VA Puget Sound Health Care System Seattle WA.
University of Washington Seattle WA.
J Am Heart Assoc. 2020 Apr 21;9(8):e014975. doi: 10.1161/JAHA.119.014975. Epub 2020 Apr 17.
Background Hospitals commonly provide a short-term supply of free P2Y inhibitors at discharge after myocardial infarction, but it is unclear if these programs improve medication persistence and outcomes. The ARTEMIS (Affordability and Real-World Antiplatelet Treatment Effectiveness After Myocardial Infarction Study) trial randomized hospitals to usual care versus waived P2Y inhibitor copayment costs for 1-year post-myocardial infarction. Whether the impact of this intervention differed between hospitals with and without pre-existing medication assistance programs is unknown. Methods and Results In this post hoc analysis of the ARTEMIS trial, we examined the associations of pre-study free medication programs and the randomized copayment voucher intervention with P2Y inhibitor persistence (measured by pharmacy fills and patient report) and major adverse cardiovascular events using logistic regression models including a propensity score. Among 262 hospitals, 129 (49%) offered pre-study free medication assistance. One-year P2Y inhibitor persistence and major adverse cardiovascular events risks were similar between patients treated at hospitals with and without free medication programs (adjusted odds ratio 0.93, 95% CI, 0.82-1.05 and hazard ratio 0.92, 95% CI, 0.80-1.07, respectively). The randomized copayment voucher intervention improved persistence, assessed by pharmacy fills, in both hospitals with (53.6% versus 44.0%, adjusted odds ratio 1.45, 95% CI, 1.20-1.75) and without (59.0% versus 48.3%, adjusted odds ratio 1.46, 95% CI, 1.25-1.70) free medication programs (=0.71). Differences in patient-reported persistence were not significant after adjustment. Conclusions While hospitals commonly report the ability to provide free short-term P2Y inhibitors, we did not find association of this with medication persistence or major adverse cardiovascular events among patients with insurance coverage for prescription medication enrolled in the ARTEMIS trial. An intervention that provided copayment assistance vouchers for 1 year was successful in improving medication persistence in hospitals with and without pre-existing short-term medication programs. Registration URL: https://www.clinicaltrials.gov/. Unique identifier: NCT02406677.
医院通常会在心肌梗死后出院时提供短期的免费 P2Y 抑制剂供应,但尚不清楚这些方案是否能提高药物的持续性和改善预后。ARTEMIS(心肌梗死后 affordability 和 real-world 抗血小板治疗效果研究)试验将医院随机分为常规护理组和免除心肌梗死后 1 年 P2Y 抑制剂共付费用组。尚不清楚这种干预措施在有无预先存在的药物援助计划的医院之间的影响是否存在差异。
在 ARTEMIS 试验的这项事后分析中,我们使用包括倾向评分的逻辑回归模型,检查研究前免费药物计划和随机共付券干预与 P2Y 抑制剂持续性(通过药房配药和患者报告来衡量)和主要不良心血管事件之间的关联。在 262 家医院中,有 129 家(49%)提供了研究前的免费药物援助。在接受治疗的患者中,接受治疗的医院有无免费药物计划,其 1 年 P2Y 抑制剂持续性和主要不良心血管事件风险相似(调整后的优势比为 0.93,95%CI,0.82-1.05 和风险比为 0.92,95%CI,0.80-1.07)。随机共付券干预改善了药房配药评估的持续性,在有(53.6%对 44.0%,调整后的优势比 1.45,95%CI,1.20-1.75)和无(59.0%对 48.3%,调整后的优势比 1.46,95%CI,1.25-1.70)免费药物计划的医院中均有改善(=0.71)。调整后,患者报告的持续性差异无统计学意义。
尽管医院通常报告有能力提供短期免费的 P2Y 抑制剂,但我们没有发现这种情况与 ARTEMIS 试验中接受处方药保险的患者的药物持续性或主要不良心血管事件之间存在关联。一项提供 1 年共付券援助的干预措施成功地提高了有无预先存在的短期药物计划的医院的药物持续性。
https://www.clinicaltrials.gov/。
NCT02406677。