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丙酸倍氯米松对哮喘气道反应性的剂量相关效应。

Dose-related effect of beclomethasone dipropionate on airway responsiveness in asthma.

作者信息

Carpentiere G, Marino S, Castello F, Baldanza C, Bonanno C T

机构信息

Istituto di Clinica Medica, Università degli Studi di Palermo, Italia.

出版信息

Respiration. 1990;57(2):100-3. doi: 10.1159/000195828.

Abstract

The effects of twice daily inhaled beclomethasone dipropionate (BDP) at two dose levels (500 and 1,000 micrograms daily) on the airway responsiveness to inhaled histamine was evaluated by a randomized, single-blind, cross-over study in 10 patients with stable asthma. The 12-week study began with a 3-week run-in period of baseline treatment, which was continued unchanged throughout the study, and the two treatment periods were separated by a 3-week placebo period. Patients attended the laboratory every 3 weeks for spirometry and histamine inhalation tests to determine the provocative concentration of histamine causing a 20% fall in forced expiratory volume in 1 s (PC20 of FEV1). There was a similar significant improvement (p less than 0.05) in mean FEV1 after both treatments. There was no significant change in PC20 after treatment with 500 micrograms daily, the geometric mean being 0.587 mg/ml after the placebo period and 0.860 mg/ml after BDP treatment. There was a significant improvement in PC20 (1.930 mg/ml) after treatment with 1,000 micrograms BDP daily in comparison with the placebo and treatment periods with 500 micrograms BDP daily (p less than 0.001). These results suggest that higher doses than usual of inhaled BDP must be used to control airway responsiveness in asthmatics.

摘要

通过一项随机、单盲、交叉研究,对10例稳定期哮喘患者评估了每日两次吸入两种剂量(分别为每日500微克和1000微克)的二丙酸倍氯米松(BDP)对吸入组胺的气道反应性的影响。这项为期12周的研究开始于为期3周的基线治疗导入期,该基线治疗在整个研究过程中保持不变,两个治疗期之间间隔3周的安慰剂期。患者每3周前往实验室进行肺活量测定和组胺吸入试验,以确定导致第1秒用力呼气量下降20%的组胺激发浓度(FEV1的PC20)。两种治疗后平均FEV1均有类似的显著改善(p<0.05)。每日500微克治疗后PC20无显著变化,安慰剂期后几何平均值为0.587毫克/毫升,BDP治疗后为0.860毫克/毫升。与安慰剂期及每日500微克BDP治疗期相比,每日1000微克BDP治疗后PC20有显著改善(1.930毫克/毫升)(p<0.001)。这些结果表明,必须使用比通常更高剂量的吸入BDP来控制哮喘患者的气道反应性。

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