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Characterization and Valuation of the Uncertainty of Calibrated Parameters in Microsimulation Decision Models
Background: We evaluated the implications of different approaches to characterize the uncertainty of calibrated parameters of microsimulation decision models (DMs) and quantified the value of such uncertainty in decision making. Methods: We calibrated the natural history model of CRC to simulated ep...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124835/ https://www.ncbi.nlm.nih.gov/pubmed/35615677 http://dx.doi.org/10.3389/fphys.2022.780917 |
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author | Alarid-Escudero, Fernando Knudsen, Amy B. Ozik, Jonathan Collier, Nicholson Kuntz, Karen M. |
author_facet | Alarid-Escudero, Fernando Knudsen, Amy B. Ozik, Jonathan Collier, Nicholson Kuntz, Karen M. |
author_sort | Alarid-Escudero, Fernando |
collection | PubMed |
description | Background: We evaluated the implications of different approaches to characterize the uncertainty of calibrated parameters of microsimulation decision models (DMs) and quantified the value of such uncertainty in decision making. Methods: We calibrated the natural history model of CRC to simulated epidemiological data with different degrees of uncertainty and obtained the joint posterior distribution of the parameters using a Bayesian approach. We conducted a probabilistic sensitivity analysis (PSA) on all the model parameters with different characterizations of the uncertainty of the calibrated parameters. We estimated the value of uncertainty of the various characterizations with a value of information analysis. We conducted all analyses using high-performance computing resources running the Extreme-scale Model Exploration with Swift (EMEWS) framework. Results: The posterior distribution had a high correlation among some parameters. The parameters of the Weibull hazard function for the age of onset of adenomas had the highest posterior correlation of −0.958. When comparing full posterior distributions and the maximum-a-posteriori estimate of the calibrated parameters, there is little difference in the spread of the distribution of the CEA outcomes with a similar expected value of perfect information (EVPI) of $653 and $685, respectively, at a willingness-to-pay (WTP) threshold of $66,000 per quality-adjusted life year (QALY). Ignoring correlation on the calibrated parameters’ posterior distribution produced the broadest distribution of CEA outcomes and the highest EVPI of $809 at the same WTP threshold. Conclusion: Different characterizations of the uncertainty of calibrated parameters affect the expected value of eliminating parametric uncertainty on the CEA. Ignoring inherent correlation among calibrated parameters on a PSA overestimates the value of uncertainty. |
format | Online Article Text |
id | pubmed-9124835 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91248352022-05-24 Characterization and Valuation of the Uncertainty of Calibrated Parameters in Microsimulation Decision Models Alarid-Escudero, Fernando Knudsen, Amy B. Ozik, Jonathan Collier, Nicholson Kuntz, Karen M. Front Physiol Physiology Background: We evaluated the implications of different approaches to characterize the uncertainty of calibrated parameters of microsimulation decision models (DMs) and quantified the value of such uncertainty in decision making. Methods: We calibrated the natural history model of CRC to simulated epidemiological data with different degrees of uncertainty and obtained the joint posterior distribution of the parameters using a Bayesian approach. We conducted a probabilistic sensitivity analysis (PSA) on all the model parameters with different characterizations of the uncertainty of the calibrated parameters. We estimated the value of uncertainty of the various characterizations with a value of information analysis. We conducted all analyses using high-performance computing resources running the Extreme-scale Model Exploration with Swift (EMEWS) framework. Results: The posterior distribution had a high correlation among some parameters. The parameters of the Weibull hazard function for the age of onset of adenomas had the highest posterior correlation of −0.958. When comparing full posterior distributions and the maximum-a-posteriori estimate of the calibrated parameters, there is little difference in the spread of the distribution of the CEA outcomes with a similar expected value of perfect information (EVPI) of $653 and $685, respectively, at a willingness-to-pay (WTP) threshold of $66,000 per quality-adjusted life year (QALY). Ignoring correlation on the calibrated parameters’ posterior distribution produced the broadest distribution of CEA outcomes and the highest EVPI of $809 at the same WTP threshold. Conclusion: Different characterizations of the uncertainty of calibrated parameters affect the expected value of eliminating parametric uncertainty on the CEA. Ignoring inherent correlation among calibrated parameters on a PSA overestimates the value of uncertainty. Frontiers Media S.A. 2022-05-09 /pmc/articles/PMC9124835/ /pubmed/35615677 http://dx.doi.org/10.3389/fphys.2022.780917 Text en Copyright © 2022 Alarid-Escudero, Knudsen, Ozik, Collier and Kuntz. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Alarid-Escudero, Fernando Knudsen, Amy B. Ozik, Jonathan Collier, Nicholson Kuntz, Karen M. Characterization and Valuation of the Uncertainty of Calibrated Parameters in Microsimulation Decision Models |
title | Characterization and Valuation of the Uncertainty of Calibrated Parameters in Microsimulation Decision Models |
title_full | Characterization and Valuation of the Uncertainty of Calibrated Parameters in Microsimulation Decision Models |
title_fullStr | Characterization and Valuation of the Uncertainty of Calibrated Parameters in Microsimulation Decision Models |
title_full_unstemmed | Characterization and Valuation of the Uncertainty of Calibrated Parameters in Microsimulation Decision Models |
title_short | Characterization and Valuation of the Uncertainty of Calibrated Parameters in Microsimulation Decision Models |
title_sort | characterization and valuation of the uncertainty of calibrated parameters in microsimulation decision models |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124835/ https://www.ncbi.nlm.nih.gov/pubmed/35615677 http://dx.doi.org/10.3389/fphys.2022.780917 |
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