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在分配使用多沙唑嗪和氯噻酮的抗高血压和降脂治疗预防心脏病发作试验(ALLHAT)参与者中对心力衰竭事件的验证

Validation of Heart Failure Events in the Antihypertensive and Lipid Lowering Treatment to Prevent Heart Attack Trial (ALLHAT) Participants Assigned to Doxazosin and Chlorthalidone.

作者信息

Piller Linda B, Davis Barry R, Cutler Jeffrey A, Cushman William C, Wright Jackson T, Williamson Jeff D, Leenen Frans HH, Einhorn Paula T, Randall Otelio S, Golden John S, Haywood L Julian

机构信息

The University of Texas School of Public Health, Houston, TX, USA.

出版信息

Curr Control Trials Cardiovasc Med. 2002 Nov 14;3(1):10. doi: 10.1186/1468-6708-3-10.

Abstract

BACKGROUND

The Antihypertensive and Lipid Lowering Treatment to Prevent Heart Attack Trial (ALLHAT) is a randomized, double-blind, active-controlled trial designed to compare the rate of coronary heart disease events in high-risk hypertensive participants initially randomized to a diuretic (chlorthalidone) versus each of three alternative antihypertensive drugs: alpha-adrenergic blocker (doxazosin), ACE-inhibitor (lisinopril), and calcium-channel blocker (amlodipine). Combined cardiovascular disease risk was significantly increased in the doxazosin arm compared to the chlorthalidone arm (RR 1.25; 95% CI, 1.17-1.33; P <.001), with a doubling of heart failure (fatal, hospitalized, or non-hospitalized but treated) (RR 2.04; 95% CI, 1.79-2.32; P <.001). Questions about heart failure diagnostic criteria led to steps to validate these events further. METHODS AND RESULTS: Baseline characteristics (age, race, sex, blood pressure) did not differ significantly between treatment groups (P <.05) for participants with heart failure events. Post-event pharmacologic management was similar in both groups and generally conformed to accepted heart failure therapy. Central review of a small sample of cases showed high adherence to ALLHAT heart failure criteria. Of 105 participants with quantitative ejection fraction measurements provided, (67% by echocardiogram, 31% by catheterization), 29/46 (63%) from the chlorthalidone group and 41/59 (70%) from the doxazosin group were at or below 40%. Two-year heart failure case-fatalities (22% and 19% in the doxazosin and chlorthalidone groups, respectively) were as expected and did not differ significantly (RR 0.96; 95% CI, 0.67-1.38; P = 0.83). CONCLUSION: Results of the validation process supported findings of increased heart failure in the ALLHAT doxazosin treatment arm compared to the chlorthalidone treatment arm.

摘要

背景

抗高血压和降脂治疗预防心脏病发作试验(ALLHAT)是一项随机、双盲、活性药物对照试验,旨在比较最初随机分配接受利尿剂(氯噻酮)治疗的高危高血压参与者与三种替代抗高血压药物(α-肾上腺素能阻滞剂多沙唑嗪、ACE抑制剂赖诺普利和钙通道阻滞剂氨氯地平)中每种药物治疗的冠心病事件发生率。与氯噻酮组相比,多沙唑嗪组的心血管疾病综合风险显著增加(RR 1.25;95%CI,1.17 - 1.33;P <.001),心力衰竭(致命、住院或未住院但接受治疗)风险翻倍(RR 2.04;95%CI,1.79 - 2.32;P <.001)。关于心力衰竭诊断标准的问题促使采取进一步措施来验证这些事件。

方法与结果

心力衰竭事件参与者的治疗组间基线特征(年龄、种族、性别、血压)无显著差异(P <.05)。两组事件发生后的药物治疗相似,且总体符合公认的心力衰竭治疗方法。对一小部分病例进行的中心审查显示,对ALLHAT心力衰竭标准的依从性很高。在提供定量射血分数测量值的105名参与者中(67%通过超声心动图,%通过心导管检查),氯噻酮组的29/46(63%)和多沙唑嗪组的41/59(70%)处于或低于40%。两年心力衰竭病死率(多沙唑嗪组和氯噻酮组分别为22%和19%)与预期相符,且无显著差异(RR 0.96;95%CI,0.67 - 1.38;P = 0.83)。

结论

验证过程的结果支持了ALLHAT试验中多沙唑嗪治疗组与氯噻酮治疗组相比心力衰竭增加的研究结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c2f/149403/3f84119ad427/1468-6708-3-10-1.jpg

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