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艾司洛尔治疗不稳定型心绞痛的安全性和有效性。

Safety and efficacy of esmolol for unstable angina pectoris.

作者信息

Wallis D E, Pope C, Littman W J, Scanlon P J

机构信息

Department of Medicine, Loyola University Medical Center, Maywood, Illinois 60153.

出版信息

Am J Cardiol. 1988 Nov 15;62(16):1033-7. doi: 10.1016/0002-9149(88)90543-7.

Abstract

Esmolol is a rapidly metabolized cardioselective beta-adrenergic blocker that provides steady state beta-adrenergic blockade when administered by continuous intravenous infusion. To determine the efficacy of esmolol in the management of unstable angina, 23 patients with known coronary artery disease, who averaged 3.7 +/- 2.7 daily episodes of chest pain at rest, were randomized to receive either a continuous infusion of esmolol (n = 12) or oral propranolol (n = 11), as an adjunct to concomitant antianginal therapy. Patients with systolic blood pressure less than 110 mm Hg, heart rate less than 60 beats/min or known contraindications to beta blockade were excluded. Esmolol was titrated in a step-wise fashion from 2 to 24 mg/min at 5-minute intervals up to a 30% reduction in heart rate and systolic blood pressure double-product. The propranolol dose was increased every 6 hours by 50 to 100% to achieve a similar reduction in heart rate and blood pressure. When compared with their 24-hour baseline periods, both groups achieved a significant reduction in episodes of chest pain, from 4.6 +/- 3.3 to 1.4 +/- 1.5 in the esmolol group (p less than 0.02) and 2.6 +/- 1.4 to 1.0 +/- 1.5 in the propranolol group (p less than 0.02) during the subsequent study period. The cardiac event rate and incidence of drug side effects were similar between the 2 groups; however, side effects seen with esmolol did not require treatment after drug discontinuation. Thus, maximally tolerated beta blockade is an effective therapy for unstable angina.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

艾司洛尔是一种代谢迅速的心脏选择性β-肾上腺素能阻滞剂,通过持续静脉输注给药时可提供稳态β-肾上腺素能阻滞作用。为确定艾司洛尔治疗不稳定型心绞痛的疗效,23例已知患有冠状动脉疾病、平均每日静息时胸痛发作3.7±2.7次的患者,被随机分为接受艾司洛尔持续输注组(n = 12)或口服普萘洛尔组(n = 11),作为辅助抗心绞痛治疗。收缩压低于110 mmHg、心率低于60次/分钟或已知有β受体阻滞剂禁忌证的患者被排除。艾司洛尔以逐步方式从2 mg/min滴定至24 mg/min,间隔5分钟,直至心率和收缩压乘积降低30%。普萘洛尔剂量每6小时增加50%至100%,以实现心率和血压的类似降低。与24小时基线期相比,在随后的研究期间,两组胸痛发作次数均显著减少,艾司洛尔组从4.6±3.3次降至1.4±1.5次(p<0.02),普萘洛尔组从2.6±1.4次降至1.0±1.5次(p<0.02)。两组的心脏事件发生率和药物副作用发生率相似;然而,艾司洛尔引起的副作用在停药后无需治疗。因此,最大耐受β受体阻滞是治疗不稳定型心绞痛的有效方法。(摘要截短至250字)

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