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An accurate prediction model to identify undiagnosed at-risk patients with COPD: a cross-sectional case-finding study
Underuse or unavailability of spirometry is one of the most important factors causing underdiagnosis of COPD. We reported the development of a COPD prediction model to identify at-risk, undiagnosed COPD patients when spirometry was unavailable. This cross-sectional study enrolled subjects aged ≥40 y...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6538645/ https://www.ncbi.nlm.nih.gov/pubmed/31138809 http://dx.doi.org/10.1038/s41533-019-0135-9 |
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author | Su, Kang-Cheng Ko, Hsin-Kuo Chou, Kun-Ta Hsiao, Yi-Han Su, Vincent Yi-Fong Perng, Diahn-Warng Kou, Yu Ru |
author_facet | Su, Kang-Cheng Ko, Hsin-Kuo Chou, Kun-Ta Hsiao, Yi-Han Su, Vincent Yi-Fong Perng, Diahn-Warng Kou, Yu Ru |
author_sort | Su, Kang-Cheng |
collection | PubMed |
description | Underuse or unavailability of spirometry is one of the most important factors causing underdiagnosis of COPD. We reported the development of a COPD prediction model to identify at-risk, undiagnosed COPD patients when spirometry was unavailable. This cross-sectional study enrolled subjects aged ≥40 years with respiratory symptoms and a smoking history (≥20 pack-years) in a medical center in two separate periods (development and validation cohorts). All subjects completed COPD assessment test (CAT), peak expiratory flow rate (PEFR) measurement, and confirmatory spirometry. A binary logistic model with calibration (Hosmer-Lemeshow test) and discrimination (area under receiver operating characteristic curve [AUROC]) was implemented. Three hundred and one subjects (development cohort) completed the study, including non-COPD (154, 51.2%) and COPD cases (147; stage I, 27.2%; II, 55.8%; III–IV, 17%). Compared with non-COPD and GOLD I cases, GOLD II-IV patients exhibited significantly higher CAT scores and lower lung function, and were considered clinically significant for COPD. Four independent variables (age, smoking pack-years, CAT score, and percent predicted PEFR) were incorporated developing the prediction model, which estimated the COPD probability (P(COPD)). This model demonstrated favorable discrimination (AUROC: 0.866/0.828; 95% CI 0.825–0.906/0.751–0.904) and calibration (Hosmer-Lemeshow P = 0.332/0.668) for the development and validation cohorts, respectively. Bootstrap validation with 1000 replicates yielded an AUROC of 0.866 (95% CI 0.821–0.905). A P(COPD) of ≥0.65 identified COPD patients with high specificity (90%) and a large proportion (91.4%) of patients with clinically significant COPD (development cohort). Our prediction model can help physicians effectively identify at-risk, undiagnosed COPD patients for further diagnostic evaluation and timely treatment when spirometry is unavailable. |
format | Online Article Text |
id | pubmed-6538645 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65386452019-05-30 An accurate prediction model to identify undiagnosed at-risk patients with COPD: a cross-sectional case-finding study Su, Kang-Cheng Ko, Hsin-Kuo Chou, Kun-Ta Hsiao, Yi-Han Su, Vincent Yi-Fong Perng, Diahn-Warng Kou, Yu Ru NPJ Prim Care Respir Med Article Underuse or unavailability of spirometry is one of the most important factors causing underdiagnosis of COPD. We reported the development of a COPD prediction model to identify at-risk, undiagnosed COPD patients when spirometry was unavailable. This cross-sectional study enrolled subjects aged ≥40 years with respiratory symptoms and a smoking history (≥20 pack-years) in a medical center in two separate periods (development and validation cohorts). All subjects completed COPD assessment test (CAT), peak expiratory flow rate (PEFR) measurement, and confirmatory spirometry. A binary logistic model with calibration (Hosmer-Lemeshow test) and discrimination (area under receiver operating characteristic curve [AUROC]) was implemented. Three hundred and one subjects (development cohort) completed the study, including non-COPD (154, 51.2%) and COPD cases (147; stage I, 27.2%; II, 55.8%; III–IV, 17%). Compared with non-COPD and GOLD I cases, GOLD II-IV patients exhibited significantly higher CAT scores and lower lung function, and were considered clinically significant for COPD. Four independent variables (age, smoking pack-years, CAT score, and percent predicted PEFR) were incorporated developing the prediction model, which estimated the COPD probability (P(COPD)). This model demonstrated favorable discrimination (AUROC: 0.866/0.828; 95% CI 0.825–0.906/0.751–0.904) and calibration (Hosmer-Lemeshow P = 0.332/0.668) for the development and validation cohorts, respectively. Bootstrap validation with 1000 replicates yielded an AUROC of 0.866 (95% CI 0.821–0.905). A P(COPD) of ≥0.65 identified COPD patients with high specificity (90%) and a large proportion (91.4%) of patients with clinically significant COPD (development cohort). Our prediction model can help physicians effectively identify at-risk, undiagnosed COPD patients for further diagnostic evaluation and timely treatment when spirometry is unavailable. Nature Publishing Group UK 2019-05-28 /pmc/articles/PMC6538645/ /pubmed/31138809 http://dx.doi.org/10.1038/s41533-019-0135-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Su, Kang-Cheng Ko, Hsin-Kuo Chou, Kun-Ta Hsiao, Yi-Han Su, Vincent Yi-Fong Perng, Diahn-Warng Kou, Yu Ru An accurate prediction model to identify undiagnosed at-risk patients with COPD: a cross-sectional case-finding study |
title | An accurate prediction model to identify undiagnosed at-risk patients with COPD: a cross-sectional case-finding study |
title_full | An accurate prediction model to identify undiagnosed at-risk patients with COPD: a cross-sectional case-finding study |
title_fullStr | An accurate prediction model to identify undiagnosed at-risk patients with COPD: a cross-sectional case-finding study |
title_full_unstemmed | An accurate prediction model to identify undiagnosed at-risk patients with COPD: a cross-sectional case-finding study |
title_short | An accurate prediction model to identify undiagnosed at-risk patients with COPD: a cross-sectional case-finding study |
title_sort | accurate prediction model to identify undiagnosed at-risk patients with copd: a cross-sectional case-finding study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6538645/ https://www.ncbi.nlm.nih.gov/pubmed/31138809 http://dx.doi.org/10.1038/s41533-019-0135-9 |
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