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β受体阻滞剂与钾通道开放剂治疗运动诱发性心绞痛的双盲对照研究

A double-blind comparison of a beta-blocker and a potassium channel opener in exercise induced angina.

作者信息

Raftery E B, Lahiri A, Hughes L O, Rose E L

机构信息

Department of Cardiology, Northwick Park Hospital, Harrow, Middlesex, U.K.

出版信息

Eur Heart J. 1993 Jul;14 Suppl B:35-9. doi: 10.1093/eurheartj/14.suppl_b.35.

Abstract

This randomized, double-blind, parallel study compared the anti-anginal effects of nicorandil and atenolol in 37 patients with exercise-induced angina pectoris. At the end of a single-blind placebo period, patients were randomized and received either atenolol 50 mg o.d. or nicorandil 10 mg b.d. for 3 weeks. On the third week, the dosage was increased (nicorandil 20 mg b.d. or atenolol 100 mg o.d.) for the final 3-week period. Treadmill exercise tolerance tests were performed immediately before and 2 h after dosing at the end of the placebo period, and at the end of the third and sixth week of active treatment. Demographic characteristics and exercise performance with placebo were comparable between both treatment groups, and at the end of the treatment periods a significant improvement in exercise time was observed: an increase in the time to peak exercise of 1.33 +/- 0.29 min (mean +/- standard error of the mean) in atenolol-treated patients (P < 0.001), and of 1.47 +/- 0.40 min (P < 0.005) in nicorandil-treated patients. While the anti-anginal activity of the two drugs was comparable, their effects on the rate-pressure product heart rate x systolic blood pressure were clearly different; atenolol induced a decrease at peak exercise, but this parameter was not changed or was slightly increased with nicorandil. One patient with severe three-vessel disease died suddenly after 3 days of treatment with nicorandil 10 mg twice daily. The most frequent adverse effect in both groups was headache, which led to discontinuation of one patient in the atenolol group and of five patients in the nicorandil group.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

这项随机、双盲、平行研究比较了尼可地尔和阿替洛尔对37例运动诱发型心绞痛患者的抗心绞痛作用。在单盲安慰剂期结束时,患者被随机分组,分别接受阿替洛尔50毫克每日一次或尼可地尔10毫克每日两次,为期3周。在第三周,剂量增加(尼可地尔20毫克每日两次或阿替洛尔100毫克每日一次),持续最后3周。在安慰剂期结束时、积极治疗的第三周和第六周结束时,给药前及给药后2小时进行跑步机运动耐力测试。两个治疗组在人口统计学特征和安慰剂治疗时的运动表现方面具有可比性,在治疗期结束时观察到运动时间有显著改善:阿替洛尔治疗的患者运动至峰值时间增加了1.33±0.29分钟(平均值±平均标准误差)(P<0.001),尼可地尔治疗的患者增加了1.47±0.40分钟(P<0.005)。虽然两种药物的抗心绞痛活性相当,但它们对心率×收缩压的速率-压力乘积的影响明显不同;阿替洛尔在运动峰值时导致降低,但该参数在尼可地尔治疗时未改变或略有增加。一名患有严重三支血管病变的患者在每日两次服用10毫克尼可地尔治疗3天后突然死亡。两组中最常见的不良反应是头痛,这导致阿替洛尔组有1例患者、尼可地尔组有5例患者停药。(摘要截断于250字)

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