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Comparability of Results from Pair and Classical Model Formulations for Different Sexually Transmitted Infections
The “classical model” for sexually transmitted infections treats partnerships as instantaneous events summarized by partner change rates, while individual-based and pair models explicitly account for time within partnerships and gaps between partnerships. We compared predictions from the classical a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3384672/ https://www.ncbi.nlm.nih.gov/pubmed/22761828 http://dx.doi.org/10.1371/journal.pone.0039575 |
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author | Ong, Jimmy Boon Som Fu, Xiuju Lee, Gary Kee Khoon Chen, Mark I-Cheng |
author_facet | Ong, Jimmy Boon Som Fu, Xiuju Lee, Gary Kee Khoon Chen, Mark I-Cheng |
author_sort | Ong, Jimmy Boon Som |
collection | PubMed |
description | The “classical model” for sexually transmitted infections treats partnerships as instantaneous events summarized by partner change rates, while individual-based and pair models explicitly account for time within partnerships and gaps between partnerships. We compared predictions from the classical and pair models over a range of partnership and gap combinations. While the former predicted similar or marginally higher prevalence at the shortest partnership lengths, the latter predicted self-sustaining transmission for gonorrhoea (GC) and Chlamydia (CT) over much broader partnership and gap combinations. Predictions on the critical level of condom use (C(c)) required to prevent transmission also differed substantially when using the same parameters. When calibrated to give the same disease prevalence as the pair model by adjusting the infectious duration for GC and CT, and by adjusting transmission probabilities for HIV, the classical model then predicted much higher C(c) values for GC and CT, while C(c) predictions for HIV were fairly close. In conclusion, the two approaches give different predictions over potentially important combinations of partnership and gap lengths. Assuming that it is more correct to explicitly model partnerships and gaps, then pair or individual-based models may be needed for GC and CT since model calibration does not resolve the differences. |
format | Online Article Text |
id | pubmed-3384672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33846722012-07-03 Comparability of Results from Pair and Classical Model Formulations for Different Sexually Transmitted Infections Ong, Jimmy Boon Som Fu, Xiuju Lee, Gary Kee Khoon Chen, Mark I-Cheng PLoS One Research Article The “classical model” for sexually transmitted infections treats partnerships as instantaneous events summarized by partner change rates, while individual-based and pair models explicitly account for time within partnerships and gaps between partnerships. We compared predictions from the classical and pair models over a range of partnership and gap combinations. While the former predicted similar or marginally higher prevalence at the shortest partnership lengths, the latter predicted self-sustaining transmission for gonorrhoea (GC) and Chlamydia (CT) over much broader partnership and gap combinations. Predictions on the critical level of condom use (C(c)) required to prevent transmission also differed substantially when using the same parameters. When calibrated to give the same disease prevalence as the pair model by adjusting the infectious duration for GC and CT, and by adjusting transmission probabilities for HIV, the classical model then predicted much higher C(c) values for GC and CT, while C(c) predictions for HIV were fairly close. In conclusion, the two approaches give different predictions over potentially important combinations of partnership and gap lengths. Assuming that it is more correct to explicitly model partnerships and gaps, then pair or individual-based models may be needed for GC and CT since model calibration does not resolve the differences. Public Library of Science 2012-06-27 /pmc/articles/PMC3384672/ /pubmed/22761828 http://dx.doi.org/10.1371/journal.pone.0039575 Text en Ong et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Ong, Jimmy Boon Som Fu, Xiuju Lee, Gary Kee Khoon Chen, Mark I-Cheng Comparability of Results from Pair and Classical Model Formulations for Different Sexually Transmitted Infections |
title | Comparability of Results from Pair and Classical Model Formulations for Different Sexually Transmitted Infections |
title_full | Comparability of Results from Pair and Classical Model Formulations for Different Sexually Transmitted Infections |
title_fullStr | Comparability of Results from Pair and Classical Model Formulations for Different Sexually Transmitted Infections |
title_full_unstemmed | Comparability of Results from Pair and Classical Model Formulations for Different Sexually Transmitted Infections |
title_short | Comparability of Results from Pair and Classical Model Formulations for Different Sexually Transmitted Infections |
title_sort | comparability of results from pair and classical model formulations for different sexually transmitted infections |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3384672/ https://www.ncbi.nlm.nih.gov/pubmed/22761828 http://dx.doi.org/10.1371/journal.pone.0039575 |
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