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Seroprevalence of hepatitis C virus markers in multi-transfused children with beta-thalassemia
BMC Infectious Diseases volume 12, Article number: P42 (2012)
Background
To study the seroprevalence of hepatitis C virus in multi-transfused children with β-thalassemia and compared with non transfused children and healthy controls. β-thalassemic children fail to thrive, with growth and developmental retardation and suffer microcytic hypochromic anemia. Since regular blood transfusions are given to maintain haemoglobin at a safe level, these children are at a high risk of acquiring hepatitis C virus through transfusions.
Methods
Study group, consisted of children 2-13 years with β-thalassemia and received more than 5 transfusions. Matched control group consisted of 30 children with β-thalassemia and no transfusion. Control group, consisted of 30 normal healthy children serum samples from all three groups were tested for antibodies to hepatitis C virus using commercial ELISA kits.
Results
Study showed 32% anti H hepatitis C virus positivity in multi-transfused and 0% in matched and healthy control groups. Hepatitis C virus infection showed a significant increase in relation to the number of transfusions received.
Conclusion
This observation is of great concern, as these children are at a risk of developing chronic hepatitis, cirrhosis and hepatocellular carcinoma. Since vaccination against hepatitis C virus is not available, highly sensitive and specific screening methods of donor blood in blood banks must be made mandatory.
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This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Madhusudhan, K., Thyagarajan, S. Seroprevalence of hepatitis C virus markers in multi-transfused children with beta-thalassemia. BMC Infect Dis 12 (Suppl 1), P42 (2012). https://doi.org/10.1186/1471-2334-12-S1-P42
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DOI: https://doi.org/10.1186/1471-2334-12-S1-P42