TY - JOUR
T1 - The Prevention of Early Asthma in Kids study
T2 - Design, rationale and methods for the Childhood Asthma Research and Education network
AU - Guilbert, Theresa W.
AU - Morgan, Wayne J.
AU - Krawiec, Marzena
AU - Lemanske, Robert F.
AU - Sorkness, Chris
AU - Szefler, Stanley J.
AU - Larsen, Gary
AU - Spahn, Joseph D.
AU - Zeiger, Robert S.
AU - Heldt, Gregory
AU - Strunk, Robert C.
AU - Bacharier, Leonard B.
AU - Bloomberg, Gordon R.
AU - Chinchilli, Vernon M.
AU - Boehmer, Susan J.
AU - Mauger, Elizabeth A.
AU - Mauger, David T.
AU - Taussig, Lynn M.
AU - Martinez, Fernando D.
PY - 2004/6
Y1 - 2004/6
N2 - 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 μg or placebo via metered-dose inhaler and Aerochamber® 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.
AB - 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 μg or placebo via metered-dose inhaler and Aerochamber® 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.
KW - Allergens
KW - Asthma predictive index
KW - Atopy
KW - Bronchial hyperresponsiveness
KW - Clinical trials
KW - Early childhood asthma
KW - Exhaled nitric oxide
KW - Fluticasone
KW - Glucocorticoids
KW - Intermittent wheezing
KW - Oscillometry
KW - Prevention of asthma
KW - Research network
KW - Spirometry
UR - http://www.scopus.com/inward/record.url?scp=2442587672&partnerID=8YFLogxK
U2 - 10.1016/j.cct.2004.03.002
DO - 10.1016/j.cct.2004.03.002
M3 - Article
C2 - 15157730
AN - SCOPUS:2442587672
SN - 0197-2456
VL - 25
SP - 286
EP - 310
JO - Controlled clinical trials
JF - Controlled clinical trials
IS - 3
ER -