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Pharmacoepidemiol Drug Saf · Jul 2013
Association of potentially inappropriate medication use with patient and prescriber characteristics in Medicare Part D.
- Holly M Holmes, Ruili Luo, Yong-Fang Kuo, Jacques Baillargeon, and James S Goodwin.
- Department of General Internal Medicine, UT MD Anderson Cancer Center, Houston, TX, USA. hholmes@mdanderson.org
- Pharmacoepidemiol Drug Saf. 2013 Jul 1;22(7):728-34.
PurposeThe use of potentially inappropriate medications (PIMs) in older people is associated with increased risk of adverse drug events and hospitalization. This study aimed to determine the contribution of primary prescribers to variation in PIM use.MethodsThis was a retrospective cohort study using 2008 Medicare Part D event files and claims data for a 100% sample of Texas beneficiaries. PIM use was defined as receiving any of 48 medications on the Beers 2003 list of PIMs. Patient characteristics associated with PIM use were determined using a multivariable model. A multilevel model for the odds of PIM use was constructed to evaluate the amount of variation in PIM use at the level of primary care prescriber, controlling for patient characteristics.ResultsOf 677,580 patients receiving prescriptions through Part D in 2008, 31.9% received a PIM. Sex, ethnicity, low-income subsidy eligibility, and hospitalization in 2007 were associated with PIM use. The strongest associations with higher PIM use were increasing number of prescribers and increasing number of medications. The odds ratio for PIM use was 1.50 (95%CI 1.47-1.53) for ≥4 prescribers versus only 1 prescriber. In the multilevel model, the adjusted average percent of patients prescribed a PIM ranged from 17.5% for the lowest decile to 28.9% for the highest decile of prescribers.ConclusionsPIM use was prevalent in Part D beneficiaries and varied among individual primary care prescribers. The association of PIM use with increasing numbers of prescribers suggests the need to reduce fragmentation of care to reduce inappropriate prescribing.Copyright © 2013 John Wiley & Sons, Ltd.
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