Bavry Anthony A, Mood Girish R, Kumbhani Dharam J, Borek Peter P, Askari Arman T, Bhatt Deepak L
Department of Cardiovascular Medicine, Cardiac, Peripheral, and Carotid Intervention, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, OH 44195, USA.
Am J Cardiovasc Drugs. 2007;7(2):135-41. doi: 10.2165/00129784-200707020-00005.
This study sought to determine if the initiation of statin (HMG-CoA reductase inhibitor) therapy during acute coronary syndromes reduces long-term mortality and other adverse cardiac outcomes.
Initiation of statin therapy during acute coronary syndromes has not been shown to reduce mortality, myocardial infarction or stroke within 4 months of follow-up.
Clinical trials that randomized patients with acute coronary syndromes to early statin therapy compared with less intensive lipid reduction (placebo/lower-dose statin/usual care), and reported long-term outcomes were included for analysis.
In all, there were seven studies (L-CAD, PTT, FLORIDA, Colivicchi et al., PROVE-IT, ESTABLISH, and A-to-Z) with 9553 patients who started statin therapy within 12 days of hospital presentation. The incidence of all-cause mortality was 3.4% in the statin group versus 4.6% in the less intensive lipid reduction group over a weighted mean follow-up of 22.9 months (relative risk [RR] 0.74; 95% CI 0.61, 0.90; p = 0.003). The number of patients needed to treat to prevent one death was 84 patients. Similarly, the incidence of cardiovascular mortality in the statin versus the less intensive lipid reduction group was 2.4% versus 3.3% (RR 0.74; 95% CI 0.58, 0.93; p = 0.010), unstable angina 4.1% versus 5.0% (RR 0.81; 95% CI 0.68, 0.98; p = 0.027), revascularization 11.2% versus 12.9% (RR 0.86; 95% CI 0.78, 0.96; p = 0.006), stroke 1.1% versus 1.2% (RR 0.90; 95% CI 0.62, 1.30; p = 0.56), and myocardial infarction 6.6% versus 7.0% (RR 0.94; 95% CI 0.81, 1.09; p = 0.41).
The benefit of early initiation of statin therapy during acute coronary syndromes slowly accrues over time so that a survival advantage is seen around 24 months. Relatively few patients need to be treated to prevent one death over this time period. Furthermore, this approach significantly reduces unstable angina and the need for revascularization.
本研究旨在确定在急性冠状动脉综合征期间启动他汀类药物(HMG-CoA还原酶抑制剂)治疗是否能降低长期死亡率和其他不良心脏结局。
在急性冠状动脉综合征期间启动他汀类药物治疗,在随访4个月内尚未显示能降低死亡率、心肌梗死或中风发生率。
纳入将急性冠状动脉综合征患者随机分为早期他汀类药物治疗组与强化降脂治疗(安慰剂/低剂量他汀类药物/常规治疗)组,并报告长期结局的临床试验进行分析。
总共7项研究(L-CAD、PTT、FLORIDA、Colivicchi等人、PROVE-IT、ESTABLISH和A-to-Z),共9553例患者在入院12天内开始他汀类药物治疗。在加权平均随访22.9个月期间,他汀类药物治疗组全因死亡率为3.4%,强化降脂治疗组为4.6%(相对风险[RR]0.74;95%置信区间0.61,0.90;p = 0.003)。预防1例死亡所需治疗的患者数为84例。同样,他汀类药物治疗组与强化降脂治疗组的心血管死亡率分别为2.4%和3.3%(RR 0.74;95%置信区间0.58,0.93;p = 0.010),不稳定型心绞痛分别为4.1%和5.0%(RR 0.81;95%置信区间0.68,0.98;p = 0.027),血运重建分别为11.2%和12.9%(RR 0.86;95%置信区间0.78,0.96;p = 0.006),中风分别为1.1%和1.2%(RR 0.90;95%置信区间0.62,1.30;p = 0.56),心肌梗死分别为6.6%和7.0%(RR 0.94;95%置信区间0.81,1.09;p = 0.41)。
在急性冠状动脉综合征期间早期启动他汀类药物治疗的益处会随着时间缓慢累积,因此在约24个月时可观察到生存优势。在此期间,预防1例死亡相对只需治疗较少患者。此外,这种方法可显著降低不稳定型心绞痛的发生率以及血运重建的需求。