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How to measure temporal changes in care pathways for chronic diseases using health care registry data
BACKGROUND: Disease trajectories for chronic diseases can span over several decades, with several time-dependent factors affecting treatment decisions. Thus, there is a need for long-term predictions of disease trajectories to inform patients and healthcare professionals on the long-term outcomes an...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543619/ https://www.ncbi.nlm.nih.gov/pubmed/31146754 http://dx.doi.org/10.1186/s12911-019-0823-y |
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author | Ventimiglia, Eugenio Van Hemelrijck, Mieke Lindhagen, Lars Stattin, Pär Garmo, Hans |
author_facet | Ventimiglia, Eugenio Van Hemelrijck, Mieke Lindhagen, Lars Stattin, Pär Garmo, Hans |
author_sort | Ventimiglia, Eugenio |
collection | PubMed |
description | BACKGROUND: Disease trajectories for chronic diseases can span over several decades, with several time-dependent factors affecting treatment decisions. Thus, there is a need for long-term predictions of disease trajectories to inform patients and healthcare professionals on the long-term outcomes and provide information on the need of future health care. Here, we propose a state transition model to describe and predict disease trajectories up to 25 years after diagnosis in men with prostate cancer (PCa), as a proof of principle. METHODS: States, state transitions, and transition probabilities were identified and estimated in Prostate Cancer data Base of Sweden (PCBaSe(Traject)), using nationwide population-based data from 118,743 men diagnosed with PCa. A state transition model in discrete time steps (i.e., 4 weeks) was developed and applied to capture all possible transitions (PCBaSe(Sim)). Transition probabilities were estimated for changes in both treatment and comorbidity. These models combined yielded parameter estimates to run an individual-level simulation based on the state-transition model to obtain prediction estimates. Predicted estimates were then compared to real world data in PCBaSe(Traject). RESULTS: PCBaSe(Sim) estimates for the cumulative incidence of first and second transitions, death from PCa and death from other causes were compared to observed transitions in PCBaSe(Traject). A good agreement was found between simulated and observed estimates. CONCLUSIONS: We developed a reliable and accurate simulation tool, PCBaSe(Sim) that provides information on disease trajectories for subjects with a chronic disease on an individual and population-based level. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12911-019-0823-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6543619 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65436192019-06-04 How to measure temporal changes in care pathways for chronic diseases using health care registry data Ventimiglia, Eugenio Van Hemelrijck, Mieke Lindhagen, Lars Stattin, Pär Garmo, Hans BMC Med Inform Decis Mak Research Article BACKGROUND: Disease trajectories for chronic diseases can span over several decades, with several time-dependent factors affecting treatment decisions. Thus, there is a need for long-term predictions of disease trajectories to inform patients and healthcare professionals on the long-term outcomes and provide information on the need of future health care. Here, we propose a state transition model to describe and predict disease trajectories up to 25 years after diagnosis in men with prostate cancer (PCa), as a proof of principle. METHODS: States, state transitions, and transition probabilities were identified and estimated in Prostate Cancer data Base of Sweden (PCBaSe(Traject)), using nationwide population-based data from 118,743 men diagnosed with PCa. A state transition model in discrete time steps (i.e., 4 weeks) was developed and applied to capture all possible transitions (PCBaSe(Sim)). Transition probabilities were estimated for changes in both treatment and comorbidity. These models combined yielded parameter estimates to run an individual-level simulation based on the state-transition model to obtain prediction estimates. Predicted estimates were then compared to real world data in PCBaSe(Traject). RESULTS: PCBaSe(Sim) estimates for the cumulative incidence of first and second transitions, death from PCa and death from other causes were compared to observed transitions in PCBaSe(Traject). A good agreement was found between simulated and observed estimates. CONCLUSIONS: We developed a reliable and accurate simulation tool, PCBaSe(Sim) that provides information on disease trajectories for subjects with a chronic disease on an individual and population-based level. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12911-019-0823-y) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-30 /pmc/articles/PMC6543619/ /pubmed/31146754 http://dx.doi.org/10.1186/s12911-019-0823-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Ventimiglia, Eugenio Van Hemelrijck, Mieke Lindhagen, Lars Stattin, Pär Garmo, Hans How to measure temporal changes in care pathways for chronic diseases using health care registry data |
title | How to measure temporal changes in care pathways for chronic diseases using health care registry data |
title_full | How to measure temporal changes in care pathways for chronic diseases using health care registry data |
title_fullStr | How to measure temporal changes in care pathways for chronic diseases using health care registry data |
title_full_unstemmed | How to measure temporal changes in care pathways for chronic diseases using health care registry data |
title_short | How to measure temporal changes in care pathways for chronic diseases using health care registry data |
title_sort | how to measure temporal changes in care pathways for chronic diseases using health care registry data |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543619/ https://www.ncbi.nlm.nih.gov/pubmed/31146754 http://dx.doi.org/10.1186/s12911-019-0823-y |
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