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J Thorac Cardiovasc Surg 2009;137:781-783
© 2009 The American Association for Thoracic Surgery
Brief Communication |
a University Clinic of Blood Group Serology and Transfusion Medicine, Medical University of Graz, Graz, Austria
b Department of Hematology and Stem Cell Transplantation, University Clinic of Internal Medicine, Medical University of Graz, Graz, Austria
c Office for Biostatistics, Center for Medical Research, Medical University of Graz, Graz, Austria
d Institute for Transfusion Medicine Dessau, Red Cross Blood Transfusion Service NSTOB, Dessau, Germany
e Clinical Department of Blood Group Serology, Medical University of Vienna, Vienna, Austria
Received for publication November 27, 2007; accepted for publication March 18, 2008. * Address for reprints: Simon Panzer, MD, Clinical Department of Blood Group Serology, Medical University of Vienna, Waehringer Guertel 18-20, A-1090 Vienna, Austria. (Email: simon.panzer@meduniwien.ac.at).
| The first 20% of the full text of this article appears below. |
Heparin-induced thrombocytopenia (HIT) is a prothrombotic condition characterized by a platelet decrease of 50% or thrombosis with a temporal relationship of 1 to 2 weeks after the initiation of heparin. These surrogate markers are useful for the clinical assessment1
but are hardly applicable in multimorbid patients with clinical conditions that mimic HIT. Platelet activation assays (heparin-induced platelet activation [HIPA] and serotonin release assay) and platelet factor 4 (PF4)/polyanion enzyme-linked immunosorbent assay (ELISA) confirm HIT.2
HIPA and serotonin release assay are highly specific, but they are laborious and require selected donor platelets and extended experience. High titer immunoglobulin (Ig)G antibodies correlate with clinical HIT,3
but ELISA is also time-consuming. The alternative heparin/PF4-antigen particle gel immunoassay (PaGIA) is easy, provides results within 1 hour, and detects mainly IgG but also IgA/M antibodies. We evaluated the specificity and sensitivity of PaGIA in relation to HIPA and ELISA in 285 patients with an undetermined likelihood for HIT with the intention to validate it as a rapid assay to exclude HIT.
Patients and Methods
Samples from 285 consecutive patients (median 71 years, range 1–97
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