heparin-induced thrombocytopenia(redirected from HIT syndrome)
heparin-induced thrombocytopeniaAcquired thrombocytopenia affecting some heparin-treated Pts–HTPs, defined as a ↓ platelet count during or shortly after heparin exposure; HIT is a markedly prothrombotic disorder seen in Pts who are at a high baseline risk for venous thrombosis DiffDx Antiphospholipid antibody syndrome, DIC, Trousseau syndrome–migratory thrombophlebitis & malignancy, TTP/HUS, thrombocytopenia and 'showers' of microthrombi Clinical HIT occurs 6-10 days after heparin exposure Diagnosis Aggregation studies using platelets from Pts known to be sensitive to antibody; quantification of serotonin release from platelets radiolabeled with serotonin in assay using Pt serum.
McGraw-Hill Concise Dictionary of Modern Medicine. © 2002 by The McGraw-Hill Companies, Inc.
Thrombocytopenia caused by an immune reaction to heparin. It may lead to widespread or potentially life-threatening blood clotting rather than bleeding. See: white-clot syndrome
CAUTION!Patients whose platelet counts drop significantly during exposure to heparin should discontinue the drug immediately.
See also: thrombocytopenia
Medical Dictionary, © 2009 Farlex and Partners
heparin-induced thrombocytopeniaA blood platelet deficiency disorder caused by a reaction to heparin. The condition is caused by antibodies, usually of the IgG class against a heparin-platelet factor IV complex on the surface of platelets. Paradoxically, the condition features thrombosis and embolism with the risk of stroke and other serious arterial occlusion effects. This is because the immune complexes formed combine with the antibody Fc receptors of platelets causing their activation and the initiation of clotting.
Collins Dictionary of Medicine © Robert M. Youngson 2004, 2005