The occurrence of antibodies to heparin-platelet factor 4 in cardiac and thoracic surgical patients receiving desirudin or heparin for postoperative venous thrombosis prophylaxis
Randomized study published in Thrombosis Research (2011)
Abstract
INTRODUCTION: This randomized, exploratory study compared the incidence of heparin-dependent antibodies associated with subcutaneous (SC) desirudin or heparin given for deep-vein thrombosis prophylaxis following cardiac and thoracic surgery. MATERIALS AND METHODS: Adult patients scheduled for elective cardiac or thoracic surgery received desirudin 15 mg SC twice daily or unfractionated heparin 5000 units SC thrice daily. Duration of thrombosis prophylaxis was determined by the treating physician. Primary outcome measure was the incidence of new antibody formation directed against platelet factor 4 (PF4)/heparin complex. Secondary outcomes included bleeding and thrombotic complications. Blood was tested for anti-PF4/heparin antibodies at baseline, after surgery prior to study drug administration, postdrug day (PDD) 2, PDD 7, and at 1 month. Doppler studies were done before discharge. RESULTS: Of 120 patients, 61 received desirudin, 59 received heparin. New PF4/heparin antibodies occurred in 10.2% and 13.6% of desirudin- and heparin-treated patients, respectively. Among desirudin patients with no heparin exposure, none (0/36) developed PF4/heparin antibodies versus 17.1% with heparin exposure. Incidence of deep venous thrombosis was 4.9% and 3.4% in the desirudin and heparin groups, respectively. Two heparin-group patients developed pulmonary embolism. Two patients per group had bleeding events; no patients required re-exploration for bleeding complications. Median chest tube output was similar with desirudin (900 mL) and heparin (692 mL) as was blood transfusion requirements of more than 2 units (5/61, desirudin; 2/59 heparin). CONCLUSIONS: The incidence of thrombotic events was low in both groups. There were no safety concerns, and desirudin was not associated with anti-PF4/heparin antibodies.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Резюме
Randomized study in 120 cardiothoracic surgery patients: 0% of patients receiving only desirudin (no heparin) developed new PF4/heparin antibodies vs 17.1% with heparin exposure, supporting recombinant hirudin as an anti-PF4-antibody-free alternative.
Почему это важно для гирудотерапии
This randomized, exploratory study of 120 patients compared subcutaneous desirudin with unfractionated heparin for postoperative deep-vein thrombosis prophylaxis after cardiac or thoracic surgery, assessing new anti-PF4/heparin antibody formation plus bleeding and thrombotic outcomes. New PF4/heparin antibodies occurred in 10.2% of desirudin patients versus 13.6% of heparin patients, and none of the 36 desirudin patients without heparin exposure developed such antibodies; thrombotic events were uncommon and no safety concerns were reported. The abstract itself does not mention leeches, hirudotherapy, or the leech secretome, so no defensible connection to ASH's hirudotherapy domain can be drawn from the abstract alone. Caveat: the study addresses a pharmaceutical anticoagulant rather than live leech therapy, and its exploratory findings would need confirmation in larger trials.
Цитирование
The occurrence of antibodies to heparin-platelet factor 4 in cardiac and thoracic surgical patients receiving desirudin or heparin for postoperative venous thrombosis prophylaxis.
Avidan MS et al. · Thrombosis Research, 2011
Связанный клинический контекст
Узнайте, как это исследование связано с клинической практикой
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