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Infantile hepatitis B in immunized children: risk for fulminant hepatitis and long-term outcomes
Yu-Ru Tseng1, Jia-Feng Wu1, Man-Shan Kong2
1Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
Insights
Infantile hepatitis B in immunized infants can lead to chronic infection. Early onset and specific maternal factors increase the risk of fulminant hepatitis B, necessitating long-term monitoring for complications like liver cancer.
Area of Science:
- Hepatology
- Pediatric Infectious Diseases
- Immunology
Background:
- Infantile hepatitis B post-neonatal immunoprophylaxis is rare but distinct.
- This study investigates long-term outcomes and risk factors in immunized infants with hepatitis B.
Purpose of the Study:
- To analyze long-term outcomes in immunized infants diagnosed with hepatitis B.
- To identify risk factors associated with infantile hepatitis B, particularly fulminant hepatitis B.
Main Methods:
- Retrospective analysis of clinical parameters and outcomes in 41 infants with hepatitis B (HBV).
- Follow-up duration of at least 6 months (median 4.4 years).
- Assessment of patient survival, hepatitis B surface antigen (HBsAg) and hepatitis B e antigen (HBeAg) status, and complications.
Main Results:
- 21 cases of fulminant hepatitis (FH) and 20 of non-fulminant hepatitis (NFH) were observed.
- Younger age of onset (<7 months) and negative maternal HBeAg were risk factors for FH.
- 47.6% mortality in FH cases; 35% of NFH cases developed chronic HBV infection. One FH survivor developed hepatocellular carcinoma.
Conclusions:
- Maternal HBsAg positivity/HBeAg negativity and early onset are risk factors for FH in immunized infants.
- Many infants with FH or NFH develop chronic HBV infection, with early HBeAg seroconversion.
- Long-term surveillance for hepatocellular carcinoma is crucial for survivors of infantile hepatitis B.
Background:
Infantile hepatitis B after neonatal immunoprophylaxis is a rare yet distinct disease. This study aimed to analyze the long-term outcomes and risk factors in immunized infants with hepatitis B.
Methods:
The clinical parameters and outcomes of 41 infants born after universal immunization, and admitted for HBV-positive hepatitis were studied. All patients were followed for at least 6 months (median = 4.4 years, range 0.6-18.1 years). Patient survival, changes of HBsAg and HBeAg status, and complications were analyzed.
Results:
Among the 41 cases (32 males, 9 females), 21 presented with fulminant hepatitis (FH), and 20 with non-fulminant hepatitis (NFH). Ninety-five percent (36/38) of the mothers were positive for hepatitis B surface antigen (HBsAg). Multivariate analyses revealed younger age of onset (age <7 months) and negative maternal hepatitis B e antigen (HBeAg) were associated with FH (p = 0.03 and p = 0.01, respectively). An infantile fulminant hepatitis B risk score using maternal/infant HBeAg positivity and onset age was proposed. Among the FH cases, the rate of mortality, HBsAg clearance, and chronic HBV infection were 47.6%, 38.1%, and 14.3%, respectively. Among the NFH cases, 35% developed chronic infection. Of the 9 chronically infected children received long-term follow-up, 8 had HBeAg seroconversion before 4 years of age. One case of FH developed hepatocellular carcinoma 14 years later.
Conclusions:
Maternal HBsAg + /HBeAg- and early onset age were risk factors for FH in immunized infants. A significant portion of patients with FH or NFH evolve to chronic HBV infection, with HBeAg seroconversion in young childhood. Close surveillance for hepatocellular carcinoma is warranted in patients surviving infantile hepatitis B.
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