Currie P J, Kelly M J, McKenzie A, Harper R W, Lim Y L, Federman J, Anderson S T, Pitt A
J Am Coll Cardiol. 1984 Jan;3(1):203-9. doi: 10.1016/s0735-1097(84)80449-0.
A double-blind crossover trial was performed to assess the effect of metoprolol in 10 patients (mean age 55 years) with severe dilated cardiomyopathy. All patients clinically had idiopathic dilated cardiomyopathy; however, at coronary angiography, four had occult coronary disease. All were in New York Heart Association functional class III with a left ventricular ejection fraction less than 35% as assessed by rest radionuclide ventriculography. Studies were performed before treatment, after 4 weeks of metoprolol therapy and after 4 weeks of placebo administration. Erect bicycle sprint exercise was used to determine maximal work load. Hemodynamic variables and radionuclide left ventricular ejection fraction were recorded at rest and during graded supine bicycle exercise. Cardiac medications were unchanged throughout the trial. The mean (+/- standard error of the mean) dose of metoprolol was 130 +/- 13 mg/day. Metoprolol did not change symptoms, chest X-ray findings or exercise tolerance (baseline 700 +/- 73, placebo 690 +/- 85, metoprolol 710 +/- 81 kilopond-meters [kpm]/min). Metoprolol produced a significant decrease in heart rate at rest and during exercise (p less than 0.001). Mean blood pressure and left ventricular filling pressure did not differ significantly in the baseline, placebo and metoprolol studies. There was a slight, but significant (p less than 0.05) decrease in cardiac index with metoprolol compared with placebo and baseline studies. The small, but significant increase in left ventricular ejection fraction from baseline to the metoprolol and placebo studies (p less than 0.001) was considered a result of spontaneous improvement rather than of therapy. No significant differences were found between the patients with and without coronary disease.(ABSTRACT TRUNCATED AT 250 WORDS)
进行了一项双盲交叉试验,以评估美托洛尔对10例(平均年龄55岁)严重扩张型心肌病患者的疗效。所有患者临床上均患有特发性扩张型心肌病;然而,在冠状动脉造影检查中,有4例存在隐匿性冠心病。所有患者均处于纽约心脏协会心功能Ⅲ级,静息放射性核素心室造影评估左心室射血分数小于35%。在治疗前、美托洛尔治疗4周后和安慰剂给药4周后进行研究。采用直立式自行车冲刺运动来确定最大工作量。记录静息和分级仰卧位自行车运动时的血流动力学变量和放射性核素左心室射血分数。在整个试验过程中,心脏药物未改变。美托洛尔的平均(±平均标准误差)剂量为130±13mg/天。美托洛尔未改变症状、胸部X线检查结果或运动耐量(基线700±73、安慰剂690±85、美托洛尔710±81千克力米[kpm]/分钟)。美托洛尔使静息和运动时的心率显著降低(p<0.001)。在基线、安慰剂和美托洛尔研究中,平均血压和左心室充盈压无显著差异。与安慰剂和基线研究相比,美托洛尔使心脏指数略有但显著降低(p<0.05)。从基线到美托洛尔和安慰剂研究,左心室射血分数虽有小幅但显著增加(p<0.001),这被认为是自发改善而非治疗的结果。在有冠心病和无冠心病的患者之间未发现显著差异。(摘要截断于250字)