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HOT TOPICS IN VIRAL HEPATITIS: Issue 23, 2012
Viral hepatitis and liver transplantation
Prophylaxis of hepatitis B reinfection after liver transplantation
Alfredo Marzano
Correspondence to:
Alfredo Marzano - MD
Head Inpatients Unit, San Giovanni Battista Hospital
Contract Professor, University of Turin
Gastro-Hepatology Division
University of Turin
San Giovanni Battista Hospital
Turin, Italy
E-mail: alfredomarzano@yahoo.it
DOI: 10.4147/HTV-122307

Abstract


In western countries, approximately 10-25% of patients undergoing liver transplantation (LT) are hepatitis B surface antigen (HBsAg) carriers. In Asia, hepatitis B virus-related liver disease is the leading indication for LT. After surgery, hepatitis B can develop in these patients, the outcome of which depends largely on the prevention of hepatitis B recurrence.
In HBsAg-positive recipients, the spontaneous risk for hepatitis B after LT is up to 70% if no prophylaxis is administered. Major advances in prophylaxis during the last 15 years have allowed achievement of very good control of post-LT hepatitis B. From the beginning of the prophylaxis era, hepatitis B immunoglobulin (HBIG) played a pivotal role, either as monotherapy or in combination with antiviral drugs. In recent years, prophylaxis using antivirals with or without HBIG has been proposed.
The analysis of the recent literature on this situation shows that HBIG maintains a significant role in the control of hepatitis B recurrence following LT in patients originally HBsAg-positive. The outcomes of antiviral therapy with or without HBIG remain controversial.

Summary


  • EPIDEMIOLOGY
  • DIFFERENT ASPECTS OF HEPATITIS B AFTER LT AND SOURCE OF INFECTION
  • PROPHYLAXIS OF HEPATITIS B RECURRENCE FOLLOWING LT
  • LT in HBsAg-positive patients receiving no prophylaxis
  • Prophylaxis with HBIG
  • Prophylaxis with one or more NUCs without HBIG
  • Combination prophylaxis (HBIG with lamivudine or other NUCs)
  • New perspectives for long-term prophylaxis
  • Prophylaxis with combined NUCs
  • HBV vaccination after LT
  • Low-dose intramuscular HBIG and NUCs
  • CONCLUSIONS
  • REFERENCES

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