Lm. Korst et al., NUCLEATED RED-BLOOD-CELLS - AN UPDATE ON THE MARKER FOR FETAL ASPHYXIA, American journal of obstetrics and gynecology, 175(4), 1996, pp. 843-846
OBJECTIVE: Our goal was to update our experience with nucleated red bl
ood cells as a marker for fetal asphyxia and to determine whether a re
lationship exists between the presence of nucleated red blood cells an
d long-term neurologic impairment. STUDY DESIGN: Nucleated red blood c
ell data from 153 singleton term neurologically impaired neonates were
compared with cord blood nucleated red blood cells of 83 term nonasph
yxiated newborns. Newborns with anemia, intrauterine growth restrictio
n, and maternal diabetes were excluded. The group of neurologically im
paired neonates was separated into the following subgroups: group I, p
ersistent nonreactive fetal heart rate pattern from admission to deliv
ery (n = 69); group II, reactive fetal heart rate on admission followe
d by tachycardia with decelerations and absent variability (n = 47); g
roup III, reactive fetal heart rate on admission followed by an acute
prolonged deceleration (n = 37). The first and highest nucleated red b
lood cell value and the time of nucleated red blood cell disappearance
were assessed. RESULTS: The mean number of initial nucleated red bloo
d cells was significantly higher in the group of neurologically impair
ed neonates (30.3 +/- 77.5, range 0 to 732 per 100 white blood cells)
than in the control group (3.4 +/- 3.0, range 0 to 12 per 100 white bl
ood cells) (p < 0.000001). When the group of neurologically impaired n
eonates was separated on the basis of timing of the neurologic impairm
ent, distinct nucleated red blood cell patterns were observed. Signifi
cant differences were obtained between each of the three groups of neu
rologically impaired neonates and the normal group, with respect to in
itial nucleated red blood cells (group 1, 48.6 +/- 106.9; group II, 11
.4 +/- 9.8; group III, 12.6 +/- 13.4; p less than or equal to 0.000002
). Maximum nucleated red blood cell values were higher in group I (mea
n 51.5 +/- 108.9) than in groups II and III combined (mean 12.7 +/- 11
.9) (p = 0.0005). Group I also had a longer clearance time (119 +/- 12
3 hours) than groups II and III combined (mean 59 +/- 64 hours) (p < 0
.001). CONCLUSION: Our ongoing study indicates that nucleated red bloo
d cells identify the presence of fetal asphyxia. When fetal asphyxia i
s present, distinct nucleated red blood cell patterns are observed tha
t relate to the timing of fetal injury. In general, intrapartum injuri
es are associated with lower nucleated red blood cell values. Thus our
data continue to support the concept that nucleated red blood cell le
vels may assist in determining the timing of fetal neurologic injury.