Kj. Moise et al., THE PREDICTIVE VALUE OF MATERNAL SERUM TESTING FOR DETECTION OF FETALANEMIA IN RED-BLOOD-CELL ALLOIMMUNIZATION, American journal of obstetrics and gynecology, 172(3), 1995, pp. 1003-1009
OBJECTIVE: Current management protocols for pregnancies complicated by
red blood cell alloimmunization use the maternal antibody titer to pr
edict the need for invasive testing for detection of fetal anemia. We
investigated the use of three maternal serum tests to assess their use
fulness in predicting fetal disease: indirect Coombs' titer, Marsh sco
re, and monocyte monolayer assay. STUDY DESIGN: Forty-seven serum samp
les from pregnant women with red blood cell antibodies associated with
fetal anemia were analyzed at cordocentesis. Fetal blood was analyzed
for hematocrit (corrected for gestational age) and antigen status. Fe
tal anemia was defined as a hematocrit value of <2 SD from the mean va
lue for gestational age. Fetuses were classified into three groups: An
tigen positive with anemia (n = 19), antigen positive without anemia (
n = 17), antigen negative (n = 11). Statistical methods included Krusk
al-Wallis test, Newman-Keuls test, Spearman's rank correlation, and re
ceiver-operator characteristic curves; p < 0.05 was considered signifi
cant. RESULTS: The median monocyte monolayer assay (phagocytosis, adhe
rence, and association) did not differ among the three groups. Both ma
ternal titers and Marsh scores were significantly higher in fetuses wi
th anemia compared with the other two groups of fetuses (256 vs 64 vs
64, p < 0.001, and 86 vs 69 vs 64, p = 0.02, respectively). Both titer
and Marsh score exhibited significant correlations with corrected fet
al hematocrit (r = -0.70, p < 0.001; r = -0.63, p < 0.001, respectivel
y). Comparison of the overall receiver-operator characteristic curves
for titer and Marsh score revealed no statistical difference; however,
a Marsh score of 57 was noted to have a superior specificity than a t
iter of 16 (p = 0.02). CONCLUSION: The maternal Marsh score can be per
formed in conjunction with standard indirect Coombs' titers to enhance
the predictability of fetal anemia.