Gerson Lauren B
Curr Gastroenterol Rep. 2013 Jun;15(6):329. doi: 10.1007/s11894-013-0329-1.
Clopidogrel, an antiplatelet agent, is increasingly prescribed for patients with recent stroke, myocardial infarction, acute coronary syndrome, and/or patients post-coronary stent insertion to prevent recurrent cardiovascular events. Since clopidogrel can increase the risk of gastrointestinal hemorrhage, co-administration of proton pump inhibitors (PPIs) has been recommended, particularly in patients at high risk. In 2009, the FDA issued warnings about potential interactions between clopidogrel and PPIs, given the fact that both drugs are metabolized via the cytochrome P450 pathway. Prior studies have demonstrated significant reduction in platelet inhibition when PPI therapy is administered to subjects on clopidogrel therapy. Two meta-analyses were published in 2010 and 2011, the first suggesting association of PPIs with adverse cardiovascular events when observational studies were examined, but noting that the results were limited by the presence of significant heterogeneity. The second meta-analysis did not find a significant increase in the risk of adverse primary events (which included all cause mortality, cardiovascular death, myocardial infarction, or stroke), and concluded that analysis of the data from two randomized controlled trials yielded a risk difference of zero. An updated literature search was performed to assess clinical studies describing interactions between PPIs and clopidogrel published from 2011-2012. The majority of these studies did not show significant interactions when primary cardiac outcomes were considered. More importantly, the newer data demonstrated that PPI usage independently was a risk factor for adverse CV outcomes, since most PPI users were older patients who were more likely to have concomitant co-morbid conditions. Two updated reviews also concluded that the presence of confounding factors likely explained differences in results between studies, and that there were no significant differences in effects on clopidogrel between individual proton pump inhibitors. Overall, clinicians can assure their patients that combination therapy is safe when indicated in a patient at high risk of GI bleeding, but they should also stop PPI therapy if it is not clinically indicated.
氯吡格雷是一种抗血小板药物,越来越多地被用于近期发生中风、心肌梗死、急性冠脉综合征的患者,和/或冠状动脉支架置入术后的患者,以预防心血管事件复发。由于氯吡格雷会增加胃肠道出血风险,因此推荐联合使用质子泵抑制剂(PPI),尤其是高风险患者。2009年,鉴于两种药物均通过细胞色素P450途径代谢,美国食品药品监督管理局(FDA)发布了关于氯吡格雷与PPI之间潜在相互作用的警告。此前的研究表明,接受氯吡格雷治疗的患者同时接受PPI治疗时,血小板抑制作用会显著降低。2010年和2011年发表了两项荟萃分析,第一项分析在检查观察性研究时提示PPI与不良心血管事件有关,但指出结果因显著异质性的存在而受到限制。第二项荟萃分析未发现主要不良事件(包括全因死亡率、心血管死亡、心肌梗死或中风)风险显著增加,并得出结论,对两项随机对照试验数据的分析得出风险差异为零。进行了一项更新的文献检索,以评估2011年至2012年发表的描述PPI与氯吡格雷之间相互作用的临床研究。当考虑主要心脏结局时,这些研究中的大多数未显示出显著的相互作用。更重要的是,新的数据表明,PPI的使用本身就是不良心血管结局的一个风险因素,因为大多数使用PPI的患者是老年患者,他们更有可能伴有合并症。两项更新的综述也得出结论,混杂因素的存在可能解释了研究结果之间的差异,并且各个质子泵抑制剂对氯吡格雷的影响没有显著差异。总体而言,临床医生可以向患者保证,在有胃肠道出血高风险的患者中,联合治疗在有指征时是安全的,但如果没有临床指征,也应停用PPI治疗。