Final Program in it's entirety - MyGirlsBlood
Final Program in it's entirety - MyGirlsBlood
Final Program in it's entirety - MyGirlsBlood
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Index of Poster Presenters cont’d<br />
09P06<br />
Prediction of Bleed<strong>in</strong>g Tendencies <strong>in</strong> Hemophilia A Patients<br />
on Prophylactic Treatment Us<strong>in</strong>g a Novel Reaction-Diffusion<br />
Assay of Hemostasis<br />
Baland<strong>in</strong>a A, Kumskova M, Kopylov K, Karamz<strong>in</strong> S, Fadeeva<br />
O, Panteleev M<br />
National Research Center for Hematology, Moscow, Russia<br />
09P07<br />
Evaluation of Hemodyne HAS Parameters <strong>in</strong> a Patient with<br />
Hemophilia A and An Inhibitor Who Has a Poor Cl<strong>in</strong>ical<br />
Response to Standard Dose rFVIIa<br />
Brophy D1 , Mart<strong>in</strong> E1 , Carr M2 , Nolte M3 , Kuhn J3 , Ezban M4 1Virg<strong>in</strong>ia Commonwealth University Coagulation<br />
Advancement Laboratory, Richmond, VA, U.S.A., 2Novo Nordisk, Inc., Pr<strong>in</strong>ceton, NJ, U.S.A., 3Central Virg<strong>in</strong>ia Center<br />
for Coagulation Disorders, Virg<strong>in</strong>ia Commonwealth University,<br />
Richmond, VA, U.S.A., 4Novo Nordisk A/S, Malov, Denmark<br />
09P08<br />
Us<strong>in</strong>g Global Hemostasis Laboratory Parameters to Identify<br />
rFVIIa Response<br />
Brophy D1 , Mart<strong>in</strong> E1 , Ezban M2 , Hedner U2 , Carr M3 , Barrett J4 1Virg<strong>in</strong>ia Commonwealth University Coagulation<br />
Advancement Laboratory, Richmond, VA, U.S.A., 2Novo Nordisk A/S, Malov, Denmark, 3Novo Nordisk, Inc., Pr<strong>in</strong>ceton,<br />
NJ, U.S.A., 4Central Virg<strong>in</strong>ia Center for Coagulation Disorders,<br />
Virg<strong>in</strong>ia Commonwealth University, Richmond, VA, U.S.A.<br />
09P09<br />
Inhibitor of Activated Prote<strong>in</strong> C as an Adjuvant for Hemophilia<br />
Treatment<br />
Butenas S1 , Whelihan M1 , Brummel-Zied<strong>in</strong>s K1 , Rivard G2 ,<br />
Mann K1 1University of Vermont, Dept. of Biochemistry, Burl<strong>in</strong>gton,<br />
VT, U.S.A., 2Hospital St. Just<strong>in</strong>e, Montreal, QC, Canada<br />
09P10<br />
Corn Tryps<strong>in</strong> Inhibitor (CTI) for Thromb<strong>in</strong> Generation (TG)<br />
Assays: To Add or Not to Add<br />
Chantarangkul V, Mancuso E, Lemma L, Clerici M,<br />
Santagost<strong>in</strong>o E, Tripodi A<br />
A Bianchi Bonomi Hemophilia and Thrombosis Center, Milan,<br />
Italy<br />
09P11<br />
Liver Transplantation with Mild Hemophilia A: Contribution<br />
of the Rotary Thromboelastography<br />
Desprez D1 , Faradji A2 , Cuby C3 , Mauvieux L1 , Grunebaum L1 1 2 Laboratory of Haematology, Regional Center for the<br />
Treatment of Haemophilia, 3Department of Anesthesiology,<br />
CHRU, Strasbourg, France<br />
09P12<br />
Pro-coagulant Activity of Lam<strong>in</strong>aria Japonica Derived<br />
Fucoidan (BAX513) Depends on the Interaction with the C-<br />
Term<strong>in</strong>us of Tissue Factor Pathway Inhibitor<br />
Palige M, Dockal M, Gerstenbauer G, Redl C, Knappe S,<br />
Ehrlich H, Scheifl<strong>in</strong>ger F,<br />
Baxter Innovations GmbH, Orth Donau, Austria<br />
09P13<br />
Quantization of Changes <strong>in</strong> VWF and FVIII Follow<strong>in</strong>g Elective<br />
Orthopedic and Coronary Artery Bypass Graft Surgery <strong>in</strong><br />
Normal Individuals<br />
Kahlon A1 , Grabell J1 , Tuttle A1 , Engen D2 , Hopman W3 ,<br />
Lillicrap D4 , James P1 1Medic<strong>in</strong>e, K<strong>in</strong>gston General Hospital, K<strong>in</strong>gston, ON, Canada,<br />
2Anesthesiology, K<strong>in</strong>gston General Hospital, K<strong>in</strong>gston, ON,<br />
Canada, 3Community Health and Epidemiology, K<strong>in</strong>gston<br />
General Hospital, K<strong>in</strong>gston, ON, Canada, 4Pathology and<br />
Molecular Medic<strong>in</strong>e, Queen’s University, K<strong>in</strong>gston, ON,<br />
Canada<br />
09P14<br />
Comb<strong>in</strong>ation of Recomb<strong>in</strong>ant Factor VIIa and Fibr<strong>in</strong>ogen<br />
Corrects the Coagulopathy of Idiopathic Thrombocytopenic<br />
Purpura<br />
Larsen OH1 , Stentoft J2 , Ingerslev J1 , Sørensen B1,3 1Centre for Haemophilia and Thrombosis, Aarhus University<br />
Hospital, Skejby, Denmark, 2Department of Haematology,<br />
Aarhus University Hospital, Aarhus, Denmark, 3Haemostasis Research Unit, St Thomas’ Hospital, London, United K<strong>in</strong>gdom<br />
09P15<br />
Discrepancy between One-Stage and Two-Stage Factor VIII<br />
Assays <strong>in</strong> Hemophilia A Patient: Molecular Genetic<br />
Background<br />
Pavlova A, Delev D, Brondke H, Vidovic N, Niemann B,<br />
Oldenburg J<br />
Institute for Experimental Haematology and Transfusion<br />
Medic<strong>in</strong>e, Bonn, Germany<br />
09P16<br />
Measurement of Factor VIII – von Willebrand Factor Complex<br />
(FVIII – VWF) by Us<strong>in</strong>g Enzyme Immunoassay (EIA) Techniques<br />
Pelzer H, Hilden I<br />
Novo Nordisk, Maaloev, Denmark<br />
09P17<br />
Guidance for the Use of Different APTT Reagents on<br />
Warfar<strong>in</strong>ised Patients<br />
Picker<strong>in</strong>g W, Brooks S, Chowdary P, Riddell A<br />
Kather<strong>in</strong>e Dormandy Haemophilia and Thrombosis Unit,<br />
Hampstead, U.K.<br />
55<br />
Posters, Sunday and Monday