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Outcomes of high-grade gastrointestinal graft-versus-host disease posthematopoietic stem cell transplantation in children

We explored the clinical course of acute high-grade gastrointestinal graft-versus-host disease in children in a single center. This was a retrospective analysis of 28 pediatric patients who presented with a clinical diagnosis of stage III and IV acute graft-versus-host disease (aGVHD) of the gastroi...

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Autores principales: Uygun, Vedat, Uygun, Dilara F.K., Daloğlu, Hayriye, Öztürkmen, Seda Irmak, Karasu, Gülsün, Hazar, Volkan, Yeşilipek, Akif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5591127/
https://www.ncbi.nlm.nih.gov/pubmed/27858879
http://dx.doi.org/10.1097/MD.0000000000005242
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author Uygun, Vedat
Uygun, Dilara F.K.
Daloğlu, Hayriye
Öztürkmen, Seda Irmak
Karasu, Gülsün
Hazar, Volkan
Yeşilipek, Akif
author_facet Uygun, Vedat
Uygun, Dilara F.K.
Daloğlu, Hayriye
Öztürkmen, Seda Irmak
Karasu, Gülsün
Hazar, Volkan
Yeşilipek, Akif
author_sort Uygun, Vedat
collection PubMed
description We explored the clinical course of acute high-grade gastrointestinal graft-versus-host disease in children in a single center. This was a retrospective analysis of 28 pediatric patients who presented with a clinical diagnosis of stage III and IV acute graft-versus-host disease (aGVHD) of the gastrointestinal system (GIS). Generally, skin involvement was the initial manifestation of aGVHD that began in the first 3 weeks of hematopoietic stem cell transplantation (HSCT); on the other hand, GIS involvement predominated after the second week of HSCT. Reported adult data show a survival rate of only 25%; however, our study showed more favorable outcomes in children with a survival rate of 55%. We monitored levels of albumin and immunoglobulin G and observed low levels overall during treatment of unresponsive patients, although only albumin levels were shown to be significantly different. We observed a significant increase in mortality with the use of antithymocyte globulin in GIS aGVHD, although antithymocyte globulin used for graft-versus-host disease prophylaxis had no demonstrable effect on GIS aGVHD mortality. Whether the significantly lower GIS aGVHD mortality among the children recruited in our study than among their historical adult counterparts is a primary result of the specific attributes of the pediatric GIS, or whether it originated from HSCT kinetics remains to be determined by future studies.
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spelling pubmed-55911272017-09-15 Outcomes of high-grade gastrointestinal graft-versus-host disease posthematopoietic stem cell transplantation in children Uygun, Vedat Uygun, Dilara F.K. Daloğlu, Hayriye Öztürkmen, Seda Irmak Karasu, Gülsün Hazar, Volkan Yeşilipek, Akif Medicine (Baltimore) 4800 We explored the clinical course of acute high-grade gastrointestinal graft-versus-host disease in children in a single center. This was a retrospective analysis of 28 pediatric patients who presented with a clinical diagnosis of stage III and IV acute graft-versus-host disease (aGVHD) of the gastrointestinal system (GIS). Generally, skin involvement was the initial manifestation of aGVHD that began in the first 3 weeks of hematopoietic stem cell transplantation (HSCT); on the other hand, GIS involvement predominated after the second week of HSCT. Reported adult data show a survival rate of only 25%; however, our study showed more favorable outcomes in children with a survival rate of 55%. We monitored levels of albumin and immunoglobulin G and observed low levels overall during treatment of unresponsive patients, although only albumin levels were shown to be significantly different. We observed a significant increase in mortality with the use of antithymocyte globulin in GIS aGVHD, although antithymocyte globulin used for graft-versus-host disease prophylaxis had no demonstrable effect on GIS aGVHD mortality. Whether the significantly lower GIS aGVHD mortality among the children recruited in our study than among their historical adult counterparts is a primary result of the specific attributes of the pediatric GIS, or whether it originated from HSCT kinetics remains to be determined by future studies. Wolters Kluwer Health 2016-11-04 /pmc/articles/PMC5591127/ /pubmed/27858879 http://dx.doi.org/10.1097/MD.0000000000005242 Text en Copyright © 2016 the Author(s). Published by Wolters Kluwer Health, Inc. All rights reserved. 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 4800
Uygun, Vedat
Uygun, Dilara F.K.
Daloğlu, Hayriye
Öztürkmen, Seda Irmak
Karasu, Gülsün
Hazar, Volkan
Yeşilipek, Akif
Outcomes of high-grade gastrointestinal graft-versus-host disease posthematopoietic stem cell transplantation in children
title Outcomes of high-grade gastrointestinal graft-versus-host disease posthematopoietic stem cell transplantation in children
title_full Outcomes of high-grade gastrointestinal graft-versus-host disease posthematopoietic stem cell transplantation in children
title_fullStr Outcomes of high-grade gastrointestinal graft-versus-host disease posthematopoietic stem cell transplantation in children
title_full_unstemmed Outcomes of high-grade gastrointestinal graft-versus-host disease posthematopoietic stem cell transplantation in children
title_short Outcomes of high-grade gastrointestinal graft-versus-host disease posthematopoietic stem cell transplantation in children
title_sort outcomes of high-grade gastrointestinal graft-versus-host disease posthematopoietic stem cell transplantation in children
topic 4800
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5591127/
https://www.ncbi.nlm.nih.gov/pubmed/27858879
http://dx.doi.org/10.1097/MD.0000000000005242
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