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一种新型β2激动剂能否降低哮喘死亡率?

Can a new beta 2-agonist reduce the mortality of asthma?

作者信息

Aldons P M

机构信息

Prince Charles Hospital, Brisbane, Queensland, Australia.

出版信息

Lung. 1990;168 Suppl:186-91. doi: 10.1007/BF02718131.

DOI:10.1007/BF02718131
PMID:1974675
Abstract

Tulobuterol is a synthetic beta-adrenergic agonist which, when administered orally, is a potent, long-acting bronchodilator. The safety and efficacy of 2 mg tulobuterol tablets taken twice daily was compared to that of 4 mg salbutamol tablets taken three times daily for a period of 12 weeks in outpatients with stable chronic asthma in a randomized, double-blind, multi-center study conducted in Australia. Strict entry criteria were employed; only those patients whose baseline FEV1 value was between 40-70% of the predicted normal value and increased at least 20% after two inhalations of a metered dose (250 micrograms per dose) of terbutaline aerosol at a screening visit were included. Treatment with active study drug was preceded by a 2 week single-blind, placebo lead-in period. The onset and duration of the bronchodilating effect was studied on the first day of the placebo lead-in period and on the first and last days of the 12 week parallel design treatment period. Of 140 patients enrolled, 73 had tulobuterol and 67 had salbutamol. Of these, 61 tulobuterol and 59 salbutamol treated patients could be evaluated for efficacy. Of the 140 patients, 129 completed the study. All patients were issued a mini peak flow meter and diary cards to record daily PEFRs and symptoms of airways obstruction throughout the study. The demographics of the patients in both treatment groups were similar in all modalities: they were comparable in age, duration of asthma, mean FEV1 (expressed as percent of predicted normal), and reversibility (as demonstrated by an increase in FEV1 after administration of a beta 2-agonist aerosol).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

妥洛特罗是一种合成的β-肾上腺素能激动剂,口服时是一种强效、长效的支气管扩张剂。在澳大利亚进行的一项随机、双盲、多中心研究中,将每日两次服用2mg妥洛特罗片的安全性和有效性与每日三次服用4mg沙丁胺醇片的安全性和有效性进行了比较,研究对象为稳定期慢性哮喘门诊患者,为期12周。采用了严格的入选标准;仅纳入那些基线第一秒用力呼气容积(FEV1)值在预测正常值的40%-70%之间,且在筛查访视时吸入两剂定量(每剂250微克)特布他林气雾剂后FEV1至少增加20%的患者。在使用活性研究药物治疗之前,有一个为期2周的单盲、安慰剂导入期。在安慰剂导入期的第一天以及12周平行设计治疗期的第一天和最后一天研究了支气管扩张作用的起效时间和持续时间。在140名入选患者中,73名服用妥洛特罗,67名服用沙丁胺醇。其中,61名服用妥洛特罗和59名服用沙丁胺醇的患者可进行疗效评估。140名患者中有129名完成了研究。在整个研究过程中,所有患者都发放了一个小型峰值流量计和日记卡,以记录每日的呼气峰值流速(PEFR)和气道阻塞症状。两个治疗组患者的人口统计学特征在所有方面都相似:他们在年龄、哮喘病程、平均FEV1(以预测正常值的百分比表示)和可逆性(通过给予β2-激动剂气雾剂后FEV1增加来证明)方面具有可比性。(摘要截短于250字)

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