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Mannitol for prevention of acute kidney injury after liver transplantation: a randomized controlled trial

BACKGROUND: Acute kidney injury (AKI) is a common complication after liver transplantation, which is associated with increased morbidity and mortality. Therefore, this study investigated mannitol as an oxygen-free radical scavenger and its role in the prevention of early AKI after living donor liver...

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Autores principales: Emara, Moataz Maher, Diab, Doaa Galal, Yassen, Amr Mohamed, Abo-Zeid, Maha A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762035/
https://www.ncbi.nlm.nih.gov/pubmed/36536282
http://dx.doi.org/10.1186/s12871-022-01936-7
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author Emara, Moataz Maher
Diab, Doaa Galal
Yassen, Amr Mohamed
Abo-Zeid, Maha A.
author_facet Emara, Moataz Maher
Diab, Doaa Galal
Yassen, Amr Mohamed
Abo-Zeid, Maha A.
author_sort Emara, Moataz Maher
collection PubMed
description BACKGROUND: Acute kidney injury (AKI) is a common complication after liver transplantation, which is associated with increased morbidity and mortality. Therefore, this study investigated mannitol as an oxygen-free radical scavenger and its role in the prevention of early AKI after living donor liver transplantation (LDLT). METHODS: A total of 84 adult patients who underwent LDLT were randomly assigned to two equal groups: the M group, where patients received 1 g/kg mannitol 20%, or the S group, where patients received an equal volume of saline. The primary outcome was the incidence of early AKI, defined as a 0.3 mg/dl increase in the serum creatinine 48 h postoperatively. Laboratory assessments of the graft and creatinine were recorded until 3 months after transplantation besides the post-reperfusion syndrome and the intraoperative hemodynamic measurements. RESULTS: The AKI incidence was comparable between groups (relative risk ratio of 1.285, 95% CI 0.598–2.759, P = 0.518). Moreover, AKI stages and serum creatinine 3 months after transplantation, P = 0.23 and P = 0.25, respectively. The incidence of the post-reperfusion syndrome was comparable in both groups, 29/39 (74.4%) and 31/41 (75.6%) in M and S groups, respectively, P = 0.897. The intraoperative hemodynamic parameters showed no significant difference between groups using the area under the curve. CONCLUSION: The current LDLT recipient sample was insufficient to demonstrate that pre-reperfusion 1 g/kg mannitol infusion would reduce the risk of early AKI or post-reperfusion syndrome. CLINICAL TRIAL REGISTRATION NUMBER: Pan African Clinical Trials Registry (PACTR202203622900599); https://pactr.samrc.ac.za/TrialDisplay.aspx?TrialID=21511. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12871-022-01936-7.
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spelling pubmed-97620352022-12-20 Mannitol for prevention of acute kidney injury after liver transplantation: a randomized controlled trial Emara, Moataz Maher Diab, Doaa Galal Yassen, Amr Mohamed Abo-Zeid, Maha A. BMC Anesthesiol Research BACKGROUND: Acute kidney injury (AKI) is a common complication after liver transplantation, which is associated with increased morbidity and mortality. Therefore, this study investigated mannitol as an oxygen-free radical scavenger and its role in the prevention of early AKI after living donor liver transplantation (LDLT). METHODS: A total of 84 adult patients who underwent LDLT were randomly assigned to two equal groups: the M group, where patients received 1 g/kg mannitol 20%, or the S group, where patients received an equal volume of saline. The primary outcome was the incidence of early AKI, defined as a 0.3 mg/dl increase in the serum creatinine 48 h postoperatively. Laboratory assessments of the graft and creatinine were recorded until 3 months after transplantation besides the post-reperfusion syndrome and the intraoperative hemodynamic measurements. RESULTS: The AKI incidence was comparable between groups (relative risk ratio of 1.285, 95% CI 0.598–2.759, P = 0.518). Moreover, AKI stages and serum creatinine 3 months after transplantation, P = 0.23 and P = 0.25, respectively. The incidence of the post-reperfusion syndrome was comparable in both groups, 29/39 (74.4%) and 31/41 (75.6%) in M and S groups, respectively, P = 0.897. The intraoperative hemodynamic parameters showed no significant difference between groups using the area under the curve. CONCLUSION: The current LDLT recipient sample was insufficient to demonstrate that pre-reperfusion 1 g/kg mannitol infusion would reduce the risk of early AKI or post-reperfusion syndrome. CLINICAL TRIAL REGISTRATION NUMBER: Pan African Clinical Trials Registry (PACTR202203622900599); https://pactr.samrc.ac.za/TrialDisplay.aspx?TrialID=21511. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12871-022-01936-7. BioMed Central 2022-12-19 /pmc/articles/PMC9762035/ /pubmed/36536282 http://dx.doi.org/10.1186/s12871-022-01936-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Emara, Moataz Maher
Diab, Doaa Galal
Yassen, Amr Mohamed
Abo-Zeid, Maha A.
Mannitol for prevention of acute kidney injury after liver transplantation: a randomized controlled trial
title Mannitol for prevention of acute kidney injury after liver transplantation: a randomized controlled trial
title_full Mannitol for prevention of acute kidney injury after liver transplantation: a randomized controlled trial
title_fullStr Mannitol for prevention of acute kidney injury after liver transplantation: a randomized controlled trial
title_full_unstemmed Mannitol for prevention of acute kidney injury after liver transplantation: a randomized controlled trial
title_short Mannitol for prevention of acute kidney injury after liver transplantation: a randomized controlled trial
title_sort mannitol for prevention of acute kidney injury after liver transplantation: a randomized controlled trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762035/
https://www.ncbi.nlm.nih.gov/pubmed/36536282
http://dx.doi.org/10.1186/s12871-022-01936-7
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