AI Article Synopsis

  • - The study examines liver-related deaths among HIV-infected patients in France, noting a rise in these deaths from 13.4% in 2000 to 15.4% in 2005, particularly highlighting a significant increase in deaths from hepatocellular carcinoma.
  • - Among deaths from hepatocellular carcinoma, the proportion of patients infected with hepatitis C (HCV) rose from 10% in 2000 to 25% in 2005, despite half of these HCV-infected individuals having received treatment.
  • - The rate of hepatitis B virus (HBV) related deaths remained stable during this period, possibly due to the effectiveness of combined antiretroviral therapy in managing co-infection in patients

Article Abstract

Background/aims: Longer exposure to hepatitis C (HCV) or B virus (HBV) and the increased use of hepatitis treatment might have an impact on liver-related deaths in patients co-infected with the Human Immunodeficiency Virus (HIV). We describe the proportion of liver-related deaths among HIV-infected patients in 2005 compared with 2000.

Methods: In a nationwide survey (341 hospital departments involved in HIV management), all deaths of HIV-infected patients were prospectively reported. Deaths from either cirrhosis, hepatocellular carcinoma or fulminant hepatitis were defined as liver-related deaths.

Results: Of the 898 deaths reported in 2005, liver-related causes accounted for 15.4%; this is compared to 13.4% in 2000. Among liver-related deaths, hepatocellular carcinoma increased from 15% to 25% (p=0.04). Among hepatocellular carcinoma-related deaths: in 2000, 10% were HCV-infected; in 2005, 25% were HCV-infected (p=0.03). Half of the HCV-related deaths had been treated for HCV but 98% remained HCV-RNA positive at time of death. The proportion of HBV-related deaths remained stable between 2000 and 2005.

Conclusions: Liver-related deaths, mainly liver cancers, have increased in HIV-infected patients in France despite wide access to HCV treatment. The stability of HBV-related deaths might be explained by the use of dually active antiretroviral drugs in co-infected patients.

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http://dx.doi.org/10.1016/j.jhep.2008.11.018DOI Listing

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