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
相关论文
共 50 条
  • [1] Inhaled Corticosteroid/Long-Acting β2-Agonist Combination Therapy for Asthma: Attitudes of Specialists in Europe
    Bousquet, Jean
    Winchester, Chris
    Papi, Alberto
    Virchow, J. Christian
    Haughney, John
    Costa, David
    Usmani, Omar
    Bjermer, Leif
    Price, David
    INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 2012, 157 (03) : 303 - 310
  • [2] Combination inhaled corticosteroid and long-acting β2-agonist use and severe asthma exacerbations
    Pedersen, Soren
    O'Byrne, Paul M.
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2012, 129 (05) : 1280 - 1281
  • [3] Role of Long-Acting Muscarinic Antagonist/Long-Acting β2-Agonist Therapy in Chronic Obstructive Pulmonary Disease
    Petite, Sarah E.
    ANNALS OF PHARMACOTHERAPY, 2017, 51 (08) : 696 - 705
  • [4] Transdermal Tulobuterol Patch, a Long-Acting β2-Agonist
    Tamura, Gen
    Ichinose, Masakazu
    Fukuchi, Yoshinosuke
    Miyamoto, Terumasa
    ALLERGOLOGY INTERNATIONAL, 2012, 61 (02) : 219 - 229
  • [5] Comparison between montelukast and tiotropium as add-on therapy to inhaled corticosteroids plus a long-acting β2-agonist in for patients with asthma
    Hoshino, Makoto
    Akitsu, Kenta
    Ohtawa, Junichi
    JOURNAL OF ASTHMA, 2019, 56 (09) : 995 - 1003
  • [6] Indacaterol: A Novel Long-Acting β2-Agonist
    Ray, Shaunta' M.
    McMillen, James C.
    Treadway, Sarah A.
    Helmer, Robert S.
    Franks, Andrea S.
    PHARMACOTHERAPY, 2012, 32 (05): : 456 - 474
  • [7] The long-acting β2-agonist salmeterol xinafoate:: effects on airway inflammation in asthma
    Roberts, JA
    Bradding, P
    Britten, KM
    Walls, AF
    Wilson, S
    Gratziou, C
    Holgate, ST
    Howarth, PH
    EUROPEAN RESPIRATORY JOURNAL, 1999, 14 (02) : 275 - 282
  • [8] Combination therapy with a long-acting β-agonist and a leukotriene antagonist in moderate asthma
    Deykin, Aaron
    Wechsler, Michael E.
    Boushey, Homer A.
    Chinchilli, Vernon M.
    Kunselman, Susan J.
    Craig, Timothy J.
    DiMango, Emily
    Fahy, John V.
    Kraft, Monica
    Leone, Frank
    Lazarus, Stephen C.
    Lemanske, Robert F., Jr.
    Martin, Richard J.
    Pesola, Gene R.
    Peters, Stephen P.
    Sorkness, Christine A.
    Szefler, Stanley J.
    Israel, Elliot
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2007, 175 (03) : 228 - 234
  • [9] Real-world effects of two inhaled corticosteroid/long-acting β2-agonist combinations in the treatment of asthma
    Yatera, Kazuhiro
    Yamasaki, Kei
    Nishida, Chinatsu
    Noguchi, Shingo
    Oda, Keishi
    Akata, Kentarou
    Nagata, Shuya
    Kawanami, Yukiko
    Kawanami, Toshinori
    Ishimoto, Hiroshi
    Mukae, Hiroshi
    JOURNAL OF ASTHMA, 2014, 51 (07) : 762 - 768
  • [10] Engineering of Crystalline Combination Inhalation Particles of a Long-Acting β2-agonist and a Corticosteroid
    Pitchayajittipong, Chonladda
    Shur, Jagdeep
    Price, Robert
    PHARMACEUTICAL RESEARCH, 2009, 26 (12) : 2657 - 2666