New Treatments of von Willebrand Disease: Plasma Derived von Willebrand Factor Concentrates

• References

• 1 Blatt PM, Brinkhous KM, Culp HR, Krauss JS, Roberts HR. Antihemophilic factor concentrate therapy in von Willebrand disease: Dissociation of bleeding-time factor and ristocetin-cofactor activities. J Am Med Ass 1976; 236: 2770-2772
• 2 Green D, Potter V E. Failure of AHF concentrate to control bleeding in von Willebrand’s disease. Am J Med 1976; 60: 357-360
• 3 Bennett E, Dormandy K. Pool’s cryoprecipitate and exhausted plasma in the treatment of von Willebrand’s disease and factor-XI deficiency. Lancet 1966; 731-732
• 4 Bumouf-Rasedovich M, Bumouf T. Chromatographic preparation of a therapeutic highly purified von Willebrand factor concentrate from human cryoprecipitate. Vox Sang 1992; 62: 01-11
• 5 Lawrie AS, Harrison P, Armstrong AL, Wilbourn BR, Dalton RG, Savidge GF. Comparison of the in vitro characteristics of von Willebrand factor in British and commercial factor VIII concentrates. Br J Haematol 1989; 73: 100-104
• 6 Fricke AW, Yu MW. Characterization of von Willebrand factor in factor VIII concentrates. Am J Hematol 1989; 31: 41-45
• 7 Morfini M, Rafanelli D, Filimberti E, Cinotti S, Piazza E, Longo G, Ferrini PR. Protein content and factor VIII complex in untreated, treated and monoclonal factor VIII concentrates. Thromb Res 1989; 56: 169-178
• 8 Mazurier C, Jorieux S, de Romeuf C, Samor B, Goudemand M. In vitro evaluation of a veiy-high-purity, solvent/detergent treated, von Willebrand factor concentrate. Vox Sang 1991; 61: 1-7
• 9 Mannucci PM, Tenconi PM, Castaman G, Rodeghiero F. Comparison of four virus-inactivated plasma concentrates for treatment of severe von Willebrand disease: A cross-over randomized trial. Blood 1992; 79: 3130-3137
• 10 Bemtorp E. Plasma product treatment in various types of von Willebrand’s disease. Haemostasis 1994; 24: 289-297
• 11 Mannucci PM, Chediak J, Byrnes J, Kessler C, Marciniak E, Hanna W, Retzios AD. and the Alphanate study Group. A high purity factor VIII concentrate in the treatment of von Willebrand’s disease. Presented at the XXII International Congress of the World Federation of Hemophilia Dublin; Ireland: 1996
• 12 Weinstein M, Deykin D. Comparison of factor VUI-related von Willebrand factor proteins prepared from human cryoprecipitate and factor VIII concentrate. Blood 1979; 53: 1095-1105
• 13 Mannucci PM, Moia M, Rebulla P, Altieri D, Monteagudo J, Castillo R. Correction of the bleeding time in treated patients with severe von Willebrand disease is not solely dependent on the normal multimeric structure of plasma von Willebrand factor. Am J Hematol 1987; 25: 55-65
• 14 Mannucci PM, Lattuada A, Ruggeri ZM. Proteolysis of von Willebrand factor in therapeutic plasma concentrates. Blood 1994; 83: 3018-3027
• 15 Menache D, Aronson DL, Darr F, Montgomery RR. and The Cooperative Study Group. Pharmacokinetics of von Willebrand factor and factor VIIIC in patients with severe von Willebrand disease (type 3 VWD): estimation of the rate of factor VIIIC synthesis. Br J Haematol 1996; 94: 740-745
• 16 Weiss HJ. Relation of von Willebrand factor to bleeding time. (Letter) N Engl J Med 1974; 291: 420
• 17 Castillo R, Monteagudo J, Escolar G, Ordinas A, Magallon M, Villar JM. Hemostatic effect of normal platelet transfusion in severe von Willebrand disease patients. Blood 1991; 77: 1901-1905
• 18 Boda Z, Pfliegler G, Harsfolvi J, Rak K. Treatment of the severe bleeding episode in type III von Willebrand’s disease by simultaneous administration of cryoprecipitate and platelet concentrate. Blood Coagul Fibrinolysis 1991; 2: 775-777
• 19 Ramstrom G, Blomback M, Egberg N, Johnsson H, Ljungberg B, Schulman S. Oral surgery in patients with hereditary bleeding disorders. A survey of treatment in the Stockholm area (1974-1985). Int J Oral Maxillofac Surg 1989; 18: 320-322
• 20 Bloom AL, Peake IR, Furlong RA, Davies BL. High potency factor VIII concentrate: more effective than cryoprecipitate in a patient with von Willebrand’s disease and inhibitor. Thromb Res 1979; 16: 847-852
• 21 Hathaway WE, Mahasandana C, Clarke S, Humbert JR. Paradoxical bleeding in intensively transfused hemophiliacs: Alteration of platelet function. Transfusion 1973; 13: 06-12
• 22 Halvorson EP, Hildgartner MW. Transient acquired defect in platelet function following therapy with AHF concentrate. Mt Sinai J Med 1978; 45: 282-287
• 23 Foster PA. The reproductive health of women with von Willebrand disease unresponsive to DDAVP: Results of an international survey. On behalf of the subcommittee on von Willebrand factor of the Scientific and Standardization Committee of the ISTH. Thromb Haemost 1995; 74: 784-790
• 24 Foster PA. A perspective on the use of FVIII concentrates and cryoprecipitate prophylactically in surgery or therapeutically in severe bleeds in patients with von Willebrand disease unresponsive to DDAVP: Results on an international survey. On behalf of the subcommittee on von Willebrand factor of the Scientific and Standardization Committee of the ISTH. Thromb Haemost 1995; 74: 1370-1378
• 25 Rodeghiero F, Castaman G, Meyer D, Mannucci PM. Replacement therapy with virus-inactivated plasma concentrates in von Willebrand disease. Vox Sang 1992; 62: 193-199
• 26 Kohler M, Hellstem P, Wenzel E. The use of heat-treated factor VIII concentrates in von Willebrand’s disease. Blut 1985; 50: 25-27
• 27 Fukui H, Nishino M, Terada S, Nishikubo T, Yoshioka A, Kinoshita S, Niinomi K, Yoshioka K. Hemostatic effect of a heat-treated factor VIII concentrate (Haemate-P) in von Willebrand’s disease. Blut 1988; 56: 171-178
• 28 Berntorp E, Nilson IM. Use of a high-purity factor VIII concentrate (Hemate P) in von Willebrand’s disease. Vox Sang 1989; 56: 212-217
• 29 Ieko M, Sakurama S, Sagawa A, Yoshikawa M, Satoh M, Yasukouchi T, Nakagawa S. Effect of factor VIII concentrate on type IIB von Willebrand’s disease-associated thrombocytopenia presenting during pregnancy in identical twin mothers. Am J Hematol 1990; 35: 26-31
• 30 Scharrer I, Vigh T, Aygoren-Pursun E. Experience with Haemate P in von Willebrand’s disease in adults. Haemostasis 1994; 24: 298-303
• 31 Kreuz W, Mentzer D, Becker S, Scharrer I, Komhuber B, Haemate P. in children with von Willebrand’s disease. Haemostasis 1994; 24: 304-310
• 32 Cumming AM, Fildes S, Cumming IR, Wensley RT, Redding OM, Bum AM. Clinical and laboratory evaluation of National Health Service factor VIII concentrate (8Y) for the treatment of von Willebrand’s disease. Br J Haematol 1990; 75: 234-239
• 33 Pasi KJ, Williams MD, Enayat MS, Hill FGH. Clinical and laboratory evaluation of the treatment of von Willebrand’s disease patients with heat-treated factor VIII concentrate (BPL 8Y). Brit J Haematol 1990; 75: 228-233
• 34 Hanna WT, Bona RD, Zimmerman CE, Carta CA, Hebert GZ, Rickies FR. The use of intermediate and high purity factor VIII products in the treatment of von Willebrand disease. Thromb Haemost 1994; 71: 173-179
• 35 Mannucci PM, Chediak J, Byrnes J, Kessler C, Marciniak E, Hanna W, Retzios AD. and the Alphanate study Group A high purity factor VIII concentrate in the treatment of von Willebrand’s disease. Blood 1996; (Suppl. 088) 1: 1309 (abst)
• 36 Goudemand J, Mazurier C, Marey A, Caron C, Coupez B, Mizon P, Goudemand M. Clinical and biological evaluation in von Willebrand’s disease of a von Willebrand factor concentrate with low factor VIII activity. Brit J Haematol 1992; 80: 214-221
• 37 Scott JP, Montgomery RR. Therapy of von Willebrand disease. Semin Thromb Hemost 1993; 19: 37-47