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Bloodless living donor liver transplantation: Risk factors, outcomes, and diagnostic predictors
Massive bleeding is often unavoidable during liver transplantation (LT). However, blood transfusions are associated with risks and should be avoided whenever possible. This study compares preoperative factors and outcomes between non-transfusion and transfusion groups to identify variables that coul...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320073/ https://www.ncbi.nlm.nih.gov/pubmed/30558025 http://dx.doi.org/10.1097/MD.0000000000013581 |
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author | Yoon, Ji-Uk Byeon, Gyeong-Jo Park, Ju Yeon Yoon, Seok Hyun Ryu, Je-Ho Ri, Hyun-Su |
author_facet | Yoon, Ji-Uk Byeon, Gyeong-Jo Park, Ju Yeon Yoon, Seok Hyun Ryu, Je-Ho Ri, Hyun-Su |
author_sort | Yoon, Ji-Uk |
collection | PubMed |
description | Massive bleeding is often unavoidable during liver transplantation (LT). However, blood transfusions are associated with risks and should be avoided whenever possible. This study compares preoperative factors and outcomes between non-transfusion and transfusion groups to identify variables that could be used to predict bloodless surgery in living donor liver transplantation (LDLT) patients. We conducted a retrospective study of 87 LDLT patients. The group of patients who did not require packed red blood cell (PRBC) transfusion (non-PRBC group, n = 44) was compared with those who did (PRBC group, n = 43). We compared risk factors, fluid management, and outcomes between the groups and identified variables for prediction of transfusion during LDLT. Compared with the PRBC group, the non-PRBC group had a lower model for end-stage liver disease (MELD) score (8.1 ± 1.1 vs 18.2 ± 8.8), international normalized ratio (INR) (1.16 ± 0.1 vs 1.80 ± 0.94), and partial thromboplastin time (PTT) (37.1 ± 6.3 vs 54.1 ± 24.0), but higher hemoglobin (Hb) (13.6 ± 1.6 vs 11.5 ± 2.2) and hematocrit (HCT) (39.1 ± 4.4 vs 32.6 ± 6.0). The non-PRBC group were more likely to receive colloid and albumin but had shorter intensive care unit (ICU) and hospital length of stay. The area under the receiver operative characteristic (ROC) curve of the MELD score was the highest (91%) using a cutoff value of 10.5. Patients without PRBC transfusion during LDLT were in better condition preoperatively and had better outcomes. The MELD score is a significant predictor for PRBC transfusion. |
format | Online Article Text |
id | pubmed-6320073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-63200732019-01-14 Bloodless living donor liver transplantation: Risk factors, outcomes, and diagnostic predictors Yoon, Ji-Uk Byeon, Gyeong-Jo Park, Ju Yeon Yoon, Seok Hyun Ryu, Je-Ho Ri, Hyun-Su Medicine (Baltimore) Research Article Massive bleeding is often unavoidable during liver transplantation (LT). However, blood transfusions are associated with risks and should be avoided whenever possible. This study compares preoperative factors and outcomes between non-transfusion and transfusion groups to identify variables that could be used to predict bloodless surgery in living donor liver transplantation (LDLT) patients. We conducted a retrospective study of 87 LDLT patients. The group of patients who did not require packed red blood cell (PRBC) transfusion (non-PRBC group, n = 44) was compared with those who did (PRBC group, n = 43). We compared risk factors, fluid management, and outcomes between the groups and identified variables for prediction of transfusion during LDLT. Compared with the PRBC group, the non-PRBC group had a lower model for end-stage liver disease (MELD) score (8.1 ± 1.1 vs 18.2 ± 8.8), international normalized ratio (INR) (1.16 ± 0.1 vs 1.80 ± 0.94), and partial thromboplastin time (PTT) (37.1 ± 6.3 vs 54.1 ± 24.0), but higher hemoglobin (Hb) (13.6 ± 1.6 vs 11.5 ± 2.2) and hematocrit (HCT) (39.1 ± 4.4 vs 32.6 ± 6.0). The non-PRBC group were more likely to receive colloid and albumin but had shorter intensive care unit (ICU) and hospital length of stay. The area under the receiver operative characteristic (ROC) curve of the MELD score was the highest (91%) using a cutoff value of 10.5. Patients without PRBC transfusion during LDLT were in better condition preoperatively and had better outcomes. The MELD score is a significant predictor for PRBC transfusion. Wolters Kluwer Health 2018-12-14 /pmc/articles/PMC6320073/ /pubmed/30558025 http://dx.doi.org/10.1097/MD.0000000000013581 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://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 (CCBY-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. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | Research Article Yoon, Ji-Uk Byeon, Gyeong-Jo Park, Ju Yeon Yoon, Seok Hyun Ryu, Je-Ho Ri, Hyun-Su Bloodless living donor liver transplantation: Risk factors, outcomes, and diagnostic predictors |
title | Bloodless living donor liver transplantation: Risk factors, outcomes, and diagnostic predictors |
title_full | Bloodless living donor liver transplantation: Risk factors, outcomes, and diagnostic predictors |
title_fullStr | Bloodless living donor liver transplantation: Risk factors, outcomes, and diagnostic predictors |
title_full_unstemmed | Bloodless living donor liver transplantation: Risk factors, outcomes, and diagnostic predictors |
title_short | Bloodless living donor liver transplantation: Risk factors, outcomes, and diagnostic predictors |
title_sort | bloodless living donor liver transplantation: risk factors, outcomes, and diagnostic predictors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320073/ https://www.ncbi.nlm.nih.gov/pubmed/30558025 http://dx.doi.org/10.1097/MD.0000000000013581 |
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