Evidence map›Paper›PMID 42087574›Full record

ArticlePediatric pulmonology2026

Real-World Effectiveness of Universal Nirsevimab on Bronchiolitis Incidence: A Regional Hub-Spoke Surveillance Analysis in Liguria, Italy.

Marcello Mariani, Giacomo Brisca, Marina Francesca Strati, Silvia Buratti, Marta Ferretti, Alberto Gaiero, Valeria Musso, Andrea Gazzolo, Francesca Ginocchio, Katiuscia Zerbini and 10 more

Abstract readMulticenter Study
In one paragraph

Article in Pediatric pulmonology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  2. Observational
  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

20 authors.

Marcello MarianiPediatric Infectious Diseases Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Giacomo BriscaEmergency Department, IRCCS Istituto Giannina Gaslini, Neonatal and Pediatric Intensive Care Unit, Intermediate Care Unit, Genoa, Italy.
Marina Francesca StratiEmergency Department, IRCCS Istituto Giannina Gaslini, Neonatal and Pediatric Intensive Care Unit, Intermediate Care Unit, Genoa, Italy.
Silvia BurattiEmergency Department, IRCCS Istituto Giannina Gaslini, Neonatal and Pediatric Intensive Care Unit, Intermediate Care Unit, Genoa, Italy.
Marta FerrettiEmergency Department, IRCCS Istituto Giannina Gaslini, Emergency Room and Pediatric Emergency Medicine, Genoa, Italy.
Alberto GaieroPediatrics and Neonatology Unit, IRCCS Istituto Giannina Gaslini, Savona, Italy.
Valeria MussoPediatrics and Neonatology Unit, IRCCS Istituto Giannina Gaslini, Savona, Italy.
Andrea GazzoloPediatrics and Neonatology Unit, IRCCS Istituto Giannina Gaslini, Lavagna, Italy.
Francesca GinocchioPediatrics and Neonatology Unit, IRCCS Istituto Giannina Gaslini, Lavagna, Italy.
Katiuscia ZerbiniPediatrics and Neonatology Unit, IRCCS Istituto Giannina Gaslini, Imperia, Italy.
Diego MinghettiPediatrics and Neonatology Unit, IRCCS Istituto Giannina Gaslini, Imperia, Italy.
Maria Franca CoronaPediatrics and Neonatology Unit, IRCCS Istituto Giannina Gaslini, La Spezia, Italy.
Laura De HofferPediatrics and Neonatology Unit, IRCCS Istituto Giannina Gaslini, La Spezia, Italy.
Daniela PirloEmergency Department, IRCCS Istituto Giannina Gaslini, Neonatal and Pediatric Intensive Care Unit, Intermediate Care Unit, Genoa, Italy.
Emanuela PiccottiEmergency Department, IRCCS Istituto Giannina Gaslini, Emergency Room and Pediatric Emergency Medicine, Genoa, Italy.
Luca Antonio RamenghiEmergency Department, IRCCS Istituto Giannina Gaslini, Neonatal and Pediatric Intensive Care Unit, Intermediate Care Unit, Genoa, Italy.
Marisa AlbertiIRCCS Istituto Giannina Gaslini, Health Management Unit, Genoa, Italy.
Raffaele SpiazziIRCCS Istituto Giannina Gaslini, Health Management Unit, Genoa, Italy.
Elio CastagnolaPediatric Infectious Diseases Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Andrea MoscatelliEmergency Department, IRCCS Istituto Giannina Gaslini, Neonatal and Pediatric Intensive Care Unit, Intermediate Care Unit, Genoa, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBronchiolitis represents a major cause of infant hospitalization, predominantly due to respiratory syncytial virus (RSV). Nirsevimab, a long-acting monoclonal antibody targeting the prefusion RSV F protein, has recently been introduced to provide season-long protection against RSV-related lower respiratory tract infection.

methodsWe conducted a multicenter, retrospective, population-based study across the Liguria Region (Northwest Italy) to assess the impact and effectiveness of the 2024-2025 nirsevimab immunization campaign. All infants under 2 years of age hospitalized with acute bronchiolitis between October 2023 and March 2025 were identified through the regional pediatric Hub-and-Spoke network. Data were compared between the pre-nirsevimab (2023-2024) and post-nirsevimab (2024-2025) seasons. Nirsevimab effectiveness (VE) against RSV-positive hospitalization was estimated using a test-negative design.

resultsA total of 858 infants were hospitalized with bronchiolitis across the two seasons. Following the introduction of nirsevimab, bronchiolitis hospitalizations decreased from 41.7 to 17.3 per 1000 admissions (Incidence Rate Ratio 0.4; 95% CI: 0.4-0.5; p < 0.001), corresponding to a 60% reduction. Estimated nirsevimab effectiveness was 65.0% (95% CI: 39.2%-79.8%) against RSV-positive hospitalization. No high-risk infants-those previously eligible for palivizumab-developed severe RSV infection requiring PICU admission. Breakthrough infections occurred in a minority of immunized infants but showed a similar clinical course to non-immunized cases.

conclusionsThe introduction of universal nirsevimab immunization in Liguria was associated with a marked reduction in RSV-related hospitalizations, confirming its strong real-world epidemiological impact. These findings support nirsevimab as an effective and feasible public health intervention to substantially reduce the burden of RSV bronchiolitis in infants.

Indexed as

Antibodies, Monoclonal, HumanizedAntiviral AgentsBronchiolitisRespiratory Syncytial Virus InfectionsFemaleHospitalizationHumansImmunization ProgramsIncidenceInfantItalyMaleRetrospective StudiesAntibodies, Monoclonal, HumanizedAntiviral Agentsbronchiolitisimmunization programnirsevimabreal‐world effectivenessrespiratory syncytial virus

Identifiers

PMID42087574
PMCPMC13383966

What OpenQuestion holds

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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.