Transfusion-Transmitted Viruses in Individuals with β Thalassemia Major at Northeastern Iran, a Retrospective Sero-Epidemiological Survey
نویسندگان
چکیده مقاله:
Background: Thalassemia syndromes are the most common genetic disorders in the world. They happen due to genetic defects in process of haemoglobin synthesis, and would be classified to many groups mainly α and β, based on the kind of defect. Anemia is the main clinical manifestation of this phenotype of disorder. In order to correct the chronic anemia in thalassaemic individuals, they may need to get 4-6 blood units per month. They are also prone to blood borne infections. Patients and Methods: We retrospectively evaluated medical records of 360 major β- thlassemic patients in northeastern Iran to find the viral blood borne status among them. Results: The findings showed that 209 (58.8%) were male and 151 (41.94%) were female. About blood borne viruses, 30 (8.33%) had positive result for anti-HCV. Eight persons (2.22%) had positive HBsAg. Twenty-two persons (6.11%) had positive HTLV-I serums. No one had positive HIV (1/2). Seven (1.94%) were positive for both HTLV-I and anti-HCV. Two ones (0.55%) had positive serums for both HTLV-I and HBsAg. Conclusion: Similar to other geographic regions, the HCV was the most common type of viral infections in northeastern Iran. Surveying the HTLV-I, the northeastern part of country is one of endemic sources for the HTLV-I and in fact 22 individuals showed it. Also HBV had infected part of major β- thalassemic patients. Fortunately there was no case with the HIV that intensified the blood safety of blood transfusion organization.
منابع مشابه
transfusion-transmitted viruses in individuals with β thalassemia major at northeastern iran, a retrospective sero-epidemiological survey
background: thalassemia syndromes are the most common genetic disorders in the world. they happen due to genetic defects in process of haemoglobin synthesis, and would be classified to many groups mainly α and β, based on the kind of defect. anemia is the main clinical manifestation of this phenotype of disorder. in order to correct the chronic anemia in thalassaemic individuals, they may need ...
متن کاملEpidemiological Investigation of a Twenty-Year Major β-Thalassemia Surveillance in Kerman, Iran
Background & Aims of the Study: Since beta-thalassemia is the most commonly inherited disease in Iran, its preventive and controlling programs are considered vitally important in the healthcare system. This study was conducted to investigate the incidence rate and epidemiology of major beta-thalassemia (MBT) over the last twenty years in Kerman, Iran. Materials and Methods: This cross-secti...
متن کاملRenal Hemosiderosis among Iranian Transfusion Dependent β-Thalassemia Major Patients
Background: In recent years, the success in management of thalassemic patients, has allowed for some previously unrecognized complications including renal abnormalities to emerge. This prospective study aimed to investigate kidney iron overload by means of MRI T2* and also renal function based on laboratory tests for early markers of glomerular and tubular dysfunction among adult Iranian transf...
متن کاملQuality of Life in Children with Β-Thalassemia Major at Center for Special Diseases
Abstract Background Knowledge of factors associated with quality of life in patients with thalassemia is necessary for creating appropriate clinical programs, social support, and improving treatment outcomes. The purpose of this study was to determine quality of life in children with thalassemia major at Center for Special Diseases of valiasr hospital in Birjand. Materials and Methods This...
متن کاملAnalysis of Survival in Patients with β-thalassemia Major in Guilan, Northern Iran
Background: Advances in treatment of thalassemia major (TM) have improved life expectancy and survival of the patients. This study was conducted to assess survival rate of these patients in Guilan province, Northern Iran. Methods: In this cross-sectional study, records of 1243 patients with TM from 2001 to March 2016 were evaluated in Guilan province. Sources of data were health centers of the...
متن کاملTransfusion suppresses erythropoiesis and increases hepcidin in adult patients with β-thalassemia major: a longitudinal study.
β-Thalassemia major causes ineffective erythropoiesis and chronic anemia and is associated with iron overload due to both transfused iron and increased iron absorption, the latter mediated by suppression of the iron-regulatory hormone hepcidin. We sought to determine whether, in β-thalassemia major, transfusion-mediated inhibition of erythropoiesis dynamically affects hepcidin. We recruited 31 ...
متن کاملمنابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ذخیره در منابع من قبلا به منابع من ذحیره شده{@ msg_add @}
عنوان ژورنال
دوره 1 شماره None
صفحات 1- 4
تاریخ انتشار 2008-09
با دنبال کردن یک ژورنال هنگامی که شماره جدید این ژورنال منتشر می شود به شما از طریق ایمیل اطلاع داده می شود.
میزبانی شده توسط پلتفرم ابری doprax.com
copyright © 2015-2023