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Predicting multi-vascular diseases in patients with coronary artery disease

Background: Because of its systemic nature, the occurrence of atherosclerosis in the coronary arteries can also indicate a risk for other vascular diseases.  However, screening program targeted for all patients with coronary artery disease (CAD) is highly ineffective and no studies have assessed the...

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Autores principales: Adiarto, Suko, Nurachman, Luthfian Aby, Dewangga, Raditya, Indriani, Suci, Taofan, Taofan, Alkatiri, Amir Aziz, Firman, Doni, Santoso, Anwar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10517298/
https://www.ncbi.nlm.nih.gov/pubmed/37744767
http://dx.doi.org/10.12688/f1000research.134648.2
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author Adiarto, Suko
Nurachman, Luthfian Aby
Dewangga, Raditya
Indriani, Suci
Taofan, Taofan
Alkatiri, Amir Aziz
Firman, Doni
Santoso, Anwar
author_facet Adiarto, Suko
Nurachman, Luthfian Aby
Dewangga, Raditya
Indriani, Suci
Taofan, Taofan
Alkatiri, Amir Aziz
Firman, Doni
Santoso, Anwar
author_sort Adiarto, Suko
collection PubMed
description Background: Because of its systemic nature, the occurrence of atherosclerosis in the coronary arteries can also indicate a risk for other vascular diseases.  However, screening program targeted for all patients with coronary artery disease (CAD) is highly ineffective and no studies have assessed the risk factors for developing multi-vascular diseases in general. This study constructed a predictive model and scoring system to enable targeted screening for multi-vascular diseases in CAD patients. Methods: This cross-sectional study includes patients with CAD, as diagnosed during coronary angiography or percutaneous coronary intervention from March 2021 to December 2021. Coronary artery stenosis (CAS) and abdominal aortic aneurysm (AAA) were diagnosed using Doppler ultrasound while peripheral artery disease (PAD) was diagnosed based on ABI score. Multivariate logistic regression was conducted to construct the predictive model and risk scores. Validation was conducted using ROC analysis and Hosmer-Lemeshow test. Results: Multivariate analysis showed that ages of >60 years (OR [95% CI] = 1.579 [1.153-2.164]), diabetes mellitus (OR = 1.412 [1.036-1.924]), cerebrovascular disease (OR = 3.656 [2.326-5.747]), and CAD3VD (OR = 1.960 [1.250-3.073]) increased the odds for multi-vascular disease. The model demonstrated good predictive capability (AUC = 0.659) and was well-calibrated (Hosmer-Lemeshow p = 0.379). Targeted screening for high-risk patients reduced the number needed to screen (NNS) from 6 in the general population to 3 and has a high specificity of 96.5% Conclusions: Targeted screening using clinical risk scores was able to decrease NNS with good predictive capability and high specificity
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spelling pubmed-105172982023-09-24 Predicting multi-vascular diseases in patients with coronary artery disease Adiarto, Suko Nurachman, Luthfian Aby Dewangga, Raditya Indriani, Suci Taofan, Taofan Alkatiri, Amir Aziz Firman, Doni Santoso, Anwar F1000Res Research Article Background: Because of its systemic nature, the occurrence of atherosclerosis in the coronary arteries can also indicate a risk for other vascular diseases.  However, screening program targeted for all patients with coronary artery disease (CAD) is highly ineffective and no studies have assessed the risk factors for developing multi-vascular diseases in general. This study constructed a predictive model and scoring system to enable targeted screening for multi-vascular diseases in CAD patients. Methods: This cross-sectional study includes patients with CAD, as diagnosed during coronary angiography or percutaneous coronary intervention from March 2021 to December 2021. Coronary artery stenosis (CAS) and abdominal aortic aneurysm (AAA) were diagnosed using Doppler ultrasound while peripheral artery disease (PAD) was diagnosed based on ABI score. Multivariate logistic regression was conducted to construct the predictive model and risk scores. Validation was conducted using ROC analysis and Hosmer-Lemeshow test. Results: Multivariate analysis showed that ages of >60 years (OR [95% CI] = 1.579 [1.153-2.164]), diabetes mellitus (OR = 1.412 [1.036-1.924]), cerebrovascular disease (OR = 3.656 [2.326-5.747]), and CAD3VD (OR = 1.960 [1.250-3.073]) increased the odds for multi-vascular disease. The model demonstrated good predictive capability (AUC = 0.659) and was well-calibrated (Hosmer-Lemeshow p = 0.379). Targeted screening for high-risk patients reduced the number needed to screen (NNS) from 6 in the general population to 3 and has a high specificity of 96.5% Conclusions: Targeted screening using clinical risk scores was able to decrease NNS with good predictive capability and high specificity F1000 Research Limited 2023-09-12 /pmc/articles/PMC10517298/ /pubmed/37744767 http://dx.doi.org/10.12688/f1000research.134648.2 Text en Copyright: © 2023 Adiarto S et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Adiarto, Suko
Nurachman, Luthfian Aby
Dewangga, Raditya
Indriani, Suci
Taofan, Taofan
Alkatiri, Amir Aziz
Firman, Doni
Santoso, Anwar
Predicting multi-vascular diseases in patients with coronary artery disease
title Predicting multi-vascular diseases in patients with coronary artery disease
title_full Predicting multi-vascular diseases in patients with coronary artery disease
title_fullStr Predicting multi-vascular diseases in patients with coronary artery disease
title_full_unstemmed Predicting multi-vascular diseases in patients with coronary artery disease
title_short Predicting multi-vascular diseases in patients with coronary artery disease
title_sort predicting multi-vascular diseases in patients with coronary artery disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10517298/
https://www.ncbi.nlm.nih.gov/pubmed/37744767
http://dx.doi.org/10.12688/f1000research.134648.2
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