Di Pasquale G, Lusa A M, Manini G L, Dominici P, Coluccini M, Bassein L, Pinelli G
G Ital Cardiol. 1984 Aug;14(8):618-20.
The relative efficacy of nicardipine and nifedipine was examined in a double-blind randomized trial. We studied 12 patients with chronic effort angina who had reproducible chest pain and greater than or equal to 1.5 mm of ST-segment depression on treadmill exercise testing performed before and after 1-week control period of single-blind placebo administration. Subsequently over a 9-week period, nicardipine 20 mg or nifedipine 10 mg or an identical placebo four times a day, was administered in a randomized double-blind crossover fashion. Treadmill exercise testing was performed at the end of each 3-week period. Both nicardipine and nifedipine reduced the frequency of anginal attacks and trinitrate consumption. Compared with placebo both drugs caused a comparable increase of the total duration of exercise (p less than 0.05 placebo versus nicardipine; p less than 0.01 placebo versus nifedipine) and of the time to the onset of angina (p less than 0.05 placebo versus nicardipine; p less than 0.01 placebo versus nifedipine) and to the appearance of 1.5 mm ST depression (p less than 0.05 placebo versus nicardipine; p less than 0.01 placebo versus nifedipine). Moreover 4 patients no longer had angina with either drug and only 1 patient with placebo. Both drugs increased resting heart rate and reduced systolic blood pressure at resting (p less than 0.01) and submaximal exercise (p less than 0.01). Peak heart rate, systolic blood pressure and rate-pressure product were similar with placebo, nicardipine and nifedipine. No important side effects were observed with either drug. We conclude that nicardipine and nifedipine produce similar haemodynamic and clinical effects in patients with stable angina.
在一项双盲随机试验中对尼卡地平与硝苯地平的相对疗效进行了研究。我们研究了12例慢性劳力性心绞痛患者,这些患者有可重复性胸痛,且在单盲安慰剂给药1周的对照期前后进行的平板运动试验中ST段压低≥1.5mm。随后在9周的时间里,以随机双盲交叉方式每天4次给予尼卡地平20mg或硝苯地平10mg或相同的安慰剂。在每3周疗程结束时进行平板运动试验。尼卡地平和硝苯地平均降低了心绞痛发作频率和硝酸酯类药物的消耗量。与安慰剂相比,两种药物均使运动总时长(安慰剂组与尼卡地平组比较,P<0.05;安慰剂组与硝苯地平组比较,P<0.01)、心绞痛发作时间(安慰剂组与尼卡地平组比较,P<0.05;安慰剂组与硝苯地平组比较,P<0.01)以及出现1.5mm ST段压低的时间(安慰剂组与尼卡地平组比较,P<0.05;安慰剂组与硝苯地平组比较,P<0.01)有类似程度的增加。此外,4例患者使用任何一种药物后均不再有心绞痛发作,而使用安慰剂的患者中只有1例不再发作。两种药物均使静息心率增加,并降低静息时(P<0.01)和次极量运动时(P<0.01)的收缩压。安慰剂、尼卡地平和硝苯地平的心率峰值、收缩压及心率-血压乘积相似。两种药物均未观察到重要的副作用。我们得出结论,尼卡地平和硝苯地平在稳定型心绞痛患者中产生相似的血流动力学和临床效果。