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Modeling causes of death: an integrated approach using CODEm
BACKGROUND: Data on causes of death by age and sex are a critical input into health decision-making. Priority setting in public health should be informed not only by the current magnitude of health problems but by trends in them. However, cause of death data are often not available or are subject to...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315398/ https://www.ncbi.nlm.nih.gov/pubmed/22226226 http://dx.doi.org/10.1186/1478-7954-10-1 |
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author | Foreman, Kyle J Lozano, Rafael Lopez, Alan D Murray, Christopher JL |
author_facet | Foreman, Kyle J Lozano, Rafael Lopez, Alan D Murray, Christopher JL |
author_sort | Foreman, Kyle J |
collection | PubMed |
description | BACKGROUND: Data on causes of death by age and sex are a critical input into health decision-making. Priority setting in public health should be informed not only by the current magnitude of health problems but by trends in them. However, cause of death data are often not available or are subject to substantial problems of comparability. We propose five general principles for cause of death model development, validation, and reporting. METHODS: We detail a specific implementation of these principles that is embodied in an analytical tool - the Cause of Death Ensemble model (CODEm) - which explores a large variety of possible models to estimate trends in causes of death. Possible models are identified using a covariate selection algorithm that yields many plausible combinations of covariates, which are then run through four model classes. The model classes include mixed effects linear models and spatial-temporal Gaussian Process Regression models for cause fractions and death rates. All models for each cause of death are then assessed using out-of-sample predictive validity and combined into an ensemble with optimal out-of-sample predictive performance. RESULTS: Ensemble models for cause of death estimation outperform any single component model in tests of root mean square error, frequency of predicting correct temporal trends, and achieving 95% coverage of the prediction interval. We present detailed results for CODEm applied to maternal mortality and summary results for several other causes of death, including cardiovascular disease and several cancers. CONCLUSIONS: CODEm produces better estimates of cause of death trends than previous methods and is less susceptible to bias in model specification. We demonstrate the utility of CODEm for the estimation of several major causes of death. |
format | Online Article Text |
id | pubmed-3315398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33153982012-04-04 Modeling causes of death: an integrated approach using CODEm Foreman, Kyle J Lozano, Rafael Lopez, Alan D Murray, Christopher JL Popul Health Metr Research BACKGROUND: Data on causes of death by age and sex are a critical input into health decision-making. Priority setting in public health should be informed not only by the current magnitude of health problems but by trends in them. However, cause of death data are often not available or are subject to substantial problems of comparability. We propose five general principles for cause of death model development, validation, and reporting. METHODS: We detail a specific implementation of these principles that is embodied in an analytical tool - the Cause of Death Ensemble model (CODEm) - which explores a large variety of possible models to estimate trends in causes of death. Possible models are identified using a covariate selection algorithm that yields many plausible combinations of covariates, which are then run through four model classes. The model classes include mixed effects linear models and spatial-temporal Gaussian Process Regression models for cause fractions and death rates. All models for each cause of death are then assessed using out-of-sample predictive validity and combined into an ensemble with optimal out-of-sample predictive performance. RESULTS: Ensemble models for cause of death estimation outperform any single component model in tests of root mean square error, frequency of predicting correct temporal trends, and achieving 95% coverage of the prediction interval. We present detailed results for CODEm applied to maternal mortality and summary results for several other causes of death, including cardiovascular disease and several cancers. CONCLUSIONS: CODEm produces better estimates of cause of death trends than previous methods and is less susceptible to bias in model specification. We demonstrate the utility of CODEm for the estimation of several major causes of death. BioMed Central 2012-01-06 /pmc/articles/PMC3315398/ /pubmed/22226226 http://dx.doi.org/10.1186/1478-7954-10-1 Text en Copyright ©2012 Foreman et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Foreman, Kyle J Lozano, Rafael Lopez, Alan D Murray, Christopher JL Modeling causes of death: an integrated approach using CODEm |
title | Modeling causes of death: an integrated approach using CODEm |
title_full | Modeling causes of death: an integrated approach using CODEm |
title_fullStr | Modeling causes of death: an integrated approach using CODEm |
title_full_unstemmed | Modeling causes of death: an integrated approach using CODEm |
title_short | Modeling causes of death: an integrated approach using CODEm |
title_sort | modeling causes of death: an integrated approach using codem |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315398/ https://www.ncbi.nlm.nih.gov/pubmed/22226226 http://dx.doi.org/10.1186/1478-7954-10-1 |
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