Aroney C N, Semigran M J, Dec G W, Boucher C A, Fifer M A
Department of Medicine, Massachusetts General Hospital, Boston 02114.
J Am Coll Cardiol. 1989 Nov 1;14(5):1331-8. doi: 10.1016/0735-1097(89)90437-3.
Nicardipine, a new dihydropyridine calcium channel blocker, has been investigated for the treatment of coronary artery disease and heart failure. To assess the inotropic effect of nicardipine in humans independent of its vasodilator effect, equihypotensive doses of intravenous nitroprusside (mean infusion rate 65 +/- 13 micrograms/min) and nicardipine (mean dose 5.2 +/- 0.4 mg) were administered to 15 patients with heart failure (New York Heart Association functional classes II to IV, radionuclide left ventricular ejection fraction 0.15 +/- 0.02). Left ventricular micromanometer pressure and simultaneous radionuclide left ventricular volume were obtained at baseline, during nitroprusside infusion, during a second baseline period and during nicardipine infusion. Heart rate did not change significantly with either nitroprusside or nicardipine. Mean systemic arterial pressure decreased by an average of 21 mm Hg with both drugs. A greater decrease in left ventricular end-diastolic pressure occurred with nitroprusside (27 +/- 2 to 14 +/- 2 mm Hg, p less than 0.01) than with nicardipine (27 +/- 2 to 23 +/- 3 mm Hg, p less than 0.05), and pulmonary capillary wedge pressure decreased significantly only with nitroprusside. Cardiac index increased from 1.8 +/- 0.1 to 2.1 +/- 0.1 liters/min per m2 (p less than 0.05) with nitroprusside and to a greater extent from 1.7 +/- 0.1 to 2.4 +/- 0.1 liters/min per m2 (p less than 0.01) with nicardipine. Left ventricular ejection fraction increased with nicardipine (0.15 +/- 0.01 to 0.19 +/- 0.01, p less than 0.01), but not with nitroprusside. Peak positive first derivative of left ventricular pressure (dP/dt) decreased by 9% with both agents.(ABSTRACT TRUNCATED AT 250 WORDS)
尼卡地平是一种新型二氢吡啶类钙通道阻滞剂,已被用于研究治疗冠状动脉疾病和心力衰竭。为了评估尼卡地平在人体中的正性肌力作用而不依赖其血管扩张作用,对15例心力衰竭患者(纽约心脏协会心功能分级II至IV级,放射性核素左心室射血分数0.15±0.02)给予等降压剂量的静脉硝普钠(平均输注速率65±13微克/分钟)和尼卡地平(平均剂量5.2±0.4毫克)。在基线期、硝普钠输注期间、第二个基线期和尼卡地平输注期间,获取左心室微压计压力和同步放射性核素左心室容积。硝普钠和尼卡地平用药后心率均无显著变化。两种药物均使平均体循环动脉压平均降低21毫米汞柱。硝普钠使左心室舒张末期压力下降幅度更大(从27±2降至14±2毫米汞柱,p<0.01),而尼卡地平使左心室舒张末期压力下降幅度较小(从27±2降至23±3毫米汞柱,p<0.05),且仅硝普钠使肺毛细血管楔压显著下降。硝普钠使心脏指数从1.8±0.1升至2.1±0.1升/分钟·每平方米(p<0.05),尼卡地平使心脏指数升高幅度更大,从1.7±0.1升至2.4±0.1升/分钟·每平方米(p<0.01)。尼卡地平使左心室射血分数升高(从0.15±0.01升至0.19±0.01,p<0.01),而硝普钠未使其升高。两种药物均使左心室压力的峰值正一阶导数(dP/dt)下降9%。(摘要截短于250字)