Kulas A, Escudier B, Hannachi N, Kolski H, Witchitz S, Acar J
Arch Mal Coeur Vaiss. 1984 Jan;77(1):92-9.
Molsidomine, one of the sydnonimine group of drugs; the object of this study was to evaluate its efforts in refractory cardiac failure. In the first part of the study, the haemodynamic effects of a single oral dose of 2 or 4 mg of molsidomine were compared with placebo controls in 23 patients. This showed molsidomine to be an active venous vasodilator reducing pulmonary artery and right atrial pressures without changing cardiac index or systemic pressures. The peak effect was observed after 1 to 1,5 hours. In the second phase, molsidomine was used in 9 patients aged 32 to 71 years (mean 47 +/- 12 years) over an average period of 19 months (3,5 to 42 months). The maintenance dose varied from 8 to 24 mg/24 hours. These patients had refractory cardiac failure secondary to primary cardiomyopathy with dilatation (6 cases) or ischemic heart disease (3 cases). The 9 patients were in functional classes IV (5 cases) or III (4 cases). Four patients were theoretically good indications for transplantation. Haemodynamic control was performed 1,8 +/- 5 months after a washout period of 8 hours, and after initial right heart catheterisation, the measurements were repeated 1 hour after oral administration of a 4 mg dose of molsidomine. Two patients did not respond initially to molsidomine; one died, the other remained in functional Class III. Another patient who responded initially was improved for over two years but died in cardiac failure after 42 months' treatment. The other six patients have been significantly improved and were in functional Class II at their last control.(ABSTRACT TRUNCATED AT 250 WORDS)
吗多明,一种亚胺基氧化吡啶类药物;本研究的目的是评估其对难治性心力衰竭的疗效。在研究的第一部分,对23例患者单次口服2毫克或4毫克吗多明的血液动力学效应与安慰剂对照组进行了比较。结果显示吗多明是一种有效的静脉血管扩张剂,可降低肺动脉和右心房压力,而不改变心脏指数或体循环压力。在1至1.5小时后观察到最大效应。在第二阶段,9例年龄在32至71岁(平均47±12岁)的患者使用吗多明,平均疗程为19个月(3.5至42个月)。维持剂量为8至24毫克/24小时。这些患者患有原发性心肌病伴扩张(6例)或缺血性心脏病(3例)继发的难治性心力衰竭。9例患者的心功能分级为IV级(5例)或III级(4例)。4例患者理论上是移植的良好适应证。在8小时的洗脱期后1.8±5个月进行血液动力学监测,在最初的右心导管检查后,口服4毫克吗多明1小时后重复测量。2例患者最初对吗多明无反应;1例死亡,另1例仍为心功能III级。另1例最初有反应的患者改善了两年多,但在治疗42个月后死于心力衰竭。其他6例患者有显著改善,在最后一次检查时的心功能分级为II级。(摘要截短于250字)