Duty vs. confidentiality

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Question: During an office visit, a patient confided in his primary care provider his intention to go on a shooting spree. When pressed, he admitted he owned a firearm, but did not truly intend to carry out the act. He denied having a specific target location or victim in mind. The primary care provider (PCP) opted to counsel the patient, and continued him on his antidepressant medication. The PCP did not make a referral to a psychiatrist. Several weeks later, the patient put his threat into action, shooting and injuring several innocent shoppers at a mall.

In a lawsuit against the PCP, which of the following is best?

A. It is unethical for the PCP to report this threat, because it violates the principle of confidentiality.

B. Failure to warn under the circumstances definitely makes the physician liable.

C. The PCP is liable under the Tarasoff doctrine.

D. Without a named victim, there is no one to warn.

E. Whether the PCP is liable may turn on the issue of foreseeability, and an immediate referral to a psychiatrist would have been a more prudent course of action.

Answer: E. One of the physician’s sacred promises is to maintain patient confidentiality. It is more than an unspoken contractual agreement; it’s a central component of trust, without which the doctor-patient relationship cannot exist. Indeed, Hippocrates had cautioned, “whatever in connection with my professional practice, or not in connection with it, I see or hear, in the life of men, which ought not to be spoken of abroad, I will not divulge as reckoning that all should be kept secret.”

Dr. S.Y. Tan
Yet in special circumstances, a doctor may be expected, even required, to violate patient confidences, as when mandated by state statute; for example, disclosure of communicable diseases and reporting of gunshot wounds and suspected child abuse. A contentious issue revolves around a physician’s duty to warn of potential harm to a third party. This has typically been in the setting where there is some control over the patient’s actions, and where there is a named or easily identifiable potential victim.

Thus, the recent expansive decision handed down by the Washington state Supreme Court stunned many mental health professionals.1 In Volk v. DeMeerleer, a clinic patient had confided in his psychiatrist over 9 years of therapy his suicidal and homicidal ideations. He eventually went on to kill his former girlfriend and one of her sons, and then committed suicide. The psychiatrist did not have full control of this clinic patient, nor had the patient named a specific victim. Nevertheless, the Volk court held that the doctor’s duty extended to any foreseeable harm by the patient, leaving it up to the jury to decide on the issue of foreseeability.

The court held that the psychiatrist had a “special relationship” with the victims, because he had a duty to exercise reasonable care to act, consistent with the standards of the mental health profession, in order to protect the foreseeable victims.

The court reasoned that some ability to control the patient’s conduct is sufficient for the “special relationship” and the consequent duty of care to exist, writing: “We find that absolute control is unnecessary, and the actions available to mental health professionals, even in the outpatient setting, weigh in favor of imposing a duty.” The court also noted that a psychiatrist’s obligation to protect third parties against patients’ violence would normally set aside confidentiality and yield to greater societal interests.

The vexing issue of compromising confidentiality in the name of protecting public safety had its genesis in the famous Tarasoff v. Regents of University of California case.2

In Tarasoff, the California court imposed a legal duty on a college psychologist to warn an intended victim of harm, even though that meant breaching confidentiality in a professional relationship. A jilted patient had confided in the university psychologist his intention to kill his ex-girlfriend. The information, though shared with campus security, was not released to the intended victim, whom the patient stabbed to death 2 months later.

The court reasoned that the protection of public safety was more important than the sanctity of the doctor-patient confidentiality relationship, pointing out: “We recognize the public interest in supporting effective treatment of mental illness and in protecting the rights of patients to privacy and the consequent public importance of safeguarding the confidential character of psychotherapeutic communication. Against this interest, however, we must weigh the public interest in safety from violent assault. ... In this risk-infested society, we can hardly tolerate the further exposure to danger that would result from a concealed knowledge of the therapist that his patient was lethal.”

Following Tarasoff, it is generally accepted that there is no affirmative duty to warn where there is no readily identifiable victim. In a subsequent case, the same court explained that “the duty to warn depends upon and arises from the existence of a prior threat to a specific identifiable victim. In those instances in which the released offender poses a predictable threat of harm to a named or readily identifiable victim or group of victims who can be effectively warned of the danger, a releasing agent may well be liable for failure to warn such persons. Despite the tragic events underlying the present complaint, plaintiffs’ decedent was not a known, identifiable victim, but rather a member of a large, amorphous public group of potential targets. Under these circumstances, we hold that County had no affirmative duty to warn plaintiffs, the police, the mother of the juvenile offender, or other local parents.”3

Commentators have suggested that such post-Tarasoff cases, coupled with the advent of state statutes that codify Tarasoff, have witnessed a retreat from imposing on clinicians a duty to warn.4 By dispensing with the control and “readily identifiable victim” elements, Volk appears to contradict this perceived trend. Foreseeability may turn out to be the dispositive issue.

Some have speculated whether Volk’s expanded view will apply to other professionals such as a family practitioner or even a school counselor. Physicians who are not experienced in treating mental health patients will do well to promptly refer their unstable patients to a specialist psychiatrist.

Volk can also be read as offering judicial insight into patients who pose a health hazard by insisting on operating a vehicle against medical advice. In its 2012 Code of Medical Ethics, the American Medical Association had this to say: “In situations where clear evidence of substantial driving impairment implies a strong threat to patient and public safety, and where the physician’s advice to discontinue driving privileges is ignored, it is desirable and ethical to notify the department of motor vehicles.”5

That is now replaced in the AMA code with a broader version covering the duty to disclose: “Physicians may disclose personal health information without the specific consent of the patient ... to other third parties situated to mitigate the threat when in the physician’s judgment there is a reasonable probability that: (i) the patient will seriously harm him/herself; or (ii) the patient will inflict serious physical harm on an identifiable individual or individuals.”6

Under Volk, physicians are now more likely to forsake confidentiality in the name of public safety – even in the absence of a readily identifiable potential victim.
 

 

 

Dr. Tan is emeritus professor of medicine and former adjunct professor of law at the University of Hawaii, Honolulu. This article is meant to be educational and does not constitute medical, ethical, or legal advice. Some of the materials have been taken from earlier columns in Internal Medicine News. For additional information, readers may contact the author at [email protected].

References

1. Volk v. DeMeerleer, 386 P.3d 254 (Wa. 2016).

2. Tarasoff v. Regents of University of California, 551 P.2d 334 (Cal. 1976).

3. Thompson v. County of Alameda, 167 Cal. Rptr. 70, 76 (1980).

4. Behav Sci Law. 2001;19(3):325-43.

5. AMA Code of Medical Ethics [2.24 (3), 2012-2013 ed].

6. AMA Code of Medical Ethics, 2017 ed. [3.2.1 Confidentiality].

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Question: During an office visit, a patient confided in his primary care provider his intention to go on a shooting spree. When pressed, he admitted he owned a firearm, but did not truly intend to carry out the act. He denied having a specific target location or victim in mind. The primary care provider (PCP) opted to counsel the patient, and continued him on his antidepressant medication. The PCP did not make a referral to a psychiatrist. Several weeks later, the patient put his threat into action, shooting and injuring several innocent shoppers at a mall.

In a lawsuit against the PCP, which of the following is best?

A. It is unethical for the PCP to report this threat, because it violates the principle of confidentiality.

B. Failure to warn under the circumstances definitely makes the physician liable.

C. The PCP is liable under the Tarasoff doctrine.

D. Without a named victim, there is no one to warn.

E. Whether the PCP is liable may turn on the issue of foreseeability, and an immediate referral to a psychiatrist would have been a more prudent course of action.

Answer: E. One of the physician’s sacred promises is to maintain patient confidentiality. It is more than an unspoken contractual agreement; it’s a central component of trust, without which the doctor-patient relationship cannot exist. Indeed, Hippocrates had cautioned, “whatever in connection with my professional practice, or not in connection with it, I see or hear, in the life of men, which ought not to be spoken of abroad, I will not divulge as reckoning that all should be kept secret.”

Dr. S.Y. Tan
Yet in special circumstances, a doctor may be expected, even required, to violate patient confidences, as when mandated by state statute; for example, disclosure of communicable diseases and reporting of gunshot wounds and suspected child abuse. A contentious issue revolves around a physician’s duty to warn of potential harm to a third party. This has typically been in the setting where there is some control over the patient’s actions, and where there is a named or easily identifiable potential victim.

Thus, the recent expansive decision handed down by the Washington state Supreme Court stunned many mental health professionals.1 In Volk v. DeMeerleer, a clinic patient had confided in his psychiatrist over 9 years of therapy his suicidal and homicidal ideations. He eventually went on to kill his former girlfriend and one of her sons, and then committed suicide. The psychiatrist did not have full control of this clinic patient, nor had the patient named a specific victim. Nevertheless, the Volk court held that the doctor’s duty extended to any foreseeable harm by the patient, leaving it up to the jury to decide on the issue of foreseeability.

The court held that the psychiatrist had a “special relationship” with the victims, because he had a duty to exercise reasonable care to act, consistent with the standards of the mental health profession, in order to protect the foreseeable victims.

The court reasoned that some ability to control the patient’s conduct is sufficient for the “special relationship” and the consequent duty of care to exist, writing: “We find that absolute control is unnecessary, and the actions available to mental health professionals, even in the outpatient setting, weigh in favor of imposing a duty.” The court also noted that a psychiatrist’s obligation to protect third parties against patients’ violence would normally set aside confidentiality and yield to greater societal interests.

The vexing issue of compromising confidentiality in the name of protecting public safety had its genesis in the famous Tarasoff v. Regents of University of California case.2

In Tarasoff, the California court imposed a legal duty on a college psychologist to warn an intended victim of harm, even though that meant breaching confidentiality in a professional relationship. A jilted patient had confided in the university psychologist his intention to kill his ex-girlfriend. The information, though shared with campus security, was not released to the intended victim, whom the patient stabbed to death 2 months later.

The court reasoned that the protection of public safety was more important than the sanctity of the doctor-patient confidentiality relationship, pointing out: “We recognize the public interest in supporting effective treatment of mental illness and in protecting the rights of patients to privacy and the consequent public importance of safeguarding the confidential character of psychotherapeutic communication. Against this interest, however, we must weigh the public interest in safety from violent assault. ... In this risk-infested society, we can hardly tolerate the further exposure to danger that would result from a concealed knowledge of the therapist that his patient was lethal.”

Following Tarasoff, it is generally accepted that there is no affirmative duty to warn where there is no readily identifiable victim. In a subsequent case, the same court explained that “the duty to warn depends upon and arises from the existence of a prior threat to a specific identifiable victim. In those instances in which the released offender poses a predictable threat of harm to a named or readily identifiable victim or group of victims who can be effectively warned of the danger, a releasing agent may well be liable for failure to warn such persons. Despite the tragic events underlying the present complaint, plaintiffs’ decedent was not a known, identifiable victim, but rather a member of a large, amorphous public group of potential targets. Under these circumstances, we hold that County had no affirmative duty to warn plaintiffs, the police, the mother of the juvenile offender, or other local parents.”3

Commentators have suggested that such post-Tarasoff cases, coupled with the advent of state statutes that codify Tarasoff, have witnessed a retreat from imposing on clinicians a duty to warn.4 By dispensing with the control and “readily identifiable victim” elements, Volk appears to contradict this perceived trend. Foreseeability may turn out to be the dispositive issue.

Some have speculated whether Volk’s expanded view will apply to other professionals such as a family practitioner or even a school counselor. Physicians who are not experienced in treating mental health patients will do well to promptly refer their unstable patients to a specialist psychiatrist.

Volk can also be read as offering judicial insight into patients who pose a health hazard by insisting on operating a vehicle against medical advice. In its 2012 Code of Medical Ethics, the American Medical Association had this to say: “In situations where clear evidence of substantial driving impairment implies a strong threat to patient and public safety, and where the physician’s advice to discontinue driving privileges is ignored, it is desirable and ethical to notify the department of motor vehicles.”5

That is now replaced in the AMA code with a broader version covering the duty to disclose: “Physicians may disclose personal health information without the specific consent of the patient ... to other third parties situated to mitigate the threat when in the physician’s judgment there is a reasonable probability that: (i) the patient will seriously harm him/herself; or (ii) the patient will inflict serious physical harm on an identifiable individual or individuals.”6

Under Volk, physicians are now more likely to forsake confidentiality in the name of public safety – even in the absence of a readily identifiable potential victim.
 

 

 

Dr. Tan is emeritus professor of medicine and former adjunct professor of law at the University of Hawaii, Honolulu. This article is meant to be educational and does not constitute medical, ethical, or legal advice. Some of the materials have been taken from earlier columns in Internal Medicine News. For additional information, readers may contact the author at [email protected].

References

1. Volk v. DeMeerleer, 386 P.3d 254 (Wa. 2016).

2. Tarasoff v. Regents of University of California, 551 P.2d 334 (Cal. 1976).

3. Thompson v. County of Alameda, 167 Cal. Rptr. 70, 76 (1980).

4. Behav Sci Law. 2001;19(3):325-43.

5. AMA Code of Medical Ethics [2.24 (3), 2012-2013 ed].

6. AMA Code of Medical Ethics, 2017 ed. [3.2.1 Confidentiality].

Question: During an office visit, a patient confided in his primary care provider his intention to go on a shooting spree. When pressed, he admitted he owned a firearm, but did not truly intend to carry out the act. He denied having a specific target location or victim in mind. The primary care provider (PCP) opted to counsel the patient, and continued him on his antidepressant medication. The PCP did not make a referral to a psychiatrist. Several weeks later, the patient put his threat into action, shooting and injuring several innocent shoppers at a mall.

In a lawsuit against the PCP, which of the following is best?

A. It is unethical for the PCP to report this threat, because it violates the principle of confidentiality.

B. Failure to warn under the circumstances definitely makes the physician liable.

C. The PCP is liable under the Tarasoff doctrine.

D. Without a named victim, there is no one to warn.

E. Whether the PCP is liable may turn on the issue of foreseeability, and an immediate referral to a psychiatrist would have been a more prudent course of action.

Answer: E. One of the physician’s sacred promises is to maintain patient confidentiality. It is more than an unspoken contractual agreement; it’s a central component of trust, without which the doctor-patient relationship cannot exist. Indeed, Hippocrates had cautioned, “whatever in connection with my professional practice, or not in connection with it, I see or hear, in the life of men, which ought not to be spoken of abroad, I will not divulge as reckoning that all should be kept secret.”

Dr. S.Y. Tan
Yet in special circumstances, a doctor may be expected, even required, to violate patient confidences, as when mandated by state statute; for example, disclosure of communicable diseases and reporting of gunshot wounds and suspected child abuse. A contentious issue revolves around a physician’s duty to warn of potential harm to a third party. This has typically been in the setting where there is some control over the patient’s actions, and where there is a named or easily identifiable potential victim.

Thus, the recent expansive decision handed down by the Washington state Supreme Court stunned many mental health professionals.1 In Volk v. DeMeerleer, a clinic patient had confided in his psychiatrist over 9 years of therapy his suicidal and homicidal ideations. He eventually went on to kill his former girlfriend and one of her sons, and then committed suicide. The psychiatrist did not have full control of this clinic patient, nor had the patient named a specific victim. Nevertheless, the Volk court held that the doctor’s duty extended to any foreseeable harm by the patient, leaving it up to the jury to decide on the issue of foreseeability.

The court held that the psychiatrist had a “special relationship” with the victims, because he had a duty to exercise reasonable care to act, consistent with the standards of the mental health profession, in order to protect the foreseeable victims.

The court reasoned that some ability to control the patient’s conduct is sufficient for the “special relationship” and the consequent duty of care to exist, writing: “We find that absolute control is unnecessary, and the actions available to mental health professionals, even in the outpatient setting, weigh in favor of imposing a duty.” The court also noted that a psychiatrist’s obligation to protect third parties against patients’ violence would normally set aside confidentiality and yield to greater societal interests.

The vexing issue of compromising confidentiality in the name of protecting public safety had its genesis in the famous Tarasoff v. Regents of University of California case.2

In Tarasoff, the California court imposed a legal duty on a college psychologist to warn an intended victim of harm, even though that meant breaching confidentiality in a professional relationship. A jilted patient had confided in the university psychologist his intention to kill his ex-girlfriend. The information, though shared with campus security, was not released to the intended victim, whom the patient stabbed to death 2 months later.

The court reasoned that the protection of public safety was more important than the sanctity of the doctor-patient confidentiality relationship, pointing out: “We recognize the public interest in supporting effective treatment of mental illness and in protecting the rights of patients to privacy and the consequent public importance of safeguarding the confidential character of psychotherapeutic communication. Against this interest, however, we must weigh the public interest in safety from violent assault. ... In this risk-infested society, we can hardly tolerate the further exposure to danger that would result from a concealed knowledge of the therapist that his patient was lethal.”

Following Tarasoff, it is generally accepted that there is no affirmative duty to warn where there is no readily identifiable victim. In a subsequent case, the same court explained that “the duty to warn depends upon and arises from the existence of a prior threat to a specific identifiable victim. In those instances in which the released offender poses a predictable threat of harm to a named or readily identifiable victim or group of victims who can be effectively warned of the danger, a releasing agent may well be liable for failure to warn such persons. Despite the tragic events underlying the present complaint, plaintiffs’ decedent was not a known, identifiable victim, but rather a member of a large, amorphous public group of potential targets. Under these circumstances, we hold that County had no affirmative duty to warn plaintiffs, the police, the mother of the juvenile offender, or other local parents.”3

Commentators have suggested that such post-Tarasoff cases, coupled with the advent of state statutes that codify Tarasoff, have witnessed a retreat from imposing on clinicians a duty to warn.4 By dispensing with the control and “readily identifiable victim” elements, Volk appears to contradict this perceived trend. Foreseeability may turn out to be the dispositive issue.

Some have speculated whether Volk’s expanded view will apply to other professionals such as a family practitioner or even a school counselor. Physicians who are not experienced in treating mental health patients will do well to promptly refer their unstable patients to a specialist psychiatrist.

Volk can also be read as offering judicial insight into patients who pose a health hazard by insisting on operating a vehicle against medical advice. In its 2012 Code of Medical Ethics, the American Medical Association had this to say: “In situations where clear evidence of substantial driving impairment implies a strong threat to patient and public safety, and where the physician’s advice to discontinue driving privileges is ignored, it is desirable and ethical to notify the department of motor vehicles.”5

That is now replaced in the AMA code with a broader version covering the duty to disclose: “Physicians may disclose personal health information without the specific consent of the patient ... to other third parties situated to mitigate the threat when in the physician’s judgment there is a reasonable probability that: (i) the patient will seriously harm him/herself; or (ii) the patient will inflict serious physical harm on an identifiable individual or individuals.”6

Under Volk, physicians are now more likely to forsake confidentiality in the name of public safety – even in the absence of a readily identifiable potential victim.
 

 

 

Dr. Tan is emeritus professor of medicine and former adjunct professor of law at the University of Hawaii, Honolulu. This article is meant to be educational and does not constitute medical, ethical, or legal advice. Some of the materials have been taken from earlier columns in Internal Medicine News. For additional information, readers may contact the author at [email protected].

References

1. Volk v. DeMeerleer, 386 P.3d 254 (Wa. 2016).

2. Tarasoff v. Regents of University of California, 551 P.2d 334 (Cal. 1976).

3. Thompson v. County of Alameda, 167 Cal. Rptr. 70, 76 (1980).

4. Behav Sci Law. 2001;19(3):325-43.

5. AMA Code of Medical Ethics [2.24 (3), 2012-2013 ed].

6. AMA Code of Medical Ethics, 2017 ed. [3.2.1 Confidentiality].

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Baseline lab data is class specific for biologics to treat psoriasis patients

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Mon, 07/01/2019 - 11:13

Don’t underestimate the importance of baseline lab tests before starting psoriasis patients on biologics, said April Armstrong, MD, of the University of Southern California, Los Angeles.

Keep class-specific considerations in mind when collecting baseline lab data to help support the success of biologics in treating psoriasis, Dr. Armstrong said at the annual Coastal Dermatology Symposium.

Dr. April Armstrong
The arsenal of current Food and Drug Administration–approved biologics for psoriasis includes tumor necrosis factor–antagonists etanercept, infliximab, and adalimumab; p40 interleukin–12/23 antagonist ustekinumab; IL-17 antagonists secukinumab, ixekizumab, and brodalumab; and the p19 IL-23 antagonist guselkumab.

When clinicians consider biologics, they must balance efficacy, safety, convenience, and costs of treatment, Dr. Armstrong said.

She addressed general considerations when selecting biologics for psoriasis and stressed the importance of assessing patients for tuberculosis and reviewing underlying cancer risk. Confirm that a patient has no active infections and consider whether a patient has completed all age-appropriate immunizations. Consider a complete blood count and metabolic panel for the following biologics:

  • Ustekinumab: Baseline HIV or pregnancy test, and a TB evaluation at baseline as well as annual monitoring.
  • Etanercept, adalimumab, infliximab: Baseline TB evaluation and screening hepatitis panel, liver function tests, and blood count, with option to add pregnancy test or HIV test. A liver function test/hepatitis panel is indicated annually, and TB should be monitored annually. Be cautious about using this class of drugs in patients with heart failure, and verify the absence of demyelinating disease in patients prior to prescribing this class of drugs.
  • Guselkumab: Baseline TB evaluation, possible pregnancy or HIV tests, followed by annual TB evaluation.
  • Secukinumab, ixekizumab, and brodalumab: Baseline TB evaluation, consider HIV or pregnancy tests, followed by annual TB evaluation. Be cautious about using this class of drugs in patients with ulcerative colitis or Crohn’s disease; assess and counsel for increased risk of suicidality when considering brodalumab.

Beyond the general considerations, several other factors can help maximize success with particular biologics, Dr. Armstrong said at the meeting, which is jointly presented by the University of Louisville and Global Academy for Medical Education.

The number of injections given in the first year, which range from 5 (ustekinumab) to 64 (etanercept) is an important consideration for some patients, Dr. Armstrong noted; the number of injections for the remaining biologics are guselkumab, 8; ixekizumab, 17; brodalumab and adalimumab, both 27, and secukinumab, 32. In addition, the IL-17 inhibitors carry some risk of oral candidiasis and inflammatory bowel disease.

This publication and the Global Academy for Medical Education are owned by Frontline Medical News.

Dr. Armstrong disclosed relationships with multiple companies including AbbVie, Janssen, Novartis, Lilly, Regeneron, Sanofi, Modernizing Medicine, and Valeant.

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Don’t underestimate the importance of baseline lab tests before starting psoriasis patients on biologics, said April Armstrong, MD, of the University of Southern California, Los Angeles.

Keep class-specific considerations in mind when collecting baseline lab data to help support the success of biologics in treating psoriasis, Dr. Armstrong said at the annual Coastal Dermatology Symposium.

Dr. April Armstrong
The arsenal of current Food and Drug Administration–approved biologics for psoriasis includes tumor necrosis factor–antagonists etanercept, infliximab, and adalimumab; p40 interleukin–12/23 antagonist ustekinumab; IL-17 antagonists secukinumab, ixekizumab, and brodalumab; and the p19 IL-23 antagonist guselkumab.

When clinicians consider biologics, they must balance efficacy, safety, convenience, and costs of treatment, Dr. Armstrong said.

She addressed general considerations when selecting biologics for psoriasis and stressed the importance of assessing patients for tuberculosis and reviewing underlying cancer risk. Confirm that a patient has no active infections and consider whether a patient has completed all age-appropriate immunizations. Consider a complete blood count and metabolic panel for the following biologics:

  • Ustekinumab: Baseline HIV or pregnancy test, and a TB evaluation at baseline as well as annual monitoring.
  • Etanercept, adalimumab, infliximab: Baseline TB evaluation and screening hepatitis panel, liver function tests, and blood count, with option to add pregnancy test or HIV test. A liver function test/hepatitis panel is indicated annually, and TB should be monitored annually. Be cautious about using this class of drugs in patients with heart failure, and verify the absence of demyelinating disease in patients prior to prescribing this class of drugs.
  • Guselkumab: Baseline TB evaluation, possible pregnancy or HIV tests, followed by annual TB evaluation.
  • Secukinumab, ixekizumab, and brodalumab: Baseline TB evaluation, consider HIV or pregnancy tests, followed by annual TB evaluation. Be cautious about using this class of drugs in patients with ulcerative colitis or Crohn’s disease; assess and counsel for increased risk of suicidality when considering brodalumab.

Beyond the general considerations, several other factors can help maximize success with particular biologics, Dr. Armstrong said at the meeting, which is jointly presented by the University of Louisville and Global Academy for Medical Education.

The number of injections given in the first year, which range from 5 (ustekinumab) to 64 (etanercept) is an important consideration for some patients, Dr. Armstrong noted; the number of injections for the remaining biologics are guselkumab, 8; ixekizumab, 17; brodalumab and adalimumab, both 27, and secukinumab, 32. In addition, the IL-17 inhibitors carry some risk of oral candidiasis and inflammatory bowel disease.

This publication and the Global Academy for Medical Education are owned by Frontline Medical News.

Dr. Armstrong disclosed relationships with multiple companies including AbbVie, Janssen, Novartis, Lilly, Regeneron, Sanofi, Modernizing Medicine, and Valeant.

Don’t underestimate the importance of baseline lab tests before starting psoriasis patients on biologics, said April Armstrong, MD, of the University of Southern California, Los Angeles.

Keep class-specific considerations in mind when collecting baseline lab data to help support the success of biologics in treating psoriasis, Dr. Armstrong said at the annual Coastal Dermatology Symposium.

Dr. April Armstrong
The arsenal of current Food and Drug Administration–approved biologics for psoriasis includes tumor necrosis factor–antagonists etanercept, infliximab, and adalimumab; p40 interleukin–12/23 antagonist ustekinumab; IL-17 antagonists secukinumab, ixekizumab, and brodalumab; and the p19 IL-23 antagonist guselkumab.

When clinicians consider biologics, they must balance efficacy, safety, convenience, and costs of treatment, Dr. Armstrong said.

She addressed general considerations when selecting biologics for psoriasis and stressed the importance of assessing patients for tuberculosis and reviewing underlying cancer risk. Confirm that a patient has no active infections and consider whether a patient has completed all age-appropriate immunizations. Consider a complete blood count and metabolic panel for the following biologics:

  • Ustekinumab: Baseline HIV or pregnancy test, and a TB evaluation at baseline as well as annual monitoring.
  • Etanercept, adalimumab, infliximab: Baseline TB evaluation and screening hepatitis panel, liver function tests, and blood count, with option to add pregnancy test or HIV test. A liver function test/hepatitis panel is indicated annually, and TB should be monitored annually. Be cautious about using this class of drugs in patients with heart failure, and verify the absence of demyelinating disease in patients prior to prescribing this class of drugs.
  • Guselkumab: Baseline TB evaluation, possible pregnancy or HIV tests, followed by annual TB evaluation.
  • Secukinumab, ixekizumab, and brodalumab: Baseline TB evaluation, consider HIV or pregnancy tests, followed by annual TB evaluation. Be cautious about using this class of drugs in patients with ulcerative colitis or Crohn’s disease; assess and counsel for increased risk of suicidality when considering brodalumab.

Beyond the general considerations, several other factors can help maximize success with particular biologics, Dr. Armstrong said at the meeting, which is jointly presented by the University of Louisville and Global Academy for Medical Education.

The number of injections given in the first year, which range from 5 (ustekinumab) to 64 (etanercept) is an important consideration for some patients, Dr. Armstrong noted; the number of injections for the remaining biologics are guselkumab, 8; ixekizumab, 17; brodalumab and adalimumab, both 27, and secukinumab, 32. In addition, the IL-17 inhibitors carry some risk of oral candidiasis and inflammatory bowel disease.

This publication and the Global Academy for Medical Education are owned by Frontline Medical News.

Dr. Armstrong disclosed relationships with multiple companies including AbbVie, Janssen, Novartis, Lilly, Regeneron, Sanofi, Modernizing Medicine, and Valeant.

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EXPERT ANALYSIS FROM THE COASTAL DERMATOLOGY SYMPOSIUM

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Trump administration narrows contraceptive mandate

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Thu, 03/28/2019 - 14:46

The Trump administration has issued new rules allowing more employers to opt out of the Affordable Care Act’s contraceptive mandate, a move that physician leaders say could sharply restrict women’s ability to access birth control and lead to more unplanned pregnancies.

 

Under two regulations, issued Oct. 6 in the Federal Register, an expanded group of employers and insurers can get out of covering contraception methods by objecting on either religious or moral grounds. The new policy will “better balance the government’s interest in promoting coverage for contraceptive and sterilization services with the government’s interests in providing conscience protections for entities with sincerely held moral convictions,” according to the rule on moral exemptions issued by the departments of Health & Human Services, Labor, and Treasury.

Gage Skidmore/Wikimedia Commons/CC BY-SA 2.0
Donald J. Trump


The American Congress of Obstetricians and Gynecologists denounced the new rules as a move that will negatively impact the health of women and families by limiting access to essential preventive care.

“Reducing access to contraceptive coverage threatens to reverse the tremendous progress our nation has made in recent years in lowering the unintended pregnancy rate,” ACOG President Haywood L. Brown said in a statement. “Instead of fulfilling its mission ‘to enhance and protect the health and well-being of all Americans,’ HHS leaders under the current administration are focused on turning back the clock on women’s health.”
Dr. Haywood L. Brown


The ACA initially required all employers to cover birth control for employees with no copayments, except for group health plans of “religious employers,” which were deemed exempt. Those religious employers were, for the most part, churches and other houses of worship. After multiple complaints and legal challenges, the Obama administration later created a workaround for another group – nonprofit religious employers – to opt out of the mandate. However, critics argued the process itself was a violation of their religious freedom. The issue led to the case of Zubik v. Burwell, a legal challenge over the mandate exemption that went before the U.S. Supreme Court in March 2016.

But the issue remained unresolved. In May 2016, the Supreme Court vacated the lower court rulings related to Zubik v. Burwell and remanded the case back to the four appeals courts that had originally ruled on the issue.

Under the new Oct. 6 regulations, any employer or insurer can halt their coverage of contraceptive services if they have religious beliefs or moral convictions against covering birth control. They need not have a specific religious affiliation to do so. States would determine how companies can make these decisions.

It’s unclear how many women and employers will be impacted. In its rule on religious exemptions, HHS estimated that 109 entities will use this voluntary accommodation moving forward. The department also estimated that the expanded religious exemptions will impact the contraceptive costs of about 31,700 women of childbearing age that use the contraception coverage.

According to research by the Kaiser Family Foundation, 1 in 10 nonprofit organizations with at least 1,000 workers sought an accommodation to not provide Affordable Care Act–required contraceptive coverage to their employees in 2015, but instead allow workers to access the copay-free coverage separately. Three percent of all nonprofits with at least 10 workers sought some kind of accommodation, according to the research. For the smallest of organizations (10-199 workers), the accommodation request rate was 2%, while 5% of organizations with 200-999 workers requested an accommodation.

The American College of Physicians expressed their disappointment with the new regulation, saying that it could lead to more out-of-pocket costs for women who currently receive free contraception.

“Our concern is grounded on our long-standing policy that all Americans should have coverage for evidence-based medical services, including preventive services like contraception,” Jack Ende, MD, ACP president said in a statement. “We are concerned that allowing employers to carve out exemptions to the ACA’s requirements that health insurance plans cover evidence-based preventive services without cost sharing, including but not necessarily limited to contraception, will create substantial barriers to patients receiving appropriate medical care as recommended by their physicians.”

In a statement, national pro-life group Susan B. Anthony List declared the new rules to be a “huge victory for conscience rights and religious liberty in America,” noting that it would exempt their group as a moral objector to contraception.

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The Trump administration has issued new rules allowing more employers to opt out of the Affordable Care Act’s contraceptive mandate, a move that physician leaders say could sharply restrict women’s ability to access birth control and lead to more unplanned pregnancies.

 

Under two regulations, issued Oct. 6 in the Federal Register, an expanded group of employers and insurers can get out of covering contraception methods by objecting on either religious or moral grounds. The new policy will “better balance the government’s interest in promoting coverage for contraceptive and sterilization services with the government’s interests in providing conscience protections for entities with sincerely held moral convictions,” according to the rule on moral exemptions issued by the departments of Health & Human Services, Labor, and Treasury.

Gage Skidmore/Wikimedia Commons/CC BY-SA 2.0
Donald J. Trump


The American Congress of Obstetricians and Gynecologists denounced the new rules as a move that will negatively impact the health of women and families by limiting access to essential preventive care.

“Reducing access to contraceptive coverage threatens to reverse the tremendous progress our nation has made in recent years in lowering the unintended pregnancy rate,” ACOG President Haywood L. Brown said in a statement. “Instead of fulfilling its mission ‘to enhance and protect the health and well-being of all Americans,’ HHS leaders under the current administration are focused on turning back the clock on women’s health.”
Dr. Haywood L. Brown


The ACA initially required all employers to cover birth control for employees with no copayments, except for group health plans of “religious employers,” which were deemed exempt. Those religious employers were, for the most part, churches and other houses of worship. After multiple complaints and legal challenges, the Obama administration later created a workaround for another group – nonprofit religious employers – to opt out of the mandate. However, critics argued the process itself was a violation of their religious freedom. The issue led to the case of Zubik v. Burwell, a legal challenge over the mandate exemption that went before the U.S. Supreme Court in March 2016.

But the issue remained unresolved. In May 2016, the Supreme Court vacated the lower court rulings related to Zubik v. Burwell and remanded the case back to the four appeals courts that had originally ruled on the issue.

Under the new Oct. 6 regulations, any employer or insurer can halt their coverage of contraceptive services if they have religious beliefs or moral convictions against covering birth control. They need not have a specific religious affiliation to do so. States would determine how companies can make these decisions.

It’s unclear how many women and employers will be impacted. In its rule on religious exemptions, HHS estimated that 109 entities will use this voluntary accommodation moving forward. The department also estimated that the expanded religious exemptions will impact the contraceptive costs of about 31,700 women of childbearing age that use the contraception coverage.

According to research by the Kaiser Family Foundation, 1 in 10 nonprofit organizations with at least 1,000 workers sought an accommodation to not provide Affordable Care Act–required contraceptive coverage to their employees in 2015, but instead allow workers to access the copay-free coverage separately. Three percent of all nonprofits with at least 10 workers sought some kind of accommodation, according to the research. For the smallest of organizations (10-199 workers), the accommodation request rate was 2%, while 5% of organizations with 200-999 workers requested an accommodation.

The American College of Physicians expressed their disappointment with the new regulation, saying that it could lead to more out-of-pocket costs for women who currently receive free contraception.

“Our concern is grounded on our long-standing policy that all Americans should have coverage for evidence-based medical services, including preventive services like contraception,” Jack Ende, MD, ACP president said in a statement. “We are concerned that allowing employers to carve out exemptions to the ACA’s requirements that health insurance plans cover evidence-based preventive services without cost sharing, including but not necessarily limited to contraception, will create substantial barriers to patients receiving appropriate medical care as recommended by their physicians.”

In a statement, national pro-life group Susan B. Anthony List declared the new rules to be a “huge victory for conscience rights and religious liberty in America,” noting that it would exempt their group as a moral objector to contraception.

The Trump administration has issued new rules allowing more employers to opt out of the Affordable Care Act’s contraceptive mandate, a move that physician leaders say could sharply restrict women’s ability to access birth control and lead to more unplanned pregnancies.

 

Under two regulations, issued Oct. 6 in the Federal Register, an expanded group of employers and insurers can get out of covering contraception methods by objecting on either religious or moral grounds. The new policy will “better balance the government’s interest in promoting coverage for contraceptive and sterilization services with the government’s interests in providing conscience protections for entities with sincerely held moral convictions,” according to the rule on moral exemptions issued by the departments of Health & Human Services, Labor, and Treasury.

Gage Skidmore/Wikimedia Commons/CC BY-SA 2.0
Donald J. Trump


The American Congress of Obstetricians and Gynecologists denounced the new rules as a move that will negatively impact the health of women and families by limiting access to essential preventive care.

“Reducing access to contraceptive coverage threatens to reverse the tremendous progress our nation has made in recent years in lowering the unintended pregnancy rate,” ACOG President Haywood L. Brown said in a statement. “Instead of fulfilling its mission ‘to enhance and protect the health and well-being of all Americans,’ HHS leaders under the current administration are focused on turning back the clock on women’s health.”
Dr. Haywood L. Brown


The ACA initially required all employers to cover birth control for employees with no copayments, except for group health plans of “religious employers,” which were deemed exempt. Those religious employers were, for the most part, churches and other houses of worship. After multiple complaints and legal challenges, the Obama administration later created a workaround for another group – nonprofit religious employers – to opt out of the mandate. However, critics argued the process itself was a violation of their religious freedom. The issue led to the case of Zubik v. Burwell, a legal challenge over the mandate exemption that went before the U.S. Supreme Court in March 2016.

But the issue remained unresolved. In May 2016, the Supreme Court vacated the lower court rulings related to Zubik v. Burwell and remanded the case back to the four appeals courts that had originally ruled on the issue.

Under the new Oct. 6 regulations, any employer or insurer can halt their coverage of contraceptive services if they have religious beliefs or moral convictions against covering birth control. They need not have a specific religious affiliation to do so. States would determine how companies can make these decisions.

It’s unclear how many women and employers will be impacted. In its rule on religious exemptions, HHS estimated that 109 entities will use this voluntary accommodation moving forward. The department also estimated that the expanded religious exemptions will impact the contraceptive costs of about 31,700 women of childbearing age that use the contraception coverage.

According to research by the Kaiser Family Foundation, 1 in 10 nonprofit organizations with at least 1,000 workers sought an accommodation to not provide Affordable Care Act–required contraceptive coverage to their employees in 2015, but instead allow workers to access the copay-free coverage separately. Three percent of all nonprofits with at least 10 workers sought some kind of accommodation, according to the research. For the smallest of organizations (10-199 workers), the accommodation request rate was 2%, while 5% of organizations with 200-999 workers requested an accommodation.

The American College of Physicians expressed their disappointment with the new regulation, saying that it could lead to more out-of-pocket costs for women who currently receive free contraception.

“Our concern is grounded on our long-standing policy that all Americans should have coverage for evidence-based medical services, including preventive services like contraception,” Jack Ende, MD, ACP president said in a statement. “We are concerned that allowing employers to carve out exemptions to the ACA’s requirements that health insurance plans cover evidence-based preventive services without cost sharing, including but not necessarily limited to contraception, will create substantial barriers to patients receiving appropriate medical care as recommended by their physicians.”

In a statement, national pro-life group Susan B. Anthony List declared the new rules to be a “huge victory for conscience rights and religious liberty in America,” noting that it would exempt their group as a moral objector to contraception.

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New psoriasis therapies coming of age

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The pathogenesis theories and treatment approaches to psoriasis have evolved over the past 3 decades, and the latest treatments continue to show safety and effectiveness, according to Alan Menter, MD, chairman of dermatology at Baylor University Medical Center, Dallas.

Dr. Alan Menter
The disease is now seen as an IL-23/Th17–mediated condition, with multiple therapeutic approaches targeting IL-12/IL-23, IL-23, IL-17, and IL-17R, he noted.

These include risankizumab, which targets the p19 subunit of IL-23 and is being studied for treatment of moderate to severe psoriasis. After one intravenous or subcutaneous dose of risankizumab in a phase 1 study, 16% of patients achieved a Psoriasis Area and Severity Index (PASI) 100, 58% achieved a PASI 90, and 87% achieved a PASI 75, and the publication of phase 2 results are pending, Dr. Menter said. The most common side effects included mild to moderate upper respiratory infections, mild nasopharyngitis, and mild to moderate headaches.

Psoriasis patients treated with guselkumab, which also targets the p19 subunit of IL-23 and was approved in July 2017 for patients with moderate to severe plaque psoriasis who are candidates for systemic therapy or phototherapy, were significantly more likely to be clear or almost clear at 16 weeks, compared with those on placebo in a phase 2 randomized, controlled trial.

“Both IL-23 and IL-17 are promising targets in the treatment of moderate to severe plaque psoriasis,” said Dr. Menter. “It is important to be vigilant in following the safety profile of these drugs both in clinical trials and in postmarketing registries to ensure their long-term safety,” he added.

Additional research on how to curb side effects associated with these new and emerging therapies should target receptors downstream along the IL-23/Th17 pathway, Dr. Menter explained. Findings from a 2015 study suggest that deficiencies in cytokines and receptors further downstream in the IL-23/Th17 pathway “are associated with fewer disorders than deficiencies in upstream components of the pathway,” he said (J Invest Dermatol. 2015 Aug;135[8]:1946-53).

Although concerns about safety remain, avoiding biologics may have a negative impact as well, as moderate to severe psoriasis patients may experience deformed joints, decreased quality of life, heart attacks, strokes, and early death, Dr. Menter said.

Dr. Menter disclosed having received research support and/or serving as a consultant and/or lecturer for AbbVie, Allergan, Amgen, Anacor, Celgene, Dermira, Eli Lilly, Galderma, Janssen Biotech, LEO Pharma, Merck, Neothetics, Novartis, Pfizer, Regeneron, Stiefel, Symbio/Maruho, Vitae, and Xenoport.

The symposium was jointly presented by the University of Louisville and Global Academy for Medical Education. This publication and Global Academy for Medical Education are both owned by Frontline Medical News.

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The pathogenesis theories and treatment approaches to psoriasis have evolved over the past 3 decades, and the latest treatments continue to show safety and effectiveness, according to Alan Menter, MD, chairman of dermatology at Baylor University Medical Center, Dallas.

Dr. Alan Menter
The disease is now seen as an IL-23/Th17–mediated condition, with multiple therapeutic approaches targeting IL-12/IL-23, IL-23, IL-17, and IL-17R, he noted.

These include risankizumab, which targets the p19 subunit of IL-23 and is being studied for treatment of moderate to severe psoriasis. After one intravenous or subcutaneous dose of risankizumab in a phase 1 study, 16% of patients achieved a Psoriasis Area and Severity Index (PASI) 100, 58% achieved a PASI 90, and 87% achieved a PASI 75, and the publication of phase 2 results are pending, Dr. Menter said. The most common side effects included mild to moderate upper respiratory infections, mild nasopharyngitis, and mild to moderate headaches.

Psoriasis patients treated with guselkumab, which also targets the p19 subunit of IL-23 and was approved in July 2017 for patients with moderate to severe plaque psoriasis who are candidates for systemic therapy or phototherapy, were significantly more likely to be clear or almost clear at 16 weeks, compared with those on placebo in a phase 2 randomized, controlled trial.

“Both IL-23 and IL-17 are promising targets in the treatment of moderate to severe plaque psoriasis,” said Dr. Menter. “It is important to be vigilant in following the safety profile of these drugs both in clinical trials and in postmarketing registries to ensure their long-term safety,” he added.

Additional research on how to curb side effects associated with these new and emerging therapies should target receptors downstream along the IL-23/Th17 pathway, Dr. Menter explained. Findings from a 2015 study suggest that deficiencies in cytokines and receptors further downstream in the IL-23/Th17 pathway “are associated with fewer disorders than deficiencies in upstream components of the pathway,” he said (J Invest Dermatol. 2015 Aug;135[8]:1946-53).

Although concerns about safety remain, avoiding biologics may have a negative impact as well, as moderate to severe psoriasis patients may experience deformed joints, decreased quality of life, heart attacks, strokes, and early death, Dr. Menter said.

Dr. Menter disclosed having received research support and/or serving as a consultant and/or lecturer for AbbVie, Allergan, Amgen, Anacor, Celgene, Dermira, Eli Lilly, Galderma, Janssen Biotech, LEO Pharma, Merck, Neothetics, Novartis, Pfizer, Regeneron, Stiefel, Symbio/Maruho, Vitae, and Xenoport.

The symposium was jointly presented by the University of Louisville and Global Academy for Medical Education. This publication and Global Academy for Medical Education are both owned by Frontline Medical News.

 

The pathogenesis theories and treatment approaches to psoriasis have evolved over the past 3 decades, and the latest treatments continue to show safety and effectiveness, according to Alan Menter, MD, chairman of dermatology at Baylor University Medical Center, Dallas.

Dr. Alan Menter
The disease is now seen as an IL-23/Th17–mediated condition, with multiple therapeutic approaches targeting IL-12/IL-23, IL-23, IL-17, and IL-17R, he noted.

These include risankizumab, which targets the p19 subunit of IL-23 and is being studied for treatment of moderate to severe psoriasis. After one intravenous or subcutaneous dose of risankizumab in a phase 1 study, 16% of patients achieved a Psoriasis Area and Severity Index (PASI) 100, 58% achieved a PASI 90, and 87% achieved a PASI 75, and the publication of phase 2 results are pending, Dr. Menter said. The most common side effects included mild to moderate upper respiratory infections, mild nasopharyngitis, and mild to moderate headaches.

Psoriasis patients treated with guselkumab, which also targets the p19 subunit of IL-23 and was approved in July 2017 for patients with moderate to severe plaque psoriasis who are candidates for systemic therapy or phototherapy, were significantly more likely to be clear or almost clear at 16 weeks, compared with those on placebo in a phase 2 randomized, controlled trial.

“Both IL-23 and IL-17 are promising targets in the treatment of moderate to severe plaque psoriasis,” said Dr. Menter. “It is important to be vigilant in following the safety profile of these drugs both in clinical trials and in postmarketing registries to ensure their long-term safety,” he added.

Additional research on how to curb side effects associated with these new and emerging therapies should target receptors downstream along the IL-23/Th17 pathway, Dr. Menter explained. Findings from a 2015 study suggest that deficiencies in cytokines and receptors further downstream in the IL-23/Th17 pathway “are associated with fewer disorders than deficiencies in upstream components of the pathway,” he said (J Invest Dermatol. 2015 Aug;135[8]:1946-53).

Although concerns about safety remain, avoiding biologics may have a negative impact as well, as moderate to severe psoriasis patients may experience deformed joints, decreased quality of life, heart attacks, strokes, and early death, Dr. Menter said.

Dr. Menter disclosed having received research support and/or serving as a consultant and/or lecturer for AbbVie, Allergan, Amgen, Anacor, Celgene, Dermira, Eli Lilly, Galderma, Janssen Biotech, LEO Pharma, Merck, Neothetics, Novartis, Pfizer, Regeneron, Stiefel, Symbio/Maruho, Vitae, and Xenoport.

The symposium was jointly presented by the University of Louisville and Global Academy for Medical Education. This publication and Global Academy for Medical Education are both owned by Frontline Medical News.

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Syphilis rates reach record high

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Novel models predict Parkinson’s disease motor progression

A new era in Parkinson’s progression prediction
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An ensemble of prediction models developed using genetic data and both baseline molecular and clinical variables from patients with Parkinson’s disease, as well as healthy controls, confirmed established predictors of the disease and identified new ones in a longitudinal cohort study.

Furthermore, the models were shown via simulated, randomized, placebo-controlled trials to have utility for clinical trial design and evaluation, as well as for clinical disease monitoring and treatment, Jeanne C. Latourelle, DSc, of GNS Healthcare, Cambridge, Mass., and her colleagues reported in Lancet Neurology.

Kuo Chun Hung/Thinkstock
The findings are important given the substantial heterogeneity in the presentation of Parkinson’s symptoms, which makes it difficult for care providers to give accurate prognoses and for researchers to develop drugs to modify the disease course, the investigators said, noting that “increasing evidence supports a complex interplay between genetic, biological, and molecular abnormalities of the disease, accounting for this heterogeneity between patients.”

“Understanding the causal and physiological factors that contribute to this variability in the evolution of symptoms of Parkinson’s disease is, therefore, a high priority area of Parkinson’s disease research,” they wrote (Lancet Neurol. 2017 Sep 25. doi: 10.1016/S1474-4422[17]30328-9).

The investigators developed the models by applying a Bayesian, machine-learning, multivariate predictive inference platform – known as Reverse Engineering and Forward Simulation – to data from the Parkinson’s Progression Markers Initiative (PPMI) study; they used these models to predict the annual rate of change in combined scores from the Movement Disorder Society–Unified Parkinson’s Disease Rating Scale (MDS-UPDRS) parts II and III. The investigators tested the overall explanatory power of the models using the coefficient of determination (R2); their models also replicated novel findings from an independent clinical cohort from the Longitudinal and Biomarker Study in Parkinson’s disease (LABS-PD).

In 117 healthy age- and sex-matched controls and 312 patients with early-stage Parkinson’s disease from the PPMI study, the model ensemble showed strong performance (fivefold cross-validated Pearson R2, 41%), the investigators said.

In the 317-patient LABS-PD validation cohort, the performance of the models was reduced, but still statistically significant (R2, 9%).

Individual predictive features – including significant replication of higher baseline motor score on MDS-UPDRS, male sex, increased age, and novel Parkinson’s disease–specific epistatic interaction, which all were indicative of faster motor progression in the disease – were confirmed in the LABS-PD cohort, they said. The most useful predictive marker of motor progression was genetic variation (R2, 2.9%), the investigators said, and the cerebrospinal fluid biomarkers at baseline also significantly affected prediction of motor progression, although more modestly (R2, 0.3%).

In 5,000 trial simulations, the incorporation of predicted rates of motor progression into the final models of treatment effect reduced the variability in study outcome, which allowed for the detection of significant differences in sample sizes up to 20% smaller than in trials of drug-naive patients.

The investigators noted that the Bayesian model inference using Reverse Engineering and Forward Simulation was particularly good at predicting Parkinson’s motor progression in early disease stages, which has “immediate relevance toward enabling more effective trial recruitment and clinical disease management.”

This study was supported by grants from the Michael J. Fox Foundation for Parkinson’s Research and the National Institute of Neurological Disorders and Stroke. PPMI is funded by the Michael J. Fox Foundation for Parkinson’s Research, and it also has many industry funding partners. Dr. Latourelle and several of her coauthors are or were employees of GNS Healthcare.

Body

 

The study by Latourelle and her colleagues adds substantial value to Parkinson’s disease research not only because of the findings but also because it introduces the topic of using multimodal data in disease prediction, an approach that is sure to grow in popularity, and one that is complex in its application and interpretation.

Although the discovery and replication efforts are of somewhat limited power – indicating a need for expansion of such efforts in terms of sample size and length of follow-up – the study marks a movement in the development of methods to predict disease progression and, therefore, assist clinicians, patients with Parkinson’s disease, and their family members with treatment and individualized disease management.

The methodology is promising, but fine-tuning and extension of current efforts are important because, while these endeavors are costly, they are vital for the development of disease-modifying therapies and the treatment of Parkinson’s disease.

Cornelis Blauwendraat, MD, and his colleagues are with the Laboratory of Neurogenetics at the National Institute on Aging. They declared having no competing interests. Their comments are taken from an editorial accompanying Dr. Latourelle and her colleagues’ report (Lancet Neurol. 2017 Sep 25. doi: 10.106/S1474-4422[17]30331-9).

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Body

 

The study by Latourelle and her colleagues adds substantial value to Parkinson’s disease research not only because of the findings but also because it introduces the topic of using multimodal data in disease prediction, an approach that is sure to grow in popularity, and one that is complex in its application and interpretation.

Although the discovery and replication efforts are of somewhat limited power – indicating a need for expansion of such efforts in terms of sample size and length of follow-up – the study marks a movement in the development of methods to predict disease progression and, therefore, assist clinicians, patients with Parkinson’s disease, and their family members with treatment and individualized disease management.

The methodology is promising, but fine-tuning and extension of current efforts are important because, while these endeavors are costly, they are vital for the development of disease-modifying therapies and the treatment of Parkinson’s disease.

Cornelis Blauwendraat, MD, and his colleagues are with the Laboratory of Neurogenetics at the National Institute on Aging. They declared having no competing interests. Their comments are taken from an editorial accompanying Dr. Latourelle and her colleagues’ report (Lancet Neurol. 2017 Sep 25. doi: 10.106/S1474-4422[17]30331-9).

Body

 

The study by Latourelle and her colleagues adds substantial value to Parkinson’s disease research not only because of the findings but also because it introduces the topic of using multimodal data in disease prediction, an approach that is sure to grow in popularity, and one that is complex in its application and interpretation.

Although the discovery and replication efforts are of somewhat limited power – indicating a need for expansion of such efforts in terms of sample size and length of follow-up – the study marks a movement in the development of methods to predict disease progression and, therefore, assist clinicians, patients with Parkinson’s disease, and their family members with treatment and individualized disease management.

The methodology is promising, but fine-tuning and extension of current efforts are important because, while these endeavors are costly, they are vital for the development of disease-modifying therapies and the treatment of Parkinson’s disease.

Cornelis Blauwendraat, MD, and his colleagues are with the Laboratory of Neurogenetics at the National Institute on Aging. They declared having no competing interests. Their comments are taken from an editorial accompanying Dr. Latourelle and her colleagues’ report (Lancet Neurol. 2017 Sep 25. doi: 10.106/S1474-4422[17]30331-9).

Title
A new era in Parkinson’s progression prediction
A new era in Parkinson’s progression prediction

An ensemble of prediction models developed using genetic data and both baseline molecular and clinical variables from patients with Parkinson’s disease, as well as healthy controls, confirmed established predictors of the disease and identified new ones in a longitudinal cohort study.

Furthermore, the models were shown via simulated, randomized, placebo-controlled trials to have utility for clinical trial design and evaluation, as well as for clinical disease monitoring and treatment, Jeanne C. Latourelle, DSc, of GNS Healthcare, Cambridge, Mass., and her colleagues reported in Lancet Neurology.

Kuo Chun Hung/Thinkstock
The findings are important given the substantial heterogeneity in the presentation of Parkinson’s symptoms, which makes it difficult for care providers to give accurate prognoses and for researchers to develop drugs to modify the disease course, the investigators said, noting that “increasing evidence supports a complex interplay between genetic, biological, and molecular abnormalities of the disease, accounting for this heterogeneity between patients.”

“Understanding the causal and physiological factors that contribute to this variability in the evolution of symptoms of Parkinson’s disease is, therefore, a high priority area of Parkinson’s disease research,” they wrote (Lancet Neurol. 2017 Sep 25. doi: 10.1016/S1474-4422[17]30328-9).

The investigators developed the models by applying a Bayesian, machine-learning, multivariate predictive inference platform – known as Reverse Engineering and Forward Simulation – to data from the Parkinson’s Progression Markers Initiative (PPMI) study; they used these models to predict the annual rate of change in combined scores from the Movement Disorder Society–Unified Parkinson’s Disease Rating Scale (MDS-UPDRS) parts II and III. The investigators tested the overall explanatory power of the models using the coefficient of determination (R2); their models also replicated novel findings from an independent clinical cohort from the Longitudinal and Biomarker Study in Parkinson’s disease (LABS-PD).

In 117 healthy age- and sex-matched controls and 312 patients with early-stage Parkinson’s disease from the PPMI study, the model ensemble showed strong performance (fivefold cross-validated Pearson R2, 41%), the investigators said.

In the 317-patient LABS-PD validation cohort, the performance of the models was reduced, but still statistically significant (R2, 9%).

Individual predictive features – including significant replication of higher baseline motor score on MDS-UPDRS, male sex, increased age, and novel Parkinson’s disease–specific epistatic interaction, which all were indicative of faster motor progression in the disease – were confirmed in the LABS-PD cohort, they said. The most useful predictive marker of motor progression was genetic variation (R2, 2.9%), the investigators said, and the cerebrospinal fluid biomarkers at baseline also significantly affected prediction of motor progression, although more modestly (R2, 0.3%).

In 5,000 trial simulations, the incorporation of predicted rates of motor progression into the final models of treatment effect reduced the variability in study outcome, which allowed for the detection of significant differences in sample sizes up to 20% smaller than in trials of drug-naive patients.

The investigators noted that the Bayesian model inference using Reverse Engineering and Forward Simulation was particularly good at predicting Parkinson’s motor progression in early disease stages, which has “immediate relevance toward enabling more effective trial recruitment and clinical disease management.”

This study was supported by grants from the Michael J. Fox Foundation for Parkinson’s Research and the National Institute of Neurological Disorders and Stroke. PPMI is funded by the Michael J. Fox Foundation for Parkinson’s Research, and it also has many industry funding partners. Dr. Latourelle and several of her coauthors are or were employees of GNS Healthcare.

An ensemble of prediction models developed using genetic data and both baseline molecular and clinical variables from patients with Parkinson’s disease, as well as healthy controls, confirmed established predictors of the disease and identified new ones in a longitudinal cohort study.

Furthermore, the models were shown via simulated, randomized, placebo-controlled trials to have utility for clinical trial design and evaluation, as well as for clinical disease monitoring and treatment, Jeanne C. Latourelle, DSc, of GNS Healthcare, Cambridge, Mass., and her colleagues reported in Lancet Neurology.

Kuo Chun Hung/Thinkstock
The findings are important given the substantial heterogeneity in the presentation of Parkinson’s symptoms, which makes it difficult for care providers to give accurate prognoses and for researchers to develop drugs to modify the disease course, the investigators said, noting that “increasing evidence supports a complex interplay between genetic, biological, and molecular abnormalities of the disease, accounting for this heterogeneity between patients.”

“Understanding the causal and physiological factors that contribute to this variability in the evolution of symptoms of Parkinson’s disease is, therefore, a high priority area of Parkinson’s disease research,” they wrote (Lancet Neurol. 2017 Sep 25. doi: 10.1016/S1474-4422[17]30328-9).

The investigators developed the models by applying a Bayesian, machine-learning, multivariate predictive inference platform – known as Reverse Engineering and Forward Simulation – to data from the Parkinson’s Progression Markers Initiative (PPMI) study; they used these models to predict the annual rate of change in combined scores from the Movement Disorder Society–Unified Parkinson’s Disease Rating Scale (MDS-UPDRS) parts II and III. The investigators tested the overall explanatory power of the models using the coefficient of determination (R2); their models also replicated novel findings from an independent clinical cohort from the Longitudinal and Biomarker Study in Parkinson’s disease (LABS-PD).

In 117 healthy age- and sex-matched controls and 312 patients with early-stage Parkinson’s disease from the PPMI study, the model ensemble showed strong performance (fivefold cross-validated Pearson R2, 41%), the investigators said.

In the 317-patient LABS-PD validation cohort, the performance of the models was reduced, but still statistically significant (R2, 9%).

Individual predictive features – including significant replication of higher baseline motor score on MDS-UPDRS, male sex, increased age, and novel Parkinson’s disease–specific epistatic interaction, which all were indicative of faster motor progression in the disease – were confirmed in the LABS-PD cohort, they said. The most useful predictive marker of motor progression was genetic variation (R2, 2.9%), the investigators said, and the cerebrospinal fluid biomarkers at baseline also significantly affected prediction of motor progression, although more modestly (R2, 0.3%).

In 5,000 trial simulations, the incorporation of predicted rates of motor progression into the final models of treatment effect reduced the variability in study outcome, which allowed for the detection of significant differences in sample sizes up to 20% smaller than in trials of drug-naive patients.

The investigators noted that the Bayesian model inference using Reverse Engineering and Forward Simulation was particularly good at predicting Parkinson’s motor progression in early disease stages, which has “immediate relevance toward enabling more effective trial recruitment and clinical disease management.”

This study was supported by grants from the Michael J. Fox Foundation for Parkinson’s Research and the National Institute of Neurological Disorders and Stroke. PPMI is funded by the Michael J. Fox Foundation for Parkinson’s Research, and it also has many industry funding partners. Dr. Latourelle and several of her coauthors are or were employees of GNS Healthcare.

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Key clinical point: A novel ensemble of prediction models confirmed established predictors of Parkinson’s disease and identified new ones in a longitudinal cohort study.

Major finding: The model ensemble showed strong performance (fivefold cross-validated Pearson R2, 41%) and remained significant in a validation cohort (R2, 9%).

Data source: A longitudinal cohort study of 429 patients and controls, as well as a validation cohort of 317 patients.

Disclosures: This study was supported by grants from the Michael J. Fox Foundation for Parkinson’s Research and the National Institute of Neurological Disorders and Stroke. The Parkinson’s Progression Markers Initiative is funded by the Michael J. Fox Foundation for Parkinson’s Research, and it also has many industry funding partners. Dr. Latourelle and several of her coauthors are or were employees of GNS Healthcare.

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Dentist-prescribed antibiotics implicated in community-acquired C. diff

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– Antibiotic prescriptions written by dentists make a substantial but largely unrecognized contribution to the risk of community-acquired Clostridium difficile (CA-CDI) infections, according to results of a public health initiative that was presented at an annual scientific meeting on infectious diseases.

When nearly 1,000 cases of CA-CDI suspected of being the result of antibiotic exposure were evaluated, it was found that 15% of the prescriptions were written by dentists, often for indications that are counter to current guidelines, reported Maria Bye, MPH, an officer in the Infectious Disease Epidemiology, Prevention, and Control Division of the Minnesota Department of Health, St. Paul.

Maria Bye
“Everyone plays a role in antibiotic stewardship. Dentists should be following the guidelines for antibiotic prophylaxis and counsel patients about the risk and symptoms of C. diff and other complications,” Ms. Bye said. She said that up until now “dentists have largely been left out of the conversation.”

In another finding from this study relevant to infection control, a substantial proportion of dentist-prescribed antibiotics associated with CA-CDI were not in the medical record. Rather, they were discovered in interviews conducted to isolate risk factors. “This is concerning since clinicians unaware of these exposures will not think about CA-CDI or other complications of antibiotic use, possibly delaying therapy,” Ms. Bye said.

The importance of dental antibiotic prescriptions in CA-CDI was identified in an ongoing infectious disease program managed by the Minnesota Department of Health in collaboration with the Centers for Disease Control and Prevention. In the years 2009-2015, medical records and interviews were conducted to identify risk factors in 1,626 confirmed cases of CA-CDI in five Minnesota counties. All cases were among patients without an overnight stay in a health care facility in the previous 12 weeks, which was an exclusion criterion.

After the review of medical records and patient interviews, 926 (57%) of the CA-CDI cases were deemed likely to be related to antibiotic exposure. Of these antibiotic exposures, 136 (15%) were from prescriptions written by dentists, a figure reached only when patients were interviewed. According to Ms. Bye, 34% of the antibiotics prescribed by dentists were not in the medical record.

There were also notable differences in antibiotic exposures stemming from dentist prescriptions relative to prescriptions from other sources. Perhaps most significantly, dental-related antibiotic prescriptions were far more likely to be for clindamycin (50% vs. 10%; P less than .001), which is commonly associated with increased risk of C. difficile, according to Ms. Bye. Fluoroquinolones (6% vs. 19%; P less than .001) and cephalosporins (7% vs. 30%; P less than .001) were significantly less likely to be prescribed by dentists. Patients who developed CA-CDI associated with antibiotics prescribed by dentists were also significantly older than were those receiving antibiotics from another source (mean age 57 years vs. 45 years; P less than .001).

For the first years of this analysis, information on the indication for dentist-prescribed antibiotics was not collected, but these data were collected beginning in 2015. In the data collected so far, a substantial proportion of prescriptions were written for prophylaxis against systemic infections, including prevention of endocarditis or infection of prosthetic joints. However, few of these prescriptions were indicated.

“The American Dental Association stated that antibiotic prophylaxis is not generally recommended in patients with prosthetic joints,” said Ms. Bye, noting that this is consistent with similar statements issued by the American Academy of Orthopedic Surgery. In 2007, the American Heart Association narrowed its recommendations for prophylactic antibiotics to patients at the highest risk of adverse consequences from endocarditis.

Of the four patients who received prophylactic antibiotics from their dentists for a cardiovascular or orthopedic indication, only one met current criteria, Ms. Bye reported.

The contribution of antibiotic exposures from dentist prescriptions to CA-CDI should not be surprising, according to Ms. Bye. In the United States, dentists prescribe 10% of all outpatient antibiotics. Although there are many valid indications for these prescriptions, Ms. Bye cited a survey that found that the proportion of dentists familiar with current guidelines and the risks of adverse events produced by antibiotics, including CA-CDI, is less than 50%.

“Dentists need to be included in antibiotic stewardship programs,” she advised. This will include educating dentists about the indications for antibiotic prophylaxis for medical conditions. She also suggested that clinicians should routinely ask patients about whether they have received antibiotics from a dentist so that this information gets into the medical record.

The event was the combined annual meetings of the Infectious Diseases Society of America, the Society for Healthcare Epidemiology of America, the HIV Medicine Association, and the Pediatric Infectious Diseases Society.

 

 

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– Antibiotic prescriptions written by dentists make a substantial but largely unrecognized contribution to the risk of community-acquired Clostridium difficile (CA-CDI) infections, according to results of a public health initiative that was presented at an annual scientific meeting on infectious diseases.

When nearly 1,000 cases of CA-CDI suspected of being the result of antibiotic exposure were evaluated, it was found that 15% of the prescriptions were written by dentists, often for indications that are counter to current guidelines, reported Maria Bye, MPH, an officer in the Infectious Disease Epidemiology, Prevention, and Control Division of the Minnesota Department of Health, St. Paul.

Maria Bye
“Everyone plays a role in antibiotic stewardship. Dentists should be following the guidelines for antibiotic prophylaxis and counsel patients about the risk and symptoms of C. diff and other complications,” Ms. Bye said. She said that up until now “dentists have largely been left out of the conversation.”

In another finding from this study relevant to infection control, a substantial proportion of dentist-prescribed antibiotics associated with CA-CDI were not in the medical record. Rather, they were discovered in interviews conducted to isolate risk factors. “This is concerning since clinicians unaware of these exposures will not think about CA-CDI or other complications of antibiotic use, possibly delaying therapy,” Ms. Bye said.

The importance of dental antibiotic prescriptions in CA-CDI was identified in an ongoing infectious disease program managed by the Minnesota Department of Health in collaboration with the Centers for Disease Control and Prevention. In the years 2009-2015, medical records and interviews were conducted to identify risk factors in 1,626 confirmed cases of CA-CDI in five Minnesota counties. All cases were among patients without an overnight stay in a health care facility in the previous 12 weeks, which was an exclusion criterion.

After the review of medical records and patient interviews, 926 (57%) of the CA-CDI cases were deemed likely to be related to antibiotic exposure. Of these antibiotic exposures, 136 (15%) were from prescriptions written by dentists, a figure reached only when patients were interviewed. According to Ms. Bye, 34% of the antibiotics prescribed by dentists were not in the medical record.

There were also notable differences in antibiotic exposures stemming from dentist prescriptions relative to prescriptions from other sources. Perhaps most significantly, dental-related antibiotic prescriptions were far more likely to be for clindamycin (50% vs. 10%; P less than .001), which is commonly associated with increased risk of C. difficile, according to Ms. Bye. Fluoroquinolones (6% vs. 19%; P less than .001) and cephalosporins (7% vs. 30%; P less than .001) were significantly less likely to be prescribed by dentists. Patients who developed CA-CDI associated with antibiotics prescribed by dentists were also significantly older than were those receiving antibiotics from another source (mean age 57 years vs. 45 years; P less than .001).

For the first years of this analysis, information on the indication for dentist-prescribed antibiotics was not collected, but these data were collected beginning in 2015. In the data collected so far, a substantial proportion of prescriptions were written for prophylaxis against systemic infections, including prevention of endocarditis or infection of prosthetic joints. However, few of these prescriptions were indicated.

“The American Dental Association stated that antibiotic prophylaxis is not generally recommended in patients with prosthetic joints,” said Ms. Bye, noting that this is consistent with similar statements issued by the American Academy of Orthopedic Surgery. In 2007, the American Heart Association narrowed its recommendations for prophylactic antibiotics to patients at the highest risk of adverse consequences from endocarditis.

Of the four patients who received prophylactic antibiotics from their dentists for a cardiovascular or orthopedic indication, only one met current criteria, Ms. Bye reported.

The contribution of antibiotic exposures from dentist prescriptions to CA-CDI should not be surprising, according to Ms. Bye. In the United States, dentists prescribe 10% of all outpatient antibiotics. Although there are many valid indications for these prescriptions, Ms. Bye cited a survey that found that the proportion of dentists familiar with current guidelines and the risks of adverse events produced by antibiotics, including CA-CDI, is less than 50%.

“Dentists need to be included in antibiotic stewardship programs,” she advised. This will include educating dentists about the indications for antibiotic prophylaxis for medical conditions. She also suggested that clinicians should routinely ask patients about whether they have received antibiotics from a dentist so that this information gets into the medical record.

The event was the combined annual meetings of the Infectious Diseases Society of America, the Society for Healthcare Epidemiology of America, the HIV Medicine Association, and the Pediatric Infectious Diseases Society.

 

 

– Antibiotic prescriptions written by dentists make a substantial but largely unrecognized contribution to the risk of community-acquired Clostridium difficile (CA-CDI) infections, according to results of a public health initiative that was presented at an annual scientific meeting on infectious diseases.

When nearly 1,000 cases of CA-CDI suspected of being the result of antibiotic exposure were evaluated, it was found that 15% of the prescriptions were written by dentists, often for indications that are counter to current guidelines, reported Maria Bye, MPH, an officer in the Infectious Disease Epidemiology, Prevention, and Control Division of the Minnesota Department of Health, St. Paul.

Maria Bye
“Everyone plays a role in antibiotic stewardship. Dentists should be following the guidelines for antibiotic prophylaxis and counsel patients about the risk and symptoms of C. diff and other complications,” Ms. Bye said. She said that up until now “dentists have largely been left out of the conversation.”

In another finding from this study relevant to infection control, a substantial proportion of dentist-prescribed antibiotics associated with CA-CDI were not in the medical record. Rather, they were discovered in interviews conducted to isolate risk factors. “This is concerning since clinicians unaware of these exposures will not think about CA-CDI or other complications of antibiotic use, possibly delaying therapy,” Ms. Bye said.

The importance of dental antibiotic prescriptions in CA-CDI was identified in an ongoing infectious disease program managed by the Minnesota Department of Health in collaboration with the Centers for Disease Control and Prevention. In the years 2009-2015, medical records and interviews were conducted to identify risk factors in 1,626 confirmed cases of CA-CDI in five Minnesota counties. All cases were among patients without an overnight stay in a health care facility in the previous 12 weeks, which was an exclusion criterion.

After the review of medical records and patient interviews, 926 (57%) of the CA-CDI cases were deemed likely to be related to antibiotic exposure. Of these antibiotic exposures, 136 (15%) were from prescriptions written by dentists, a figure reached only when patients were interviewed. According to Ms. Bye, 34% of the antibiotics prescribed by dentists were not in the medical record.

There were also notable differences in antibiotic exposures stemming from dentist prescriptions relative to prescriptions from other sources. Perhaps most significantly, dental-related antibiotic prescriptions were far more likely to be for clindamycin (50% vs. 10%; P less than .001), which is commonly associated with increased risk of C. difficile, according to Ms. Bye. Fluoroquinolones (6% vs. 19%; P less than .001) and cephalosporins (7% vs. 30%; P less than .001) were significantly less likely to be prescribed by dentists. Patients who developed CA-CDI associated with antibiotics prescribed by dentists were also significantly older than were those receiving antibiotics from another source (mean age 57 years vs. 45 years; P less than .001).

For the first years of this analysis, information on the indication for dentist-prescribed antibiotics was not collected, but these data were collected beginning in 2015. In the data collected so far, a substantial proportion of prescriptions were written for prophylaxis against systemic infections, including prevention of endocarditis or infection of prosthetic joints. However, few of these prescriptions were indicated.

“The American Dental Association stated that antibiotic prophylaxis is not generally recommended in patients with prosthetic joints,” said Ms. Bye, noting that this is consistent with similar statements issued by the American Academy of Orthopedic Surgery. In 2007, the American Heart Association narrowed its recommendations for prophylactic antibiotics to patients at the highest risk of adverse consequences from endocarditis.

Of the four patients who received prophylactic antibiotics from their dentists for a cardiovascular or orthopedic indication, only one met current criteria, Ms. Bye reported.

The contribution of antibiotic exposures from dentist prescriptions to CA-CDI should not be surprising, according to Ms. Bye. In the United States, dentists prescribe 10% of all outpatient antibiotics. Although there are many valid indications for these prescriptions, Ms. Bye cited a survey that found that the proportion of dentists familiar with current guidelines and the risks of adverse events produced by antibiotics, including CA-CDI, is less than 50%.

“Dentists need to be included in antibiotic stewardship programs,” she advised. This will include educating dentists about the indications for antibiotic prophylaxis for medical conditions. She also suggested that clinicians should routinely ask patients about whether they have received antibiotics from a dentist so that this information gets into the medical record.

The event was the combined annual meetings of the Infectious Diseases Society of America, the Society for Healthcare Epidemiology of America, the HIV Medicine Association, and the Pediatric Infectious Diseases Society.

 

 

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Key clinical point: A public health initiative tracking community-acquired Clostridium difficile infections suggests dental antibiotic prescribing is a significant source.

Major finding: When traced, 15% of the antibiotics related to community-acquired C. difficile infections were from a dentist prescription.

Data source: Population-based surveillance study.

Disclosures: Ms. Bye reported that she has no financial relationships relevant to this topic.

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It’s too soon to discard cotesting in cervical cancer

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In their new cervical cancer screening draft recommendation statement, the U.S. Preventive Services Task Force recommends screening for cervical cancer every 3 years with cervical cytology alone in women aged 21-29 years, and either continuing 3-year cytology screening or 5-year high-risk human papillomavirus (HPV) screening in women aged 30-65 years.1 They arrived at the conclusion primarily based on an analysis of benefits and harms of each of the currently used screening modalities. Cytology plus HPV cotesting was considered but rejected based on the benefits versus harms calculations. However, some of the assumptions in their modeling are wrong and this has led them to faulty conclusions.

The USPSTF correctly identified CIN-2/3 and CIN-3+ detected and cervical cancer cases and deaths prevented as benefits. But they used the number of colposcopies and the number of tests conducted as their proxy for harms, primarily because these were more easily measured. They identified other harms, such as greater psychological distress related to being told of a positive HPV result (compared with being told of an abnormal cytology or cotest result), but these harms were not numerical and so they could not be incorporated into their modeling. They also did not measure the psychological distress associated with an extended screening interval or HPV-only screening.

Dr. Mark Spitzer
In their modeling, the USPSTF assumed that colposcopy is 100% sensitive.2 This is clearly untrue but convenient for their analysis. Current management guidelines take advantage of the relative strengths of each complementary set of tools to detect cervical disease (cytology, HPV testing, and colposcopy). What is missed by one modality often is detected by another. For example, in a patient with high-grade squamous intraepithelial lesion cytology but negative colposcopy, a loop electrosurgical excisional procedure is recommended. The colposcopy is assumed to be falsely negative. In the USPSTF’s modeling for primary HPV screening, they relied on “perfect” colposcopy to detect the disease. But, in the real world, the absence of cytology screening (as part of cotesting) would result in a missed diagnosis.

The USPSTF also primarily relied on evidence from seven large, randomly controlled trials of primary screening, mostly conducted in Europe.3 Of the seven trials, two of them (SWEDESCREEN and POBASCAM) used HPV testing by a polymerase chain reaction methodology that is not approved by the U.S. Food and Drug Administration, not commercially available in the United States, and has different sensitivity and specificity does than FDA-approved tests.

Most of the studies also were done with conventional cytology that is, for the most part, no longer used in the United States. The age range in some of the studies was also very narrow (SWEDESCREEN evaluated women aged 32-38 years only) while extending to very young ages in others (ARTISTIC evaluated women as young as age 20 years). It may not be possible to extrapolate from these results to the U.S. experience. On the other hand, the USPSTF elected not to use data from very large retrospective U.S. trials, such as the data from more than 1 million women from Kaiser Permanente Northern California, which helped form the foundation of current guidelines.4

Although screening has dramatically reduced the incidence of cervical cancer in the United States, most screening in this country is opportunistic and lacks population-based registries or regular invitations to screening. The USPSTF notes that a sizable proportion of the U.S.-based female population is not routinely screened. In fact, 11.4% of 21- to 65-year-old women have not been screened in the previous 5 years and the percentages are higher among minority and disadvantaged populations. Although the numbers seem relatively small, more than half of women with cervical cancer are found in this population. These women also are at greater risk of being lost to follow-up. Unlike the patients in the European trials, there is no current mechanism in the United States to assure that patients will return in 5 years. In fact, the USPSTF notes this limitation in their evidence, but doesn’t provide a remedy. These women may not get rescreened for many years after the 5-year interval has passed, and there is no evidence that this interval is safe.

Finally, the USPSTF recommendations for HPV primary screening relied in whole or in part on cytology triage of positive results. There is no U.S. experience for the use of cytology within this context, and many experts have argued that the test performance of cytology in a triage setting would be different than in a screening setting and would further be different in a vaccinated population. Since the modeling on which these draft recommendations are based did not account for these changed performance characteristics, their assumptions must be wrong.

Five years have not yet passed since publication of the last set of guidelines, and we have no idea how this extended screening interval functions in our opportunistic screening system. Stated simply, these draft recommendations have gone too far and too fast and should be reconsidered.

 

 

Dr. Spitzer is a professor of obstetrics and gynecology at Hofstra Northwell School of Medicine, Hempstead, N.Y., and a past president of the American Society for Colposcopy and Cervical Pathology. He reported receiving royalties from Elsevier, and consulting fees from Hologic, Biop Medical, Illumigen, and Merck.


References

1. Draft Recommendation Statement: Cervical Cancer: Screening. U.S. Preventive Services Task Force. September 2017.

2. Screening for Cervical Cancer in Primary Care: A Decision Analysis for the U.S. Preventive Services Task Force. 2017.

3. Screening for Cervical Cancer With High-Risk Human Papillomavirus Testing: A Systematic Evidence Review for the U.S. Preventive Services Task Force. 2017.

4. J Natl Cancer Inst. 2014 Jul 18;106(8). pii: dju153.
 

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In their new cervical cancer screening draft recommendation statement, the U.S. Preventive Services Task Force recommends screening for cervical cancer every 3 years with cervical cytology alone in women aged 21-29 years, and either continuing 3-year cytology screening or 5-year high-risk human papillomavirus (HPV) screening in women aged 30-65 years.1 They arrived at the conclusion primarily based on an analysis of benefits and harms of each of the currently used screening modalities. Cytology plus HPV cotesting was considered but rejected based on the benefits versus harms calculations. However, some of the assumptions in their modeling are wrong and this has led them to faulty conclusions.

The USPSTF correctly identified CIN-2/3 and CIN-3+ detected and cervical cancer cases and deaths prevented as benefits. But they used the number of colposcopies and the number of tests conducted as their proxy for harms, primarily because these were more easily measured. They identified other harms, such as greater psychological distress related to being told of a positive HPV result (compared with being told of an abnormal cytology or cotest result), but these harms were not numerical and so they could not be incorporated into their modeling. They also did not measure the psychological distress associated with an extended screening interval or HPV-only screening.

Dr. Mark Spitzer
In their modeling, the USPSTF assumed that colposcopy is 100% sensitive.2 This is clearly untrue but convenient for their analysis. Current management guidelines take advantage of the relative strengths of each complementary set of tools to detect cervical disease (cytology, HPV testing, and colposcopy). What is missed by one modality often is detected by another. For example, in a patient with high-grade squamous intraepithelial lesion cytology but negative colposcopy, a loop electrosurgical excisional procedure is recommended. The colposcopy is assumed to be falsely negative. In the USPSTF’s modeling for primary HPV screening, they relied on “perfect” colposcopy to detect the disease. But, in the real world, the absence of cytology screening (as part of cotesting) would result in a missed diagnosis.

The USPSTF also primarily relied on evidence from seven large, randomly controlled trials of primary screening, mostly conducted in Europe.3 Of the seven trials, two of them (SWEDESCREEN and POBASCAM) used HPV testing by a polymerase chain reaction methodology that is not approved by the U.S. Food and Drug Administration, not commercially available in the United States, and has different sensitivity and specificity does than FDA-approved tests.

Most of the studies also were done with conventional cytology that is, for the most part, no longer used in the United States. The age range in some of the studies was also very narrow (SWEDESCREEN evaluated women aged 32-38 years only) while extending to very young ages in others (ARTISTIC evaluated women as young as age 20 years). It may not be possible to extrapolate from these results to the U.S. experience. On the other hand, the USPSTF elected not to use data from very large retrospective U.S. trials, such as the data from more than 1 million women from Kaiser Permanente Northern California, which helped form the foundation of current guidelines.4

Although screening has dramatically reduced the incidence of cervical cancer in the United States, most screening in this country is opportunistic and lacks population-based registries or regular invitations to screening. The USPSTF notes that a sizable proportion of the U.S.-based female population is not routinely screened. In fact, 11.4% of 21- to 65-year-old women have not been screened in the previous 5 years and the percentages are higher among minority and disadvantaged populations. Although the numbers seem relatively small, more than half of women with cervical cancer are found in this population. These women also are at greater risk of being lost to follow-up. Unlike the patients in the European trials, there is no current mechanism in the United States to assure that patients will return in 5 years. In fact, the USPSTF notes this limitation in their evidence, but doesn’t provide a remedy. These women may not get rescreened for many years after the 5-year interval has passed, and there is no evidence that this interval is safe.

Finally, the USPSTF recommendations for HPV primary screening relied in whole or in part on cytology triage of positive results. There is no U.S. experience for the use of cytology within this context, and many experts have argued that the test performance of cytology in a triage setting would be different than in a screening setting and would further be different in a vaccinated population. Since the modeling on which these draft recommendations are based did not account for these changed performance characteristics, their assumptions must be wrong.

Five years have not yet passed since publication of the last set of guidelines, and we have no idea how this extended screening interval functions in our opportunistic screening system. Stated simply, these draft recommendations have gone too far and too fast and should be reconsidered.

 

 

Dr. Spitzer is a professor of obstetrics and gynecology at Hofstra Northwell School of Medicine, Hempstead, N.Y., and a past president of the American Society for Colposcopy and Cervical Pathology. He reported receiving royalties from Elsevier, and consulting fees from Hologic, Biop Medical, Illumigen, and Merck.


References

1. Draft Recommendation Statement: Cervical Cancer: Screening. U.S. Preventive Services Task Force. September 2017.

2. Screening for Cervical Cancer in Primary Care: A Decision Analysis for the U.S. Preventive Services Task Force. 2017.

3. Screening for Cervical Cancer With High-Risk Human Papillomavirus Testing: A Systematic Evidence Review for the U.S. Preventive Services Task Force. 2017.

4. J Natl Cancer Inst. 2014 Jul 18;106(8). pii: dju153.
 

 

In their new cervical cancer screening draft recommendation statement, the U.S. Preventive Services Task Force recommends screening for cervical cancer every 3 years with cervical cytology alone in women aged 21-29 years, and either continuing 3-year cytology screening or 5-year high-risk human papillomavirus (HPV) screening in women aged 30-65 years.1 They arrived at the conclusion primarily based on an analysis of benefits and harms of each of the currently used screening modalities. Cytology plus HPV cotesting was considered but rejected based on the benefits versus harms calculations. However, some of the assumptions in their modeling are wrong and this has led them to faulty conclusions.

The USPSTF correctly identified CIN-2/3 and CIN-3+ detected and cervical cancer cases and deaths prevented as benefits. But they used the number of colposcopies and the number of tests conducted as their proxy for harms, primarily because these were more easily measured. They identified other harms, such as greater psychological distress related to being told of a positive HPV result (compared with being told of an abnormal cytology or cotest result), but these harms were not numerical and so they could not be incorporated into their modeling. They also did not measure the psychological distress associated with an extended screening interval or HPV-only screening.

Dr. Mark Spitzer
In their modeling, the USPSTF assumed that colposcopy is 100% sensitive.2 This is clearly untrue but convenient for their analysis. Current management guidelines take advantage of the relative strengths of each complementary set of tools to detect cervical disease (cytology, HPV testing, and colposcopy). What is missed by one modality often is detected by another. For example, in a patient with high-grade squamous intraepithelial lesion cytology but negative colposcopy, a loop electrosurgical excisional procedure is recommended. The colposcopy is assumed to be falsely negative. In the USPSTF’s modeling for primary HPV screening, they relied on “perfect” colposcopy to detect the disease. But, in the real world, the absence of cytology screening (as part of cotesting) would result in a missed diagnosis.

The USPSTF also primarily relied on evidence from seven large, randomly controlled trials of primary screening, mostly conducted in Europe.3 Of the seven trials, two of them (SWEDESCREEN and POBASCAM) used HPV testing by a polymerase chain reaction methodology that is not approved by the U.S. Food and Drug Administration, not commercially available in the United States, and has different sensitivity and specificity does than FDA-approved tests.

Most of the studies also were done with conventional cytology that is, for the most part, no longer used in the United States. The age range in some of the studies was also very narrow (SWEDESCREEN evaluated women aged 32-38 years only) while extending to very young ages in others (ARTISTIC evaluated women as young as age 20 years). It may not be possible to extrapolate from these results to the U.S. experience. On the other hand, the USPSTF elected not to use data from very large retrospective U.S. trials, such as the data from more than 1 million women from Kaiser Permanente Northern California, which helped form the foundation of current guidelines.4

Although screening has dramatically reduced the incidence of cervical cancer in the United States, most screening in this country is opportunistic and lacks population-based registries or regular invitations to screening. The USPSTF notes that a sizable proportion of the U.S.-based female population is not routinely screened. In fact, 11.4% of 21- to 65-year-old women have not been screened in the previous 5 years and the percentages are higher among minority and disadvantaged populations. Although the numbers seem relatively small, more than half of women with cervical cancer are found in this population. These women also are at greater risk of being lost to follow-up. Unlike the patients in the European trials, there is no current mechanism in the United States to assure that patients will return in 5 years. In fact, the USPSTF notes this limitation in their evidence, but doesn’t provide a remedy. These women may not get rescreened for many years after the 5-year interval has passed, and there is no evidence that this interval is safe.

Finally, the USPSTF recommendations for HPV primary screening relied in whole or in part on cytology triage of positive results. There is no U.S. experience for the use of cytology within this context, and many experts have argued that the test performance of cytology in a triage setting would be different than in a screening setting and would further be different in a vaccinated population. Since the modeling on which these draft recommendations are based did not account for these changed performance characteristics, their assumptions must be wrong.

Five years have not yet passed since publication of the last set of guidelines, and we have no idea how this extended screening interval functions in our opportunistic screening system. Stated simply, these draft recommendations have gone too far and too fast and should be reconsidered.

 

 

Dr. Spitzer is a professor of obstetrics and gynecology at Hofstra Northwell School of Medicine, Hempstead, N.Y., and a past president of the American Society for Colposcopy and Cervical Pathology. He reported receiving royalties from Elsevier, and consulting fees from Hologic, Biop Medical, Illumigen, and Merck.


References

1. Draft Recommendation Statement: Cervical Cancer: Screening. U.S. Preventive Services Task Force. September 2017.

2. Screening for Cervical Cancer in Primary Care: A Decision Analysis for the U.S. Preventive Services Task Force. 2017.

3. Screening for Cervical Cancer With High-Risk Human Papillomavirus Testing: A Systematic Evidence Review for the U.S. Preventive Services Task Force. 2017.

4. J Natl Cancer Inst. 2014 Jul 18;106(8). pii: dju153.
 

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New treatments up the ante against acne

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Acne remains “an equal opportunity annoyance,” according to Hilary E. Baldwin, MD, of Rutgers Robert Wood Johnson Medical School, Newark, NJ.

However, acne medications also work equally well across age, gender, and skin type groups, and new systemic and topical options are emerging, said Dr. Baldwin, who serves as medical director of The Acne Treatment and Research Center in Morristown, NJ.

Several products that entered the market in 2016 have demonstrated success, she said in a presentation on acne at the annual Coastal Dermatology Symposium. She cited data on dapsone 7.5% gel (Aczone) applied daily, which showed significant improvements in moderate facial acne and lesion counts compared with vehicle.

A noteworthy new potential acne treatment combines 200 mg doxycycline with topical adapalene 0.3%/benzoyl peroxide 2.5%, Dr. Baldwin said. In a small but promising 12-week open-label study of patients aged 12 years and older with severe facial acne considered candidates for isotretinoin, inflammatory, noninflammatory, and overall total lesion counts reduced significantly from baseline, she said.

Other acne treatments in the pipeline include a nitric oxide gel, a topical sebum inhibitor, and minocycline gel and foam formulations.

Sarecycline, a tetracycline class antibiotic, has generated some excitement after a phase 2 dose ranging study presented at the 2017 American Academy of Dermatology’s annual meeting showed significant improvement in inflammatory lesion counts among acne patients who received 1.5 mg/kg or 3 mg/kg once a day compared with placebo patients, after 12 weeks. Noninflammatory lesion counts were not significantly improved compared with placebo. Potential advantages of sarecycline include improved efficacy with fewer side effects and possibly, a lower risk of antibiotic resistance, Dr. Baldwin said. Phase 3 study results of the 1.5 mg/kg dose are pending.

Data on the potential role of diet in acne continue to evolve, she noted. A recent study of 225 teens with acne suggested that skim and/or low-fat dairy products are associated with acne and that reducing consumption of these products might help (J Am Acad Dermatol. 2016 Aug;75[2]:318-22). Another small study of 64 adults involving a nutritional survey showed that those with moderate to severe acne consumed significantly more carbohydrates than did those without acne, an indication that clinicians could consider recommending that acne patients reduce their carbohydrate intake to see whether it makes a difference.

The symposium was jointly presented by the University of Louisville and Global Academy for Medical Education. This publication and Global Academy for Medical Education are both owned by Frontline Medical News. Dr. Baldwin is a speaker and advisor for Allergan, Galderma, and Valeant; and is an investigator for Dermira, Galderma, Novan, and Valeant.

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Acne remains “an equal opportunity annoyance,” according to Hilary E. Baldwin, MD, of Rutgers Robert Wood Johnson Medical School, Newark, NJ.

However, acne medications also work equally well across age, gender, and skin type groups, and new systemic and topical options are emerging, said Dr. Baldwin, who serves as medical director of The Acne Treatment and Research Center in Morristown, NJ.

Several products that entered the market in 2016 have demonstrated success, she said in a presentation on acne at the annual Coastal Dermatology Symposium. She cited data on dapsone 7.5% gel (Aczone) applied daily, which showed significant improvements in moderate facial acne and lesion counts compared with vehicle.

A noteworthy new potential acne treatment combines 200 mg doxycycline with topical adapalene 0.3%/benzoyl peroxide 2.5%, Dr. Baldwin said. In a small but promising 12-week open-label study of patients aged 12 years and older with severe facial acne considered candidates for isotretinoin, inflammatory, noninflammatory, and overall total lesion counts reduced significantly from baseline, she said.

Other acne treatments in the pipeline include a nitric oxide gel, a topical sebum inhibitor, and minocycline gel and foam formulations.

Sarecycline, a tetracycline class antibiotic, has generated some excitement after a phase 2 dose ranging study presented at the 2017 American Academy of Dermatology’s annual meeting showed significant improvement in inflammatory lesion counts among acne patients who received 1.5 mg/kg or 3 mg/kg once a day compared with placebo patients, after 12 weeks. Noninflammatory lesion counts were not significantly improved compared with placebo. Potential advantages of sarecycline include improved efficacy with fewer side effects and possibly, a lower risk of antibiotic resistance, Dr. Baldwin said. Phase 3 study results of the 1.5 mg/kg dose are pending.

Data on the potential role of diet in acne continue to evolve, she noted. A recent study of 225 teens with acne suggested that skim and/or low-fat dairy products are associated with acne and that reducing consumption of these products might help (J Am Acad Dermatol. 2016 Aug;75[2]:318-22). Another small study of 64 adults involving a nutritional survey showed that those with moderate to severe acne consumed significantly more carbohydrates than did those without acne, an indication that clinicians could consider recommending that acne patients reduce their carbohydrate intake to see whether it makes a difference.

The symposium was jointly presented by the University of Louisville and Global Academy for Medical Education. This publication and Global Academy for Medical Education are both owned by Frontline Medical News. Dr. Baldwin is a speaker and advisor for Allergan, Galderma, and Valeant; and is an investigator for Dermira, Galderma, Novan, and Valeant.

Acne remains “an equal opportunity annoyance,” according to Hilary E. Baldwin, MD, of Rutgers Robert Wood Johnson Medical School, Newark, NJ.

However, acne medications also work equally well across age, gender, and skin type groups, and new systemic and topical options are emerging, said Dr. Baldwin, who serves as medical director of The Acne Treatment and Research Center in Morristown, NJ.

Several products that entered the market in 2016 have demonstrated success, she said in a presentation on acne at the annual Coastal Dermatology Symposium. She cited data on dapsone 7.5% gel (Aczone) applied daily, which showed significant improvements in moderate facial acne and lesion counts compared with vehicle.

A noteworthy new potential acne treatment combines 200 mg doxycycline with topical adapalene 0.3%/benzoyl peroxide 2.5%, Dr. Baldwin said. In a small but promising 12-week open-label study of patients aged 12 years and older with severe facial acne considered candidates for isotretinoin, inflammatory, noninflammatory, and overall total lesion counts reduced significantly from baseline, she said.

Other acne treatments in the pipeline include a nitric oxide gel, a topical sebum inhibitor, and minocycline gel and foam formulations.

Sarecycline, a tetracycline class antibiotic, has generated some excitement after a phase 2 dose ranging study presented at the 2017 American Academy of Dermatology’s annual meeting showed significant improvement in inflammatory lesion counts among acne patients who received 1.5 mg/kg or 3 mg/kg once a day compared with placebo patients, after 12 weeks. Noninflammatory lesion counts were not significantly improved compared with placebo. Potential advantages of sarecycline include improved efficacy with fewer side effects and possibly, a lower risk of antibiotic resistance, Dr. Baldwin said. Phase 3 study results of the 1.5 mg/kg dose are pending.

Data on the potential role of diet in acne continue to evolve, she noted. A recent study of 225 teens with acne suggested that skim and/or low-fat dairy products are associated with acne and that reducing consumption of these products might help (J Am Acad Dermatol. 2016 Aug;75[2]:318-22). Another small study of 64 adults involving a nutritional survey showed that those with moderate to severe acne consumed significantly more carbohydrates than did those without acne, an indication that clinicians could consider recommending that acne patients reduce their carbohydrate intake to see whether it makes a difference.

The symposium was jointly presented by the University of Louisville and Global Academy for Medical Education. This publication and Global Academy for Medical Education are both owned by Frontline Medical News. Dr. Baldwin is a speaker and advisor for Allergan, Galderma, and Valeant; and is an investigator for Dermira, Galderma, Novan, and Valeant.

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PrEP is not main driver in STI epidemic, says expert

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– Increased use of pre-exposure prophylaxis (PrEP) to prevent HIV transmission has accelerated but is not the main reason for surging rates of sexually transmitted infections in the United States, Kenneth Mayer, MD, said during an oral presentation at an annual scientific meeting on infectious diseases.

Public health officials are seeing unprecedented rises in STIs such as syphilis and gonorrhea in both HIV-negative and HIV-positive individuals, and these trends predate the advent of PrEP, said Dr. Mayer of the Fenway Institute and Harvard University in Boston, Mass. “An overall level of behavioral disinhibition is fueling this epidemic and is not necessarily associated with PrEP,” he said.

Dr. Kenneth Mayer
In the United States, de novo uptake of PrEP rose sevenfold between the third quarters of 2012 and 2016, noted Dr. Mayer. But rather than considering PreP a red flag for high-risk behavior, providers should use it as an opportunity to increase early diagnosis of STI, he said. Instead of siloing HIV and STI testing and management, they can advocate for more “user-friendly” approaches, such as housing PrEP and proactive STI screening under one roof, offering home-based testing for HIV and STIs, and supporting phone apps that educate high-risk individuals and link them to screening and treatment, he said.

Several studies suggest that being on PrEP does not increase the likelihood of acquiring or transmitting an STI, Dr. Mayer emphasized. In the open-label PROUD trial of PrEP in men who have sex with men (MSM), “rates of STI were extremely high and remained so, but did not go up after PrEP was initiated,” he noted. Importantly, the incidence of HIV infection was only 1.6 per 100 person-years when MSM received PrEP immediately but was 9.4 cases per 100 person-years when MSM were randomly assigned to a 1-year wait list (rate ratio, 6.0). In the randomized ANRS IPERGAY trial, 70% of high-risk MSM prescribed PrEP reported engaging in condomless anal intercourse during their most recent sexual encounter, but that proportion remained stable over 24 subsequent months of follow-up.

Providers also should understand that oral PrEP is just as effective at preventing HIV transmission when patients have STIs, Dr. Mayer said. In five recent studies, PrEP was equally efficacious among MSM regardless of whether they had syphilis or other STIs, and bacterial vaginosis in women also did not decrease the efficacy of oral PrEP. “There is no evidence to indicate that the efficacy of PrEP is lower among persons with STIs,” Dr. Mayer said.

Finally, providers should consider screening high-risk individuals for STIs more frequently than every 6 months as recommended by the Centers for Disease Control and Prevention, said Dr. Mayer. “For men who have sex with men, who are sexually active, and are on PrEP, quarterly screening makes exceedingly good sense from a cost-effectiveness standpoint,” he said.

“Screening less frequently than quarterly means that these individuals are having STIs for a longer period of time. When they are sexually active, we have a better chance of interrupting the transmission chain if we detect closer to the time of infection.”

Dr. Mayer disclosed support from the National Institutes of Health and Gilead Sciences, which makes some of the medications used in PrEP regimens.

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– Increased use of pre-exposure prophylaxis (PrEP) to prevent HIV transmission has accelerated but is not the main reason for surging rates of sexually transmitted infections in the United States, Kenneth Mayer, MD, said during an oral presentation at an annual scientific meeting on infectious diseases.

Public health officials are seeing unprecedented rises in STIs such as syphilis and gonorrhea in both HIV-negative and HIV-positive individuals, and these trends predate the advent of PrEP, said Dr. Mayer of the Fenway Institute and Harvard University in Boston, Mass. “An overall level of behavioral disinhibition is fueling this epidemic and is not necessarily associated with PrEP,” he said.

Dr. Kenneth Mayer
In the United States, de novo uptake of PrEP rose sevenfold between the third quarters of 2012 and 2016, noted Dr. Mayer. But rather than considering PreP a red flag for high-risk behavior, providers should use it as an opportunity to increase early diagnosis of STI, he said. Instead of siloing HIV and STI testing and management, they can advocate for more “user-friendly” approaches, such as housing PrEP and proactive STI screening under one roof, offering home-based testing for HIV and STIs, and supporting phone apps that educate high-risk individuals and link them to screening and treatment, he said.

Several studies suggest that being on PrEP does not increase the likelihood of acquiring or transmitting an STI, Dr. Mayer emphasized. In the open-label PROUD trial of PrEP in men who have sex with men (MSM), “rates of STI were extremely high and remained so, but did not go up after PrEP was initiated,” he noted. Importantly, the incidence of HIV infection was only 1.6 per 100 person-years when MSM received PrEP immediately but was 9.4 cases per 100 person-years when MSM were randomly assigned to a 1-year wait list (rate ratio, 6.0). In the randomized ANRS IPERGAY trial, 70% of high-risk MSM prescribed PrEP reported engaging in condomless anal intercourse during their most recent sexual encounter, but that proportion remained stable over 24 subsequent months of follow-up.

Providers also should understand that oral PrEP is just as effective at preventing HIV transmission when patients have STIs, Dr. Mayer said. In five recent studies, PrEP was equally efficacious among MSM regardless of whether they had syphilis or other STIs, and bacterial vaginosis in women also did not decrease the efficacy of oral PrEP. “There is no evidence to indicate that the efficacy of PrEP is lower among persons with STIs,” Dr. Mayer said.

Finally, providers should consider screening high-risk individuals for STIs more frequently than every 6 months as recommended by the Centers for Disease Control and Prevention, said Dr. Mayer. “For men who have sex with men, who are sexually active, and are on PrEP, quarterly screening makes exceedingly good sense from a cost-effectiveness standpoint,” he said.

“Screening less frequently than quarterly means that these individuals are having STIs for a longer period of time. When they are sexually active, we have a better chance of interrupting the transmission chain if we detect closer to the time of infection.”

Dr. Mayer disclosed support from the National Institutes of Health and Gilead Sciences, which makes some of the medications used in PrEP regimens.

– Increased use of pre-exposure prophylaxis (PrEP) to prevent HIV transmission has accelerated but is not the main reason for surging rates of sexually transmitted infections in the United States, Kenneth Mayer, MD, said during an oral presentation at an annual scientific meeting on infectious diseases.

Public health officials are seeing unprecedented rises in STIs such as syphilis and gonorrhea in both HIV-negative and HIV-positive individuals, and these trends predate the advent of PrEP, said Dr. Mayer of the Fenway Institute and Harvard University in Boston, Mass. “An overall level of behavioral disinhibition is fueling this epidemic and is not necessarily associated with PrEP,” he said.

Dr. Kenneth Mayer
In the United States, de novo uptake of PrEP rose sevenfold between the third quarters of 2012 and 2016, noted Dr. Mayer. But rather than considering PreP a red flag for high-risk behavior, providers should use it as an opportunity to increase early diagnosis of STI, he said. Instead of siloing HIV and STI testing and management, they can advocate for more “user-friendly” approaches, such as housing PrEP and proactive STI screening under one roof, offering home-based testing for HIV and STIs, and supporting phone apps that educate high-risk individuals and link them to screening and treatment, he said.

Several studies suggest that being on PrEP does not increase the likelihood of acquiring or transmitting an STI, Dr. Mayer emphasized. In the open-label PROUD trial of PrEP in men who have sex with men (MSM), “rates of STI were extremely high and remained so, but did not go up after PrEP was initiated,” he noted. Importantly, the incidence of HIV infection was only 1.6 per 100 person-years when MSM received PrEP immediately but was 9.4 cases per 100 person-years when MSM were randomly assigned to a 1-year wait list (rate ratio, 6.0). In the randomized ANRS IPERGAY trial, 70% of high-risk MSM prescribed PrEP reported engaging in condomless anal intercourse during their most recent sexual encounter, but that proportion remained stable over 24 subsequent months of follow-up.

Providers also should understand that oral PrEP is just as effective at preventing HIV transmission when patients have STIs, Dr. Mayer said. In five recent studies, PrEP was equally efficacious among MSM regardless of whether they had syphilis or other STIs, and bacterial vaginosis in women also did not decrease the efficacy of oral PrEP. “There is no evidence to indicate that the efficacy of PrEP is lower among persons with STIs,” Dr. Mayer said.

Finally, providers should consider screening high-risk individuals for STIs more frequently than every 6 months as recommended by the Centers for Disease Control and Prevention, said Dr. Mayer. “For men who have sex with men, who are sexually active, and are on PrEP, quarterly screening makes exceedingly good sense from a cost-effectiveness standpoint,” he said.

“Screening less frequently than quarterly means that these individuals are having STIs for a longer period of time. When they are sexually active, we have a better chance of interrupting the transmission chain if we detect closer to the time of infection.”

Dr. Mayer disclosed support from the National Institutes of Health and Gilead Sciences, which makes some of the medications used in PrEP regimens.

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