e-Posters List

Talk codeTitlePresenting Author
PO001A NOVEL CHROMOGENIC METHOD FOR MEASURING FACTOR VIII ACTIVITY IN THE PRESENCE OF THE BISPECIFIC ANTIBODY EMICIZUMABAlfred Weber
PO002ACQUIRED FACTOR X DEFICIENCY IN A PATIENT WITH MULTIPLE MYELOMA WITHOUT ASSOCIATED AMYLOIDOSIS.Marina De la Torre de LA Paz
PO003ACQUIRED HEMOPHILIA : A PRESENTING AS GROSS HEMATURIA WITH FATAL OUTCOMENesrin Bensaid
PO004ASSESSING FACTOR VIII ACTIVITY IN THE PRESENCE OF MIM8 VIA CHROMOGENIC ASSAYSWilliam Pickering
PO005DOSE OPTIMISATION AND RISK MITIGATION DURING CONCIZUMAB PROPHYLAXIS IN PATIENTS WITH HAEMOPHILIA A/B WITH AND WITHOUT INHIBITORS IN PHASE 3 CLINICAL TRIALSPratima Chowdary
PO006EFFECT OF PLASMA-DERIVED FACTOR VIII/VON WILLEBRAND FACTOR IN PATIENTS WITH SEVERE HEMOPHILIA A ON PROPHYLAXIS WITH EMICIZUMAB: AN EX VIVO EVALUATION WITH A THROMBIN GENERATION ASSAYMaria-Isabel Bravo
PO007IMPACT OF ANTITHROMBIN REDUCTION IN PLASMA ON COAGULATION ASSAYSEkta Seth Chhabra
PO008INDUCTION OF NEONATAL FC RECEPTOR-MEDIATED TOLERANCE TO THERAPEUTIC FACTOR VIII IN HEMOPHILIA AAlejandra Reyes-Ruiz
PO009INDUCTION OF TOLERANCE TO THERAPEUTIC FACTOR VIII IN HA BY MODIFICATION WITH A2,3 SIALIC ACIDEleonora Nardini
PO010LIVER SINUSOIDAL CELLS AS A NEW TARGET FOR TOLERANCE INDUCTION TO FVIIIMichela Leoni
PO011MUTATION ANALYSIS OF COHORT OF RUSSIAN PATIENTS WITH HEMOPHILIA AValentina Salomashkina
PO012ONE STAGE CHRONOMETRIC FVIII ASSAY OR TWO STAGE CHROMOGENIC FVIII ASSAY TO DIAGNOSE HAEMOPHILIA A?Birgit Frotscher
PO013POST-INFUSION MONITORING OF FVIII REPLACEMENT THERAPY – DATA FROM THE UK NEQAS BC EQA PROGRAMME 2021.Christopher Reilly-Stitt
PO014POTENTIAL USE OF FIX CONCENTRATES TO REGULATE THE PROCOAGULANT EFFECT OF EMICIZUMABElena Arias-Salgado
PO016SELECTION OF THE METHOD OF DETERMINATION THE ACTIVITY OF THE FACTOR VIII BLOOD COAGULATION WITH THE APPLICATION OF VIRUS-INACTIVATING AGENTSNataliia Shurko
PO017THIRD-GENERATION FVIII-SPECIFIC CAR CONSTRUCTS RESULT IN VARIABLE CAR SURFACE EXPRESSION AND UPREGULATION OF ACTIVATION MARKERS UPON FVIII STIMULATIONSarah Scatigna
PO018USEFULNESS OF PHARMACOKINETICS DATA FOR PERSONALIZED DOSING REGIMENS IN PROPHYLAXIS WITH EXTENDED HALF-LIFE FACTOR. A CASE REPORTDiana Carneiro-Leão
PO019DEVELOPMENT OF A PATIENT-REPORTED OUTCOME (PRO) TOOL TO SUPPORT JOINT HEALTH MANAGEMENT FOR PATIENTS WITH HAEMOPHILIA B AGED 8 YEARS AND OLDERNisa Khan
PO020LARGE-SCALE MAPPING OF CD4 T-CELL EPITOPES OF RECOMBINANT FULL LENGTH FVIII IN HEALTHY INDIVIDUALS.Valeria Porcheddu
PO021NEARLY PICTURE PERFECT": A MIXED-METHOD STUDY ON EXPERIENCES WITH HEMOPHILIA CARE IN THE NETHERLANDS"Martijn Brands
PO022"WHY DOES IT ALWAYS HAVE TO BE HEMOPHILIA FAULT?"Carola Sella
PO023A BOY WITH HEMOPHILIA A WITHOUT INHIBITORS IN PROPHYLAXIS WITH EMICIZUMAB IN PORTUGAL: IS HE THE FIRST OF MANY?Soraia Campaniço
PO024A PROSPECTIVE, OBSERVATIONAL, ITALIAN STUDY TO ASSESS LONG-TERM EFFECTIVENESS OF DAMOCTOCOG ALFA PEGOL PROPHYLAXIS ON JOINT HEALTH IN ADULTS WITH HAEMOPHILIA A (JOIHA)Matteo Nicola Dario Di Minno
PO025A SINGLE CENTRE, OPEN LABEL, PILOT STUDY EVALUATING THE EFFECTS OF HYALURONIC ACID ON PAIN AND FUNCTIONALITY WHEN INJECTED INTO THE ANKLE JOINT IN PATIENTS WITH HAEMOPHILIC ARTHROPATHYStephanie Taylor
PO026ADHERENCE TO PROPHYLAXIS IN MODERATE AND SEVERE HAEMOPHILIA IN A PANDEMIC LIFE SETTINGFatma Keklik Karadağ
PO027AN INDIVIDUALIZED APPROACH TO REDUCE INHIBITOR RISK IN PUPS WITH SEVERE HEMOPHILIA ASusan Halimeh
PO028ANKLE JOINT IN PEOPLE WITH HAEMOPHILIA: THE ASSOCIATION BETWEEN STRUCTURE, FUNCTION AND PAIN: A CROSS-SECTIONAL STUDYValerie-Anne Chantrain
PO029ANNUALIZED BLEEDING RATE IN HAEMOPHILIA A AND B ON PROPHYLAXIS: ECOLOGICAL STUDY COLOMBIA, 2020.Jesús Ardila
PO030ANTI-EMICIZUMAB ANTIBODIES DO NOT CROSS-REACT WITH MIM8 IN VITRORoberta Gualtierotti
PO031APPLICATION OF EMICIZUMAB IN CUBAN PATIENTS WITH HEMOPHILIA ADunia Castillo
PO032AREA UNDER THE CURVE: INDIRECT PRODUCT COMPARISONS BETWEEN FACTOR VIII REPLACEMENT THERAPIES IN HAEMOPHILIA AErik Berntorp
PO033ASSESSING THE IMPACT OF COVID-19 ON PEOPLE WITH HEMOPHILIA (PWH) AGED ≥40 YEARS AND THE HTCS THAT CARE FOR THEM: AN OBSERVATIONAL COHORT STUDY FROM THE ADVANCE WORKING GROUPCedric Hermans
PO034ASSOCIATION BETWEEN ANNUAL BLEEDING EVENTS AND HEALTH-RELATED QUALITY OF LIFE IN ADULTS WITH HAEMOPHILIA A PRESCRIBED PROPHYLAXISLisa Young
PO035ATHN 16: SAFETY OF COAGULATION FACTOR VIIA (RECOMBINANT)-JNCW FOR THE TREATMENT OF BLEEDING EVENTS IN PATIENTS WITH CONGENITAL HEMOPHILIA A OR B WITH INHIBITORS WITH OR WITHOUT PROPHYLACTIC TREATMENTTammuella Chrisentery-Singleton
PO036BIOEQUIVALENCE (BE) OF MARSTACIMAB PREFILLED PEN (PFP) DEVICE AND PREFILLED SYRINGE (PFS) DEVICE FOLLOWING SUBCUTANEOUS (SC) ADMINISTRATION IN HEALTHY ADULT MALESSangeeta Raje
PO039BONE MINERAL DENSITY IN YOUNG ADULT PATIENTS WITH SEVERE HEMOPHILIA A -A SINGLE-CENTER STUDYHristina Ivanova
PO040BUDGET IMPACT OF RVIII-SINGLECHAIN IN MODERATE AND SEVERE HAEMOPHILIA A TREATMENT IN ITALYRadovan Tomic
PO041CANADIAN CLINICAL EXPERIENCE ON SWITCHING FROM OCTOCOG ALFA TO EXTENDED-HALF-LIFE FVIII DAMOCTOCOG ALFA PEGOL IN PATIENTS WITH SEVERE HAEMOPHILIA ADavide Matino
PO042CARDIAC SURGERY IN HAEMOPHILIA – AN EXPERIENCE OF A CHALLENGING PERIOPERATIVE HEMOSTATIC APPROACHCristina Emilia Ursu
PO043CLEARANCE OF GIROCTOCOGENE FITELPARVOVEC VECTOR DNA IN ADULTS WITH SEVERE HAEMOPHILIA APatrick Fogarty
PO044CLINICAL APPLICATION OF EXTENDED HALF-LIFE PEGYLATED FACTOR VIII IN CHILDREN WITH SEVERE HAEMOPHILIA AAthina Dettoraki
PO045CLINICAL OUTCOMES FOLLOWING PROPHYLAXIS WITH RURIOCTOCOG ALFA PEGOL IN PATIENTS WITH HEMOPHILIA A: REAL-WORLD OBSERVATIONAL DATA FROM THE AHEAD INTERNATIONAL STUDYMargareth Ozelo
PO046COMPARTMENT SYNDROME MANAGEMENT IN SEVERE HEMOPHILIA A WITH INHIBITORSAslı Turgutoğlu Yılmaz
PO047CURRENT OPINIONS ON THE MANAGEMENT OF ACS IN PEOPLE WITH HEMOPHILIA A: A SURVEY OF THE ADVANCE WORKING GROUPRobert Klamroth
PO048DESIGN OF A REAL-WOLRD STUDY TO EVALUATE THE EFFECTIVENESS AND SAFETY OF OMFILOCTOCOG ALFA IN PATIENTS RECEIVING PROPHYLACTIC TREATMENT FOR MODERATE OR SEVERE HEMOPHILIA ASen Yu
PO049DOSE SELECTION AND STUDY DESIGN FOR B-LIEVE, A PHASE 1/2 DOSE CONFIRMATION CLINICAL TRIAL OF FLT180A GENE THERAPY FOR PATIENTS WITH HAEMOPHILIA BGuy Young
PO050EFFICACY AND SAFETY OF RURIOCTOCOG ALFA PEGOL IN PERIOPERATIVE MANAGEMENT: INTERIM RESULTS FROM AN OPEN-LABEL MULTICENTER CLINICAL TRIAL IN PREVIOUSLY UNTREATED PATIENTS WITH SEVERE HEMOPHILIA AFlora Peyvandi
PO051EFFICACY AND SAFETY OF TUROCTOCOG ALFA IN PATIENTS WITH HAEMOPHILIA A REQUIRING SURGICAL PROCEDURES: A FRENCH SINGLE CENTRE RETROSPECTIVE STUDYPierre-Olivier Bertho
PO052EMICIZUMAB AND INITIATION OF TREATMENT IN SEVERE HAEMOPHILIA A CHILDREN: ABOUT A CLINICAL CASEHortense Maynadié
PO053EMICIZUMAB PROPHYLAXIS IN PEOPLE WITH HAEMOPHILIA A (PWHA), AGED ≥50 YEARS, WITH COMORBIDITIES - POOLED DATA FROM FOUR PHASE 3 STUDIES (HAVEN 1, 3, 4, AND STASEY)Victor Jiménez-Yuste
PO054EMICIZUMAB PROPHYLAXIS IN SEVERE HAEMOPHILIA A WITHOUT INHIBITORS: OUTCOME AND INDICATIONS. FROM THE UK HAEMOPHILIA CENTRE DOCTORS’ ORGANISATIONCaroline Wall
PO055EMICIZUMAB THERAPY IN REAL-LIFE CLINICAL SETTING: DRAMATIC REDUCTION OF BLEEDING RATES IN CHILDREN WITH HEMOPHILIA A WITH INHIBITORS.Pavel Zharkov
PO056ESSENTIAL THROMBOCYTHEMIA IN PATIENTS WITH HEMOPHILIA: HIGH THROMBOTIC AND HEMORRHAGIC RISKFrancisco-Jose Lopez-Jaime
PO057EVALUATION OF CAI’S FORMULA IN CHINESE PREVIOUSLY TREATED PATIENTS WITH SEVERE HEMOPHILIA A RECEIVING TUROCTOCOG ALFACai Lisheng
PO058EXPERIENCE OF IMMUNE TOLERANCE INDUCTION THERAPY FOR HEMOPHILIA A PATIENTS WITH INHIBITORS FROM A SINGLE CENTER IN ALGERIAWassila Messadi
PO059EXPLORING THE TREATMENT EXPERIENCES OF ADOLESCENT AND ADULT PATIENTS WITH HAEMOPHILIA A: EXIT INTERVIEW FINDINGS FROM THE PATHFINDER 8 TRIALMeryl Bord
PO060FIX PRODUCT AT FIRST EXPOSURE IN CHILDREN WITH SEVERE HAEMOPHILIA B BETWEEN 2000-2020: DATA FROM PEDNETMarijke Van den Berg
PO061FUNCTIONAL INDEPENDENCE OF ADOLESCENTS WITH HEMOPHILIA FROM A BRAZILIAN HEMOPHILIA TREATMENT CENTERRicardo Mesquita Camelo
PO062FVIII PRODUCT AT FIRST EXPOSURE IN CHILDREN WITH SEVERE HAEMOPHILIA A BETWEEN 2000-2020: DATA FROM PEDNETMarijke Van den Berg
PO063GENE THERAPY FOR HAEMOPHILIA: THE EXIGENCY PROGRAMMESimon Fletcher
PO064GENETIC AND NON-GENETIC DETERMINANTS OF THE OUTCOME OF IMMUNE TOLERANCE INDUCTION IN PATIENTS WITH HEMOPHILIA A AND INHIBITORS –A SYSTEMATIC REVIEWIlja Oomen
PO065HAEMOPHILIA B PATIENTS UNDER RIX-FP PROPHYLAXIS: CLINICAL EXPERIENCE AT HOSPITAL UNIVERSITARIO LA PAZMaria Teresa Álvarez Román
PO066HAEMOPHILIA GENE THERAPY (GT) OUTCOMES: INTEGRATION OF THE HAEMOPHILIA VALUE FRAMEWORK WITH COREHEMMark Skinner
PO067HEALTH-RELATED QUALITY OF LIFE (HRQOL) IMPROVES IN PEOPLE WITH HEMOPHILIA A OR B (PWHA/B) WITH INHIBITORS RECEIVING FITUSIRAN PROPHYLAXIS: RESULTS OF PHASE 3 ATLAS-INHClaude Négrier
PO068HEALTH-RELATED QUALITY OF LIFE (HRQOL) OUTCOMES IN PEOPLE WITH HEMOPHILIA A (PWHA) FROM THE A-LONG/ASPIRE STUDIES OF RECOMBINANT FACTOR VIII FC FUSION PROTEIN (RFVIIIFC)Alex Cockerham
PO069HEMOPHILIA AND CANCER - TWO CASE REPORTSWassila Messadi
PO070HEMOPHILIA HEALTH SERVICES IN LIMITED RESOURCES CLINIC DURING COVID-19 PANDEMIC: MANADO EXPERIENCEIrene Maryauw
PO071HEMOPHILIA REGISTRY IN CUBA, DATA OF ALL PATIENTS.Dunia Castillo
PO072IDEAL STUDY: A REAL-WORLD ASSESSMENT OF TREATMENT REGIMENS, FACTOR IX TROUGH LEVELS AND CONCENTRATE CONSUMPTION IN HAEMOPHILIA B PATIENTS RECEIVING ALBUTREPENONACOG ALFA IN ITALYGiancarlo Castaman
PO073IDENTIFYING PERFORMANCE-BASED OUTCOME MEASURES OF PHYSICAL FUNCTION IN PEOPLE WITH HAEMOPHILIA (IPOP)David Stephensen
PO074ILLNESS PERCEPTIONS RELATED TO JOINT PAIN IN ADULT PEOPLE WITH HEMOPHILIA.Anthe Foubert
PO075IMPACT OF EXTENDED HALF-LIFE FACTORS ON THE QUALITY OF LIFE OF PATIENTS WITH HEMOPHILIA B AND CAREGIVERS. EXPERIENCE IN OUR CENTER.Jose Carlos De La Rosa Garcia
PO076IMPACT OF RFVIII-SC ON JOINT HEALTH-CLINICAL CASE REPORTOlga Benitez Hidalgo
PO077IMPACT OF VALOCTOCOGENE ROXAPARVOVEC GENE TRANSFER FOR SEVERE HAEMOPHILIA A ON HEALTH-RELATED QUALITY OF LIFEBrian O'Mahony
PO078INHERETED HEMOPHILIA WITH INHIBITORS TO FACTORS VIII AND IXTatsiana Talako
PO079INNOVATIVE BREAKTHROUGH TREATMENT, THE FINANCING OF EDUCATIONAL PROGRAMMES IS THE RESPONSIBILITY OF MANUFACTURERS, A FIRST IN FRANCE WITH THE EXAMPLE OF EMICIZUMABThomas Sannié
PO080INTERIM BASELINE DATA ON THE 48-MONTH PROSPECTIVE, OBSERVATIONAL A-MORE STUDY EVALUATING LONG-TERM EFFECTIVENESS OF RFVIIIFC ON JOINT HEALTHJan Astermark
PO081INTERIM DATA FROM A CHART REVIEW STUDY OF PATIENTS WITH HAEMOPHILIA A WITH INHIBITORS TREATED WITH RECOMBINANT FACTOR VIII FC FUSION PROTEIN (RFVIIIFC) FOR IMMUNE TOLERANCE INDUCTIONRobert Klamroth
PO082INVASIVE PROCEDURES IN PATIENTS WITH HAEMOPHILIA ON EMICIZUMAB PROPHYLAXIS: REAL-WORLD CLINICAL EXPERIENCE IN SLOVENIAKarla Rener
PO083JOINT HEALTH IN YOUNG ADULTS WITH SEVERE HAEMOPHILIA RECEIVING PRIMARY PROPHYLAXIS: AN INSIGHT FROM THE CHESS II EUROPEAN STUDYSharmila Kar
PO084JOINT HEALTH STATUS ASSESSMENT OF HAEMOPHILIA PATIENTS NOT TREATED WITH PROPHYLAXISBolívar Luis Díaz Jordán
PO085JOINT STATUS OF PATIENTS WITH NON-SEVERE HEMOPHILIA AAnne-Fleur Zwagemaker
PO086LIVING WITH HAEMOPHILIA A IN PORTUGAL: PRELIMINARY RESULTS OF A QUALITATIVE MARKET RESEARCH STUDYSusana Nobre Fernandes
PO087LONG TERM FOLLOW UP OF LOW DOSE PROPHYLAXIS IN TUNISIAN CHILDREN WITH HAEMOPHILIARabeb Jaied
PO088LONG-TERM EFFECT OF TUROCTOCOG ALFA PEGOL ON TREATMENT SATISFACTION IN PREVIOUSLY TREATED PATIENTS WITH HAEMOPHILIA A: RESULTS FROM PATHFINDER8Azusa Nagao
PO089MAJOR ORTHOPEDIC SURGERIES USING EXTENDED HALF-LIFE (EHL) COAGULATION REPLACEMENT FACTORS: THE EXPERIENCE OF A GREEK COMPREHENSIVE HAEMOPHILIA TREATMENT CENTER (CHTC)Anna Kouramba
PO090MANAGEMENT OF ACQUIRED HEMOPHILIA A:REVIEW OF OUR EXPERIENCE OF THE LAST 15 YEARSGianluca Sottilotta
PO091MANAGEMENT OF BREAKTHROUGH BLEEDS DURING CONCIZUMAB PROPHYLAXIS IN PATIENTS WITH HAEMOPHILIA A/B WITH AND WITHOUT INHIBITORS IN PHASE 3 CLINICAL TRIALSJan Astermark
PO092MANAGEMENT OF FACTOR XI DEFICIENCY TREATMENT IN A CASE WITH CRANIOPHARYNGIOMASerap Karaman
PO093MANAGEMENT OF INTRACRANIAL HEMORRHAGE IN HEMOPHILIA A PATIENTSWassila Messadi
PO094MEDICAL AND SOCIO-PSYCHOLOGICAL EFFECTS OF THE PANDEMIC ON PATIENTS WITH HEREDITER BLEEDING DISORDERS AND THEIR TREATERSBulent Zulfikar
PO095MINOR SURGERIES IN PATIENTS RECEIVING PROPHYLAXIS WITH CONCIZUMAB: EXPERIENCE IN OUR CENTERAna-Maria Mena-Santano
PO096MONITORING OF EMICIZUMAB USING A PATIENT REGISTRYGeertje Goedhart
PO097MOROCTOCOG ALFA (AF-CC) PROPHYLAXIS AND TREATMENT OF BLEEDING EPISODES IN PREVIOUSLY TREATED PATIENTS WITH MODERATE OR SEVERE HEMOPHILIA A IN INDIADamien Simoneau
PO098MULTIPLE-YEAR DURABILITY DATA FROM A PHASE 2B TRIAL OF GENE THERAPY WITH ETRANACOGENE DEZAPARVOVEC IN PATIENTS WITH HEMOPHILIA BEsteban Gomez
PO099PAIN RELIEF WITH EPTACOG BETA IN HEMOPHILIA PATIENTS WITH INHIBITORSCédric Hermans
PO100PATIENT-ORIENTED APPROACH IN THE MANAGEMENT OF HEMOPHILIA; A MULTICENTER SURVEY ON INJECTIONS WITHOUT A VIAL IN PLACEHaluk Zulfikar
PO101PERIOPERATIVE MANAGEMENT AND TROMBOELASTOMETRY MONITORING IN A CASE OF HEMOPHILIA A WITH INHIBITOR ON EMIZICUMAB PROPHYLAXISAbel Dos Santos Ortas
PO102PERIOPERATIVE MANAGEMENT IN “NON-SEVERE” HEMOPHILIA PATIENTSCarmen Rodríguez Lefler
PO103PERIOPERATIVE USE OF EXTENDED HALF-LIFE (EHL) FVIII AND FIX CONCENTRATES IN CHILDREN WITH HAEMOPHILIA A AND BAikaterini Michalopoulou
PO104PHARMACOKINETIC MODEL-BASED DOSE SETTING FOR PROPHYLAXIS WITH FACTOR IX PRODUCTS IN SEVERE HAEMOPHILIA BKaren Pinachyan
PO105PHARMACOKINETIC-GUIDED PROPHYLAXIS WITH RECOMBINANT ANTIHEMOPHILIC FACTOR IMPROVES BLEEDING RATES IN PATIENTS WITH MODERATE HEMOPHILIA: REAL-WORLD OBSERVATIONAL DATA FROM THE AHEAD GERMAN STUDYRobert Klamroth
PO106PK-GUIDED PROPHYLAXIS VERSUS STANDARD PROPHYLAXIS REGIMENS IN SEVERE HEMOPHILIADaniel Kraemmer
PO107PRESENTATION OF 5 CASES WITH ACQUIRED HEMOPHILIA A TREATED AT THE CLINIC OF HEMATOLOGY IN SKOPJESvetlana Stankovikj
PO108PREVIOUSLY UNTREATED PATIENTS IN GERMANY 2017 - 2021 – A CROSS-SECTIONAL ANALYSIS OF 249 PATIENTS FROM THE GEPHARD COHORTChristoph Bidlingmaier
PO109PROPHYLAXIS AND ZERO BLEED FOR ALL ADULT PATIENTS WITH SEVERE HEMOPHILIA: AN ACHIEVABLE AMBITION WITH NEW TREATMENT OPTIONSCedric Hermans
PO110PROPHYLAXIS WITH DAMOCTOCOG ALFA PEGOL: REAL WORLD USAGE AND EFFECTIVENESS IN PATIENTS WITH HEMOPHILIA A OF A PORTUGUESE HEMOPHILIA REFERENCE CENTRESoraia Campaniço
PO111PROTECTIVE AND RISK FACTOR FOR PERIODONTAL DISEASES IN A BLEEDING DISORDERS POPULATIONLaura Isidro
PO112QUALITATIVE RESEARCH EVALUATING PATIENT PREFERENCE FOR HAEMOPHILIA THERAPYWolfgang Miesbach
PO113REAL WORLD DATA ON BLEEDING PATTERN IN A COHORT OF HEMOPHILIA A PATIENTS TREATED WITH EMICIZUMABSarina Levy-Mendelovich
PO114REAL-WORLD DATA ON EMICIZUMAB PROPHYLAXIS IN THE MILAN COHORT: A SINGLE-CENTER EXPERIENCESara Arcudi
PO115RELATIONSHIP OF FUNCTIONAL FIBRINOGEN WITH CLOT FIRMNESS AND JOINT HEALTH IN PATIENTS WITH SEVERE HEMOPHILIAPaula Acuña
PO116REMOTE COORDINATION OF THE MULTIDISCIPLINARY HAEMOPHILIA TEAM WITH SKELETAL IMAGING SUPPORT. BEYOND THE PANDEMICA.Patricia Nally
PO117RIX-FP PROPHYLAXIS IN PATIENTS WITH HAEMOPHILIA B: REAL-WORLD EVIDENCE FROM A SPANISH REFERENCE CENTEROlga Benítez Hidalgo
PO118RVIII-SINGLECHAIN FOR TREATMENT OF PREVIOUSLY UNTREATED PATIENTS WITH SEVERE HAEMOPHILIA A: A SINGLE-CENTRE EXPERIENCESusana Nobre Fernandes
PO119SAFE AND EFFICACIOUS USE OF EFMOROCTOCOG ALFA IN A PREGNANT WOMAN WITH HAEMOPHILIA A.David Quinn
PO120SAFETY AND EFFECTIVENESS OF RECOMBINANT B-DOMAIN–DELETED PORCINE-SEQUENCE FACTOR VIII FOR ACQUIRED HEMOPHILIA A IN A REAL-WORLD SETTINGWolfgang Miesbach
PO121SAFETY AND EFFICACY OF DAMOCTOCOG ALFA PEGOL PROPHYLAXIS IN PATIENTS WITH SEVERE HAEMOPHILIA A: INTERIM RESULTS OF A POST-MARKETING, INTERVENTIONAL STUDYPål Andrè Holme
PO122SAFETY AND EFFICACY OF MARSTACIMAB FOR PREVENTION OF BLEEDING EPISODES IN PAEDIATRIC PATIENTS WITH SEVERE HAEMOPHILIA A OR MODERATELY SEVERE TO SEVERE HAEMOPHILIA B WITH OR WITHOUT INHIBITORSJohn Teeter
PO123SAFETY AND EFFICACY OF NONACOG ALFA PROPHYLAXIS AND TREATMENT OF BLEEDING EPISODES IN PREVIOUSLY TREATED PATIENTS WITH MODERATELY SEVERE OR SEVERE HEMOPHILIA B IN INDIADamien Simoneau
PO124SECOND INTERIM ANALYSIS OF THE PHASE IV HEM-POWR STUDY EVALUATING THE REAL-WORLD EFFECTIVENESS AND SAFETY OF DAMOCTOCOG ALFA PEGOL IN PREVIOUSLY TREATED PATIENTS WITH HAEMOPHILIA AMark Reding
PO125SEVERE HAEMOPHILIA A AND FACTOR V LEIDEN: A CASE REPORTCatarina Almeida
PO126SHOCK INDEX AS HEMARTHROSIS MARKER IN HEMOPHILIA PATIENTS IN COLOMBIA: A PROGNOSTIC APPROACHMario-Miguel Barbosa
PO127SPINAL EPIDURAL HEMATOMA IN A SEVERE HEMOPHILIA A WITH A HIGH TITER INHIBITORSelin Aytac
PO129SURGERIES AND DIAGNOSTIC PROCEDURES IN HAEMOPHILIA PATIENTS ON CONCIZUMAB PROPHYLAXIS IN PHASE 2 CLINICAL TRIALSAllison Wheeler
PO130SURGICAL MANAGEMENT IN PATIENT WITH SEVERE HAEMOPHILIA B RECEIVING RFIX-FC: CASE REPORTOlga Benitez Hidalgo
PO131SYSTEMATIC JOINT EXAMINATION IN PATIENTS WITH HAEMOPHILIA A IN FRANCE: INTERIM BASELINE RESULTS FROM THE A-MOVE STUDYBrigitte Pan-Petesch
PO132THE CLINICAL AND ECONOMIC IMPACT OF RECOMBINANT FACTOR VIII FC FUSION PROTEIN (RFVIIIFC) ON LONG-TERM JOINT HEALTH IN PEOPLE WITH HEMOPHILIA A (PWHA)Katharine Batt
PO133THE CLINICAL PHENOTYPE OF PATIENTS WITH NON-SEVERE HEMOPHILIA A AND BF.R. Kloosterman
PO134THE HEM-CORE SURVEY: PSYCHOLOGICAL REACTION OF HEMOPHILIA PATIENTS DURING COVID-19Gianluca Sottilotta
PO135THE IMPACT OF COVID19 PANDEMIC ON HEMOPHILIA CARE: EXPERIENCE OF A SINGLE PEDIATRIC TREATMENT CENTERMaria Vousvouki
PO136THE IMPACT OF SEVERE HAEMOPHILIA ON EVERYDAY LIFE AMONG ADULTS: REPORTS FROM THE CHESS II STUDY ACROSS EUROPESharmila Kar
PO137THE TOOL STUDY. PRELIMINARY RESULTS FROM A MULTICENTER COHORT OF HAEMOPHILIA A PATIENTS SWITCHING TO AN EXTENDED HALF-LIFE AGENT.Helen Pergantou
PO138THE USE OF PAEDIATRIC PROMIS® ITEM BANKS IN DUTCH BOYS WITH HAEMOPHILIALorynn Teela
PO139THE WORLD FEDERATION OF HEMOPHILIA GENE THERAPY REGISTRY – A GLOBAL RESOURCE FOR THE LONG-TERM FOLLOW-UP OF HEMOPHILIA PATIENTS TREATED WITH GENE THERAPYMayss Naccache
PO140TRANSITION READINESS AMONG ADOLESCENTS AND YOUNG ADULTS WITH HAEMOPHILIA IN THE NETHERLANDSMartijn Brands
PO141TREATMENT SATISFACTION SURVEY FOR HEMOPHILIA A IN ADULT PATIENTS IN RUSSIANadezhda Ivanovna Zozulya
PO142UNMET NEEDS IN HEMOPHILIA B: PERSPECTIVES FROM PEOPLE LIVING WITH HEMOPHILIA B, HEALTHCARE PROFESSIONALS AND THE HEALTHCARE INDUSTRYKaren Pinachyan
PO143UPDATE FROM THE PHASE 3 HOPE-B GENE THERAPY TRIAL: STABLE STEADY-STATE EFFICACY AND SAFETY OF ETRANACOGENE DEZAPARVOVEC IN ADULTS WITH SEVERE OR MODERATELY SEVERE HEMOPHILIA BWolfgang Miesbach
PO144USE OF SUSOCTOCOG ALFA AS POST-OPERATIVE BLEEDING PREVENTION IN A PATIENT WITH ACQUIRED HEMOPHILIA A AND ANTI-PORCINE FVIII ANTIBODIES: A CASE REPORTMarco Bardetta
PO145USING COMBINED LIMITED SAMPLING STRATEGIES TO MAKE PHARMACOKINETIC-GUIDED SWITCHING BETWEEN FACTOR VIII CONCENTRATES MORE EFFICIENTLaura Bukkems
PO146VALOCTOCOGENE ROXAPARVOVEC GENE TRANSFER IN PARTICIPANTS WITH HIVMargaret Ragni
PO147WHEN A BRAIN HEMORRHAGE REVEALS OTHER PROBLEMSFilipa Martins Pereira
PO148ALLOANTIBODIES IN VON WILLEBRAND DISEASE IN SOUTH OF TUNISIARahma Mallek
PO149DIAGNOSIS OF VON WILLEBRAND DISEASE IN RUSSIA: EXPERIENCE IN CENTRALIZED DIAGNOSTICS.Aleksandr Poletaev
PO150ESTABLISHMENT OF REFERENCE INTERVALS FOR THE VON WILLEBRAND FACTOR ANTIGEN IN ALGERIAN ADULTS ACCORDING TO BLOOD GROUP ABOMalika BELKACEMI
PO151PLATELET AGGREGATION ABNORMALITIES IN PATIENTS VON WILLEBRAND DISEASE TYPE 2B.Yuly Paola Martínez
PO152VON WILLEBRAND DISEASE (VWD) INCIDENCE AMONG PATIENTS WITH BLEEDING MANIFESTATIONS FROM MULTI HAEMOPHILIA TREATMENT CENTERS (HTCS) IN EGYPT: DATA FROM VWD REGISTRYSonia Adolf
PO153VWF GENE PATHOGENIC VARIANTS SPECTRUM IN RUSSIAN PATIENTS WITH VON WILLEBRAND DISEASEDaria Chernetskaya
PO154A VERY COMPLICATED COURSE AFTER VAGINAL DELIVERY IN TYPE 3 VON WILLEBRAND DISEASE WITH ALLOANTIBODIES TO VON WILLEBRAND FACTOR AND FACTOR VIIILize van Vulpen
PO155ACQUIRED VON WILLEBRAND DISEASE AND CHRONIC LYMPHOCYTIC LEUKAEMIA: REMISSION AFTER ALLOGENEIC HEMATOPOIETIC CELL TRANSPLANTATIONFrancisco-Jose Lopez-Jaime
PO156AN UNUSUAL CASE OF A YOUNG WOMAN WITH TYPE 2A VON WILLEBRAND DISEASE DEVELOPING ANTI VWF ANTIBODIESBirgit Frotscher
PO157ASSESSMENT OF PATIENTS WITH VON WILLEBRAND DISEASE WITH ISTH-BAT IN SOUTHERN TUNISIARahma Mallek
PO158EFFICACY AND SAFETY OF HIGH RATIO HVWF/FVIII CONCENTRATE (VONCENTO®) FOR THE TREATMENT OF BLEEDING EPISODES IN PATIENTS WITH VON WILLEBRAND DISEASE: THE OPALE FRENCH EXPERIENCERoseline d’Oiron
PO159LIFE THREATENING BLEEDINGS IN VON WILLEBRAND DISEASE IN SOUTHERN TUNISIARahma Mallek
PO160RECURRENT EPISTAXIS IN PATIENT WITH ACQURED VON WILLEBRAND SYNDROME AND MONOCLONAL GAMMOPATHY OF UNDETERMINATED SIGNIFICANCEAna Rosa Carranco Falcón
PO161THE PROGNOSTIC VALUE OF THE APPLICATION OF THE ISTH-BAT CLINICAL SCORE IN VON WILLEBRAND DISEASE : SERIES OF 20 PATIENTS FOLLOWED AT THE UNIVERSITY HOSPITAL OF ORANReda Messaoudi
PO162TREATMENT COMPLIANCE IN PATIENTS WITH VON WILLEBRAND'S DISEASENadezhda Ivanovna Zozulya
PO163TREATMENT WITH A PLASMA-DERIVED VON WILLEBRAND FACTOR (VWF) ALMOST DEVOID OF FACTOR VIII IN ELDERLY PATIENTS WITH VON WILLEBRAND DISEASE (VWD): A POOLED ANALYSISJenny Goudemand
PO164VONICOG ALFA IN PREGNANCY IS SAFE AND EFFICACIOUSDavid Quinn
PO165A SUCCESSFUL 11-YEAR TREATMENT WITH TOPICAL PLASMINOGEN, SURGERY AND PROSTHETIC EYE FITTING IN SEVERE LIGNEOUS CONJUNCTIVITISAntonella Coretti
PO166ACCESS TO PREGNANCY FOR WOMEN WITH TYPE 1 GLANZMANN'S THROMBASTHENIA: A SYSTEMATIC APPROACHGuillaume Morelle
PO167ACCIDENTAL DISCOVERY OF AN UNUSUAL CONSTITUTIONAL DYSFIBRINOGENEMIA: LONGMONT FIBRINOGENAhlem Raissi
PO168ACQUIRED FACTOR V INHIBITOR ASSOCIATED TO CHRONIC LYMPHATIC LEUKAEMIA (CLL). A CASE REPORT.Alberto Porro Camarero
PO169ACQUIRED HAEMOPHILIA A ASSOCIATED TO POSTPARTUM PERIOD: A CASE REPORT OF A DELAYED DIAGNOSISRebeca Jurado Tapiador
PO170APPLICATION OF THE ISTH-BAT HEMORRHAGIC SCORE IN CONSTITUTIONAL BLEEDING DISORDERSReda Messaoudi
PO171CLINICAL PHENOTYPE IN PATIENTS WITH HEREDITARY FACTOR XII DEFICIENCYNadezhda Zozulya
PO172COEXISTENCE OF PLATELET GLYCOPROTEIN IV DEFICIENCY AND VON WILLEBRAND DISEASE: UNIQUE CLINICAL AND MOLECULAR CHARACTERISTICS.Mohamed Elshinawy
PO173EPIDEMIOLOGY AND CHARACTERISTICS OF SEVERE RARE HEREDITARY BLEEDING DISORDERS AT A REFERENCE CENTER IN SPAINMaría Fernanda Martínez García
PO174EVALUATION OF HEMORRHAGIC OR THROMBOTIC PROFILE IN PATIENTS WITH DYSFIBRINOGENEMIAVirginie Barbay
PO175FACTOR V MUTATION PREVIOUSLY NOT DESCRIBED – A CASE REPORTLiliana Fonseca
PO176FEMALE PATIENTS WITH BLEEDING DISORDERS: SINGLE CENTER RESULTSCanan Albayrak
PO177FIVE PATIENTS WITH COMBINED FACTOR V AND FACTOR VIII DEFICIENCY: EXPERIENCE OF TWO CENTERS IN SAMSUN-TURKEYCanan Albayrak
PO178INHERITED (HYPO)DYSFIBRINOGENEMIA AND THROMBOSIS IN TWO FAMILIES CAUSED BY THE SAME NOVEL GLY318SER SUBSTITUTION IN THE FIBRINOGEN GAMMA CHAINEugénia Cruz
PO179INVASIVE MAJOR SURGERY IN PATIENTS WITH FXII DEFICIENCY – TWO CENTERS EXPERIENCEInes Vaide
PO180LONGITUDINAL COMPARATIVE STUDY OF CHILDREN WITH IMMUNE THROMBOCYTOPENIA (ITP): A SINGLE CENTRE EXPERIENCEAikaterini Michalopoulou
PO181MENSTRUAL PROBLEMS IN CHRONIC IMMUNE THROMBOCYTOPENIA: A MONTHLY CHALLENGE - A COHORT STUDY AND REVIEWWobke Van Dijk
PO182NOVEL VARIANTS IN ETV6 AND FYB1 GENES: TWO CHILDREN WITH RARE INHERITED THROMBOCYTOPENIAVeysel Gök
PO183PREDICTION VALUE OF PEDIATRIC BLEEDING QUESTIONNAIRE (PBQ) FOR CHILDREN WITH DIFFERENT BLEEDING DISODERSTatyana Yafoshkina
PO184RETROSPECTIVE COMPARATIVE ANALYSIS OF HEMORRHAGIC SYNDROME SEVERITY IN CHILDREN WITH GLANZMANN THROMBASTHENIA AND OTHER BLEEDING DISORDERSMaria Ustinova
PO185SEVERE FACTOR XI DEFICIENCY – A CASE REPORTLiliana Fonseca
PO186THROMBOTIC EVENTS IN CHILDREN AND ADOLESCENTS DURING THE COVID-19 PANDEMIC PERIOD. DATA OF A REFERENCE CENTER IN GREECELoukia Ioannidou
PO187WEAKENING OF THE PROCOAGULANT ACTIVITY OF PLATELETS AND THE SEVERITY OF HEMORRHAGIC SYNDROME IN CHILDREN WITH INHERITED THROMBOCYTOPENIASDmitrii Polokhov
PO188EFFECTS OF MULTIMODAL EXERCISES PROGRAM ON BALANCE, FUNCTIONALITY, RISK OF FALLS AND STRENGTH IN PEOPLE WITH HAEMOPHILIAAna Chimeno-Hernández
PO189IMMERSIVE MOVEMENT VISUALIZATION IN PATIENTS WITH HEMOPHILIC ARTHROPATHY: A POSSIBLE THERAPEUTIC ALTERNATIVE IN HEMOPHILIA?Roberto Ucero-Lozano
PO190MAY SELF-INDUCED MYOFASCIAL RELEASE BE SAFE AND EFFECTIVE IN PATIENTS WITH HEMOPHILIC ANKLE ARTHROPATHY?Elena Donoso-Úbeda
PO191PHYSIOTHERAPEUTIC EVALUATION OF JOINT HEALTH OF HEMOPHILIAC PATIENTS THROUGH HJHS, REFERRED TO RADIOACTIVE SYNOVECTOMY – BRAZIL EXPERIENCE.Fernando Zikan
PO192PHYSIOTHERAPY, HEMOPHILIA AND INTERNATIONAL CLASSIFICATION OF FUNCTIONALITY - DO WE HAVE SCIENTIFIC EVIDENCE AVAILABLE?Fernando Zikan
PO193SELF-INDUCED MYOFASCIAL RELEASE: EFFECTIVENESS IN THE HOME APPROACH TO HEMOPHILIC KNEE ARTHROPATHY.Raúl Pérez-Llanes
PO194THE HISTORICAL EVOLUTION OF PHYSIOTHERAPY FOR THE MULTIDISCIPLINARY MANAGEMENT OF PATIENTS WITH HAEMOPHILIA (PWH)Valentina Begnozzi
PO195EHCUCATE: DEVELOPING AN ENGAGING AND ACCESSIBLE NOVEL THERAPIES EDUCATIONAL APPFiona Robinson
PO196REHABILITATION OF PATIENTS WITH BLEEDING DISORDERS BY MULTIDISCIPLINARY CARE TEAM IN ESTONIA IN KURESSAAREInes Vaide
PO197VIRTUAL REALITY: INCREASING EMPOWERMENT IN THE SELF-TREATMENT OF PEOPLE WITH HEMOPHILIA WITH NEW TECHNOLOGIESAmparo Santamaria
PO198WORDS IN HEMOPHILIA: A PROJECT FOR A BETTER PATIENT ENGAGEMENTSerena Barello