Randomised controlled trial of montelukast plus inhaled budesonide versus double dose inhaled budesonide in adult patients with asthma

被引:141
作者
Price, DB
Hernandez, D
Magyar, P
Fiterman, J
Beeh, KM
James, IG
Konstantopoulos, S
Rojas, R
van Noord, JA
Pons, M
Gilles, L
Leff, JA
机构
[1] Univ Aberdeen, Foresterhill Hlth Ctr, Dept Gen Practice & Primary Care, Aberdeen AB25 2AY, Scotland
[2] Hosp Civil Guadalajara, Guadalajara, Jalisco, Mexico
[3] Semmelweis Univ, Dept Pulmonol, H-1085 Budapest, Hungary
[4] Pucrs Med Sch, Porto Alegre, RS, Brazil
[5] Univ Hosp Mainz, Div Pulm, Mainz, Germany
[6] Spring House Surg, Bolton, Lancs, England
[7] Univ Hosp Ioannina, Sch Med, Pneumonol Clin, Ioannina, Greece
[8] Univ Nacl Tucuman, RA-4000 San Miguel De Tucuman, Tucuman, Argentina
[9] Atrium Med Ctr, Dept Pulmonol, Heerlen, Netherlands
[10] Osped Civ, Lugano, Switzerland
[11] Merck & Co Inc, Whitehouse Stn, NJ USA
关键词
LEUKOTRIENE RECEPTOR ANTAGONIST; QUALITY-OF-LIFE; DOUBLE-BLIND; FLUTICASONE PROPIONATE; BECLOMETHASONE; INFLAMMATION; SALMETEROL; CHILDREN; HYPERRESPONSIVENESS; DISEASE;
D O I
10.1136/thorax.58.3.211
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Inhaled corticosteroids (ICS) affect many inflammatory pathways in asthma but have little impact on cysteinyl leukotrienes. This may partly explain persistent airway inflammation during chronic ICS treatment and failure to achieve adequate asthma control in some patients. This double blind, randomised, parallel group, non-inferiority, multicentre 16 week study compared the clinical benefits of adding montelukast to budesonide with doubling the budesonide dose in adults with asthma. Methods: After a 1 month single blind run in period, patients inadequately controlled on inhaled budesonide (800 mug/day) were randomised to receive montelukast 10 mg + inhaled budesonide 800 mug/day (n=448) or budesonicle 1600 mug/day (n=441) for 12 weeks. Results: Both groups showed progressive improvement in several measures of asthma control compared with baseline. Mean morning peak expiratory flow (AM PEF) improved similarly in the last 10 weeks of treatment compared with baseline in both the montelukast + budesonide group and in the double dose budesonide group (33.5 v 30.1 l/min). During days 1-3 after start of treatment, the change in AM PEF from baseline was significantly greater in the montelukast + budesonide group than in the double dose budesonicle group (20.1 v 9.6 l/min, p<0.001), indicating faster onset of action in the montelukast group. Both groups showed similar improvements with respect to "as needed" 0 agonist use, mean daytime symptom score, nocturnal awakenings, exacerbations, asthma free days, peripheral eosinophil counts, and asthma specific quality of life. Both montelukast + buclesonide and double dose budesonide were generally well tolerated. Conclusion: The addition of montelukast to inhaled budesonide is an effective and well tolerated alternative to doubling the dose of inhaled budesonicle in adult asthma patients experiencing symptoms and inadequate control on budesonide alone.
引用
收藏
页码:211 / 216
页数:6
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