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Chronic hepatitis in haemophilia
1Department of Haematology, Royal Hallamshire Hospital, Sheffield, UK.
Blood Reviews
|December 1, 1993
Summary
Most hemophiliacs treated with clotting factors develop chronic hepatitis C (HCV). While interferon therapy helps some, liver transplantation offers a cure for advanced liver disease and hemophilia.
Area of Science:
- Hepatology
- Virology
- Hematology
Background:
- Chronic hepatitis impacts nearly all hemophiliacs receiving non-virally inactivated clotting factor concentrates.
- Hepatitis C virus (HCV) is the primary cause, with most patients exhibiting non-neutralizing antibodies and circulating virus.
- Hepatitis B virus (HBV) infection is common, but chronic carriage (HBsAg) affects less than 5%.
Purpose of the Study:
- To investigate the prevalence and impact of chronic hepatitis C in hemophiliacs.
- To evaluate treatment outcomes for chronic hepatitis C in this population.
- To explore the role of liver transplantation in managing advanced liver disease and hemophilia.
Main Methods:
- Analysis of patient data on hepatitis C and B infection markers.
- Assessment of liver function in patients undergoing treatment.
- Review of outcomes for patients treated with interferon alpha and liver transplantation.
Main Results:
- Chronic hepatitis C is nearly universal in hemophiliacs treated with clotting factors.
- Subcutaneous recombinant interferon alpha normalizes liver function in 50% of patients, with 50% relapsing post-treatment.
- Liver transplantation is effective for advanced liver disease and provides a phenotypic cure for hemophilia.
Conclusions:
- Chronic hepatitis C is a significant complication in hemophilia treatment.
- Interferon therapy offers temporary remission, necessitating further treatment strategies.
- Liver transplantation presents a viable option for severe cases, addressing both liver disease and hemophilia.