Down-titration from high-dose combination therapy in asthma: Removal of long-acting β2-agonist

被引:52
|
作者
Reddel, Helen K. [1 ]
Gibson, Peter G. [2 ]
Peters, Matthew J. [3 ]
Wark, Peter A. B. [2 ]
Sand, Ingrid B. [4 ]
Hoyos, Camilla M. [1 ]
Jenkins, Christine R. [1 ]
机构
[1] Woolcock Inst Med Res, Camperdown, NSW 2050, Australia
[2] John Hunter Hosp, Hunter Med Res Inst, New Lambton, NSW 2305, Australia
[3] Concord Repatriat Gen Hosp, Concord, NSW 2139, Australia
[4] GlaxoSmithKline Australia, Boronia, Vic 3155, Australia
关键词
Asthma; Down-titration; Combination ICS/LABA therapy; Treatment outcomes; QUALITY-OF-LIFE; INHALED CORTICOSTEROIDS; INDUCED SPUTUM; RESPONSIVENESS; EXACERBATIONS; QUESTIONNAIRE; BUDESONIDE; MARKERS; ADULTS; SCALE;
D O I
10.1016/j.rmed.2010.04.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Asthma guidelines recommend reducing inhaled corticosteroids (ICS) to the minimum effective dose, but the timing of long-acting beta(2)-agonist (LABA) withdrawal is unclear. Recent FDA guidelines recommend LABA withdrawal once asthma is well-controlled. This 13-month double-blind study of patients taking high-dose combination therapy investigated the effect of discontinuation of LABA before ICS down-titration. Methods: Adults using salmeterol/fluticasone combination (SFC) 50/500 mu g bd were randomized to SFC 50/500 mu g bd or fluticasone propionate (FP) 500 mu g bd, with subsequent ICS down-titration 8-weekly using a clinical algorithm. The primary outcome was mean daily FP dose, including ICS for exacerbations. Results: 82 subjects were randomized. Asthma was well-controlled at baseline, with mean FEV1 84.8% predicted and Asthma Control Questionnaire (ACQ) score 0.9. There was no significant difference in mean daily FP dose (SFC: 721 mu g, FP:816 mu g, p = 0.3), but final dose was lower with SFC (534 mu g cf. 724 mu g, p = 0.005). ICS dose was reduced by >= 80% in 41% SFC and 15% FP patients. Ambulatory lung function was significantly higher with SFC, but there were no differences between groups in rescue beta(2)-agonist use, clinic spirometry, airway responsiveness, ACQ, sputum eosinophils or FeNO. Baseline airway responsiveness, and pre-reduction blood eosinophils, were significant predictors of mean daily FP dose and dose reduction failure respectively. Conclusions: Many patients prescribed high-dose combination therapy may be over-treated. Substantial reductions in dose can be achieved with a clinical algorithm, reaching lower FP doses with SFC than FP without losing asthma control or increasing disease activity. Trial Registration: This study was commenced before mandatory registration of clinical trials. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1110 / 1120
页数:11
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