Parodi O, Simonetti I, Michelassi C, Carpeggiani C, Biagini A, L'Abbate A, Maseri A
Am J Cardiol. 1986 Apr 15;57(11):899-906. doi: 10.1016/0002-9149(86)90727-7.
The effects of oral verapamil (V), 400 mg/day, oral propranolol (P), 300 mg/day, and placebo were compared in 10 patients admitted to the coronary care unit because of frequent attacks of angina at rest. Testing was done according to a randomized, double-blind, multiple-crossover, placebo-controlled trial, consisting of 8 consecutive 48-hour treatment periods with V or P or placebo. Three patients had variant angina, 5 had episodes of both ST-segment elevation and depression and 2 had only ST-segment depression. One patient had no critical coronary stenoses, 1 had 1-vessel disease, 7 had 2-vessel disease and 1 had 3-vessel disease. Electrocardiographic monitoring and tape recording were continued during the 16 days of the trial. A total of 1,602 episodes of transient diagnostic ST shift were recorded during the trial (1,309 episodes of ST-segment elevation, 293 of ST-segment depression); 43% were painless. Mean blood levels of V and P at the end of the active phases were 161 +/- 89 and 120 +/- 45 ng/ml, respectively. In the group as a whole, the average number of diagnostic ischemic ST-segment shifts per 24 hours was significantly reduced relative to corresponding placebo periods during V (2.6 +/- 2.4 vs 11.9 +/- 8.6; p less than 0.01) but not during P treatment (11.9 +/- 8.6 vs 12.0 +/- 7.3). Similar statistically significant reductions were observed in the number of anginal attacks and nitroglycerin tablets consumed. Considering individual patients, V reduced ischemic episodes during both active phases in all patients, whereas P was effective only in 1.(ABSTRACT TRUNCATED AT 250 WORDS)
对10名因静息时频繁心绞痛发作而入住冠心病监护病房的患者,比较了口服维拉帕米(V)(400毫克/天)、口服普萘洛尔(P)(300毫克/天)和安慰剂的效果。试验按照随机、双盲、多次交叉、安慰剂对照试验进行,包括连续8个48小时的V、P或安慰剂治疗期。3例患者有变异型心绞痛,5例有ST段抬高和压低发作,2例仅有ST段压低。1例患者无严重冠状动脉狭窄,1例有单支血管病变,7例有双支血管病变,1例有三支血管病变。在试验的16天内持续进行心电图监测和磁带记录。试验期间共记录到1602次短暂诊断性ST段移位发作(1309次ST段抬高发作,293次ST段压低发作);43%为无痛性。活跃期结束时V和P的平均血药浓度分别为161±89和120±45纳克/毫升。总体而言,与相应安慰剂期相比,V治疗期间每24小时诊断性缺血性ST段移位的平均次数显著减少(2.6±2.4对11.9±8.6;p<0.01),而P治疗期间未减少(11.9±8.6对12.0±7.3)。心绞痛发作次数和硝酸甘油片消耗量也有类似的统计学显著减少。就个体患者而言,V在所有患者的两个活跃期均减少了缺血发作,而P仅对1例患者有效。(摘要截短于250字)