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Development and Evaluation of a Prediction Model for Ascertaining Rheumatic Heart Disease Status in Administrative Data
BACKGROUND: Previous research has raised substantial concerns regarding the validity of the International Statistical Classification of Diseases and Related Health Problems (ICD) codes (ICD-10 I05–I09) for rheumatic heart disease (RHD) due to likely misclassification of non-rheumatic valvular diseas...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7358074/ https://www.ncbi.nlm.nih.gov/pubmed/32753974 http://dx.doi.org/10.2147/CLEP.S241588 |
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author | Bond-Smith, D Seth, R de Klerk, N Nedkoff, L Anderson, M Hung, J Cannon, J Griffiths, K Katzenellenbogen, J M |
author_facet | Bond-Smith, D Seth, R de Klerk, N Nedkoff, L Anderson, M Hung, J Cannon, J Griffiths, K Katzenellenbogen, J M |
author_sort | Bond-Smith, D |
collection | PubMed |
description | BACKGROUND: Previous research has raised substantial concerns regarding the validity of the International Statistical Classification of Diseases and Related Health Problems (ICD) codes (ICD-10 I05–I09) for rheumatic heart disease (RHD) due to likely misclassification of non-rheumatic valvular disease (non-rheumatic VHD) as RHD. There is currently no validated, quantitative approach for reliable case ascertainment of RHD in administrative hospital data. METHODS: A comprehensive dataset of validated Australian RHD cases was compiled and linked to inpatient hospital records with an RHD ICD code (2000–2018, n=7555). A prediction model was developed based on a generalized linear mixed model structure considering an extensive range of demographic and clinical variables. It was validated internally using randomly selected cross-validation samples and externally. Conditional optimal probability cutpoints were calculated, maximising discrimination separately for high-risk versus low-risk populations. RESULTS: The proposed model reduced the false-positive rate (FPR) from acute rheumatic fever (ARF) cases misclassified as RHD from 0.59 to 0.27; similarly for non-rheumatic VHD from 0.77 to 0.22. Overall, the model achieved strong discriminant capacity (AUC: 0.93) and maintained a similar robust performance during external validation (AUC: 0.88). It can also be used when only basic demographic and diagnosis data are available. CONCLUSION: This paper is the first to show that not only misclassification of non-rheumatic VHD but also of ARF as RHD yields substantial FPRs. Both sources of bias can be successfully addressed with the proposed model which provides an effective solution for reliable RHD case ascertainment from hospital data for epidemiological disease monitoring and policy evaluation. |
format | Online Article Text |
id | pubmed-7358074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-73580742020-08-03 Development and Evaluation of a Prediction Model for Ascertaining Rheumatic Heart Disease Status in Administrative Data Bond-Smith, D Seth, R de Klerk, N Nedkoff, L Anderson, M Hung, J Cannon, J Griffiths, K Katzenellenbogen, J M Clin Epidemiol Original Research BACKGROUND: Previous research has raised substantial concerns regarding the validity of the International Statistical Classification of Diseases and Related Health Problems (ICD) codes (ICD-10 I05–I09) for rheumatic heart disease (RHD) due to likely misclassification of non-rheumatic valvular disease (non-rheumatic VHD) as RHD. There is currently no validated, quantitative approach for reliable case ascertainment of RHD in administrative hospital data. METHODS: A comprehensive dataset of validated Australian RHD cases was compiled and linked to inpatient hospital records with an RHD ICD code (2000–2018, n=7555). A prediction model was developed based on a generalized linear mixed model structure considering an extensive range of demographic and clinical variables. It was validated internally using randomly selected cross-validation samples and externally. Conditional optimal probability cutpoints were calculated, maximising discrimination separately for high-risk versus low-risk populations. RESULTS: The proposed model reduced the false-positive rate (FPR) from acute rheumatic fever (ARF) cases misclassified as RHD from 0.59 to 0.27; similarly for non-rheumatic VHD from 0.77 to 0.22. Overall, the model achieved strong discriminant capacity (AUC: 0.93) and maintained a similar robust performance during external validation (AUC: 0.88). It can also be used when only basic demographic and diagnosis data are available. CONCLUSION: This paper is the first to show that not only misclassification of non-rheumatic VHD but also of ARF as RHD yields substantial FPRs. Both sources of bias can be successfully addressed with the proposed model which provides an effective solution for reliable RHD case ascertainment from hospital data for epidemiological disease monitoring and policy evaluation. Dove 2020-07-09 /pmc/articles/PMC7358074/ /pubmed/32753974 http://dx.doi.org/10.2147/CLEP.S241588 Text en © 2020 Bond-Smith et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Bond-Smith, D Seth, R de Klerk, N Nedkoff, L Anderson, M Hung, J Cannon, J Griffiths, K Katzenellenbogen, J M Development and Evaluation of a Prediction Model for Ascertaining Rheumatic Heart Disease Status in Administrative Data |
title | Development and Evaluation of a Prediction Model for Ascertaining Rheumatic Heart Disease Status in Administrative Data |
title_full | Development and Evaluation of a Prediction Model for Ascertaining Rheumatic Heart Disease Status in Administrative Data |
title_fullStr | Development and Evaluation of a Prediction Model for Ascertaining Rheumatic Heart Disease Status in Administrative Data |
title_full_unstemmed | Development and Evaluation of a Prediction Model for Ascertaining Rheumatic Heart Disease Status in Administrative Data |
title_short | Development and Evaluation of a Prediction Model for Ascertaining Rheumatic Heart Disease Status in Administrative Data |
title_sort | development and evaluation of a prediction model for ascertaining rheumatic heart disease status in administrative data |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7358074/ https://www.ncbi.nlm.nih.gov/pubmed/32753974 http://dx.doi.org/10.2147/CLEP.S241588 |
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