Thrombocytopenia detected during pregnancy addresses the issue of its mecha
nism and of the possible occurrence of neonatal thrombocytopenia. To furthe
r investigate these issues, 50 women referred to us because of thrombocytop
enia detected during pregnancy (platelet count, <150 x 10(9)/L), were exten
sively studied, as well as their offspring. Among these thrombocytopenic wo
men, we used the threshold of 70 x 10(9)/L to differentiate between mild an
d severe thrombocytopenia. Whatever the severity of thrombocytopenia, we fo
und biological features of an autoimmune disorder in 48% of the women, and
chronic thrombocytopenia in 55%. A familial thrombocytopenia was evidenced
in 1 case. These 50 women gave birth to 63 neonates, among whom 24 were thr
ombocytopenic, either at birth or during the first week of life. Neonatal t
hrombocytopenia could only be predicted in multiparous women, on the basis
of previous neonatal thrombocytopenia in older siblings, and/or when matern
al platelet life span study, performed before pregnancy, had evidenced an a
utoimmune thrombocytopenia (AITP)-like profile. These results suggest that,
in case of pregnancy-associated thrombocytopenia, familial and immunologic
al studies, combined with postdelivery iterative platelet counts, should be
performed to properly characterize the thrombocytopenia. Moreover, the pla
telet count of the neonate should be carefully assessed at birth and during
the following days, a platelet life span study should be performed after d
elivery in the mother, because these two parameters are likely to bring val
uable information regarding the forthcoming pregnancies and the risk of neo
natal thrombocytopenia. (C) 1998 by The American Society of Hematology.