Medical education lacks emphasis on adverse drug reactions,
Georgetown research finds
Although studies have reported that adverse drug reactions may cause more
than 100,000 deaths annually in the United States, only a small percentage of
the curriculum at many medical schools is dedicated to recognizing and reporting
adverse drug reactions, according to a study conducted at Georgetown University
Medical Center and published in the current issue of Clinical Pharmacology &
Therapeutics. The study also found that residentsnewly minted physicians in
specialty trainingreceive only a modest amount of education in this area. The
lack of time dedicated to clinical pharmacology and adverse drug reactions
curriculum seems out of proportion to their importance to society and health
care, the study noted.
The Georgetown researchers surveyed 105 directors of third-year internal
medicine clerkships (programs for medical students), and the directors of 420
internal medicine residency programs (post-MD degree training), choosing
internal medicine programs because internal medicine programs train future
physicians to care for patients with complex medical problems usually
necessitating use of multiple medications, they reported. This type of patient
would be prone to experiencing an adverse drug reaction.
Each program director completed a two-page survey that asked questions about
the percentage of their institutions curriculum dedicated to adverse drug
reactions or interactions. They were also asked whether they felt that these
topics should be added to the curriculum if not already included; and about
their familiarity with a widely publicized Institute of Medicine report on
medical errors.
The Georgetown study found that 53% of the medical schools did not offer
training in clinical pharmacology or adverse drug reactions to third- and
fourth-year medical students, and of those schools at which such training was
available, only 8% of these rotations were mandatory. While more than 60% of
residency programs offered lectures in adverse drug reactions, 25% of residency
program directors surveyed had never reported an adverse drug reaction, the
study found. Additionally, 23% believed adverse drug reactions were difficult to
report, and 18% did not review adverse drug reactions during their regular
mortality and morbidity conferences.
The study also found that while many medical educators were willing to
incorporate courses in clinical pharmacology, including the study of adverse
drug reactions, into their curricula, they themselves lacked training in the
field.
Educators have little incentive to incorporate clinical pharmacology into
their curricula, the study concluded, because this discipline is not included as
an independent topic in the medical licensing examinations that all American
physicians must pass, nor is it included in the specialty certification
examinations for internists. And despite results of studies revealing that
involving clinical pharmacists as part of the health care team results in
improvements in health care outcome, fewer than 50% of internal medicine
residents are exposed to this expertise and culture, the study reported.
The majority of respondents to the study survey indicated a willingness to
incorporate drug reaction education into their curricula if educational modules
were available. Georgetown researchers, in collaboration with the U.S. Food and
Drug Administration, have recently developed such a module for use in medical
schools and residency programs. This was done as part of Georgetowns mission as
one of seven Centers for Education and Research on Therapeutics (CERTs)
nationwide. CERTs were created by the Agency for Healthcare Research and
Quality, an agency of the U.S. Department of Health and Human Services, to
improve the outcomes and quality of health care, reduce its costs, address
patient safety and medical errors, and broaden access to effective services.
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Support for the study published in Clinical Pharmacology & Therapeutics was
provided by the National Institutes of Health (NIH) and the Agency for
Healthcare Research and Quality (AHRQ). The study authors were Curtis J.
Rosebraugh, MD, MPH, medical officer in the FDA Division of Pulmonary and
Allergy Drug Products who led this research during a clinical pharmacology
fellowship at Georgetown; Peter K. Honig, MD, MPH, director of the FDAs Office
of Postmarketing Drug Risk Assessment and clinical assistant professor of
medicine at Georgetown; Sally Usdin Yasuda, MS, PharmD, assistant professor of
pharmacology at Georgetown; John C. Pezzullo, PhD, associate professor of
pharmacology and biostatistics at Georgetown; and Raymond L. Woosley, MD, PhD,
former associate dean for clinical research at Georgetown, currently vice
president for health sciences at the University of Arizona Health Sciences
Center, and director of the Arizona CERTs (which was formerly at Georgetown).
Georgetown University Medical Center includes the nationally ranked School of
Medicine, School of Nursing and Health Studies, the Lombardi Cancer Center and a
biomedical research enterprise. For more information, visit
www.georgetown.edu/gumc.
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