Emergency department visits and hospital readmissions after a deprescribing intervention among hospitalized older adults

Author:

Lee Ji Won12ORCID,Hollingsworth Emily Kay3,Shah Avantika Saraf4,Szanton Sarah L.1ORCID,Perrin Nancy1,Mixon Amanda S.35,Vasilevskis Eduard Eric356,Boyd Cynthia M.7,Han Hae‐Ra1,Green Ariel R.7ORCID,Taylor Janiece L.1ORCID,Simmons Sandra Faye35

Affiliation:

1. Johns Hopkins School of Nursing Baltimore Maryland USA

2. Columbia University School of Nursing New York USA

3. Division of Geriatrics, Vanderbilt Center for Quality Aging Vanderbilt University Medical Center Nashville Tennessee USA

4. Department of Health Policy and Management Johns Hopkins Bloomberg School of Public Health Baltimore Maryland USA

5. VA Tennessee Valley Healthcare System Geriatric Research Education and Clinical Center Nashville Tennessee USA

6. Division of Hospital Medicine, School of Medicine and Public Health University of Wisconsin – Madison Madison Wisconsin USA

7. Johns Hopkins School of Medicine Center for Transformative Geriatric Research Baltimore Maryland USA

Abstract

AbstractBackgroundDeprescribing is the planned/supervised method of dose reduction or cessation of medications that might be harmful, or no longer be beneficial. Though benefits of deprescribing are debatable in improving clinical outcomes, it has been associated with decreased number of potentially inappropriate medications, which may potentially reduce the risk of adverse events among hospitalized older adults. With unclear evidence for deprescribing in this population, this study aimed to examine time‐to‐first unplanned healthcare utilization, which included 90‐day emergency department (ED) visits or hospital readmission and associated predictors, during a deprescribing intervention.MethodsA secondary data analysis of a clinical trial (Shed‐MEDS NCT02979353) was performed. Cox regression was used to compare the time‐to‐first 90‐day ED visit/readmission/death from hospital discharge for the intervention and control groups. Additionally, we performed exploratory analysis of predictors (comorbidities, functional health status, drug burden index (DBI), hospital length of stay, health literacy, food insecurity, and financial burden) associated with the time‐to‐first 90‐day ED visit/readmission/death.ResultsThe hazard of first 90‐day ED visits/readmissions/death was 15% lower in the intervention versus the control group (95% CI: 0.61–1.19, p = 0.352, respectively); however, this difference was not statistically significant. For every additional number of comorbidities (Hazard ratio (HR): 1.12, 95% CI: 1.04–1.21) and each additional day of hospital length of stay (HR: 1.04, 95% CI: 1.01–1.07) were significantly associated with a higher hazard of 90‐day ED visit/readmission/death in the intervention group; whereas for each unit of increase in pre‐hospital DBI score (HR: 1.08 and HR 1.16, respectively) was significantly associated with a higher hazard of 90‐day ED visit/readmission/death in the control group.ConclusionsThe intervention and control groups had comparable time‐to‐first 90‐day ED visit/readmission/death during a deprescribing intervention. This finding suggests that deprescribing did not result in a higher risk of ED visit/readmission/death during the 90‐day period following hospital discharge.

Funder

National Institute on Aging

National Center for Advancing Translational Sciences

School of Nursing, Johns Hopkins University

Publisher

Wiley

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