Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Su, Kang-Cheng, Ko, Hsin-Kuo, Chou, Kun-Ta, Hsiao, Yi-Han, Su, Vincent Yi-Fong, Perng, Diahn-Warng, Kou, Yu Ru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
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
_version_ 1783422207200854016
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
work_keys_str_mv AT sukangcheng anaccuratepredictionmodeltoidentifyundiagnosedatriskpatientswithcopdacrosssectionalcasefindingstudy
AT kohsinkuo anaccuratepredictionmodeltoidentifyundiagnosedatriskpatientswithcopdacrosssectionalcasefindingstudy
AT choukunta anaccuratepredictionmodeltoidentifyundiagnosedatriskpatientswithcopdacrosssectionalcasefindingstudy
AT hsiaoyihan anaccuratepredictionmodeltoidentifyundiagnosedatriskpatientswithcopdacrosssectionalcasefindingstudy
AT suvincentyifong anaccuratepredictionmodeltoidentifyundiagnosedatriskpatientswithcopdacrosssectionalcasefindingstudy
AT perngdiahnwarng anaccuratepredictionmodeltoidentifyundiagnosedatriskpatientswithcopdacrosssectionalcasefindingstudy
AT kouyuru anaccuratepredictionmodeltoidentifyundiagnosedatriskpatientswithcopdacrosssectionalcasefindingstudy
AT sukangcheng accuratepredictionmodeltoidentifyundiagnosedatriskpatientswithcopdacrosssectionalcasefindingstudy
AT kohsinkuo accuratepredictionmodeltoidentifyundiagnosedatriskpatientswithcopdacrosssectionalcasefindingstudy
AT choukunta accuratepredictionmodeltoidentifyundiagnosedatriskpatientswithcopdacrosssectionalcasefindingstudy
AT hsiaoyihan accuratepredictionmodeltoidentifyundiagnosedatriskpatientswithcopdacrosssectionalcasefindingstudy
AT suvincentyifong accuratepredictionmodeltoidentifyundiagnosedatriskpatientswithcopdacrosssectionalcasefindingstudy
AT perngdiahnwarng accuratepredictionmodeltoidentifyundiagnosedatriskpatientswithcopdacrosssectionalcasefindingstudy
AT kouyuru accuratepredictionmodeltoidentifyundiagnosedatriskpatientswithcopdacrosssectionalcasefindingstudy