Ka. Louden et al., NEONATAL PLATELET REACTIVITY AND SERUM THROMBOXANE B-2 PRODUCTION IN WHOLE-BLOOD - THE EFFECT OF MATERNAL LOW-DOSE ASPIRIN, British journal of obstetrics and gynaecology, 101(3), 1994, pp. 203-208
Objectives Concern has been expressed about possible neonatal side eff
ects after the use of maternal anti-platelet agents in pregnancy, part
icularly low dose aspirin treatment. We have studied neonatal platelet
behaviour using whole blood techniques, and assessed the neonatal eff
ect of the maternal ingestion of 60 mg aspirin daily. Design Cross sec
tional and randomised, double-blind, placebo-controlled. Setting Unive
rsity hospital. Subjects 1. Eight normal women, studied before concept
ion, and their infants. 2. Twenty-four infants whose mothers had been
randomised to receive either 60 mg aspirin daily, or placebo, in doubl
e-blind fashion. Methods The Clay Adams Ultra Flo 100 whole blood sing
le platelet counter was employed to measure platelet aggregation in re
sponse to Various agonists. The platelet release reaction was also mea
sured in whole blood, and serum thromboxane B-2 (TxB(2)) production wa
s measured by radio-immunoassay. Umbilical cord blood samples were obt
ained at delivery. Results 1. Neonatal platelet aggregation induced by
adrenaline, ADP and platelet activating factor was reduced in compari
son with their mothers (P < 0.01), whereas the neonatal platelet relea
se reaction was reduced when stimulated by collagen and U46619 (a thro
mboxane mimetic) (P < 0.01). Serum TxB(2) production was similar in mo
thers and babies. 2. Neonatal platelet aggregation, release reaction a
nd serum TxB(2) production were not significantly reduced in infants e
xposed to maternal aspirin in comparison with those neonates exposed t
o maternal placebo. This is in contrast to the effect on maternal plat
elets. Conclusions Although only a small number of patients were studi
ed, we interpret this as a relative sparing of neonatal platelet react
ivity due to the presystemic action of low dose aspirin.