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强化他汀类药物治疗与中等剂量治疗预防心血管事件的比较:超过 40000 例患者的荟萃分析。

Intensive statin therapy compared with moderate dosing for prevention of cardiovascular events: a meta-analysis of >40 000 patients.

机构信息

Faculty of Health Sciences, University of Ottawa, Ottawa, Ontario, Canada V5Z 4B4 K1n6X1.

出版信息

Eur Heart J. 2011 Jun;32(11):1409-15. doi: 10.1093/eurheartj/ehr035. Epub 2011 Mar 8.

Abstract

AIMS

Statin therapy is associated with important benefits for patients at risk of, and with, established cardiovascular disease. There is widespread interest in whether intensive dosing of statins yields larger treatment effects. We aimed to determine if intensive dosing is clinically important using a meta-analysis of randomized clinical trials (RCTs).

METHODS

We conducted comprehensive searches of electronic databases from inception to December 2010. We included any RCT evaluating a larger dose with a clinically common dose. Two reviewers independently extracted data, in duplicate. We performed random-effects meta-analysis and a trial sequential analysis.

RESULTS

We identified 10 RCTs enrolling a total of 41 778 participants. Trials followed patients for a mean of 2.5 years. We did not find statistically significant effects on all-cause mortality [relative risk (RR) 0.92, 95% confidence interval (CI), 0.83-1.03, P = 0.14, I(2) = 38%] or cardiovascular disease (CVD) deaths (RR 0.89, 95% CI, 0.78-1.01, P = 0.07, I(2) = 34%). When we pooled the composite endpoint of coronary heart disease (CHD) death plus non-fatal myocardial infarction (MI), we found a significant protective effect of intensive statin dosing (RR 0.90, 95% CI, 0.84-0.96, P ≤ 0.0001, I(2) = 0%). We also found a significant effect on non-fatal MIs (RR 0.82, 95% CI, 0.76-0.89, P ≤ 0.0001, I(2) = 0%) and a significant reduction in the composite of fatal and non-fatal strokes (excluding transient ischaemic attacks) reported in 10 RCTs (RR 0.86, 95% CI, 0.77-0.96, P = 0.006, I(2) = 0%). A subgroup analysis of three trials examining acute coronary syndrome patients found significant effects on all-cause (RR 0.75, 95% CI, 0.61-0.91, P = 0.005, I(2) = 0%) and CVD mortality (RR 0.74, 95% CI, 0.59-0.94, P = 0.013, I(2) = 0%) with intensive dosing. Applying an analysis of optimal information size on the primary analysis, we found that the evidence for CHD death plus non-fatal MIs is conclusive. The evidence for CVD deaths alone is not yet conclusive.

CONCLUSIONS

Available evidence suggests that intensive statin therapy reduces the risk of non-fatal events and may have a role in reducing mortality.

摘要

目的

他汀类药物治疗与有或无已确立心血管疾病风险的患者的重要益处相关。人们广泛关注他汀类药物的强化剂量是否会产生更大的治疗效果。我们旨在通过对随机临床试验(RCT)的荟萃分析来确定强化剂量是否具有临床意义。

方法

我们对电子数据库进行了全面搜索,检索时间从建库至 2010 年 12 月。我们纳入了所有评估较大剂量与临床常用剂量的 RCT。两名审查员独立重复提取数据。我们进行了随机效应荟萃分析和试验序贯分析。

结果

我们确定了 10 项 RCT,共纳入了 41778 名参与者。试验随访患者的平均时间为 2.5 年。我们没有发现全因死亡率(RR 0.92,95%置信区间[CI],0.83-1.03,P=0.14,I²=38%)或心血管疾病(CVD)死亡率(RR 0.89,95%CI,0.78-1.01,P=0.07,I²=34%)的统计学显著影响。当我们汇总冠心病(CHD)死亡加非致死性心肌梗死(MI)的复合终点时,我们发现强化他汀类药物剂量具有显著的保护作用(RR 0.90,95%CI,0.84-0.96,P≤0.0001,I²=0%)。我们还发现非致死性 MI(RR 0.82,95%CI,0.76-0.89,P≤0.0001,I²=0%)和致命和非致命性卒中(不包括短暂性脑缺血发作)的复合终点(RR 0.86,95%CI,0.77-0.96,P=0.006,I²=0%)也有显著降低,这是在 10 项 RCT 中报告的(RR 0.86,95%CI,0.77-0.96,P=0.006,I²=0%)。对三项研究急性冠状动脉综合征患者的亚组分析发现,全因死亡率(RR 0.75,95%CI,0.61-0.91,P=0.005,I²=0%)和 CVD 死亡率(RR 0.74,95%CI,0.59-0.94,P=0.013,I²=0%)的强化剂量有显著影响。对主要分析进行最佳信息大小的分析,我们发现 CHD 死亡加非致死性 MI 的证据是结论性的。单独 CVD 死亡的证据尚未得出结论。

结论

现有证据表明,强化他汀类药物治疗可降低非致死性事件的风险,并且可能在降低死亡率方面发挥作用。

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