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Predictors of exposure to high-priority drug-drug interactions among non-elderly adults in Quebec, Canada [Prescribing and pharmacotherapeutics]

Annals of Family Medicine

Drug reimbursement claims were used to identify periods of overlapping exposure to 2 or more prescription drugs between April 1, 2015 and March 31, 2016. Results: Our cohort included 63,834 individuals aged 19-64 (mean age 44.9 Study design and Analysis: Retrospective cohort study using provincial administrative health databases.

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Stress management interventions may help individual health care workers for at least a year

Medical Xpress

Interventions aimed at reducing work-related stress for individual health care workers may lead to improvements in how people cope with stress up to a year later.

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Q&A: Cannabis Use Tied to Reduced Working Memory

Physician's Weekly

Gowin and his colleagues analyzed data from 1,003 adults between 22 and 36 years of age who had functional magnetic resonance imaging (fMRI), urine toxicology, and cannabis use results collected at one academic site between 2012 and 2015 as part of the Human Connectome Project. The cohort (mean age, 28.7

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Risking It All For a New Business Model at Family Physicians of St. Joe

Family Physicians of St. Joseph

In 2007, Dr. Mancini joined the practice, followed by Dr. Meadows in 2012, and Dr. Gendernalik in 2015. The individuals who make up the practice impact the community in a variety of ways. Eggebrecht joined in 1993, at a time when family doctors still rounded in the hospital and delivered babies.

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Episode 293 – Antiracism in Medicine Series – Episode 22 – Live from SGIM 2023: Best of Antiracism Research at the Society of General Internal Medicine’s 2023 Annual Meeting

The Clinical Problem Solvers

Describe difficulties and examples of how to measure unconscious race bias in medical practice. Identify strategies to mitigate bias and stigma in the electronic health record as a trainee and medical practitioner. She also is the 2017 recipient of the George L.

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A Question 30 Years in the Making: Would a Final LDT Rule Withstand Judicial Scrutiny?

FDA Law Blog

Lenz, Principal Medical Device Regulation Expert & Sophia R. Gibbs — For more than three decades, FDA has claimed that the Federal Food, Drug & Cosmetic (FD&C Act) gives the agency legal authority to regulate laboratory developed tests (LDTs) as medical devices (see our prior post here ). Gaulkin & Jeffrey N.

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eMDR System Enhancements

FDA Law Blog

By Véronique Li, Senior Medical Device Regulation Expert — On March 17, 2023, enhancements to FDA’s electronic Medical Device Reporting (eMDR) system will go live. Since the final rule took effect on August 14, 2015, medical device manufacturers and importers have been required to submit MDRs in an electronic format.