Emergency management of patients with bleeding disorders: Practical points for the emergency physician

Transfusion and Apheresis Science - Tập 58 - Trang 553-562 - 2019
Adrienne Lee1
1Departments of Medicine, Cumming School of Medicine, University of Calgary and the Southern Alberta Rare Blood and Bleeding Disorders Comprehensive Care Program, Foothills Medical Centre, Alberta Health Services, 1403-29th Street NW, Calgary, AB T2N 2T9, Canada

Tài liệu tham khảo

Bowman, 2008, Generation and validation of the condensed MCMDM-1VWD bleeding questionnaire for von Willebrand disease, J Thromb Haemost, 6, 2062, 10.1111/j.1538-7836.2008.03182.x Rodeghiero, 2010, ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders, J Thromb Haemost, 8, 2063, 10.1111/j.1538-7836.2010.03975.x Pryzdial, 2018, Blood coagulation dissected, Transfus Apher Sci, 57, 449, 10.1016/j.transci.2018.07.003 Gailani, 2011, A cofactor for factor XI activation, Blood, 118, 6730, 10.1182/blood-2011-10-385336 Franchini, 2017, Acquired hemophilia A: a review of recent data and new therapeutic options, Hematology, 22, 514, 10.1080/10245332.2017.1319115 Hay, 2006, The diagnosis and management of factor VIII and IX inhibitors: a guideline from the United Kingdom Haemophilia Centre Doctors Organisation, Br J Haematol, 133, 591, 10.1111/j.1365-2141.2006.06087.x Charlebois, 2018, Management of acquired hemophilia A: review of current evidence, Transfus Apher Sci, 57, 717, 10.1016/j.transci.2018.10.011 Bowman, 2009, Evaluation of the diagnostic utility for von Willebrand disease of a pediatric bleeding questionnaire, J Thromb Haemost, 7, 1418, 10.1111/j.1538-7836.2009.03499.x Lee, 2018, Inherited platelet functional disorders: general principles and practical aspects of management, Transfus Apher Sci, 57, 494, 10.1016/j.transci.2018.07.010 Rand, 2018, Laboratory diagnosis of inherited platelet function disorders, Transfus Apher Sci, 57, 485, 10.1016/j.transci.2018.07.009 Srivastava, 2013, Guidelines for the management of hemophilia, Haemophilia, 19, e1, 10.1111/j.1365-2516.2012.02909.x Hanley, 2017, Guidelines for the management of acute joint bleeds and chronic synovitis in haemophilia: a United Kingdom Haemophilia Centre Doctors’ Organisation (UKHCDO) guideline, Haemophilia, 23, 511, 10.1111/hae.13201 Poon, 2018, Hemophilia, BMJ Best Pract Fullerton, 2011, Evidence-based emergent management of bleeding disorders, Pediatr Emerg Med Pract, 8, 1 Schwartz, 2015, Hemophilia von Willebrand disease in children: emergency department evaluation and management, Pediatr Emerg Med Pract, 12, 1 Franchini, 2018, Non-factor replacement therapy for haemophilia: a current update, Blood Transfus, 16, 457 James, 2007, Bleeding events and other complications during pregnancy and childbirth in women with von Willebrand disease, J Thromb Haemost, 5, 1165, 10.1111/j.1538-7836.2007.02563.x Revel-Vilk, 2003, Desmopressin (DDAVP) responsiveness in children with von Willebrand disease, J Pediatr Hematol Oncol, 25, 874, 10.1097/00043426-200311000-00010 Archer, 2015, The utility of the DDAVP challenge test in children with low von Willebrand factor, Br J Haematol, 170, 884, 10.1111/bjh.13331 Siew, 2014, Desmopressin responsiveness at a capped dose of 15 mug in type 1 von Willebrand disease and mild hemophilia A, Blood Coagul Fibrinolysis, 25, 820, 10.1097/MBC.0000000000000158