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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

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