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新型抗血小板药物在预防复发性心肌梗死中的效果。

Effectiveness of new antiplatelets in the prevention of recurrent myocardial infarction.

机构信息

Pharmacoepidemiology, PGRx Study Group, PGRx, Paris, France.

London School of Hygiene and Tropical Medicine, London, UK.

出版信息

Heart. 2018 Oct;104(19):1583-1592. doi: 10.1136/heartjnl-2017-312534. Epub 2018 Mar 13.

Abstract

OBJECTIVE

To compare ticagrelor and prasugrel with clopidogrel for recurrent fatal and non-fatal myocardial infarction (reMI) in real-life conditions.

METHODS

Case-referent study using the Pharmacoepidemiological General Research eXtension (PGRx)-acute coronary syndrome (ACS) registry. Cases were patients with reMI from a cohort with index ACS or external to the cohort (same sites). Referents from the cohort, without recurrent event, were matched on index ACS type and date, age and sex with reMI cases. Multivariate conditional logistic regression assessed the OR (95% CI) for reMI associated with ticagrelor and prasugrel vs clopidogrel, adjusted for aspirin use and cardiovascular risk factors.

RESULTS

1047 cases and 2234 matched referents were included. Compared with clopidogrel, ticagrelor and prasugrel were associated with respective ORs of 0.65 (95% CI 0.52 to 0.81) and 0.71 (95% CI 0.53 to 0.96) for reMI occurrence. ORs for ticagrelor and prasugrel vs clopidogrel were: 0.50 (95% CI 0.38 to 0.67) and 0.66 (95% CI 0.45 to 0.95), 0.39 (95% CI 0.24 to 0.62) and 0.44 (95% CI 0.26 to 0.75), 0.63 (95% CI 0.43 to 0.92) and 1.20 (95% CI 0.69 to 2.07), 1.11 (95% CI 0.72 to 1.72) and 0.82 (95% CI 0.44 to 1.54) when index ACS was a first MI, a first ST-elevated MI (STEMI), a first non-STEMI and a recurrent ACS, respectively, and 0.63 (95% CI 0.45 to 0.87) and 0.77 (95% CI 0.41 to 1.45) for patients aged ≥70  years.

CONCLUSIONS

This real-world study showed a significant reduction of reMI with new antiplatelets compared with clopidogrel, ticagrelor being associated with a greater decrease of risk notably for first, either STEMI or non-STEMI. The larger magnitude of effect may be attributed to potential residual confounding or higher effectiveness compared with efficacy reported in trials (EMA Post Authorisation Study Registry Number EUPAS5905).

摘要

目的

比较替格瑞洛和普拉格雷与氯吡格雷在真实情况下复发性致命和非致命性心肌梗死(再 MI)的疗效。

方法

采用 Pharmacoepidemiological General Research eXtension(PGRx)-急性冠状动脉综合征(ACS)登记处的病例对照研究。病例为指数 ACS 或指数 ACS 之外的队列中有再 MI 的患者(同一地点)。参照队列中无复发事件的患者,按指数 ACS 类型和日期、年龄和性别与再 MI 病例匹配。多变量条件逻辑回归评估了替格瑞洛和普拉格雷与氯吡格雷相比再 MI 的比值比(95%置信区间),调整了阿司匹林的使用和心血管危险因素。

结果

纳入 1047 例病例和 2234 例匹配的对照。与氯吡格雷相比,替格瑞洛和普拉格雷的再 MI 发生率的相应比值比(95%CI)分别为 0.65(95%CI 0.52 至 0.81)和 0.71(95%CI 0.53 至 0.96)。替格瑞洛和普拉格雷与氯吡格雷的比值比分别为:0.50(95%CI 0.38 至 0.67)和 0.66(95%CI 0.45 至 0.95),0.39(95%CI 0.24 至 0.62)和 0.44(95%CI 0.26 至 0.75),0.63(95%CI 0.43 至 0.92)和 1.20(95%CI 0.69 至 2.07),1.11(95%CI 0.72 至 1.72)和 0.82(95%CI 0.44 至 1.54),当指数 ACS 分别为首次心肌梗死、首次 ST 段抬高型心肌梗死(STEMI)、首次非 ST 段抬高型心肌梗死和复发性 ACS 时。对于年龄≥70 岁的患者,比值比分别为 0.63(95%CI 0.45 至 0.87)和 0.77(95%CI 0.41 至 1.45)。

结论

这项真实世界的研究表明,与氯吡格雷相比,新型抗血小板药物可显著降低再 MI 的风险,其中替格瑞洛与风险降低的相关性更大,特别是首次发生 STEMI 或非 STEMI 时。这种更大的效应可能归因于潜在的残余混杂因素或与试验报告的疗效相比更高的有效性(EMA 事后授权研究注册号 EUPAS5905)。

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