Caralis D G, Kyriakides Z
Division of Cardiology, St. Louis University Hospital, Missouri 63104.
Cardiovasc Drugs Ther. 1988 May;2(1):79-82. doi: 10.1007/BF00054256.
We studied the acute hemodynamic effects of molsidomine, a selective preload reducing agent, and nifedipine, a selective afterload reducing agent. Thirty-two patients with stable angina pectoris and angiographically significant coronary artery disease were randomized into two groups: group A patients received 4 mg of molsidomine, and group B patients received 20 mg of nifedipine orally. Molsidomine was associated with a significant reduction of the left ventricular end-diastolic pressure and an increase in Vcf. Nifedipine caused a significant reduction of the mean arterial pressure and an increase of the heart rate. Hemodynamic parameters associated with chronic exertional angina pectoris in patients with angiographically significant coronary artery disease improved more with a preload reducing agent, like molsidomine.
我们研究了选择性降低前负荷药物吗多明和选择性降低后负荷药物硝苯地平的急性血流动力学效应。32例患有稳定型心绞痛且冠状动脉造影显示有明显冠状动脉疾病的患者被随机分为两组:A组患者口服4毫克吗多明,B组患者口服20毫克硝苯地平。吗多明可使左心室舒张末期压力显著降低,心室周径纤维缩短速度(Vcf)增加。硝苯地平可使平均动脉压显著降低,心率增加。对于冠状动脉造影显示有明显冠状动脉疾病的慢性劳力性心绞痛患者,与使用硝苯地平这类后负荷降低药物相比,使用像吗多明这样的前负荷降低药物能使相关血流动力学参数得到更大改善。