The Effectiveness of the Palivizumab Programme in Reducing the Risk of Paediatric Asthma: A Population‐Based Study in Ontario, Canada

BACKGROUND: Palivizumab was introduced in Canada in 1998 as a publicly funded programme to reduce respiratory syncytial virus (RSV) disease in high-risk children. Severe early-life RSV infections are associated with increased asthma risk. Thus, palivizumab may also indirectly reduce paediatric asthma. OBJECTIVE: To evaluate the effectiveness of Ontario, Canada's palivizumab programme in decreasing paediatric asthma. METHODS: We used multiple linked population-based administrative databases to identify all children born in Ontario between 1993 and 2013, with follow-up through March 2020. Our primary outcome was physician-diagnosed asthma by age 7. Controlled interrupted time-series analysis was used to compare changes in annual asthma incidence (by birth year) before and after palivizumab's introduction, according to programme eligibility (clearly, possibly, or ineligible). Socio-demographic differences were explored via stratification. RESULTS: Nearly 3 million children were included in this study, including 406,596 (14.6%) diagnosed with asthma by age 7. Asthma incidence substantially declined over the study period, with the greatest declines among palivizumab-ineligible children (35.3%, 95% confidence interval [CI] 28.3, 42.6, versus 18.1%, 95% CI 13.9, 22.9 among clearly eligible children). However, relative to ineligible children, post-palivizumab declines were most apparent among possibly eligible children, with an additional annual decline of 2.0% (95% CI 0.3, 3.7) in asthma. Socio demographic differences in asthma incidence and post-palivizumab declines were noted. Particularly, incidence was higher among children born to teenage mothers than among those aged 19+ years; this gap narrowed over time, especially among possibly eligible children. CONCLUSIONS: Asthma incidence declined over this 20-year study; however, smaller declines were observed among children clearly eligible for palivizumab relative to ineligible children. However, exploratory evidence was suggestive of reduced social inequities in asthma post-palivizumab, particularly among possibly eligible children. Larger reductions in asthma might be realized with the introduction of population-based RSV immunization programmes through broader programme eligibility and reductions in severe RSV disease.

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Publication Details

Journal
Paediatric and Perinatal Epidemiology
Published
2026-03-31
DOI
https://doi.org/10.1111/ppe.70141
Citations
1
Primary Topic
Respiratory viral infections research
Type
article
Field-Weighted Citation Impact
19.14

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article

The Effectiveness of the Palivizumab Programme in Reducing the Risk of Paediatric Asthma: A Population‐Based Study in Ontario, Canada

Dougal Hargreaves, Steven Hawken, Michelle C. Dimitris, Tiffany Fitzpatrick et al.
1 citations
Paediatric and Perinatal Epidemiology
Respiratory viral infections research
19.14
article

The Effectiveness of the Palivizumab Programme in Reducing the Risk of Paediatric Asthma: A Population‐Based Study in Ontario, Canada

Dougal Hargreaves, Steven Hawken, Michelle C. Dimitris, Tiffany Fitzpatrick, Sarah Swayze, Sonia K Saxena, Justin Kwong, Kimberley Foley, Sarah A. Buchan, Dayre McNally
article en
1 citations

Abstract

BACKGROUND: Palivizumab was introduced in Canada in 1998 as a publicly funded programme to reduce respiratory syncytial virus (RSV) disease in high-risk children. Severe early-life RSV infections are associated with increased asthma risk. Thus, palivizumab may also indirectly reduce paediatric asthma. OBJECTIVE: To evaluate the effectiveness of Ontario, Canada's palivizumab programme in decreasing paediatric asthma. METHODS: We used multiple linked population-based administrative databases to identify all children born in Ontario between 1993 and 2013, with follow-up through March 2020. Our primary outcome was physician-diagnosed asthma by age 7. Controlled interrupted time-series analysis was used to compare changes in annual asthma incidence (by birth year) before and after palivizumab's introduction, according to programme eligibility (clearly, possibly, or ineligible). Socio-demographic differences were explored via stratification. RESULTS: Nearly 3 million children were included in this study, including 406,596 (14.6%) diagnosed with asthma by age 7. Asthma incidence substantially declined over the study period, with the greatest declines among palivizumab-ineligible children (35.3%, 95% confidence interval [CI] 28.3, 42.6, versus 18.1%, 95% CI 13.9, 22.9 among clearly eligible children). However, relative to ineligible children, post-palivizumab declines were most apparent among possibly eligible children, with an additional annual decline of 2.0% (95% CI 0.3, 3.7) in asthma. Socio demographic differences in asthma incidence and post-palivizumab declines were noted. Particularly, incidence was higher among children born to teenage mothers than among those aged 19+ years; this gap narrowed over time, especially among possibly eligible children. CONCLUSIONS: Asthma incidence declined over this 20-year study; however, smaller declines were observed among children clearly eligible for palivizumab relative to ineligible children. However, exploratory evidence was suggestive of reduced social inequities in asthma post-palivizumab, particularly among possibly eligible children. Larger reductions in asthma might be realized with the introduction of population-based RSV immunization programmes through broader programme eligibility and reductions in severe RSV disease.

Paediatric and Perinatal Epidemiology
Dalhousie University (CA), University of Ottawa (CA), University of Toronto (CA), Children's Hospital of Eastern Ontario (CA), Ottawa Hospital (CA), NIHR Imperial Biomedical Research Centre (GB), Public Health Ontario (CA), Centre for Disability Prevention and Rehabilitation (CA), Institute for Work & Health (CA), Ottawa Hospital Research Institute (CA), Imperial College London (GB)
Canadian Institutes of Health Research
Openalex Percentile: Top 1%
Respiratory viral infections research
19.14
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