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随机分配至普伐他汀组与常规治疗组的轻至中度高胆固醇血症高血压患者的长期随访:抗高血压和降脂治疗预防心脏病发作试验(ALLHAT-LLT)。

Long-term follow-up of moderately hypercholesterolemic hypertensive patients following randomization to pravastatin vs usual care: the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT-LLT).

机构信息

Health Partners Institute for Education and Research, Minneapolis, MN, USA.

出版信息

J Clin Hypertens (Greenwich). 2013 Aug;15(8):542-54. doi: 10.1111/jch.12139. Epub 2013 Jun 10.

Abstract

The authors conducted a randomized, controlled, multicenter trial, in which they assigned well-controlled hypertensive participants aged 55 years and older with moderate hypercholesterolemia to receive pravastatin (n=5170) or usual care (n=5185) for 4 to 8 years, when trial therapy was discontinued. Passive surveillance using national databases to ascertain deaths and hospitalizations continued for a total follow-up of 8 to 13 years to assess whether mortality and morbidity differences persisted or new differences developed. During the post-trial period, fatal and nonfatal outcomes were available for 98% and 64% of participants, respectively. The primary outcome was all-cause mortality and the secondary outcomes included cardiovascular mortality, coronary heart disease (CHD), stroke, heart failure, cardiovascular disease, and end-stage renal disease. No significant differences appeared in mortality for pravastatin vs usual care (hazard ratio [HR], 0.96; 95% confidence interval [CI], 0.89-1.03) or other secondary outcomes. Similar to the previously reported in-trial result, there was a significant treatment effect for CHD in black patients (HR, 0.79; 95% CI, 0.64-0.98). However, the in-trial result showing a significant treatment by race effect did not remain significant during the entire follow-up (P=.08). These findings are consistent with evidence from other large trials that show statins prevent CHD and add evidence that they are effective for CHD prevention in black patients.

摘要

作者开展了一项随机、对照、多中心试验,将 55 岁及以上、血压控制良好且伴有中度高胆固醇血症的高血压患者随机分为普伐他汀组(n=5170)和常规治疗组(n=5185),分别接受为期 4 至 8 年的治疗,试验治疗结束后停止用药。通过国家数据库进行被动监测以确定死亡和住院情况,总随访时间为 8 至 13 年,以评估死亡率和发病率差异是否持续存在或是否出现新的差异。在试验后期间,分别有 98%和 64%的参与者可获得致命和非致命结局的数据。主要结局是全因死亡率,次要结局包括心血管死亡率、冠心病、中风、心力衰竭、心血管疾病和终末期肾病。普伐他汀与常规治疗相比,死亡率无显著差异(风险比 [HR],0.96;95%置信区间 [CI],0.89-1.03)或其他次要结局。与之前报告的试验内结果相似,黑种人患者的冠心病有显著的治疗效果(HR,0.79;95% CI,0.64-0.98)。然而,在整个随访期间,试验内显示种族治疗效果显著的结果不再显著(P=.08)。这些发现与其他大型试验的证据一致,表明他汀类药物可预防冠心病,并进一步证明其对黑种人患者的冠心病预防有效。

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本文引用的文献

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Mortality and morbidity during and after the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial.
J Clin Hypertens (Greenwich). 2012 Jan;14(1):20-31. doi: 10.1111/j.1751-7176.2011.00568.x. Epub 2011 Dec 9.
4
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Cochrane Database Syst Rev. 2009 Apr 15(2):CD007784. doi: 10.1002/14651858.CD007784.
8
The Anglo-Scandinavian Cardiac Outcomes Trial lipid lowering arm: extended observations 2 years after trial closure.
Eur Heart J. 2008 Feb;29(4):499-508. doi: 10.1093/eurheartj/ehm583. Epub 2008 Jan 5.
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N Engl J Med. 2007 Oct 11;357(15):1477-86. doi: 10.1056/NEJMoa065994.

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