Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/39009
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dc.contributor.authorMOGELMOSE, Signe-
dc.contributor.authorNeels, Karel-
dc.contributor.authorHENS, Niel-
dc.date.accessioned2022-12-06T09:49:11Z-
dc.date.available2022-12-06T09:49:11Z-
dc.date.issued2022-
dc.date.submitted2022-12-01T12:47:28Z-
dc.identifier.citationBMC INFECTIOUS DISEASES, 22 (1) (Art N° 862)-
dc.identifier.urihttp://hdl.handle.net/1942/39009-
dc.description.abstractBackground An increasing number of infectious disease models consider demographic change in the host population, but the demographic methods and assumptions vary considerably. We carry out a systematic review of the methods and assumptions used to incorporate dynamic populations in infectious disease models. Methods We systematically searched PubMed and Web of Science for articles on infectious disease transmission in dynamic host populations. We screened the articles and extracted data in accordance with the guidelines of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). Results We identified 46 articles containing 53 infectious disease models with dynamic populations. Population dynamics were modelled explicitly in 71% of the disease transmission models using cohort-component-based models (CCBMs) or individual-based models (IBMs), while 29% used population prospects as an external input. Fertility and mortality were in most cases age- or age-sex-specific, but several models used crude fertility rates (40%). Households were incorporated in 15% of the models, which were IBMs except for one model using external population prospects. Finally, 17% of the infectious disease models included demographic sensitivity analyses. Conclusions We find that most studies model fertility, mortality and migration explicitly. Moreover, population-level modelling was more common than IBMs. Demographic characteristics beyond age and sex are cumbersome to implement in population-level models and were for that reason only incorporated in IBMs. Several IBMs included households and networks, but the granularity of the underlying demographic processes was often similar to that of CCBMs. We describe the implications of the most common assumptions and discuss possible extensions.-
dc.description.sponsorshipThe results reported herein correspond to the specifc aims of Grant 682540— TransMID to investigator Niel Hens from the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation program.-
dc.language.isoen-
dc.publisherBMC-
dc.rightsThe Author(s) 2022. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativeco mmons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.-
dc.subject.otherDemography-
dc.subject.otherPopulation dynamics-
dc.subject.otherDemographic change-
dc.subject.otherInfectious diseases-
dc.subject.otherTransmission-
dc.subject.otherMathematical epidemiology-
dc.titleIncorporating human dynamic populations in models of infectious disease transmission: a systematic review-
dc.typeJournal Contribution-
dc.identifier.issue1-
dc.identifier.volume22-
local.bibliographicCitation.jcatA1-
dc.description.notesMogelmose, S (corresponding author), Hasselt Univ, Interuniv Inst Biostat & Statist Bioinformat, Data Sci Inst, Hasselt, Belgium.; Mogelmose, S (corresponding author), Univ Antwerp, Ctr Populat Family & Hlth, Antwerp, Belgium.-
dc.description.notessigne.mogelmose@uhasselt.be-
local.publisher.placeCAMPUS, 4 CRINAN ST, LONDON N1 9XW, ENGLAND-
local.type.refereedRefereed-
local.type.specifiedReview-
local.bibliographicCitation.artnr862-
local.type.programmeH2020-
local.relation.h2020682540-
dc.identifier.doi10.1186/s12879-022-07842-0-
dc.identifier.pmid36401210-
dc.identifier.isi000885309800001-
local.provider.typewosris-
local.description.affiliation[Mogelmose, Signe; Hens, Niel] Hasselt Univ, Interuniv Inst Biostat & Statist Bioinformat, Data Sci Inst, Hasselt, Belgium.-
local.description.affiliation[Mogelmose, Signe; Neels, Karel] Univ Antwerp, Ctr Populat Family & Hlth, Antwerp, Belgium.-
local.description.affiliation[Hens, Niel] Univ Antwerp, Ctr Hlth Econ Res & Modelling Infect Dis, Vaccine & Infect Dis Inst, Antwerp, Belgium.-
local.uhasselt.internationalno-
item.validationecoom 2023-
item.fulltextWith Fulltext-
item.accessRightsOpen Access-
item.fullcitationMOGELMOSE, Signe; Neels, Karel & HENS, Niel (2022) Incorporating human dynamic populations in models of infectious disease transmission: a systematic review. In: BMC INFECTIOUS DISEASES, 22 (1) (Art N° 862).-
item.contributorMOGELMOSE, Signe-
item.contributorNeels, Karel-
item.contributorHENS, Niel-
crisitem.journal.eissn1471-2334-
Appears in Collections:Research publications
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