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Incorporating human dynamic populations in models of infectious disease transmission: a systematic review
BACKGROUND: 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 disea...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673416/ https://www.ncbi.nlm.nih.gov/pubmed/36401210 http://dx.doi.org/10.1186/s12879-022-07842-0 |
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author | Møgelmose, Signe Neels, Karel Hens, Niel |
author_facet | Møgelmose, Signe Neels, Karel Hens, Niel |
author_sort | Møgelmose, Signe |
collection | PubMed |
description | BACKGROUND: 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-022-07842-0. |
format | Online Article Text |
id | pubmed-9673416 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-96734162022-11-19 Incorporating human dynamic populations in models of infectious disease transmission: a systematic review Møgelmose, Signe Neels, Karel Hens, Niel BMC Infect Dis Research BACKGROUND: 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-022-07842-0. BioMed Central 2022-11-18 /pmc/articles/PMC9673416/ /pubmed/36401210 http://dx.doi.org/10.1186/s12879-022-07842-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Møgelmose, Signe Neels, Karel Hens, Niel Incorporating human dynamic populations in models of infectious disease transmission: a systematic review |
title | Incorporating human dynamic populations in models of infectious disease transmission: a systematic review |
title_full | Incorporating human dynamic populations in models of infectious disease transmission: a systematic review |
title_fullStr | Incorporating human dynamic populations in models of infectious disease transmission: a systematic review |
title_full_unstemmed | Incorporating human dynamic populations in models of infectious disease transmission: a systematic review |
title_short | Incorporating human dynamic populations in models of infectious disease transmission: a systematic review |
title_sort | incorporating human dynamic populations in models of infectious disease transmission: a systematic review |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673416/ https://www.ncbi.nlm.nih.gov/pubmed/36401210 http://dx.doi.org/10.1186/s12879-022-07842-0 |
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