Hemophilia Daily - Tuesday, July 10, 2012 - (Page 4)
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HEMOPHILIA DAILY
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TUESDAY, JULY 10, 2012 • PARIS
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Guidelines For The Management Of Hemophilia: New Edition
Revised second edition now available free online in Haemophilia.
• Fully revised and updated • Clinical practice recommendations supported by graded evidence • Prepared and reviewed by the world’s leading experts in the diagnosis and treatment of hemophilia
Media centre
Haemophilia (2012), 1–47
DOI: 10.1111/j.1365-2516.2012.02909.x
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GUIDELINES
Guidelines for the management of hemophilia
A. SRIVASTAVA,* A. K. BREWER,† E. P. MAUSER-BUNSCHOTEN,‡ N. S. KEY,§ S. KITCHEN,¶ A . L L I N A S , * * C . A . L U D L A M , † † J . N . M A H L A N G U , ‡ ‡ K . M U L D E R , § § M . C . P O O N ¶ ¶ and A. STREET***; TREATMENT GUIDELINES WORKING GROUP ON BEHALF OF THE WORLD FEDERATION OF HEMOPHILIA
*Department of Hematology, Christian Medical College, Vellore, India; †Department of Oral Surgery, The Royal Infirmary, Glasgow, Scotland; ‡Van Creveldkliniek and Department of Hematology, University Medical Center Utrecht, Utrecht, The Netherlands; §Department of Medicine, University of North Carolina, Chapel Hill, NC USA; ¶Sheffield Haemophilia and Thrombosis Centre, Royal Hallamshire Hospital, Sheffield, UK; **Department of Orthopaedics and Traumatology, Fundacion ´ ´ ´ Santa Fe University Hospital Fundacion Cosme y Damian and Universidad de los Andes and Universidad del Rosario, Bogota, ´ Colombia; ††Comprehensive Care Haemophilia and Thrombosis Centre, Royal Infirmary, Edinburgh, UK; ‡‡Haemophilia Comprehensive Care Centre, Johannesburg Hospital and Department of Molecular Medicine and Haematology, Faculty of Health Sciences, National Health Laboratory Services and University of the Witwatersrand, Johannesburg, South Africa; §§Bleeding Disorders Clinic, Health Sciences Center, Winnipeg, Canada; ¶¶Departments of Medicine, Pediatrics and Oncology, and Southern Alberta Rare Blood and Bleeding Disorders Comprehensive Care Program, University of Calgary, Foothills Hospital and Calgary Health Region, Calgary, Canada; and ***Haematology, Alfred Hospital, Melbourne, Victoria Australia
Summary. Hemophilia is a rare disorder that is complex to diagnose and to manage. These evidencebased guidelines offer practical recommendations on the diagnosis and general management of hemophilia, as well as the management of complications including musculoskeletal issues, inhibitors, and transfusiontransmitted infections. By compiling these guidelines, the World Federation of Hemophilia aims to assist
healthcare providers maintain hemophilia practice harmonization recommendations lack appropriate studies.
seeking to initiate and/or care programs, encourage around the world and, where adequate evidence, stimulate
Keywords: bleeding disorders, guidelines, hemophilia, management, treatment
TODAY’S PROGRAM UPDATES
Free papers 4: Product and clinical trials 2 (FP-TU-01.1—Medical): Henning Stennicke will be presenting the topic, “GlycoPEGylated rFVIII (N8-GP) has prolonged hemostatic effect in hemophilia A mice” Preparing future generations (S-TU-01.3—Multidisciplinary): Dhawal Yogesh Bhanushali will be presenting the topic, “Youth programs and concepts from an emerging country” In today’s “Late-breaking session I” (LB-TU-04.1—Medical), 16:30 – 18:00, the following presenters are scheduled: Treatment for life: Prophylaxis in hemophilia A is more cost-effective than ondemand therapy in a cost-utility model Albert Farrugia
Correspondence: Dr. Alok Srivastava, Christian Medical College, Vellore 632004, India. Tel.: +91 416 228 2472; fax: +91 416 222 6449; e-mail: aloks@cmcvellore.ac.in Accepted after revision 6 June 2012 © 2012 Blackwell Publishing Ltd
U.K. product switch Charles R. M. Hay
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Safety and efficacy of turoctocog alfa during prevention and treatment of bleeds in adult and adolescent patients with severe hemophilia A Steven Lentz Safety and efficacy of turoctocog alfa during prevention and treatment of bleeds in pediatric patients with severe hemophilia A and below 12 years of age Elena Santagostino A view of the Aledort-Iorio debate concerning the immunogenicity of B-domain-deleted and full-length recombinant FVIII products from a mechanistic personalized medicine perspective Tom Howard
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Table of Contents for the Digital Edition of Hemophilia Daily - Tuesday, July 10, 2012
Hemophilia Daily - Tuesday, July 10, 2012
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