Rk. Zimmerman et al., HEPATITIS-B VIRUS-INFECTION, HEPATITIS-B VACCINE, AND HEPATITIS-B IMMUNE GLOBULIN, Journal of family practice, 45(4), 1997, pp. 295-315
Hepatitis B virus (HBV) infection is a major health problem in the Uni
ted States; in 1995, approximately 128,000 cases occurred. Transmissio
n of HBV occurs primarily by blood exchange (ey, by shared needles dur
ing injection drug use) and by sexual contact, Persons infected early
in life are much more likely to become chronically infected than those
infected during adulthood: as many as 90% of infants infected perinat
ally develop chronic infection and up to 25% will die of HBV-related c
hronic liver disease as adults. Clinical signs of acute hepatitis occu
r in about 50% of infected adults but in only 5% of infected preschool
-aged children. In the United States, hepatitis B vaccine is currently
made by recombinant DNA technology using baker's yeast, Preexposure v
accination results in protective antibody levels in almost all infants
and children (>95%) and healthy adults younger than 40 years of age (
>90%). The most common adverse event following administration of hepat
itis B vaccine is pain at the injection site, which occurs in 13% to 2
9% of adults and 3% to 9% of children. A comprehensive hepatitis B vac
cination policy is now recommended that includes (1) routine infant va
ccination; (2) catch-up vaccination of 11- to 12-year-olds who were no
t previously vaccinated; (3) catch-up vaccination of young children at
high risk for infection; (4) vaccination of adolescents and adults ba
sed on lifestyle or environmental, medical, and occupational situation
s that place them at risk; and (5) prevention of perinatal HBV infecti
on.