More than a decade has gone by since the detailed clinical description
of the Antiphospholipid (Hughes) Syndrome. Because of the wide spectr
um of manifestations, virtually any physician may encounter patients w
ith this potentially treatable condition. Because of limited controlle
d, prospective data, current therapy remains empirical and directed at
coagulation mechanisms, immune mechanisms, or both. There is now good
evidence that patients with antiphospholipid-associated thrombosis wi
ll be subject to recurrences and require prophylactic therapy. Althoug
h most authorities agree about the efficacy of warfarin alone or warfa
rin plus low-dose aspirin in preventing recurrences of venous and arte
rial thrombosis, there is still doubt regarding the intensity and dura
tion of warfarin therapy. Steroids and immunosuppressive drugs have no
t provided longterm benefit. Controlled clinical trials of the treatme
nt of pregnant women with antiphospholipid antibody demonstrated that
prednisolone is ineffective, and possibly detrimental, in treatment of
recurrent pregnancy loss and that heparin plus low-dose aspirin is be
neficial.