Abstract
Three cases of the heparin-induced thrombocytopenia syndrome are presented. Two of the patients died of thrombotic sequelae and 1 patient survived but suffered a significant bleeding complication. Several significant features are identified: (1) clinical presentation of the syndrome was apparent just before a fall in the platelet count; (2) platelet counts below 100,000/mm3 were not necessary for complications to occur; (3) antiplatelet IgM antibody was identified with the bleeding complication, as opposed to IgG in the thrombotic complication ; (4) despite cessation of heparin and institution of coumadin in 1 patient, platelet counts remained depressed and thrombotic complications continued to occur; and (5) superior vena cava thrombosis occurred in 1 patient, a condition previously unreported. These findings offer a means of suspecting the diagnosis before complications occur, raise questions regarding mechanism and management of the disorder, and add to the spectrum of thrombohemorrhagic sequelae associated with this syndrome.
Get full access to this article
View all access options for this article.
