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The Effect and Safety of Prostaglandin Administration in Pediatric Liver Transplantation
BACKGROUND: Prostaglandins are often administered after liver transplantation (LT) to diminish ischemia-reperfusion injury (IRI), to favor liver recovery and to prevent vascular thrombosis. Possible beneficial effects in adult liver recipients are controversial, but the single existing pediatric sma...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5464782/ https://www.ncbi.nlm.nih.gov/pubmed/28620647 http://dx.doi.org/10.1097/TXD.0000000000000682 |
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author | Lironi, Céline McLin, Valérie A. Wildhaber, Barbara E. |
author_facet | Lironi, Céline McLin, Valérie A. Wildhaber, Barbara E. |
author_sort | Lironi, Céline |
collection | PubMed |
description | BACKGROUND: Prostaglandins are often administered after liver transplantation (LT) to diminish ischemia-reperfusion injury (IRI), to favor liver recovery and to prevent vascular thrombosis. Possible beneficial effects in adult liver recipients are controversial, but the single existing pediatric small case series shows no significant impact of prostaglandin administration after LT. The purpose of this study was to analyze the effect of the prostaglandin dinoprostone in pediatric liver recipients. METHODS: A retrospective analysis of 41 children (<16 years) who underwent LT between March 2008 and December 2013 was performed. Dinoprostone was administered at a rate from 0.1 to a maximum of 0.6 μg/kg per hour immediately after LT and for a maximum of 5 days. Effect of dinoprostone on post-LT IRI and hepatic function up to 60 postoperative days and number of hypotensive episodes were analyzed. RESULTS: The median cumulative dose of dinoprostone was 28 μg/kg (interquartile range, 23.2). Dinoprostone had no significant effect on post-LT liver function tests and factor V levels at any of the administered dosages. There was no significant association between the total quantity of vasopressor given and the number of hypotensive episodes observed in 8 patients. One patient showed a short-lasting hypotension, possibly related to the administration of dinoprostone. CONCLUSIONS: This study did not show, at any dosage between 0.1 and 0.6 μg/kg per hour, any differences in beneficial or harmful effects of high- or low-dose dinoprostone administered immediately after pediatric LT on markers of IRI, hepatic function, or hypotension. |
format | Online Article Text |
id | pubmed-5464782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-54647822017-06-15 The Effect and Safety of Prostaglandin Administration in Pediatric Liver Transplantation Lironi, Céline McLin, Valérie A. Wildhaber, Barbara E. Transplant Direct Liver Transplantation BACKGROUND: Prostaglandins are often administered after liver transplantation (LT) to diminish ischemia-reperfusion injury (IRI), to favor liver recovery and to prevent vascular thrombosis. Possible beneficial effects in adult liver recipients are controversial, but the single existing pediatric small case series shows no significant impact of prostaglandin administration after LT. The purpose of this study was to analyze the effect of the prostaglandin dinoprostone in pediatric liver recipients. METHODS: A retrospective analysis of 41 children (<16 years) who underwent LT between March 2008 and December 2013 was performed. Dinoprostone was administered at a rate from 0.1 to a maximum of 0.6 μg/kg per hour immediately after LT and for a maximum of 5 days. Effect of dinoprostone on post-LT IRI and hepatic function up to 60 postoperative days and number of hypotensive episodes were analyzed. RESULTS: The median cumulative dose of dinoprostone was 28 μg/kg (interquartile range, 23.2). Dinoprostone had no significant effect on post-LT liver function tests and factor V levels at any of the administered dosages. There was no significant association between the total quantity of vasopressor given and the number of hypotensive episodes observed in 8 patients. One patient showed a short-lasting hypotension, possibly related to the administration of dinoprostone. CONCLUSIONS: This study did not show, at any dosage between 0.1 and 0.6 μg/kg per hour, any differences in beneficial or harmful effects of high- or low-dose dinoprostone administered immediately after pediatric LT on markers of IRI, hepatic function, or hypotension. Lippincott Williams & Wilkins 2017-05-18 /pmc/articles/PMC5464782/ /pubmed/28620647 http://dx.doi.org/10.1097/TXD.0000000000000682 Text en Copyright © 2017 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc. 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) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , 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 | Liver Transplantation Lironi, Céline McLin, Valérie A. Wildhaber, Barbara E. The Effect and Safety of Prostaglandin Administration in Pediatric Liver Transplantation |
title | The Effect and Safety of Prostaglandin Administration in Pediatric Liver Transplantation |
title_full | The Effect and Safety of Prostaglandin Administration in Pediatric Liver Transplantation |
title_fullStr | The Effect and Safety of Prostaglandin Administration in Pediatric Liver Transplantation |
title_full_unstemmed | The Effect and Safety of Prostaglandin Administration in Pediatric Liver Transplantation |
title_short | The Effect and Safety of Prostaglandin Administration in Pediatric Liver Transplantation |
title_sort | effect and safety of prostaglandin administration in pediatric liver transplantation |
topic | Liver Transplantation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5464782/ https://www.ncbi.nlm.nih.gov/pubmed/28620647 http://dx.doi.org/10.1097/TXD.0000000000000682 |
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