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ABSTRACT: Purpose
Our aim is to determine if propoxyphene withdrawal from the US market was associated with opioid continuation, continued chronic opioid use, and secondary propoxyphene-related adverse events (emergency department visits, opioid-related events, and acetaminophen toxicity).Methods
Medical service use and pharmacy data from 19/11/08 to 19/11/11 were collected from the national Veterans Healthcare Administration healthcare databases. A quasi-experimental pre-post retrospective cohort design utilizing a historical comparison group provided the study framework. Logistic regression controlling for baseline covariates was used to estimate the effect of propoxyphene withdrawal.Results
There were 24,328 subjects (policy affected n = 10,747; comparison n = 13,581) meet
SUBMITTER: Hayes CJ
PROVIDER: S-EPMC5305002 | biostudies-literature | 2015 Nov
REPOSITORIES: biostudies-literature