Brandon M L
JAMA. 1976 Feb 16;235(7):736-7.
The bronchodilator efficacy and safety of metaproterenol sulfate were evaluated by double-blind crossover tests against placebo at three intervals during a 90-day treatment period in 50 asthmatic children. One group of 25 patients was continuously treated with metaproterenol syrup, and the other 25 with placebo syrup. Pulmonary function tests showed statistically significant improvements in forced expiratory volume, forced expiratory volume in one second, and peak expiratory flow rate after metaproterenol administration as compared with those measurements after treatment with placebo. Biweekly global evaluations of responses to metaproterenol administration were consistently more favorable than responses to placebo. Tachycardia and blood pressure changes after metaproterenol administration were consistent with the pharmacologic properties of beta-sympathomimetic stimulants. Side effects during metaproterenol treatment were minimal and laboratory data remained normal.
在50名哮喘儿童的90天治疗期内,通过双盲交叉试验,在三个时间间隔对硫酸间羟异丙肾上腺素与安慰剂进行对照,评估了其支气管扩张疗效和安全性。一组25名患者持续接受间羟异丙肾上腺素糖浆治疗,另一组25名患者接受安慰剂糖浆治疗。肺功能测试显示,与安慰剂治疗后的测量值相比,间羟异丙肾上腺素给药后,用力呼气量、一秒用力呼气量和呼气峰值流速有统计学上的显著改善。对间羟异丙肾上腺素给药反应的每两周一次的总体评估始终比对安慰剂的反应更有利。间羟异丙肾上腺素给药后的心动过速和血压变化与β-拟交感神经兴奋剂的药理特性一致。间羟异丙肾上腺素治疗期间的副作用最小,实验室数据保持正常。