Evidence map›Paper›PMID 40627354›Full record

ArticleJAMA network open2025

RSV Hospital Admissions During the First 2 Seasons Among Children With Chronic Medical Conditions.

Marina Viñeta Paramo, Allison W Watts, Jeffrey N Bone, Manish Sadarangani, Julie A Bettinger, Claire Seaton, Alfonso Solimano, Matthew O Wiens, Danuta M Skowronski, Hind Sbihi and 1 more

Abstract read
In one paragraph

Article in JAMA network open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Marina Viñeta ParamoDepartment of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada.
Allison W WattsDepartment of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada.
Jeffrey N BoneBritish Columbia Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
Manish SadaranganiDepartment of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada.
Julie A BettingerDepartment of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada.
Claire SeatonDepartment of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada.
Alfonso SolimanoDepartment of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada.
Matthew O WiensBritish Columbia Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
Danuta M SkowronskiImmunization Programs and Vaccine Preventable Diseases Service, British Columbia Centre for Disease Control, Vancouver, British Columbia, Canada.
Hind SbihiData and Analytics Services, British Columbia Centre for Disease Control, Vancouver, British Columbia, Canada.
Pascal M LavoieDepartment of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: National Immunization Technical Advisory Groups recommend long-acting monoclonal antibody prophylaxis for the prevention of respiratory syncytial virus (RSV) disease for children at high risk in the first season, regardless of RSV vaccination during pregnancy, and for those who remain at increased risk in the second season. Objective: This study assessed which groups of children with chronic medical conditions (CMCs) are at higher risk of RSV hospitalization during their first and second RSV seasons. Design, Setting, and Participants: This retrospective, population-based, season-stratified cohort analysis was conducted among children who were born between April 1, 2013, and March 31, 2023, in British Columbia, Canada (population of 5.7 million in 2024), and were enrolled in the provincial medical service plan and followed up until the day before their third RSV season or April 1, 2024, whichever occurred first. Exposure: Any CMC diagnosed in the first 2 years of life. Main Outcomes and Measures: Respiratory syncytial virus-related hospitalizations. Results: The final cohort consisted of 431 937 children (32 959 [7.6%] born at <37 weeks' gestation; 222 207 boys [51.4%]) followed up for a median of 728 days (IQR, 642-729 days), including 25 452 children (5.9%) diagnosed with at least 1 of 1116 distinct CMCs. In total, 4567 children (1.1%) experienced a combined total of 4592 RSV hospitalizations, combining data from the first and second RSV seasons. In the first RSV season, the RSV hospitalization rate per 1000 person-years for children with CMCs was 15.9 (95% CI, 14.2-17.6) and for children without CMCs was 8.0 (95% CI, 7.7-8.3). In the second RSV season, the RSV hospitalization rate per 1000 person-years for children with CMCs was 7.8 (95% CI, 6.7-8.8) and for children without CMCs was 2.2 (95% CI, 2.1-2.3). Children with multisystem CMCs, particularly those affecting the respiratory, cardiovascular, or gastrointestinal systems, had second-season RSV hospitalization rates that were at least 2-fold higher than the rate among all children in the first season. Second-season rates among children with Down syndrome or those who were born prematurely (<28 weeks of gestation) were 5-fold higher than for all children in the first season. Conclusions and Relevance: This population-based retrospective cohort study identified specific groups of higher-risk children with CMCs who could most benefit from prophylaxis with long-acting monoclonal antibodies in their first and second RSV seasons. This study supports expanded eligibility criteria for long-acting monoclonal antibody prophylaxis.

Indexed as

HospitalizationRespiratory Syncytial Virus InfectionsBritish ColumbiaChild, PreschoolChronic DiseaseFemaleHumansInfantInfant, NewbornMaleRetrospective StudiesSeasons

Identifiers

PMID40627354
PMCPMC12238895

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.