Veterans Affairs North Texas Health Care System, Dallas, TX, USA.
Am J Cardiol. 2011 Mar 15;107(6):871-8. doi: 10.1016/j.amjcard.2010.10.073. Epub 2011 Jan 19.
The aim of the present study was to analyze the effect of drug exposure patterns of clopidogrel and proton pump inhibitors (PPIs) on the clinical outcomes after percutaneous coronary intervention (PCI). Previous analyses predominantly included discharge medications and did not explore the effect of the drug exposure patterns. We analyzed all-cause death, nonfatal myocardial infarction, repeat revascularization, and major adverse cardiovascular events (MACE) in a cohort of 23,200 post-PCI patients (January 2003 to December 2008) using a multivariate adjusted Cox model and propensity-matched case-control analysis. The adjusted hazard ratio for MACE on PPI according to the exposure patterns of clopidogrel after PCI for 6 years was 1.24 (95% confidence interval [CI] 1.11 to 1.38) and 1.12 (95% CI 1.03 to 1.22) for "continuous" (consistent clopidogrel with or without PPIs) and "switched" (clopidogrel with or without varying PPIs) respectively. However, the propensity score adjusted odds ratios for MACE on PPI use was 0.97 (95% CI 0.65 to 1.44) for "continuous" and 1.04 (95% CI 0.87 to 1.25) for "switched." Moreover, in the first year after PCI, the use of "rescue" (≤30 days before MACE) nitroglycerin was greater in the patients taking clopidogrel and PPIs than in those taking clopidogrel alone, as was the overall use of rescue PPIs (p <0.001). In conclusion, PPI use in clopidogrel-treated post-PCI patients was not associated with an increased risk of MACE after controlling for the confounding effect of PPI use with propensity matching. A potential for the misdiagnosis of angina symptoms and rescue use of nitroglycerin and PPIs in post-PCI patients exists, a finding that might have confounded previous observational analyses.
本研究旨在分析氯吡格雷和质子泵抑制剂(PPIs)的药物暴露模式对经皮冠状动脉介入治疗(PCI)后的临床结局的影响。先前的分析主要包括出院时的药物治疗,并未探讨药物暴露模式的影响。我们使用多变量调整 Cox 模型和倾向匹配病例对照分析,对 23200 例 PCI 后患者(2003 年 1 月至 2008 年 12 月)的全因死亡、非致死性心肌梗死、再次血运重建和主要不良心血管事件(MACE)进行了分析。根据 PCI 后 6 年氯吡格雷暴露模式,PPI 的调整后 MACE 危险比分别为 1.24(95%置信区间 [CI] 1.11 至 1.38)和 1.12(95%CI 1.03 至 1.22)对于“连续”(一致使用氯吡格雷和/或 PPI)和“切换”(氯吡格雷和/或不同的 PPI)。然而,PPI 使用的倾向评分调整后 MACE 比值比(OR)分别为 0.97(95%CI 0.65 至 1.44)和 1.04(95%CI 0.87 至 1.25)。此外,在 PCI 后第一年,服用氯吡格雷和 PPI 的患者比单独服用氯吡格雷的患者更常使用“挽救”(MACE 前≤30 天)硝酸甘油,同时使用挽救性 PPI 的总体比例也更高(p<0.001)。总之,在控制 PPI 使用的混杂效应并进行倾向匹配后,接受 PCI 的氯吡格雷治疗患者使用 PPI 与 MACE 风险增加无关。接受 PCI 的患者存在心绞痛症状误诊和硝酸甘油和 PPI 挽救性使用的可能性,这可能会混淆以前的观察性分析。