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dc.contributor.authorHazari, S
dc.contributor.authorPanda, SK
dc.contributor.authorGupta, SD
dc.contributor.authorBatra, Y
dc.contributor.authorSingh, R
dc.contributor.authorAcharya, KS
dc.date.accessioned2013-07-03T14:51:20Z
dc.date.available2013-07-03T14:51:20Z
dc.date.issued2004
dc.identifier.citationKIRTDA, DRACHARYAS. 2004. Hazari S, Panda SK, Gupta SD, Batra Y, Singh R, Acharya SK.Treatment of hepatitis C virus infection in patients of northern India.J Gastroenterol Hepatol. 2004 Sep;19(9):1058-65..en
dc.identifier.urihttp://profiles.uonbi.ac.ke/sacharya/publications/hazari-s-panda-sk-gupta-sd-batra-y-singh-r-acharya-sktreatment-hepatitis-c-vir
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/44858
dc.description.abstractBACKGROUND AND AIM: The purpose of the present study was to evaluate the therapeutic response of north Indian patients with chronic hepatitis C (CH-C) to two different treatment regimens of interferon and ribavirin. METHODS: Consecutive patients with a diagnosis of CH-C attending the Liver Clinic at the All India Institute of Medical Sciences, New Delhi between April 1999 and April 2002 were included in the study. A competitive reverse transcription-polymerase chain reaction (RT-PCR) method developed in the authors' laboratory was used for quantification of hepatitis C virus (HCV)-RNA. Genotyping of HCV was also determined. The clinical, biochemical, virological and histological parameters were used to assess the therapeutic response among a clinical cohort of patients with chronic hepatitis C. They were treated with two different protocols (interferon [IFN]-alpha-2b, 3 million units daily and ribavirin 10.6 mg/kg daily in two divided doses for 6 months or IFN-alpha-2b, 3 million units thrice weekly and ribavirin 10.6 mg/kg daily for 6 months). RESULTS: Sixty-five patients with CH-C were included in the study. Blood transfusion (n = 28, 43%) and community-acquired (n = 23, 35%) HCV infections were the commonest. The mean HCV load was high (24.14 +/- 12.5 x 10(8) copies/mL). Genotype 2 and 3 were prevalent in 80% (41/51) of the patients. Forty-five patients received 3 million units of IFN thrice weekly and 20 received the same dose daily. All received the same dose of ribavirin. A sustained virological response (SVR) of 95% (19/20) was achieved among patients receiving daily IFN, whereas 64.4% (29/45) of those who received IFN thrice weekly had SVR. The virological relapse was significantly lower among patients who received daily IFN than in those treated with thrice weekly IFN (n = 1/20, 5% vs 10/39, 25.6%; P = 0.015). The proportion of patients receiving daily IFN among those achieving SVR (19/48, 40%) was significantly higher than the proportion of patients receiving similar therapy among patients without SVR (1/17, 6%; P = 0.02). CONCLUSIONS: Transfusion and community-acquired HCV infection were the major causes of CH-C. Genotype 2 and 3 HCV were most prevalent among these patients. Despite high viral load, these patients responded well to a combination of daily IFN-alpha-2b and ribavirin. Copyright 2004 Blackwell Publishing Asia Pty Ltden
dc.language.isoenen
dc.titleTreatment of hepatitis C virus infection in patients of northern Indiaen
dc.typeArticleen
local.publisherDepartment of Medicine, College of Health Sciences, University of Nairobien


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