Heparin-induced thrombocytopenia with or without thrombosis has been recogn
ized increasingly as a serious complication of heparin use. This article re
views type II heparin-induced thrombocytopenia, which is mediated by an ant
ibody that in most cases has specificity for a complex between heparin and
platelet factor 4, a secreted platelet alpha-granule protein. The antibody-
heparin-platelet factor 4 complex can activate platelets and endothelial ce
lls, thereby initiating thrombosis. Clinical thrombosis in this syndrome ma
y be arterial or venous. Treatment of the syndrome requires discontinuation
of heparin and institution of an alternative anticoagulant.