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Hepatitis C virus infection is a risk factor for liver failure from veno-occlusive disease after bone marrow transplantation [see comments]
- Source :
- Blood. 83:1998-2004
- Publication Year :
- 1994
- Publisher :
- American Society of Hematology, 1994.
-
Abstract
- The contribution of hepatitis C virus (HCV) infection to liver disease after bone marrow transplantation (BMT) was retrospectively evaluated in 61 patients treated with BMT. HCV genome, as well as antibodies to HCV, was analyzed in sera collected before and serially after BMT. Six patients had been infected with HCV before BMT and three patients acquired the infection during or shortly after BMT. All patients infected before BMT died within 10 weeks after transplantation. Five of these six patients (83%) died of veno-occlusive disease (VOD), compared with nine of 52 patients (17%) not infected with HCV (P < .005). Risk factors for VOD other than HCV were not more prevalent in these patients compared with uninfected patients. Parallel to the development of VOD, replication of HCV increased, as demonstrated by rising concentrations of viral RNA in serum. HCV infection acquired during or after BMT caused only mild acute hepatitis C, which progressed to chronic hepatitis C in one patient surviving 10 years after BMT. These data suggest that patients with liver disease caused by HCV infection are at high risk of developing lethal VOD after BMT.
- Subjects :
- medicine.medical_specialty
Hepatitis C virus
Immunology
chemical and pharmacologic phenomena
medicine.disease_cause
Gastroenterology
Biochemistry
Liver disease
immune system diseases
Internal medicine
medicine
Risk factor
Aplastic anemia
Fulminant hepatitis
business.industry
virus diseases
Cell Biology
Hematology
medicine.disease
digestive system diseases
Transplantation
surgical procedures, operative
Viral disease
Viral hepatitis
business
Subjects
Details
- ISSN :
- 15280020 and 00064971
- Volume :
- 83
- Database :
- OpenAIRE
- Journal :
- Blood
- Accession number :
- edsair.doi.dedup.....b06beb6cab92ac45e1f16e6b1590ed04
- Full Text :
- https://doi.org/10.1182/blood.v83.7.1998.bloodjournal8371998