C. Hammerman et al., INTRAVENOUS IMMUNE GLOBULIN IN NEONATAL ABO ISOIMMUNIZATION - FACTORSASSOCIATED WITH CLINICAL EFFICACY, Biology of the neonate, 70(2), 1996, pp. 69-74
Objective: Intravenous immune globulin (IVIG) reduces jaundice in many
but not all cases of neonatal isoimmunization. We sought to elucidate
the type of infant most likely to benefit from IVIG administration by
attempting to define pretreatment parameters associated with both cli
nical symptomatology and therapeutic responsiveness to IVIG. Methods:
Term, healthy Coombs-positive infants were studied prospectively. IVIG
was administered if, despite phototherapy, serum bilirubin reached gr
eater than or equal to 222 mu mol/l (13 mg/dl) at less than or equal t
o 24 h of age and/or greater than or equal to 274 mu mol/l (16 mg/dl)
at > 24 h of age. Clinical data including serial serum total bilirubin
levels, rate of bilirubin rise on day 1 of life, serial corrected car
boxyhemoglobin levels (a sensitive indicator of hemolysis) and total h
emoglobin (tHb) levels were collected. Results: Infants were classifie
d as IVIG responders (n = 18), those in whom total serum bilirubin lev
els either remained stable or decreased following IVIG administration;
IVIG nonresponders (n = 5), those who developed a total serum bilirub
in of greater than or equal to 2 mg/dl greater than pre-IVIG bilirubin
levels within the first 24 h after IVIG administration, or nontreated
, those not meeting IVIG treatment criteria (n = 13). Four of the five
nonresponders proceeded to require exchange transfusion vs. none of t
he others (p < 0.001). Four of the five nonresponders had a pretreatme
nt rate of bilirubin rise of greater than or equal to 1 mg/dl/h as com
pared with only 1 of 18 responders and none of the nontreated (p < 0.0
01). Pretreatment tHb levels were also different (13.2 +/- 1.3 vs. 15.
5 +/- 2.3 vs. 17.7 +/- 2.4 g/dl for nonresponders vs. responders vs, n
ontreated infants, respectively; p < 0.005). The highest pretreatment
COHbc levels were seen in the nonresponders (1.8 +/- 0.7 vs. 1.4 +/- 0
.3 vs. 0.9 +/- 0.3% tHb, respectively). Conclusions: Our 3 groups repr
esent a spectrum of hemolysis, ranging from severe to moderate to mild
. This spectrum appears to relate not only to the severity of hemolysi
s, but also to the therapeutic responsiveness to IVIG. We speculate th
at some or all of the factors identified can be used prospectively to
predict the subsequent clinical course of ABO-incompatible infants and
to facilitate optimal management.