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急性冠状动脉综合征患者早期启动他汀治疗及其预后

Early statin initiation and outcomes in patients with acute coronary syndromes.

作者信息

Newby L Kristin, Kristinsson Arni, Bhapkar Manjushri V, Aylward Philip E, Dimas Alexios P, Klein Werner W, McGuire Darren K, Moliterno David J, Verheugt Freek W A, Weaver W Douglas, Califf Robert M

机构信息

Duke Clinical Research Institute, Duke University Medical Center, PO Box 17969, Durham, NC 27715, USA.

出版信息

JAMA. 2002 Jun 19;287(23):3087-95. doi: 10.1001/jama.287.23.3087.

Abstract

CONTEXT

The secondary prevention benefit of therapy with 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors (statins) has been clearly demonstrated; however, the role of early initiation of statins after acute coronary syndromes (ACSs) is unknown.

OBJECTIVE

To evaluate the association of early statin initiation (< or = 7 days) after ACS with 90-day and 1-year outcomes.

DESIGN

Observational cohort from databases of 2 randomized clinical trials, SYMPHONY and 2nd SYMPHONY.

SETTING

Nine hundred thirty-one clinical centers in 37 countries.

PATIENTS

A total of 12,365 ACS patients randomized from August 1997 to August 1999 who were not taking statins prior to the index ACS and who either started statin therapy early (median, 2.0 [interquartile range, 1.0-3.1] days after ACS; n = 3952) or survived more than 5 days after ACS and never received statin therapy (n = 8413).

MAIN OUTCOME MEASURES

Ninety-day incidence of death; death or myocardial infarction (MI); and death, MI, or severe recurrent ischemia; as well as 1-year incidence of death.

RESULTS

Ninety-day and 1-year unadjusted mortality comparison suggested early statin benefit (1.2% for early statins vs 2.1% for no statins; hazard ratio [HR], 0.58; 95% confidence interval [CI], 0.42-0.81 for 90-day comparisons and 2.3% for early statins vs 4.4% for no statins; HR, 0.52; 95% CI, 0.40-0.68 for 1-year comparison). However, no benefit was evident for 90-day death or MI (6.5% vs 6.9%; HR, 0.95; 95% CI, 0.82-1.11) or death, MI, or severe recurrent ischemia (9.2% vs 8.9%; HR, 1.04; 95% CI, 0.92-1.18). After propensity and covariate adjustment, there were no 90-day or 1-year differences between the early-statin group and the no-statin group. The 90-day adjusted HR for death was 1.08 (95% CI, 0.75-1.56); for death or MI, 1.08 (95% CI, 0.91-1.29); and for death, MI, or severe recurrent ischemia, 1.15 (95% CI, 0.99-1.34). One-year mortality-adjusted HR was 0.99 (95% CI, 0.73-1.33). Among 2711 patients with core laboratory lipid analysis, early statin was associated with higher adjusted risk for death or death or MI at cholesterol levels below treatment guidelines but was more favorable at higher levels.

CONCLUSIONS

In this study, there was no relationship between early initiation of statin therapy and improved outcomes although our subset analysis suggests that outcomes after early statin initiation may vary with cholesterol levels. Confirmation of early treatment effects of statins on outcomes awaits the results of adequately powered randomized clinical trials.

摘要

背景

3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂(他汀类药物)的二级预防益处已得到明确证实;然而,急性冠状动脉综合征(ACS)后早期开始使用他汀类药物的作用尚不清楚。

目的

评估ACS后早期(≤7天)开始使用他汀类药物与90天和1年预后的相关性。

设计

来自两项随机临床试验SYMPHONY和第二次SYMPHONY数据库的观察性队列研究。

地点

37个国家的931个临床中心。

患者

共有12365例于1997年8月至1999年8月随机分组的ACS患者,这些患者在首次ACS发作前未服用他汀类药物,其中部分患者早期开始他汀类药物治疗(ACS发作后中位数为2.0天[四分位间距为1.0 - 3.1天];n = 3952),另一部分患者在ACS发作后存活超过5天且从未接受他汀类药物治疗(n = 8413)。

主要结局指标

90天死亡发生率;死亡或心肌梗死(MI);死亡、MI或严重复发性缺血;以及1年死亡发生率。

结果

90天和1年的未调整死亡率比较显示早期使用他汀类药物有益(早期使用他汀类药物的死亡率为1.2%,未使用他汀类药物的为2.1%;风险比[HR]为0.58;90天比较的95%置信区间[CI]为0.42 - 0.81;早期使用他汀类药物的死亡率为2.3%,未使用他汀类药物的为4.4%;1年比较的HR为0.52;95% CI为0.40 - 0.68)。然而,90天死亡或MI(6.5%对6.9%;HR为0.95;95% CI为0.82 - 1.11)或死亡、MI或严重复发性缺血(9.2%对8.9%;HR为1.04;95% CI为0.92 - 1.18)并无明显益处。在进行倾向评分和协变量调整后,早期使用他汀类药物组与未使用他汀类药物组在90天或1年时并无差异。调整后90天死亡的HR为1.08(95% CI为0.75 - 1.56);死亡或MI为1.08(95% CI为0.91 - 1.29);死亡、MI或严重复发性缺血为1.15(95% CI为0.99 - 1.34)。1年死亡率调整后的HR为0.99(95% CI为0.73 - 1.33)。在2711例进行核心实验室血脂分析的患者中,早期使用他汀类药物与胆固醇水平低于治疗指南时死亡或死亡或MI的调整后风险较高相关,但在较高水平时更有益。

结论

在本研究中,早期开始他汀类药物治疗与改善预后之间并无关联,尽管我们的亚组分析表明早期开始使用他汀类药物后的预后可能随胆固醇水平而变化。他汀类药物对预后的早期治疗效果有待充分有力的随机临床试验结果证实。

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