INFECTIONS IN THALASSEMIA AND HEMOGLOBINOPATHIES

<p class="MsoNormalCxSpFirst" style="margin: 0cm 70.9pt 0pt 0cm; text-indent: 0cm; line-height: 200%; text-align: justify; mso-add-space: auto;"><span style="font-size: 12pt; line-height: 200%; font-family: ";Times New Roman";,";serif"...

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Main Authors: Deborah Rund, Arturo Di Girolamo, Bianca Maria Ricerca
Format: Article
Language:English
Published: PAGEPress Publications 2009-06-01
Series:Mediterranean Journal of Hematology and Infectious Diseases
Subjects:
Online Access:http://www.mjhid.org/article/view/5229
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spelling doaj-01947e97665d4b79a3a86128d2c549e32020-11-24T23:36:35ZengPAGEPress PublicationsMediterranean Journal of Hematology and Infectious Diseases2035-30062009-06-0111e2009028e2009028INFECTIONS IN THALASSEMIA AND HEMOGLOBINOPATHIESDeborah RundArturo Di GirolamoBianca Maria Ricerca<p class="MsoNormalCxSpFirst" style="margin: 0cm 70.9pt 0pt 0cm; text-indent: 0cm; line-height: 200%; text-align: justify; mso-add-space: auto;"><span style="font-size: 12pt; line-height: 200%; font-family: ";Times New Roman";,";serif";; mso-ansi-language: EN-US;" lang="EN-US"> </span></p><span style="font-size: 12pt; font-family: ";Times New Roman";,";serif";; mso-ansi-language: EN-US; mso-fareast-font-family: Calibri; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;" lang="EN-US">The clinical approach to thalassemia and hemoglobinopathies, specifically Sickle Cell Disease (SCD), based on transfusions, iron chelation and bone marrow transplantation has ameliorated their prognosis. Nevertheless, infections still may cause serious complications in these patients. The susceptibility to infections in thalassemia and SCD arises both from a large spectrum of immunological abnormalities and from exposure to specific infectious agents. Four fundamental issues will be focused upon as central causes of immune dysfunction: the diseases themselves; iron overload, transfusion therapy and the role of the spleen. Thalassemia and SCD differ in their pathogenesis and clinical course. It will be outlined how these differences affect immune dysfunction, the risk of infections and the types of most frequent infections in each disease. Moreover, since transfusions are a fundamental tool for treating these patients, their safety is paramount in reducing the risks of infections. In recent years, careful surveillance worldwide and improvements in laboratory tests reduced greatly transfusion transmitted infections, but the problem is not completely resolved. Finally, selected topics will be discussed regarding Parvovirus B19 and transfusion transmitted infections as well as the prevention of infectious risk postsplenectomy or in presence of functional asplenia.</span>http://www.mjhid.org/article/view/5229Infectious diseases, Thalassemia, Sickle cell disease, Immune dysfunction, iron overload, allogenic blood transfusions, splenectomy
collection DOAJ
language English
format Article
sources DOAJ
author Deborah Rund
Arturo Di Girolamo
Bianca Maria Ricerca
spellingShingle Deborah Rund
Arturo Di Girolamo
Bianca Maria Ricerca
INFECTIONS IN THALASSEMIA AND HEMOGLOBINOPATHIES
Mediterranean Journal of Hematology and Infectious Diseases
Infectious diseases, Thalassemia, Sickle cell disease, Immune dysfunction, iron overload, allogenic blood transfusions, splenectomy
author_facet Deborah Rund
Arturo Di Girolamo
Bianca Maria Ricerca
author_sort Deborah Rund
title INFECTIONS IN THALASSEMIA AND HEMOGLOBINOPATHIES
title_short INFECTIONS IN THALASSEMIA AND HEMOGLOBINOPATHIES
title_full INFECTIONS IN THALASSEMIA AND HEMOGLOBINOPATHIES
title_fullStr INFECTIONS IN THALASSEMIA AND HEMOGLOBINOPATHIES
title_full_unstemmed INFECTIONS IN THALASSEMIA AND HEMOGLOBINOPATHIES
title_sort infections in thalassemia and hemoglobinopathies
publisher PAGEPress Publications
series Mediterranean Journal of Hematology and Infectious Diseases
issn 2035-3006
publishDate 2009-06-01
description <p class="MsoNormalCxSpFirst" style="margin: 0cm 70.9pt 0pt 0cm; text-indent: 0cm; line-height: 200%; text-align: justify; mso-add-space: auto;"><span style="font-size: 12pt; line-height: 200%; font-family: ";Times New Roman";,";serif";; mso-ansi-language: EN-US;" lang="EN-US"> </span></p><span style="font-size: 12pt; font-family: ";Times New Roman";,";serif";; mso-ansi-language: EN-US; mso-fareast-font-family: Calibri; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;" lang="EN-US">The clinical approach to thalassemia and hemoglobinopathies, specifically Sickle Cell Disease (SCD), based on transfusions, iron chelation and bone marrow transplantation has ameliorated their prognosis. Nevertheless, infections still may cause serious complications in these patients. The susceptibility to infections in thalassemia and SCD arises both from a large spectrum of immunological abnormalities and from exposure to specific infectious agents. Four fundamental issues will be focused upon as central causes of immune dysfunction: the diseases themselves; iron overload, transfusion therapy and the role of the spleen. Thalassemia and SCD differ in their pathogenesis and clinical course. It will be outlined how these differences affect immune dysfunction, the risk of infections and the types of most frequent infections in each disease. Moreover, since transfusions are a fundamental tool for treating these patients, their safety is paramount in reducing the risks of infections. In recent years, careful surveillance worldwide and improvements in laboratory tests reduced greatly transfusion transmitted infections, but the problem is not completely resolved. Finally, selected topics will be discussed regarding Parvovirus B19 and transfusion transmitted infections as well as the prevention of infectious risk postsplenectomy or in presence of functional asplenia.</span>
topic Infectious diseases, Thalassemia, Sickle cell disease, Immune dysfunction, iron overload, allogenic blood transfusions, splenectomy
url http://www.mjhid.org/article/view/5229
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AT arturodigirolamo infectionsinthalassemiaandhemoglobinopathies
AT biancamariaricerca infectionsinthalassemiaandhemoglobinopathies
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