The antiphospholipid syndrome (APS) is an autoimmune disease
characterized by the appearance of antiphospholipid antibodies
(APA) and at least one clinical manifestation like venous
and arterial thrombosis or recurrent miscarriages and fetal
loss in the second and third trimester. This most common acquired
thrombophilia can also cause placental insufficiency,
preeclampsia, intrauterine growth retardation, and placental
abruption. Several potential pathogenic pathways leading to a
procoagulant state by activation of endothelial cells, monocytes
or platelets and inhibition of the protein C activation pathway
have been identified. These are supposed to be responsible for
thrombosis and obstetric complications. Failed trophoblast differentiation
and invasiveness, with subsequently hampered
uteroplacental development, as well as thrombosis in the placental
vessels are further pathogenic pathways for observed
complications specific for pregnancy. Tests for anticardiolipin
antibodies and lupus anticoagulant are most commonly used in
clinical practice although antiphospholipid antibodies are a heterogeneous
group. Current criteria for the classification of APS
recommend the use of standardized ELISAs that measure ß2-
glycoprotein I-dependent IgG and IgM anticardiolipin antibodies
and/or lupus anticoagulant. Current recommendations regarding
prophylactic and therapeutic strategies in pregnancy
are based on a systematic Cochrane review. Although APS is an
autoimmune disease, anticoagulant therapy is the favored strategy
to prevent thromboembolic events, miscarriages, or other
pregnancy complications. The recommended therapy is the
combination of heparin and low-dose aspirin reducing pregnancy
loss by 54%. Aspirin alone, prednisone, or intravenous
immunoglobulin infusion had no significant beneficial effect on
pregnancy outcome, but rather a higher rate of side effects.
Oral anticoagulants are contraindicated during pregnancy because
of substantial embryotoxic side effects. Currently lowmolecular-
weight heparin replaces unfractionated heparin as
drug of choice because of safe use for mother and fetus as well
as fewer side effects as several studies have shown. Our experience
has taught us that prophylaxis should be initiated as soon
as pregnancy has been recognized in order to prevent the described
pathologies in placental development.