Type II heparin-induced thrombocytopenia (HIT) is an immunological disorder
characterized by antibodies to heparin-platelet factor 4 complexes and a h
igh risk of thrombotic complications. Here, we present illustrative case hi
stories to educate the reader on evaluation and management of this complex
syndrome. Cases include typical and unusual presentations of the syndrome,
and commonly encountered problems and pitfalls of therapy Major points illu
strated are, (1) occurrence of HIT with any dose or form of heparin; (2) mi
sperceptions on the diagnostic criteria; (3) correct (thrombin inhibitors)
and incorrect (platelet transfusions and warfarin) management; (4) influenc
e of management strategy on clinical outcomes; (5) severity of the syndrome
; and (6) potential for both anamnestic response to heparin and disappearan
ce of HIT antibodies over time. Effective therapy of WIT involves both the
prompt recognition of the syndrome and its proper management.