Many persons with hemophilia were infected with hepatitis C and B viruses (HCV, HBV) and HIV, but the consequences of these transfusion-acquired infections are poorly defined. We estimated the risk of HCV-related end-stage liver disease (ESLD) and the associations of age, HBV, and HIV with that risk. All 1816 HCV-seropositive hemophilic patients at 16 centers were followed for up to 16 years. Of these, 624 were HIV- and 1192 were HIV-coinfected; 135 had persistent HBV surface antigenemia, 1374 had resolved HBV infection, and 287 were HBV-uninfected. ESLD was defined as bleeding esophageal vaHces, hepatic ehcephalopathy, persistent ascites, or death excluding nonhepatic causes of these conditions. Competing risk models were used to estimate the annual hazard rate and cumulative incidence of ESLD. Proportional hazards models were used to estimate relative hazards of ESLD with covariates. ESLD developed in 127 of the HCV/HIV-coinfected participants, with an estimated 16-year cumulative incidence of 14.0% (95% confidence interval [CI], 11.6%-16.4%). Without HIV, 10 HCV-infected participants developed ESLD, for a significantly lower cumulative incidence of 2.6% (95% Cl, 1.0%-4.3%, P < .0001). ESLD risk increase steeply with age in both groups. With HIV, ESLD risk was increased 8.1-fold (95% Cl, 1.9-35.2) with HBV surface antigenemia, 2.1-fold (95% Cl, 1.3-3.3) with fewer than 0.2 × 109/L (200/μL) CD4+ lymphocytes, and 1.04-fold (95% Cl, 1.03-1.06) per year of age. Thus, HIV Is associated with a markedly increased risk of HCV-related ESLD for persons with hemophilia, particularly with HBV infection, low CD4+ lymphocytes, or older age.
|Original language||English (US)|
|Number of pages||6|
|Publication status||Published - Sep 1 2002|
All Science Journal Classification (ASJC) codes
- Cell Biology