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Prognostic value of CHADS(2) and CHA(2)DS(2)-VASc scores for post-discharge outcomes in patients with acute coronary syndrome undergoing percutaneous coronary intervention
The CHADS(2) and CHA(2)DS(2)-VASc scores were initially developed to assess the risk of stroke or systemic embolism in patients with atrial fibrillation (AF). Recently, these two scoring systems have been demonstrated to predict long- and short-term cardiovascular (CV) outcomes in many patient cohor...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Wolters Kluwer Health
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387006/ https://www.ncbi.nlm.nih.gov/pubmed/32791726 http://dx.doi.org/10.1097/MD.0000000000021321 |
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author | Ma, Xiaoteng Shao, Qiaoyu Dong, Lisha Cheng, Yujing Lv, Sai Shen, Hua Liang, Jing Wang, Zhijian Zhou, Yujie |
author_facet | Ma, Xiaoteng Shao, Qiaoyu Dong, Lisha Cheng, Yujing Lv, Sai Shen, Hua Liang, Jing Wang, Zhijian Zhou, Yujie |
author_sort | Ma, Xiaoteng |
collection | PubMed |
description | The CHADS(2) and CHA(2)DS(2)-VASc scores were initially developed to assess the risk of stroke or systemic embolism in patients with atrial fibrillation (AF). Recently, these two scoring systems have been demonstrated to predict long- and short-term cardiovascular (CV) outcomes in many patient cohorts. However, to the best of our knowledge, their prognostic value has not been fully elucidated in patients with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI). This study aimed to investigate the association of CHADS(2) and CHA(2)DS(2)-VASc scores with CV outcomes in such patients. We included a total of 915 ACS patients undergoing PCI in this study. CHADS(2) and CHA(2)DS(2)-VASc scores were calculated from data collected before discharge. The primary endpoint was defined as a composite of major adverse CV events (MACE) including overall death, nonfatal stroke, nonfatal myocardial infarction (MI) and unplanned repeat revascularization. We assessed MACE's relationship to CHADS(2) and CHA(2)DS(2)-VASc scores using Cox proportional-hazard regression analyses. Mean follow-up duration was 918 days. MACE occurred in 167 (18.3%) patients. A higher CHADS(2) score was associated with reduced event-free survival (EFS) from MACE (logrank test, P = .007) with differences potentiated if stratified by CHA(2)DS(2)-VASc score (logrank test, P < .001). Univariate analysis showed that both CHADS(2) and CHA(2)DS(2)-VASc scores were good predictors of MACE. In the multivariate Cox proportional-hazard regression analysis, CHA(2)DS(2)-VASc score (hazard ratio [HR], 1.15; 95% confidence interval [CI] 1.04–1.27; P = .007) remained a useful predictor of MACE; however, CHADS(2) score was no longer associated with increased risk of MACE. C-statistics for CHA(2)DS(2)-VASc score, GRACE (Global Registry of Acute Coronary Events) hospital discharge risk score (GRACE Score) and SYNTAX (Synergy between PCI with TAXUS and Cardiac Surgery) Score II (SS II) in predicting MACE were 0.614, 0.598, and 0.609, respectively. CHA(2)DS(2)-VASc score was an independent and significant predictor of MACE in ACS patients undergoing PCI, and its discriminatory performance was not inferior to those of GRACE Score and SS II. |
format | Online Article Text |
id | pubmed-7387006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-73870062020-08-05 Prognostic value of CHADS(2) and CHA(2)DS(2)-VASc scores for post-discharge outcomes in patients with acute coronary syndrome undergoing percutaneous coronary intervention Ma, Xiaoteng Shao, Qiaoyu Dong, Lisha Cheng, Yujing Lv, Sai Shen, Hua Liang, Jing Wang, Zhijian Zhou, Yujie Medicine (Baltimore) 3400 The CHADS(2) and CHA(2)DS(2)-VASc scores were initially developed to assess the risk of stroke or systemic embolism in patients with atrial fibrillation (AF). Recently, these two scoring systems have been demonstrated to predict long- and short-term cardiovascular (CV) outcomes in many patient cohorts. However, to the best of our knowledge, their prognostic value has not been fully elucidated in patients with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI). This study aimed to investigate the association of CHADS(2) and CHA(2)DS(2)-VASc scores with CV outcomes in such patients. We included a total of 915 ACS patients undergoing PCI in this study. CHADS(2) and CHA(2)DS(2)-VASc scores were calculated from data collected before discharge. The primary endpoint was defined as a composite of major adverse CV events (MACE) including overall death, nonfatal stroke, nonfatal myocardial infarction (MI) and unplanned repeat revascularization. We assessed MACE's relationship to CHADS(2) and CHA(2)DS(2)-VASc scores using Cox proportional-hazard regression analyses. Mean follow-up duration was 918 days. MACE occurred in 167 (18.3%) patients. A higher CHADS(2) score was associated with reduced event-free survival (EFS) from MACE (logrank test, P = .007) with differences potentiated if stratified by CHA(2)DS(2)-VASc score (logrank test, P < .001). Univariate analysis showed that both CHADS(2) and CHA(2)DS(2)-VASc scores were good predictors of MACE. In the multivariate Cox proportional-hazard regression analysis, CHA(2)DS(2)-VASc score (hazard ratio [HR], 1.15; 95% confidence interval [CI] 1.04–1.27; P = .007) remained a useful predictor of MACE; however, CHADS(2) score was no longer associated with increased risk of MACE. C-statistics for CHA(2)DS(2)-VASc score, GRACE (Global Registry of Acute Coronary Events) hospital discharge risk score (GRACE Score) and SYNTAX (Synergy between PCI with TAXUS and Cardiac Surgery) Score II (SS II) in predicting MACE were 0.614, 0.598, and 0.609, respectively. CHA(2)DS(2)-VASc score was an independent and significant predictor of MACE in ACS patients undergoing PCI, and its discriminatory performance was not inferior to those of GRACE Score and SS II. Wolters Kluwer Health 2020-07-24 /pmc/articles/PMC7387006/ /pubmed/32791726 http://dx.doi.org/10.1097/MD.0000000000021321 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 3400 Ma, Xiaoteng Shao, Qiaoyu Dong, Lisha Cheng, Yujing Lv, Sai Shen, Hua Liang, Jing Wang, Zhijian Zhou, Yujie Prognostic value of CHADS(2) and CHA(2)DS(2)-VASc scores for post-discharge outcomes in patients with acute coronary syndrome undergoing percutaneous coronary intervention |
title | Prognostic value of CHADS(2) and CHA(2)DS(2)-VASc scores for post-discharge outcomes in patients with acute coronary syndrome undergoing percutaneous coronary intervention |
title_full | Prognostic value of CHADS(2) and CHA(2)DS(2)-VASc scores for post-discharge outcomes in patients with acute coronary syndrome undergoing percutaneous coronary intervention |
title_fullStr | Prognostic value of CHADS(2) and CHA(2)DS(2)-VASc scores for post-discharge outcomes in patients with acute coronary syndrome undergoing percutaneous coronary intervention |
title_full_unstemmed | Prognostic value of CHADS(2) and CHA(2)DS(2)-VASc scores for post-discharge outcomes in patients with acute coronary syndrome undergoing percutaneous coronary intervention |
title_short | Prognostic value of CHADS(2) and CHA(2)DS(2)-VASc scores for post-discharge outcomes in patients with acute coronary syndrome undergoing percutaneous coronary intervention |
title_sort | prognostic value of chads(2) and cha(2)ds(2)-vasc scores for post-discharge outcomes in patients with acute coronary syndrome undergoing percutaneous coronary intervention |
topic | 3400 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7387006/ https://www.ncbi.nlm.nih.gov/pubmed/32791726 http://dx.doi.org/10.1097/MD.0000000000021321 |
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