Vanderbilt University School of Medicine and Veterans Affairs Tennessee Valley Healthcare System, Nashville, Tennessee, USA.
Ann Intern Med. 2010 Mar 16;152(6):337-45. doi: 10.7326/0003-4819-152-6-201003160-00003.
Proton-pump inhibitors (PPIs) and clopidogrel are frequently coprescribed, although the benefits and harms of their concurrent use are unclear.
To examine the association between concurrent use of PPIs and clopidogrel and the risks for hospitalizations for gastroduodenal bleeding and serious cardiovascular disease.
Retrospective cohort study using automated data to identify patients who received clopidogrel between 1999 through 2005 after hospitalization for coronary heart disease.
Tennessee Medicaid program.
20,596 patients (including 7593 concurrent users of clopidogrel and PPIs) hospitalized for myocardial infarction, coronary artery revascularization, or unstable angina pectoris.
Baseline and follow-up drug use was assessed from automated records of dispensed prescriptions. Primary outcomes were hospitalizations for gastroduodenal bleeding and serious cardiovascular disease (fatal or nonfatal myocardial infarction or sudden cardiac death, stroke, or other cardiovascular death).
Pantoprazole and omeprazole accounted for 62% and 9% of concurrent PPI use, respectively. Adjusted incidence of hospitalization for gastroduodenal bleeding in concurrent PPI users was 50% lower than that in nonusers (hazard ratio, 0.50 [95% CI, 0.39 to 0.65]). For patients at highest risk for bleeding, PPI use was associated with an absolute reduction of 28.5 (CI, 11.7 to 36.9) hospitalizations for gastroduodenal bleeding per 1000 person-years. The hazard ratio associated with concurrent PPI use for risk for serious cardiovascular disease was 0.99 (CI, 0.82 to 1.19) for the entire cohort and 1.01 (CI, 0.76 to 1.34) for the subgroup of patients who had percutaneous coronary interventions with stenting during the qualifying hospitalization.
Unmeasured confounding and misclassification of exposure (no information on adherence or over-the-counter use of drugs) and end points (not confirmed by medical record review) were possible. Because many patients entered the cohort from hospitals with relatively few cohort members, the analysis relied on the assumption that after adjustment for observed covariates, PPI users from one such hospital could be compared with nonusers from a different hospital.
In patients with serious coronary heart disease treated with clopidogrel, concurrent PPI use was associated with reduced incidence of hospitalizations for gastroduodenal bleeding. The corresponding point estimate for serious cardiovascular disease was not increased; however, the 95% CI included a clinically important increased risk.
Agency for Healthcare Research and Quality and National Heart, Lung, and Blood Institute.
质子泵抑制剂 (PPI) 和氯吡格雷经常同时使用,尽管其同时使用的益处和危害尚不清楚。
研究质子泵抑制剂与氯吡格雷同时使用与住院胃肠道出血和严重心血管疾病风险之间的关系。
使用自动化数据回顾性队列研究,以确定在因冠心病住院后于 1999 年至 2005 年期间接受氯吡格雷治疗的患者。
田纳西州医疗补助计划。
20596 名患者(包括 7593 名氯吡格雷和 PPI 同时使用者)因心肌梗死、冠状动脉血运重建或不稳定型心绞痛住院。
从处方配药的自动记录中评估基线和随访药物使用情况。主要结局是住院胃肠道出血和严重心血管疾病(致命或非致命性心肌梗死或心源性猝死、中风或其他心血管死亡)。
泮托拉唑和奥美拉唑分别占同时使用 PPI 的 62%和 9%。与非使用者相比,同时使用 PPI 的住院胃肠道出血发生率降低 50%(危险比,0.50 [95%CI,0.39 至 0.65])。对于出血风险最高的患者,PPI 治疗与每 1000 人年减少 28.5 例(CI,11.7 至 36.9)胃肠道出血住院相关。对于整个队列,同时使用 PPI 与严重心血管疾病风险相关的危险比为 0.99(CI,0.82 至 1.19),对于在合格住院期间接受经皮冠状动脉介入治疗和支架置入的亚组患者,该危险比为 1.01(CI,0.76 至 1.34)。
可能存在未测量的混杂因素和暴露(无药物依从性或非处方使用的信息)和终点(未经病历审查证实)的错误分类。由于许多患者从住院人数相对较少的医院进入队列,因此该分析依赖于这样的假设,即调整观察协变量后,来自一家医院的 PPI 使用者可以与来自另一家医院的非使用者进行比较。
在接受氯吡格雷治疗的严重冠心病患者中,同时使用质子泵抑制剂与胃肠道出血住院发生率降低相关。严重心血管疾病的相应点估计值没有增加;然而,95%CI 包括临床意义上的风险增加。
医疗保健研究与质量局和国家心肺血液研究所。