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溴沙特罗(Z.1170),一种新型口服β2受体激动剂,与沙丁胺醇的比较。

Broxaterol (Z.1170), a new oral beta 2-agonist compared with salbutamol.

作者信息

Perruchoud A P, Bründler H, Godly R, Imhof E, Herzog H

出版信息

Respiration. 1987;51(2):113-8. doi: 10.1159/000195177.

Abstract

The bronchodilating activity and tolerability of a single 0.5-mg oral dose of broxaterol (Z.1170) were evaluated in 18 patients with reversible bronchial obstruction. Salbutamol 4.0 mg and placebo were used as controls. The study design was double-blind within patients. The forced expiratory volume in 1 s (FEV1), pulse rate, and blood pressure were measured immediately before and 0.5, 1, 2, 3, 4, 5, and 6 h after each treatment. At the same time clinical controls were made to detect the possible presence of side effects. Both broxaterol and salbutamol caused significant increases in FEV1 until the 5th hour as compared to baseline values and until the 2nd hour as compared to placebo. No significant difference was reported between the effects of broxaterol and those of salbutamol at all the times considered. The tolerability of broxaterol was good, as was that of salbutamol. The pulse rate and blood pressure did not show any significant clinical variations. The side effect reported most frequently was tremor.

摘要

对18例可逆性支气管阻塞患者评估了单次口服0.5毫克溴沙特罗(Z.1170)的支气管扩张活性和耐受性。使用4.0毫克沙丁胺醇和安慰剂作为对照。研究设计为患者内双盲。在每次治疗前以及治疗后0.5、1、2、3、4、5和6小时立即测量1秒用力呼气量(FEV1)、脉搏率和血压。同时进行临床对照以检测可能出现的副作用。与基线值相比,溴沙特罗和沙丁胺醇均使FEV1在第5小时前显著增加,与安慰剂相比在第2小时前显著增加。在所有考虑的时间点,溴沙特罗和沙丁胺醇的效果之间均未报告有显著差异。溴沙特罗的耐受性良好,沙丁胺醇也是如此。脉搏率和血压未显示任何显著的临床变化。最常报告的副作用是震颤。

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