Evidence map›Paper›PMID 38485425›Full record

ArticleThe Lancet. Global health2024

Estimating the health effects of COVID-19-related immunisation disruptions in 112 countries during 2020-30: a modelling study.

Anna-Maria Hartner, Xiang Li, Susy Echeverria-Londono, Jeremy Roth, Kaja Abbas, Megan Auzenbergs, Margaret J de Villiers, Matthew J Ferrari, Keith Fraser, Han Fu and 31 more

Open access · goldAbstract read
In one paragraph

Article in The Lancet. Global health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
8.7field-weighted citation impact, top 1% of its field
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

14 citing papers in PubMed, 22 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

41 authors at 17 institutions in 11 countries.

Anna-Maria HartnerMedical Research Council Centre for Global Infectious Disease Analysis, Jameel Institute School of Public Health, Imperial College London, London, UK; Centre for Artificial Intelligence in Public Health Research, Robert Koch Institute, Wildau, Germany.
Xiang LiMedical Research Council Centre for Global Infectious Disease Analysis, Jameel Institute School of Public Health, Imperial College London, London, UK.
Susy Echeverria-LondonoMedical Research Council Centre for Global Infectious Disease Analysis, Jameel Institute School of Public Health, Imperial College London, London, UK.
Jeremy RothMedical Research Council Centre for Global Infectious Disease Analysis, Jameel Institute School of Public Health, Imperial College London, London, UK.
Kaja AbbasLondon School of Hygiene & Tropical Medicine, London, UK; School of Tropical Medicine and Global Health, Nagasaki University, Nagasaki, Japan.
Megan AuzenbergsLondon School of Hygiene & Tropical Medicine, London, UK.
Margaret J de VilliersMedical Research Council Centre for Global Infectious Disease Analysis, Jameel Institute School of Public Health, Imperial College London, London, UK.
Matthew J FerrariCenter for Infectious Disease Dynamics, Pennsylvania State University, Pennsylvania, PA, USA.
Keith FraserMedical Research Council Centre for Global Infectious Disease Analysis, Jameel Institute School of Public Health, Imperial College London, London, UK.
Han FuLondon School of Hygiene & Tropical Medicine, London, UK.
Timothy HallettMedical Research Council Centre for Global Infectious Disease Analysis, Jameel Institute School of Public Health, Imperial College London, London, UK.
Wes HinsleyMedical Research Council Centre for Global Infectious Disease Analysis, Jameel Institute School of Public Health, Imperial College London, London, UK.
Mark JitLondon School of Hygiene & Tropical Medicine, London, UK; School of Public Health, University of Hong Kong, Hong Kong Special Administrative Region, China.
Andromachi KarachaliouVeterinary Medicine, University of Cambridge, Cambridge, UK.
Sean M MooreDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN, USA.
Shevanthi NayagamMedical Research Council Centre for Global Infectious Disease Analysis, Jameel Institute School of Public Health, Imperial College London, London, UK; Section of Hepatology and Gastroenterology, Department of Metabolism, Digestion, and Reproduction, Imperial College London, London, UK.
Timos PapadopoulosUK Health Security Agency, London, UK.
T Alex PerkinsDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN, USA.
Allison PortnoyCenter for Health Decision Science, T H Chan School of Public Health, Harvard University, Boston, MA, USA.
Quan Tran MinhDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN, USA.
Emilia VynnyckyUK Health Security Agency, London, UK.
Amy K WinterDepartment of Epidemiology and Biostatistics and Center for the Ecology of Infectious Diseases, University of Georgia, Athens, GA, USA.
Holly BurrowsSchool of Public Health, Yale University, New Haven, CT, USA.
Cynthia ChenSaw Swee Hock School of Public Health, National University of Singapore, Singapore.
Hannah E ClaphamSaw Swee Hock School of Public Health, National University of Singapore, Singapore; Oxford University Clinical Research Unit, Ho Chi Minh City, Viet Nam; Nuffield Department of Medicine, Oxford University, Oxford, UK.
Aniruddha DeshpandeRollins School of Public Health, Emory University, Atlanta, GA, USA.
Sarah HauryskiCenter for Infectious Disease Dynamics, Pennsylvania State University, Pennsylvania, PA, USA.
John HuberDepartment of Biological Sciences, University of Notre Dame, Notre Dame, IN, USA; School of Medicine, Washington University, St Louis, MO, USA.
Kevin JeanLaboratoire Modélisation, épidémiologie, et surveillance des risques sanitaires and Unit Cnam risques infectieux et émergents, Institut Pasteur, Conservatoire National des Arts et Metiers, Paris, France.
Chaelin KimInternational Vaccine Institute, Seoul, South Korea.
Jong-Hoon KimInternational Vaccine Institute, Seoul, South Korea.
Jemima KohSaw Swee Hock School of Public Health, National University of Singapore, Singapore.
Benjamin A LopmanRollins School of Public Health, Emory University, Atlanta, GA, USA.
Virginia E PitzerSchool of Public Health, Yale University, New Haven, CT, USA.
Yvonne TamBloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA.
Philipp LambachDepartment of Immunization, Vaccines, and Biologicals, WHO, Geneva, Switzerland.
So Yoon SimDepartment of Immunization, Vaccines, and Biologicals, WHO, Geneva, Switzerland.
Kim WoodruffMedical Research Council Centre for Global Infectious Disease Analysis, Jameel Institute School of Public Health, Imperial College London, London, UK.
Neil M FergusonMedical Research Council Centre for Global Infectious Disease Analysis, Jameel Institute School of Public Health, Imperial College London, London, UK.
Caroline L TrotterMedical Research Council Centre for Global Infectious Disease Analysis, Jameel Institute School of Public Health, Imperial College London, London, UK; Veterinary Medicine, University of Cambridge, Cambridge, UK.
Katy A M GaythorpeMedical Research Council Centre for Global Infectious Disease Analysis, Jameel Institute School of Public Health, Imperial College London, London, UK. Electronic address: k.gaythorpe@imperial.ac.uk.
Imperial College London · GBUniversity of Notre Dame · USLondon School of Hygiene & Tropical Medicine · GBNational University of Singapore · SGEmory University · USInternational Vaccine Institute · KRPennsylvania State University · USUK Health Security Agency · GBUniversity of Cambridge · GBWorld Health Organization · CHYale University · USConservatoire National des Arts et Métiers · FRHarvard University · USJohns Hopkins University · USRobert Koch Institute · DEUniversity of Georgia · USUniversity of London · GB

Funding

World Health Organization 001
6 · The paper itself

Abstract

backgroundThere have been declines in global immunisation coverage due to the COVID-19 pandemic. Recovery has begun but is geographically variable. This disruption has led to under-immunised cohorts and interrupted progress in reducing vaccine-preventable disease burden. There have, so far, been few studies of the effects of coverage disruption on vaccine effects. We aimed to quantify the effects of vaccine-coverage disruption on routine and campaign immunisation services, identify cohorts and regions that could particularly benefit from catch-up activities, and establish if losses in effect could be recovered.

methodsFor this modelling study, we used modelling groups from the Vaccine Impact Modelling Consortium from 112 low-income and middle-income countries to estimate vaccine effect for 14 pathogens. One set of modelling estimates used vaccine-coverage data from 1937 to 2021 for a subset of vaccine-preventable, outbreak-prone or priority diseases (ie, measles, rubella, hepatitis B, human papillomavirus [HPV], meningitis A, and yellow fever) to examine mitigation measures, hereafter referred to as recovery runs. The second set of estimates were conducted with vaccine-coverage data from 1937 to 2020, used to calculate effect ratios (ie, the burden averted per dose) for all 14 included vaccines and diseases, hereafter referred to as full runs. Both runs were modelled from Jan 1, 2000, to Dec 31, 2100. Countries were included if they were in the Gavi, the Vaccine Alliance portfolio; had notable burden; or had notable strategic vaccination activities. These countries represented the majority of global vaccine-preventable disease burden. Vaccine coverage was informed by historical estimates from WHO-UNICEF Estimates of National Immunization Coverage and the immunisation repository of WHO for data up to and including 2021. From 2022 onwards, we estimated coverage on the basis of guidance about campaign frequency, non-linear assumptions about the recovery of routine immunisation to pre-disruption magnitude, and 2030 endpoints informed by the WHO Immunization Agenda 2030 aims and expert consultation. We examined three main scenarios: no disruption, baseline recovery, and baseline recovery and catch-up.

findingsWe estimated that disruption to measles, rubella, HPV, hepatitis B, meningitis A, and yellow fever vaccination could lead to 49 119 additional deaths (95% credible interval [CrI] 17 248-134 941) during calendar years 2020-30, largely due to measles. For years of vaccination 2020-30 for all 14 pathogens, disruption could lead to a 2·66% (95% CrI 2·52-2·81) reduction in long-term effect from 37 378 194 deaths averted (34 450 249-40 241 202) to 36 410 559 deaths averted (33 515 397-39 241 799). We estimated that catch-up activities could avert 78·9% (40·4-151·4) of excess deaths between calendar years 2023 and 2030 (ie, 18 900 [7037-60 223] of 25 356 [9859-75 073]).

interpretationOur results highlight the importance of the timing of catch-up activities, considering estimated burden to improve vaccine coverage in affected cohorts. We estimated that mitigation measures for measles and yellow fever were particularly effective at reducing excess burden in the short term. Additionally, the high long-term effect of HPV vaccine as an important cervical-cancer prevention tool warrants continued immunisation efforts after disruption.

fundingThe Vaccine Impact Modelling Consortium, funded by Gavi, the Vaccine Alliance and the Bill & Melinda Gates Foundation. TRANSLATIONS: For the Arabic, Chinese, French, Portguese and Spanish translations of the abstract see Supplementary Materials section.

Indexed as

COVID-19Hepatitis BMeaslesMeningitisPapillomavirus InfectionsPapillomavirus VaccinesRubellaVaccine-Preventable DiseasesYellow FeverHumansImmunizationPandemicsVaccinationPapillomavirus Vaccines

Identifiers

PMID38485425
PMCPMC10951961
OpenAlexW4392728662

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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.