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钙通道阻滞剂作为稳定型心绞痛的主要治疗方法。维拉帕米与普萘洛尔的双盲安慰剂对照比较。

Calcium channel blockade as primary therapy for stable angina pectoris. A double-blind placebo-controlled comparison of verapamil and propranolol.

作者信息

Subramanian V B, Bowles M J, Davies A B, Raftery E B

出版信息

Am J Cardiol. 1982 Nov;50(5):1158-63. doi: 10.1016/0002-9149(82)90437-4.

Abstract

The effectiveness and safety of the beta-adrenergic blocking agent propranolol and the calcium channel antagonist verapamil were compared in 22 patients with chronic stable angina pectoris using a double-blind randomized placebo-controlled crossover protocol. The double-blind phase was preceded by a 2 week single-blind placebo period, followed by randomization to either 4 weeks' therapy with verapamil, 360 mg/day, or propranolol, 240 mg/day, followed by crossover to the other drug. Both verapamil and propranolol increased exercise tolerance (5.5 +/- 0.4 minutes with placebo, 7.8 +/- 0.5 minutes with propranolol [p less than 0.001], and 9.1 +/- 0.5 minutes with verapamil [p less than 0.001]), but the increase with verapamil was significantly greater (p less than 0.01). Both drugs prolonged the exercise duration to 1 mm S-T depression (3.3 +/- 0.4 minutes with placebo, 5.7 +/- 0.5 minutes with propranolol [p less than 0.001] and 5.5 +/- 0.6 minutes with verapamil [p less than 0.001]); the degree of improvement was similar with both active drugs. Both drugs decreased the resting heart rate (76 +/- 3 beats/min with placebo, 56 +/- 2 beats/min with propranolol [p less than 0.001], and 71 +/- 3 beats/min with verapamil [p less than 0.01]), but the heart rate decreased more with propranolol than with verapamil (p less than 0.001). Neither drug produced significant adverse reactions. This study, along with 8 similar double-blind placebo-controlled randomized investigations which have compared verapamil with propranolol, indicate that verapamil is as effective and safe as propranolol in relieving symptoms and improving exercise tolerance in patients with chronic stable angina pectoris and may be considered a first-line therapeutic agent in patients with ischemic heart disease.

摘要

采用双盲随机安慰剂对照交叉试验方案,对22例慢性稳定型心绞痛患者比较了β-肾上腺素能阻滞剂普萘洛尔和钙通道拮抗剂维拉帕米的有效性和安全性。双盲阶段之前有2周单盲安慰剂期,随后随机分为接受维拉帕米(360mg/天)或普萘洛尔(240mg/天)治疗4周,之后交叉使用另一种药物。维拉帕米和普萘洛尔均提高了运动耐量(安慰剂组为5.5±0.4分钟,普萘洛尔组为7.8±0.5分钟[p<0.001],维拉帕米组为9.1±0.5分钟[p<0.001]),但维拉帕米组的增加更为显著(p<0.01)。两种药物均将运动持续时间延长至ST段压低1mm(安慰剂组为3.3±0.4分钟,普萘洛尔组为5.7±0.5分钟[p<0.001],维拉帕米组为5.5±0.6分钟[p<0.001]);两种活性药物的改善程度相似。两种药物均降低了静息心率(安慰剂组为76±3次/分钟,普萘洛尔组为56±2次/分钟[p<0.001],维拉帕米组为71±3次/分钟[p<0.01]),但普萘洛尔使心率降低的幅度大于维拉帕米(p<0.001)。两种药物均未产生明显不良反应。本研究以及另外8项比较维拉帕米和普萘洛尔的类似双盲安慰剂对照随机研究表明,在缓解慢性稳定型心绞痛患者症状和提高运动耐量方面,维拉帕米与普萘洛尔同样有效和安全,可被视为缺血性心脏病患者的一线治疗药物。

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