A history of thromboembolism is associated with an increased risk of new th
romboembolic events during pregnancy. Prophylaxis with heparin during pregn
ancy implicates long-term treatment with daily injections with either unfra
ctionated heparin (UFH) or low molecular mass heparin (LMMH). Prolonged tre
atment with heparin may result in endothelial absorption and drug accumulat
ion. In order to test this hypothesis, anti-FXa activity during pregnancy w
as measured in four women allergic to conventional UFH, who were treated wi
th LMMH (dalteparin; Pharmacia). It was found that, at the commencement of
treatment, it took more than 8 days to reach a steady maximum peak value, l
ocated 3 h after the given dose. One daily dosage of 5000 IU anti-Xa result
ed in a measurable level of FXa for 24 h in pregnancy week 40, compared wit
h 17 h at pregnancy week 37. The implications of an elevated anti-FXa activ
ity during pregnancy, especially during the third trimester and at partus,
are discussed. We present a reduced dose regime near term and during delive
ry. (C) 2001 Lippincott Williams & Wilkins.