scholarly journals Prevalence of Transfusion Transmissible Infection among Healthy Blood Donors at Dongola Specialized Hospital, Sudan, 2010–2015

Author(s):  
Mohamed Abdelaziz

Background: Blood transfusion saves lives but carries the risk of transmission of infections. Screening donors for transfusion transmissible infection (TTI) is mandatory. Objectives: To study the prevalence of TTI among blood donors at Dongola Specialized hospital, Northern State, Sudan. Materials and Methods: Retrospective study performed on blood donors at the blood bank of Dongola Specialized Hospital during the period 2010–2015. Demographic data and results of screening tests for all donors in the study period were included. Data were analyzed using SPSS and results were presented in percentages. Results: The total number of donors were 6,489, of which 6,433 (99.1%) were included in the study. All donors were males and family donors. Mean age (SD) was 27.9 (6.516) years. hepatitis B virus was detected in 85 (1.3%), syphilis in 68 (1.1%), hepatitis virus in 45 (0.7%), and human immunodeficiency virus in 3 (0.05%) donors. Coinfections of hepatitis B with syphilis and hepatitis B with hepatitis C were found in 0.05% and 0.03% of the donors, respectively.  Conclusion: The prevalence of TTI is low compared to national and international figures. These findings may reflect low prevalence rates of the studied infections in the community. Key words: blood donors, Northern State, Sudan, transfusion transmissible infection

2000 ◽  
Vol 44 (7) ◽  
pp. 1964-1969 ◽  
Author(s):  
Karl Y. Hostetler ◽  
James R. Beadle ◽  
William E. Hornbuckle ◽  
Christine A. Bellezza ◽  
Ilia A. Tochkov ◽  
...  

ABSTRACT Acyclovir triphosphate is a potent inhibitor of hepatitis B virus DNA polymerase, but acyclovir treatment provides no benefit in patients with hepatitis B virus infection. This is due in part to the fact that hepatitis B virus, unlike herpes simplex virus, does not code for a viral thymidine kinase which catalyzes the initial phosphorylation of acyclovir. We synthesized 1-O-octadecyl-sn-glycero-3-phospho (3-P)-acyclovir and found that it was highly active in reducing hepatitis B virus replication in 2.2.15 cells, while acyclovir was inactive. The greater antiviral activity of 1-O-octadecyl-sn-glycero-3-P-acyclovir appeared to be due to liver cell metabolism of the compound to acyclovir monophosphate (K. Y. Hostetler et al., Biochem. Pharmacol. 53:1815–1822, 1997). However, a closely related compound without a hydroxyl group at the sn-2 position of glycerol, 1-O-hexadecylpropanediol-3-P-acyclovir, was more active and selective in 2.2.15 cells in vitro. In this study, we treated woodchucks chronically infected with woodchuck hepatitis virus with increasing oral doses of 1-O-hexadecylpropanediol-3-P-acyclovir and assessed the response to therapy versus acyclovir or a placebo. At a dosage of 10 mg/kg of body weight twice a day, the test compound significantly inhibited viral replication in vivo, as indicated by a 95% reduction in serum woodchuck hepatitis virus DNA levels and by a 54% reduction in levels of woodchuck hepatitis virus replicative intermediates in the liver. Higher doses were somewhat less effective. In contrast, 20 mg of acyclovir/kg twice daily, a 5.3-fold-higher molar dosage, had no demonstrable activity against woodchuck hepatitis virus. Oral 1-O-hexadecylpropanediol-3-P-acyclovir appeared to be safe and effective in chronic woodchuck hepatitis virus infection.


2007 ◽  
Vol 66 (3) ◽  
pp. 278-282 ◽  
Author(s):  
M. El-Zaatari ◽  
H. Kazma ◽  
M. Naboulsi-Majzoub ◽  
M. Haidar ◽  
F. Ramlawi ◽  
...  

1980 ◽  
Vol 6 (4) ◽  
pp. 323-332 ◽  
Author(s):  
R.S. Tedder ◽  
C.H. Cameron ◽  
Ruth Wilson-Croome ◽  
D.R. Howell ◽  
Anne Colgrove ◽  
...  

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