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Risk stratification for early bacteremia after living donor liver transplantation: a retrospective observational cohort study

BACKGROUND: This study investigated perioperative clinical risk factors for early post-transplant bacteremia in patients undergoing living donor liver transplantation (LDLT). Additionally, postoperative outcomes were compared between patients with and without early post-transplant bacteremia. METHOD...

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Autores principales: Park, Jaesik, Kim, Bae Wook, Choi, Ho Joong, Hong, Sang Hyun, Park, Chul Soo, Choi, Jong Ho, Chae, Min Suk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066734/
https://www.ncbi.nlm.nih.gov/pubmed/32160890
http://dx.doi.org/10.1186/s12893-019-0658-6
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author Park, Jaesik
Kim, Bae Wook
Choi, Ho Joong
Hong, Sang Hyun
Park, Chul Soo
Choi, Jong Ho
Chae, Min Suk
author_facet Park, Jaesik
Kim, Bae Wook
Choi, Ho Joong
Hong, Sang Hyun
Park, Chul Soo
Choi, Jong Ho
Chae, Min Suk
author_sort Park, Jaesik
collection PubMed
description BACKGROUND: This study investigated perioperative clinical risk factors for early post-transplant bacteremia in patients undergoing living donor liver transplantation (LDLT). Additionally, postoperative outcomes were compared between patients with and without early post-transplant bacteremia. METHODS: Clinical data of 610 adult patients who underwent elective LDLT between January 2009 and December 2018 at Seoul St. Mary’s Hospital were retrospectively collected. The exclusion criteria included overt signs of infection within 1 month before surgery. A total of 596 adult patients were enrolled in this study. Based on the occurrence of a systemic bacterial infection after surgery, patients were classified into non-infected and infected groups. RESULTS: The incidence of bacteremia at 1 month after LDLT was 9.7% (57 patients) and Enterococcus faecium (31.6%) was the most commonly cultured bacterium in the blood samples. Univariate analysis showed that preoperative psoas muscle index (PMI), model for end-stage disease score, utility of continuous renal replacement therapy (CRRT), ascites, C-reactive protein to albumin ratio, neutrophil to lymphocyte ratio (NLR), platelet to lymphocyte ratio, and sodium level, as well as intraoperative post-reperfusion syndrome, mean central venous pressure, requirement for packed red blood cells and fresh frozen plasma, hourly fluid infusion and urine output, and short-term postoperative early allograft dysfunction (EAD) were associated with the risk of early post-transplant bacteremia. Multivariate analysis revealed that PMI, the CRRT requirement, the NLR, and EAD were independently associated with the risk of early post-transplant bacteremia (area under the curve: 0.707; 95% confidence interval: 0.667–0.745; p < 0.001). The overall survival rate was better in the non-infected patient group. Among patients with bacteremia, anti-bacterial treatment was unable to resolve infection in 34 patients, resulting in an increased risk of patient mortality. Among the factors included in the model, EAD was significantly correlated with non-resolving infection. CONCLUSIONS: We propose a prognostic model to identify patients at high risk for a bloodstream bacterial infection; furthermore, our findings support the notion that skeletal muscle depletion, CRRT requirement, systemic inflammatory response, and delayed liver graft function are associated with a pathogenic vulnerability in cirrhotic patients who undergo LDLT.
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spelling pubmed-70667342020-03-18 Risk stratification for early bacteremia after living donor liver transplantation: a retrospective observational cohort study Park, Jaesik Kim, Bae Wook Choi, Ho Joong Hong, Sang Hyun Park, Chul Soo Choi, Jong Ho Chae, Min Suk BMC Surg Research Article BACKGROUND: This study investigated perioperative clinical risk factors for early post-transplant bacteremia in patients undergoing living donor liver transplantation (LDLT). Additionally, postoperative outcomes were compared between patients with and without early post-transplant bacteremia. METHODS: Clinical data of 610 adult patients who underwent elective LDLT between January 2009 and December 2018 at Seoul St. Mary’s Hospital were retrospectively collected. The exclusion criteria included overt signs of infection within 1 month before surgery. A total of 596 adult patients were enrolled in this study. Based on the occurrence of a systemic bacterial infection after surgery, patients were classified into non-infected and infected groups. RESULTS: The incidence of bacteremia at 1 month after LDLT was 9.7% (57 patients) and Enterococcus faecium (31.6%) was the most commonly cultured bacterium in the blood samples. Univariate analysis showed that preoperative psoas muscle index (PMI), model for end-stage disease score, utility of continuous renal replacement therapy (CRRT), ascites, C-reactive protein to albumin ratio, neutrophil to lymphocyte ratio (NLR), platelet to lymphocyte ratio, and sodium level, as well as intraoperative post-reperfusion syndrome, mean central venous pressure, requirement for packed red blood cells and fresh frozen plasma, hourly fluid infusion and urine output, and short-term postoperative early allograft dysfunction (EAD) were associated with the risk of early post-transplant bacteremia. Multivariate analysis revealed that PMI, the CRRT requirement, the NLR, and EAD were independently associated with the risk of early post-transplant bacteremia (area under the curve: 0.707; 95% confidence interval: 0.667–0.745; p < 0.001). The overall survival rate was better in the non-infected patient group. Among patients with bacteremia, anti-bacterial treatment was unable to resolve infection in 34 patients, resulting in an increased risk of patient mortality. Among the factors included in the model, EAD was significantly correlated with non-resolving infection. CONCLUSIONS: We propose a prognostic model to identify patients at high risk for a bloodstream bacterial infection; furthermore, our findings support the notion that skeletal muscle depletion, CRRT requirement, systemic inflammatory response, and delayed liver graft function are associated with a pathogenic vulnerability in cirrhotic patients who undergo LDLT. BioMed Central 2020-03-12 /pmc/articles/PMC7066734/ /pubmed/32160890 http://dx.doi.org/10.1186/s12893-019-0658-6 Text en © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Park, Jaesik
Kim, Bae Wook
Choi, Ho Joong
Hong, Sang Hyun
Park, Chul Soo
Choi, Jong Ho
Chae, Min Suk
Risk stratification for early bacteremia after living donor liver transplantation: a retrospective observational cohort study
title Risk stratification for early bacteremia after living donor liver transplantation: a retrospective observational cohort study
title_full Risk stratification for early bacteremia after living donor liver transplantation: a retrospective observational cohort study
title_fullStr Risk stratification for early bacteremia after living donor liver transplantation: a retrospective observational cohort study
title_full_unstemmed Risk stratification for early bacteremia after living donor liver transplantation: a retrospective observational cohort study
title_short Risk stratification for early bacteremia after living donor liver transplantation: a retrospective observational cohort study
title_sort risk stratification for early bacteremia after living donor liver transplantation: a retrospective observational cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066734/
https://www.ncbi.nlm.nih.gov/pubmed/32160890
http://dx.doi.org/10.1186/s12893-019-0658-6
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