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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Rerksuppaphol S. | |
dc.contributor.author | Hardikar W. | |
dc.contributor.author | Dore G.J. | |
dc.date.accessioned | 2021-04-05T04:32:49Z | - |
dc.date.available | 2021-04-05T04:32:49Z | - |
dc.date.issued | 2004 | |
dc.identifier.issn | 8159319 | |
dc.identifier.other | 2-s2.0-11144222222 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/15169 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-11144222222&doi=10.1111%2fj.1440-1746.2004.03463.x&partnerID=40&md5=9d4403c8057eb59a0fded0ac3ddce083 | |
dc.description.abstract | Background and Aim: To determine the natural history of perinatally acquired hepatitis C virus (HCV) infection, clinical and laboratory outcomes among 31 children with HCV infection were retrospectively reviewed. Fifteen children had acquired HCV by blood transfusion (BT) prior to 6 months of age and 16 had vertically acquired (VT) HCV. Methods: Demographic data, clinical symptoms and signs, liver biochemistry, HCV antibody, HCV-RNA and liver histology were evaluated. Results: Mean age at last visit was 13.0 years (range 9.0-16.8 years) in the BT group and 8.6 years (range 0.5-18.1 years) in the VT group. There were no abnormal clinical findings of chronic liver disease in either group. Estimated HCV-RNA clearance rate was 19%, with no significant difference between the groups. In HCV-RNA-negative children (n = 6), two lost anti-HCV antibody and two developed indeterminate anti-HCV antibody results, while all HCV-RNA-positive children (n = 25) remained both anti-HCV antibody positive and HCV-RNA positive throughout follow up. The alanine aminotransferase level was significantly higher in the VT group than in the BT group during the first 5 years of life. Liver biopsy, which was carried out in four children, revealed mild to moderate fibrosis and/or necroinflammatory activity, but no cirrhosis. Conclusions: Outcomes among children with HCV acquired in infancy demonstrate asymptomatic and slowly progressive disease, at least for the initial decade of infection. Mode of acquisition appears to have a limited impact on outcomes, with similar viral clearance and anti-HCV antibody seroreversion rates in vertical and transfusion acquired infection. © 2004 Blackwell Publishing Asia Pty Ltd. | |
dc.subject | alanine aminotransferase | |
dc.subject | adolescent | |
dc.subject | antibody detection | |
dc.subject | antiinflammatory activity | |
dc.subject | article | |
dc.subject | blood transfusion | |
dc.subject | child | |
dc.subject | chronic liver disease | |
dc.subject | clinical article | |
dc.subject | female | |
dc.subject | hepatitis C | |
dc.subject | Hepatitis C virus | |
dc.subject | human | |
dc.subject | infection risk | |
dc.subject | liver biopsy | |
dc.subject | liver cirrhosis | |
dc.subject | liver histology | |
dc.subject | male | |
dc.subject | outcomes research | |
dc.subject | priority journal | |
dc.subject | seroconversion | |
dc.subject | vertical transmission | |
dc.title | Long-term outcome of vertically acquired and post-transfusion hepatitis C infection in children | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Journal of Gastroenterology and Hepatology (Australia). Vol 19, No.12 (2004), p.1357-1362 | |
dc.identifier.doi | 10.1111/j.1440-1746.2004.03463.x | |
Appears in Collections: | Scopus 1983-2021 |
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