Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
Pharmacotherapy. 2017 Oct;37(10):1322-1327. doi: 10.1002/phar.2018. Epub 2017 Sep 19.
To describe contemporary trends of P2Y12 inhibitor use in patients with acute coronary syndrome (ACS) and comorbid diabetes mellitus (DM) and/or chronic kidney disease (CKD) who have a higher risk of recurring ACS and may benefit from treatment with higher efficacy third-generation agents (prasugrel and ticagrelor).
Observational cohort study.
A large U.S. commercial insurance program (2009-2015).
P2Y12 inhibitor initiated within 2 weeks after an ACS event.
We identified 98,649 P2Y12 inhibitor initiators, of whom 24.5% had comorbid DM (no CKD), 10.5% had CKD (no DM), and 12.6% had DM and CKD. Overall, 85.2% of patients initiated clopidogrel, followed by prasugrel (11.6%) and ticagrelor (3.2%). Prasugrel use decreased over time irrespective of preexisting DM and/or CKD; ticagrelor use increased. In logistic regression models accounting for patient demographics and clinical covariates, preexisting DM alone was not associated with prasugrel or ticagrelor versus clopidogrel treatment initiation; however, having CKD with or without DM significantly reduced the likelihood of receiving prasugrel versus clopidogrel (odds ratio [OR] 0.81, 95% confidence interval [CI] 0.74-0.88 for CKD alone; OR 0.91, 95% CI 0.83-0.98 for DM and CKD). Comorbid DM and CKD reduced the odds of initiating ticagrelor versus clopidogrel (OR 0.80, 95% CI 0.70-0.92).
We observed lower or similar use of prasugrel and ticagrelor compared with clopidogrel in patients with ACS and comorbid DM and/or CKD. Given the potential for worse clinical outcomes with clopidogrel in these patients, our findings highlight the need to investigate the implications of these trends on recurrent ACS and bleeding events.
描述急性冠脉综合征(ACS)合并糖尿病(DM)和/或慢性肾脏病(CKD)的患者中 P2Y12 抑制剂的当代使用趋势,这些患者复发 ACS 的风险较高,可能受益于更高疗效的第三代药物(普拉格雷和替格瑞洛)的治疗。
观察性队列研究。
美国一个大型商业保险计划(2009-2015 年)。
ACS 事件后 2 周内开始使用 P2Y12 抑制剂。
我们确定了 98649 名 P2Y12 抑制剂使用者,其中 24.5%合并 DM(无 CKD),10.5%有 CKD(无 DM),12.6%有 DM 和 CKD。总体而言,85.2%的患者开始使用氯吡格雷,其次是普拉格雷(11.6%)和替格瑞洛(3.2%)。普拉格雷的使用随着时间的推移而减少,无论是否存在预先存在的 DM 和/或 CKD;替格瑞洛的使用增加了。在考虑患者人口统计学和临床协变量的逻辑回归模型中,单独存在 DM 与氯吡格雷相比,与普拉格雷或替格瑞洛的治疗起始无关;然而,合并 CKD 或不合并 DM 显著降低了接受普拉格雷而非氯吡格雷治疗的可能性(优势比 [OR] 0.81,95%置信区间 [CI] 0.74-0.88 用于单独 CKD;OR 0.91,95%CI 0.83-0.98 用于 DM 和 CKD)。合并 DM 和 CKD 降低了起始替格瑞洛与氯吡格雷相比的几率(OR 0.80,95%CI 0.70-0.92)。
我们观察到 ACS 合并 DM 和/或 CKD 的患者中,普拉格雷和替格瑞洛的使用率低于或与氯吡格雷相似。鉴于这些患者使用氯吡格雷可能会导致更差的临床结局,我们的发现强调了需要研究这些趋势对复发 ACS 和出血事件的影响。