OBJECTIVE INDICATORS OF SEVERITY OF ASTHMA

被引:13
作者
PERIN, PV
WELDON, D
MCGEADY, SJ
机构
[1] THOMAS JEFFERSON UNIV,DIV CLIN IMMUNOL & ALLERGY,PHILADELPHIA,PA 19107
[2] CHILDRENS REHABIL HOSP,PHILADELPHIA,PA
关键词
D O I
10.1016/0091-6749(94)90208-9
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Subjects with asthma who are intensively treated in residential care facilities frequently demonstrate marked clinical improvement in their disease, with fewer attacks and improved well being. Despite their improved status it is known that pulmonary function test results often remain abnormal in patients with asthma. This prospective study on children with asthma receiving residential care was carried out to determine which pulmonary function parameter best reflected clinical improvement through correlation with the duration of complete freedom from wheezing. Evaluated in 42 children were spirometry values including forced vital capacity forced expiratory volume in 1 second, peak expiratory pow rate, forced expiratory pow (between 25% and 75% of forced vital capacity), and lung volumes as reflected by residual volume/total lung capacity. Bronchial hyperreactivity as reflected by bimonthly provocative concentration causing a 20% fall in FEV(1) in response to methacholine inhalation was evaluated in 18 patients. All pulmonary function test results were correlated with days since last wheezing episode. Results indicate that only peak expiratory pow rate (r = 0.91; p < 0.001), forced expiratory volume in 1 second (r = 0.69; p < 0.01), and forced expiratory flow (r = 0.62; p < 0.05) demonstrated significant correlation with the number of days since last wheezing episode. Of particular interest was the failure of bronchial hyperreactivity to improve despite intensive therapy with bronchodilators and corticosteroids. Persistence of bronchial hyperreactivity despite intensive therapy with corticosteroids suggests that in at least some children with severe asthma, bronchial hyperreactivity may be especially long-lived may be perpetuated by inhaled beta(2) agonists, or may exist independently of airway inflammation.
引用
收藏
页码:517 / 522
页数:6
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