Asthma exacerbations and sputum eosinophil counts: a randomised controlled trial

被引:1349
作者
Green, RH [1 ]
Brightling, CE [1 ]
McKenna, S [1 ]
Hargadon, B [1 ]
Parker, D [1 ]
Bradding, P [1 ]
Wardlaw, AJ [1 ]
Pavord, ID [1 ]
机构
[1] Glenfield Hosp, Inst Lung Hlth, Dept Resp Med & Thorac Surg, Leicester LE3 9PQ, Leics, England
关键词
D O I
10.1016/S0140-6736(02)11679-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Treatment decisions in asthma are based on assessments of symptoms and simple measures of lung function, which do not relate closely to underlying eosinophilic airway inflammation. We aimed to assess whether a management strategy that minimises eosinophilic inflammation reduces asthma exacerbations compared with a standard management strategy. Methods We recruited 74 patients with moderate to severe asthma from hospital clinics and randomly allocated them to management either by standard British Thoracic Society asthma guidelines (BTS management group) or by normalisation of the induced sputum eosinophil count and reduction of symptoms (sputum management group). We assessed patients nine times over 12 months. The results were used to manage those in the sputum management group, but were not disclosed in the BTS group. The primary outcomes were the number of severe exacerbations and control of eosinophilic inflammation, measured by induced sputum eosinophil count. Analyses were by intention to treat. Findings The sputum eosinophil count was 63% (95% CI 24-100) lower over 12 months in the sputum management group than in the BTS management group (p=0.002). Patients in the sputum management group had significantly fewer severe asthma exacerbations than did patients in the BTS management group (35 vs 109; p=0.01) and significantly fewer patients were admitted to hospital with asthma (one vs six, p=0.047). The average daily dose of inhaled or oral corticosteroids did not differ between the two groups. Interpretation A treatment strategy directed at normalisation of the induced sputum eosinophil count reduces asthma exacerbations and admissions without the need for additional anti-inflammatory treatment.
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页码:1715 / 1721
页数:7
相关论文
共 32 条
[11]  
Juniper E, 1994, HISTAMINE METHACHOLI
[12]   MEASURING QUALITY-OF-LIFE IN ASTHMA [J].
JUNIPER, EF ;
GUYATT, GH ;
FERRIE, PJ ;
GRIFFITH, LE .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1993, 147 (04) :832-838
[13]   Exhaled and nasal nitric oxide measurements: Recommendations [J].
Kharitonov, S ;
Alving, K ;
Barnes, PJ .
EUROPEAN RESPIRATORY JOURNAL, 1997, 10 (07) :1683-1693
[14]   Effects of an interleukin-5 blocking monoclonal antibody on eosinophils, airway hyper-responsiveness, and the late asthmatic response [J].
Leckie, MJ ;
ten Brinke, A ;
Khan, J ;
Diamant, Z ;
O'Connor, BJ ;
Walls, CM ;
Mathur, AK ;
Cowley, HC ;
Chung, KF ;
Djukanovic, R ;
Hansel, TT ;
Holgate, T ;
Sterk, PJ ;
Barnes, PJ .
LANCET, 2000, 356 (9248) :2144-2148
[15]  
Louis R, 2000, CLIN EXP ALLERGY, V30, P1151
[16]  
NETTON A, 2001, UNIT COSTS HLTH SOCI
[17]  
*NHS, 2001, NEW NHS 2001 REF COS
[18]   Clinical judgement of airway inflammation versus sputum cell counts in patients with asthma [J].
Parameswaran, K ;
Pizzichini, E ;
Pizzichini, MM ;
Hussack, P ;
Efthimiadis, A ;
Hargreave, FE .
EUROPEAN RESPIRATORY JOURNAL, 2000, 15 (03) :486-490
[19]   Effect of inhaled formoterol and budesonide on exacerbations of asthma [J].
Pauwels, RA ;
Lofdahl, CG ;
Postma, DS ;
Tattersfield, AE ;
OByrne, P ;
Barnes, PJ ;
Ullman, A .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (20) :1405-1411
[20]   Non-eosinophilic corticosteroid unresponsive asthma [J].
Pavord, ID ;
Brightling, CE ;
Woltmann, G ;
Wardlaw, AJ .
LANCET, 1999, 353 (9171) :2213-2214