الأربعاء، 28 مارس 2012

Transfusion-transmitted diseases


Transfusion-transmitted diseases

Hepatitis B virus infection, once a serious problem in thalassaemics, is now very uncommon, due to the com­bined efficacy of Ihe hepatitis B surface antigen screening in blood donors and the implementation of vaccination.




The vast majority of the patients who are now more than 10 years old are anti-HCV-positive from early child­hood, as a consequence of the transmission of HCV from infected blood donors before the introduction of anti-HCV screening. In 1992, Ihe prevalence of confirmed sec­ond-generation anii-HCV reactivity in a cohort of 1,481 Italian Ihalassaemics was 85% [8], with a frequency of persistent viraemia of approximately 70% [D. Prati, un- published data]. On liver biopsy, substantial fibrosis or cirrhosis are found in 15% of adult viraemic patients [58]. Cryoglobufinaemia, an extrahepatic manifestation of HCV infection, is present in 66% of thalassaemics, and seems lo be particularly frequent in cirrhotic patients [59]. Even after the introduction of anti-HCV screening, however, primary HCV infection remains an important cause of morbidity among thalassaemics. The current incidence - 4.27 cases/1,000 person-years - is 40-fold higher than that observed among low-risk adults from the same geographic area. This incidence translates into an infection risk substantially different from that expected on the basis of the incidence/window period model (I/ 7100 vs. 1/50,000 units) [8, 60], which seems to indicate that a proportion of HCV cases currently occurring among Ihalassaemics may not be related to blood transfu­sion, but may be acquired in the community or through the nosocomial route (8).

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