Jm. O'Riordan et al., Risk of hepatitis C infection in neonates transfused with blood from donors infected with hepatitis C, TRANSFUS M, 8(4), 1998, pp. 303-308
This look-back study was undertaken to identify newborn infants who had bee
n infected with the hepatitis C virus (HCV) as a result of transfusions rec
eived before the introduction of routine screening in 1991 and to determine
the transmission rates and persistence of transfusion-transmitted HCV infe
ction acquired in the neonatal period.
A total of 24 infants, transfused between 1980 and 1991, were identified as
having received potentially infected blood from 11 blood donors. Ten of th
e donors had been administered batches of anti-D in 1977 known to have tran
smitted HCV genotype Ib infection. HCV RNA was detected in five of these do
nors when tested in 1994-95; the past donations of five of the donors, who
had received anti-D immunoglobulin and had serological evidence of previous
HCV infection but who were PCR negative when tested in 1994-95, were consi
dered of lower risk. The source and time of acquisition of HCV infection fo
r the one remaining donor in the study was not determined.
Twenty-one (88%) of the 24 children were living at time of lookback. The me
dian age at transfusion was 12 days. The median age at time of testing was
6.3 years. One child, who tested negative, was excluded from further analys
is of HCV transmission, due to incomplete transfusion records. Overall, 12
of 20 (60%) children tested were positive for anti-HCV and seven (35%) were
HCV RNA positive. Twelve (71%) of the 17 recipients of viraemic blood were
ELISA positive and seven (41%) were PCR positive. Resolved HCV infection,
as determined by ELISA pos, RIBA pos or indeterminate and PCR negativity, o
ccurred in five of 12 (42%). In many instances there was more than one reci
pient per HCV infected donation. All of the reported children are clinicall
y asymptomatic. However, the duration of HCV infection is relatively short
and there is evidence of a degree of hepatitis in five of the seven childre
n who are HCV RNA positive as judged by mildly elevated transaminase levels
. The three who have undergone liver biopsy show mild hepatitis.
The lower rates of persistence of HCV infection in this study may be due to
the young age at exposure or to the source of infection which for all but
one of the children was linked to one HCV genotype from female donors. Shar
ing of units of blood among multiple infants should be discouraged.