One of the most important adverse drug reactions that physicians encounter is the
life- and limb-threatening prothrombotic syndrome known as heparin-induced thrombocytopenia
(HIT). Unfractionated heparin (UFH), administered during cardiopulmonary bypass (CPB),
is highly immunogenic. Heparin-dependent antibodies can develop in 25 to 50% of UFH-treated
cardiac surgery patients within 5 to 10 days. These antibodies can activate platelets
and are considered the causative agents of HIT. HIT is a relatively common complication,
occurring in 1 to 3% of cardiovascular surgery patients when UFH administration is
continued postoperatively. It is strongly associated with new thromboembolic events
leading to limb amputation and death. In acute or recent (< 100 days) HIT, alternative
anticoagulatory regimens are needed during CPB surgery for prevention of HIT-related
thrombosis. Treatment options for such patients now generally include the use of alternative
anticoagulants such as lepirudin, bivalirudin, or danaparoid, as well as a combined
treatment with platelet-function inhibitors and heparin. In patients with a history
of HIT and no detectable antibodies, heparin is currently the safest approach for
high-dose anticoagulation during CPB. Before and after surgery, however, alternative
anticoagulants should be used. The risk of clinical HIT after heart surgery could
potentially be reduced by using low-molecular-weight heparins for postsurgery anticoagulation.
KEYWORDS
Anticoagulation - cardiopulmonary bypass - lepirudin - HIT - thrombocytopenia
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Prof. Dr. med.
Andreas Greinacher
Institut für Immunologie und Transfusionsmedizin, Ernst-Moritz-Arndt-Universität,
Diagnostikzentrum, Sauerbruchstraße
17487 Greifswald, Germany
Email: greinach@uni-greifswald.de