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Prognostic value of CAD-RADS classification by coronary CTA in patients with suspected CAD

BACKGROUND: The study sought to compare Coronary Artery Disease Reporting and Data System (CAD-RADS) classification with traditional coronary artery disease (CAD) classifications and Duke Prognostic CAD Index for predicting the risk of all-cause mortality in patients with suspected CAD. METHODS: 962...

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Autores principales: Huang, Zengfa, Zhang, Shutong, Jin, Nan, Hu, Yun, Xiao, Jianwei, Li, Zuoqin, Yang, Yang, Sun, Ruihong, Wang, Zheng, Li, Xiang, Xie, Yuanliang, Wang, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487531/
https://www.ncbi.nlm.nih.gov/pubmed/34602055
http://dx.doi.org/10.1186/s12872-021-02286-x
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author Huang, Zengfa
Zhang, Shutong
Jin, Nan
Hu, Yun
Xiao, Jianwei
Li, Zuoqin
Yang, Yang
Sun, Ruihong
Wang, Zheng
Li, Xiang
Xie, Yuanliang
Wang, Xiang
author_facet Huang, Zengfa
Zhang, Shutong
Jin, Nan
Hu, Yun
Xiao, Jianwei
Li, Zuoqin
Yang, Yang
Sun, Ruihong
Wang, Zheng
Li, Xiang
Xie, Yuanliang
Wang, Xiang
author_sort Huang, Zengfa
collection PubMed
description BACKGROUND: The study sought to compare Coronary Artery Disease Reporting and Data System (CAD-RADS) classification with traditional coronary artery disease (CAD) classifications and Duke Prognostic CAD Index for predicting the risk of all-cause mortality in patients with suspected CAD. METHODS: 9625 consecutive suspected CAD patients were assessed by coronary CTA for CAD-RADS classification, traditional CAD classifications and Duke Prognostic CAD Index. Kaplan–Meier and multivariable Cox models were used to estimate all-cause mortality. Discriminatory ability of classifications was assessed using time dependent receiver-operating characteristic (ROC) curves and The Hosmer–Lemeshow goodness-of-fit test was employed to evaluate calibration. RESULTS: A total of 540 patients died from all causes with a median follow-up of 4.3 ± 2.1 years. Kaplan–Meier survival curves showed the cumulative events increased significantly associated with CAD-RADS, three traditional CAD classifications and Duke Prognostic CAD Index. In multivariate Cox regressions, the risk for the all-cause death increased from HR 0.861 (95% CI 0.420–1.764) for CAD-RADS 1 to HR 2.761 (95% CI 1.961–3.887) for CAD-RADS 4B&5, using CAD-RADS 0 as the reference group. The relative HRs for all-cause death increased proportionally with the grades of the three traditional CAD classifications and Duke Prognostic CAD Index. The area under the time dependent ROC curve for prediction of all-cause death was 0.7917, 0.7805, 0.7991for CAD-RADS in 1 year, 3 year, 5 year, respectively, which was non-inferior to the traditional CAD classifications and Duke Prognostic CAD Index. CONCLUSIONS: The CAD-RADS classification provided important prognostic information for patients with suspected CAD with noninvasive evaluation, which was non-inferior than Duke Prognostic CAD Index and traditional stenosis-based grading schemes in prognostic value of all-cause mortality. Traditional and simplest CAD classification should be preferable, given the more number of groups and complexity of CAD-RADS and Duke prognostic index, without using more time consuming classification. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12872-021-02286-x.
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spelling pubmed-84875312021-10-04 Prognostic value of CAD-RADS classification by coronary CTA in patients with suspected CAD Huang, Zengfa Zhang, Shutong Jin, Nan Hu, Yun Xiao, Jianwei Li, Zuoqin Yang, Yang Sun, Ruihong Wang, Zheng Li, Xiang Xie, Yuanliang Wang, Xiang BMC Cardiovasc Disord Research BACKGROUND: The study sought to compare Coronary Artery Disease Reporting and Data System (CAD-RADS) classification with traditional coronary artery disease (CAD) classifications and Duke Prognostic CAD Index for predicting the risk of all-cause mortality in patients with suspected CAD. METHODS: 9625 consecutive suspected CAD patients were assessed by coronary CTA for CAD-RADS classification, traditional CAD classifications and Duke Prognostic CAD Index. Kaplan–Meier and multivariable Cox models were used to estimate all-cause mortality. Discriminatory ability of classifications was assessed using time dependent receiver-operating characteristic (ROC) curves and The Hosmer–Lemeshow goodness-of-fit test was employed to evaluate calibration. RESULTS: A total of 540 patients died from all causes with a median follow-up of 4.3 ± 2.1 years. Kaplan–Meier survival curves showed the cumulative events increased significantly associated with CAD-RADS, three traditional CAD classifications and Duke Prognostic CAD Index. In multivariate Cox regressions, the risk for the all-cause death increased from HR 0.861 (95% CI 0.420–1.764) for CAD-RADS 1 to HR 2.761 (95% CI 1.961–3.887) for CAD-RADS 4B&5, using CAD-RADS 0 as the reference group. The relative HRs for all-cause death increased proportionally with the grades of the three traditional CAD classifications and Duke Prognostic CAD Index. The area under the time dependent ROC curve for prediction of all-cause death was 0.7917, 0.7805, 0.7991for CAD-RADS in 1 year, 3 year, 5 year, respectively, which was non-inferior to the traditional CAD classifications and Duke Prognostic CAD Index. CONCLUSIONS: The CAD-RADS classification provided important prognostic information for patients with suspected CAD with noninvasive evaluation, which was non-inferior than Duke Prognostic CAD Index and traditional stenosis-based grading schemes in prognostic value of all-cause mortality. Traditional and simplest CAD classification should be preferable, given the more number of groups and complexity of CAD-RADS and Duke prognostic index, without using more time consuming classification. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12872-021-02286-x. BioMed Central 2021-10-03 /pmc/articles/PMC8487531/ /pubmed/34602055 http://dx.doi.org/10.1186/s12872-021-02286-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Huang, Zengfa
Zhang, Shutong
Jin, Nan
Hu, Yun
Xiao, Jianwei
Li, Zuoqin
Yang, Yang
Sun, Ruihong
Wang, Zheng
Li, Xiang
Xie, Yuanliang
Wang, Xiang
Prognostic value of CAD-RADS classification by coronary CTA in patients with suspected CAD
title Prognostic value of CAD-RADS classification by coronary CTA in patients with suspected CAD
title_full Prognostic value of CAD-RADS classification by coronary CTA in patients with suspected CAD
title_fullStr Prognostic value of CAD-RADS classification by coronary CTA in patients with suspected CAD
title_full_unstemmed Prognostic value of CAD-RADS classification by coronary CTA in patients with suspected CAD
title_short Prognostic value of CAD-RADS classification by coronary CTA in patients with suspected CAD
title_sort prognostic value of cad-rads classification by coronary cta in patients with suspected cad
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487531/
https://www.ncbi.nlm.nih.gov/pubmed/34602055
http://dx.doi.org/10.1186/s12872-021-02286-x
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