Iron Overload in Patients Undergoing Hematopoietic Stem Cell Transplantation

Recipients of hematopoietic stem cell transplantation (HSCT) frequently have iron overload resulting from chronic transfusion therapy for anemia. In some cases, for example, in patients with myelodysplastic syndromes and thalassemia, this can be further exacerbated by increased absorption of iron fr...

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Main Author: Vinod Pullarkat
Format: Article
Language:English
Published: Hindawi Limited 2010-01-01
Series:Advances in Hematology
Online Access:http://dx.doi.org/10.1155/2010/345756
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spelling doaj-2fdce075573048bfa8308a4b147981fa2021-07-02T15:45:43ZengHindawi LimitedAdvances in Hematology1687-91041687-91122010-01-01201010.1155/2010/345756345756Iron Overload in Patients Undergoing Hematopoietic Stem Cell TransplantationVinod Pullarkat0Department of Hematology and Hematopoietic Cell Transplantation, City of Hope Medical Center, 150 East Duarte Road, Duarte, CA 91010, USARecipients of hematopoietic stem cell transplantation (HSCT) frequently have iron overload resulting from chronic transfusion therapy for anemia. In some cases, for example, in patients with myelodysplastic syndromes and thalassemia, this can be further exacerbated by increased absorption of iron from the gut as a result of ineffective erythropoiesis. Accumulating evidence has established the negative impact of elevated pretransplantation serum ferritin, a surrogate marker of iron overload, on overall survival and nonrelapse mortality after HSCT. Complications of HSCT associated with iron overload include increased bacterial and fungal infections as well as sinusoidal obstruction syndrome and possibly other regimen-related toxicities. Based on current evidence, particular attention should be paid to prevention and management of iron overload in allogeneic HSCT candidates, especially in patients with thalassemia and myelodysplastic syndromes. The pathophysiology of iron overload in the HSCT patient and optimum strategies to deal with iron overload during and after HSCT require further study.http://dx.doi.org/10.1155/2010/345756
collection DOAJ
language English
format Article
sources DOAJ
author Vinod Pullarkat
spellingShingle Vinod Pullarkat
Iron Overload in Patients Undergoing Hematopoietic Stem Cell Transplantation
Advances in Hematology
author_facet Vinod Pullarkat
author_sort Vinod Pullarkat
title Iron Overload in Patients Undergoing Hematopoietic Stem Cell Transplantation
title_short Iron Overload in Patients Undergoing Hematopoietic Stem Cell Transplantation
title_full Iron Overload in Patients Undergoing Hematopoietic Stem Cell Transplantation
title_fullStr Iron Overload in Patients Undergoing Hematopoietic Stem Cell Transplantation
title_full_unstemmed Iron Overload in Patients Undergoing Hematopoietic Stem Cell Transplantation
title_sort iron overload in patients undergoing hematopoietic stem cell transplantation
publisher Hindawi Limited
series Advances in Hematology
issn 1687-9104
1687-9112
publishDate 2010-01-01
description Recipients of hematopoietic stem cell transplantation (HSCT) frequently have iron overload resulting from chronic transfusion therapy for anemia. In some cases, for example, in patients with myelodysplastic syndromes and thalassemia, this can be further exacerbated by increased absorption of iron from the gut as a result of ineffective erythropoiesis. Accumulating evidence has established the negative impact of elevated pretransplantation serum ferritin, a surrogate marker of iron overload, on overall survival and nonrelapse mortality after HSCT. Complications of HSCT associated with iron overload include increased bacterial and fungal infections as well as sinusoidal obstruction syndrome and possibly other regimen-related toxicities. Based on current evidence, particular attention should be paid to prevention and management of iron overload in allogeneic HSCT candidates, especially in patients with thalassemia and myelodysplastic syndromes. The pathophysiology of iron overload in the HSCT patient and optimum strategies to deal with iron overload during and after HSCT require further study.
url http://dx.doi.org/10.1155/2010/345756
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