Evidence map›Paper›PMID 41165704›Full record

ArticleJAMA network open2025

Nirsevimab Treatment of RSV Bronchiolitis in Pediatric Emergency Departments.

Lea Lenglart, Corinne Levy, Romain Basmaci, Karine Levieux, Rolf Kramer, Pauline De Mari, Stéphane Béchet, Elise Launay, Lise Martin Perceval, Laure Cohen and 5 more

Abstract readMulticenter Study
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 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. Article
  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

15 authors.

Lea LenglartPediatric Emergency Department, Robert Debré Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
Corinne LevyAssociation Clinique et Thérapeutique Infantile du Val de Marne, Créteil, France.
Romain BasmaciInfection, Antimicrobials, Modelling, Evolution, INSERM UMR 1137, Paris Cité University, Paris, France.
Karine LevieuxPediatric Emergency Department, Nantes University Hospital, Nantes, France.
Rolf KramerSanofi Pasteur, Lyon, France.
Pauline De MariSanofi Pasteur, Lyon, France.
Stéphane BéchetAssociation Clinique et Thérapeutique Infantile du Val de Marne, Créteil, France.
Elise LaunayGroupe de Pathologie Infectieuse Pédiatrique, Paris, France.
Lise Martin PercevalDepartment of Pediatrics, Nantes University Hospital, Nantes, France.
Laure CohenPediatric Emergency Department, Louis Mourier Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
Camille AupiaisGroupe de Pathologie Infectieuse Pédiatrique, Paris, France.
Loic de PontualGroupe de Pathologie Infectieuse Pédiatrique, Paris, France.
Alexis RybakAssociation Clinique et Thérapeutique Infantile du Val de Marne, Créteil, France.
Naim OuldaliInfection, Antimicrobials, Modelling, Evolution, INSERM UMR 1137, Paris Cité University, Paris, France.
Robert CohenAssociation Clinique et Thérapeutique Infantile du Val de Marne, Créteil, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: New resistant mutations of respiratory syncytial virus type B (RSV-B) have been observed during the first year of implementation nirsevimab treatment. During the second season of implementation of nirsevimab treatment in France, RSV-B was predominant. Objectives: To assess and compare the effectiveness of nirsevimab treatment in preventing RSV bronchiolitis in pediatric emergency departments during the first and second seasons of implementation of treatment in France. Design, Setting, and Participants: This a multicenter test-negative case-control study included 636 infants younger than 1 year who received a diagnosis of a first bronchiolitis episode in 5 pediatric emergency departments in France during the 2 first seasons of implementation of nirsevimab treatment (from October 5, 2023, to February 29, 2024, and from October 15, 2024, to January 31, 2025) and underwent a nasopharyngeal test for RSV. Main Outcomes and Measures: The main outcome of the study was the RSV status of the bronchiolitis cases. Multivariable logistic regression was performed with nirsevimab as the explanatory variable, adjusted on age, sex, risk factors of bronchiolitis, type of childcare, month, and center of inclusion. Effectiveness was calculated for each season and compared using the likelihood ratio test. Subgroup analysis by age and severity as well as sensitivity analyses were performed. Results: The study included 636 patients with bronchiolitis (median age, 3.0 months [IQR, 1.4-5.0 months]; 333 boys [52.4%]). In both seasons, 162 of 636 patients (25.5%) were immunized with nirsevimab. During the first season of implementation, 273 of 384 patients (71.1%) tested positive for RSV; during the second season, 181 of 252 patients (71.8%) tested positive for RSV. The effectiveness of nirsevimab treatment against RSV bronchiolitis was estimated to be 83.2% (95% CI, 68.0%-91.4%) during the first season and 89.3% (95% CI, 77.8%-95.1%) during the second season; no statistically significant difference in effectiveness was found between the 2 seasons (P = .97). Subgroup and sensitivity analyses provided similar results. Conclusions and Relevance: In this test-negative case-control study of nirsevimab treatment, its effectiveness in reducing pediatric emergency department visits for RSV bronchiolitis during the second season of national immunization was high and comparable with that observed in the first season. Although RSV-B resistant strains had been recently identified, it did not appear to have important clinical consequences to date. Continued close monitoring of RSV epidemiology in the context of the widespread nirsevimab use remains essential.

Indexed as

Antibodies, Monoclonal, HumanizedAntiviral AgentsBronchiolitisBronchiolitis, ViralEmergency Service, HospitalRespiratory Syncytial Virus InfectionsCase-Control StudiesFemaleFranceHumansInfantInfant, NewbornMaleRespiratory Syncytial Virus, HumanAntibodies, Monoclonal, HumanizedAntiviral Agents

Identifiers

PMID41165704
PMCPMC12576487

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.