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哮喘患者吸入糖皮质激素后支气管反应性变化的时间进程。

Time course of change in bronchial reactivity with an inhaled corticosteroid in asthma.

作者信息

Vathenen A S, Knox A J, Wisniewski A, Tattersfield A E

机构信息

Respiratory Medicine Unit, City Hospital, Nottingham, England.

出版信息

Am Rev Respir Dis. 1991 Jun;143(6):1317-21. doi: 10.1164/ajrccm/143.6.1317.

Abstract

The time course of change in FEV1, bronchial reactivity, and daily measures of asthma control (peak expiratory flow, symptoms, and beta 2-agonist inhaler use) was determined during 6 wk of treatment with inhaled budesonide, 800 micrograms twice a day, and for 2 wk following cessation of treatment in 40 asthmatic subjects in a double-blind, placebo-controlled, parallel group study. Histamine reactivity, expressed as the provocative dose of histamine causing a 20% fall in FEV1 (PD20), was measured at intervals during the 8 wk of the study, with more frequent measurements after the first and last dose of drug to provide a detailed profile of change at the start and end of treatment. The first dose of budesonide caused a small increase in median values of FEV1 (0.2 L) and PD20 (1.0 doubling dose of histamine), which was maximum at 6 h. There was a further increase in FEV1 and PD20 over the 6 wk in the budesonide group relative to placebo, the maximum increases (0.53 L, 3.4 doubling doses of histamine) being recorded 6 h after the last dose on Day 42. Following cessation of treatment, FEV1 and PD20 declined and PD20 returned to placebo values at 1 wk. Median PEF increased by 40 and 30 L/min in the morning and evening, respectively, with budesonide treatment. Symptom scores and beta 2-agonist inhaler use were lower in the budesonide group than the placebo group during treatment but tended to be similar (symptom scores) or higher (beta 2-agonist) in the 2 wk following cessation of treatment.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在一项双盲、安慰剂对照、平行组研究中,对40名哮喘患者进行了为期6周的治疗,每日两次吸入800微克布地奈德,并在停药后2周进行观察,以确定第一秒用力呼气容积(FEV1)、支气管反应性和哮喘控制的日常指标(呼气峰值流速、症状和β2受体激动剂吸入器使用情况)随时间的变化过程。在研究的8周内定期测量组胺反应性,以引起FEV1下降20%的组胺激发剂量(PD20)表示,在首次和末次给药后更频繁测量,以提供治疗开始和结束时变化的详细情况。布地奈德的首剂使FEV1中位数(0.2升)和PD20(组胺加倍剂量1.0)略有增加,6小时时达到最大值。与安慰剂相比,布地奈德组在6周内FEV1和PD20进一步增加,在第42天末次给药后6小时记录到最大增加量(0.53升,组胺加倍剂量3.4)。停药后,FEV1和PD20下降,1周时PD20恢复到安慰剂值。布地奈德治疗使早晨和晚上的呼气峰值流速中位数分别增加40和30升/分钟。治疗期间布地奈德组的症状评分和β2受体激动剂吸入器使用次数低于安慰剂组,但停药后2周症状评分(趋于相似)或β2受体激动剂使用次数(更高)。(摘要截短于250字)

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