From the Department of Neurology, West Virginia University-Charleston Division (K.M.); Second Department of Neurology, National and Kapodistrian University of Athens, "Attikon" University Hospital, Greece (A.H.K., G.T.); Department of Neurology, University of Ioannina School of Medicine, Greece (A.H.K.); Department of Gastroenterology & Hepatology, University of Texas Medical Branch, Galveston (M.B.); and Department of Neurology, University of Tennessee Health Science Center, Memphis (M.F.I., N.G., G.T.).
Stroke. 2018 Feb;49(2):312-318. doi: 10.1161/STROKEAHA.117.019166. Epub 2018 Jan 16.
Pharmacokinetic and prior studies on thienopyridine and proton pump inhibitors (PPI) coadministration provide conflicting data for cardiovascular outcomes, whereas there is no established evidence on the association of concomitant use of PPI and thienopyridines with adverse cerebrovascular outcomes.
We conducted a systematic review and meta-analysis of randomized controlled trials and cohort studies from inception to July 2017, reporting following outcomes among patients treated with thienopyridine and PPI versus thienopyridine alone (1) ischemic stroke, (2) combined ischemic or hemorrhagic stroke, (3) composite outcome of stroke, myocardial infarction (MI), and cardiovascular death, (4) MI, (5) all-cause mortality, and (6) major or minor bleeding events. After the unadjusted analyses of risk ratios, we performed additional analyses of studies reporting hazard ratios adjusted for potential confounders.
We identified 22 studies (12 randomized controlled trials and 10 cohort studies) comprising 131 714 patients. Concomitant use of PPI with thienopyridines was associated with increased risk of ischemic stroke (risk ratio, 1.74; 95% confidence interval [CI], 1.41-2.16; <0.001), composite stroke/MI/cardiovascular death (risk ratio, 1.14; 95% CI, 1.01-1.29; =0.04), and MI (risk ratio, 1.19; 95% CI, 1.00-1.40; =0.05). Likewise, in adjusted analyses concomitant use of PPI with thienopyridines was again associated with increased risk of stroke (hazard ratios adjusted, 1.30; 95% CI, 1.04-1.61; =0.02), composite stroke/MI/cardiovascular death (hazard ratios adjusted, 1.23; 95% CI, 1.03-1.47; =0.02), but not with MI (hazard ratios adjusted, 1.19; 95% CI, 0.93-1.52; =0.16).
Co-prescription of PPI and thienopyridines increases the risk of incident ischemic strokes and composite stroke/MI/cardiovascular death. Our findings corroborate the current guidelines for PPI deprescription and pharmacovigilance, especially in patients treated with thienopyridines.
噻吩吡啶和质子泵抑制剂(PPI)联合应用的药代动力学和既往研究结果对心血管结局提供了相互矛盾的数据,而关于 PPI 与噻吩吡啶联合应用与不良脑血管结局之间的相关性,尚无确定的证据。
我们对从开始到 2017 年 7 月的随机对照试验和队列研究进行了系统评价和荟萃分析,报告了噻吩吡啶和 PPI 联合治疗与噻吩吡啶单独治疗的患者以下结果:(1)缺血性卒中;(2)缺血性或出血性卒中合并;(3)卒中、心肌梗死(MI)和心血管死亡的复合结局;(4)MI;(5)全因死亡率;(6)主要或次要出血事件。在对风险比进行未调整分析后,我们对报告了经潜在混杂因素调整后的危险比的研究进行了进一步分析。
我们确定了 22 项研究(12 项随机对照试验和 10 项队列研究),共纳入 131714 名患者。PPI 与噻吩吡啶联合使用与缺血性卒中风险增加相关(风险比,1.74;95%置信区间[CI],1.41-2.16;<0.001)、卒中/MI/心血管死亡的复合结局风险增加(风险比,1.14;95%CI,1.01-1.29;=0.04)和 MI 风险增加(风险比,1.19;95%CI,1.00-1.40;=0.05)。同样,在调整分析中,PPI 与噻吩吡啶联合使用与卒中风险增加再次相关(调整后的危险比,1.30;95%CI,1.04-1.61;=0.02)、卒中/MI/心血管死亡的复合结局风险增加(调整后的危险比,1.23;95%CI,1.03-1.47;=0.02),但与 MI 无关(调整后的危险比,1.19;95%CI,0.93-1.52;=0.16)。
PPI 和噻吩吡啶联合处方增加了缺血性卒中事件和卒中/MI/心血管死亡的复合结局的风险。我们的研究结果证实了目前关于 PPI 撤药和药物警戒的指南,特别是在使用噻吩吡啶的患者中。