TY - JOUR
T1 - Modeling asthma exacerbations through lung function in children
AU - Wu, Ann Chen
AU - Gregory, Martin
AU - Kymes, Steven
AU - Lambert, Dennis
AU - Edler, Joshua
AU - Stwalley, Dustin
AU - Fuhlbrigge, Anne L.
PY - 2012/11
Y1 - 2012/11
N2 - Background: Formal economic evaluation using a model-based approach is playing an increasingly important role in health care decision making. Objective: To develop a model by using an objective measure of lung function - prebronchodilator FEV1 as a percent of predicted (FEV1% predicted) - as the primary independent factor to predict the frequency of adverse events related to the exacerbation of asthma on a population level. Methods: We developed a Markov simulation model of childhood asthma by using data from the Childhood Asthma Management Program. The primary outcomes were the result of asthma exacerbations defined as hospitalizations, emergency department (ED) visits, and the need for oral corticosteroid therapy. Predicted monthly frequencies for each acute event were based on negative binomial regression equations estimated from the placebo arm of the Childhood Asthma Management Program with covariates of age, prebronchodilator FEV1% predicted, time in study, prior hospitalizations, and prior nocturnal awakenings. Results: Simulated versus observed mean number of acute events were similar within the placebo and treatment groups. While the trial demonstrated treatment effects of 48% reduction in hospitalizations, 46% reduction in ED visits, and 44% reduction in the need for oral corticosteroid therapy at 48 months, the model simulated similar reductions of 49% in hospitalizations, 41% in ED visits, and 46% in the need for oral corticosteroid therapy. Conclusions: Our findings suggest that longitudinal intervention effects may be modeled through FEV1% predicted to estimate hospitalizations, ED visits, and need for oral corticosteroid therapy in childhood asthma for planning and evaluation purposes.
AB - Background: Formal economic evaluation using a model-based approach is playing an increasingly important role in health care decision making. Objective: To develop a model by using an objective measure of lung function - prebronchodilator FEV1 as a percent of predicted (FEV1% predicted) - as the primary independent factor to predict the frequency of adverse events related to the exacerbation of asthma on a population level. Methods: We developed a Markov simulation model of childhood asthma by using data from the Childhood Asthma Management Program. The primary outcomes were the result of asthma exacerbations defined as hospitalizations, emergency department (ED) visits, and the need for oral corticosteroid therapy. Predicted monthly frequencies for each acute event were based on negative binomial regression equations estimated from the placebo arm of the Childhood Asthma Management Program with covariates of age, prebronchodilator FEV1% predicted, time in study, prior hospitalizations, and prior nocturnal awakenings. Results: Simulated versus observed mean number of acute events were similar within the placebo and treatment groups. While the trial demonstrated treatment effects of 48% reduction in hospitalizations, 46% reduction in ED visits, and 44% reduction in the need for oral corticosteroid therapy at 48 months, the model simulated similar reductions of 49% in hospitalizations, 41% in ED visits, and 46% in the need for oral corticosteroid therapy. Conclusions: Our findings suggest that longitudinal intervention effects may be modeled through FEV1% predicted to estimate hospitalizations, ED visits, and need for oral corticosteroid therapy in childhood asthma for planning and evaluation purposes.
KW - Asthma
KW - FEV% predicted
KW - emergency department visits
KW - hospitalizations
KW - lung function
KW - model
KW - pediatric patients
UR - http://www.scopus.com/inward/record.url?scp=84869143758&partnerID=8YFLogxK
U2 - 10.1016/j.jaci.2012.08.009
DO - 10.1016/j.jaci.2012.08.009
M3 - Article
C2 - 23021884
AN - SCOPUS:84869143758
SN - 0091-6749
VL - 130
SP - 1065
EP - 1070
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 5
ER -