Evidence map›Paper›PMID 41031614›Full record

ArticleInfluenza and other respiratory viruses2025

Cost-Effectiveness Analysis of Nirsevimab for Respiratory Syncytial Virus Disease Prevention in Newborns of Hong Kong.

Yingcheng Wang, Mingjun Rui, Qiran Wei, Ting Fan Leung, Joyce H S You

Abstract read
In one paragraph

Article in Influenza and other respiratory viruses, 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

5 authors.

Yingcheng WangSchool of Pharmacy, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China.
Mingjun RuiSchool of Pharmacy, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China.
Qiran WeiSchool of Pharmacy, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China.
Ting Fan LeungDepartment of Paediatrics, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China.ORCID 0000-0002-6469-1926
Joyce H S YouSchool of Pharmacy, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China.ORCID 0000-0002-5763-7403

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNirsevimab, a long-acting monoclonal antibody, was shown to prevent respiratory syncytial virus (RSV) infections in newborns. We evaluated the cost-effectiveness of nirsevimab strategies for newborns from the societal perspective in Hong Kong.

methodsA Markov model was developed to simulate outcomes of four nirsevimab strategies in newborns: (1) year-round, (2) seasonal, (3) catch-up, and (4) no nirsevimab. Primary outcomes included RSV lower respiratory tract infections (LRTI) related events, direct and indirect costs, quality-adjusted life year (QALY) loss, and incremental cost per QALY (ICER).

resultsIn base-case analysis, all strategies with nirsevimab reduced RSV-LRTI-related events. The catch-up group had the lowest QALY loss per 100,000 infants (38.82), followed by year-round (45.71), seasonal (60.60), and no intervention groups (81.52). Three nirsevimab cost levels were examined: 10%, 25%, and 50% of the US cost. At 10% US cost (USD52), all strategies were cost-saving versus no intervention. At 25% US cost (USD130), the ICER of the catch-up group (vs. no intervention) was 141,925 USD/QALY. At 50% US cost (USD260), all nirsevimab strategies were not cost-effective versus no intervention at a willingness-to-pay of 162,401 USD/QALY. Influential factors with thresholds were identified for RSV-LRTI incidence, RSV-related hospitalization and mortality, and nirsevimab effectiveness at the 25% US cost level (USD130). In probabilistic sensitivity analysis, the catch-up and no intervention strategies were cost-effective 100% of the time at 10% (USD52) and 50% (USD260) US cost, respectively. At 25% US cost (USD130), the catch-up strategy was cost-effective 58.56% of the time.

conclusionsThe cost-effectiveness acceptance of nirsevimab was highly subject to drug cost and effectiveness of nirsevimab, RSV-LRTI incidence, and RSV-LRTI-related consequences.

Indexed as

Antibodies, Monoclonal, HumanizedAntiviral AgentsCost-Benefit AnalysisRespiratory Syncytial Virus InfectionsCost-Effectiveness AnalysisFemaleHong KongHumansInfantInfant, NewbornMaleMarkov ChainsQuality-Adjusted Life YearsAntibodies, Monoclonal, HumanizedAntiviral Agentscatch‐up schedulecost‐effectivenessnewbornsnirsevimabseasonal immunization scheduleyear‐round immunization schedule

Identifiers

PMID41031614
PMCPMC12485666

What Socratic holds

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LicenceCC BY
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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 Socratic graph.