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硝苯地平联合β受体阻滞剂治疗重度心绞痛的症状及客观疗效。

The symptomatic and objective effects of nifedipine in combination with beta-blocker therapy in severe angina pectoris.

作者信息

Jenkins R M, Nagle R E

出版信息

Postgrad Med J. 1982 Nov;58(685):697-700. doi: 10.1136/pgmj.58.685.697.

Abstract

Nine patients with severe coronary artery disease and disabling angina receiving either regular metoprolol or oxprenolol, together with glyceryl trinitrate tablets as required for chest pain, were studied. Nifedipine 10 mg three times per day was compared to placebo in a double blind randomized control trial, using patient diary cards and exercise tests. The number of recorded episodes of angina during the placebo period of 15.0 +/- 2.1 (mean +/- s.e.m.) per patient per week was significantly reduced to 11.2 +/- 2.5 during the nifedipine period (P less than 0.05). Similarly, the recorded number of glyceryl trinitrate tablets consumed during the placebo period of 12.6 +/- 2.1 was significantly reduced to 9.1 +/- 2.0 tablets per patient per week during the nifedipine period (P less than 0.05). There was a statistically significant increase in both the duration of exercise to onset of chest pain (from 241 +/- 16.3 seconds on placebo to 306 +/- 38.4 seconds on nifedipine (P less than 0.05)) and the total work performed to the onset of chest pain during the nifedipine period compared to the control and placebo periods (P less than 0.05). There was a significant increase (P less than 0.05) in exercise time before the onset of appreciable ST depression (greater than 1 mm) on exercise testing during the nifedipine period (66.2 +/- 4.2 sec) compared to the control period (51.2 +/- 3.0 sec) and placebo periods (58.7 +/- 3.5 sec). Although nifedipine was generally well tolerated, one patient experienced a severe episode of angina whilst taking the drug, which required admission to hospital.

摘要

对9例患有严重冠状动脉疾病且心绞痛症状严重的患者进行了研究,这些患者正在接受常规美托洛尔或氧烯洛尔治疗,并根据胸痛情况按需服用硝酸甘油片。在一项双盲随机对照试验中,将每日三次每次10毫克硝苯地平与安慰剂进行比较,试验采用患者日记卡和运动试验。每位患者每周在安慰剂期记录的心绞痛发作次数为15.0±2.1(均值±标准误),在硝苯地平期显著减少至11.2±2.5(P<0.05)。同样,每位患者每周在安慰剂期消耗的硝酸甘油片记录数量为12.6±2.1,在硝苯地平期显著减少至9.1±2.0片(P<0.05)。与对照组和安慰剂组相比,硝苯地平期胸痛发作前的运动持续时间(从安慰剂组的241±16.3秒增加到硝苯地平组的306±38.4秒(P<0.05))以及胸痛发作前完成的总工作量均有统计学显著增加(P<0.05)。与对照组(51.2±3.0秒)和安慰剂组(58.7±3.5秒)相比,硝苯地平期运动试验中出现明显ST段压低(大于1毫米)之前的运动时间显著增加(P<0.05)(66.2±4.2秒)。尽管硝苯地平总体耐受性良好,但有1例患者在服用该药时经历了一次严重心绞痛发作,需要住院治疗。

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