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孟鲁司特对预防运动性支气管收缩的时间效应。

Time-effect of montelukast on protection against exercise-induced bronchoconstriction.

机构信息

Pediatric Department, University of Verona, Verona, Italy.

出版信息

Respir Med. 2011 Dec;105(12):1790-7. doi: 10.1016/j.rmed.2011.08.007. Epub 2011 Aug 23.

Abstract

INTRODUCTION

Montelukast has been proven to assure a protective effect against exercise-induced bronchoconstriction.

AIM

To verify exactly when montelukast begins protection in asthmatic children by evaluating different time intervals between dosing and challenge.

METHODS

In a double blind, placebo-controlled, three day doses, crossover study, patients were randomized to receive in sequence treatment with either a placebo or montelukast and assigned to one of seven groups that were tested 1, 2, 3, 4, 5, 6 and 8 h after drug administration, respectively. For each group, the exercise challenge was always performed at the same hour on the first and third days of treatment.

RESULTS

Sixty-nine asthmatic children took part in the study. On day 3, the mean FEV(1) % fall from baseline was 25.54 (95% CI = 21.63/29.46) and 14.89 (95% CI = 11.85/17.92) for the placebo and active drug (p < 0.05), respectively. On day 1, the mean fall of FEV(1) was 28.20 (95% CI = 24.46/31.94) and 19.01 (95% CI = 15.71/22.31) for the placebo and montelukast (p < 0.05), respectively. Clinical protection was achieved in 21 (30%) and 33 (48%) subjects by montelukast on the first and third days, respectively.

CONCLUSIONS

Montelukast assured protection against exercise-induced bronchoconstriction from the first through the eighth hour from the first day of treatment. However, individual susceptibility to protection was evident since some individuals were not protected at any time. We conclude that in clinical use individual responses to the drug should be carefully evaluated in the follow-up management.

摘要

简介

孟鲁司特已被证明能预防运动引起的支气管收缩。

目的

通过评估不同的给药和激发时间间隔,精确地确定孟鲁司特在哮喘儿童中何时开始发挥保护作用。

方法

在一项双盲、安慰剂对照、三天剂量的交叉研究中,患者随机顺序接受安慰剂或孟鲁司特治疗,并分为七组,分别在给药后 1、2、3、4、5、6 和 8 小时进行检测。对于每组,第一次和第三次治疗的第一天,运动激发总是在同一时间进行。

结果

69 名哮喘儿童参与了这项研究。第 3 天,安慰剂组和活性药物组的 FEV1 从基线的平均下降率分别为 25.54%(95%可信区间为 21.63/29.46)和 14.89%(95%可信区间为 11.85/17.92)(p<0.05)。第 1 天,安慰剂组和孟鲁司特组的 FEV1 平均下降率分别为 28.20%(95%可信区间为 24.46/31.94)和 19.01%(95%可信区间为 15.71/22.31)(p<0.05)。在第一天和第三天,孟鲁司特分别使 21 名(30%)和 33 名(48%)受试者获得临床保护。

结论

孟鲁司特从第一天开始的第一到第八小时都能预防运动引起的支气管收缩。然而,个体对保护的敏感性是明显的,因为有些人在任何时候都没有得到保护。我们的结论是,在临床应用中,应该在随访管理中仔细评估个体对药物的反应。

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