Keyriläinen O, Uusitalo A
Acta Med Scand. 1976;199(6):491-7.
Eighteen patients with angina pectoris, who had previously participated in a cross-over study with 20 mg metoprolol t.i.d. and placebo, have been included in this study. During an introductory six-month open tolerability study, all patients were treated with 50 mg metoprolol t.i.d. and during a subsequent cross-over study, the efficacy of this dose was compared with that of placebo under double-blind conditions. An exercise was performed at the end of each cross-over period. Metoprolol, in a dose of 50 mg t.i.d., gave a significant improvement compared with placebo in respect of the number of anginal attacks, nitroglycerin consumption and daily subjective assessment of the patients' anginal symptoms. Metoprolol also gave a significant increase in exercise capacity, both until the appearance of 1 mm ST segment depression and until the end of exercise. Heart rate and blood pressure were reduced both at rest and during exercise. No severe unwanted effects were observed during this study ranging over eight months, and none of the patients had any signs or symptoms of cardiac failure or pulmonary dysfunction on any occasion. Unwanted effects reported were mild to moderate, and the frequency was the same as during placebo treatment. No abnormal laboratory findings were observed and the relative heart volume was not significantly changed. Administration of 50 mg metoprolol t.i.d. seems to be of greater benefit than 20 mg metoprolol t.i.d., previously investigated in these patients.
18名曾参与过美托洛尔20mg每日三次与安慰剂交叉对照研究的心绞痛患者被纳入本研究。在为期6个月的初始开放耐受性研究中,所有患者均接受美托洛尔50mg每日三次治疗,随后在交叉对照研究中,在双盲条件下将该剂量的疗效与安慰剂进行比较。在每个交叉对照期结束时进行运动试验。与安慰剂相比,美托洛尔50mg每日三次的剂量在心绞痛发作次数、硝酸甘油消耗量以及患者心绞痛症状的每日主观评估方面均有显著改善。美托洛尔在运动能力方面也有显著提高,无论是在出现1mm ST段压低之前还是运动结束时。静息和运动时心率及血压均降低。在为期8个月的本研究期间未观察到严重不良反应,任何时候均无患者出现心力衰竭或肺功能障碍的体征或症状。报告的不良反应为轻至中度,其发生率与安慰剂治疗期间相同。未观察到异常实验室检查结果,相对心脏容积也无显著变化。美托洛尔50mg每日三次的给药似乎比之前在这些患者中研究过的美托洛尔20mg每日三次更有益。