Verma S P, Taylor S H
Z Kardiol. 1985;74 Suppl 2:37-42.
This is an interim report of haemodynamic studies with oral muzolimine in male patients under 70 yr with haemodynamically confirmed left ventricular failure complicating acute myocardial infarction. All were in sinus rhythm and without hypotension (SBP 100 mmHg) and were studied by conventional intravascular haemodynamic methods within 18 hr of onset of symptoms of acute myocardial infarction. A preliminary dose-finding study in four patients indicated that both 60 and 120 mg oral muzolimine induced substantial diuresis but only the latter dose was associated with an appreciable reduction in left heart filling pressure within 2 hr. The aims of the main study are to determine the haemodynamic effects of oral muzolimine 120 mg given once daily for 10 days in these high risk patients. Thereafter patients are randomised to continued oral muzolimine or placebo for a period of three months. The effects of such treatment on their haemodynamic profile at rest and during dynamic exercise are being measured by comparison with the 10 day measurements. In the first six patients entered into the main study, 120 mg oral muzolimine resulted in a progressive reduction in the elevated left heart filling pressure without tachycardia or any other major haemodynamic change over 8 hr on both Day 1 and Day 2. These potentially advantageous haemodynamic effects await confirmation from further results in this on-going study.
这是一项关于口服莫唑胺对70岁以下男性急性心肌梗死合并血流动力学确诊的左心室衰竭患者血流动力学研究的中期报告。所有患者均为窦性心律,无低血压(收缩压≥100 mmHg),并在急性心肌梗死症状发作后18小时内采用传统血管内血流动力学方法进行研究。对4名患者进行的初步剂量探索研究表明,口服60 mg和120 mg莫唑胺均能引起大量利尿,但只有后者剂量在2小时内可使左心充盈压明显降低。主要研究的目的是确定在这些高危患者中,每天口服120 mg莫唑胺,连续服用10天的血流动力学效应。此后,患者被随机分为继续口服莫唑胺组或安慰剂组,为期三个月。通过与第10天的测量结果进行比较,来测定这种治疗对患者静息和动态运动时血流动力学状况的影响。在进入主要研究的前6名患者中,口服120 mg莫唑胺导致升高的左心充盈压逐渐降低,在第1天和第2天的8小时内均未出现心动过速或任何其他主要血流动力学变化。这些潜在的有利血流动力学效应有待于这项正在进行的研究的进一步结果证实。