Pediatric Fulminant Hepatic Failure in Endemic Areas of Hepatitis B Infection: 15 Years after Universal Hepatitis B Vaccination
Journal
Hepatology
Journal Volume
39
Journal Issue
1
Pages
58-63
Date Issued
2004
Author(s)
Chang C.-J.
Kong M.-S.
Huang F.-C.
Lee H.-C.
Lin C.-C.
Liu C.-C.
Lee I.-H.
Wu T.-C.
Wu S.-F.
Chen D.-S.
Abstract
To investigate the role of hepatitis B virus (HBV) infection in pediatric fulminant hepatic failure (FHF) after the launch of universal HBV vaccination, the authors analyzed the data from patients with FHF collected from a nationwide collaborative study group. Children aged 1 month to 15 years who were diagnosed with FHF (62 males and 33 females) between 1985-1999 were included. HBV infection (hepatitis B surface antigen [HBsAg] and/or immunoglobulin M hepatitis B core antibody [IgM anti-HBc] seropositive) accounted for 46% (43 of 95 cases) of all the cases of FHF. The average annual incidence of FHF in the time period 1985-1999 was 0.053/100,000 in the group of patients ages 1-15 years and 1.29/100,000 in those patients age < 1 year. Approximately 61% (58 of 95 cases) of all FHF cases were infants. The percentage of HBV infection was found to be higher in infants (57%) compared with children ages 1-15 years (27%) (P = 0.004). The incidence rate ratio of those patients age < 1 year to those ages 1-15 years was 54.2 for HBV-positive FHF and 15.2 for HBV-negative FHF. Maternal HBsAg was found to be positive in 97% of the infants with HBV-positive FHF, and hepatitis B e antigen (HBeAg) was found to be negative in 84% of these infants. Approximately 74% of all HBV-positive FHF patients and 81% of the infantile HBV-positive patients had been vaccinated. In conclusion, within the first 15 years of universal vaccination, HBV was found to rarely cause FHF in children age > 1 year but remained a significant cause of FHF in infants. HBV-positive FHF was prone to develop in infants born to HBeAg-negative, HBsAg-carrier mothers; these infants had not received hepatitis B immunoglobulin according to the vaccination program in place.
SDGs
Other Subjects
hepatitis B antibody; hepatitis B core antibody; hepatitis B surface antigen; hepatitis B vaccine; immunoglobulin M; hepatitis B vaccine; adolescent; article; child; endemic disease; female; hepatitis B; high risk population; human; incidence; infant; liver failure; major clinical study; male; maternal serum; priority journal; treatment outcome; vaccination; adult; age distribution; hepatitis B; mortality; mother; preschool child; register; sex ratio; Taiwan; virology; Adolescent; Adult; Age Distribution; Child; Child, Preschool; Endemic Diseases; Female; Hepatitis B Vaccines; Hepatitis B, Chronic; Humans; Incidence; Infant; Liver Failure; Male; Mothers; Registries; Sex Distribution; Taiwan
Type
journal article