Analytica International, New York, New York 72223, USA.
Pharmacotherapy. 2012 Sep;32(9):809-18. doi: 10.1002/j.1875-9114.2012.01112.x. Epub 2012 Jun 28.
To examine the effect of the drug interaction between clopidogrel and proton pump inhibitors (PPIs) on the risk of an adverse cardiovascular event.
Population-based, retrospective cohort study.
IMS LifeLink Health Plan administrative claims database.
A total of 10,101 patients aged 18 years or older with a diagnosis of acute coronary syndrome (ACS) made during a hospitalization or emergency department visit between 2001 and 2008 and who had their first clopidogrel prescription within 90 days after their ACS diagnosis were included in the study. Patients were stratified according to concurrent use (clopidogrel plus PPI group) or no use (clopidogrel alone group) of the following PPIs: esomeprazole, lansoprazole, omeprazole, pantoprazole, or rabeprazole.
Data were collected on baseline patient demographic and clinical characteristics. Patients were followed from their first clopidogrel prescription until they experienced an adverse cardiovascular event, defined as inpatient hospitalization or emergency department visits for myocardial infarction, percutaneous coronary intervention, or intermediate coronary syndrome; were disenrolled; discontinued clopidogrel; or reached the end of the study period. Using a propensity scoring method, the clopidogrel plus PPI group was matched in a 1:1 ratio with the clopidogrel alone group. Exposure to overlapping clopidogrel-PPI prescriptions was modeled as a time-dependent covariate. The Cox hazards regression model was used to estimate the risk of an adverse cardiovascular event in the clopidogrel plus PPI group versus the clopidogrel alone group. Propensity score matching resulted in 2674 patient pairs. In the propensity score-matched sample, the mean age was 61.30 years, with a mean follow-up of 268 days, and 70.04% were male. Concurrent use of clopidogrel with a PPI was associated with a significantly increased risk of a cardiovascular adverse event (hazard ratio 1.438, 95% confidence interval 1.237-1.671) compared with clopidogrel alone.
Concurrent use of clopidogrel plus a PPI was associated with a significant increase in risk of an adverse cardiovascular event in patients with ACS. Large randomized studies are needed to confirm this finding. Until then, clinicians should prescribe the concurrent use of these two drugs cautiously.
研究氯吡格雷与质子泵抑制剂(PPIs)药物相互作用对不良心血管事件风险的影响。
基于人群的回顾性队列研究。
IMS LifeLink 健康计划管理索赔数据库。
共纳入 10101 名年龄在 18 岁或以上的患者,他们在 2001 年至 2008 年期间因急性冠状动脉综合征(ACS)住院或急诊就诊,并在 ACS 诊断后 90 天内首次开氯吡格雷处方。根据是否同时使用(氯吡格雷加 PPI 组)或不使用(氯吡格雷单药组)以下 PPIs 将患者分层:埃索美拉唑、兰索拉唑、奥美拉唑、泮托拉唑或雷贝拉唑。
收集基线患者人口统计学和临床特征的数据。从患者首次氯吡格雷处方开始,随访至发生不良心血管事件,定义为因心肌梗死、经皮冠状动脉介入治疗或中间冠状动脉综合征住院或急诊就诊;失访;停止使用氯吡格雷;或达到研究期末。使用倾向评分法,将氯吡格雷加 PPI 组按 1:1 比例与氯吡格雷单药组匹配。重叠氯吡格雷-PPI 处方的暴露被建模为时间依赖性协变量。使用 Cox 风险回归模型估计氯吡格雷加 PPI 组与氯吡格雷单药组发生不良心血管事件的风险。倾向评分匹配产生了 2674 对患者。在倾向评分匹配样本中,平均年龄为 61.30 岁,平均随访 268 天,70.04%为男性。与氯吡格雷单药相比,同时使用氯吡格雷加 PPI 与心血管不良事件风险显著增加相关(风险比 1.438,95%置信区间 1.237-1.671)。
与氯吡格雷单药相比,ACS 患者同时使用氯吡格雷加 PPI 与不良心血管事件风险显著增加相关。需要进行大型随机研究来证实这一发现。在那之前,临床医生应谨慎开这两种药物的同时使用。