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Development and Validation of Nomogram for the Prediction of Malignant Ventricular Arrhythmia Including Circulating Inflammatory Cells in Patients with Acute ST-Segment Elevation Myocardial Infarction
BACKGROUND: Malignant ventricular arrhythmia (MVA) can seriously affect the hemodynamic changes of the body. In this study, we developed and validated a nomogram to predict the in-hospital MVA risk in patients with STEMI after emergency PCI. METHODS: The multivariable logistic regression analysis in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10389081/ https://www.ncbi.nlm.nih.gov/pubmed/37529768 http://dx.doi.org/10.2147/JIR.S420305 |
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author | Wang, Liang Yang, Liting Li, Tao Geng, Shanshan |
author_facet | Wang, Liang Yang, Liting Li, Tao Geng, Shanshan |
author_sort | Wang, Liang |
collection | PubMed |
description | BACKGROUND: Malignant ventricular arrhythmia (MVA) can seriously affect the hemodynamic changes of the body. In this study, we developed and validated a nomogram to predict the in-hospital MVA risk in patients with STEMI after emergency PCI. METHODS: The multivariable logistic regression analysis included variables with a P<0.05 in the univariate logistic regression analysis and investigated the independent predictors affecting in-hospital MVA after PCI in patients with STEMI in the training cohort. The construction of a nomogram model used independent predictors to predict the risk of in-hospital MVA, and C-index, Hosmer-Lemeshow (HL) test, calibration curves, decision curve analysis (DCA), and receiver operating characteristic (ROC) were used to validate the nomogram. RESULTS: Killip class [OR=5.034 (95% CI: 1.596–15.809), P=0.005], CK-MB [OR=1.002 (95% CI: 1.001–1.004), P=0.022], serum potassium [OR=0.618 (95% CI: 0.406–0.918), P=0.020], NLR [OR=1.073 (95% CI: 1.034–1.115), P<0.001], and monocyte [OR=1.974 (95% CI: 1.376–2.925), P<0.001] were the independent predictors of in-hospital MVA after PCI in patients with STEMI. A nomogram including the 5 independent predictors was developed to predict the risk of in-hospital MVA. The C-index, equivalent to the area under the ROC curve (AUC), was 0.803 (95% confidence interval [CI]: 0.738–0.868) in the training cohort, and 0.801 (95% CI:0.692–0.911) in the validation cohort, showing that the nomogram had a good discrimination. The HL test (χ(2)=8.439, P=0.392 in the training cohort; χ(2)=9.730, P=0.285 in the validation cohort) revealed a good calibration. The DCA suggested an obvious clinical net benefit. CONCLUSION: Killip class, CK-MB, serum potassium, NLR, and monocyte were independent factors for in-hospital MVA after PCI in patients with STEMI. The nomogram model constructed based on the above factors to predict the risk of in-hospital MVA had satisfactory discrimination, calibration, and clinical effectiveness, and was an excellent tool for early prediction of the risk of in-hospital MVA after PCI in patients with STEMI. |
format | Online Article Text |
id | pubmed-10389081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-103890812023-08-01 Development and Validation of Nomogram for the Prediction of Malignant Ventricular Arrhythmia Including Circulating Inflammatory Cells in Patients with Acute ST-Segment Elevation Myocardial Infarction Wang, Liang Yang, Liting Li, Tao Geng, Shanshan J Inflamm Res Original Research BACKGROUND: Malignant ventricular arrhythmia (MVA) can seriously affect the hemodynamic changes of the body. In this study, we developed and validated a nomogram to predict the in-hospital MVA risk in patients with STEMI after emergency PCI. METHODS: The multivariable logistic regression analysis included variables with a P<0.05 in the univariate logistic regression analysis and investigated the independent predictors affecting in-hospital MVA after PCI in patients with STEMI in the training cohort. The construction of a nomogram model used independent predictors to predict the risk of in-hospital MVA, and C-index, Hosmer-Lemeshow (HL) test, calibration curves, decision curve analysis (DCA), and receiver operating characteristic (ROC) were used to validate the nomogram. RESULTS: Killip class [OR=5.034 (95% CI: 1.596–15.809), P=0.005], CK-MB [OR=1.002 (95% CI: 1.001–1.004), P=0.022], serum potassium [OR=0.618 (95% CI: 0.406–0.918), P=0.020], NLR [OR=1.073 (95% CI: 1.034–1.115), P<0.001], and monocyte [OR=1.974 (95% CI: 1.376–2.925), P<0.001] were the independent predictors of in-hospital MVA after PCI in patients with STEMI. A nomogram including the 5 independent predictors was developed to predict the risk of in-hospital MVA. The C-index, equivalent to the area under the ROC curve (AUC), was 0.803 (95% confidence interval [CI]: 0.738–0.868) in the training cohort, and 0.801 (95% CI:0.692–0.911) in the validation cohort, showing that the nomogram had a good discrimination. The HL test (χ(2)=8.439, P=0.392 in the training cohort; χ(2)=9.730, P=0.285 in the validation cohort) revealed a good calibration. The DCA suggested an obvious clinical net benefit. CONCLUSION: Killip class, CK-MB, serum potassium, NLR, and monocyte were independent factors for in-hospital MVA after PCI in patients with STEMI. The nomogram model constructed based on the above factors to predict the risk of in-hospital MVA had satisfactory discrimination, calibration, and clinical effectiveness, and was an excellent tool for early prediction of the risk of in-hospital MVA after PCI in patients with STEMI. Dove 2023-07-27 /pmc/articles/PMC10389081/ /pubmed/37529768 http://dx.doi.org/10.2147/JIR.S420305 Text en © 2023 Wang et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Wang, Liang Yang, Liting Li, Tao Geng, Shanshan Development and Validation of Nomogram for the Prediction of Malignant Ventricular Arrhythmia Including Circulating Inflammatory Cells in Patients with Acute ST-Segment Elevation Myocardial Infarction |
title | Development and Validation of Nomogram for the Prediction of Malignant Ventricular Arrhythmia Including Circulating Inflammatory Cells in Patients with Acute ST-Segment Elevation Myocardial Infarction |
title_full | Development and Validation of Nomogram for the Prediction of Malignant Ventricular Arrhythmia Including Circulating Inflammatory Cells in Patients with Acute ST-Segment Elevation Myocardial Infarction |
title_fullStr | Development and Validation of Nomogram for the Prediction of Malignant Ventricular Arrhythmia Including Circulating Inflammatory Cells in Patients with Acute ST-Segment Elevation Myocardial Infarction |
title_full_unstemmed | Development and Validation of Nomogram for the Prediction of Malignant Ventricular Arrhythmia Including Circulating Inflammatory Cells in Patients with Acute ST-Segment Elevation Myocardial Infarction |
title_short | Development and Validation of Nomogram for the Prediction of Malignant Ventricular Arrhythmia Including Circulating Inflammatory Cells in Patients with Acute ST-Segment Elevation Myocardial Infarction |
title_sort | development and validation of nomogram for the prediction of malignant ventricular arrhythmia including circulating inflammatory cells in patients with acute st-segment elevation myocardial infarction |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10389081/ https://www.ncbi.nlm.nih.gov/pubmed/37529768 http://dx.doi.org/10.2147/JIR.S420305 |
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