The immunological type of heparin-associated thromocytopenia (HAT II)
is a severe complication of heparin treatment and is associated with a
rterial and venous thrombosis. Only patients with absolute thrombocyto
penia have prompted suspicion of HAT in clinical practice. We report o
n a 44-year-old male who developed thromboembolic episodes after coron
ary angiography such as reinfarction and thrombotic episodes of A. bra
chialis. Fibrinolytic therapy combined with i. v. unfractionated hepar
in treatment was the therapy of choice and was followed by severe furt
her thromboembolic adverse effects. Besides an impaired fibrinolytic r
esponse and elevated antiphospholipid antibodies, we diagnosed HAT typ
e II In HIPA and ELISA (Stage, Boehringer-Mannheim). This special pati
ent had platelet counts within a normal range, when developing the thr
omboembolic episodes. It appears that the normal platelet count during
the thromboembolic episodes reflect a relative thrombocytopenia. From
a clinical point of view we recommend the use of a lab panel to exclu
de HAT type II in patients with thromboembolic episodes under therapy
with fractionated or unfractionated heparin. Platelet counts within a
normal range are not absolute exclusion criterion for HAT II.