Pandhi P, Sethi V, Sharma B K, Wahi P L, Sharma P L
Int J Clin Pharmacol Ther Toxicol. 1985 Nov;23(11):598-600.
Twenty-four patients with classical angina of effort completed this double-blind cross-over clinical trial of acebutolol and propranolol. Both acebutolol (100-400 mg) and propranolol (40-160 mg) three times a day produced a significant reduction in the incidence of anginal attacks, consumption of nitroglycerine tablets and increased exercise tolerance. Both drugs produced mild and tolerable side effects which did not require any reduction of doses of the drugs being used. No change in laboratory parameters assessing the function of the liver, the kidneys and the hemopoietic system was found. The commonly accepted dose ratio of 1:2.5 propranolol and acebutolol, respectively, was found to be true in less than 50% of the patients. Therefore, for optimal effect, the dose of acebutolol should be individualized depending upon the response.
24例典型劳力型心绞痛患者完成了醋丁洛尔与普萘洛尔的双盲交叉临床试验。醋丁洛尔(100 - 400毫克)和普萘洛尔(40 - 160毫克)每日三次服用均能显著降低心绞痛发作的发生率、硝酸甘油片的消耗量并提高运动耐量。两种药物均产生了轻微且可耐受的副作用,无需减少所用药物的剂量。未发现评估肝脏、肾脏和造血系统功能的实验室参数有变化。分别为普萘洛尔与醋丁洛尔的1:2.5这一普遍接受的剂量比,在不到50%的患者中被证实。因此,为达到最佳效果,醋丁洛尔的剂量应根据反应个体化调整。