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. 2016 Mar 3;11(3):e0150621.
doi: 10.1371/journal.pone.0150621. eCollection 2016.

Associations between Anticholinergic Burden and Adverse Health Outcomes in Parkinson Disease

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Associations between Anticholinergic Burden and Adverse Health Outcomes in Parkinson Disease

James A G Crispo et al. PLoS One. .

Abstract

Background: Elderly adults should avoid medications with anticholinergic effects since they may increase the risk of adverse events, including falls, delirium, and cognitive impairment. However, data on anticholinergic burden are limited in subpopulations, such as individuals with Parkinson disease (PD). The objective of this study was to determine whether anticholinergic burden was associated with adverse outcomes in a PD inpatient population.

Methods: Using the Cerner Health Facts® database, we retrospectively examined anticholinergic medication use, diagnoses, and hospital revisits within a cohort of 16,302 PD inpatients admitted to a Cerner hospital between 2000 and 2011. Anticholinergic burden was computed using the Anticholinergic Risk Scale (ARS). Primary outcomes were associations between ARS score and diagnosis of fracture and delirium. Secondary outcomes included associations between ARS score and 30-day hospital revisits.

Results: Many individuals (57.8%) were prescribed non-PD medications with moderate to very strong anticholinergic potential. Individuals with the greatest ARS score (≥ 4) were more likely to be diagnosed with fractures (adjusted odds ratio (AOR): 1.56, 95% CI: 1.29-1.88) and delirium (AOR: 1.61, 95% CI: 1.08-2.40) relative to those with no anticholinergic burden. Similarly, inpatients with the greatest ARS score were more likely to visit the emergency department (adjusted hazard ratio (AHR): 1.32, 95% CI: 1.10-1.58) and be readmitted (AHR: 1.16, 95% CI: 1.01-1.33) within 30-days of discharge.

Conclusions: We found a positive association between increased anticholinergic burden and adverse outcomes among individuals with PD. Additional pharmacovigilance studies are needed to better understand risks associated with anticholinergic medication use in PD.

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Conflict of interest statement

Competing Interests: Mr. Crispo, Dr. Willis, Mr. Thibault, Mr. Fortin, Dr. Bjerre, and Dr. Kohen report no disclosures. Dr. McNair and Mr. Hays are employed by the Cerner Corporation. Dr. Perez-Lloret served as a consultant for Aguettant Laboratories in 2014. Drs. Mattison and Krewski serve as Chief Medical Officer and Chief Risk Scientist of Risk Sciences International, a Canadian company formed in partnership with the University of Ottawa in 2006 (www.risksciences.com) that conducts risk assessment work for public and private sector clients in Canada and internationally. To date, RSI has not conducted work on the subject of the present research paper. Dr. Krewski holds a Natural Sciences and Engineering Council of Canada (NSERC) Industrial Research Chair in Risk Science, through a peer-reviewed university-industry partnerships program administered by NSERC. None of the industrial partners in this program are from the pharmaceutical industry. Commercial affiliation with the Cerner Corporation and Risk Sciences International does not alter the authors' adherence to PLOS ONE policies on sharing data and materials.

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