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Comparison and validation of two computational models of Chagas disease: A thirty year perspective from Venezuela

BACKGROUND: Mathematical models can help aid public health responses to Chagas disease. Models are typically developed to fulfill a particular need, and comparing outputs from different models addressing the same question can help identify the strengths and weaknesses of the models in answering part...

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Autores principales: Bartsch, Sarah M., Peterson, Jennifer K., Hertenstein, Daniel L, Skrip, Laura, Ndeffo-Mbah, Martial, Galvani, Alison P., Dobson, Andrew P., Lee, Bruce Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5549789/
https://www.ncbi.nlm.nih.gov/pubmed/28279459
http://dx.doi.org/10.1016/j.epidem.2017.02.004
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author Bartsch, Sarah M.
Peterson, Jennifer K.
Hertenstein, Daniel L
Skrip, Laura
Ndeffo-Mbah, Martial
Galvani, Alison P.
Dobson, Andrew P.
Lee, Bruce Y.
author_facet Bartsch, Sarah M.
Peterson, Jennifer K.
Hertenstein, Daniel L
Skrip, Laura
Ndeffo-Mbah, Martial
Galvani, Alison P.
Dobson, Andrew P.
Lee, Bruce Y.
author_sort Bartsch, Sarah M.
collection PubMed
description BACKGROUND: Mathematical models can help aid public health responses to Chagas disease. Models are typically developed to fulfill a particular need, and comparing outputs from different models addressing the same question can help identify the strengths and weaknesses of the models in answering particular questions, such as those for achieving the 2020 goals for Chagas disease. METHODS: Using two separately developed models (PHICOR/CIDMA model and Princeton model), we simulated dynamics for domestic transmission of Trypanosoma cruzi (T. cruzi). We compared how well the models targeted the last 9 years and last 19 years of the 1968–1998 historical seroprevalence data from Venezuela. RESULTS: Both models were able to generate the T. cruzi seroprevalence for the next time period within reason to the historical data. The PHICOR/CIDMA model estimates of the total population seroprevalence more closely followed the trends seen in the historic data, while the Princeton model estimates of the age-specific seroprevalence more closely followed historic trends when simulating over 9 years. Additionally, results from both models overestimated T. cruzi seroprevalence among younger age groups, while underestimating the seroprevalence of T. cruzi in older age groups. CONCLUSION: The PHICOR/CIDMA and Princeton models differ in level of detail and included features, yet both were able to generate the historical changes in T. cruzi seroprevalence in Venezuela over 9 and 19-year time periods. Our model comparison has demonstrated that different model structures can be useful in evaluating disease transmission dynamics and intervention strategies.
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spelling pubmed-55497892018-03-01 Comparison and validation of two computational models of Chagas disease: A thirty year perspective from Venezuela Bartsch, Sarah M. Peterson, Jennifer K. Hertenstein, Daniel L Skrip, Laura Ndeffo-Mbah, Martial Galvani, Alison P. Dobson, Andrew P. Lee, Bruce Y. Epidemics Article BACKGROUND: Mathematical models can help aid public health responses to Chagas disease. Models are typically developed to fulfill a particular need, and comparing outputs from different models addressing the same question can help identify the strengths and weaknesses of the models in answering particular questions, such as those for achieving the 2020 goals for Chagas disease. METHODS: Using two separately developed models (PHICOR/CIDMA model and Princeton model), we simulated dynamics for domestic transmission of Trypanosoma cruzi (T. cruzi). We compared how well the models targeted the last 9 years and last 19 years of the 1968–1998 historical seroprevalence data from Venezuela. RESULTS: Both models were able to generate the T. cruzi seroprevalence for the next time period within reason to the historical data. The PHICOR/CIDMA model estimates of the total population seroprevalence more closely followed the trends seen in the historic data, while the Princeton model estimates of the age-specific seroprevalence more closely followed historic trends when simulating over 9 years. Additionally, results from both models overestimated T. cruzi seroprevalence among younger age groups, while underestimating the seroprevalence of T. cruzi in older age groups. CONCLUSION: The PHICOR/CIDMA and Princeton models differ in level of detail and included features, yet both were able to generate the historical changes in T. cruzi seroprevalence in Venezuela over 9 and 19-year time periods. Our model comparison has demonstrated that different model structures can be useful in evaluating disease transmission dynamics and intervention strategies. 2017-03 /pmc/articles/PMC5549789/ /pubmed/28279459 http://dx.doi.org/10.1016/j.epidem.2017.02.004 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Bartsch, Sarah M.
Peterson, Jennifer K.
Hertenstein, Daniel L
Skrip, Laura
Ndeffo-Mbah, Martial
Galvani, Alison P.
Dobson, Andrew P.
Lee, Bruce Y.
Comparison and validation of two computational models of Chagas disease: A thirty year perspective from Venezuela
title Comparison and validation of two computational models of Chagas disease: A thirty year perspective from Venezuela
title_full Comparison and validation of two computational models of Chagas disease: A thirty year perspective from Venezuela
title_fullStr Comparison and validation of two computational models of Chagas disease: A thirty year perspective from Venezuela
title_full_unstemmed Comparison and validation of two computational models of Chagas disease: A thirty year perspective from Venezuela
title_short Comparison and validation of two computational models of Chagas disease: A thirty year perspective from Venezuela
title_sort comparison and validation of two computational models of chagas disease: a thirty year perspective from venezuela
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5549789/
https://www.ncbi.nlm.nih.gov/pubmed/28279459
http://dx.doi.org/10.1016/j.epidem.2017.02.004
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