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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.
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页码:1110 / 1120
页数:11
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