Evidence map›Paper›PMID 39788540›Full record

ArticleAmerican journal of perinatology2026

Increased Respiratory Syncytial Virus-Associated Hospitalizations and Ambulatory Visits in Very Preterm Infants in the First Year of Life following Discontinuation of Access to Palivizumab.

Yolanda Evong, Jiaxin Luo, Lingyun Ye, John Fahey, Janis L Breeze, Rebecca Attenborough, Kenny Wong, Joanne M Langley

Abstract read
In one paragraph

Article in American journal of perinatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

8 authors.

Yolanda EvongDepartment of Pediatrics, Dalhousie University Faculty of Medicine, Izaak Walton Killam Health Centre, Halifax, Nova Scotia, Canada.
Jiaxin LuoCanadian Center for Vaccinology (Dalhousie University, IWK Health and Nova Scotia Health), Halifax, Nova Scotia, Halifax, Nova Scotia, Canada.
Lingyun YeCanadian Centre for Vaccinology, Dalhousie University, Halifax, Nova Scotia, Canada.
John FaheyDepartment of Reproductive Care of Nova Scotia, IWK Health Centre, Halifax, Nova Scotia, Canada.
Janis L BreezeCanadian Centre for Vaccinology, Dalhousie University, Halifax, Nova Scotia, Canada.
Rebecca AttenboroughDepartment of Reproductive Care of Nova Scotia, IWK Health Centre, Halifax, Nova Scotia, Canada.
Kenny WongDivision of Pediatric Cardiology, Department of Pediatrics, Dalhousie University Faculty of Medicine, IWK Health Centre, Halifax, Nova Scotia, Canada.
Joanne M LangleyCanadian Center for Vaccinology (Dalhousie University, IWK Health and Nova Scotia Health), Halifax, Nova Scotia, Halifax, Nova Scotia, Canada.ORCID 0000-0003-3270-7345

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

From 2002 to 2023, palivizumab was the only intervention to reduce respiratory syncytial virus (RSV)-associated hospitalizations in high-risk infants in Canada but advances in RSV prevention are drastically changing this landscape. Eligibility criteria for this monoclonal antibody for preterm infants varied over time across each of 10 Canadian provinces and 3 territories. The National Professional Pediatric Association (Canadian Pediatric Society) revised its eligibility recommendations in 2015, removing access for preterm infants 30 to 32 weeks gestation (WG). The province of Nova Scotia followed these recommendations the next season. This study aimed to determine if the removal of access to palivizumab in these previously eligible infants was associated with a change in hospital admissions, deaths, or ambulatory visits associated with RSV.We identified a retrospective cohort of Nova Scotia infants born between 30 and 32 WG, without other risk factors for RSV-H, from April 2012 to September 2019 by linking six population-based provincial databases, and followed each infant through the first year of life. Episodes of RSV-associated hospitalization (RSV-H), ambulatory visits (RSV-A), or death were identified by the International Statistical Classification of Diseases and Related Health Disorders (ICD) RSV-associated diagnostic codes.Of 4,835 infants born during the study period, 250 were 30 to 32 WG and eligible for the cohort. RSV-H increased approximately 10-fold following restricted access to palivizumab (from no RSV-H (0/123) to 9.4%; 95% CI 5.0, 15.9; risk difference 9.4), but no RSV-associated deaths occurred. RSV-A also increased from 5.7 to 17.3% (risk difference 11.6).Discontinuation of access to a prophylactic anti-RSV monoclonal antibody in very preterm infants was associated with a higher risk of RSV-H and RSV-A. Evaluation of health care policy change on patient well-being is essential to assess the impact and guide future decision-making at the population level. · Discontinuation of access to a prophylactic anti-RSV monoclonal antibody in very preterm infants 30 to 32 WG was associated with a higher risk of RSV-H and RSV-A. Evaluation of changes to health care policy on patient well-being is essential to assess impact and guide future decision-making at the population level.. · Removing access to palivizumab led to higher RSV admissions in 30 to 32 WG infants.. · The effect of health care policy changes on child well-being should be assessed routinely.. · No deaths associated with RSV were identified prior to or after the policy change..

Indexed as

Ambulatory CareAntiviral AgentsHospitalizationInfant, Premature, DiseasesPalivizumabRespiratory Syncytial Virus InfectionsFemaleGestational AgeHumansInfantInfant, Extremely PrematureInfant, NewbornInfant, PrematureMaleNova ScotiaRetrospective StudiesAntiviral AgentsPalivizumab

Identifiers

PMID39788540
PMCPMC12688655

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.