Evidence map›Paper›PMID 40046840›Full record

ArticleLancet regional health. Americas2025

Assessing the impact of revising MenACWY vaccination schedule for adolescents in the United States: a modelling study.

Affan Shoukat, Chad R Wells, Thomas Shin, Lilia Potter-Schwartz, Alison P Galvani, Seyed M Moghadas

Abstract read
In one paragraph

Article in Lancet regional health. Americas, 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

6 authors.

Affan ShoukatDepartment of Mathematics and Statistics, University of Regina, Regina, Canada.
Chad R WellsCenter for Infectious Disease Modeling and Analysis, Yale School of Public Health, New Haven, USA.
Thomas ShinHealth Economics and Outcomes Research, Sanofi, New Jersey, USA.
Lilia Potter-SchwartzCenter for Infectious Disease Modeling and Analysis, Yale School of Public Health, New Haven, USA.
Alison P GalvaniCenter for Infectious Disease Modeling and Analysis, Yale School of Public Health, New Haven, USA.
Seyed M MoghadasAgent-Based Modelling Laboratory, York University, Toronto, Ontario, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The current recommendation for MenACWY vaccination against invasive meningococcal disease (IMD) in the United States (US) includes two doses: the first dose at ages 11-12 and a booster dose at age 16. The Advisory Committee on Immunization Practices has proposed options for revising this schedule by either eliminating the first dose or adjusting the timing of the first dose to age 15 and the booster to ages 17-18. The impact of these alternative schedules on IMD incidence remains undetermined. Methods: We developed an age-stratified, agent-based Monte-Carlo simulation model of meningococcal transmission dynamics, parameterised with US age demographics, to assess the impact of the proposed changes to the MenACWY vaccination schedules. Excluding serogroup A, absent in the US for decades, the model included serogroups C, W, and Y for asymptomatic infection (carriage) and vaccine effectiveness against IMD. We calibrated serogroup-specific transmission and IMD development probabilities by fitting the model to reported IMD cases from 1997 to 2004, before vaccine introduction. The calibrated model then simulated the current vaccination schedule (CVS) starting in 2005 and alternative schedules from January 1, 2025 to December 31, 2035, comparing outcomes over the same period. Findings: Switching from the CVS to a single-dose program at age 16 with 61% vaccine uptake (as reported for the booster in 2022) would result in 1062 (95% Uncertainty Range [UR]: 724-1419) additional IMD cases during the 11-year study period. With a case fatality rate of 14.5%, this change could cause an estimated 154 (95% UR: 105-206) additional deaths. Even if vaccine uptake increased to 90% at age 16, the program would still result in 934 (95% UR: 640-1242) additional cases and 135 (95% UR: 93-180) more deaths compared to the CVS. The second alternative schedule (i.e. first dose at age 15, booster at ages 17-18) also increased IMD cases, notably shifting a substantial burden to adolescents aged 11-15 years. Interpretation: Our findings indicate that the current MenACWY vaccination program remains more effective than the proposed alternatives, even with increased vaccine uptake during late adolescence. Improving the uptake rate of the booster at age 16 while maintaining the 11-12-year dose within the existing program would reduce the IMD burden among high-risk adolescents and young adults. Funding: This study was in part supported by Sanofi. Seyed M. Moghadas acknowledges support from the Natural Sciences and Engineering Research Council of Canada Discovery Grant and Alliance Grant (ALLRP 576914-22). Alison P. Galvani acknowledges support from The Notsew Orm Sands Foundation.

Indexed as

MenACWY vaccinationMeningococcal diseaseSimulationTransmission dynamics

Identifiers

PMID40046840
PMCPMC11880592

What OpenQuestion holds

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LicenceCC BY-NC
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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.