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阿替洛尔作为福辛普利的附加疗法治疗心力衰竭的效果。

Effects of atenolol as add-on therapy to fosinopril in heart failure.

作者信息

Pacher R, Hülsmann M, Berger R, Koller-Strametz J, Kos T, Frey B, Dukat A, Stanek B

机构信息

Department of Cardiology, University of Vienna, Austria.

出版信息

Wien Klin Wochenschr. 1997 Apr 11;109(7):232-8.

PMID:9141231
Abstract

Several trials have demonstrated functional benefit with beta-blockers in patients with chronic heart failure. The aim of this observational study was to investigate if additional beneficial effects can be obtained from beta-blockade in a heart failure population that is already receiving high-dose ACE-inhibitor therapy. Atenolol is a long-acting cardioselective beta-blocking agent and is devoid of additional vasodilatory properties. Twenty-five male patients with class II or III heart failure and background therapy of digitalis, furosemide and 20 mg fosinopril per day were treated with 40 mg fosinopril per day and additional 75 mg atenolol per day (beta-blocker group) or with 40 mg fosinopril per day alone (control group). At the end of one year, changes in left ventricular function, exercise parameters and plasma neurohumoral variables reflecting vasoconstriction (noradrenaline, big endothelin) were measured and compared in the two treatment groups. Nineteen patients completed the study. Drop-outs were due to death (4 patients) and non-compliance (2 patients) with no significant difference between the groups. There was a beta-blocker related improvement in left ventricular ejection fraction (p < 0.05 between groups) and an increase in peak oxygen consumption in the control group only (p < 0.05 between groups). Thus, in a heart failure population receiving high-dose ACE inhibitor background therapy beta-blockade with atenolol produced additional benefit by reversing left ventricular dysfunction.

摘要

多项试验已证明β受体阻滞剂对慢性心力衰竭患者具有功能益处。这项观察性研究的目的是调查在已经接受高剂量ACE抑制剂治疗的心力衰竭人群中,β受体阻滞剂是否能带来额外的有益效果。阿替洛尔是一种长效心脏选择性β受体阻滞剂,不具有额外的血管舒张特性。25名患有II级或III级心力衰竭且接受洋地黄、呋塞米和每日20毫克福辛普利作为背景治疗的男性患者,被分为两组,一组每天接受40毫克福辛普利及额外75毫克阿替洛尔治疗(β受体阻滞剂组),另一组仅每天接受40毫克福辛普利治疗(对照组)。一年结束时,测量并比较了两组患者左心室功能、运动参数以及反映血管收缩的血浆神经体液变量(去甲肾上腺素、大内皮素)的变化。19名患者完成了研究。退出研究的原因是死亡(4例患者)和不依从(2例患者),两组之间无显著差异。β受体阻滞剂组的左心室射血分数有改善(组间p<0.05),且仅对照组的峰值耗氧量增加(组间p<0.05)。因此,在接受高剂量ACE抑制剂背景治疗的心力衰竭人群中,阿替洛尔进行β受体阻滞通过逆转左心室功能障碍产生了额外的益处。

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