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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PAGEPress Publications
2009-06-01
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Series: | Mediterranean Journal of Hematology and Infectious Diseases |
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Online Access: | http://www.mjhid.org/article/view/5229 |
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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 |
work_keys_str_mv |
AT deborahrund infectionsinthalassemiaandhemoglobinopathies AT arturodigirolamo infectionsinthalassemiaandhemoglobinopathies AT biancamariaricerca infectionsinthalassemiaandhemoglobinopathies |
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