S. Haas et al., Heparin-induced thrombocytopenia: Clinical considerations of alternative anticoagulation with various glycosaminoglycans and thrombin inhibitors, CL APPL T-H, 5(1), 1999, pp. 52-59
Heparin-induced thrombocytopenia (HIT), the most common complication of hep
arin therapy, is also the most common form of the drug-induced thrombocytop
enias. HIT is classified as type I and type II, the first being benign and
the latter severe. HIT type II is attributed to an immune response characte
rized by complexes of heparin and platelet factor (PF) 4. Enzyme-linked imm
unosorbent assays allow easy and simple determination of these antibody tit
ers; however, because specificity and sensitivity is not optimal, there is
concern that the clinical relevance may be low. In clinical trials many pat
ients were shown to form HIT-IgG in response to heparin without developing
manifestations of HIT-type II. Therefore, routine screening of clinically a
symptomatic patients for antiheparin/PF 4 antibodies is not recommended. HI
T type TT is a clinicopathologic syndrome that ideally should be confirmed
by laboratory testing. If any clinical suspicion arises, however, heparin a
nd low molecular weight heparin therapy should be discontinued and an alter
native anticoagulant therapy started. Alternative drugs have been evaluated
in significant numbers of patients including danaparoid and thrombin inhib
itors. In the case of danaparoid, it is highly recommended that an in vitro
test for cross-reactivity be performed before the onset of therapy. If tes
ting cannot be performed, immediate administration of a thrombin inhibitor
is preferred.