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Acute-On-Chronic Liver Failure: The Role of Prognostic Scores in a Single-Center Experience

BACKGROUND: Acute-on-chronic liver failure (ACLF) is associated with multi-organ failure and high short-term mortality. We evaluated the role of currently available prognostic scores for prediction of 90-day mortality in ACLF patients. MATERIAL/METHODS: Fifty-five (M/F=40/15, mean age 60.0±11.1years...

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Autores principales: Niewiński, Grzegorz, Morawiec, Szymon, Janik, Maciej K., Grąt, Michał, Graczyńska, Agata, Zieniewicz, Krzysztof, Raszeja-Wyszomirska, Joanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7249742/
https://www.ncbi.nlm.nih.gov/pubmed/32415953
http://dx.doi.org/10.12659/MSM.922121
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author Niewiński, Grzegorz
Morawiec, Szymon
Janik, Maciej K.
Grąt, Michał
Graczyńska, Agata
Zieniewicz, Krzysztof
Raszeja-Wyszomirska, Joanna
author_facet Niewiński, Grzegorz
Morawiec, Szymon
Janik, Maciej K.
Grąt, Michał
Graczyńska, Agata
Zieniewicz, Krzysztof
Raszeja-Wyszomirska, Joanna
author_sort Niewiński, Grzegorz
collection PubMed
description BACKGROUND: Acute-on-chronic liver failure (ACLF) is associated with multi-organ failure and high short-term mortality. We evaluated the role of currently available prognostic scores for prediction of 90-day mortality in ACLF patients. MATERIAL/METHODS: Fifty-five (M/F=40/15, mean age 60.0±11.1years) consecutive cirrhotic patients with severe liver insufficiency (mean MELD 28.4±9.0, Child-Pugh score – C-12) were enrolled into the study. MELD variants and SOFA, CLIF-SOFA, and CLIF-C scores were calculated, mortality predicting factors were identified, and clinical comparisons between ACLF and AD patients were performed. RESULTS: In total, 30 (55%) patients were transplanted (22 ACLF and 8 AD), and 20 (30%) died (19 ACLF and 1 AD). Five (9%) patients survived without liver transplantation (LT) (3 ACLF and 2 AD), and 3 transplant recipients died within 1 month. SOFA, CLIF-SOFA, CLIF-C OF, and INR were significantly associated with the incidence of 90-day mortality in competing risk regression analysis (all p<0.001). The model based on SOFA had the lowest BIC, with the optimal cut-off for 90-day mortality prediction ≥12, with the area under the receiver operating characteristic (AUROC) of 0.901 (95% CI 0.779–1.000; p<0.001), and corresponding incidence of transplantation rates of 85.5% and 11.8%, respectively (p<0.001). Of note, the important role of 24-h urine output is emphasized. CONCLUSIONS: In this series of ACLF patients, SOFA score outperformed the CLIF-C scores in predicting 90-day mortality. Multi-organ failure scores performed better in predicting patient mortality than conventional liver function assessment. LT is possible and remains effective in selected ACLF patients.
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spelling pubmed-72497422020-05-29 Acute-On-Chronic Liver Failure: The Role of Prognostic Scores in a Single-Center Experience Niewiński, Grzegorz Morawiec, Szymon Janik, Maciej K. Grąt, Michał Graczyńska, Agata Zieniewicz, Krzysztof Raszeja-Wyszomirska, Joanna Med Sci Monit Clinical Research BACKGROUND: Acute-on-chronic liver failure (ACLF) is associated with multi-organ failure and high short-term mortality. We evaluated the role of currently available prognostic scores for prediction of 90-day mortality in ACLF patients. MATERIAL/METHODS: Fifty-five (M/F=40/15, mean age 60.0±11.1years) consecutive cirrhotic patients with severe liver insufficiency (mean MELD 28.4±9.0, Child-Pugh score – C-12) were enrolled into the study. MELD variants and SOFA, CLIF-SOFA, and CLIF-C scores were calculated, mortality predicting factors were identified, and clinical comparisons between ACLF and AD patients were performed. RESULTS: In total, 30 (55%) patients were transplanted (22 ACLF and 8 AD), and 20 (30%) died (19 ACLF and 1 AD). Five (9%) patients survived without liver transplantation (LT) (3 ACLF and 2 AD), and 3 transplant recipients died within 1 month. SOFA, CLIF-SOFA, CLIF-C OF, and INR were significantly associated with the incidence of 90-day mortality in competing risk regression analysis (all p<0.001). The model based on SOFA had the lowest BIC, with the optimal cut-off for 90-day mortality prediction ≥12, with the area under the receiver operating characteristic (AUROC) of 0.901 (95% CI 0.779–1.000; p<0.001), and corresponding incidence of transplantation rates of 85.5% and 11.8%, respectively (p<0.001). Of note, the important role of 24-h urine output is emphasized. CONCLUSIONS: In this series of ACLF patients, SOFA score outperformed the CLIF-C scores in predicting 90-day mortality. Multi-organ failure scores performed better in predicting patient mortality than conventional liver function assessment. LT is possible and remains effective in selected ACLF patients. International Scientific Literature, Inc. 2020-05-16 /pmc/articles/PMC7249742/ /pubmed/32415953 http://dx.doi.org/10.12659/MSM.922121 Text en © Med Sci Monit, 2020 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Clinical Research
Niewiński, Grzegorz
Morawiec, Szymon
Janik, Maciej K.
Grąt, Michał
Graczyńska, Agata
Zieniewicz, Krzysztof
Raszeja-Wyszomirska, Joanna
Acute-On-Chronic Liver Failure: The Role of Prognostic Scores in a Single-Center Experience
title Acute-On-Chronic Liver Failure: The Role of Prognostic Scores in a Single-Center Experience
title_full Acute-On-Chronic Liver Failure: The Role of Prognostic Scores in a Single-Center Experience
title_fullStr Acute-On-Chronic Liver Failure: The Role of Prognostic Scores in a Single-Center Experience
title_full_unstemmed Acute-On-Chronic Liver Failure: The Role of Prognostic Scores in a Single-Center Experience
title_short Acute-On-Chronic Liver Failure: The Role of Prognostic Scores in a Single-Center Experience
title_sort acute-on-chronic liver failure: the role of prognostic scores in a single-center experience
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7249742/
https://www.ncbi.nlm.nih.gov/pubmed/32415953
http://dx.doi.org/10.12659/MSM.922121
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