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An analysis of long term prophylaxis of virus recurrence with antiviral treatment in HBV infected liver transplant recipient patients / 中华肝脏病杂志
Chinese Journal of Hepatology ; (12): 663-666, 2007.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-354673
Responsible library: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>No optimal prophylactic protocol of hepatitis B immunoglobulin (HBIG) combined with nucleos(t)ide analogue for HBV recurrence has been established yet. By investigating the alterations of HBV markers in HBV related liver disease patients, recipients of a liver transplant, under lamivudine or/and HBIG prophylaxis, we aim to explore the possible HBV recurrence mechanism involved and to find a new option in the prophylaxis of HBV recurrence and to tailor individualized therapy.</p><p><b>METHODS</b>Serial liver biopsy specimens and sera were obtained intraoperationally and at definite time points during follow-up. ELISA and chemiluminescent microparticle immunoassay, HBV DNA fluorescent quantification, immunohistochemistry staining and HBV DNA in situ hybridization were performed. Alterations of HBV markers in specimens of 96 liver transplant recipients were investigated retrospectively.</p><p><b>RESULTS</b>All 17 cases had HBV recurrence (median 37 months) which occurred in the follow-up period after liver transplantation. The overall actual HBV recurrence rate at 2 years was 22% with a significant difference between that of the active and inactive groups (P<0.05); 82.4% HBV recurrence took place within the first 3 years after the operation, and the recurrence ratio of first 3 years to 3 years later after transplantation was 4.7 (P<0.01). The HBV DNA positive patients accounted for 78.6% of the total number of recurrences within the first 3 years. HBcAb and HBeAb positive rates went down with time, but their positivity remained.</p><p><b>CONCLUSION</b>HBV recurrence happens after liver transplantation. In inactive HBV replicative patients with strictly combined prophylaxis and availability of other medications and using 3 years after liver transplantation as a point of time, we think that tapering down the dosage of HBIG and tailoring individualized treatment methods based on virological and immunological situations of each recipient are worth trying.</p>
Subject(s)
Full text: Available Health context: SDG3 - Health and Well-Being / SDG3 - Target 3.3 End transmission of communicable diseases Health problem: Target 3.3: End transmission of communicable diseases / Hepatitis Database: WPRIM (Western Pacific) Main subject: Antiviral Agents / Postoperative Period / Prognosis / Immunoglobulins / Retrospective Studies / Liver Transplantation / Treatment Outcome / Lamivudine / Therapeutic Uses / Drug Therapy Type of study: Practice guideline / Observational study / Prognostic study Limits: Adolescent / Adult / Aged / Child / Female / Humans / Male Language: Chinese Journal: Chinese Journal of Hepatology Year: 2007 Document type: Article
Full text: Available Health context: SDG3 - Health and Well-Being / SDG3 - Target 3.3 End transmission of communicable diseases Health problem: Target 3.3: End transmission of communicable diseases / Hepatitis Database: WPRIM (Western Pacific) Main subject: Antiviral Agents / Postoperative Period / Prognosis / Immunoglobulins / Retrospective Studies / Liver Transplantation / Treatment Outcome / Lamivudine / Therapeutic Uses / Drug Therapy Type of study: Practice guideline / Observational study / Prognostic study Limits: Adolescent / Adult / Aged / Child / Female / Humans / Male Language: Chinese Journal: Chinese Journal of Hepatology Year: 2007 Document type: Article
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