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首页> 外文期刊>Thorax: The Journal of the British Thoracic Society >Dose response study of ipratropium bromide aerosol on maximum exercise performance in stable patients with chronic obstructive pulmonary disease.
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Dose response study of ipratropium bromide aerosol on maximum exercise performance in stable patients with chronic obstructive pulmonary disease.

机译:异丙托溴铵气雾剂对稳定的慢性阻塞性肺疾病患者最大运动能力的剂量反应研究。

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BACKGROUND: Although the bronchodilating effect of inhaled anticholinergics has been established in patients with chronic obstructive pulmonary disease (COPD), their effects on exercise capacity are still controversial. Previous studies have suggested that the standard dosage hardly affects exercise tolerance, whereas higher doses might elicit an improvement. The aim of the present study was to determine the dose of ipratropium bromide aerosol that improves exercise performance using progressive cycle ergometry in patients with stable COPD. METHODS: Twenty men with stable COPD of mean (SD) age 69.2 (4.6) years and forced expiratory volume in one second (FEV1) 1.00 (0.37) 1 were studied in a randomised double blind manner. Each patient received ipratropium bromide in doses of 240 micrograms, 160 micrograms, 80 micrograms, 40 micrograms, and placebo from a metered dose inhaler (MDI) with an InspirEase spacer on five separate days. Spirometric parameters were assessed before and at 30, 60, 90, and 120 minutes after each inhalation, and pulse rate and blood pressure were also measured immediately before each spirometric measurement. Symptom limited progressive (20 watts/min) cycle ergometer exercise tests were performed 90 minutes after each inhalation. RESULTS: Ipratropium bromide in doses of 160 micrograms and 240 micrograms produced a greater increase in FEV1 than 40 micrograms or 80 micrograms ipratropium bromide at all time points. Doses of 160 micrograms and 240 micrograms ipratropium bromide also produced greater increases in maximal work load and maximal oxygen consumption than placebo, whereas 40 micrograms and 80 micrograms ipratropium bromide did not. There was a weak correlation between the change in FEV1 and the change in maximal work load (r = 0.45). No differences were found in pulse rate or blood pressure between the treatment and placebo groups, and no side effects were noted throughout the study. CONCLUSIONS: A dose of at least four times the standard dose of ipratropium bromide from an MDI with a spacer device was necessary to improve maximal cycle exercise capacity in patients with stable COPD. Although the data from cycle ergometry cannot be directly applied to exercise performed during day to day activities, it is conceivable that the recommended doses of ipratropium bromide do not elicit the optimal clinical benefits.
机译:背景:尽管已在慢性阻塞性肺疾病(COPD)患者中确立了吸入抗胆碱能药物的支气管扩张作用,但其对运动能力的影响仍存在争议。先前的研究表明,标准剂量几乎不会影响运动耐力,而更高的剂量可能会引起改善。本研究的目的是使用渐进式循环测力法确定稳定COPD患者的异丙托溴铵气雾剂的剂量,该剂量可改善运动表现。方法:采用随机双盲方法研究了20名平均COPD稳定(SD)平均年龄(SD)为69.2(4.6)岁,一秒用力呼气量(FEV1)1.00(0.37)1的男性。每位患者在五天内分别从带有InspirEase间隔物的定量吸入器(MDI)接受剂量为240微克,160微克,80微克,40微克和安慰剂的异丙托溴铵。在每次吸入之前和之后30、60、90和120分钟评估肺活量参数,并在每次进行肺活量测量之前立即测量脉搏率和血压。每次吸入后90分钟进行症状受限的渐进式(20瓦特/分钟)测功计运动测试。结果:在所有时间点,异丙托溴铵分别为160微克和240微克,其FEV1的增加大于40微克或80微克溴托普铵。 160毫克和240毫克异丙托溴铵的剂量也比安慰剂产生了更大的最大工作负荷和最大耗氧量的增加,而40毫克和80毫克异丙托溴铵却没有。 FEV1的变化与最大工作负荷的变化之间存在弱关联(r = 0.45)。在治疗组和安慰剂组之间未发现脉搏率或血压方面的差异,并且在整个研究中均未发现副作用。结论:使用间隔器从MDI注射异丙托溴铵的剂量至少应为标准剂量的四倍,以提高稳定COPD患者的最大循环运动能力。尽管来自循环测功的数据无法直接应用于日常活动中进行的锻炼,但可以想象推荐剂量的异丙托溴铵不能带来最佳的临床益处。

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