HEPARIN-INDUCED THROMBOCYTOPENIA - IGG BINDING TO PF4-HEPARIN COMPLEXES IN THE FLUID-PHASE AND CROSS-REACTIVITY WITH LOW-MOLECULAR-WEIGHT HEPARIN AND HEPARINOID
Pm. Newman et al., HEPARIN-INDUCED THROMBOCYTOPENIA - IGG BINDING TO PF4-HEPARIN COMPLEXES IN THE FLUID-PHASE AND CROSS-REACTIVITY WITH LOW-MOLECULAR-WEIGHT HEPARIN AND HEPARINOID, Thrombosis and haemostasis, 80(2), 1998, pp. 292-297
Early diagnosis of heparin-induced thrombocytopenia (HIT) is essential
to reduce morbidity and mortality. We report an enzyme immunoassay wh
ich detects the binding of HIT IgG to PF4-heparin in the fluid phase.
Our fluid phase assay produces consistently low background and can det
ect low levels of anti-PF4-heparin. It is suited to testing alternativ
e anticoagulants because, unlike in an ELISA, a clearly defined amount
of antigen is available for antibody binding. We were able to detect
anti-PF4-heparin IgG in 26/28 (93%) HIT patients. We investigated cros
s-reactivity of anti-PF4-heparin antibodies with PF4 complexed to alte
rnative heparin-like anticoagulants. Low molecular weight heparins cro
ss-reacted with 23/26 (88%) of the sera from HIT patients while half o
f the HIT sera weakly cross-reacted with PF4-danaparoid (Orgaran). The
thrombocytopenia and thrombosis of most of these patients resolved du
ring danaparoid therapy, indicating that detection of low affinity ant
ibodies to PF4-danaparoid by immunoassay may not be an absolute contra
indication for danaparoid administration.