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哮喘患者每日两次使用沙美特罗后对沙丁胺醇的支气管扩张剂敏感性降低。

Bronchodilator subsensitivity to salbutamol after twice daily salmeterol in asthmatic patients.

作者信息

Grove A, Lipworth B J

机构信息

Department of Clinical Pharmacology, Ninewells Hospital, University of Dundee, UK.

出版信息

Lancet. 1995 Jul 22;346(8969):201-6. doi: 10.1016/s0140-6736(95)91265-7.

Abstract

In view of current concerns about use of regular beta-2 agonists, and the place of the newer long-acting drugs, we decided to evaluate whether continuous exposure to twice daily salmeterol results in a blunting of the acute bronchodilator response to repeated doses of salbutamol, as might be administered in the management of an acute asthma attack. After a 2 week run-in without beta-2 agonists, 17 asthmatic patients (mean [SE] age 34 [3] years, mean forced expiratory volume in 1 s [FEV1] 64 [2.7]% of predicted) were randomised to receive salmeterol 50 micrograms twice daily or placebo for 4 weeks in a double-blind cross-over fashion. A histamine challenge test was done 12 h after the last dose of each treatment period, and dose-response curves to inhaled salbutamol (200-3200 micrograms) were constructed 36 h after the last dose. Patients treated with salmeterol had reduced bronchodilator responses to salbutamol in terms of FEV1 and peak expiratory flow rate (PEFR) than those treated with placebo. The reduction in response equated with a 2.5-fold and a fourfold greater dose of salbutamol being required to produce a given FEV1 and PEFR, respectively. There was a significant reduction in lymphocyte beta-2 adrenoceptor density after salmeterol compared with placebo and run-in. Salmeterol remained effective in terms of disease control, with a significant improvement in morning PEFR compared with placebo that was maintained over the 4 week treatment period.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

鉴于目前对常规β2激动剂使用的关注以及新型长效药物的地位,我们决定评估每日两次持续使用沙美特罗是否会导致对重复剂量沙丁胺醇的急性支气管扩张反应减弱,因为在急性哮喘发作的治疗中可能会使用沙丁胺醇。在无β2激动剂的2周导入期后,17例哮喘患者(平均[标准误]年龄34[3]岁,平均第1秒用力呼气量[FEV1]为预测值的64[2.7]%)以双盲交叉方式随机接受每日两次50微克沙美特罗或安慰剂治疗4周。在每个治疗期的最后一剂后12小时进行组胺激发试验,并在最后一剂后36小时绘制吸入沙丁胺醇(200 - 3200微克)的剂量反应曲线。与接受安慰剂治疗的患者相比,接受沙美特罗治疗的患者在FEV1和呼气峰值流速(PEFR)方面对沙丁胺醇的支气管扩张反应降低。反应降低相当于分别需要2.5倍和4倍剂量的沙丁胺醇才能产生给定的FEV1和PEFR。与安慰剂和导入期相比,沙美特罗治疗后淋巴细胞β2肾上腺素能受体密度显著降低。沙美特罗在疾病控制方面仍然有效,与安慰剂相比,早晨PEFR有显著改善,并在4周治疗期内维持。(摘要截断于250字)

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