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Current issues in the management of paediatric viral hepatitis
Latifa T F Yeung1, Eve A Roberts
1Rouge Valley Health System, Centenary Health Centre, Galaxy 12 Child & Teen Clinic, Scarborough, ON, Canada. fung.yeung@utoronto.ca
Insights
Vaccines for hepatitis A (HAV), E (HEV), and B (HBV) offer protection for children. Early detection and treatment of hepatitis C virus (HCV) infection are crucial for preventing liver disease progression.
Area of Science:
- Pediatric infectious diseases
- Hepatology
- Vaccinology
Background:
- Viral hepatitis presents significant challenges in pediatric populations.
- Hepatitis A virus (HAV) can cause acute liver failure in preschoolers, necessitating preventive strategies.
- Hepatitis E virus (HEV) poses risks to pregnant women, impacting fetal health.
Purpose of the Study:
- To review current strategies and outcomes for managing viral hepatitis in children.
- To highlight the role of vaccination in preventing HAV, HEV, and HBV infections.
- To discuss the management and treatment of chronic hepatitis B (HBV) and C (HCV) in pediatric patients.
Main Methods:
- Review of existing literature on viral hepatitis in children.
- Analysis of vaccine efficacy for HAV, HEV, and HBV.
- Evaluation of diagnostic and therapeutic approaches for chronic HBV and HCV infections.
Main Results:
- HAV vaccination is effective for post-exposure prophylaxis and reducing mortality in endemic areas.
- Hepatitis B vaccine provides ongoing protection against serious liver disease.
- Undetectable HBV DNA levels are a key outcome measure for chronic HBV infection, with low pretreatment levels predicting interferon-alpha response in Taiwanese children.
- HCV RNA testing at 1 month is recommended for infants born to infected mothers.
- Combination therapy for genotypes 2 or 3 HCV in children shows high success rates.
Conclusions:
- Vaccination is a cornerstone in preventing viral hepatitis in children.
- Monitoring viral load (HBV DNA, HCV RNA) is critical for managing chronic infections.
- Effective treatments exist for chronic HCV in children, with ongoing research into optimal HBV management.
Abstract:
Viral hepatitis poses important problems for children. In preschoolers, hepatitis A virus (HAV) infection frequently causes acute liver failure. Vaccinating toddlers against HAV in countries with high endemicity is expected to decrease mortality. HAV vaccine demonstrates efficacy (comparable to immunoglobulin) as post-exposure prophylaxis. A recently developed vaccine against hepatitis E virus (HEV) may benefit fetal health, because pregnant women are most prone to acute liver failure as a result of HEV. Hepatitis B vaccine continues to demonstrate value and versatility for preventing serious liver disease. With chronic infection, undetectable levels of serum HBV DNA complement e-seroconversion as the preferred outcome measure; suppressed viral load correlates with long-term complications better than HBeAg status. Among Taiwanese children, low pretreatment HBV DNA (<2 x 10(8) copies/ml) strongly predicted response to interferon-alpha. Future paediatric studies must incorporate HBV DNA levels. The rationale for routine treatment of immunotolerant hepatitis B during childhood remains uncertain. Any treatment of chronic hepatitis B in childhood requires consideration of the risks and benefits. Childhood hepatitis C virus (HCV) infection results mainly from mother-to-infant transmission. Babies of HCV-infected women should be tested for serum HCV RNA at 1 month of age. If negative, confirmatory anti-HCV antibody testing may be performed between 12 and 15 months of age. Children with chronic hepatitis C may develop progressive fibrosis/cirrhosis, particularly in the setting of obesity and insulin resistance. Treatment of children chronically infected with genotype 2 or 3 is highly successful: combination therapy of pegylated interferon-alpha and ribavirin is well tolerated and superior to pegylated interferon-alpha alone.
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