4.2 Article

An observational study examining the effect of comorbidity on the rates of persistence and adherence to newly initiated oral anti-hyperglycaemic agents

期刊

PHARMACOEPIDEMIOLOGY AND DRUG SAFETY
卷 22, 期 12, 页码 1336-1344

出版社

WILEY
DOI: 10.1002/pds.3535

关键词

type 2 diabetes; comorbidity; adherence; persistence; oral anti-hyperglycaemic therapy; pharmacoepidemiology

资金

  1. European Commission [223075]
  2. Health Research Board (HRB) Scholars Programme in Health Services Research [PHD/2007/16]

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PurposeTo examine whether the type of comorbid condition affects medication persistence and adherence in patients initiating oral anti-hyperglycaemic (OAH) therapy. MethodsThe Irish Health Services Executive pharmacy claims database was used to identify a cohort of incident OAH therapy users (anatomical therapeutic chemical A10B), 25years, between June 2009 and December 2010. Persistence and adherence were examined at 6 and 12months post-therapy initiation. Comorbidity was ascertained using modified versions of the RxRisk and RxRisk-V indices and classified as either concordant or discordant with diabetes. Adjusted odds ratios (ORs) and 95% confidence intervals (95%CIs) were determined in relation to comorbidity using logistic regression analysis, adjusting for age, gender and type of OAH prescribed. ResultsIn the study cohort (n=21280), persistence was 74.0% and 62.6% and adherence was 70.0% and 66.7% for all OAHs at 6 and 12months, respectively. Patients with only concordant comorbidity were significantly more likely to be persistent at 6 (OR 1.45, 95%CI 1.28, 1.65) and 12months (OR 1.22, 95%CI 1.09, 1.38). Patients with only discordant comorbidity were significantly less likely to be persistent at 6 (OR 0.40, 95%CI 0.35, 0.46) and 12months (OR 0.43 95%CI 0.38, 0.50) (p<0.0001). Results were similar for adherence. ConclusionThe study suggests that the persistence and adherence of OAH therapy in incident users are affected by the type of comorbidity present; this may help in identifying effective interventions aimed at optimising medication use. Copyright (c) 2013 John Wiley & Sons, Ltd.

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