Cv. Towers et al., A BLOODLESS CESAREAN-SECTION AND PERINATAL TRANSMISSION OF THE HUMAN-IMMUNODEFICIENCY-VIRUS, American journal of obstetrics and gynecology, 179(3), 1998, pp. 708-714
OBJECTIVE: Perinatal transmission of the human immunodeficiency virus
is the main pathway for children to become infected with this virus; h
owever, the relative contribution and timing of this transmission, whe
ther transplacental or by exposure through the birth process, have not
yet been elucidated. An obvious question is whether the mode of deliv
ery has an impact on this transmission rate. However, a routine cesare
an section will primarily diminish the duration of exposure of materna
l bodily fluids to the neonate but does not prevent the baby from bein
g exposed to maternal blood coming from the uterine incision. The purp
ose of this study was to determine whether the rate of perinatal trans
mission of human immunodeficiency virus could be significantly lowered
by delivering the baby with minimal to no exposure to maternal blood
or bodily fluids by the use of a surgical technique termed a ''bloodle
ss cesarean section''. STUDY DESIGN: We performed a prospective cohort
study in a group of pregnant women infected with human immunodeficien
cy virus and evaluated the rate of transmission of this virus to the n
eonate on the basis of the mode of delivery. One group of patients was
delivered by means of a ''bloodless cesarean section,'' in which the
baby was delivered and not exposed to any maternal blood or bodily flu
id. The control group gave birth either by vaginal delivery or by rout
ine cesarean section. All of the newborns were followed up for a minim
um of 15 months or until negative findings were confirmed. Multiple an
tenatal, intrapartum, and postdelivery variables were collected and an
alyzed. RESULTS: A total of 108 patients were included in this study a
nd 14 neonates became infected with human immunodeficiency virus (13%)
. Three of 53 infants delivered by a bloodless cesarean section (5.7%)
became infected compared with 11 of 55 control patients (20.0%). This
was significant at P=.02 and represented an absolute difference in pe
rcentage between the 2 groups of 14.3%, which corresponds to a 71.5% r
elative reduction in transmission risk (z=2.27, P=.012). Since the use
of zidovudine greatly influences the perinatal transmission rate of h
uman immunodeficiency virus, the study data were reanalyzed with the e
xclusion of patients who used antenatal or intrapartum zidovudine. Two
of 32 infants in the bloodless cesarean section group (6.3%) were inf
ected compared with 9 of 38 in the control group (23.7%). This was sig
nificant at P=.04 and revealed an absolute difference in percentage of
17.4%, which corresponds to a 73.4% relative reduction in transmissio
n risk (z=2.15, P=.016). There was no difference in the transmission r
ate between the bloodless cesarean section patients who did not use zi
dovudine (2/32, 6.3%) and the patients who did use zidovudine from the
entire study population (3/38, 7.9%). CONCLUSION: In the absence of z
idovudine usage, these data show that 70% to 75% of the perinatal tran
smission of human immunodeficiency virus to a newborn occurs from expo
sure to maternal blood and bodily fluids at the time of birth. This in
formation is important for patients unable to take zidovudine or other
antiretroviral agents, but more important, it introduces the concept
of other treatment options for the future.