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Updated: Jun 6, 2026

Real-Time Polymerase Chain Reaction-Based Detection and Quantification of Hepatitis B Virus DNA
Published on: December 15, 2023
Trends in mortality after diagnosis of hepatitis B or C infection: 1992-2006
Scott R Walter1, Hla-Hla Thein, Janaki Amin
1National Centre in HIV Epidemiology and Clinical Research, The University of New South Wales, Sydney, Australia.
Insights
Chronic hepatitis B and C infections increase mortality risk, especially from liver and drug-related causes. Improved HBV treatment reduced liver deaths, while HCV drug-related deaths remain low due to harm reduction strategies.
Area of Science:
- Hepatology
- Infectious Diseases
- Public Health
Background:
- Chronic hepatitis B (HBV) and hepatitis C (HCV) infections are linked to increased mortality.
- Liver- and drug-related causes contribute significantly to excess deaths in these populations.
Purpose of the Study:
- To investigate specific causes of death in HBV and HCV cohorts.
- To identify areas of excess mortality risk.
- To analyze trends in mortality over time.
Main Methods:
- Linked HBV and HCV case notifications (1992-2006) with cause of death and HIV/AIDS data in New South Wales.
- Calculated mortality rates and standardized mortality ratios (SMRs) using person-time methodology.
- Compared cohort mortality to the general New South Wales population.
Main Results:
- The cohort included 42,480 HBV and 82,034 HCV mono-infected individuals.
- HIV co-infection increased mortality 3-10 fold.
- High excess mortality risk for liver-related deaths (HBV SMR 10.0, HCV SMR 15.8) and drug-related deaths (HCV SMR 15.4).
- Hepatocellular carcinoma (HCC) mortality remained stable; non-HCC liver deaths decreased in HBV but not HCV.
- HCV drug-related mortality stabilized after a 1999-2002 decrease.
Conclusions:
- Improved HBV treatment likely reduced non-HCC liver mortality.
- HCV drug-related mortality remains low, potentially due to improved harm reduction and opiate supply changes.
- Continued monitoring and intervention are crucial for managing mortality risks in chronic viral hepatitis.
Background & Aims:
Chronic hepatitis B (HBV) or C (HCV) virus infection has been associated with increased risk of death, particularly from liver- and drug-related causes. We examined specific causes of death among a population-based cohort of people infected with HBV or HCV to identify areas of excess risk and examine trends in mortality.
Methods:
HBV and HCV cases notified to the New South Wales (NSW) Health Department between 1992 and 2006 were linked to cause of death data and HIV/AIDS notifications. Mortality rates and standardised mortality ratios (SMRs) were calculated using person time methodology, with NSW population rates used as a comparison.
Results:
The study cohort comprised 42,480 individuals with HBV mono-infection and 82,034 with HCV mono-infection. HIV co-infection increased the overall mortality rate three to 10-fold compared to mono-infected groups. Liver-related deaths were associated with high excess risk of mortality in both HBV and HCV groups (SMR 10.0, 95% CI 9.0-11.1; 15.8, 95% CI 14.8-16.8). Drug-related deaths among the HCV group also represented an elevated excess risk (SMR 15.4, 95% CI 14.5-16.3). Rates of hepatocellular carcinoma (HCC)-related death remained steady in both groups. A decrease in non-HCC liver-related deaths was seen in the HBV group between 1997 and 2006, but not in the HCV group. After a sharp decrease between 1999 and 2002, drug-related mortality rates in the HCV group have been stable.
Conclusions:
Improvements in HBV treatment and uptake have most likely reduced non-HCC liver-related mortality. Encouragingly, HCV drug-related mortality remained low compared to pre-2002 levels, likely due to changes in opiate supply, and maintenance or improvement in harm reduction strategies.
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