The prevention of early asthma in kids study: design, rationale and methods for the childhood asthma research and education network
被引:146
作者:
Guilbert, TW
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Guilbert, TW
Morgan, WJ
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Morgan, WJ
Krawiec, M
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Krawiec, M
Lemanske, RF
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Lemanske, RF
Sorkness, C
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Sorkness, C
Szefler, SJ
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Szefler, SJ
Larsen, G
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Larsen, G
Spahn, JD
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Spahn, JD
Zeiger, RS
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Zeiger, RS
Heldt, G
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Heldt, G
Strunk, RC
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Strunk, RC
Bacharier, LB
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Bacharier, LB
Bloomberg, GR
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Bloomberg, GR
Chinchilli, VM
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Chinchilli, VM
Boehmer, SJ
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Boehmer, SJ
Mauger, EA
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Mauger, EA
Mauger, DT
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Mauger, DT
Taussig, LM
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Taussig, LM
Martinez, FD
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机构:Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
Martinez, FD
机构:
[1] Univ Arizona, Arizona Resp Ctr, Div Pediat Pulm Med, Tucson, AZ 85724 USA
[2] Univ Wisconsin, Madison, WI USA
[3] New Jewish Med & Res Ctr, Denver, CO USA
[4] Univ Calif San Diego, San Diego, CA 92103 USA
[5] Kaiser Permanente, San Diego, CA USA
[6] Washington Univ, St Louis, MO USA
[7] Penn State Univ, Hershey, PA USA
来源:
CONTROLLED CLINICAL TRIALS
|
2004年
/
25卷
/
03期
关键词:
allergens;
asthma predictive index;
atopy;
bronchial hyperresponsiveness;
clinical trials;
early childhood asthma;
exhaled nitric oxide;
fluticasone;
glucocorticoids;
intermittent wheezing;
oscillometry;
spirometry;
prevention of asthma;
research network;
D O I:
10.1016/j.cct.2004.03.002
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Pediatric asthma remains an important public health concern as its prevalence and cost to the health care system is rising. In order to promote innovative research in asthma therapies, the National Heart, Lung and Blood Institute created the Childhood Asthma Research and Education Network in 1999. As its first study, the steering committee of the Childhood Asthma Research and Education Network designed a randomized clinical trial to determine if persistent asthma could be prevented in children at a high risk to develop the disease. This communication presents the design of its first clinical trial, the Prevention of Asthma in Kids (PEAK) trial and the organization of the Childhood Asthma Research and Education Network that developed and implemented this trial. Studies of the natural history of asthma have shown that, in persistent asthma, the initial asthma-like symptoms and loss of lung function occur predominately during the first years of life. Therefore, in the Prevention of Asthma in Kids study, children 2 and 3 years old with a positive asthma predictive index were randomized to twice daily treatment with fluticasone 88 mug or placebo via metered-dose inhaler and Aerochamber(R) for 2 years. The double blind treatment period was followed by a 1-year observational period. Lung function was measured by spirometry and oscillometry technique at 4-month intervals throughout the study. Bronchodilator reversibility and exhaled nitric oxide (ENO) studies were performed at the end of the treatment and observation periods. The primary outcome measure was the number of asthma-free days. Other secondary outcomes included number of exacerbations, use of asthma medications and lung function. These measures were chosen to reflect the progression of the disease from intermittent wheezing to persistent asthma and measurement of the extent of airflow limitation and airway reactivity. (C) 2004 Elsevier Inc. All rights reserved.