Ikeda A, Nishimura K, Koyama H, Izumi T
Chest Disease Research Institute, Kyoto University, Japan.
Thorax. 1995 Jan;50(1):62-6. doi: 10.1136/thx.50.1.62.
Inhaled anticholinergics and beta agonists are widely used in the treatment of patients with chronic obstructive pulmonary disease (COPD). However, dosage requirements have not been thoroughly evaluated and comparative dose-response data for these agents are limited.
Twenty men with stable COPD of mean (SD) age 69.4 (5.8) years and FEV1 0.93 (0.38) litres were studied in randomised, double blind, crossover, placebo controlled experiments. All of the patients received two, four, eight, and 16 puffs of ipratropium bromide (20 micrograms/puff), flutropium bromide (30 micrograms/puff), oxitropium bromide (100 micrograms/puff), fenoterol (200 micrograms/puff), or placebo in random order on five separate days. Doses were administered by a metered dose inhaler at intervals of 60 minutes to give cumulative doses of two, six, 14, and 30 puffs. Five mg of nebulised salbutamol was administered 60 minutes after the patient had received the final 16 puffs of each regimen. Forced expiratory volume in one second (FEV1), forced vital capacity (FVC), heart rate, and blood pressure were measured five minutes before each treatment and 30 minutes after treatment with nebulised salbutamol.
FEV1 and FVC reached a plateau after administration of a cumulative dose of 14 puffs of ipratropium bromide (280 micrograms) or flutropium bromide (420 micrograms), and after six puffs of oxitropium bromide (600 micrograms). There were no differences with respect to maximum increases in FEV1 and FVC amongst the three anticholinergic agents. However, after six puffs oxitropium bromide produced a greater increase in FEV1 than either ipratropium bromide or flutropium bromide. Fenoterol caused a greater increase in both FEV1 and FVC than the three anticholinergic agents after six puffs, as well as a greater increase in pulse rate. Oxitropium bromide produced a greater increase in pulse rate than the other anticholinergics after 14 puffs. The incidence of side effects was dose-related and notable adverse effects were reported after 30 puffs of ipratropium bromide, 14 puffs of oxitropium bromide, and two puffs of fenoterol.
Oxitropium bromide produced a greater bronchodilator effect than either ipratropium bromide or flutropium bromide when used at doses of less than six puffs, without apparent side effects. There were, however, no differences in maximal response between these drugs. Fenoterol may have a greater peak bronchodilator effect than the anticholinergic agents but it causes more adverse effects, even at lower doses. Depending upon the balance between efficacy and side effects, oxitropium bromide may be preferred in the treatment of patients with COPD.
吸入性抗胆碱能药物和β受体激动剂广泛用于慢性阻塞性肺疾病(COPD)患者的治疗。然而,剂量需求尚未得到充分评估,且这些药物的比较剂量反应数据有限。
在随机、双盲、交叉、安慰剂对照实验中,对20名平均(标准差)年龄为69.4(5.8)岁、第一秒用力呼气容积(FEV1)为0.93(0.38)升的稳定期COPD男性患者进行了研究。所有患者在五个不同的日子里,以随机顺序接受两次、四次、八次和十六次异丙托溴铵(20微克/喷)、氟托溴铵(30微克/喷)、氧托溴铵(100微克/喷)、非诺特罗(200微克/喷)或安慰剂吸入。剂量通过定量吸入器每隔60分钟给药一次,累积剂量分别为两次、六次、十四次和三十次喷量。在患者接受每种方案的最后16次喷量后60分钟,给予5毫克雾化沙丁胺醇。在每次治疗前5分钟和雾化沙丁胺醇治疗后30分钟,测量第一秒用力呼气容积(FEV1)、用力肺活量(FVC)、心率和血压。
累积给予14次喷量的异丙托溴铵(280微克)或氟托溴铵(420微克),以及6次喷量的氧托溴铵(600微克)后,FEV1和FVC达到平台期。三种抗胆碱能药物在FEV1和FVC的最大增加量方面没有差异。然而,6次喷量后,氧托溴铵使FEV1的增加量大于异丙托溴铵或氟托溴铵。6次喷量后,非诺特罗使FEV1和FVC的增加量均大于三种抗胆碱能药物,且使脉搏率增加更多。14次喷量后,氧托溴铵使脉搏率的增加量大于其他抗胆碱能药物。副作用的发生率与剂量相关,在给予30次喷量的异丙托溴铵、14次喷量的氧托溴铵和2次喷量的非诺特罗后,报告了明显的不良反应。
当氧托溴铵使用剂量小于6次喷量时,其支气管扩张作用大于异丙托溴铵或氟托溴铵,且无明显副作用。然而,这些药物之间的最大反应没有差异。非诺特罗的支气管扩张峰值效应可能大于抗胆碱能药物,但即使在较低剂量下也会引起更多不良反应。根据疗效和副作用之间的平衡,氧托溴铵可能是治疗COPD患者的首选药物。