CURRENT PERSPECTIVES IN HEPATITIS ¨C C

Mathur YC

Aditya Children¡¯s Hospital, Hyderabad ¨C 500 004. A.P. India

 

Hepatitis C is a major health problem worldwide. Hepatitis C infects nearly 170 million people in the world. HCV prevalence ranges from 0.1 to 5% in different countries. The incidence in India ranges from 0.1 to 2.5%. 25% sero positivity was found in multitransfused thalassaemics & hemophiliacs.

Transmission: The low prevalence of HCV infection in childhood is most probably because of the fact that the most common routes of transmission by parenteral or percutaneous are less frequent in children than is adults. The risk of infection through household contacts is low (average 1.8%) although higher when the mother is the index case (about 3%) and lower when it is the father (0.6%). In most cases it is not possible to identify the risk factor or the route of infection. The overall risk of vertical transmission has been estimated to be about 5% (0-25%). If the mother is only anti HCV positive, the risk of vertical transmission varies from 5-10%. This increases to 9-50% if she is HCVRNA positive. If the mother is also HIV co infected then the transmission rate rises to 14% (9-100%. The identification of fewer quasi species explains the mild form of the disease the infants show. Most studies have indicated that caesarean section does not decrease the risk of perinatal transmission of HCV but rather increases in relation to the time between membrane rupture and delivery.

Screening: All children with prolonged jaundice, multiple blood transfusions, hemodialysis and recurrent injections should be screened for HCV infection. Screening is not recommended for all pregnant women. However all babies born to women sho are HCV positive should be tested for infection. Testing for Anti HCV should be delayed for 12-18 months to allow for maternally derived IgG to clear from the blood of the infant.

Natural History of Hepatitis C: The natural history in children has not been established & varies in children from adults because of different mode of transmission, age of acquisition and immunological response. Progress to chronicity was seen in 90-100% of the children of mothers with HCV infection who had elevated aminotransferase levels & were HCVRN positive. The disease is milder in children. 40-50% of the children after transfusion associated HCV infection clear the virus & 20% remain asymptomatic.

Diagnosis: Diagnosis should be based on at least 2 serum samples that are HCV RNA positive two months apart, with ALT levels. Anti HCV should be tested only in children after the first year of life. Screening should be based on a single 2nd or 3rd generation EIA and a repeat 2 months later for confirmed positively. Qualitative HCV RNA by PCR should be done for week positive EIA samples, chronic liver disease of HCV, chronic hepatitis C with normal ALT and a in diagnosis of vertical transmission.

Treatment: At our center we have treated 16 children with chronic HCV (mean age range 7.1 yrs.). 14 were treated with interferon alone while 2 were treated with a combination of IFN + Ribavarin. There was sustained response in 25%. In 6 children repeat biopsy were performed after 6 months to 2 years after therapy, showed significant improvement in histological activity. Both the children on the combination therapy showed response. Therapy had to be stopped in 2 children and one child was lost in follow up.

There is not known intervention capable of interrupting the spread of HCV from mother to child. In future we need drugs that have greater specificity for HCV with less system side effects and which are compatible with detection and quantification of HCV.

Vaccination: HCV is a worthy adversary changing continuously to avoid the surveillance by the host. A traditional vaccine is unlikely to be effective and experiments with DNA based vaccines offers a promising approach.

 
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