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A nomogram to predict the in‐hospital mortality of patients with congestive heart failure and chronic kidney disease

AIMS: Patients with congestive heart failure (CHF) may also suffer from chronic kidney disease (CKD), and the two conditions may interact to increase the risk of death. The purpose of this study was to investigate the risk factors contributing to in‐hospital mortality in patients with CHF and CKD an...

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Autores principales: Chen, Jiamin, Li, Ying, Liu, Peng, Wu, Huihui, Su, Guohai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9715887/
https://www.ncbi.nlm.nih.gov/pubmed/35765720
http://dx.doi.org/10.1002/ehf2.14042
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author Chen, Jiamin
Li, Ying
Liu, Peng
Wu, Huihui
Su, Guohai
author_facet Chen, Jiamin
Li, Ying
Liu, Peng
Wu, Huihui
Su, Guohai
author_sort Chen, Jiamin
collection PubMed
description AIMS: Patients with congestive heart failure (CHF) may also suffer from chronic kidney disease (CKD), and the two conditions may interact to increase the risk of death. The purpose of this study was to investigate the risk factors contributing to in‐hospital mortality in patients with CHF and CKD and to develop a nomogram to predict the risk of in‐hospital mortality. METHODS AND RESULTS: This retrospective study used data from the Marketplace for Medical Information in Intensive Care (MIMIC‐IV, version 1.0). Patients diagnosed with CHF and CKD in MIMIC‐IV were included in this study. The least absolute shrinkage and selection operator (LASSO) logistic regression is used to select risk variables for the nomogram model, and bootstrap is used for internal validation. Simplified Acute Physiology Score II (SAPS II) and Logistic Organ Dysfunction Score (LODS) were compared with the nomogram model by the area under the receiver operating characteristic curve (AUC) and decision curve analysis (DCA). A total of 4638 adult patients with CHF and CKD were included in the final cohort; of them, 707 (15.2%) died and 3931 (84.8%) survived during hospitalization. Our final model included the following 13 variables: age, acute kidney injury, myocardial infarction, anaemia, heart rate ≥ 100 b.p.m., systolic blood pressure ≥ 130 mmHg, anion gap (AG) ≥ 20 mEq/L, sodium ≥ 145 mEq/L, red blood cell distribution width (RDW) ≥ 15.5%, white blood cell count ≥ 10 K/μL, continuous renal replacement therapy (CRRT), angiotensin‐converting enzyme inhibitors/angiotensin receptor blockers, and beta‐blocker. The corrected C‐statistic of the nomogram was 0.767, and the calibration curve indicating good concordance between the predicted and observed values. The nomogram demonstrated good accuracy for predicting the in‐hospital mortality with an AUC of 0.771 (95% CI: 0.752–0.790), while the AUC for SAPS II and LODS was 0.747 (95% CI: 0.726–0.767) and 0.752 (95% CI: 0.730–0.773), respectively. DCA found that when the threshold probability was 0.05 to 0.41, the nomogram model could provide a greater net benefit than SAPS II. CONCLUSIONS: In this retrospective cohort analysis of patients with CHF and CKD, we identified 13 independent variables associated with in‐hospital mortality using LASSO logistic regression. RDW, AG, and CRRT were reported to play a significant role in in‐hospital mortality among patients with CHF and CKD for the first time. Based on a simplified model including 13 variables, a nomogram was drawn to predict the risk of in‐hospital mortality. In comparison with SAPS II and LODS, the nomogram model performed well.
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spelling pubmed-97158872022-12-05 A nomogram to predict the in‐hospital mortality of patients with congestive heart failure and chronic kidney disease Chen, Jiamin Li, Ying Liu, Peng Wu, Huihui Su, Guohai ESC Heart Fail Original Articles AIMS: Patients with congestive heart failure (CHF) may also suffer from chronic kidney disease (CKD), and the two conditions may interact to increase the risk of death. The purpose of this study was to investigate the risk factors contributing to in‐hospital mortality in patients with CHF and CKD and to develop a nomogram to predict the risk of in‐hospital mortality. METHODS AND RESULTS: This retrospective study used data from the Marketplace for Medical Information in Intensive Care (MIMIC‐IV, version 1.0). Patients diagnosed with CHF and CKD in MIMIC‐IV were included in this study. The least absolute shrinkage and selection operator (LASSO) logistic regression is used to select risk variables for the nomogram model, and bootstrap is used for internal validation. Simplified Acute Physiology Score II (SAPS II) and Logistic Organ Dysfunction Score (LODS) were compared with the nomogram model by the area under the receiver operating characteristic curve (AUC) and decision curve analysis (DCA). A total of 4638 adult patients with CHF and CKD were included in the final cohort; of them, 707 (15.2%) died and 3931 (84.8%) survived during hospitalization. Our final model included the following 13 variables: age, acute kidney injury, myocardial infarction, anaemia, heart rate ≥ 100 b.p.m., systolic blood pressure ≥ 130 mmHg, anion gap (AG) ≥ 20 mEq/L, sodium ≥ 145 mEq/L, red blood cell distribution width (RDW) ≥ 15.5%, white blood cell count ≥ 10 K/μL, continuous renal replacement therapy (CRRT), angiotensin‐converting enzyme inhibitors/angiotensin receptor blockers, and beta‐blocker. The corrected C‐statistic of the nomogram was 0.767, and the calibration curve indicating good concordance between the predicted and observed values. The nomogram demonstrated good accuracy for predicting the in‐hospital mortality with an AUC of 0.771 (95% CI: 0.752–0.790), while the AUC for SAPS II and LODS was 0.747 (95% CI: 0.726–0.767) and 0.752 (95% CI: 0.730–0.773), respectively. DCA found that when the threshold probability was 0.05 to 0.41, the nomogram model could provide a greater net benefit than SAPS II. CONCLUSIONS: In this retrospective cohort analysis of patients with CHF and CKD, we identified 13 independent variables associated with in‐hospital mortality using LASSO logistic regression. RDW, AG, and CRRT were reported to play a significant role in in‐hospital mortality among patients with CHF and CKD for the first time. Based on a simplified model including 13 variables, a nomogram was drawn to predict the risk of in‐hospital mortality. In comparison with SAPS II and LODS, the nomogram model performed well. John Wiley and Sons Inc. 2022-06-28 /pmc/articles/PMC9715887/ /pubmed/35765720 http://dx.doi.org/10.1002/ehf2.14042 Text en © 2022 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Chen, Jiamin
Li, Ying
Liu, Peng
Wu, Huihui
Su, Guohai
A nomogram to predict the in‐hospital mortality of patients with congestive heart failure and chronic kidney disease
title A nomogram to predict the in‐hospital mortality of patients with congestive heart failure and chronic kidney disease
title_full A nomogram to predict the in‐hospital mortality of patients with congestive heart failure and chronic kidney disease
title_fullStr A nomogram to predict the in‐hospital mortality of patients with congestive heart failure and chronic kidney disease
title_full_unstemmed A nomogram to predict the in‐hospital mortality of patients with congestive heart failure and chronic kidney disease
title_short A nomogram to predict the in‐hospital mortality of patients with congestive heart failure and chronic kidney disease
title_sort nomogram to predict the in‐hospital mortality of patients with congestive heart failure and chronic kidney disease
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9715887/
https://www.ncbi.nlm.nih.gov/pubmed/35765720
http://dx.doi.org/10.1002/ehf2.14042
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