72.

7. “ ‘How many people have to die?’ SC mental health patients endure nightmare transport.” The News & Observer. 2019 May 29.

8. 42 C.F.R. Part 482. Part IV. Department of Health and Human Services. Medicare & Medicaid programs; Hospital conditions of participation; Patients’ rights; Final rule. 2006 Dec 8.

Publications
Publications
Topics
Article Type
Sections
Disallow All Ads
Content Gating
No Gating (article Unlocked/Free)
Alternative CME
Disqus Comments
Default
Use ProPublica
Hide sidebar & use full width
render the right sidebar.
Conference Recap Checkbox
Not Conference Recap
Clinical Edge
Display the Slideshow in this Article
Medscape Article
Display survey writer
Reuters content
Disable Inline Native ads
WebMD Article

Welcome Editorial

Article Type
Changed
Mon, 02/24/2020 - 10:39

It’s an honor and a great pleasure to take on this new role as editor in chief for Hematology News. When I got the call from our outgoing editor Matt Kalaycio, MD, a year ago asking me to consider stepping into his shoes a few things flashed through my mind. Will I do this role justice? Do I have what it takes to be a great editor in chief?

Dr. Ifeyinwa (Ify) Osunkwo, a sickle cell disease specialist at Levine Cancer Institute in Charlotte, N.C.
Dr. Ifeyinwa (Ify) Osunkwo

Then I thought – will there be time to learn the ropes or will this be like most of my career positions where you jump into the water first and figure out how to swim later? I never once thought: “Oh no … I cannot do this and I’m going to say no!” So here I am today, reporting for duty as the editor in chief of Hematology News.

I was once accused of being “intellectually restless” which is a badge I wear with honor and is perhaps a trait I learned from my mom who was a public health nurse in Nigeria back in the seventies. She broke a lot of glass ceilings in her day – Cornell University–trained advanced practice nurse, mother of five girls, with a degree in textile and design and business accounting. She also got a certificate in baking and cake decorating and she used all her skills and certifications to raise her daughters to believe the sky was the limit.

Mom started one of the first licensed practical nursing (LPN) schools in Nigeria and I learned from her to never back down from a challenge – on a dare I got my LPN certification before I went to medical school.

You see I love a challenge and an adventure and serving as the editor in chief for Hematology News provides me with an amazing platform and opportunity to achieve a lot of firsts and satisfy that hunger to make a global difference that has always guided my career.

I’ve thought long and hard about what and how I envision this role shaping out. What do I want our readers to take away from this newspaper under my leadership? What common themes will be woven in every edition? I want our readers to be challenged and keep learning. Not just about hematologic disorders and the latest scientific breakthroughs that drive improved patient outcomes for blood disorders but also about the intersectionality between hematology and other life disciplines.

I remember taking an art class in high school learning about dimensions and proportions of buildings and I dreamt of becoming an architect. Fast forward 2 decades later, I attended a medical conference at Georgia Institute of Technology in Atlanta and was enthralled at how various sessions demonstrated how art, engineering and architecture played a role in the development and design of orthopedic prosthesis used in amputees. I learned how engineering shaped our understanding of microfluidics, something that is now being leveraged in drug delivery science and in the field of hematology.

I want our readers to keep learning not just from esteemed scientists and clinicians but from various stakeholders – the patient, the high school student, the spouse of the hematologist, not to mention our residents and fellows, who are the future of our discipline. Furthermore, I want our readers to see the human side of hematology – the face behind the scientist or clinician and the reality of what joys and tolls we experience in this field.

A Fall 2019 Medscape survey cited the prevalence of physician burnout among hematology oncology physicians: 32% of oncologists were burned out, 4% were depressed, and 9% were both burned out and depressed. These are statistics that cannot be ignored or minimized a they ultimately have a profound impact on patient outcomes. You see, I really believe that much of the success we have in healing our patients relies not just on the medications we prescribe or on the procedures we perform or the science we leverage. Much of healing in medicine and in hematology is based on the secret sauce of being humane – defined by Merriam-Webster dictionary as the character trait that is “marked by demonstrating compassion, sympathy, or consideration for humans or animals.”

So, to sum up what to expect in the coming year from your editor in chief? Look out for some thought-provoking, fun, and unusual perspectives that are aimed to keep us learning, growing, and remaining humane in our interactions with our patients, each other, but more importantly with ourselves. #bringit2020 #HematologyNews #NewEditorInChiefPerspectives.

Ifeyinwa (Ify) Osunkwo, MD, MPH, is a professor of medicine and the director of the Sickle Cell Disease Enterprise at the Levine Cancer Institute, Atrium Health, Charlotte, N.C. She is the editor in chief of Hematology News.

Publications
Topics
Sections

It’s an honor and a great pleasure to take on this new role as editor in chief for Hematology News. When I got the call from our outgoing editor Matt Kalaycio, MD, a year ago asking me to consider stepping into his shoes a few things flashed through my mind. Will I do this role justice? Do I have what it takes to be a great editor in chief?

Dr. Ifeyinwa (Ify) Osunkwo, a sickle cell disease specialist at Levine Cancer Institute in Charlotte, N.C.
Dr. Ifeyinwa (Ify) Osunkwo

Then I thought – will there be time to learn the ropes or will this be like most of my career positions where you jump into the water first and figure out how to swim later? I never once thought: “Oh no … I cannot do this and I’m going to say no!” So here I am today, reporting for duty as the editor in chief of Hematology News.

I was once accused of being “intellectually restless” which is a badge I wear with honor and is perhaps a trait I learned from my mom who was a public health nurse in Nigeria back in the seventies. She broke a lot of glass ceilings in her day – Cornell University–trained advanced practice nurse, mother of five girls, with a degree in textile and design and business accounting. She also got a certificate in baking and cake decorating and she used all her skills and certifications to raise her daughters to believe the sky was the limit.

Mom started one of the first licensed practical nursing (LPN) schools in Nigeria and I learned from her to never back down from a challenge – on a dare I got my LPN certification before I went to medical school.

You see I love a challenge and an adventure and serving as the editor in chief for Hematology News provides me with an amazing platform and opportunity to achieve a lot of firsts and satisfy that hunger to make a global difference that has always guided my career.

I’ve thought long and hard about what and how I envision this role shaping out. What do I want our readers to take away from this newspaper under my leadership? What common themes will be woven in every edition? I want our readers to be challenged and keep learning. Not just about hematologic disorders and the latest scientific breakthroughs that drive improved patient outcomes for blood disorders but also about the intersectionality between hematology and other life disciplines.

I remember taking an art class in high school learning about dimensions and proportions of buildings and I dreamt of becoming an architect. Fast forward 2 decades later, I attended a medical conference at Georgia Institute of Technology in Atlanta and was enthralled at how various sessions demonstrated how art, engineering and architecture played a role in the development and design of orthopedic prosthesis used in amputees. I learned how engineering shaped our understanding of microfluidics, something that is now being leveraged in drug delivery science and in the field of hematology.

I want our readers to keep learning not just from esteemed scientists and clinicians but from various stakeholders – the patient, the high school student, the spouse of the hematologist, not to mention our residents and fellows, who are the future of our discipline. Furthermore, I want our readers to see the human side of hematology – the face behind the scientist or clinician and the reality of what joys and tolls we experience in this field.

A Fall 2019 Medscape survey cited the prevalence of physician burnout among hematology oncology physicians: 32% of oncologists were burned out, 4% were depressed, and 9% were both burned out and depressed. These are statistics that cannot be ignored or minimized a they ultimately have a profound impact on patient outcomes. You see, I really believe that much of the success we have in healing our patients relies not just on the medications we prescribe or on the procedures we perform or the science we leverage. Much of healing in medicine and in hematology is based on the secret sauce of being humane – defined by Merriam-Webster dictionary as the character trait that is “marked by demonstrating compassion, sympathy, or consideration for humans or animals.”

So, to sum up what to expect in the coming year from your editor in chief? Look out for some thought-provoking, fun, and unusual perspectives that are aimed to keep us learning, growing, and remaining humane in our interactions with our patients, each other, but more importantly with ourselves. #bringit2020 #HematologyNews #NewEditorInChiefPerspectives.

Ifeyinwa (Ify) Osunkwo, MD, MPH, is a professor of medicine and the director of the Sickle Cell Disease Enterprise at the Levine Cancer Institute, Atrium Health, Charlotte, N.C. She is the editor in chief of Hematology News.

It’s an honor and a great pleasure to take on this new role as editor in chief for Hematology News. When I got the call from our outgoing editor Matt Kalaycio, MD, a year ago asking me to consider stepping into his shoes a few things flashed through my mind. Will I do this role justice? Do I have what it takes to be a great editor in chief?

Dr. Ifeyinwa (Ify) Osunkwo, a sickle cell disease specialist at Levine Cancer Institute in Charlotte, N.C.
Dr. Ifeyinwa (Ify) Osunkwo

Then I thought – will there be time to learn the ropes or will this be like most of my career positions where you jump into the water first and figure out how to swim later? I never once thought: “Oh no … I cannot do this and I’m going to say no!” So here I am today, reporting for duty as the editor in chief of Hematology News.

I was once accused of being “intellectually restless” which is a badge I wear with honor and is perhaps a trait I learned from my mom who was a public health nurse in Nigeria back in the seventies. She broke a lot of glass ceilings in her day – Cornell University–trained advanced practice nurse, mother of five girls, with a degree in textile and design and business accounting. She also got a certificate in baking and cake decorating and she used all her skills and certifications to raise her daughters to believe the sky was the limit.

Mom started one of the first licensed practical nursing (LPN) schools in Nigeria and I learned from her to never back down from a challenge – on a dare I got my LPN certification before I went to medical school.

You see I love a challenge and an adventure and serving as the editor in chief for Hematology News provides me with an amazing platform and opportunity to achieve a lot of firsts and satisfy that hunger to make a global difference that has always guided my career.

I’ve thought long and hard about what and how I envision this role shaping out. What do I want our readers to take away from this newspaper under my leadership? What common themes will be woven in every edition? I want our readers to be challenged and keep learning. Not just about hematologic disorders and the latest scientific breakthroughs that drive improved patient outcomes for blood disorders but also about the intersectionality between hematology and other life disciplines.

I remember taking an art class in high school learning about dimensions and proportions of buildings and I dreamt of becoming an architect. Fast forward 2 decades later, I attended a medical conference at Georgia Institute of Technology in Atlanta and was enthralled at how various sessions demonstrated how art, engineering and architecture played a role in the development and design of orthopedic prosthesis used in amputees. I learned how engineering shaped our understanding of microfluidics, something that is now being leveraged in drug delivery science and in the field of hematology.

I want our readers to keep learning not just from esteemed scientists and clinicians but from various stakeholders – the patient, the high school student, the spouse of the hematologist, not to mention our residents and fellows, who are the future of our discipline. Furthermore, I want our readers to see the human side of hematology – the face behind the scientist or clinician and the reality of what joys and tolls we experience in this field.

A Fall 2019 Medscape survey cited the prevalence of physician burnout among hematology oncology physicians: 32% of oncologists were burned out, 4% were depressed, and 9% were both burned out and depressed. These are statistics that cannot be ignored or minimized a they ultimately have a profound impact on patient outcomes. You see, I really believe that much of the success we have in healing our patients relies not just on the medications we prescribe or on the procedures we perform or the science we leverage. Much of healing in medicine and in hematology is based on the secret sauce of being humane – defined by Merriam-Webster dictionary as the character trait that is “marked by demonstrating compassion, sympathy, or consideration for humans or animals.”

So, to sum up what to expect in the coming year from your editor in chief? Look out for some thought-provoking, fun, and unusual perspectives that are aimed to keep us learning, growing, and remaining humane in our interactions with our patients, each other, but more importantly with ourselves. #bringit2020 #HematologyNews #NewEditorInChiefPerspectives.

Ifeyinwa (Ify) Osunkwo, MD, MPH, is a professor of medicine and the director of the Sickle Cell Disease Enterprise at the Levine Cancer Institute, Atrium Health, Charlotte, N.C. She is the editor in chief of Hematology News.

Publications
Publications
Topics
Article Type
Sections
Disallow All Ads
Content Gating
No Gating (article Unlocked/Free)
Alternative CME
Disqus Comments
Default
Use ProPublica
Hide sidebar & use full width
render the right sidebar.

Chronic Diarrhea in an Adolescent Girl With a Genetic Skin Condition

Article Type
Changed
Mon, 02/24/2020 - 11:31
Display Headline
Chronic Diarrhea in an Adolescent Girl With a Genetic Skin Condition

The Diagnosis: Netherton Syndrome  

Netherton syndrome (NS) is a rare autosomal-recessive disorder characterized by a clinical triad of ichthyosis linearis circumflexa; atopic diathesis; and hair shaft abnormalities, most classically trichorrhexis invaginata.1 Netherton syndrome is caused by a loss-of-function mutation in the serine peptidase inhibitor Kazal-type gene, SPINK5, which encodes LEKTI proteins and is found in all stratified epithelia as well as the thymus.2 A lack of functional LEKTI leads to the activation of a cascade of allergy and inflammation as well as uncontrolled proteolytic activity in the stratum corneum, which causes increased desquamation.1  

Netherton syndrome presents with serpiginous or circinate scaling plaques with double-edged scale referred to as ichthyosis linearis circumflexa (quiz image). Skin plaques are intensely pruritic and migratory with fluctuating severity. Alternately, patients may have a generalized scaling erythroderma. Infants are at an especially high risk for recurrent infections, sepsis, hypernatremic dehydration, and failure to thrive.2  

Netherton syndrome often gradually improves over time, though adults with NS usually have intensely pruritic, localized patches of redness, scaling, or ichthyosis linearis circumflexa. Lichenification and eczematous plaques of the popliteal and antecubital fossae also are common.1 Therapeutic options for NS include emollients, topical steroids, phototherapy, and intravenous immunoglobulin for severe cases.3 Because there is skin barrier dysfunction in NS, supratherapeutic serum levels of tacrolimus following topical application have been reported.4 Topical pimecrolimus has been demonstrated as an effective and safer application.5 Trichorrhexis invaginata (also known as bamboo hair) of the hair and eyebrows is a pathognomonic finding in NS, involving invagination of the distal hair shaft into the proximal shaft on light microscopy examination.1 

Histopathology is variable and nonspecific with psoriasiform hyperplasia as the most frequent finding. Other histologic findings include incomplete keratinization of the epidermis, incomplete cornification with a severely reduced granular layer, and mild to moderate inflammatory dermal infiltrate.6 LEKTI immunostaining is confirmatory and shows the reduction or complete absence of LEKTI in the granular layer and inner root sheath of follicles.1 Patchy LEKTI staining would be suggestive of atopic dermatitis and psoriasis instead of NS.2 

Atopic manifestations include angioedema, urticaria, and anaphylaxis, as well as chronic diarrhea or vomiting due to food allergies.1 Elevated IgE levels for staple foods (eg, milk, wheat), elevated total serum IgE, and eosinophilia frequently are seen.7 Biopsy of the esophagus and colon likely would show mucosal eosinophilia.7,8 Elimination of major food triggers through specific serum IgE testing and oral allergen desensitization can lead to the reduction of digestive symptoms.9 Cisapride and omeprazole are effective treatments for gastroesophageal reflux and poor feeding.8 Biopsy of the intestines in this patient likely would not have shown total villous atrophy, which is rare and primarily reported in infants with NS who have failure to thrive.10 There is a limited association between NS and intestinal metaplasia, intraepithelial lymphocytes, and bacterial overgrowth. 

The primary morphology of dyskeratosis follicularis includes keratotic papules developing in sebaceous areas of the skin rather than scaly serpiginous plaques as seen in NS. Elastosis perforans serpiginosa is a perforating disorder seen in the context of several genetic conditions. It has a serpiginous appearance but, unlike NS, tends to be localized and features keratotic papules rather than patches with scale. Erythema marginatum is an uncommon feature of rheumatic fever and appears as pink annular macules and tends not to be pruritic. Subacute cutaneous lupus does feature scaly annular and serpiginous plaques but features trailing scale without the double-edge appearance of NS and is acquired rather than genetic.

References
  1. Hovnanian A. Netherton syndrome: skin inflammation and allergy by loss of protease inhibition. Cell Tissue Res. 2013;351:289-300. 
  2. Bitoun E, Micheloni A, Lamant L, et al. LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome. Human Mol Genet. 2003;12:2417-2430. 
  3. Yan AC, Honig PJ, Ming ME, et al. The safety and efficacy of pimecrolimus, 1%, cream for the treatment of Netherton syndrome: results from an exploratory study. Arch Dermatol. 2010;146:57-62. 
  4. Shah KN, Yan AC. Low but detectable serum levels of tacrolimus seen with the use of very dilute, extemporaneously compounded formulations of tacrolimus ointment in the treatment of patients with Netherton syndrome. Arch Dermatol. 2006;142:1362-1363. 
  5. Yan AC, Honig PJ, Ming ME, et al. The safety and efficacy of pimecrolimus, 1%, cream for the treatment of Netherton syndrome: results from an exploratory study. Arch Dermatol. 2010;146:57-62. 
  6. Leclerc-Mercier S, Bodemer C, Furio L, et al. Skin biopsy in Netherton syndrome: a histological review of a large series and new findings. Am J Dermatopathol. 2016;38:83-91. 
  7. Pauluel-Marmont C, Bellon N, Barbet P, et al. Eosinophilic esophagitis and colonic mucosal eosinophilia in Netherton syndrome. J Allergy Clin Immunol. 2017;139:2003-2005.e1. 
  8. Hannula-Jouppi K, Laasanen SL, Heikkila H, et al. IgE allergen component-based profiling and atopic manifestations in patients with Netherton syndrome. J Allergy Clin Immunol. 2014;134:985-988. 
  9. Kagalwalla AF, Sentongo TA, Ritz S, et al. Effect of six-food elimination diet on clinical and histologic outcomes in eosinophilic esophagitis. Clin Gastroenterol Hepatol. 2006;4:1097-1102. 
  10. Judge MR, Morgan G , Harper JI. A clinical and immunological study of Netherton's syndrome. Br J Dermatol. 1994;131:615-21.
Article PDF
Author and Disclosure Information

Ms. Liao is from Pennsylvania State University College of Medicine, Hershey. Drs. Zaenglein and Foulke are from the Department of Dermatology, Pennsylvania State Medical Center, Hershey. Dr. Zaengelin also is from the Department of Pediatrics.

The authors report no conflict of interest.

Correspondence: Galen T. Foulke, MD, 500 University Dr HU14, Hershey, PA 17033 (gfoulke@pennstatehealth.psu.edu).

Issue
Cutis - 105(2)
Publications
Topics
Page Number
E18-E19
Sections
Author and Disclosure Information

Ms. Liao is from Pennsylvania State University College of Medicine, Hershey. Drs. Zaenglein and Foulke are from the Department of Dermatology, Pennsylvania State Medical Center, Hershey. Dr. Zaengelin also is from the Department of Pediatrics.

The authors report no conflict of interest.

Correspondence: Galen T. Foulke, MD, 500 University Dr HU14, Hershey, PA 17033 (gfoulke@pennstatehealth.psu.edu).

Author and Disclosure Information

Ms. Liao is from Pennsylvania State University College of Medicine, Hershey. Drs. Zaenglein and Foulke are from the Department of Dermatology, Pennsylvania State Medical Center, Hershey. Dr. Zaengelin also is from the Department of Pediatrics.

The authors report no conflict of interest.

Correspondence: Galen T. Foulke, MD, 500 University Dr HU14, Hershey, PA 17033 (gfoulke@pennstatehealth.psu.edu).

Article PDF
Article PDF
Related Articles

The Diagnosis: Netherton Syndrome  

Netherton syndrome (NS) is a rare autosomal-recessive disorder characterized by a clinical triad of ichthyosis linearis circumflexa; atopic diathesis; and hair shaft abnormalities, most classically trichorrhexis invaginata.1 Netherton syndrome is caused by a loss-of-function mutation in the serine peptidase inhibitor Kazal-type gene, SPINK5, which encodes LEKTI proteins and is found in all stratified epithelia as well as the thymus.2 A lack of functional LEKTI leads to the activation of a cascade of allergy and inflammation as well as uncontrolled proteolytic activity in the stratum corneum, which causes increased desquamation.1  

Netherton syndrome presents with serpiginous or circinate scaling plaques with double-edged scale referred to as ichthyosis linearis circumflexa (quiz image). Skin plaques are intensely pruritic and migratory with fluctuating severity. Alternately, patients may have a generalized scaling erythroderma. Infants are at an especially high risk for recurrent infections, sepsis, hypernatremic dehydration, and failure to thrive.2  

Netherton syndrome often gradually improves over time, though adults with NS usually have intensely pruritic, localized patches of redness, scaling, or ichthyosis linearis circumflexa. Lichenification and eczematous plaques of the popliteal and antecubital fossae also are common.1 Therapeutic options for NS include emollients, topical steroids, phototherapy, and intravenous immunoglobulin for severe cases.3 Because there is skin barrier dysfunction in NS, supratherapeutic serum levels of tacrolimus following topical application have been reported.4 Topical pimecrolimus has been demonstrated as an effective and safer application.5 Trichorrhexis invaginata (also known as bamboo hair) of the hair and eyebrows is a pathognomonic finding in NS, involving invagination of the distal hair shaft into the proximal shaft on light microscopy examination.1 

Histopathology is variable and nonspecific with psoriasiform hyperplasia as the most frequent finding. Other histologic findings include incomplete keratinization of the epidermis, incomplete cornification with a severely reduced granular layer, and mild to moderate inflammatory dermal infiltrate.6 LEKTI immunostaining is confirmatory and shows the reduction or complete absence of LEKTI in the granular layer and inner root sheath of follicles.1 Patchy LEKTI staining would be suggestive of atopic dermatitis and psoriasis instead of NS.2 

Atopic manifestations include angioedema, urticaria, and anaphylaxis, as well as chronic diarrhea or vomiting due to food allergies.1 Elevated IgE levels for staple foods (eg, milk, wheat), elevated total serum IgE, and eosinophilia frequently are seen.7 Biopsy of the esophagus and colon likely would show mucosal eosinophilia.7,8 Elimination of major food triggers through specific serum IgE testing and oral allergen desensitization can lead to the reduction of digestive symptoms.9 Cisapride and omeprazole are effective treatments for gastroesophageal reflux and poor feeding.8 Biopsy of the intestines in this patient likely would not have shown total villous atrophy, which is rare and primarily reported in infants with NS who have failure to thrive.10 There is a limited association between NS and intestinal metaplasia, intraepithelial lymphocytes, and bacterial overgrowth. 

The primary morphology of dyskeratosis follicularis includes keratotic papules developing in sebaceous areas of the skin rather than scaly serpiginous plaques as seen in NS. Elastosis perforans serpiginosa is a perforating disorder seen in the context of several genetic conditions. It has a serpiginous appearance but, unlike NS, tends to be localized and features keratotic papules rather than patches with scale. Erythema marginatum is an uncommon feature of rheumatic fever and appears as pink annular macules and tends not to be pruritic. Subacute cutaneous lupus does feature scaly annular and serpiginous plaques but features trailing scale without the double-edge appearance of NS and is acquired rather than genetic.

The Diagnosis: Netherton Syndrome  

Netherton syndrome (NS) is a rare autosomal-recessive disorder characterized by a clinical triad of ichthyosis linearis circumflexa; atopic diathesis; and hair shaft abnormalities, most classically trichorrhexis invaginata.1 Netherton syndrome is caused by a loss-of-function mutation in the serine peptidase inhibitor Kazal-type gene, SPINK5, which encodes LEKTI proteins and is found in all stratified epithelia as well as the thymus.2 A lack of functional LEKTI leads to the activation of a cascade of allergy and inflammation as well as uncontrolled proteolytic activity in the stratum corneum, which causes increased desquamation.1  

Netherton syndrome presents with serpiginous or circinate scaling plaques with double-edged scale referred to as ichthyosis linearis circumflexa (quiz image). Skin plaques are intensely pruritic and migratory with fluctuating severity. Alternately, patients may have a generalized scaling erythroderma. Infants are at an especially high risk for recurrent infections, sepsis, hypernatremic dehydration, and failure to thrive.2  

Netherton syndrome often gradually improves over time, though adults with NS usually have intensely pruritic, localized patches of redness, scaling, or ichthyosis linearis circumflexa. Lichenification and eczematous plaques of the popliteal and antecubital fossae also are common.1 Therapeutic options for NS include emollients, topical steroids, phototherapy, and intravenous immunoglobulin for severe cases.3 Because there is skin barrier dysfunction in NS, supratherapeutic serum levels of tacrolimus following topical application have been reported.4 Topical pimecrolimus has been demonstrated as an effective and safer application.5 Trichorrhexis invaginata (also known as bamboo hair) of the hair and eyebrows is a pathognomonic finding in NS, involving invagination of the distal hair shaft into the proximal shaft on light microscopy examination.1 

Histopathology is variable and nonspecific with psoriasiform hyperplasia as the most frequent finding. Other histologic findings include incomplete keratinization of the epidermis, incomplete cornification with a severely reduced granular layer, and mild to moderate inflammatory dermal infiltrate.6 LEKTI immunostaining is confirmatory and shows the reduction or complete absence of LEKTI in the granular layer and inner root sheath of follicles.1 Patchy LEKTI staining would be suggestive of atopic dermatitis and psoriasis instead of NS.2 

Atopic manifestations include angioedema, urticaria, and anaphylaxis, as well as chronic diarrhea or vomiting due to food allergies.1 Elevated IgE levels for staple foods (eg, milk, wheat), elevated total serum IgE, and eosinophilia frequently are seen.7 Biopsy of the esophagus and colon likely would show mucosal eosinophilia.7,8 Elimination of major food triggers through specific serum IgE testing and oral allergen desensitization can lead to the reduction of digestive symptoms.9 Cisapride and omeprazole are effective treatments for gastroesophageal reflux and poor feeding.8 Biopsy of the intestines in this patient likely would not have shown total villous atrophy, which is rare and primarily reported in infants with NS who have failure to thrive.10 There is a limited association between NS and intestinal metaplasia, intraepithelial lymphocytes, and bacterial overgrowth. 

The primary morphology of dyskeratosis follicularis includes keratotic papules developing in sebaceous areas of the skin rather than scaly serpiginous plaques as seen in NS. Elastosis perforans serpiginosa is a perforating disorder seen in the context of several genetic conditions. It has a serpiginous appearance but, unlike NS, tends to be localized and features keratotic papules rather than patches with scale. Erythema marginatum is an uncommon feature of rheumatic fever and appears as pink annular macules and tends not to be pruritic. Subacute cutaneous lupus does feature scaly annular and serpiginous plaques but features trailing scale without the double-edge appearance of NS and is acquired rather than genetic.

References
  1. Hovnanian A. Netherton syndrome: skin inflammation and allergy by loss of protease inhibition. Cell Tissue Res. 2013;351:289-300. 
  2. Bitoun E, Micheloni A, Lamant L, et al. LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome. Human Mol Genet. 2003;12:2417-2430. 
  3. Yan AC, Honig PJ, Ming ME, et al. The safety and efficacy of pimecrolimus, 1%, cream for the treatment of Netherton syndrome: results from an exploratory study. Arch Dermatol. 2010;146:57-62. 
  4. Shah KN, Yan AC. Low but detectable serum levels of tacrolimus seen with the use of very dilute, extemporaneously compounded formulations of tacrolimus ointment in the treatment of patients with Netherton syndrome. Arch Dermatol. 2006;142:1362-1363. 
  5. Yan AC, Honig PJ, Ming ME, et al. The safety and efficacy of pimecrolimus, 1%, cream for the treatment of Netherton syndrome: results from an exploratory study. Arch Dermatol. 2010;146:57-62. 
  6. Leclerc-Mercier S, Bodemer C, Furio L, et al. Skin biopsy in Netherton syndrome: a histological review of a large series and new findings. Am J Dermatopathol. 2016;38:83-91. 
  7. Pauluel-Marmont C, Bellon N, Barbet P, et al. Eosinophilic esophagitis and colonic mucosal eosinophilia in Netherton syndrome. J Allergy Clin Immunol. 2017;139:2003-2005.e1. 
  8. Hannula-Jouppi K, Laasanen SL, Heikkila H, et al. IgE allergen component-based profiling and atopic manifestations in patients with Netherton syndrome. J Allergy Clin Immunol. 2014;134:985-988. 
  9. Kagalwalla AF, Sentongo TA, Ritz S, et al. Effect of six-food elimination diet on clinical and histologic outcomes in eosinophilic esophagitis. Clin Gastroenterol Hepatol. 2006;4:1097-1102. 
  10. Judge MR, Morgan G , Harper JI. A clinical and immunological study of Netherton's syndrome. Br J Dermatol. 1994;131:615-21.
References
  1. Hovnanian A. Netherton syndrome: skin inflammation and allergy by loss of protease inhibition. Cell Tissue Res. 2013;351:289-300. 
  2. Bitoun E, Micheloni A, Lamant L, et al. LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome. Human Mol Genet. 2003;12:2417-2430. 
  3. Yan AC, Honig PJ, Ming ME, et al. The safety and efficacy of pimecrolimus, 1%, cream for the treatment of Netherton syndrome: results from an exploratory study. Arch Dermatol. 2010;146:57-62. 
  4. Shah KN, Yan AC. Low but detectable serum levels of tacrolimus seen with the use of very dilute, extemporaneously compounded formulations of tacrolimus ointment in the treatment of patients with Netherton syndrome. Arch Dermatol. 2006;142:1362-1363. 
  5. Yan AC, Honig PJ, Ming ME, et al. The safety and efficacy of pimecrolimus, 1%, cream for the treatment of Netherton syndrome: results from an exploratory study. Arch Dermatol. 2010;146:57-62. 
  6. Leclerc-Mercier S, Bodemer C, Furio L, et al. Skin biopsy in Netherton syndrome: a histological review of a large series and new findings. Am J Dermatopathol. 2016;38:83-91. 
  7. Pauluel-Marmont C, Bellon N, Barbet P, et al. Eosinophilic esophagitis and colonic mucosal eosinophilia in Netherton syndrome. J Allergy Clin Immunol. 2017;139:2003-2005.e1. 
  8. Hannula-Jouppi K, Laasanen SL, Heikkila H, et al. IgE allergen component-based profiling and atopic manifestations in patients with Netherton syndrome. J Allergy Clin Immunol. 2014;134:985-988. 
  9. Kagalwalla AF, Sentongo TA, Ritz S, et al. Effect of six-food elimination diet on clinical and histologic outcomes in eosinophilic esophagitis. Clin Gastroenterol Hepatol. 2006;4:1097-1102. 
  10. Judge MR, Morgan G , Harper JI. A clinical and immunological study of Netherton's syndrome. Br J Dermatol. 1994;131:615-21.
Issue
Cutis - 105(2)
Issue
Cutis - 105(2)
Page Number
E18-E19
Page Number
E18-E19
Publications
Publications
Topics
Article Type
Display Headline
Chronic Diarrhea in an Adolescent Girl With a Genetic Skin Condition
Display Headline
Chronic Diarrhea in an Adolescent Girl With a Genetic Skin Condition
Sections
Questionnaire Body

A 17-year-old adolescent girl visited our clinic to establish care for her genetic skin condition. She exhibited red scaly plaques and patches over much of the body surface area consistent with atopic dermatitis but also had areas on the trunk with serpiginous red plaques with scale on the leading and trailing edges. She also noted fragile hair with sparse eyebrows. The patient reported that she had experienced chronic diarrhea and abdominal pain since childhood. She asked if it could be related to her genetic condition.  

Disallow All Ads
Content Gating
No Gating (article Unlocked/Free)
Alternative CME
Disqus Comments
Default
Gate On Date
Mon, 02/24/2020 - 10:30
Un-Gate On Date
Mon, 02/24/2020 - 10:30
Use ProPublica
CFC Schedule Remove Status
Mon, 02/24/2020 - 10:30
Hide sidebar & use full width
render the right sidebar.
Article PDF Media

Unilateral Vesicular Eruption in a Neonate

Article Type
Changed
Mon, 02/24/2020 - 11:33
Display Headline
Unilateral Vesicular Eruption in a Neonate

The Diagnosis: Incontinentia Pigmenti 

The patient was diagnosed clinically with the vesicular stage of incontinentia pigmenti (IP), a rare, X-linked dominant neuroectodermal dysplasia that usually is lethal in males. The genetic mutation has been identified in the IKBKG gene (inhibitor of nuclear factor κB; formally NEMO), which leads to a truncated and defective nuclear factor κB. Female infants survive and display characteristic findings on examination due to X-inactivation leading to mosaicism.1 Worldwide, there are approximately 27.6 new cases of IP per year. Although it is heritable, the majority (65%-75%) of cases are due to sporadic mutations, with the remaining minority (25%-35%) representing familial disease.1 

Cutaneous findings of IP classically progress through 4 stages, though individual patients often do not develop the characteristic lesions of each of the 4 stages. The vesicular stage (stage 1) presented in our patient (quiz image). This stage presents within 2 weeks of birth in 90% of patients and typically disappears when the patient is approximately 4 months of age.1-3 Although the clinical presentation is striking, it is essential to rule out herpes simplex virus infection, which can mimic vesicular IP. Localized herpes simplex virus is most commonly seen in clusters on the scalp and often is not present at birth. Alternatively, IP is most often seen on the extremities in bands or whorls of distribution along Blaschko lines,4 as in this patient. 

Stage 2 (the verrucous stage) presents with verrucous papules or pustules in a similar blaschkoid distribution. Areas previously involved in stage 1 are not always the same areas affected in stage 2. Approximately 70% of patients develop stage 2 lesions, usually at 2 to 6 weeks of age.1-3 Erythema toxicum neonatorum presents in the first week of life with pustules often on the trunk or extremities, but these lesions are not confined to Blaschko lines, differentiating it from IP.

The third stage (hyperpigmented stage) lends the disease its name and occurs in 90% to 95% of patients with IP. Linear and whorled hyperpigmentation develops in early infancy and can either persist or fade by adolescence.1 Pustules and hyperpigmentation in transient neonatal pustular melanosis may be similar to this stage of IP, but the distribution is more variable and progression to other lesions is not seen.5 

The fourth and final stage is the hypopigmented stage, whereby blaschkoid linear and whorled lines of hypopigmentation with or without both atrophy and alopecia develop in 75% of patients. This is the last finding, beginning in adolescence and often persisting into adulthood.1 Goltz syndrome is another X-linked dominant disorder with features similar to IP. Verrucous and atrophic lesions along Blaschko lines are reminiscent of the second and fourth stages of IP but are differentiated in Goltz syndrome because they present concurrently rather than in sequential stages such as IP. Similar extracutaneous organs are affected such as the eyes, teeth, and nails; however, Goltz syndrome may be associated with more distinguishing systemic signs such as sweating and skeletal abnormalities.6 

Given its unique appearance, physicians usually diagnose IP clinically after identification of characteristic linear lesions along the lines of Blaschko in an infant or neonate. Skin biopsy is confirmatory, which would differ depending on the stage of disease biopsied. The vesicular stage is characterized by eosinophilic spongiosis and is differentiated from other items on the histologic differential diagnosis by the presence of dyskeratosis.7 Genetic testing is available and should be performed along with a physical examination of the mother for counseling  purposes.1 

Proper diagnosis is critical because of the potential multisystem nature of the disease with implications for longitudinal care and prognosis in patients. As in other neurocutaneous disease, IP can affect the hair, nails, teeth, central nervous system, and eyes. All IP patients receive a referral to ophthalmology at the time of diagnosis for a dilated fundus examination, with repeat examinations every several months initially--every 3 months for a year, every 6 months from 1 to 3 years of age--and annually thereafter. Dental evaluation should occur at 6 months of age or whenever the first tooth erupts.1 Mental retardation, seizures, and developmental delay can occur and usually are evident in the first year of life. Patients should have developmental milestones closely  monitored and be referred to appropriate specialists if signs or symptoms develop consistent with neurologic involvement.1 

References
  1. Greene-Roethke C. Incontinentia pigmenti: a summary review of this rare ectodermal dysplasia with neurologic manifestations, including treatment protocols. J Pediatr Health Care. 2017;31:e45-e52. 
  2. Shah KN. Incontinentia pigmenti clinical presentation. Medscape. https://emedicine.medscape.com/article/1114205-clinical. Updated March 5, 2019. Accessed August 2, 2019. 
  3. Poziomczyk CS, Recuero JK, Bringhenti L, et al. Incontinentia pigmenti. An Bras Dermatol. 2014;89:23-36. 
  4. Mathes E, Howard RM. Vesicular, pustular, and bullous lesions in the newborn and infant. UpToDate. https://www.uptodate.com/contents/vesicular-pustular-and-bullous-lesions-in-the-newborn-and-infant. Updated December 3, 2018. Accessed February 20, 2020. 
  5. Ghosh S. Neonatal pustular dermatosis: an overview. Indian J Dermatol. 2015;60:211. 
  6. Temple IK, MacDowall P, Baraitser M, et al. Focal dermal hypoplasia (Goltz syndrome). J Med Genet. 1990;27:180-187. 
  7. Ferringer T. Genodermatoses. In: Elston D, Ferringer T, Ko CJ, et al, eds. Dermatology. 2nd ed. Philadelphia, PA: Elsevier Saunders; 2014:208-213.
Article PDF
Author and Disclosure Information

Mr. Thomas is from Kansas City University College of Osteopathic Medicine, Missouri. Drs. Whitsitt and Rajpara are from the Division of Dermatology, University of Kansas Medical Center, Kansas City.

The authors report no conflict of interest.

Correspondence: Jacob Whitsitt, MD, Division of Dermatology, University of Kansas Medical Center, 3901 Rainbow Blvd, Kansas City, KS 66160 (j10327@kumc.edu).

Issue
Cutis - 105(2)
Publications
Topics
Page Number
E16-E17
Sections
Author and Disclosure Information

Mr. Thomas is from Kansas City University College of Osteopathic Medicine, Missouri. Drs. Whitsitt and Rajpara are from the Division of Dermatology, University of Kansas Medical Center, Kansas City.

The authors report no conflict of interest.

Correspondence: Jacob Whitsitt, MD, Division of Dermatology, University of Kansas Medical Center, 3901 Rainbow Blvd, Kansas City, KS 66160 (j10327@kumc.edu).

Author and Disclosure Information

Mr. Thomas is from Kansas City University College of Osteopathic Medicine, Missouri. Drs. Whitsitt and Rajpara are from the Division of Dermatology, University of Kansas Medical Center, Kansas City.

The authors report no conflict of interest.

Correspondence: Jacob Whitsitt, MD, Division of Dermatology, University of Kansas Medical Center, 3901 Rainbow Blvd, Kansas City, KS 66160 (j10327@kumc.edu).

Article PDF
Article PDF
Related Articles

The Diagnosis: Incontinentia Pigmenti 

The patient was diagnosed clinically with the vesicular stage of incontinentia pigmenti (IP), a rare, X-linked dominant neuroectodermal dysplasia that usually is lethal in males. The genetic mutation has been identified in the IKBKG gene (inhibitor of nuclear factor κB; formally NEMO), which leads to a truncated and defective nuclear factor κB. Female infants survive and display characteristic findings on examination due to X-inactivation leading to mosaicism.1 Worldwide, there are approximately 27.6 new cases of IP per year. Although it is heritable, the majority (65%-75%) of cases are due to sporadic mutations, with the remaining minority (25%-35%) representing familial disease.1 

Cutaneous findings of IP classically progress through 4 stages, though individual patients often do not develop the characteristic lesions of each of the 4 stages. The vesicular stage (stage 1) presented in our patient (quiz image). This stage presents within 2 weeks of birth in 90% of patients and typically disappears when the patient is approximately 4 months of age.1-3 Although the clinical presentation is striking, it is essential to rule out herpes simplex virus infection, which can mimic vesicular IP. Localized herpes simplex virus is most commonly seen in clusters on the scalp and often is not present at birth. Alternatively, IP is most often seen on the extremities in bands or whorls of distribution along Blaschko lines,4 as in this patient. 

Stage 2 (the verrucous stage) presents with verrucous papules or pustules in a similar blaschkoid distribution. Areas previously involved in stage 1 are not always the same areas affected in stage 2. Approximately 70% of patients develop stage 2 lesions, usually at 2 to 6 weeks of age.1-3 Erythema toxicum neonatorum presents in the first week of life with pustules often on the trunk or extremities, but these lesions are not confined to Blaschko lines, differentiating it from IP.

The third stage (hyperpigmented stage) lends the disease its name and occurs in 90% to 95% of patients with IP. Linear and whorled hyperpigmentation develops in early infancy and can either persist or fade by adolescence.1 Pustules and hyperpigmentation in transient neonatal pustular melanosis may be similar to this stage of IP, but the distribution is more variable and progression to other lesions is not seen.5 

The fourth and final stage is the hypopigmented stage, whereby blaschkoid linear and whorled lines of hypopigmentation with or without both atrophy and alopecia develop in 75% of patients. This is the last finding, beginning in adolescence and often persisting into adulthood.1 Goltz syndrome is another X-linked dominant disorder with features similar to IP. Verrucous and atrophic lesions along Blaschko lines are reminiscent of the second and fourth stages of IP but are differentiated in Goltz syndrome because they present concurrently rather than in sequential stages such as IP. Similar extracutaneous organs are affected such as the eyes, teeth, and nails; however, Goltz syndrome may be associated with more distinguishing systemic signs such as sweating and skeletal abnormalities.6 

Given its unique appearance, physicians usually diagnose IP clinically after identification of characteristic linear lesions along the lines of Blaschko in an infant or neonate. Skin biopsy is confirmatory, which would differ depending on the stage of disease biopsied. The vesicular stage is characterized by eosinophilic spongiosis and is differentiated from other items on the histologic differential diagnosis by the presence of dyskeratosis.7 Genetic testing is available and should be performed along with a physical examination of the mother for counseling  purposes.1 

Proper diagnosis is critical because of the potential multisystem nature of the disease with implications for longitudinal care and prognosis in patients. As in other neurocutaneous disease, IP can affect the hair, nails, teeth, central nervous system, and eyes. All IP patients receive a referral to ophthalmology at the time of diagnosis for a dilated fundus examination, with repeat examinations every several months initially--every 3 months for a year, every 6 months from 1 to 3 years of age--and annually thereafter. Dental evaluation should occur at 6 months of age or whenever the first tooth erupts.1 Mental retardation, seizures, and developmental delay can occur and usually are evident in the first year of life. Patients should have developmental milestones closely  monitored and be referred to appropriate specialists if signs or symptoms develop consistent with neurologic involvement.1 

The Diagnosis: Incontinentia Pigmenti 

The patient was diagnosed clinically with the vesicular stage of incontinentia pigmenti (IP), a rare, X-linked dominant neuroectodermal dysplasia that usually is lethal in males. The genetic mutation has been identified in the IKBKG gene (inhibitor of nuclear factor κB; formally NEMO), which leads to a truncated and defective nuclear factor κB. Female infants survive and display characteristic findings on examination due to X-inactivation leading to mosaicism.1 Worldwide, there are approximately 27.6 new cases of IP per year. Although it is heritable, the majority (65%-75%) of cases are due to sporadic mutations, with the remaining minority (25%-35%) representing familial disease.1 

Cutaneous findings of IP classically progress through 4 stages, though individual patients often do not develop the characteristic lesions of each of the 4 stages. The vesicular stage (stage 1) presented in our patient (quiz image). This stage presents within 2 weeks of birth in 90% of patients and typically disappears when the patient is approximately 4 months of age.1-3 Although the clinical presentation is striking, it is essential to rule out herpes simplex virus infection, which can mimic vesicular IP. Localized herpes simplex virus is most commonly seen in clusters on the scalp and often is not present at birth. Alternatively, IP is most often seen on the extremities in bands or whorls of distribution along Blaschko lines,4 as in this patient. 

Stage 2 (the verrucous stage) presents with verrucous papules or pustules in a similar blaschkoid distribution. Areas previously involved in stage 1 are not always the same areas affected in stage 2. Approximately 70% of patients develop stage 2 lesions, usually at 2 to 6 weeks of age.1-3 Erythema toxicum neonatorum presents in the first week of life with pustules often on the trunk or extremities, but these lesions are not confined to Blaschko lines, differentiating it from IP.

The third stage (hyperpigmented stage) lends the disease its name and occurs in 90% to 95% of patients with IP. Linear and whorled hyperpigmentation develops in early infancy and can either persist or fade by adolescence.1 Pustules and hyperpigmentation in transient neonatal pustular melanosis may be similar to this stage of IP, but the distribution is more variable and progression to other lesions is not seen.5 

The fourth and final stage is the hypopigmented stage, whereby blaschkoid linear and whorled lines of hypopigmentation with or without both atrophy and alopecia develop in 75% of patients. This is the last finding, beginning in adolescence and often persisting into adulthood.1 Goltz syndrome is another X-linked dominant disorder with features similar to IP. Verrucous and atrophic lesions along Blaschko lines are reminiscent of the second and fourth stages of IP but are differentiated in Goltz syndrome because they present concurrently rather than in sequential stages such as IP. Similar extracutaneous organs are affected such as the eyes, teeth, and nails; however, Goltz syndrome may be associated with more distinguishing systemic signs such as sweating and skeletal abnormalities.6 

Given its unique appearance, physicians usually diagnose IP clinically after identification of characteristic linear lesions along the lines of Blaschko in an infant or neonate. Skin biopsy is confirmatory, which would differ depending on the stage of disease biopsied. The vesicular stage is characterized by eosinophilic spongiosis and is differentiated from other items on the histologic differential diagnosis by the presence of dyskeratosis.7 Genetic testing is available and should be performed along with a physical examination of the mother for counseling  purposes.1 

Proper diagnosis is critical because of the potential multisystem nature of the disease with implications for longitudinal care and prognosis in patients. As in other neurocutaneous disease, IP can affect the hair, nails, teeth, central nervous system, and eyes. All IP patients receive a referral to ophthalmology at the time of diagnosis for a dilated fundus examination, with repeat examinations every several months initially--every 3 months for a year, every 6 months from 1 to 3 years of age--and annually thereafter. Dental evaluation should occur at 6 months of age or whenever the first tooth erupts.1 Mental retardation, seizures, and developmental delay can occur and usually are evident in the first year of life. Patients should have developmental milestones closely  monitored and be referred to appropriate specialists if signs or symptoms develop consistent with neurologic involvement.1 

References
  1. Greene-Roethke C. Incontinentia pigmenti: a summary review of this rare ectodermal dysplasia with neurologic manifestations, including treatment protocols. J Pediatr Health Care. 2017;31:e45-e52. 
  2. Shah KN. Incontinentia pigmenti clinical presentation. Medscape. https://emedicine.medscape.com/article/1114205-clinical. Updated March 5, 2019. Accessed August 2, 2019. 
  3. Poziomczyk CS, Recuero JK, Bringhenti L, et al. Incontinentia pigmenti. An Bras Dermatol. 2014;89:23-36. 
  4. Mathes E, Howard RM. Vesicular, pustular, and bullous lesions in the newborn and infant. UpToDate. https://www.uptodate.com/contents/vesicular-pustular-and-bullous-lesions-in-the-newborn-and-infant. Updated December 3, 2018. Accessed February 20, 2020. 
  5. Ghosh S. Neonatal pustular dermatosis: an overview. Indian J Dermatol. 2015;60:211. 
  6. Temple IK, MacDowall P, Baraitser M, et al. Focal dermal hypoplasia (Goltz syndrome). J Med Genet. 1990;27:180-187. 
  7. Ferringer T. Genodermatoses. In: Elston D, Ferringer T, Ko CJ, et al, eds. Dermatology. 2nd ed. Philadelphia, PA: Elsevier Saunders; 2014:208-213.
References
  1. Greene-Roethke C. Incontinentia pigmenti: a summary review of this rare ectodermal dysplasia with neurologic manifestations, including treatment protocols. J Pediatr Health Care. 2017;31:e45-e52. 
  2. Shah KN. Incontinentia pigmenti clinical presentation. Medscape. https://emedicine.medscape.com/article/1114205-clinical. Updated March 5, 2019. Accessed August 2, 2019. 
  3. Poziomczyk CS, Recuero JK, Bringhenti L, et al. Incontinentia pigmenti. An Bras Dermatol. 2014;89:23-36. 
  4. Mathes E, Howard RM. Vesicular, pustular, and bullous lesions in the newborn and infant. UpToDate. https://www.uptodate.com/contents/vesicular-pustular-and-bullous-lesions-in-the-newborn-and-infant. Updated December 3, 2018. Accessed February 20, 2020. 
  5. Ghosh S. Neonatal pustular dermatosis: an overview. Indian J Dermatol. 2015;60:211. 
  6. Temple IK, MacDowall P, Baraitser M, et al. Focal dermal hypoplasia (Goltz syndrome). J Med Genet. 1990;27:180-187. 
  7. Ferringer T. Genodermatoses. In: Elston D, Ferringer T, Ko CJ, et al, eds. Dermatology. 2nd ed. Philadelphia, PA: Elsevier Saunders; 2014:208-213.
Issue
Cutis - 105(2)
Issue
Cutis - 105(2)
Page Number
E16-E17
Page Number
E16-E17
Publications
Publications
Topics
Article Type
Display Headline
Unilateral Vesicular Eruption in a Neonate
Display Headline
Unilateral Vesicular Eruption in a Neonate
Sections
Questionnaire Body

A 4-day-old female neonate presented to the dermatology clinic with a vesicular eruption on the left leg of 1 day's duration. The eruption was asymptomatic without any extracutaneous findings. This term infant was born without complication, and the mother denied any symptoms consistent with herpes simplex virus infection. Physical examination revealed yellow-red vesicles on an erythematous base in a blaschkoid distribution on the left leg. The rest of the examination was unremarkable. Herpes simplex virus polymerase chain reaction testing was negative.  

Disallow All Ads
Content Gating
No Gating (article Unlocked/Free)
Alternative CME
Disqus Comments
Default
Gate On Date
Mon, 02/24/2020 - 10:15
Un-Gate On Date
Mon, 02/24/2020 - 10:15
Use ProPublica
CFC Schedule Remove Status
Mon, 02/24/2020 - 10:15
Hide sidebar & use full width
render the right sidebar.
Article PDF Media

June Medical Services v. Russo: Understanding this high-stakes abortion case

Article Type
Changed
Fri, 02/28/2020 - 14:16
Display Headline
June Medical Services v. Russo: Understanding this high-stakes abortion case

On March 4, 2020, the Supreme Court of the United States (SCOTUS) will hear opening arguments for June Medical Services v. Russo. (Please note that this case was originally referred to as June Medical Services v. Gee. However, Secretary Rebekah Gee resigned from her position on January 31, 2020, and was replaced by Interim Secretary Stephen Russo.) The case will examine a Louisiana law (Louisiana Act 620, or LA 620), originally passed in 2014, that requires physicians to have hospital admitting privileges within 30 miles of where they provide abortion services.1 When LA 620 was signed into law in 2014, 5 of Louisiana’s 6 abortion clinics would not have met the standards created by this legislation and would have been forced to close, potentially leaving the vast majority of women in Louisiana without access to an abortion provider, and disproportionately impacting poor and rural women. Prior to enactment of this law, physicians at these 5 clinics attempted to obtain admitting privileges, and all were denied. The denials occurred due to two main reasons—because the providers admitted too few patients each year to qualify for hospital privileges or simply because they provided abortion care.2 Shortly after this legislation was signed into law, the Center for Reproductive Rights (CRR) challenged the law, citing the undue burden it created for patients attempting to access abortion care.
 

Prior case also considered question of hospital privileges for abortion providers

Interestingly, SCOTUS already has ruled on this very question. In 1992, the Court ruled in Planned Parenthood of Southeastern Pennsylvania v. Casey that it is unconstitutional for a state to create an “undue burden” on a woman’s right to abortion prior to fetal viability.3 And in 2016, when considering whether or not requiring abortion providers to obtain hospital privileges creates an undue burden in Whole Women’s Health (WWH) v. Hellerstedt, the Supreme Court’s answer was yes, it does. WWH, with legal aid from CRR, challenged Texas House Bill 2 (H.B. 2), which similar to LA 620, required abortion providers to have local admitting privileges. Based largely on the precedent set in Casey, SCOTUS ruled 5-3 in favor of WWH.

The Louisiana law currently in question was written and challenged in district court simultaneous to the Supreme Court’s review of WWH. The district court declared LA 620 invalid and permanently enjoined its enforcement, finding the law would “drastically burden women’s right to choose abortions.”4 However, the US Court of Appeals for the Fifth Circuit reviewed the case and overturned the district court decision, finding the lower court’s analysis erroneous and stating, “no clinics will likely be forced to close on account of [LA 620].” The Fifth Circuit panel ruled that, despite the precedent of WWH, LA 620 did not create an undue burden because of state-level differences in admitting privileges, demographics, and geography. They also found that only 30% of the 2 million women living in Louisiana would be impacted by the law, predominantly via longer wait times, and argued that this does not represent significant burden. The plaintiffs filed for an emergency stay with SCOTUS, who granted the stay pending a full hearing. On March 4, the Supreme Court will hear arguments to determine if the Fifth Circuit was correct in drawing a distinction between LA 620 and the SCOTUS verdict in WWH.

 

 

Targeted restrictions on abortion providers

LA 620 joins a long series of laws meant to enact targeted restrictions on abortion providers, or “TRAP” laws. TRAP laws are written to limit access to abortion under the guise of improving patient safety, despite ample evidence to the contrary, and include such various regulations as admitting privileges, facilities requirements, waiting periods, and parental or partner notification. Many such laws have been enacted in the last decade, and many struck down based on judicial precedent.

How the Supreme Court has ruled in the past

When a case is appealed to the Supreme Court, the court can either decline to hear the case, thereby leaving the lower courts’ ruling in place, or choose to hear the case in full and either affirm or overturn the lower court’s decision. After issuing a ruling in WWH, the 2016-2017 Roberts Court declined to hear challenges from other states with similarly overturned laws, leaving the laws struck down. In electing to hear June Medical Services v. Russo, the court has the opportunity to uphold or overturn the Fifth Circuit Court’s decision. However, today’s Supreme Court differs greatly from the Supreme Court in 2016.

In 2016, the court ruled 5-3 to overturn H.B. 2 in WWH shortly after the death of Justice Antonin Scalia. Scalia was replaced by Justice Neil Gorsuch, a Constitutional originalist who has never directly ruled on an abortion case.5 In 2018, Justice Anthony Kennedy, who authored the court’s majority opinion on Casey and was among the majority on WWH, retired, and was replaced by Justice Brett Kavanaugh. Kavanaugh has ruled once on the right to abortion in Garza v. Hargan in 2017, where he argued that precedent states that the government has “permissible interests in favoring fetal life…and refraining from facilitating abortion,” and that significant delay in care did not constitute undue burden.6 In regard to the 5-4 stay issued by the court in June Medical Services, Kavanaugh joined Gorsuch in voting to deny the application for stay, and was the only justice to issue an opinion alongside the ruling, arguing that because the doctors in question had not applied for and been denied admitting privileges since the WWH ruling, the case hinges on theoretical rather than demonstrable undue burden.7 Appointed by President Donald Trump, both Gorsuch and Kavanaugh are widely considered to be conservative judges, and while neither has a strong judicial record on abortion rights, both are anticipated to side with the conservative majority on the court.

The Supreme Court rarely overturns its own precedent, but concerns are high

The question of precedent will be central in SCOTUS hearing June Medical Services v. Russo so quickly after the WWH decision. Additionally, in hearing this case, the court will have the opportunity to reexamine all relevant precedent, including the Planned Parenthood of Southeastern Pennsylvania v. Casey decision and even Roe v. Wade. With a conservative court and an increasingly charged political environment, reproductive rights advocates fear that the June Medical Services v. Russo ruling may be the first step toward dismantling judicial protection of abortion rights in the United States.

 

 

If SCOTUS rules against June Medical Services, stating that admitting privileges do not cause an undue burden for women seeking to access abortion care, other states likely will introduce and enact similar legislation. These TRAP laws have the potential to limit or eliminate access to abortion for 25 million people of reproductive age. Numerous studies have demonstrated that limiting access to abortion care does not decrease the number of abortions but can result in patients using unsafe means to obtain an abortion.8

The medical community recognizes the danger of enacting restrictive legislation. The American College of Obstetricians and Gynecologists (ACOG), along with the American Medical Association, the Society of Maternal-Fetal Medicine, the Association for Sexual and Reproductive Medicine, the American Association of Family Practitioners, and many others, filed an amicus curiae in support of the June Medical Services plaintiffs.9 These brief filings are critical to ensuring the courts hear physician voices in this important legal decision, and ACOG’s briefs have been quoted in several previous Supreme Court opinions, concurrences, and dissents.
 

Action items

  • Although June Medical Services v. Russo’s decision will not be made until early summer 2020, we can continue to use our voices and expertise to speak out against laws designed to limit access to abortion—at the state and federal levels. As women’s health clinicians, we see the impact abortion restrictions have on our patients, especially our low income and rural patients. Sharing these stories with our legislators, testifying for or against legislation, and speaking out in our communities can have a powerful impact. Check with your local ACOG chapter or with ACOG’s state and government affairs office for more information.
  • Follow along with this case at SCOTUS Blog.
  • Lastly, make sure you are registered to vote. We are in an election year, and using our voices in and out of the ballot box is critical. You can register here.
References
  1. HB338. Louisiana State Legislature. 2014. http://www.legis.la.gov/legis/BillInfo.aspx?s=14RS&b=ACT620&sbi=y. Accessed February 19, 2020.
  2. Nash E, Donovan MK. Admitting priveleges are back at the U.S. Supreme Court with serious implications for abortion access. Guttmacher Institute. Updated December 3, 2019.
  3. Planned Parenthood of Southeastern Pennsylvania v. Casey. Cornell Law School Legal Information Institute. https://www.law.cornell.edu/supremecourt/text/505/833. Accessed February 20, 2020.
  4. June Medical Services LLC v Gee. Oyez. www.oyez.org/cases/2019/18-1323. Accessed February 20, 2020.
  5. Neil Gorsuch. Oyez. https://www.oyez.org/justices/neil_gorsuch. Accessed February 20, 2020.
  6. Judge Kavanaugh’s Judicial Record on the Right to Abortion. Center for Reproductive Rights. https://www.reproductiverights.org/sites/crr.civicactions.net/files/documents/factsheets/Judge-Kavanaugh-Judicial-Record-on-the-Right-to-Abortion2.pdf. Accessed February 20, 2020.
  7. Kavanaugh B. (2019, February 7). June Medical Services, L.L.C, v. Gee, 586 U.S. ____ (2019). Supreme Court of the United States. https://www.supremecourt.gov/opinions/18pdf/18a774_3ebh.pdf. Accessed February 20, 2020.
  8. Cohen SA. Facts and consequences: Legality, incidence and safety of abortion worldwide. November 20, 2009.
  9. June Medical Services, LLC v. Russo. SCOTUSblog. February 6, 2020. https://www.scotusblog.com/case-files/cases/june-medical-services-llc-v-russo/. Accessed February 20, 2020.
Author and Disclosure Information

Dr. Trammel is ObGyn Resident, Tufts Medical Center, Boston, Massachusetts.

Dr. Evans is Assistant Professor, Tufts University School of Medicine, and Associate Program Director, Department of Obstetrics and Gynecology, Tufts Medical Center.

The authors report no financial relationships relevant to this article.

Issue
OBG Management - 32(2)
Publications
Topics
Sections
Author and Disclosure Information

Dr. Trammel is ObGyn Resident, Tufts Medical Center, Boston, Massachusetts.

Dr. Evans is Assistant Professor, Tufts University School of Medicine, and Associate Program Director, Department of Obstetrics and Gynecology, Tufts Medical Center.

The authors report no financial relationships relevant to this article.

Author and Disclosure Information

Dr. Trammel is ObGyn Resident, Tufts Medical Center, Boston, Massachusetts.

Dr. Evans is Assistant Professor, Tufts University School of Medicine, and Associate Program Director, Department of Obstetrics and Gynecology, Tufts Medical Center.

The authors report no financial relationships relevant to this article.

On March 4, 2020, the Supreme Court of the United States (SCOTUS) will hear opening arguments for June Medical Services v. Russo. (Please note that this case was originally referred to as June Medical Services v. Gee. However, Secretary Rebekah Gee resigned from her position on January 31, 2020, and was replaced by Interim Secretary Stephen Russo.) The case will examine a Louisiana law (Louisiana Act 620, or LA 620), originally passed in 2014, that requires physicians to have hospital admitting privileges within 30 miles of where they provide abortion services.1 When LA 620 was signed into law in 2014, 5 of Louisiana’s 6 abortion clinics would not have met the standards created by this legislation and would have been forced to close, potentially leaving the vast majority of women in Louisiana without access to an abortion provider, and disproportionately impacting poor and rural women. Prior to enactment of this law, physicians at these 5 clinics attempted to obtain admitting privileges, and all were denied. The denials occurred due to two main reasons—because the providers admitted too few patients each year to qualify for hospital privileges or simply because they provided abortion care.2 Shortly after this legislation was signed into law, the Center for Reproductive Rights (CRR) challenged the law, citing the undue burden it created for patients attempting to access abortion care.
 

Prior case also considered question of hospital privileges for abortion providers

Interestingly, SCOTUS already has ruled on this very question. In 1992, the Court ruled in Planned Parenthood of Southeastern Pennsylvania v. Casey that it is unconstitutional for a state to create an “undue burden” on a woman’s right to abortion prior to fetal viability.3 And in 2016, when considering whether or not requiring abortion providers to obtain hospital privileges creates an undue burden in Whole Women’s Health (WWH) v. Hellerstedt, the Supreme Court’s answer was yes, it does. WWH, with legal aid from CRR, challenged Texas House Bill 2 (H.B. 2), which similar to LA 620, required abortion providers to have local admitting privileges. Based largely on the precedent set in Casey, SCOTUS ruled 5-3 in favor of WWH.

The Louisiana law currently in question was written and challenged in district court simultaneous to the Supreme Court’s review of WWH. The district court declared LA 620 invalid and permanently enjoined its enforcement, finding the law would “drastically burden women’s right to choose abortions.”4 However, the US Court of Appeals for the Fifth Circuit reviewed the case and overturned the district court decision, finding the lower court’s analysis erroneous and stating, “no clinics will likely be forced to close on account of [LA 620].” The Fifth Circuit panel ruled that, despite the precedent of WWH, LA 620 did not create an undue burden because of state-level differences in admitting privileges, demographics, and geography. They also found that only 30% of the 2 million women living in Louisiana would be impacted by the law, predominantly via longer wait times, and argued that this does not represent significant burden. The plaintiffs filed for an emergency stay with SCOTUS, who granted the stay pending a full hearing. On March 4, the Supreme Court will hear arguments to determine if the Fifth Circuit was correct in drawing a distinction between LA 620 and the SCOTUS verdict in WWH.

 

 

Targeted restrictions on abortion providers

LA 620 joins a long series of laws meant to enact targeted restrictions on abortion providers, or “TRAP” laws. TRAP laws are written to limit access to abortion under the guise of improving patient safety, despite ample evidence to the contrary, and include such various regulations as admitting privileges, facilities requirements, waiting periods, and parental or partner notification. Many such laws have been enacted in the last decade, and many struck down based on judicial precedent.

How the Supreme Court has ruled in the past

When a case is appealed to the Supreme Court, the court can either decline to hear the case, thereby leaving the lower courts’ ruling in place, or choose to hear the case in full and either affirm or overturn the lower court’s decision. After issuing a ruling in WWH, the 2016-2017 Roberts Court declined to hear challenges from other states with similarly overturned laws, leaving the laws struck down. In electing to hear June Medical Services v. Russo, the court has the opportunity to uphold or overturn the Fifth Circuit Court’s decision. However, today’s Supreme Court differs greatly from the Supreme Court in 2016.

In 2016, the court ruled 5-3 to overturn H.B. 2 in WWH shortly after the death of Justice Antonin Scalia. Scalia was replaced by Justice Neil Gorsuch, a Constitutional originalist who has never directly ruled on an abortion case.5 In 2018, Justice Anthony Kennedy, who authored the court’s majority opinion on Casey and was among the majority on WWH, retired, and was replaced by Justice Brett Kavanaugh. Kavanaugh has ruled once on the right to abortion in Garza v. Hargan in 2017, where he argued that precedent states that the government has “permissible interests in favoring fetal life…and refraining from facilitating abortion,” and that significant delay in care did not constitute undue burden.6 In regard to the 5-4 stay issued by the court in June Medical Services, Kavanaugh joined Gorsuch in voting to deny the application for stay, and was the only justice to issue an opinion alongside the ruling, arguing that because the doctors in question had not applied for and been denied admitting privileges since the WWH ruling, the case hinges on theoretical rather than demonstrable undue burden.7 Appointed by President Donald Trump, both Gorsuch and Kavanaugh are widely considered to be conservative judges, and while neither has a strong judicial record on abortion rights, both are anticipated to side with the conservative majority on the court.

The Supreme Court rarely overturns its own precedent, but concerns are high

The question of precedent will be central in SCOTUS hearing June Medical Services v. Russo so quickly after the WWH decision. Additionally, in hearing this case, the court will have the opportunity to reexamine all relevant precedent, including the Planned Parenthood of Southeastern Pennsylvania v. Casey decision and even Roe v. Wade. With a conservative court and an increasingly charged political environment, reproductive rights advocates fear that the June Medical Services v. Russo ruling may be the first step toward dismantling judicial protection of abortion rights in the United States.

 

 

If SCOTUS rules against June Medical Services, stating that admitting privileges do not cause an undue burden for women seeking to access abortion care, other states likely will introduce and enact similar legislation. These TRAP laws have the potential to limit or eliminate access to abortion for 25 million people of reproductive age. Numerous studies have demonstrated that limiting access to abortion care does not decrease the number of abortions but can result in patients using unsafe means to obtain an abortion.8

The medical community recognizes the danger of enacting restrictive legislation. The American College of Obstetricians and Gynecologists (ACOG), along with the American Medical Association, the Society of Maternal-Fetal Medicine, the Association for Sexual and Reproductive Medicine, the American Association of Family Practitioners, and many others, filed an amicus curiae in support of the June Medical Services plaintiffs.9 These brief filings are critical to ensuring the courts hear physician voices in this important legal decision, and ACOG’s briefs have been quoted in several previous Supreme Court opinions, concurrences, and dissents.
 

Action items

  • Although June Medical Services v. Russo’s decision will not be made until early summer 2020, we can continue to use our voices and expertise to speak out against laws designed to limit access to abortion—at the state and federal levels. As women’s health clinicians, we see the impact abortion restrictions have on our patients, especially our low income and rural patients. Sharing these stories with our legislators, testifying for or against legislation, and speaking out in our communities can have a powerful impact. Check with your local ACOG chapter or with ACOG’s state and government affairs office for more information.
  • Follow along with this case at SCOTUS Blog.
  • Lastly, make sure you are registered to vote. We are in an election year, and using our voices in and out of the ballot box is critical. You can register here.

On March 4, 2020, the Supreme Court of the United States (SCOTUS) will hear opening arguments for June Medical Services v. Russo. (Please note that this case was originally referred to as June Medical Services v. Gee. However, Secretary Rebekah Gee resigned from her position on January 31, 2020, and was replaced by Interim Secretary Stephen Russo.) The case will examine a Louisiana law (Louisiana Act 620, or LA 620), originally passed in 2014, that requires physicians to have hospital admitting privileges within 30 miles of where they provide abortion services.1 When LA 620 was signed into law in 2014, 5 of Louisiana’s 6 abortion clinics would not have met the standards created by this legislation and would have been forced to close, potentially leaving the vast majority of women in Louisiana without access to an abortion provider, and disproportionately impacting poor and rural women. Prior to enactment of this law, physicians at these 5 clinics attempted to obtain admitting privileges, and all were denied. The denials occurred due to two main reasons—because the providers admitted too few patients each year to qualify for hospital privileges or simply because they provided abortion care.2 Shortly after this legislation was signed into law, the Center for Reproductive Rights (CRR) challenged the law, citing the undue burden it created for patients attempting to access abortion care.
 

Prior case also considered question of hospital privileges for abortion providers

Interestingly, SCOTUS already has ruled on this very question. In 1992, the Court ruled in Planned Parenthood of Southeastern Pennsylvania v. Casey that it is unconstitutional for a state to create an “undue burden” on a woman’s right to abortion prior to fetal viability.3 And in 2016, when considering whether or not requiring abortion providers to obtain hospital privileges creates an undue burden in Whole Women’s Health (WWH) v. Hellerstedt, the Supreme Court’s answer was yes, it does. WWH, with legal aid from CRR, challenged Texas House Bill 2 (H.B. 2), which similar to LA 620, required abortion providers to have local admitting privileges. Based largely on the precedent set in Casey, SCOTUS ruled 5-3 in favor of WWH.

The Louisiana law currently in question was written and challenged in district court simultaneous to the Supreme Court’s review of WWH. The district court declared LA 620 invalid and permanently enjoined its enforcement, finding the law would “drastically burden women’s right to choose abortions.”4 However, the US Court of Appeals for the Fifth Circuit reviewed the case and overturned the district court decision, finding the lower court’s analysis erroneous and stating, “no clinics will likely be forced to close on account of [LA 620].” The Fifth Circuit panel ruled that, despite the precedent of WWH, LA 620 did not create an undue burden because of state-level differences in admitting privileges, demographics, and geography. They also found that only 30% of the 2 million women living in Louisiana would be impacted by the law, predominantly via longer wait times, and argued that this does not represent significant burden. The plaintiffs filed for an emergency stay with SCOTUS, who granted the stay pending a full hearing. On March 4, the Supreme Court will hear arguments to determine if the Fifth Circuit was correct in drawing a distinction between LA 620 and the SCOTUS verdict in WWH.

 

 

Targeted restrictions on abortion providers

LA 620 joins a long series of laws meant to enact targeted restrictions on abortion providers, or “TRAP” laws. TRAP laws are written to limit access to abortion under the guise of improving patient safety, despite ample evidence to the contrary, and include such various regulations as admitting privileges, facilities requirements, waiting periods, and parental or partner notification. Many such laws have been enacted in the last decade, and many struck down based on judicial precedent.

How the Supreme Court has ruled in the past

When a case is appealed to the Supreme Court, the court can either decline to hear the case, thereby leaving the lower courts’ ruling in place, or choose to hear the case in full and either affirm or overturn the lower court’s decision. After issuing a ruling in WWH, the 2016-2017 Roberts Court declined to hear challenges from other states with similarly overturned laws, leaving the laws struck down. In electing to hear June Medical Services v. Russo, the court has the opportunity to uphold or overturn the Fifth Circuit Court’s decision. However, today’s Supreme Court differs greatly from the Supreme Court in 2016.

In 2016, the court ruled 5-3 to overturn H.B. 2 in WWH shortly after the death of Justice Antonin Scalia. Scalia was replaced by Justice Neil Gorsuch, a Constitutional originalist who has never directly ruled on an abortion case.5 In 2018, Justice Anthony Kennedy, who authored the court’s majority opinion on Casey and was among the majority on WWH, retired, and was replaced by Justice Brett Kavanaugh. Kavanaugh has ruled once on the right to abortion in Garza v. Hargan in 2017, where he argued that precedent states that the government has “permissible interests in favoring fetal life…and refraining from facilitating abortion,” and that significant delay in care did not constitute undue burden.6 In regard to the 5-4 stay issued by the court in June Medical Services, Kavanaugh joined Gorsuch in voting to deny the application for stay, and was the only justice to issue an opinion alongside the ruling, arguing that because the doctors in question had not applied for and been denied admitting privileges since the WWH ruling, the case hinges on theoretical rather than demonstrable undue burden.7 Appointed by President Donald Trump, both Gorsuch and Kavanaugh are widely considered to be conservative judges, and while neither has a strong judicial record on abortion rights, both are anticipated to side with the conservative majority on the court.

The Supreme Court rarely overturns its own precedent, but concerns are high

The question of precedent will be central in SCOTUS hearing June Medical Services v. Russo so quickly after the WWH decision. Additionally, in hearing this case, the court will have the opportunity to reexamine all relevant precedent, including the Planned Parenthood of Southeastern Pennsylvania v. Casey decision and even Roe v. Wade. With a conservative court and an increasingly charged political environment, reproductive rights advocates fear that the June Medical Services v. Russo ruling may be the first step toward dismantling judicial protection of abortion rights in the United States.

 

 

If SCOTUS rules against June Medical Services, stating that admitting privileges do not cause an undue burden for women seeking to access abortion care, other states likely will introduce and enact similar legislation. These TRAP laws have the potential to limit or eliminate access to abortion for 25 million people of reproductive age. Numerous studies have demonstrated that limiting access to abortion care does not decrease the number of abortions but can result in patients using unsafe means to obtain an abortion.8

The medical community recognizes the danger of enacting restrictive legislation. The American College of Obstetricians and Gynecologists (ACOG), along with the American Medical Association, the Society of Maternal-Fetal Medicine, the Association for Sexual and Reproductive Medicine, the American Association of Family Practitioners, and many others, filed an amicus curiae in support of the June Medical Services plaintiffs.9 These brief filings are critical to ensuring the courts hear physician voices in this important legal decision, and ACOG’s briefs have been quoted in several previous Supreme Court opinions, concurrences, and dissents.
 

Action items

  • Although June Medical Services v. Russo’s decision will not be made until early summer 2020, we can continue to use our voices and expertise to speak out against laws designed to limit access to abortion—at the state and federal levels. As women’s health clinicians, we see the impact abortion restrictions have on our patients, especially our low income and rural patients. Sharing these stories with our legislators, testifying for or against legislation, and speaking out in our communities can have a powerful impact. Check with your local ACOG chapter or with ACOG’s state and government affairs office for more information.
  • Follow along with this case at SCOTUS Blog.
  • Lastly, make sure you are registered to vote. We are in an election year, and using our voices in and out of the ballot box is critical. You can register here.
References
  1. HB338. Louisiana State Legislature. 2014. http://www.legis.la.gov/legis/BillInfo.aspx?s=14RS&b=ACT620&sbi=y. Accessed February 19, 2020.
  2. Nash E, Donovan MK. Admitting priveleges are back at the U.S. Supreme Court with serious implications for abortion access. Guttmacher Institute. Updated December 3, 2019.
  3. Planned Parenthood of Southeastern Pennsylvania v. Casey. Cornell Law School Legal Information Institute. https://www.law.cornell.edu/supremecourt/text/505/833. Accessed February 20, 2020.
  4. June Medical Services LLC v Gee. Oyez. www.oyez.org/cases/2019/18-1323. Accessed February 20, 2020.
  5. Neil Gorsuch. Oyez. https://www.oyez.org/justices/neil_gorsuch. Accessed February 20, 2020.
  6. Judge Kavanaugh’s Judicial Record on the Right to Abortion. Center for Reproductive Rights. https://www.reproductiverights.org/sites/crr.civicactions.net/files/documents/factsheets/Judge-Kavanaugh-Judicial-Record-on-the-Right-to-Abortion2.pdf. Accessed February 20, 2020.
  7. Kavanaugh B. (2019, February 7). June Medical Services, L.L.C, v. Gee, 586 U.S. ____ (2019). Supreme Court of the United States. https://www.supremecourt.gov/opinions/18pdf/18a774_3ebh.pdf. Accessed February 20, 2020.
  8. Cohen SA. Facts and consequences: Legality, incidence and safety of abortion worldwide. November 20, 2009.
  9. June Medical Services, LLC v. Russo. SCOTUSblog. February 6, 2020. https://www.scotusblog.com/case-files/cases/june-medical-services-llc-v-russo/. Accessed February 20, 2020.
References
  1. HB338. Louisiana State Legislature. 2014. http://www.legis.la.gov/legis/BillInfo.aspx?s=14RS&b=ACT620&sbi=y. Accessed February 19, 2020.
  2. Nash E, Donovan MK. Admitting priveleges are back at the U.S. Supreme Court with serious implications for abortion access. Guttmacher Institute. Updated December 3, 2019.
  3. Planned Parenthood of Southeastern Pennsylvania v. Casey. Cornell Law School Legal Information Institute. https://www.law.cornell.edu/supremecourt/text/505/833. Accessed February 20, 2020.
  4. June Medical Services LLC v Gee. Oyez. www.oyez.org/cases/2019/18-1323. Accessed February 20, 2020.
  5. Neil Gorsuch. Oyez. https://www.oyez.org/justices/neil_gorsuch. Accessed February 20, 2020.
  6. Judge Kavanaugh’s Judicial Record on the Right to Abortion. Center for Reproductive Rights. https://www.reproductiverights.org/sites/crr.civicactions.net/files/documents/factsheets/Judge-Kavanaugh-Judicial-Record-on-the-Right-to-Abortion2.pdf. Accessed February 20, 2020.
  7. Kavanaugh B. (2019, February 7). June Medical Services, L.L.C, v. Gee, 586 U.S. ____ (2019). Supreme Court of the United States. https://www.supremecourt.gov/opinions/18pdf/18a774_3ebh.pdf. Accessed February 20, 2020.
  8. Cohen SA. Facts and consequences: Legality, incidence and safety of abortion worldwide. November 20, 2009.
  9. June Medical Services, LLC v. Russo. SCOTUSblog. February 6, 2020. https://www.scotusblog.com/case-files/cases/june-medical-services-llc-v-russo/. Accessed February 20, 2020.
Issue
OBG Management - 32(2)
Issue
OBG Management - 32(2)
Publications
Publications
Topics
Article Type
Display Headline
June Medical Services v. Russo: Understanding this high-stakes abortion case
Display Headline
June Medical Services v. Russo: Understanding this high-stakes abortion case
Sections
Disallow All Ads
Content Gating
No Gating (article Unlocked/Free)
Alternative CME
Disqus Comments
Default
Eyebrow Default
ADVOCACY COLUMN
Use ProPublica
Hide sidebar & use full width
render the right sidebar.

Study implicates gut bacteria in PAH

Article Type
Changed
Tue, 02/25/2020 - 11:33

Model finds microbiota highly predictive

A unique collection of bacteria in the gut may have a strong association with pulmonary arterial hypertension and could be highly predictive of the disease in undiagnosed patients, according to a study published in the journal Hypertension.

Dr. Mohan Raizada

This is the first study to show that people with PAH have a common specific gut microbiota profile, wrote lead study author Mohan Raizada, PhD, distinguished professor in the department of physiology and functional genomics at the University of Florida, Gainesville.

The findings have the potential to change how cardiologists diagnose and treat PAH, he added. “While current PAH treatments focus on the lungs, looking at the lung/gut axis could open the door to new therapies centered in the digestive system,” Dr. Raizada said.

The researchers developed a model that found the specific microbiota profile was 83% accurate in predicting the presence or absence of PAH. If a larger study can validate the findings, the researchers wrote, this could lead to a new test for diagnosing PAH that’s less invasive than cardiac catheterization. It could also lead to new treatments that target the gut microbiome.

Study investigators collected stool samples from 18 PAH patients and 12 people without a history of cardiopulmonary disease. The microbiota DNA from the stool samples were isolated and sequenced. The analysis revealed that PAH patients had reduced richness and evenness of the gut bacteria, known as alpha diversity. They had increased levels of bacteria associated with atherosclerosis, and healthy patients had increased levels of bacteria that produced short-chain fatty acids.

Although recent studies have begun to show potential associations between the gut microbiome and cardiovascular diseases, this research is in its infancy, Mariell Jessup, MD, commented. “Even though the study by Dr. Raizada and colleagues predicted pulmonary arterial hypertension based on an individual’s microbiome with some accuracy, it is an observational study, so it does not prove cause and effect. Many other factors, especially diet, affect the gut microbiome,” added Dr. Jessup, Chief Science and Medical Officer for the American Heart Association.

Dr. Mariell Jessup


She stressed that, “In addition, even if studies confirm an association between the gut microbiome and cardiovascular diseases such as PAH, more research is needed to determine if improving gut microbiota could directly impact PAH or other cardiovascular diseases. The findings of this study will not impact clinical practice.”

Dr. Raizada and his coinvestigators offered two possible mechanisms through which the gut microbiome influences pulmonary physiology. One is that lower levels of bacteria that produce the short-chain fatty acid butyrate, such as Coprococcus, Butyrivibrio, Lachnospiraceae, and Eubacterium, along with Clostridia in the gut of PAH patients, may increase gut permeability. Reduced butyrate weakens gut barrier function and can induce inflammation and leakage. This can allow microbial metabolites to enter the circulatory system, disrupting metabolism and immunity and affecting pulmonary vessels.

The second potential mechanism is that increased Collinsella in the PAH cohort may be the culprit that increases gut permeability, resulting in the ensuing gut barrier dysfunction and inflammation. The study noted Collinsella contributed most of the increased genes for the biosynthesis on the amino acid proline in these patients, and that a previous study implicated Collinsella and its parent, Cariobacteriales, in trimethylamine/trimethylamine N-oxide production (TMA/TMAO) in atherosclerosis (Cell. 2015;163[7]:1585-95). The non-PAH patients had higher levels of bacteria that had a low correlation with TMA/TMAO.

“We were very surprised to see such an association within a small group of study subjects,” wrote Dr. Raizada and associates. “It usually requires hundreds of patients to achieve such significance.”

More research is needed to determine if the specific microbiota associated with PAH causes the disease or is a result of it, they concluded.

The study was funded by grants from the National Institutes of Health, the NIH National Center for Research Resources, and the U.S. Department of Defense. Dr. Raizada and coauthors reported no relevant financial relationships.

SOURCE: Raizada MK et al. Hypertension. 2020. doi: 10.1161/HYPERTENSIONAHA.119.14294.

Publications
Topics
Sections

Model finds microbiota highly predictive

Model finds microbiota highly predictive

A unique collection of bacteria in the gut may have a strong association with pulmonary arterial hypertension and could be highly predictive of the disease in undiagnosed patients, according to a study published in the journal Hypertension.

Dr. Mohan Raizada

This is the first study to show that people with PAH have a common specific gut microbiota profile, wrote lead study author Mohan Raizada, PhD, distinguished professor in the department of physiology and functional genomics at the University of Florida, Gainesville.

The findings have the potential to change how cardiologists diagnose and treat PAH, he added. “While current PAH treatments focus on the lungs, looking at the lung/gut axis could open the door to new therapies centered in the digestive system,” Dr. Raizada said.

The researchers developed a model that found the specific microbiota profile was 83% accurate in predicting the presence or absence of PAH. If a larger study can validate the findings, the researchers wrote, this could lead to a new test for diagnosing PAH that’s less invasive than cardiac catheterization. It could also lead to new treatments that target the gut microbiome.

Study investigators collected stool samples from 18 PAH patients and 12 people without a history of cardiopulmonary disease. The microbiota DNA from the stool samples were isolated and sequenced. The analysis revealed that PAH patients had reduced richness and evenness of the gut bacteria, known as alpha diversity. They had increased levels of bacteria associated with atherosclerosis, and healthy patients had increased levels of bacteria that produced short-chain fatty acids.

Although recent studies have begun to show potential associations between the gut microbiome and cardiovascular diseases, this research is in its infancy, Mariell Jessup, MD, commented. “Even though the study by Dr. Raizada and colleagues predicted pulmonary arterial hypertension based on an individual’s microbiome with some accuracy, it is an observational study, so it does not prove cause and effect. Many other factors, especially diet, affect the gut microbiome,” added Dr. Jessup, Chief Science and Medical Officer for the American Heart Association.

Dr. Mariell Jessup


She stressed that, “In addition, even if studies confirm an association between the gut microbiome and cardiovascular diseases such as PAH, more research is needed to determine if improving gut microbiota could directly impact PAH or other cardiovascular diseases. The findings of this study will not impact clinical practice.”

Dr. Raizada and his coinvestigators offered two possible mechanisms through which the gut microbiome influences pulmonary physiology. One is that lower levels of bacteria that produce the short-chain fatty acid butyrate, such as Coprococcus, Butyrivibrio, Lachnospiraceae, and Eubacterium, along with Clostridia in the gut of PAH patients, may increase gut permeability. Reduced butyrate weakens gut barrier function and can induce inflammation and leakage. This can allow microbial metabolites to enter the circulatory system, disrupting metabolism and immunity and affecting pulmonary vessels.

The second potential mechanism is that increased Collinsella in the PAH cohort may be the culprit that increases gut permeability, resulting in the ensuing gut barrier dysfunction and inflammation. The study noted Collinsella contributed most of the increased genes for the biosynthesis on the amino acid proline in these patients, and that a previous study implicated Collinsella and its parent, Cariobacteriales, in trimethylamine/trimethylamine N-oxide production (TMA/TMAO) in atherosclerosis (Cell. 2015;163[7]:1585-95). The non-PAH patients had higher levels of bacteria that had a low correlation with TMA/TMAO.

“We were very surprised to see such an association within a small group of study subjects,” wrote Dr. Raizada and associates. “It usually requires hundreds of patients to achieve such significance.”

More research is needed to determine if the specific microbiota associated with PAH causes the disease or is a result of it, they concluded.

The study was funded by grants from the National Institutes of Health, the NIH National Center for Research Resources, and the U.S. Department of Defense. Dr. Raizada and coauthors reported no relevant financial relationships.

SOURCE: Raizada MK et al. Hypertension. 2020. doi: 10.1161/HYPERTENSIONAHA.119.14294.

A unique collection of bacteria in the gut may have a strong association with pulmonary arterial hypertension and could be highly predictive of the disease in undiagnosed patients, according to a study published in the journal Hypertension.

Dr. Mohan Raizada

This is the first study to show that people with PAH have a common specific gut microbiota profile, wrote lead study author Mohan Raizada, PhD, distinguished professor in the department of physiology and functional genomics at the University of Florida, Gainesville.

The findings have the potential to change how cardiologists diagnose and treat PAH, he added. “While current PAH treatments focus on the lungs, looking at the lung/gut axis could open the door to new therapies centered in the digestive system,” Dr. Raizada said.

The researchers developed a model that found the specific microbiota profile was 83% accurate in predicting the presence or absence of PAH. If a larger study can validate the findings, the researchers wrote, this could lead to a new test for diagnosing PAH that’s less invasive than cardiac catheterization. It could also lead to new treatments that target the gut microbiome.

Study investigators collected stool samples from 18 PAH patients and 12 people without a history of cardiopulmonary disease. The microbiota DNA from the stool samples were isolated and sequenced. The analysis revealed that PAH patients had reduced richness and evenness of the gut bacteria, known as alpha diversity. They had increased levels of bacteria associated with atherosclerosis, and healthy patients had increased levels of bacteria that produced short-chain fatty acids.

Although recent studies have begun to show potential associations between the gut microbiome and cardiovascular diseases, this research is in its infancy, Mariell Jessup, MD, commented. “Even though the study by Dr. Raizada and colleagues predicted pulmonary arterial hypertension based on an individual’s microbiome with some accuracy, it is an observational study, so it does not prove cause and effect. Many other factors, especially diet, affect the gut microbiome,” added Dr. Jessup, Chief Science and Medical Officer for the American Heart Association.

Dr. Mariell Jessup


She stressed that, “In addition, even if studies confirm an association between the gut microbiome and cardiovascular diseases such as PAH, more research is needed to determine if improving gut microbiota could directly impact PAH or other cardiovascular diseases. The findings of this study will not impact clinical practice.”

Dr. Raizada and his coinvestigators offered two possible mechanisms through which the gut microbiome influences pulmonary physiology. One is that lower levels of bacteria that produce the short-chain fatty acid butyrate, such as Coprococcus, Butyrivibrio, Lachnospiraceae, and Eubacterium, along with Clostridia in the gut of PAH patients, may increase gut permeability. Reduced butyrate weakens gut barrier function and can induce inflammation and leakage. This can allow microbial metabolites to enter the circulatory system, disrupting metabolism and immunity and affecting pulmonary vessels.

The second potential mechanism is that increased Collinsella in the PAH cohort may be the culprit that increases gut permeability, resulting in the ensuing gut barrier dysfunction and inflammation. The study noted Collinsella contributed most of the increased genes for the biosynthesis on the amino acid proline in these patients, and that a previous study implicated Collinsella and its parent, Cariobacteriales, in trimethylamine/trimethylamine N-oxide production (TMA/TMAO) in atherosclerosis (Cell. 2015;163[7]:1585-95). The non-PAH patients had higher levels of bacteria that had a low correlation with TMA/TMAO.

“We were very surprised to see such an association within a small group of study subjects,” wrote Dr. Raizada and associates. “It usually requires hundreds of patients to achieve such significance.”

More research is needed to determine if the specific microbiota associated with PAH causes the disease or is a result of it, they concluded.

The study was funded by grants from the National Institutes of Health, the NIH National Center for Research Resources, and the U.S. Department of Defense. Dr. Raizada and coauthors reported no relevant financial relationships.

SOURCE: Raizada MK et al. Hypertension. 2020. doi: 10.1161/HYPERTENSIONAHA.119.14294.

Publications
Publications
Topics
Article Type
Click for Credit Status
Ready
Sections
Article Source

FROM HYPERTENSION

Disallow All Ads
Content Gating
No Gating (article Unlocked/Free)
Alternative CME
Disqus Comments
Default
Use ProPublica
Hide sidebar & use full width
render the right sidebar.

Guidance defines vaping-related respiratory syndrome

Article Type
Changed
Wed, 04/08/2020 - 13:26

– Knowledge of vaping devices, familiarity with terminology, and the ability to quickly pinpoint individuals at risk of lung injury are just a few skills that can help critical care professionals confronted with patients who may have vaping-associated lung disease, according to a new guidance document.

Dr. Craig M. Lilly, professor of medicine, anesthesiology, and surgery at the University of Massachusetts, Worcester
Andrew D. Bowser/MDedge News
Dr. Craig M. Lilly

The guidance offers a risk-stratification system that classifies patients into groups based on exposure, symptoms, and imaging results, and provides specific evaluation needs and management strategies for each. The guidance is designed to help critical care professionals efficiently identify those at high risk of respiratory failure.

Physicians also need to communicate with patients to identify what substances are being vaped and develop effective methods to encourage abstinence, according to the authors, led by Craig M. Lilly, MD, FCCP, professor of medicine, anesthesiology, and surgery at the University of Massachusetts, Worcester.

“I would encourage every intensivist, when they leave their intensive care unit at night, [to ask], ‘have I advised against vaping today?’ ” Dr. Lilly said at the Critical Care Congress sponsored by the Society of Critical Care Medicine.

The guidelines, concurrently published as a review article in Critical Care Explorations, propose the term vaping-associated respiratory distress syndrome (VARDS), which the authors say constitutes an acute and progressive respiratory syndrome marked by pathologic changes of lung injury and potentially life-threatening hypoxemic respiratory failure.

They also introduce the three-group Worcester classification system, which is intended to triage vaping-exposed individuals for risk of VARDS based on the presence or absence of vaping-related symptoms and infiltrates, and normal or abnormal oxygen saturation.

“It’s very simple,” said Dr. Lilly, who added that the risk stratification model was developed at the request of Massachusetts public health officials.

Patients with vaping exposure but no symptoms attributable to vaping, such as cough, chest pain, or weight loss, are classified as Worcester Low Risk and testing is not recommended, he said.

By contrast, individuals are considered Worcester Medium Risk if they have vaping exposure, symptoms, and a vaping-associated abnormal pattern on imaging, but no hypoxemia; the presence of hypoxemia would tip the scale toward Worcester High Risk.

“Most patients that have died from vaping have been sent out of emergency rooms when they were noted to be hypoxic,” Dr. Lilly told meeting attendees.

 

 


Louella B. Amos, MD, a pediatric pulmonologist at Children’s Hospital of Wisconsin in Milwaukee, said she expects the guidance and risk stratification system will be useful not only for critical care specialists, but for other health care providers as well.

“It’s important to make decisions relatively quickly, depending on the severity of symptoms, and I think this is nice and simple,” Dr. Amos said in an interview.

“We always triage when we see patients, either at the door or in our clinic, or behind that, even in the hospital,” she said. “So I think this can be a great tool for everybody, not only the intensivist, but people who are triaging at the front.”

Management of individuals at low risk of VARDS begins with encouragement of abstinence. “We think that every vaping patient should be advised to quit vaping,” Dr. Lilly said. Patients who are interested in quitting who have not yet worked with someone in their health care team whom they trust can be referred to their primary care physicians for counseling, he added, while those struggling with addiction, unable to quit, and unable to partner with a primary care physician can be referred to an addiction medicine specialist.

For moderate-risk patients, vaping cessation is “absolutely mandatory,” said Dr. Lilly, who recommended monitoring of vaping abstinence, outpatient evaluation based on imaging studies, and adequate follow-up to ensure symptoms resolve, tests normalize, and daily activities bounce back to baseline levels.

The guidance offers more extensive recommendations for the VARDS high-risk group, including supervised vaping abstinence, continuous pulse oximetry, and early intervention with noninvasive ventilation, and mechanical ventilation if required, Dr. Lilly said.

Judging vaping exposure is challenging, requiring clinicians to have a familiarity with the many different devices that are available.

Beyond device type, he added, it’s important to know the various terms for devices and lingo that patients may use to describe them, what solutions are vaped, whether those solutions are commercially prepared or off the street, the dose the device delivers, and a number of other factors, he said.

Clinical evaluation typically comes down to unexplained cough, chest pain, weight loss, fatigue, or dyspnea, though one other clue is whether there are gastrointestinal symptoms: “The same way that aerosols can go down to the lungs, they also go into the GI tract, and when nausea, vomiting, or cramping abdominal pain is tightly associated with vaping exposure, one should assume that the patient has been toxin exposed,” he explained.

Dr. Lilly said he had no financial relationships to disclose.
Meeting/Event
Publications
Topics
Sections
Meeting/Event
Meeting/Event

– Knowledge of vaping devices, familiarity with terminology, and the ability to quickly pinpoint individuals at risk of lung injury are just a few skills that can help critical care professionals confronted with patients who may have vaping-associated lung disease, according to a new guidance document.

Dr. Craig M. Lilly, professor of medicine, anesthesiology, and surgery at the University of Massachusetts, Worcester
Andrew D. Bowser/MDedge News
Dr. Craig M. Lilly

The guidance offers a risk-stratification system that classifies patients into groups based on exposure, symptoms, and imaging results, and provides specific evaluation needs and management strategies for each. The guidance is designed to help critical care professionals efficiently identify those at high risk of respiratory failure.

Physicians also need to communicate with patients to identify what substances are being vaped and develop effective methods to encourage abstinence, according to the authors, led by Craig M. Lilly, MD, FCCP, professor of medicine, anesthesiology, and surgery at the University of Massachusetts, Worcester.

“I would encourage every intensivist, when they leave their intensive care unit at night, [to ask], ‘have I advised against vaping today?’ ” Dr. Lilly said at the Critical Care Congress sponsored by the Society of Critical Care Medicine.

The guidelines, concurrently published as a review article in Critical Care Explorations, propose the term vaping-associated respiratory distress syndrome (VARDS), which the authors say constitutes an acute and progressive respiratory syndrome marked by pathologic changes of lung injury and potentially life-threatening hypoxemic respiratory failure.

They also introduce the three-group Worcester classification system, which is intended to triage vaping-exposed individuals for risk of VARDS based on the presence or absence of vaping-related symptoms and infiltrates, and normal or abnormal oxygen saturation.

“It’s very simple,” said Dr. Lilly, who added that the risk stratification model was developed at the request of Massachusetts public health officials.

Patients with vaping exposure but no symptoms attributable to vaping, such as cough, chest pain, or weight loss, are classified as Worcester Low Risk and testing is not recommended, he said.

By contrast, individuals are considered Worcester Medium Risk if they have vaping exposure, symptoms, and a vaping-associated abnormal pattern on imaging, but no hypoxemia; the presence of hypoxemia would tip the scale toward Worcester High Risk.

“Most patients that have died from vaping have been sent out of emergency rooms when they were noted to be hypoxic,” Dr. Lilly told meeting attendees.

 

 


Louella B. Amos, MD, a pediatric pulmonologist at Children’s Hospital of Wisconsin in Milwaukee, said she expects the guidance and risk stratification system will be useful not only for critical care specialists, but for other health care providers as well.

“It’s important to make decisions relatively quickly, depending on the severity of symptoms, and I think this is nice and simple,” Dr. Amos said in an interview.

“We always triage when we see patients, either at the door or in our clinic, or behind that, even in the hospital,” she said. “So I think this can be a great tool for everybody, not only the intensivist, but people who are triaging at the front.”

Management of individuals at low risk of VARDS begins with encouragement of abstinence. “We think that every vaping patient should be advised to quit vaping,” Dr. Lilly said. Patients who are interested in quitting who have not yet worked with someone in their health care team whom they trust can be referred to their primary care physicians for counseling, he added, while those struggling with addiction, unable to quit, and unable to partner with a primary care physician can be referred to an addiction medicine specialist.

For moderate-risk patients, vaping cessation is “absolutely mandatory,” said Dr. Lilly, who recommended monitoring of vaping abstinence, outpatient evaluation based on imaging studies, and adequate follow-up to ensure symptoms resolve, tests normalize, and daily activities bounce back to baseline levels.

The guidance offers more extensive recommendations for the VARDS high-risk group, including supervised vaping abstinence, continuous pulse oximetry, and early intervention with noninvasive ventilation, and mechanical ventilation if required, Dr. Lilly said.

Judging vaping exposure is challenging, requiring clinicians to have a familiarity with the many different devices that are available.

Beyond device type, he added, it’s important to know the various terms for devices and lingo that patients may use to describe them, what solutions are vaped, whether those solutions are commercially prepared or off the street, the dose the device delivers, and a number of other factors, he said.

Clinical evaluation typically comes down to unexplained cough, chest pain, weight loss, fatigue, or dyspnea, though one other clue is whether there are gastrointestinal symptoms: “The same way that aerosols can go down to the lungs, they also go into the GI tract, and when nausea, vomiting, or cramping abdominal pain is tightly associated with vaping exposure, one should assume that the patient has been toxin exposed,” he explained.

Dr. Lilly said he had no financial relationships to disclose.

– Knowledge of vaping devices, familiarity with terminology, and the ability to quickly pinpoint individuals at risk of lung injury are just a few skills that can help critical care professionals confronted with patients who may have vaping-associated lung disease, according to a new guidance document.

Dr. Craig M. Lilly, professor of medicine, anesthesiology, and surgery at the University of Massachusetts, Worcester
Andrew D. Bowser/MDedge News
Dr. Craig M. Lilly

The guidance offers a risk-stratification system that classifies patients into groups based on exposure, symptoms, and imaging results, and provides specific evaluation needs and management strategies for each. The guidance is designed to help critical care professionals efficiently identify those at high risk of respiratory failure.

Physicians also need to communicate with patients to identify what substances are being vaped and develop effective methods to encourage abstinence, according to the authors, led by Craig M. Lilly, MD, FCCP, professor of medicine, anesthesiology, and surgery at the University of Massachusetts, Worcester.

“I would encourage every intensivist, when they leave their intensive care unit at night, [to ask], ‘have I advised against vaping today?’ ” Dr. Lilly said at the Critical Care Congress sponsored by the Society of Critical Care Medicine.

The guidelines, concurrently published as a review article in Critical Care Explorations, propose the term vaping-associated respiratory distress syndrome (VARDS), which the authors say constitutes an acute and progressive respiratory syndrome marked by pathologic changes of lung injury and potentially life-threatening hypoxemic respiratory failure.

They also introduce the three-group Worcester classification system, which is intended to triage vaping-exposed individuals for risk of VARDS based on the presence or absence of vaping-related symptoms and infiltrates, and normal or abnormal oxygen saturation.

“It’s very simple,” said Dr. Lilly, who added that the risk stratification model was developed at the request of Massachusetts public health officials.

Patients with vaping exposure but no symptoms attributable to vaping, such as cough, chest pain, or weight loss, are classified as Worcester Low Risk and testing is not recommended, he said.

By contrast, individuals are considered Worcester Medium Risk if they have vaping exposure, symptoms, and a vaping-associated abnormal pattern on imaging, but no hypoxemia; the presence of hypoxemia would tip the scale toward Worcester High Risk.

“Most patients that have died from vaping have been sent out of emergency rooms when they were noted to be hypoxic,” Dr. Lilly told meeting attendees.

 

 


Louella B. Amos, MD, a pediatric pulmonologist at Children’s Hospital of Wisconsin in Milwaukee, said she expects the guidance and risk stratification system will be useful not only for critical care specialists, but for other health care providers as well.

“It’s important to make decisions relatively quickly, depending on the severity of symptoms, and I think this is nice and simple,” Dr. Amos said in an interview.

“We always triage when we see patients, either at the door or in our clinic, or behind that, even in the hospital,” she said. “So I think this can be a great tool for everybody, not only the intensivist, but people who are triaging at the front.”

Management of individuals at low risk of VARDS begins with encouragement of abstinence. “We think that every vaping patient should be advised to quit vaping,” Dr. Lilly said. Patients who are interested in quitting who have not yet worked with someone in their health care team whom they trust can be referred to their primary care physicians for counseling, he added, while those struggling with addiction, unable to quit, and unable to partner with a primary care physician can be referred to an addiction medicine specialist.

For moderate-risk patients, vaping cessation is “absolutely mandatory,” said Dr. Lilly, who recommended monitoring of vaping abstinence, outpatient evaluation based on imaging studies, and adequate follow-up to ensure symptoms resolve, tests normalize, and daily activities bounce back to baseline levels.

The guidance offers more extensive recommendations for the VARDS high-risk group, including supervised vaping abstinence, continuous pulse oximetry, and early intervention with noninvasive ventilation, and mechanical ventilation if required, Dr. Lilly said.

Judging vaping exposure is challenging, requiring clinicians to have a familiarity with the many different devices that are available.

Beyond device type, he added, it’s important to know the various terms for devices and lingo that patients may use to describe them, what solutions are vaped, whether those solutions are commercially prepared or off the street, the dose the device delivers, and a number of other factors, he said.

Clinical evaluation typically comes down to unexplained cough, chest pain, weight loss, fatigue, or dyspnea, though one other clue is whether there are gastrointestinal symptoms: “The same way that aerosols can go down to the lungs, they also go into the GI tract, and when nausea, vomiting, or cramping abdominal pain is tightly associated with vaping exposure, one should assume that the patient has been toxin exposed,” he explained.

Dr. Lilly said he had no financial relationships to disclose.
Publications
Publications
Topics
Article Type
Sections
Article Source

REPORTING FROM CCC49

Disallow All Ads
Content Gating
No Gating (article Unlocked/Free)
Alternative CME
Disqus Comments
Default
Use ProPublica
Hide sidebar & use full width
render the right sidebar.

Prioritize oral health in children with DEB

Article Type
Changed
Sun, 02/23/2020 - 12:54

Preventive oral health should be high on the agenda when managing babies and children with dystrophic epidermolysis bullosa (DEB), pediatric dentist Susanne Krämer told attendees at the first EB World Congress.

Dr. Susanne Krämer, a pediatric dentist in Santiago, Chile
Sara Freeman/MDedge News
Dr. Susanne Krämer

While it may not be the first thing on the minds of families coming to terms with their children having a chronic and potentially debilitating skin disease, it is important to consider oral health early to ensure healthy dentition and mouth function, both of which will affect the ability to eat and thus nutrition.

When there are a lot of other health issues, “dentistry is not a priority,” Dr. Krämer acknowledged in an interview at the meeting, organized by the Dystrophic Epidermolysis Bullosa Association (DEBRA). 

Something as simple as brushing teeth can be very distressing for parents of a child with EB, she observed, especially if there is dysphagia and toothpaste may be getting into the airways accidentally.

Oral health was one of the topics that patients with EB and their families said would be good to have some guidance on when they were surveyed by DEBRA International. This led the charity to develop its first clinical practice guideline in 2012. Dr. Krämer was the lead author of the guidelines, which are about to be updated and republished.

The “Oral Health for Patients with Epidermolysis Bullosa – Best Clinical Practice Guidelines” (Int J Paediatr Dent. 2012;22 Suppl 1:1-35) are in the final stages of being revised, said Dr. Krämer, who is head of the department of pediatric dentistry at the University of Chile in Santiago. Although there is not much new evidence since the guidelines were first published, “we do have a lot of new technologies within dentistry that can aid the care of EB,” she said.

 

 


An important addition to the upcoming 2020 guidelines is a chapter on the patient-clinician partnership. This was added because “you can have fantastic technologies, but if you don’t have a confident relationship with the family and the patient, you won’t be able to proceed.” Dr. Krämer explained: “Patients with EB are so fragile and so afraid of being hurt that they won’t open their mouth unless there is a confidence with the clinician and they trust [him or her]; once they trust, they [will] open the mouth and you can work.”

Dr. Krämer noted that timing of the first dental appointment will depend on the referral pathway for every country and then every service. In her specialist practice the aim is to see newly diagnosed babies before the age of 3 months. “Lots of people would argue they don’t have teeth, but I need to educate the families on several aspects of oral health from early on.”

Older patients with EB may be more aware of the importance of a healthy mouth from a functional point of view and the need to eat and swallow normally, Dr. Krämer said, adding that the “social aspects of having a healthy smile are very important as well.”

Oral care in EB has come a long way since the 1970s when teeth extraction was recommended as the primary dental treatment option. “If you refer to literature in the 90s, that said we can actually restore the teeth in the patients with EB, and what we are now saying is that we have to prevent oral disease,” Dr. Krämer said.

Can oral disease be prevented completely? Yes, she said, but only in a few patients. “We still have decay in a lot of our patients, but far less than what we have had before. It will depend on the compliance of the family and the patient,” Dr. Krämer noted.

Compliance also is a factor in improving mouth function after surgery, which may be done to prevent the tongue from fusing to the bottom of the mouth and to relieve or prevent microstomia, which limits mouth opening.

“We are doing a lot of surgeries to release the fibrotic scars ... we have done it in both children and adults, but there have been better results in adults, because they are able to comply with the course of exercises” after surgery, Dr. Krämer said.

Results of an as-yet unpublished randomized controlled trial of postoperative mouth exercises demonstrate that patients who did the exercises, which involved using a device to stretch the mouth three times a day for 3 months, saw improvements in mouth opening. Once they stopped doing the exercises, however, these improvements faded. Considering the time spent on dressing changes and other exercises, this is perhaps understandable, she acknowledged.

Prevention, education, continual follow-up, and early referral are key to good oral health, Dr. Krämer emphasized. “If there is patient-clinician partnership confidence, they can have regular checkups with dental cleaning, with a fluoride varnish, different preventive strategies so they do not need to get to the point where they need general anesthesia or extractions.” Extractions still will be done, she added, but more for orthodontic reasons, because the teeth do not fit in the mouth. “That is our ideal world, that is where we want to go.”
Meeting/Event
Publications
Topics
Sections
Meeting/Event
Meeting/Event

Preventive oral health should be high on the agenda when managing babies and children with dystrophic epidermolysis bullosa (DEB), pediatric dentist Susanne Krämer told attendees at the first EB World Congress.

Dr. Susanne Krämer, a pediatric dentist in Santiago, Chile
Sara Freeman/MDedge News
Dr. Susanne Krämer

While it may not be the first thing on the minds of families coming to terms with their children having a chronic and potentially debilitating skin disease, it is important to consider oral health early to ensure healthy dentition and mouth function, both of which will affect the ability to eat and thus nutrition.

When there are a lot of other health issues, “dentistry is not a priority,” Dr. Krämer acknowledged in an interview at the meeting, organized by the Dystrophic Epidermolysis Bullosa Association (DEBRA). 

Something as simple as brushing teeth can be very distressing for parents of a child with EB, she observed, especially if there is dysphagia and toothpaste may be getting into the airways accidentally.

Oral health was one of the topics that patients with EB and their families said would be good to have some guidance on when they were surveyed by DEBRA International. This led the charity to develop its first clinical practice guideline in 2012. Dr. Krämer was the lead author of the guidelines, which are about to be updated and republished.

The “Oral Health for Patients with Epidermolysis Bullosa – Best Clinical Practice Guidelines” (Int J Paediatr Dent. 2012;22 Suppl 1:1-35) are in the final stages of being revised, said Dr. Krämer, who is head of the department of pediatric dentistry at the University of Chile in Santiago. Although there is not much new evidence since the guidelines were first published, “we do have a lot of new technologies within dentistry that can aid the care of EB,” she said.

 

 


An important addition to the upcoming 2020 guidelines is a chapter on the patient-clinician partnership. This was added because “you can have fantastic technologies, but if you don’t have a confident relationship with the family and the patient, you won’t be able to proceed.” Dr. Krämer explained: “Patients with EB are so fragile and so afraid of being hurt that they won’t open their mouth unless there is a confidence with the clinician and they trust [him or her]; once they trust, they [will] open the mouth and you can work.”

Dr. Krämer noted that timing of the first dental appointment will depend on the referral pathway for every country and then every service. In her specialist practice the aim is to see newly diagnosed babies before the age of 3 months. “Lots of people would argue they don’t have teeth, but I need to educate the families on several aspects of oral health from early on.”

Older patients with EB may be more aware of the importance of a healthy mouth from a functional point of view and the need to eat and swallow normally, Dr. Krämer said, adding that the “social aspects of having a healthy smile are very important as well.”

Oral care in EB has come a long way since the 1970s when teeth extraction was recommended as the primary dental treatment option. “If you refer to literature in the 90s, that said we can actually restore the teeth in the patients with EB, and what we are now saying is that we have to prevent oral disease,” Dr. Krämer said.

Can oral disease be prevented completely? Yes, she said, but only in a few patients. “We still have decay in a lot of our patients, but far less than what we have had before. It will depend on the compliance of the family and the patient,” Dr. Krämer noted.

Compliance also is a factor in improving mouth function after surgery, which may be done to prevent the tongue from fusing to the bottom of the mouth and to relieve or prevent microstomia, which limits mouth opening.

“We are doing a lot of surgeries to release the fibrotic scars ... we have done it in both children and adults, but there have been better results in adults, because they are able to comply with the course of exercises” after surgery, Dr. Krämer said.

Results of an as-yet unpublished randomized controlled trial of postoperative mouth exercises demonstrate that patients who did the exercises, which involved using a device to stretch the mouth three times a day for 3 months, saw improvements in mouth opening. Once they stopped doing the exercises, however, these improvements faded. Considering the time spent on dressing changes and other exercises, this is perhaps understandable, she acknowledged.

Prevention, education, continual follow-up, and early referral are key to good oral health, Dr. Krämer emphasized. “If there is patient-clinician partnership confidence, they can have regular checkups with dental cleaning, with a fluoride varnish, different preventive strategies so they do not need to get to the point where they need general anesthesia or extractions.” Extractions still will be done, she added, but more for orthodontic reasons, because the teeth do not fit in the mouth. “That is our ideal world, that is where we want to go.”

Preventive oral health should be high on the agenda when managing babies and children with dystrophic epidermolysis bullosa (DEB), pediatric dentist Susanne Krämer told attendees at the first EB World Congress.

Dr. Susanne Krämer, a pediatric dentist in Santiago, Chile
Sara Freeman/MDedge News
Dr. Susanne Krämer

While it may not be the first thing on the minds of families coming to terms with their children having a chronic and potentially debilitating skin disease, it is important to consider oral health early to ensure healthy dentition and mouth function, both of which will affect the ability to eat and thus nutrition.

When there are a lot of other health issues, “dentistry is not a priority,” Dr. Krämer acknowledged in an interview at the meeting, organized by the Dystrophic Epidermolysis Bullosa Association (DEBRA). 

Something as simple as brushing teeth can be very distressing for parents of a child with EB, she observed, especially if there is dysphagia and toothpaste may be getting into the airways accidentally.

Oral health was one of the topics that patients with EB and their families said would be good to have some guidance on when they were surveyed by DEBRA International. This led the charity to develop its first clinical practice guideline in 2012. Dr. Krämer was the lead author of the guidelines, which are about to be updated and republished.

The “Oral Health for Patients with Epidermolysis Bullosa – Best Clinical Practice Guidelines” (Int J Paediatr Dent. 2012;22 Suppl 1:1-35) are in the final stages of being revised, said Dr. Krämer, who is head of the department of pediatric dentistry at the University of Chile in Santiago. Although there is not much new evidence since the guidelines were first published, “we do have a lot of new technologies within dentistry that can aid the care of EB,” she said.

 

 


An important addition to the upcoming 2020 guidelines is a chapter on the patient-clinician partnership. This was added because “you can have fantastic technologies, but if you don’t have a confident relationship with the family and the patient, you won’t be able to proceed.” Dr. Krämer explained: “Patients with EB are so fragile and so afraid of being hurt that they won’t open their mouth unless there is a confidence with the clinician and they trust [him or her]; once they trust, they [will] open the mouth and you can work.”

Dr. Krämer noted that timing of the first dental appointment will depend on the referral pathway for every country and then every service. In her specialist practice the aim is to see newly diagnosed babies before the age of 3 months. “Lots of people would argue they don’t have teeth, but I need to educate the families on several aspects of oral health from early on.”

Older patients with EB may be more aware of the importance of a healthy mouth from a functional point of view and the need to eat and swallow normally, Dr. Krämer said, adding that the “social aspects of having a healthy smile are very important as well.”

Oral care in EB has come a long way since the 1970s when teeth extraction was recommended as the primary dental treatment option. “If you refer to literature in the 90s, that said we can actually restore the teeth in the patients with EB, and what we are now saying is that we have to prevent oral disease,” Dr. Krämer said.

Can oral disease be prevented completely? Yes, she said, but only in a few patients. “We still have decay in a lot of our patients, but far less than what we have had before. It will depend on the compliance of the family and the patient,” Dr. Krämer noted.

Compliance also is a factor in improving mouth function after surgery, which may be done to prevent the tongue from fusing to the bottom of the mouth and to relieve or prevent microstomia, which limits mouth opening.

“We are doing a lot of surgeries to release the fibrotic scars ... we have done it in both children and adults, but there have been better results in adults, because they are able to comply with the course of exercises” after surgery, Dr. Krämer said.

Results of an as-yet unpublished randomized controlled trial of postoperative mouth exercises demonstrate that patients who did the exercises, which involved using a device to stretch the mouth three times a day for 3 months, saw improvements in mouth opening. Once they stopped doing the exercises, however, these improvements faded. Considering the time spent on dressing changes and other exercises, this is perhaps understandable, she acknowledged.

Prevention, education, continual follow-up, and early referral are key to good oral health, Dr. Krämer emphasized. “If there is patient-clinician partnership confidence, they can have regular checkups with dental cleaning, with a fluoride varnish, different preventive strategies so they do not need to get to the point where they need general anesthesia or extractions.” Extractions still will be done, she added, but more for orthodontic reasons, because the teeth do not fit in the mouth. “That is our ideal world, that is where we want to go.”
Publications
Publications
Topics
Article Type
Sections
Article Source

REPORTING FROM EB 2020

Disallow All Ads
Content Gating
No Gating (article Unlocked/Free)
Alternative CME
Disqus Comments
Default
Use ProPublica
Hide sidebar & use full width
render the right sidebar.

Medicare beneficiaries get few home health visits after ICU stay

Article Type
Changed
Mon, 02/24/2020 - 09:50

Medicare beneficiaries are receiving a low number of rehabilitation visits in the early posthospitalization period after critical illness, an analysis of hospital and home health claims data suggests.

The beneficiaries, all discharged directly to home health after an intensive care unit stay, received an average of less than one visit per week in the ensuing month, while a full third received no visits at all, according to authors of the analysis, presented at the Critical Care Congress sponsored by the Society of Critical Care Medicine.

Living alone and living in a rural area were associated with significantly fewer home health rehabilitation visits, according to investigator Jason Raymond Falvey, PT, DPT, PhD, of Yale University, New Haven, Conn.

“We identified that these patients are receiving low doses of rehabilitation in home health care settings, and perhaps doses low enough to not be physiologically adequate to overcome the deconditioning and aerobic capacity concerns that these patients have,” Dr. Falvey said.

These findings reflect an “underrecognition” of the importance of rehabilitation both outside and inside the hospital setting, according to Patricia J. Posa, RN, of Saint Joseph Mercy Hospital, Northville, Mich.

“We even struggle to provide sufficient rehabilitation while they’re in the hospital,” Ms. Posa said in an interview. “So I think that we still have a major gap in providing rehab services across the continuum, and part of that is recognizing the deficits that patients, especially our elderly patients, might be leaving the hospital with.”

Medicare beneficiaries who survive a critical illness are often discharged with referrals for physical, occupational, or speech therapy, yet there are not much data on the delivery of that care or how many visits actually take place, according to Dr. Falvey.

 

 


He and coinvestigators analyzed data on 3,176 Medicare beneficiaries discharged to home health right after an acute hospitalization with an ICU stay of at least 24 hours. To do this, they linked 2012 Medicare hospital and home health claims data with Medicare demographic and patient assessment data.

They found that the beneficiaries received just 3.5 home rehabilitation visits in 30 days, while 33% had no visits on record.

The factors most strongly associated with receiving fewer rehabilitation visits, in adjusted models, included living in a rural setting, with a rate ratio (RR) of 0.87 and living alone, with an RR of 0.88.

Higher comorbidity count also was associated with fewer visits (RR, 0.98), according to the investigators.

On the other hand, Medicare beneficiaries who received more visits were more likely to be older (RR, 1.03; 1.01-1.04; for every 5 years), more likely to have higher disability scores (RR, 1.03; 1.02-1.04; per point on the Elixhauser Comorbidity Index), and more likely to have reported severe dyspnea (RR, 1.12; 1.04-1.21), according to the report.

More research will be needed to determine the appropriate number of home health rehabilitation visits for older hospitalized patients, according to Ms. Pena, a member of the Society of Critical Care Medicine’s ICU Liberation initiative, which aims to free patients from the harmful effects of pain, agitation/sedation, delirium, immobility, and sleep disruption in the ICU, as well as improve patient outcomes after an ICU stay.

The literature is already fairly robust, she said, on how frequently visits are warranted following specific scenarios such as postsurgical hip or knee replacement or stroke.

“For the general hospitalized patients that are just losing function because they were sick and didn’t get out of bed enough, we don’t really have good data to say, ‘you know, they need three visits a week, or they need two visits a week for an hour in order to improve,’ ” she said, “so the science is still not caught up with the frequency.”

In the absence of data, the number of visits may be left up to an individual clinician’s knowledge and past experience as well as what insurance will pay for, Ms. Pena said.

Dr. Falvey reported royalties related to an online continuing education course on hospital readmissions. No other disclosures were reported.

SOURCE: Falvey J et al. Crit Care Med. 2020 Jan;48(1):28.

Meeting/Event
Publications
Topics
Sections
Meeting/Event
Meeting/Event

Medicare beneficiaries are receiving a low number of rehabilitation visits in the early posthospitalization period after critical illness, an analysis of hospital and home health claims data suggests.

The beneficiaries, all discharged directly to home health after an intensive care unit stay, received an average of less than one visit per week in the ensuing month, while a full third received no visits at all, according to authors of the analysis, presented at the Critical Care Congress sponsored by the Society of Critical Care Medicine.

Living alone and living in a rural area were associated with significantly fewer home health rehabilitation visits, according to investigator Jason Raymond Falvey, PT, DPT, PhD, of Yale University, New Haven, Conn.

“We identified that these patients are receiving low doses of rehabilitation in home health care settings, and perhaps doses low enough to not be physiologically adequate to overcome the deconditioning and aerobic capacity concerns that these patients have,” Dr. Falvey said.

These findings reflect an “underrecognition” of the importance of rehabilitation both outside and inside the hospital setting, according to Patricia J. Posa, RN, of Saint Joseph Mercy Hospital, Northville, Mich.

“We even struggle to provide sufficient rehabilitation while they’re in the hospital,” Ms. Posa said in an interview. “So I think that we still have a major gap in providing rehab services across the continuum, and part of that is recognizing the deficits that patients, especially our elderly patients, might be leaving the hospital with.”

Medicare beneficiaries who survive a critical illness are often discharged with referrals for physical, occupational, or speech therapy, yet there are not much data on the delivery of that care or how many visits actually take place, according to Dr. Falvey.

 

 


He and coinvestigators analyzed data on 3,176 Medicare beneficiaries discharged to home health right after an acute hospitalization with an ICU stay of at least 24 hours. To do this, they linked 2012 Medicare hospital and home health claims data with Medicare demographic and patient assessment data.

They found that the beneficiaries received just 3.5 home rehabilitation visits in 30 days, while 33% had no visits on record.

The factors most strongly associated with receiving fewer rehabilitation visits, in adjusted models, included living in a rural setting, with a rate ratio (RR) of 0.87 and living alone, with an RR of 0.88.

Higher comorbidity count also was associated with fewer visits (RR, 0.98), according to the investigators.

On the other hand, Medicare beneficiaries who received more visits were more likely to be older (RR, 1.03; 1.01-1.04; for every 5 years), more likely to have higher disability scores (RR, 1.03; 1.02-1.04; per point on the Elixhauser Comorbidity Index), and more likely to have reported severe dyspnea (RR, 1.12; 1.04-1.21), according to the report.

More research will be needed to determine the appropriate number of home health rehabilitation visits for older hospitalized patients, according to Ms. Pena, a member of the Society of Critical Care Medicine’s ICU Liberation initiative, which aims to free patients from the harmful effects of pain, agitation/sedation, delirium, immobility, and sleep disruption in the ICU, as well as improve patient outcomes after an ICU stay.

The literature is already fairly robust, she said, on how frequently visits are warranted following specific scenarios such as postsurgical hip or knee replacement or stroke.

“For the general hospitalized patients that are just losing function because they were sick and didn’t get out of bed enough, we don’t really have good data to say, ‘you know, they need three visits a week, or they need two visits a week for an hour in order to improve,’ ” she said, “so the science is still not caught up with the frequency.”

In the absence of data, the number of visits may be left up to an individual clinician’s knowledge and past experience as well as what insurance will pay for, Ms. Pena said.

Dr. Falvey reported royalties related to an online continuing education course on hospital readmissions. No other disclosures were reported.

SOURCE: Falvey J et al. Crit Care Med. 2020 Jan;48(1):28.

Medicare beneficiaries are receiving a low number of rehabilitation visits in the early posthospitalization period after critical illness, an analysis of hospital and home health claims data suggests.

The beneficiaries, all discharged directly to home health after an intensive care unit stay, received an average of less than one visit per week in the ensuing month, while a full third received no visits at all, according to authors of the analysis, presented at the Critical Care Congress sponsored by the Society of Critical Care Medicine.

Living alone and living in a rural area were associated with significantly fewer home health rehabilitation visits, according to investigator Jason Raymond Falvey, PT, DPT, PhD, of Yale University, New Haven, Conn.

“We identified that these patients are receiving low doses of rehabilitation in home health care settings, and perhaps doses low enough to not be physiologically adequate to overcome the deconditioning and aerobic capacity concerns that these patients have,” Dr. Falvey said.

These findings reflect an “underrecognition” of the importance of rehabilitation both outside and inside the hospital setting, according to Patricia J. Posa, RN, of Saint Joseph Mercy Hospital, Northville, Mich.

“We even struggle to provide sufficient rehabilitation while they’re in the hospital,” Ms. Posa said in an interview. “So I think that we still have a major gap in providing rehab services across the continuum, and part of that is recognizing the deficits that patients, especially our elderly patients, might be leaving the hospital with.”

Medicare beneficiaries who survive a critical illness are often discharged with referrals for physical, occupational, or speech therapy, yet there are not much data on the delivery of that care or how many visits actually take place, according to Dr. Falvey.

 

 


He and coinvestigators analyzed data on 3,176 Medicare beneficiaries discharged to home health right after an acute hospitalization with an ICU stay of at least 24 hours. To do this, they linked 2012 Medicare hospital and home health claims data with Medicare demographic and patient assessment data.

They found that the beneficiaries received just 3.5 home rehabilitation visits in 30 days, while 33% had no visits on record.

The factors most strongly associated with receiving fewer rehabilitation visits, in adjusted models, included living in a rural setting, with a rate ratio (RR) of 0.87 and living alone, with an RR of 0.88.

Higher comorbidity count also was associated with fewer visits (RR, 0.98), according to the investigators.

On the other hand, Medicare beneficiaries who received more visits were more likely to be older (RR, 1.03; 1.01-1.04; for every 5 years), more likely to have higher disability scores (RR, 1.03; 1.02-1.04; per point on the Elixhauser Comorbidity Index), and more likely to have reported severe dyspnea (RR, 1.12; 1.04-1.21), according to the report.

More research will be needed to determine the appropriate number of home health rehabilitation visits for older hospitalized patients, according to Ms. Pena, a member of the Society of Critical Care Medicine’s ICU Liberation initiative, which aims to free patients from the harmful effects of pain, agitation/sedation, delirium, immobility, and sleep disruption in the ICU, as well as improve patient outcomes after an ICU stay.

The literature is already fairly robust, she said, on how frequently visits are warranted following specific scenarios such as postsurgical hip or knee replacement or stroke.

“For the general hospitalized patients that are just losing function because they were sick and didn’t get out of bed enough, we don’t really have good data to say, ‘you know, they need three visits a week, or they need two visits a week for an hour in order to improve,’ ” she said, “so the science is still not caught up with the frequency.”

In the absence of data, the number of visits may be left up to an individual clinician’s knowledge and past experience as well as what insurance will pay for, Ms. Pena said.

Dr. Falvey reported royalties related to an online continuing education course on hospital readmissions. No other disclosures were reported.

SOURCE: Falvey J et al. Crit Care Med. 2020 Jan;48(1):28.

Publications
Publications
Topics
Article Type
Sections
Article Source

REPORTING FROM CCC49

Disallow All Ads
Content Gating
No Gating (article Unlocked/Free)
Alternative CME
Disqus Comments
Default
Use ProPublica
Hide sidebar & use full width
render the right sidebar.

Target plantar keratoderma when managing ‘mild’ EBS

Article Type
Changed
Sun, 02/23/2020 - 11:15

– Hardened feet are a major determinant of the clinical course of epidermolysis bullosa simplex (EBS), according to research presented by a German team of investigators at the EB World Congress.

In a study of 157 individuals with EBS, 75.8% had plantar keratoderma, a condition associated with a vicious circle of pain, reduced mobility, subsequent weight gain, and further foot problems.

“EBS has severe impacts on various aspects of everyday life,” Antonia Reimer, MD, and associates at the University of Freiburg, Germany, reported in a poster presentation. “Plantar involvement and [plantar keratoderma] are serious complications of all EBS subtypes, correlating with excessive weight gain, pain, local infections, and limited mobility.”

The researchers suggested that “targeting [plantar keratoderma] should be a priority in EBS therapy and research.”

In their retrospective cohort study, clinical and molecular data were retrieved from patient records, and major determinants of the clinical course of EBS investigated. As such, the researchers looked at how weight changes affected EBS, the effect of hardening skin on the feet, pain, mobility, and working life.

“EB simplex is generally regarded as the ‘mildest’ EB type,” Dr. Reimer and colleagues wrote, “however, individuals with EBS report a high disease burden and frequent pain.” The team found that just under 30% of patients (n = 46) experienced frequent pain, particularly those with localized and severe EBS. Of the patients experiencing pain, the majority (75.2%) had plantar keratoderma. Furthermore, those with blisters underneath the hardened skin reported having the most painful lesions.

Palmoplantar hyperhidrosis was present in slightly more than 40% of cases, and was especially common in individuals with localized EBS, Dr. Reimer and colleagues found. They also found that bacterial and fungal infections occurred in 14% and 7% of patients, respectively, and this correlated significantly with diffuse plantar keratoderma.

A third of patients experience mobility problems, and 8.2% required a wheelchair; 16.4% “were in occupational disability,” the team reported.

“Hyperkeratosis is important because it isn’t just about treating the hyperkeratosis, it’s also looking at the mechanical balance of the foot,” Tariq Khan, PhD, said during an unrelated oral presentation. Dr. Khan, a consultant podiatrist specializing in EB at Great Ormond Street Hospital NHS Foundation Trust in London, discussed how to best manage the feet of people with EB.

“Podiatry technology and how we treat can often be detrimental to an EB patient,” Dr. Khan cautioned at the meeting, which was organized by the Dystrophic Epidermolysis Bullosa Association (DEBRA).

For example, “certain devices, certain types of material, will add more friction and pressure and cause more blistering,” he added, making treatment challenging.

 

 


Having worked with the EB community for the past 22 years, he noted that he had seen how podiatry practices had been refined to deal with this patient population. Dr. Khan is one of several experts behind EB podiatry guidelines issued by DEBRA International last year (Br J Dermatol. 2019 Aug 9. doi: 10.1111/bjd.18381) and has run the charity’s first practical EB podiatry skills course to educate more podiatrists on the intricacies of managing EB feet.

During his talk, Dr. Kahn mentioned several innovations that came about by working with external companies, such as the production of special cotton socks containing silver fibers to help reduce the symptom of hot feet, and development of a cooling insole that helped draw moisture and odor away from the foot while providing comfort to the wearer.

One of the main problems for those with EB is finding comfortable footwear that doesn’t aggravate their symptoms, Dr. Khan emphasized.

According to the EB podiatry guidelines, footwear needs to be supportive, and “its primary focus should be aimed at minimizing blistering by reducing friction.” If blisters are already present, the guidelines note that dressings and topical antiseptics or antibiotics might be used until the blisters heal. “Therefore, suitable shoes or footwear are essential to accommodate dressings and not lead to further trauma to the damaged area. Footwear that is adjustable may be beneficial in these circumstances.”

What constitutes appropriate footwear is open to debate and was the topic of a separate poster presentation at meeting. Mark O’Sullivan, EB team podiatrist at Solihull and Birmingham Women’s and Children’s NHS Foundation Trust, and associates looked at whether wearing rocker bottom footwear could ease the formation of blisters in patients with EBS.

The team studied nine patients who reported regular plantar blistering. An in-shoe measurement system was devised to measure patients’ plantar pressure while they were wearing their existing footwear and then again when they were wearing new footwear with a rocker bottom. Participants completed questionnaires about the development of blisters on their feet, their activity levels, and pain.

The rocker bottom footwear reduced the peak plantar pressure by 30.5% and the total plantar pressure by 31.8%, compared with regular footwear. A shift in the average pressure under the foot was seen, moving from the heels of the feet to the midfoot area, while remaining similar in the front foot area.

“Patient feedback has been mixed,” Mr. O’Sullivan said when presenting the poster. “Patients state that blisters have often reduced in the heels and forefoot, but new blisters have developed in the midfoot.” As a result, some study participants chose to alternate wearing the rocker bottom footwear with their normal shoes, to even out the places where blisters might form.
 

 


Although the jury is still out on the benefit of rocker bottom footwear, one thing that might help those with EBS who develop regular foot blisters may be to keep their weight in check. In a separate poster presentation given by Lynn Hubbard, a specialist EB dietitian in the department of nutrition and dietetics at St. Thomas’ Hospital in London, it was shown that almost a third of patients with EB simplex were obese, compared with 26% of adults in the general U.K. population.

“People with EBS are known to have hyperkeratosis and foot-blistering,” Ms. Hubbard observed in the poster. This can lead to reduce mobility and pain, which “may in turn have an impact on body weight, and an increased BMI [body mass index] may further affect mobility.”

Data were collected on 90 patients who attended a U.K. EBS clinic over an 11-month period. While 45.5% of patients had a normal weight, the majority was overweight (21.1%), obese (21.1%), or morbidly obese (10%).

Fifteen patients completed questionnaires about their mobility, and almost all felt that their weight had an adverse effect on their feet, as did EBS. Several also noted problems with their EBS, in the skin folds around the bra, waist, and sock lines.

“We now plan to begin a pilot study to establish a supportive weight management program for people with EBS and evaluate both weight loss and impact on mobility,” Ms. Hubbard reported.

No conflicts of interest were declared by any of the speakers.

SOURCES: EB 2020. Reimer A et al. Poster 26; Khan T. oral presentation; O’Sullivan M et al. Poster 93; Hubbard L. Poster 19.

Meeting/Event
Publications
Topics
Sections
Meeting/Event
Meeting/Event

– Hardened feet are a major determinant of the clinical course of epidermolysis bullosa simplex (EBS), according to research presented by a German team of investigators at the EB World Congress.

In a study of 157 individuals with EBS, 75.8% had plantar keratoderma, a condition associated with a vicious circle of pain, reduced mobility, subsequent weight gain, and further foot problems.

“EBS has severe impacts on various aspects of everyday life,” Antonia Reimer, MD, and associates at the University of Freiburg, Germany, reported in a poster presentation. “Plantar involvement and [plantar keratoderma] are serious complications of all EBS subtypes, correlating with excessive weight gain, pain, local infections, and limited mobility.”

The researchers suggested that “targeting [plantar keratoderma] should be a priority in EBS therapy and research.”

In their retrospective cohort study, clinical and molecular data were retrieved from patient records, and major determinants of the clinical course of EBS investigated. As such, the researchers looked at how weight changes affected EBS, the effect of hardening skin on the feet, pain, mobility, and working life.

“EB simplex is generally regarded as the ‘mildest’ EB type,” Dr. Reimer and colleagues wrote, “however, individuals with EBS report a high disease burden and frequent pain.” The team found that just under 30% of patients (n = 46) experienced frequent pain, particularly those with localized and severe EBS. Of the patients experiencing pain, the majority (75.2%) had plantar keratoderma. Furthermore, those with blisters underneath the hardened skin reported having the most painful lesions.

Palmoplantar hyperhidrosis was present in slightly more than 40% of cases, and was especially common in individuals with localized EBS, Dr. Reimer and colleagues found. They also found that bacterial and fungal infections occurred in 14% and 7% of patients, respectively, and this correlated significantly with diffuse plantar keratoderma.

A third of patients experience mobility problems, and 8.2% required a wheelchair; 16.4% “were in occupational disability,” the team reported.

“Hyperkeratosis is important because it isn’t just about treating the hyperkeratosis, it’s also looking at the mechanical balance of the foot,” Tariq Khan, PhD, said during an unrelated oral presentation. Dr. Khan, a consultant podiatrist specializing in EB at Great Ormond Street Hospital NHS Foundation Trust in London, discussed how to best manage the feet of people with EB.

“Podiatry technology and how we treat can often be detrimental to an EB patient,” Dr. Khan cautioned at the meeting, which was organized by the Dystrophic Epidermolysis Bullosa Association (DEBRA).

For example, “certain devices, certain types of material, will add more friction and pressure and cause more blistering,” he added, making treatment challenging.

 

 


Having worked with the EB community for the past 22 years, he noted that he had seen how podiatry practices had been refined to deal with this patient population. Dr. Khan is one of several experts behind EB podiatry guidelines issued by DEBRA International last year (Br J Dermatol. 2019 Aug 9. doi: 10.1111/bjd.18381) and has run the charity’s first practical EB podiatry skills course to educate more podiatrists on the intricacies of managing EB feet.

During his talk, Dr. Kahn mentioned several innovations that came about by working with external companies, such as the production of special cotton socks containing silver fibers to help reduce the symptom of hot feet, and development of a cooling insole that helped draw moisture and odor away from the foot while providing comfort to the wearer.

One of the main problems for those with EB is finding comfortable footwear that doesn’t aggravate their symptoms, Dr. Khan emphasized.

According to the EB podiatry guidelines, footwear needs to be supportive, and “its primary focus should be aimed at minimizing blistering by reducing friction.” If blisters are already present, the guidelines note that dressings and topical antiseptics or antibiotics might be used until the blisters heal. “Therefore, suitable shoes or footwear are essential to accommodate dressings and not lead to further trauma to the damaged area. Footwear that is adjustable may be beneficial in these circumstances.”

What constitutes appropriate footwear is open to debate and was the topic of a separate poster presentation at meeting. Mark O’Sullivan, EB team podiatrist at Solihull and Birmingham Women’s and Children’s NHS Foundation Trust, and associates looked at whether wearing rocker bottom footwear could ease the formation of blisters in patients with EBS.

The team studied nine patients who reported regular plantar blistering. An in-shoe measurement system was devised to measure patients’ plantar pressure while they were wearing their existing footwear and then again when they were wearing new footwear with a rocker bottom. Participants completed questionnaires about the development of blisters on their feet, their activity levels, and pain.

The rocker bottom footwear reduced the peak plantar pressure by 30.5% and the total plantar pressure by 31.8%, compared with regular footwear. A shift in the average pressure under the foot was seen, moving from the heels of the feet to the midfoot area, while remaining similar in the front foot area.

“Patient feedback has been mixed,” Mr. O’Sullivan said when presenting the poster. “Patients state that blisters have often reduced in the heels and forefoot, but new blisters have developed in the midfoot.” As a result, some study participants chose to alternate wearing the rocker bottom footwear with their normal shoes, to even out the places where blisters might form.
 

 


Although the jury is still out on the benefit of rocker bottom footwear, one thing that might help those with EBS who develop regular foot blisters may be to keep their weight in check. In a separate poster presentation given by Lynn Hubbard, a specialist EB dietitian in the department of nutrition and dietetics at St. Thomas’ Hospital in London, it was shown that almost a third of patients with EB simplex were obese, compared with 26% of adults in the general U.K. population.

“People with EBS are known to have hyperkeratosis and foot-blistering,” Ms. Hubbard observed in the poster. This can lead to reduce mobility and pain, which “may in turn have an impact on body weight, and an increased BMI [body mass index] may further affect mobility.”

Data were collected on 90 patients who attended a U.K. EBS clinic over an 11-month period. While 45.5% of patients had a normal weight, the majority was overweight (21.1%), obese (21.1%), or morbidly obese (10%).

Fifteen patients completed questionnaires about their mobility, and almost all felt that their weight had an adverse effect on their feet, as did EBS. Several also noted problems with their EBS, in the skin folds around the bra, waist, and sock lines.

“We now plan to begin a pilot study to establish a supportive weight management program for people with EBS and evaluate both weight loss and impact on mobility,” Ms. Hubbard reported.

No conflicts of interest were declared by any of the speakers.

SOURCES: EB 2020. Reimer A et al. Poster 26; Khan T. oral presentation; O’Sullivan M et al. Poster 93; Hubbard L. Poster 19.

– Hardened feet are a major determinant of the clinical course of epidermolysis bullosa simplex (EBS), according to research presented by a German team of investigators at the EB World Congress.

In a study of 157 individuals with EBS, 75.8% had plantar keratoderma, a condition associated with a vicious circle of pain, reduced mobility, subsequent weight gain, and further foot problems.

“EBS has severe impacts on various aspects of everyday life,” Antonia Reimer, MD, and associates at the University of Freiburg, Germany, reported in a poster presentation. “Plantar involvement and [plantar keratoderma] are serious complications of all EBS subtypes, correlating with excessive weight gain, pain, local infections, and limited mobility.”

The researchers suggested that “targeting [plantar keratoderma] should be a priority in EBS therapy and research.”

In their retrospective cohort study, clinical and molecular data were retrieved from patient records, and major determinants of the clinical course of EBS investigated. As such, the researchers looked at how weight changes affected EBS, the effect of hardening skin on the feet, pain, mobility, and working life.

“EB simplex is generally regarded as the ‘mildest’ EB type,” Dr. Reimer and colleagues wrote, “however, individuals with EBS report a high disease burden and frequent pain.” The team found that just under 30% of patients (n = 46) experienced frequent pain, particularly those with localized and severe EBS. Of the patients experiencing pain, the majority (75.2%) had plantar keratoderma. Furthermore, those with blisters underneath the hardened skin reported having the most painful lesions.

Palmoplantar hyperhidrosis was present in slightly more than 40% of cases, and was especially common in individuals with localized EBS, Dr. Reimer and colleagues found. They also found that bacterial and fungal infections occurred in 14% and 7% of patients, respectively, and this correlated significantly with diffuse plantar keratoderma.

A third of patients experience mobility problems, and 8.2% required a wheelchair; 16.4% “were in occupational disability,” the team reported.

“Hyperkeratosis is important because it isn’t just about treating the hyperkeratosis, it’s also looking at the mechanical balance of the foot,” Tariq Khan, PhD, said during an unrelated oral presentation. Dr. Khan, a consultant podiatrist specializing in EB at Great Ormond Street Hospital NHS Foundation Trust in London, discussed how to best manage the feet of people with EB.

“Podiatry technology and how we treat can often be detrimental to an EB patient,” Dr. Khan cautioned at the meeting, which was organized by the Dystrophic Epidermolysis Bullosa Association (DEBRA).

For example, “certain devices, certain types of material, will add more friction and pressure and cause more blistering,” he added, making treatment challenging.

 

 


Having worked with the EB community for the past 22 years, he noted that he had seen how podiatry practices had been refined to deal with this patient population. Dr. Khan is one of several experts behind EB podiatry guidelines issued by DEBRA International last year (Br J Dermatol. 2019 Aug 9. doi: 10.1111/bjd.18381) and has run the charity’s first practical EB podiatry skills course to educate more podiatrists on the intricacies of managing EB feet.

During his talk, Dr. Kahn mentioned several innovations that came about by working with external companies, such as the production of special cotton socks containing silver fibers to help reduce the symptom of hot feet, and development of a cooling insole that helped draw moisture and odor away from the foot while providing comfort to the wearer.

One of the main problems for those with EB is finding comfortable footwear that doesn’t aggravate their symptoms, Dr. Khan emphasized.

According to the EB podiatry guidelines, footwear needs to be supportive, and “its primary focus should be aimed at minimizing blistering by reducing friction.” If blisters are already present, the guidelines note that dressings and topical antiseptics or antibiotics might be used until the blisters heal. “Therefore, suitable shoes or footwear are essential to accommodate dressings and not lead to further trauma to the damaged area. Footwear that is adjustable may be beneficial in these circumstances.”

What constitutes appropriate footwear is open to debate and was the topic of a separate poster presentation at meeting. Mark O’Sullivan, EB team podiatrist at Solihull and Birmingham Women’s and Children’s NHS Foundation Trust, and associates looked at whether wearing rocker bottom footwear could ease the formation of blisters in patients with EBS.

The team studied nine patients who reported regular plantar blistering. An in-shoe measurement system was devised to measure patients’ plantar pressure while they were wearing their existing footwear and then again when they were wearing new footwear with a rocker bottom. Participants completed questionnaires about the development of blisters on their feet, their activity levels, and pain.

The rocker bottom footwear reduced the peak plantar pressure by 30.5% and the total plantar pressure by 31.8%, compared with regular footwear. A shift in the average pressure under the foot was seen, moving from the heels of the feet to the midfoot area, while remaining similar in the front foot area.

“Patient feedback has been mixed,” Mr. O’Sullivan said when presenting the poster. “Patients state that blisters have often reduced in the heels and forefoot, but new blisters have developed in the midfoot.” As a result, some study participants chose to alternate wearing the rocker bottom footwear with their normal shoes, to even out the places where blisters might form.
 

 


Although the jury is still out on the benefit of rocker bottom footwear, one thing that might help those with EBS who develop regular foot blisters may be to keep their weight in check. In a separate poster presentation given by Lynn Hubbard, a specialist EB dietitian in the department of nutrition and dietetics at St. Thomas’ Hospital in London, it was shown that almost a third of patients with EB simplex were obese, compared with 26% of adults in the general U.K. population.

“People with EBS are known to have hyperkeratosis and foot-blistering,” Ms. Hubbard observed in the poster. This can lead to reduce mobility and pain, which “may in turn have an impact on body weight, and an increased BMI [body mass index] may further affect mobility.”

Data were collected on 90 patients who attended a U.K. EBS clinic over an 11-month period. While 45.5% of patients had a normal weight, the majority was overweight (21.1%), obese (21.1%), or morbidly obese (10%).

Fifteen patients completed questionnaires about their mobility, and almost all felt that their weight had an adverse effect on their feet, as did EBS. Several also noted problems with their EBS, in the skin folds around the bra, waist, and sock lines.

“We now plan to begin a pilot study to establish a supportive weight management program for people with EBS and evaluate both weight loss and impact on mobility,” Ms. Hubbard reported.

No conflicts of interest were declared by any of the speakers.

SOURCES: EB 2020. Reimer A et al. Poster 26; Khan T. oral presentation; O’Sullivan M et al. Poster 93; Hubbard L. Poster 19.

Publications
Publications
Topics
Article Type
Sections
Article Source

REPORTING FROM EB 2020

Disallow All Ads
Content Gating
No Gating (article Unlocked/Free)
Alternative CME
Disqus Comments
Default
Use ProPublica
Hide sidebar & use full width
render the right sidebar.