We performed a prospective study on the incidence of thrombocytopenia (t-pe
nia) and its immunological origin in unselected 26,275 mothers and 24,101 n
ewborns. Platelet antibodies were examined by the platelet immunofluorescen
ce test (PIFT) and the monoclonal antibody immobilisation of platelet antig
ens assay (MAIPA). T-penia (platelet count < 100 x 10(9)/l) was found in 12
4 (0.5%) mothers (in 0.04% severe, <50 x 10(9)/l) and in 116 (0.5%) newborn
s (in 0.15% severe); 90 (72.6%) and 112 (96.6%), respectively, were availab
le for further studies. In both groups non-immune t-penia was diagnosed abo
ut 4.5 times more often than the immune t-penia. Among 90 mothers, t-penia
was severe in 11.1%, antibodies were detected in 17.8%; both factors were n
ot prognostic for delivering thrombocytopenic newborns. Among 112 babies, 2
1 were delivered by thrombocytopenic mothers and 91 fry mothers with normal
platelet count; among newborns with immune t-penia the proportion of alloi
mmune (NAIT) to autoimmune was equal(10 with NAIT, 10 with autoimmune, 4 of
them born by mothers with hidden autoimmune t-penia). In 33% of the neonat
es t-penia was severe, most often among NAIT. In conclusion, although t-pen
ia in mothers as well as in infants is not frequent and severe, and an immu
ne origin not often found, the search for antibodies, in particular alloant
ibodies, should be done. Even if the serological results are not helpful at
the moment, they can Be of importance in subsequent pregnancy and for rela
ted pregnant women.