Background/objective: Medication changes at transitions of care and polypharmacy are growing concerns that adversely impact optimal drug use. We aimed to describe transitions and patterns of medication use before and 1 year after older patients were hospitalized for community-acquired pneumonia, the second-most common reason for admission in North America. Materials and methods: This was an analysis of a population-based clinical registry of patients treated in any of the six hospitals or seven emergency departments in Edmonton, Alberta, Canada, comprising 2, 105 patients 65 years and older with community-acquired pneumonia who had survived at least 1 year. The prevalence of polypharmacy (five or more unique prescription drugs), as well as new use and persistence of common drug classes were assessed. Results: The mean age was 78 years (standard deviation 8 years), 50% were female, 62% were hospitalized, and 58% had severe pneumonia. Among the 2, 105 patients, 949 (45%) were using five or more medications prior to hospitalization, increasing to 1, 559 (74%) within 90 days postdischarge and remaining over 70% at 1 year. Overall, 1, 690 (80%) patients newly started and 1, 553 (74%) patients stopped at least one medication in the first 90 days of follow-up. The prevalence of the most common drug classes (ie, cardiovascular, alimentary/metabolism) remained stable, with the exception of anti-infective agents, whereby 25% of patients were dispensed an anti-infective agent 3 months to 1 year after hospitalization. Conclusion: Most older patients with pneumonia are subject to polypharmacy, and almost every patient had a medication started or stopped during 1-year follow-up, with 25% using antibiotics again. The period following an episode of pneumonia represents an opportunity potentially to optimize pharmacotherapy. © 2014 Gamble et al.
CITATION STYLE
Gamble, J. M., Hall, J. J., Marrie, T. J., Sadowski, C. A., Majumdar, S. R., & Eurich, D. T. (2014). Medication transitions and polypharmacy in older adults following acute care. Therapeutics and Clinical Risk Management, 10(1), 189–196. https://doi.org/10.2147/TCRM.S58707
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