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Liver cirrhosis affects serum lactate level measurement while assessing disease severity in patients with sepsis
BACKGROUND: Elevated serum lactate is associated with higher mortality in sepsis, whereas liver dysfunction is associated with higher serum lactate levels. We assessed the predictive ability of serum lactate in patients with liver cirrhosis and sepsis. METHODS: This retrospective study included 12 2...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Lippincott Williams And Wilkins
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8322043/ https://www.ncbi.nlm.nih.gov/pubmed/32576767 http://dx.doi.org/10.1097/MEG.0000000000001826 |
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author | Cheng, Chi-Yung Kung, Chia-Te Wu, Kuan-Han Chen, Fu-Cheng Cheng, Hsien-Hung Cheng, Fu-Jen Huang, Jyun-Bin Su, Chih-Min |
author_facet | Cheng, Chi-Yung Kung, Chia-Te Wu, Kuan-Han Chen, Fu-Cheng Cheng, Hsien-Hung Cheng, Fu-Jen Huang, Jyun-Bin Su, Chih-Min |
author_sort | Cheng, Chi-Yung |
collection | PubMed |
description | BACKGROUND: Elevated serum lactate is associated with higher mortality in sepsis, whereas liver dysfunction is associated with higher serum lactate levels. We assessed the predictive ability of serum lactate in patients with liver cirrhosis and sepsis. METHODS: This retrospective study included 12 281 cases of suspected infection with initial serum blood lactate drawn during January 2007–December 2013. RESULTS: Using one-to-two propensity score matching analysis, 1053 and 2106 septic patients with and without underlying liver cirrhosis, respectively, were successfully matched. Lactate levels of survivors and nonsurvivors were 2.58 and 5.93 mmol/L, respectively, in patients without liver cirrhosis (WLC), 2.96 and 7.29 mmol/L, respectively, in patients with nondecompensated liver cirrhosis (NDLC), and 4.08 and 7.16 mmol/L, respectively, in patients with decompensated liver cirrhosis (DLC). In receiver operating characteristic curve analysis, the sensitivity and specificity for predicting mortality were 0.81 and 0.55, respectively, in the WLC group, 0.85 and 0.45, respectively, in the NDLC group, and 0.86 and 0.33, respectively, in the DLC group, using serum lactate levels >2.0 mmol/L. CONCLUSIONS: The serum lactate level can be used to predict the severity of sepsis in patients with liver cirrhosis; however, its specificity would be lower at a cutoff of 2.0 mmol/L. |
format | Online Article Text |
id | pubmed-8322043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Lippincott Williams And Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-83220432021-08-02 Liver cirrhosis affects serum lactate level measurement while assessing disease severity in patients with sepsis Cheng, Chi-Yung Kung, Chia-Te Wu, Kuan-Han Chen, Fu-Cheng Cheng, Hsien-Hung Cheng, Fu-Jen Huang, Jyun-Bin Su, Chih-Min Eur J Gastroenterol Hepatol Original Articles: Hepatology BACKGROUND: Elevated serum lactate is associated with higher mortality in sepsis, whereas liver dysfunction is associated with higher serum lactate levels. We assessed the predictive ability of serum lactate in patients with liver cirrhosis and sepsis. METHODS: This retrospective study included 12 281 cases of suspected infection with initial serum blood lactate drawn during January 2007–December 2013. RESULTS: Using one-to-two propensity score matching analysis, 1053 and 2106 septic patients with and without underlying liver cirrhosis, respectively, were successfully matched. Lactate levels of survivors and nonsurvivors were 2.58 and 5.93 mmol/L, respectively, in patients without liver cirrhosis (WLC), 2.96 and 7.29 mmol/L, respectively, in patients with nondecompensated liver cirrhosis (NDLC), and 4.08 and 7.16 mmol/L, respectively, in patients with decompensated liver cirrhosis (DLC). In receiver operating characteristic curve analysis, the sensitivity and specificity for predicting mortality were 0.81 and 0.55, respectively, in the WLC group, 0.85 and 0.45, respectively, in the NDLC group, and 0.86 and 0.33, respectively, in the DLC group, using serum lactate levels >2.0 mmol/L. CONCLUSIONS: The serum lactate level can be used to predict the severity of sepsis in patients with liver cirrhosis; however, its specificity would be lower at a cutoff of 2.0 mmol/L. Lippincott Williams And Wilkins 2020-06-22 2021-09 /pmc/articles/PMC8322043/ /pubmed/32576767 http://dx.doi.org/10.1097/MEG.0000000000001826 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) (CC-BY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Original Articles: Hepatology Cheng, Chi-Yung Kung, Chia-Te Wu, Kuan-Han Chen, Fu-Cheng Cheng, Hsien-Hung Cheng, Fu-Jen Huang, Jyun-Bin Su, Chih-Min Liver cirrhosis affects serum lactate level measurement while assessing disease severity in patients with sepsis |
title | Liver cirrhosis affects serum lactate level measurement while assessing disease severity in patients with sepsis |
title_full | Liver cirrhosis affects serum lactate level measurement while assessing disease severity in patients with sepsis |
title_fullStr | Liver cirrhosis affects serum lactate level measurement while assessing disease severity in patients with sepsis |
title_full_unstemmed | Liver cirrhosis affects serum lactate level measurement while assessing disease severity in patients with sepsis |
title_short | Liver cirrhosis affects serum lactate level measurement while assessing disease severity in patients with sepsis |
title_sort | liver cirrhosis affects serum lactate level measurement while assessing disease severity in patients with sepsis |
topic | Original Articles: Hepatology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8322043/ https://www.ncbi.nlm.nih.gov/pubmed/32576767 http://dx.doi.org/10.1097/MEG.0000000000001826 |
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