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依那普利治疗重度充血性心力衰竭。一项双盲研究。

Enalapril for severe congestive heart failure. A double-blind study.

作者信息

Jennings G, Kiat H, Nelson L, Kelly M J, Kalff V, Johns J

出版信息

Med J Aust. 1984 Nov 24;141(11):723-6.

PMID:6094995
Abstract

The effects of the new, orally administered converting-enzyme inhibitor, enalapril (MK-421), were studied in 12 ambulatory patients with severe cardiac failure who were also receiving digoxin and diuretic agents. The study was double-blind, parallel, placebo-controlled and randomized. The clinical characteristics and pretreatment exercise performance were similar in the two groups of patients. All vasodilator drugs had been withdrawn two weeks before the start of the trial. At 12 weeks, the patients receiving enalapril showed a significant improvement in the functional class of the disease, exercise time (P less than 0.01), and maximum workload achieved, and experienced relief of symptoms. Blood pressure fell in patients receiving active treatment suggesting a reduction of afterload. Left ventricular ejection fraction was unchanged in enalapril-treated patients, but fell in patients on placebo (P less than 0.001). Enalapril was well tolerated without apparent adverse effects. It was effective when used with digoxin and diuretic agents in the treatment of severe cardiac failure, and its efficacy was maintained throughout 12 weeks of therapy.

摘要

对12例门诊重度心力衰竭患者进行了研究,这些患者同时还在服用地高辛和利尿剂,研究新型口服转换酶抑制剂依那普利(MK - 421)的效果。该研究为双盲、平行、安慰剂对照且随机分组。两组患者的临床特征和治疗前运动表现相似。在试验开始前两周停用了所有血管扩张剂。12周时,接受依那普利治疗的患者在疾病功能分级、运动时间(P<0.01)和达到的最大工作量方面有显著改善,并症状缓解。接受积极治疗的患者血压下降,提示后负荷降低。依那普利治疗的患者左心室射血分数未改变,但安慰剂组患者的左心室射血分数下降(P<0.001)。依那普利耐受性良好,无明显不良反应。与地高辛和利尿剂联合使用时,它在治疗重度心力衰竭方面有效,且在整个12周的治疗过程中疗效持续存在。

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