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Serum cystatin C as a predictor of 90‐day mortality among patients admitted with complications of cirrhosis
BACKGROUND AND AIM: Cystatin C (Cys) is not affected by age, sex, and muscle mass. We evaluated to compare the predictive performance of serum Cys level and model for end‐stage liver disease (MELD) score and developed a new model to predict 90‐day mortality among patients admitted with cirrhosis com...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Publishing Asia Pty Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8114990/ https://www.ncbi.nlm.nih.gov/pubmed/34013062 http://dx.doi.org/10.1002/jgh3.12543 |
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author | Suksamai, Anuchit Chaiprasert, Amnart Chirapongsathorn, Sakkarin |
author_facet | Suksamai, Anuchit Chaiprasert, Amnart Chirapongsathorn, Sakkarin |
author_sort | Suksamai, Anuchit |
collection | PubMed |
description | BACKGROUND AND AIM: Cystatin C (Cys) is not affected by age, sex, and muscle mass. We evaluated to compare the predictive performance of serum Cys level and model for end‐stage liver disease (MELD) score and developed a new model to predict 90‐day mortality among patients admitted with cirrhosis complications. METHODS: A prospective cohort study was performed from December 2018 to December 2019. All cirrhotic patients admitted with acute decompensated liver cirrhosis or acute on chronic liver failure had laboratory values measured within 48 h of admission. RESULTS: A cohort of 225 patients with cirrhosis was admitted during the study period. Sixty‐five patients were eligible for analysis. Twenty‐seven of these patients (41.4%) died within 90 days of follow‐up. The median of MELD score was 20.5 (15, 24). Serum Cys level of >1.45 mg/L had the highest 90‐day mortality prediction with the sensitivity and specificity of 66.7% and 68.4%, respectively. Cys and MELD scores were predictive of 90‐day mortality: Cys hazard ratio (HR) = 2.04 (95% CI 1.01–4.14, P = 0.048); MELD score HR = 1.01 (95% CI 0.51–2.01, P = 0.970). C‐statistic of Cys, MELD score, model for end‐stage liver disease‐cystatin C (MELD‐Cys) score, combined Cys with MELD‐Cys score to predict 90‐day mortality were 0.67, 0.58, 0.58, and 0.63, respectively. Adding Cys to the MELD score did not improve the predictive of 90‐day mortality. CONCLUSION: Serum Cys is superior to MELD score, and the new MELD‐Cys model is comparable to the MELD score in predicting mortality among patients with cirrhosis admitted with complications. |
format | Online Article Text |
id | pubmed-8114990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wiley Publishing Asia Pty Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-81149902021-05-18 Serum cystatin C as a predictor of 90‐day mortality among patients admitted with complications of cirrhosis Suksamai, Anuchit Chaiprasert, Amnart Chirapongsathorn, Sakkarin JGH Open Original Articles BACKGROUND AND AIM: Cystatin C (Cys) is not affected by age, sex, and muscle mass. We evaluated to compare the predictive performance of serum Cys level and model for end‐stage liver disease (MELD) score and developed a new model to predict 90‐day mortality among patients admitted with cirrhosis complications. METHODS: A prospective cohort study was performed from December 2018 to December 2019. All cirrhotic patients admitted with acute decompensated liver cirrhosis or acute on chronic liver failure had laboratory values measured within 48 h of admission. RESULTS: A cohort of 225 patients with cirrhosis was admitted during the study period. Sixty‐five patients were eligible for analysis. Twenty‐seven of these patients (41.4%) died within 90 days of follow‐up. The median of MELD score was 20.5 (15, 24). Serum Cys level of >1.45 mg/L had the highest 90‐day mortality prediction with the sensitivity and specificity of 66.7% and 68.4%, respectively. Cys and MELD scores were predictive of 90‐day mortality: Cys hazard ratio (HR) = 2.04 (95% CI 1.01–4.14, P = 0.048); MELD score HR = 1.01 (95% CI 0.51–2.01, P = 0.970). C‐statistic of Cys, MELD score, model for end‐stage liver disease‐cystatin C (MELD‐Cys) score, combined Cys with MELD‐Cys score to predict 90‐day mortality were 0.67, 0.58, 0.58, and 0.63, respectively. Adding Cys to the MELD score did not improve the predictive of 90‐day mortality. CONCLUSION: Serum Cys is superior to MELD score, and the new MELD‐Cys model is comparable to the MELD score in predicting mortality among patients with cirrhosis admitted with complications. Wiley Publishing Asia Pty Ltd 2021-04-07 /pmc/articles/PMC8114990/ /pubmed/34013062 http://dx.doi.org/10.1002/jgh3.12543 Text en © 2021 The Authors. JGH Open published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Suksamai, Anuchit Chaiprasert, Amnart Chirapongsathorn, Sakkarin Serum cystatin C as a predictor of 90‐day mortality among patients admitted with complications of cirrhosis |
title | Serum cystatin C as a predictor of 90‐day mortality among patients admitted with complications of cirrhosis |
title_full | Serum cystatin C as a predictor of 90‐day mortality among patients admitted with complications of cirrhosis |
title_fullStr | Serum cystatin C as a predictor of 90‐day mortality among patients admitted with complications of cirrhosis |
title_full_unstemmed | Serum cystatin C as a predictor of 90‐day mortality among patients admitted with complications of cirrhosis |
title_short | Serum cystatin C as a predictor of 90‐day mortality among patients admitted with complications of cirrhosis |
title_sort | serum cystatin c as a predictor of 90‐day mortality among patients admitted with complications of cirrhosis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8114990/ https://www.ncbi.nlm.nih.gov/pubmed/34013062 http://dx.doi.org/10.1002/jgh3.12543 |
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