Chatterjee K, Parmley W W, Cohn J N, Levine T B, Awan N A, Mason D T, Faxon D P, Creager M, Gavras H P, Fouad F M
Am Heart J. 1985 Aug;110(2):439-47. doi: 10.1016/0002-8703(85)90167-x.
The acute hemodynamic effects, long-term clinical efficacy, and safety of the oral angiotensin-converting enzyme inhibitor, captopril, were assessed in a multicenter cooperative study of 124 patients with heart failure resistant to digitalis and diuretics. The cardiac status of most patients was deteriorating prior to the study. Favorable acute hemodynamic effects consistently occurred with captopril. Maximal mean percentage increases in cardiac index, stroke index, and stroke work index were, respectively, 35%, 44%, and 34%. Systemic and pulmonary vascular resistances were each decreased by approximately 40%, as were the filling pressures of the right and left heart. Infusion of nitroprusside in some of the same patients to an end point of a pulmonary capillary wedge pressure of 12 to 18 mm Hg (equivalent to that after captopril) revealed no significant difference in the effect of either drug on the other hemodynamic parameters. Recatheterization after 8 weeks of captopril therapy revealed sustained hemodynamic changes. Significant and sustained improvements in clinical status were observed in most patients as measured by changes in New York Heart Association (NYHA) functional classification and exercise tolerance times. Seventy-nine percent of patients for whom there were adequate NYHA class data improved. Twenty percent remained unchanged and 1% deteriorated. Those patients who had both pretreatment and post-treatment exercise stress testing exhibited a highly significant mean increase in exercise tolerance times of 34% (317 +/- 32 seconds pretreatment to 425 +/- 34 seconds, final measurement). There was no evidence of tachyphylaxis over an 18-month period.(ABSTRACT TRUNCATED AT 250 WORDS)
在一项针对124例对洋地黄和利尿剂耐药的心力衰竭患者的多中心合作研究中,评估了口服血管紧张素转换酶抑制剂卡托普利的急性血流动力学效应、长期临床疗效和安全性。大多数患者在研究前心脏状况正在恶化。卡托普利始终产生有利的急性血流动力学效应。心脏指数、每搏指数和每搏作功指数的最大平均百分比增加分别为35%、44%和34%。全身和肺血管阻力均降低约40%,左右心的充盈压也降低。在一些相同患者中输注硝普钠至肺毛细血管楔压达到12至18 mmHg(与卡托普利治疗后相当)的终点,结果显示两种药物对其他血流动力学参数的影响无显著差异。卡托普利治疗8周后再次进行心导管检查显示血流动力学变化持续存在。根据纽约心脏协会(NYHA)功能分级和运动耐量时间的变化衡量,大多数患者的临床状况有显著且持续的改善。有足够NYHA分级数据的患者中,79%病情改善。20%病情不变,1%病情恶化。那些在治疗前和治疗后都进行运动应激测试的患者,运动耐量时间平均显著增加34%(从治疗前的317±32秒增加到最终测量的425±34秒)。在18个月的时间里没有快速耐受的证据。(摘要截短于250字)