RECOMMENDATIONS ON NEWBORN SCREENING FOR HEPATITIS C VIRUS INFECTION
OVERVIEW
The hepatitis C virus (HCV) is a leading cause of death from liver
disease and a major public health problem in adults in the United
States. In the general US population, the prevalence of HCV infection is
estimated to be 1.8%. In children, however, the seroprevalence ranges
from 0.2% in children younger than 12 years to 0.4% in adolescents aged
12-19 years. This leads to an estimated 240,000 children with antibodies
to HCV in the United States. Perinatal transmission from infected
mothers is a recognized mode of transmission of HCV infection and is
currently the most common route of infection in children. In this
newsletter, we present the current screening recommendations for
newborns born to mothers infected with HCV. We also review
considerations specific for children infected with HCV.
PERINATAL TRANSMISSION OF HCV INFECTION
In the United States, the seroprevalence of HCV infection in pregnant
women is approximately 1-2%. Perinatal transmission of HCV infection
occurs only from mothers who are positive for HCV RNA at the time of
delivery. The risk of perinatal transmission is about 5-6%. If the
mother is co-infected with human immunodeficiency virus (HIV) and has
especially high levels of HCV RNA, the rate of transmission may increase
up to 19%.
RECOMMENDATIONS FOR INFANTS BORN TO MOTHERS INFECTED WITH HCV
According to the Centers for Disease Control and Prevention (CDC),
children born to mothers infected with HCV are at intermediate risk of
infection. The current screening practice as recommended by the CDC and
the Report of the Committee on Infectious Diseases published by the
American Academy of Pediatrics (AAP) is as follows:
-
All children born to mothers infected with HCV should be tested for HCV
infection.
-
Testing is performed by detecting the presence of antibodies (anti-HCV).
However, because of the presence of passive maternal antibodies in
infants aged 18 months or younger, testing should be delayed until after
that time.
-
Reverse transcriptase-polymerase chain reaction (RT-PCR) assays for
detection of HCV RNA may be performed at age 1-2 months, if earlier
diagnosis is desired.
-
All infected children should be vaccinated against hepatitis A virus (HAV)
and hepatitis B virus (HBV) to prevent superinfection, which can lead to
life-threatening clinical hepatitis.
IMPORTANT CONSIDERATIONS IN CHILDREN
Breastfeeding of infants born to mothers infected with HCV
Maternal HCV infection is not a contraindication to breastfeeding,
according to the current guidelines of the US Public Health Service and
the AAP. HCV transmission through breastfeeding has not been
demonstrated in anti-HCV positive, anti-HIV negative mothers. Rates of
transmission are similar between breastfed infants and bottle-fed
infants. However, transmission through breastfeeding is, theoretically,
possible. Antibodies to HCV and HCV RNA have been detected in breast
milk from mothers infected with HCV. Mothers with cracked and bleeding
nipples should consider abstaining from breastfeeding. A mother who is
infected with HCV should decide whether or not to breastfeed her infant
after an informed discussion with her health care professionals.
Child care of children infected with HCV
Exclusion of children infected with HCV from child care centers is not
indicated, nor is restriction from school attendance or contact sports.
FUTURE DIRECTIONS
Improvements are needed in the diagnosis, treatment, and, most
importantly, prevention of HCV in children. Stricter strategies are
needed to screen and identify infected children. A prophylactic vaccine,
as currently present for HAV and HBV, may be an effective control for
HCV infection in children.
In addition, further research is needed to study the course of HCV
infection in children, specifically the chronicity of the infection,
presentation of symptoms, and the response to treatment. At this time, very
little is known about the course of HCV infection in children who are
infected perinatally. Current methods of treatment in adults also need to be
better studied in children. This is especially true in children younger than
3 years, in whom current therapies are contraindicated at this time.
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