Montelukast and fluticasone compared with salmeterol and fluticasone in protecting against asthma exacerbation in adults: one year, double blind, randomised, comparative trial

被引:137
作者
Bjermer, L
Bisgaard, H
Bousquet, J
Fabbri, LM
Greening, AP
Haahtela, T
Holgate, ST
Picado, C
Menten, J
Dass, SB
Leff, JA
Polos, PG
机构
[1] Merck & Co Inc, Whitehouse Stn, NJ 08889 USA
[2] Univ Hosp, Dept Resp Med & Allergol, SE-22185 Lund, Sweden
[3] Univ Copenhagen Hosp, Dept Paediat, DK-2900 Copenhagen, Denmark
[4] Hosp Arnaud Villeneuve, Serv Malad Resp, F-34295 Montpellier 5, France
[5] Univ Modena, Dept Resp Dis, I-41100 Modena, Italy
[6] Western Gen Hosp, Resp Med Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[7] Helsinki Univ Hosp, Dept Allergol, FIN-00029 Helsinki, Finland
[8] Southampton Gen Hosp, Resp Cell & Mol Biol Res Div, Southampton SO16 6YD, Hants, England
[9] Univ Barcelona, Hosp Clin, Inst Pneumol, Serv Pneumol, E-08036 Barcelona, Spain
来源
BMJ-BRITISH MEDICAL JOURNAL | 2003年 / 327卷 / 7420期
关键词
D O I
10.1136/bmj.327.7420.891
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives To assess the effect of montelukast versus salmeterol added to inhaled fluticasone propionate on asthma exacerbation in patients whose symptoms are inadequately controlled with fluticasone alone. Design and setting A 52 week, two period, double blind, multicentre trial during which patients whose symptoms remained uncontrolled by inhaled corticosteroids were randomised to add montelukast or salmeterol. Participants Patients (15-72 years; n = 1490) had a clinical history of chronic asthma for greater than or equal to1 year, a baseline forced expiratory volume in one second (FEV1) value 50-90% predicted, and a beta agonist improvement of greater than or equal to 12% in FEV1. Main outcome measures The primary end point was the percentage of patients with at least one asthma exacerbation. Results 20.1% of the patients in the group receiving montelukast and fluticasone had an asthma exacerbation compared with 19.1% in the group receiving salmeterol and fluticasone; the difference was 1% (95% confidence interval - 3.1% to 5.0%). With a risk ratio (montelukast-fluticasone/ salmeterol-fluticasone) of 1.05 (0.86 to 1.29), treatment with montelukast and fluticasone was shown to be non-inferior to treatment with salmeterol and fluticasone. Salmeterol and fluticasonc significantly increased FEV1 before a beta agonist was used and morning peak expiratory flow compared with montelukast and fluticasone (P less than or equal to0.001), whereas FEV1 after a beta agonist was used and improvements in asthma specific quality of life and nocturnal awakenings were similar between the groups. Montelukast and fluticasone significantly (P = 0.011) reduced peripheral blood eosinophil counts compared with salmeterol and fluticasone. Both treatments were generally well tolerated. Conclusion The addition of montelukast in patients whose symptoms remain uncontrolled by inhaled fluticasone could provide equivalent clinical control to salmeterol.
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收藏
页码:891 / 895
页数:7
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