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Validating and updating a risk model for pneumonia – a case study

BACKGROUND: The development of risk prediction models is of increasing importance in medical research - their use in practice, however, is rare. Among other reasons this might be due to the fact that thorough validation is often lacking. This study focuses on two Bayesian approaches of how to valida...

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Autores principales: Held, Ulrike, Bové, Daniel Sabanes, Steurer, Johann, Held, Leonhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3441433/
https://www.ncbi.nlm.nih.gov/pubmed/22817850
http://dx.doi.org/10.1186/1471-2288-12-99
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author Held, Ulrike
Bové, Daniel Sabanes
Steurer, Johann
Held, Leonhard
author_facet Held, Ulrike
Bové, Daniel Sabanes
Steurer, Johann
Held, Leonhard
author_sort Held, Ulrike
collection PubMed
description BACKGROUND: The development of risk prediction models is of increasing importance in medical research - their use in practice, however, is rare. Among other reasons this might be due to the fact that thorough validation is often lacking. This study focuses on two Bayesian approaches of how to validate a prediction rule for the diagnosis of pneumonia, and compares them with established validation methods. METHODS: Expert knowledge was used to derive a risk prediction model for pneumonia. Data on more than 600 patients presenting with cough and fever at a general practitioner’s practice in Switzerland were collected in order to validate the expert model and to examine the predictive performance of it. Additionally, four modifications of the original model including shrinkage of the regression coefficients, and two Bayesian approaches with the expert model used as prior mean and different weights for the prior covariance matrix were fitted. We quantify the predictive performance of the different methods with respect to calibration and discrimination, using cross-validation. RESULTS: The predictive performance of the unshrinked regression coefficients was poor when applied to the Swiss cohort. Shrinkage improved the results, but a Bayesian model formulation with unspecified weight of the informative prior lead to large AUC and small Brier score, naïve and after cross-validation. The advantage of this approach is the flexibility in case of a prior-data conflict. CONCLUSIONS: Published risk prediction rules in clinical research need to be validated externally before they can be used in new settings. We propose to use a Bayesian model formulation with the original risk prediction rule as prior. The posterior means of the coefficients, given the validation data showed best predictive performance with respect to cross-validated calibration and discriminative ability.
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spelling pubmed-34414332012-09-18 Validating and updating a risk model for pneumonia – a case study Held, Ulrike Bové, Daniel Sabanes Steurer, Johann Held, Leonhard BMC Med Res Methodol Research Article BACKGROUND: The development of risk prediction models is of increasing importance in medical research - their use in practice, however, is rare. Among other reasons this might be due to the fact that thorough validation is often lacking. This study focuses on two Bayesian approaches of how to validate a prediction rule for the diagnosis of pneumonia, and compares them with established validation methods. METHODS: Expert knowledge was used to derive a risk prediction model for pneumonia. Data on more than 600 patients presenting with cough and fever at a general practitioner’s practice in Switzerland were collected in order to validate the expert model and to examine the predictive performance of it. Additionally, four modifications of the original model including shrinkage of the regression coefficients, and two Bayesian approaches with the expert model used as prior mean and different weights for the prior covariance matrix were fitted. We quantify the predictive performance of the different methods with respect to calibration and discrimination, using cross-validation. RESULTS: The predictive performance of the unshrinked regression coefficients was poor when applied to the Swiss cohort. Shrinkage improved the results, but a Bayesian model formulation with unspecified weight of the informative prior lead to large AUC and small Brier score, naïve and after cross-validation. The advantage of this approach is the flexibility in case of a prior-data conflict. CONCLUSIONS: Published risk prediction rules in clinical research need to be validated externally before they can be used in new settings. We propose to use a Bayesian model formulation with the original risk prediction rule as prior. The posterior means of the coefficients, given the validation data showed best predictive performance with respect to cross-validated calibration and discriminative ability. BioMed Central 2012-07-20 /pmc/articles/PMC3441433/ /pubmed/22817850 http://dx.doi.org/10.1186/1471-2288-12-99 Text en Copyright ©2012 Held et al.; http://creativecommons.org/licenses/by/2.0 licensee BioMed Central Ltd. 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 Article
Held, Ulrike
Bové, Daniel Sabanes
Steurer, Johann
Held, Leonhard
Validating and updating a risk model for pneumonia – a case study
title Validating and updating a risk model for pneumonia – a case study
title_full Validating and updating a risk model for pneumonia – a case study
title_fullStr Validating and updating a risk model for pneumonia – a case study
title_full_unstemmed Validating and updating a risk model for pneumonia – a case study
title_short Validating and updating a risk model for pneumonia – a case study
title_sort validating and updating a risk model for pneumonia – a case study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3441433/
https://www.ncbi.nlm.nih.gov/pubmed/22817850
http://dx.doi.org/10.1186/1471-2288-12-99
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