PMID- 16788093 OWN - NLM STAT- MEDLINE DCOM- 20070221 LR - 20220321 IS - 1060-0280 (Print) IS - 1060-0280 (Linking) VI - 40 IP - 7-8 DP - 2006 Jul-Aug TI - Fondaparinux for thromboembolic treatment and prophylaxis of heparin-induced thrombocytopenia. PG - 1383-7 AB - OBJECTIVE: To review literature evaluating the use of fondaparinux for thromboembolic treatment and prophylaxis in patients with heparin-induced thrombocytopenia (HIT). DATA SOURCES: A MEDLINE search (1966-February 2006) was conducted using the search terms fondaparinux, heparin, low-molecular-weight heparin, and thrombocytopenia to identify English-language articles. Additional sources were identified from bibliographies of select articles and the manufacturer. DATA SYNTHESIS: Fondaparinux, a pentasaccharide that selectively inhibits factor Xa, has been reported to have negligible or no cross-reactivity in vitro with HIT antibodies. Thromboembolic treatment and prophylaxis with fondaparinux in patients with HIT has been described. Three cases reported patients who were successfully treated for thromboembolic events with fondaparinux after developing HIT during therapy with unfractionated heparin (UFH) or low-molecular-weight heparin (LMWH). Another report showed positive outcomes using fondaparinux for prophylaxis in a patient who had previously developed HIT after receiving UFH. Moreover, 2 case series, one using fondaparinux for prophylaxis in patients with a previous diagnosis of HIT and the other using fondaparinux for treatment in patients who developed HIT while receiving UFH or LMWH, reported normal platelet counts during fondaparinux treatment. Finally, results of a retrospective review demonstrated that fondaparinux prevented thromboembolic events or recurrent thrombocytopenia in patients with a prior HIT diagnosis. CONCLUSIONS: Limited data support the use of fondaparinux for thromboembolic treatment or prophylaxis in patients with antibody assay-confirmed HIT who do not have a contraindication for fondaparinux use. Randomized controlled trials have not been published; therefore, questions remain regarding efficacy, safety, optimal doses, treatment duration, and incidence of thromboembolic events when fondaparinux is used in this setting. Prospective trials evaluating the efficacy and safety of fondaparinux in this patient population need to be conducted to answer these questions. FAU - Efird, Leigh E AU - Efird LE AD - Virginia Commonwealth University Medical Center/Medical College of Virginia Hospitals, Richmond, 23298, USA. lefird@mcvh-vcu.edu FAU - Kockler, Denise R AU - Kockler DR LA - eng PT - Journal Article PT - Review DEP - 20060620 PL - United States TA - Ann Pharmacother JT - The Annals of pharmacotherapy JID - 9203131 RN - 0 (Anticoagulants) RN - 0 (Polysaccharides) RN - 9005-49-6 (Heparin) RN - J177FOW5JL (Fondaparinux) SB - IM MH - Anticoagulants/*therapeutic use MH - Fondaparinux MH - Heparin/adverse effects MH - Humans MH - Polysaccharides/*therapeutic use MH - Thrombocytopenia/chemically induced/*drug therapy MH - Thromboembolism/drug therapy/prevention & control RF - 34 EDAT- 2006/06/22 09:00 MHDA- 2007/02/22 09:00 CRDT- 2006/06/22 09:00 PHST- 2006/06/22 09:00 [pubmed] PHST- 2007/02/22 09:00 [medline] PHST- 2006/06/22 09:00 [entrez] AID - aph.1G738 [pii] AID - 10.1345/aph.1G738 [doi] PST - ppublish SO - Ann Pharmacother. 2006 Jul-Aug;40(7-8):1383-7. doi: 10.1345/aph.1G738. Epub 2006 Jun 20.