Why the study?
The study aims to quantify asthma risk by age 5 and 10 years after high-dose corticosteroid and epinephrine treatment for infant bronchiolitis, identify risk factors, and build prediction models.
Does combined therapy of high-dose corticosteroids and nebulised epinephrine for bronchiolitis during infancy affect the risk of developing asthma by age 5 and 10 years?
Does combined therapy of high-dose corticosteroids and nebulised epinephrine for bronchiolitis during infancy affect the risk of developing asthma by age 5 and 10 years?
This study protocol outlines a longitudinal cohort study to determine if early treatment of bronchiolitis with high-dose corticosteroids and epinephrine affects the long-term risk of developing asthma.
Protocol to quantify asthma risk after infant bronchiolitis treatment leaves open long-term effects; prospective data needed before practice implications.
INTRODUCTION: The Canadian Bronchiolitis Epinephrine Steroid Trial (CanBEST) and the Bronchiolitis Severity Cohort (BSC) study enrolled infants with bronchiolitis during the first year of life. The CanBEST trial suggested that treatment of infants with a combined therapy of high-dose corticosteroids and nebulised epinephrine reduced the risk of admission to hospital. Our study aims to-(1) quantify the risk of developing asthma by age 5 and 10 years in children treated with high-dose corticosteroid and epinephrine for bronchiolitis during infancy, (2) identify risk factors associated with development of asthma in children with bronchiolitis during infancy, (3) develop asthma prediction models for children diagnosed with bronchiolitis during infancy. METHODS AND ANALYSIS: We propose a longitudinal cohort study in which we will link data from the CanBEST and BSC study with routinely collected data from provincial health administrative databases. Our outcome is asthma incidence measured using a validated health administrative data algorithm. Primary exposure will be treatment with a combined therapy of high-dose corticosteroids and nebulised epinephrine for bronchiolitis. Covariates will include type of viral pathogen, disease severity, medication use, maternal, prenatal, postnatal and demographic factors and variables related to health service utilisation for acute lower respiratory tract infection. The risk associated with development of asthma in children treated with high-dose corticosteroid and epinephrine for bronchiolitis will be assessed using multivariable Cox proportional hazards regression models. Prediction models will be developed using multivariable logistic regression analysis and internally validated using a bootstrap approach. ETHICS AND DISSEMINATION: Our study has been approved by the ethics board of all four participating sites of the CanBEST and BSC study. Finding of the study will be disseminated to the academic community and relevant stakeholders through conferences and peer-reviewed publications. TRIAL REGISTRATION NUMBER: ISRCTN56745572; Post-results.
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Abdullah et al. (2021) studied this question.
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