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Risk factors and prediction nomogram model for 1-year readmission for major adverse cardiovascular events in patients with STEMI after PCI

To identify risk factors and develop a risk-prediction nomogram model for 1-year readmission due to major adverse cardiovascular events (MACEs) in patients with acute ST-segment elevation myocardial infarction (STEMI) after primary percutaneous coronary intervention (PCI). This was a single-center,...

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Autores principales: Yao, Wensen, Li, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9676288/
https://www.ncbi.nlm.nih.gov/pubmed/36380508
http://dx.doi.org/10.1177/10760296221137847
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author Yao, Wensen
Li, Jie
author_facet Yao, Wensen
Li, Jie
author_sort Yao, Wensen
collection PubMed
description To identify risk factors and develop a risk-prediction nomogram model for 1-year readmission due to major adverse cardiovascular events (MACEs) in patients with acute ST-segment elevation myocardial infarction (STEMI) after primary percutaneous coronary intervention (PCI). This was a single-center, retrospective cohort study. A total of 526 eligible participants were enrolled, which included 456 non-readmitted and 70 readmitted patients. Multivariate logistical regressions were performed to identify the independent risk factors for readmission, and a prediction nomogram model was developed based on the results of the regression analysis. The receiver operating characteristic curve, Hosmer-Lemeshow test, calibration plot, and decision curve analysis (DCA) were used to evaluate the performance of the nomogram. Female (OR = 2.426; 95% CI: 1.395–4.218), hypertension (OR = 1.898; 95% CI: 1.100–3.275), 3-vessel disease (OR = 2.632; 95% CI: 1.332–5.201), in-hospital Ventricular arrhythmias (VA) (OR = 3.143; 95% CI: 1.305–7.574), peak cTnI (OR = 1.003; 95% CI: 1.001–1.004) and baseline NT-proBNP (OR = 1.001; 95% CI: 1.000–1.002) were independent risk factors for readmission (all P < 0.05). The nomogram exhibited good discrimination with the area under the curve (AUC) of 0.723, calibration (Hosmer-Lemeshow test; χ(2) = 15.396, P = 0.052), and clinical usefulness. Female gender, hypertension, in-hospital VA, 3-vessel disease, baseline NT-proBNP, and peak cTnI were independent risk factors for readmission. The nomogram helped clinicians to identify the patients at risk of readmission before their hospital discharge, which may help reduce readmission rates.
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spelling pubmed-96762882022-11-22 Risk factors and prediction nomogram model for 1-year readmission for major adverse cardiovascular events in patients with STEMI after PCI Yao, Wensen Li, Jie Clin Appl Thromb Hemost Original Manuscript To identify risk factors and develop a risk-prediction nomogram model for 1-year readmission due to major adverse cardiovascular events (MACEs) in patients with acute ST-segment elevation myocardial infarction (STEMI) after primary percutaneous coronary intervention (PCI). This was a single-center, retrospective cohort study. A total of 526 eligible participants were enrolled, which included 456 non-readmitted and 70 readmitted patients. Multivariate logistical regressions were performed to identify the independent risk factors for readmission, and a prediction nomogram model was developed based on the results of the regression analysis. The receiver operating characteristic curve, Hosmer-Lemeshow test, calibration plot, and decision curve analysis (DCA) were used to evaluate the performance of the nomogram. Female (OR = 2.426; 95% CI: 1.395–4.218), hypertension (OR = 1.898; 95% CI: 1.100–3.275), 3-vessel disease (OR = 2.632; 95% CI: 1.332–5.201), in-hospital Ventricular arrhythmias (VA) (OR = 3.143; 95% CI: 1.305–7.574), peak cTnI (OR = 1.003; 95% CI: 1.001–1.004) and baseline NT-proBNP (OR = 1.001; 95% CI: 1.000–1.002) were independent risk factors for readmission (all P < 0.05). The nomogram exhibited good discrimination with the area under the curve (AUC) of 0.723, calibration (Hosmer-Lemeshow test; χ(2) = 15.396, P = 0.052), and clinical usefulness. Female gender, hypertension, in-hospital VA, 3-vessel disease, baseline NT-proBNP, and peak cTnI were independent risk factors for readmission. The nomogram helped clinicians to identify the patients at risk of readmission before their hospital discharge, which may help reduce readmission rates. SAGE Publications 2022-11-15 /pmc/articles/PMC9676288/ /pubmed/36380508 http://dx.doi.org/10.1177/10760296221137847 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Manuscript
Yao, Wensen
Li, Jie
Risk factors and prediction nomogram model for 1-year readmission for major adverse cardiovascular events in patients with STEMI after PCI
title Risk factors and prediction nomogram model for 1-year readmission for major adverse cardiovascular events in patients with STEMI after PCI
title_full Risk factors and prediction nomogram model for 1-year readmission for major adverse cardiovascular events in patients with STEMI after PCI
title_fullStr Risk factors and prediction nomogram model for 1-year readmission for major adverse cardiovascular events in patients with STEMI after PCI
title_full_unstemmed Risk factors and prediction nomogram model for 1-year readmission for major adverse cardiovascular events in patients with STEMI after PCI
title_short Risk factors and prediction nomogram model for 1-year readmission for major adverse cardiovascular events in patients with STEMI after PCI
title_sort risk factors and prediction nomogram model for 1-year readmission for major adverse cardiovascular events in patients with stemi after pci
topic Original Manuscript
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9676288/
https://www.ncbi.nlm.nih.gov/pubmed/36380508
http://dx.doi.org/10.1177/10760296221137847
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