Cleland J G, Dargie H J, Ball S G, Gillen G, Hodsman G P, Morton J J, East B W, Robertson I, Ford I, Robertson J I
Br Heart J. 1985 Sep;54(3):305-12. doi: 10.1136/hrt.54.3.305.
Several studies have shown symptomatic and haemodynamic improvement after the introduction of angiotensin converting enzyme inhibitors in patients with heart failure treated with diuretics. The concomitant long term effects of the new orally effective long acting angiotensin converting enzyme inhibitor, enalapril, on symptoms, exercise performance, cardiac function, arrhythmias, hormones, electrolytes, body composition, and renal function have been further assessed in a placebo controlled double blind cross over trial with treatment periods of eight weeks. Twenty patients with New York Heart Association functional class II to IV heart failure who were clinically stable on digoxin and diuretic therapy were studied. Apart from the introduction of enalapril, regular treatment was not changed over the study period; no order or period effects were noted. Enalapril treatment significantly improved functional class, symptom score for breathlessness, and exercise tolerance. Systolic blood pressure was significantly lower on enalapril treatment. Echocardiographic assessment indicated a reduction in left ventricular dimensions and an improvement in systolic time intervals. In response to enalapril, the plasma concentration of angiotensin II was reduced and that of active renin rose; plasma concentrations of aldosterone, vasopressin, and noradrenaline fell. There were significant increases in serum potassium and serum magnesium on enalapril. Glomerular filtration rate measured both by isotopic techniques and by creatinine clearance declined on enalapril while serum urea and creatinine rose and effective renal plasma flow increased. Body weight and total body sodium were unchanged indicating that there was no overall diuresis. There was a statistically insignificant rise in total body potassium, though the increase was related directly to pretreatment plasma renin (r = 0.5). On enalapril the improvement in symptoms, exercise performance, fall in plasma noradrenaline, and rise in serum potassium coincided with a decline in the frequency of ventricular extrasystoles recorded during ambulatory monitoring. Adverse effects were few. In patients with heart failure, enalapril had a beneficial effect on symptoms and functional capacity. The decline in glomerular filtration rate on enalapril may not be beneficial in early heart failure.
多项研究表明,在接受利尿剂治疗的心力衰竭患者中引入血管紧张素转换酶抑制剂后,症状和血流动力学得到改善。新型口服长效血管紧张素转换酶抑制剂依那普利对症状、运动能力、心功能、心律失常、激素、电解质、身体组成和肾功能的长期伴随影响,已在一项安慰剂对照双盲交叉试验中进一步评估,治疗期为8周。研究了20例纽约心脏协会心功能II至IV级的心力衰竭患者,这些患者在洋地黄和利尿剂治疗下临床稳定。除了引入依那普利外,在研究期间常规治疗不变;未发现顺序或周期效应。依那普利治疗显著改善了心功能分级、呼吸困难症状评分和运动耐量。依那普利治疗时收缩压显著降低。超声心动图评估显示左心室尺寸减小,收缩时间间期改善。对依那普利的反应是,血浆血管紧张素II浓度降低,活性肾素浓度升高;血浆醛固酮、血管加压素和去甲肾上腺素浓度下降。依那普利治疗时血清钾和血清镁显著升高。用同位素技术和肌酐清除率测量的肾小球滤过率在依那普利治疗时下降,而血清尿素和肌酐升高,有效肾血浆流量增加。体重和总体钠不变,表明没有总体利尿作用。总体钾有统计学上无显著意义的升高,尽管升高与治疗前血浆肾素直接相关(r = 0.5)。服用依那普利时,症状改善、运动能力提高、血浆去甲肾上腺素下降和血清钾升高与动态监测期间记录的室性早搏频率下降同时出现。不良反应很少。在心力衰竭患者中,依那普利对症状和功能能力有有益作用。依那普利治疗时肾小球滤过率下降在早期心力衰竭中可能并无益处。