在使用医疗保险处方药数据时,考虑不可观察的暴露时间偏差。

Medicare & medicaid research review Pub Date : 2013-11-15 eCollection Date: 2013-01-01 DOI:10.5600/mmrr.003.04.a01
Elizabeth A Cook, Kathleen M Schneider, Elizabeth Chrischilles, John M Brooks
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引用次数: 12

摘要

目的:在使用医疗保险D部分数据的研究中,描述不可观察药物暴露时间的患病率及其相关性,并推荐最小化偏倚的方法。样本:2007年或2008年因急性心肌梗死住院的179,065名医疗保险患者。方法:我们比较了两种使用急症出院日期和急症出院日期创建药物暴露观察期的方法。我们通过对观察天数要求不同的阈值,或在观察期使用协变量来检验增加队列规模的选择。我们计算了未观察到的医疗保险D部分暴露时间的程度和健康状况的相关性,并检查了其与接受β受体阻滞剂的关系。结果:39%的患者在急性护理后30天暴露评估期间出现不可观测时间;他们明显年龄较大,有更多的合并症和较长的急性护理时间,1年生存率较差,并且被归类为受体阻滞剂使用者的可能性明显较低。使用替代暴露评估窗口,只有29%的样本有不可观察的时间,组间差异不太明显。通过限制或控制暴露评估期间所需的可观测天数,可获得样本量的显著增加。结论:不可观察的暴露时间在医疗保险D部分受益人中很常见,并且他们通常健康状况较差。为了保留暴露时间不可观察的患者,我们建议对接受急性后设施护理的患者进行分层,计算和使用可观察天数作为协变量,并且在适当的情况下,使用连续急性后设施护理的出院日期开始暴露评估期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Accounting for unobservable exposure time bias when using Medicare prescription drug data.

Accounting for unobservable exposure time bias when using Medicare prescription drug data.

Accounting for unobservable exposure time bias when using Medicare prescription drug data.

Accounting for unobservable exposure time bias when using Medicare prescription drug data.

Objective: To describe the prevalence and correlates of unobservable medication exposure time, and to recommend approaches for minimizing bias, in studies using Medicare Part D data..

Sample: 179,065 Medicare patients hospitalized for an AMI in 2007 or 2008.

Methods: We compared two methods for creating medication exposure observation periods using acute care discharge vs. post-acute care discharge dates. We examined options for increasing cohort sizes by requiring different thresholds for observable days, or by using as a covariate, in the observation period. We calculated the extent and health status correlates of unobserved Medicare Part D exposure time and examined its association with receipt of beta-blockers.

Results: 39% of patients had unobservable time during the 30 day exposure assessment period following acute care; they were significantly older, had more comorbidity and longer acute care stays, had worse 1-year survival, and were significantly less likely to be classified as beta-blocker users. Using the alternative exposure assessment window, only 29% of the sample had unobservable time, and differences between groups were less pronounced. Significant gains in sample size can be obtained by restricting or controlling for the number of observable days required in the exposure assessment period.

Conclusions: Unobservable exposure time is common among Medicare Part D beneficiaries, and they are often in worse health. To retain patients with unobservable exposure time, we recommend stratifying patients on receipt of post-acute facility-based care, calculating and using observable days as a covariate and, when appropriate, using the discharge date from contiguous post-acute facility care for beginning the exposure assessment period.

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