非诺特罗加异丙托溴铵(Duovent)气雾剂和粉剂在哮喘和慢性支气管炎患者中的应用比较。

Pharmatherapeutica Pub Date : 1988-01-01
G I Town
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引用次数: 0

摘要

对15名稳定型哮喘患者和5名部分可逆性气流阻塞患者进行了一项研究,以比较单剂量200微克非诺特罗加80微克异丙托普溴化铵('Duovent')的疗效和耐受性,这两种剂量分别是通过计量气溶胶或作为干粉制剂用于吸入('Inhalets')。采用双假人技术,患者在1周内的2天随机接受每种制剂。在给药后6小时内进行肺活量测定。结果显示,每一种给药方法的平均FEV1峰值改善达35%,且反应之间无统计学差异。25%的改善持续超过4小时,两种制剂对脉搏率和震颤的影响相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison between aerosol and powder delivery system of fenoterol plus ipratropium bromide ('Duovent') in patients with asthma and chronic bronchitis.

A study was carried out in 15 stable asthmatics and 5 patients with partially reversible airflow obstruction to compare the efficacy and tolerability of a single dose of 200 micrograms fenoterol plus 80 micrograms ipratropium bromide ('Duovent') administered either by metered dose aerosol or as a dry powder preparation for inhalation ('Inhalets'). Using a double-dummy technique, patients received each formulation, in random order, on 2 separate days within 1 week. Spirometric measurements were made over a period of 6 hours after the dose. The results showed that a 35% peak improvement in mean FEV1 occurred with each method of administration and there was no statistical difference between responses. Improvements of 25% were sustained for over 4 hours and effects on pulse rate and tremor were similar for both preparations.

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