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普伐他汀和阿司匹林降低心血管疾病风险的附加益处:二级预防试验的随机和观察性比较及其荟萃分析

Additive benefits of pravastatin and aspirin to decrease risks of cardiovascular disease: randomized and observational comparisons of secondary prevention trials and their meta-analyses.

作者信息

Hennekens Charles H, Sacks Frank M, Tonkin Andrew, Jukema J Wouter, Byington Robert P, Pitt Bertram, Berry Donald A, Berry Scott M, Ford Neville F, Walker Andrew J, Natarajan Kannan, Sheng-Lin Chen, Fiedorek Frederick T, Belder Rene

机构信息

Mount Sinai Medical Center-Miami Heart Institute, Department of Medicine & Epidemiology and Public Health, University of Miami School of Medicine, Boca Raton, FL 33432, USA.

出版信息

Arch Intern Med. 2004 Jan 12;164(1):40-4. doi: 10.1001/archinte.164.1.40.

Abstract

BACKGROUND

In randomized trials of secondary prevention, pravastatin sodium and aspirin reduce risks of cardiovascular disease. Pravastatin has a predominantly delayed antiatherogenic effect, and aspirin has an immediate antiplatelet effect, raising the possibility of additive clinical benefits.

METHODS

In 5 randomized trials of secondary prevention with pravastatin (40 mg/d), comprising 73 900 patient-years of observation, aspirin use was also prescribed in varying frequencies, and data were available on a large number of confounding variables. We tested whether pravastatin and aspirin have additive benefits in the 2 large trials (Long-term Intervention With Pravastatin in Ischaemic Disease trial and the Cholesterol and Recurrent Events trial) that were designed to test clinical benefits. We also performed meta-analyses of these 2 trials and 3 smaller angiographic trials that collected clinical end points. In all analyses, multivariate models were used to adjust for a large number of cardiovascular disease risk factors.

RESULTS

Individual trials and all meta-analyses demonstrated similar additive benefits of pravastatin and aspirin on cardiovascular disease. In meta-analysis, the relative risk reductions for fatal or nonfatal myocardial infarction were 31% for pravastatin plus aspirin vs aspirin alone and 26% for pravastatin plus aspirin vs pravastatin alone. For ischemic stroke, the corresponding relative risk reductions were 29% and 31%. For the composite end point of coronary heart disease death, nonfatal myocardial infarction, coronary artery bypass graft, percutaneous transluminal coronary angioplasty, or ischemic stroke, the relative risk reductions were 24% and 13%. All relative risk reductions were statistically significant.

CONCLUSION

More widespread and appropriate combined use of statins and aspirin in secondary prevention of cardiovascular disease will avoid large numbers of premature deaths.

摘要

背景

在二级预防的随机试验中,普伐他汀钠和阿司匹林可降低心血管疾病风险。普伐他汀主要具有延迟的抗动脉粥样硬化作用,而阿司匹林具有即时的抗血小板作用,这增加了临床获益相加的可能性。

方法

在5项使用普伐他汀(40mg/d)进行二级预防的随机试验中,共观察了73900患者年,阿司匹林的使用频率也各不相同,并且有大量混杂变量的数据。我们在两项旨在测试临床获益的大型试验(普伐他汀长期干预缺血性疾病试验和胆固醇与再发事件试验)中检验了普伐他汀和阿司匹林是否具有相加获益。我们还对这两项试验以及另外3项收集临床终点的小型血管造影试验进行了荟萃分析。在所有分析中,使用多变量模型来调整大量心血管疾病风险因素。

结果

个体试验和所有荟萃分析均显示普伐他汀和阿司匹林在心血管疾病方面具有相似的相加获益。在荟萃分析中,普伐他汀加阿司匹林组与单用阿司匹林组相比,致命或非致命心肌梗死的相对风险降低31%;普伐他汀加阿司匹林组与单用普伐他汀组相比,相对风险降低26%。对于缺血性卒中,相应的相对风险降低分别为29%和31%。对于冠心病死亡、非致命心肌梗死、冠状动脉搭桥术、经皮冠状动脉腔内血管成形术或缺血性卒中的复合终点,相对风险降低分别为24%和13%。所有相对风险降低均具有统计学意义。

结论

在心血管疾病二级预防中更广泛且适当地联合使用他汀类药物和阿司匹林将避免大量过早死亡。

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