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Volumn 32, Issue 5, 2006, Pages 529-536

Composition, quality control, and labeling of plasma-derived products for the treatment of von Willebrand disease

Author keywords

Collagen binding activity; Factor concentrates; Ristocetin cofactor activity; Von Willebrand disease (vWD); Von Willebrand factor (vWF)

Indexed keywords

BIOSTATE; BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 8 CONCENTRATE; CONFACT F; EMOCLOT; FANDHI; KOATE DVI; VON WILLEBRAND FACTOR; WILATE; WILFACTIN;

EID: 33746595318     PISSN: 00946176     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-947868     Document Type: Article
Times cited : (15)

References (33)
  • 1
    • 33746639092 scopus 로고
    • A pilot plant for the preparation of a human plasma fraction containing the human antihaemophilic factor a (factor VIII) and von Willebrand's factor
    • Jorpes JE, Blombäck B, Blombäck M, et al. A pilot plant for the preparation of a human plasma fraction containing the human antihaemophilic factor A (factor VIII) and von Willebrand's factor. Acta Med Scand 1962;379(suppl): 7-21
    • (1962) Acta Med Scand , vol.379 , Issue.SUPPL. , pp. 7-21
    • Jorpes, J.E.1    Blombäck, B.2    Blombäck, M.3
  • 2
    • 0014123936 scopus 로고
    • Correction of the hemostatic effects in von Willebrand's disease
    • Perkins HA. Correction of the hemostatic effects in von Willebrand's disease. Blood 1967;30:375-380
    • (1967) Blood , vol.30 , pp. 375-380
    • Perkins, H.A.1
  • 3
    • 12344287493 scopus 로고
    • Antihemophilic factor concentrate therapy in von Willebrand disease: Dissociation of bleeding-time factor and ristocetin-cofactor activities
    • Blatt PM, Brinkhous KM, Culp HR, et al. Antihemophilic factor concentrate therapy in von Willebrand disease: dissociation of bleeding-time factor and ristocetin-cofactor activities. JAMA 1976;236:2770-2772
    • (1976) JAMA , vol.236 , pp. 2770-2772
    • Blatt, P.M.1    Brinkhous, K.M.2    Culp, H.R.3
  • 4
    • 0017106261 scopus 로고
    • Failure of AHF concentrate to control bleeding in von Willebrand's disease
    • Green D, Potter EV. Failure of AHF concentrate to control bleeding in von Willebrand's disease. Am J Med 1976;60: 357-360
    • (1976) Am J Med , vol.60 , pp. 357-360
    • Green, D.1    Potter, E.V.2
  • 5
    • 0025780906 scopus 로고
    • In vitro evaluation of a very-high-purity solvent/detergent treated, von Willebrand factor concentrate
    • Mazurier C, Jorieux S, de Romeuf C, et al. In vitro evaluation of a very-high-purity solvent/detergent treated, von Willebrand factor concentrate. Vox Sang 1991;61:1-7
    • (1991) Vox Sang , vol.61 , pp. 1-7
    • Mazurier, C.1    Jorieux, S.2    De Romeuf, C.3
  • 6
    • 0030736701 scopus 로고    scopus 로고
    • In vivo characterization of recombinant von Willebrand factor in dogs with von Willebrand disease
    • Turecek PL, Gritsch H, Pichler L, et al. In vivo characterization of recombinant von Willebrand factor in dogs with von Willebrand disease. Blood 1997;90:3555-3567
    • (1997) Blood , vol.90 , pp. 3555-3567
    • Turecek, P.L.1    Gritsch, H.2    Pichler, L.3
  • 7
    • 10744220312 scopus 로고    scopus 로고
    • Successful treatment for patients with von Willebrand disease undergoing urgent surgery using factor VIII/VWF concentrate (Humate P)
    • Thompson AR, Gill JC, Ewenstein BM, et al. Successful treatment for patients with von Willebrand disease undergoing urgent surgery using factor VIII/VWF concentrate (Humate P). Haemophilia 2004;10:42-51
    • (2004) Haemophilia , vol.10 , pp. 42-51
    • Thompson, A.R.1    Gill, J.C.2    Ewenstein, B.M.3
  • 8
    • 10744230522 scopus 로고    scopus 로고
    • Successful treatment of urgent bleeding in von Willebrand disease with factor VIII/VWF concentrate (Humate-P®): Use of the ristocetin cofactor assay (VWF:RCo) to measure potency and to guide therapy
    • Gill JC, Ewenstein BM, Thompson AR, et al. Successful treatment of urgent bleeding in von Willebrand disease with factor VIII/VWF concentrate (Humate-P®): use of the ristocetin cofactor assay (VWF:RCo) to measure potency and to guide therapy. Haemophilia 2003;9:688-695
    • (2003) Haemophilia , vol.9 , pp. 688-695
    • Gill, J.C.1    Ewenstein, B.M.2    Thompson, A.R.3
  • 9
    • 0037079717 scopus 로고    scopus 로고
    • Treatment of von Willebrand disease with a high-purity factor VIII/von Willebrand factor concentrate: A prospective, multicenter study
    • Mannucci PM, Chediak J, Hanna W, et al. Treatment of von Willebrand disease with a high-purity factor VIII/von Willebrand factor concentrate: a prospective, multicenter study. Blood 2002;99:450-456
    • (2002) Blood , vol.99 , pp. 450-456
    • Mannucci, P.M.1    Chediak, J.2    Hanna, W.3
  • 10
    • 0036166457 scopus 로고    scopus 로고
    • Efficacy and safety of the factor VIII/von Willebrand factor concentrate, Haemate-P/Humate-P: Ristocetin cofactor unit dosing in patients with von Willebrand disease
    • Lillicrap D, Poon MC, Walker I, et al. Efficacy and safety of the factor VIII/von Willebrand factor concentrate, Haemate-P/Humate-P: ristocetin cofactor unit dosing in patients with von Willebrand disease. Thromb Haemost 2002;87:224-230
    • (2002) Thromb Haemost , vol.87 , pp. 224-230
    • Lillicrap, D.1    Poon, M.C.2    Walker, I.3
  • 11
    • 6644224638 scopus 로고    scopus 로고
    • Management of von Willebrand disease: A survey on current clinical practice from the haemophilia centres of North America
    • Cohen AJ, Kessler CM, Ewenstein BM, et al. Management of von Willebrand disease: a survey on current clinical practice from the haemophilia centres of North America. Haemophilia 2001;7:235-241
    • (2001) Haemophilia , vol.7 , pp. 235-241
    • Cohen, A.J.1    Kessler, C.M.2    Ewenstein, B.M.3
  • 12
    • 0036119808 scopus 로고    scopus 로고
    • Successful surgical hemostasis in patients with von Willebrand disease following infusion of Koate® DVI
    • Srivastava A, Mathews V, Bhurani D, et al. Successful surgical hemostasis in patients with von Willebrand disease following infusion of Koate® DVI. Thromb Haemost 2002;87:541-543
    • (2002) Thromb Haemost , vol.87 , pp. 541-543
    • Srivastava, A.1    Mathews, V.2    Bhurani, D.3
  • 13
    • 19944386220 scopus 로고    scopus 로고
    • Management of von Willebrand disease with factor VIII/von Willebrand factor concentrates: Results from current studies and surveys
    • Federici AB. Management of von Willebrand disease with factor VIII/von Willebrand factor concentrates: results from current studies and surveys. Blood Coagul Fibrinolysis 2005; 16:S17-S21
    • (2005) Blood Coagul Fibrinolysis , vol.16
    • Federici, A.B.1
  • 16
    • 2342591992 scopus 로고    scopus 로고
    • A comparative in vitro evaluation of six von Willebrand factor concentrates
    • Lethagen S, Carlson M, Hillarp A. A comparative in vitro evaluation of six von Willebrand factor concentrates. Haemophilia 2004;10:243-249
    • (2004) Haemophilia , vol.10 , pp. 243-249
    • Lethagen, S.1    Carlson, M.2    Hillarp, A.3
  • 17
    • 0034490066 scopus 로고    scopus 로고
    • Von Willebrand factor-cleaving protease activity in congenital thrombotic thrombocytopenic purpura
    • Allford SL, Harrison P, Lawrie AS, et al. Von Willebrand factor-cleaving protease activity in congenital thrombotic thrombocytopenic purpura. Br J Haematol 2000;111:1215-1222
    • (2000) Br J Haematol , vol.111 , pp. 1215-1222
    • Allford, S.L.1    Harrison, P.2    Lawrie, A.S.3
  • 18
    • 0036713595 scopus 로고    scopus 로고
    • Venous thrombosis following the use of intermediate purity FVIII concentrate to treat patients with von Willebrand's disease
    • Makris M, Colvin B, Gupta V, et al. Venous thrombosis following the use of intermediate purity FVIII concentrate to treat patients with von Willebrand's disease. Thromb Haemost 2002;88:387-388
    • (2002) Thromb Haemost , vol.88 , pp. 387-388
    • Makris, M.1    Colvin, B.2    Gupta, V.3
  • 19
    • 0036712293 scopus 로고    scopus 로고
    • Venous thromboembolism in von Willebrand disease
    • Mannucci PM. Venous thromboembolism in von Willebrand disease. Thromb Haemost 2002;88:378-379
    • (2002) Thromb Haemost , vol.88 , pp. 378-379
    • Mannucci, P.M.1
  • 20
    • 1842524080 scopus 로고    scopus 로고
    • In vitro study of a triple-secured von Willebrand factor concentrate
    • Mazurier C, Poulle M, Samor B, et al. In vitro study of a triple-secured von Willebrand factor concentrate. Vox Sang 2004;86:100-104
    • (2004) Vox Sang , vol.86 , pp. 100-104
    • Mazurier, C.1    Poulle, M.2    Samor, B.3
  • 21
    • 0036120805 scopus 로고    scopus 로고
    • A comparative multi-laboratory assessment of three factor VIII/von Willebrand factor concentrates
    • Favaloro EJ, Bukuya M, Martinelli T, et al. A comparative multi-laboratory assessment of three factor VIII/von Willebrand factor concentrates. Thromb Haemost 2002;87:466-476
    • (2002) Thromb Haemost , vol.87 , pp. 466-476
    • Favaloro, E.J.1    Bukuya, M.2    Martinelli, T.3
  • 22
    • 0030748121 scopus 로고    scopus 로고
    • New treatments of von Willebrand disease: Plasma derived von Willebrand factor concentrates
    • Menache D, Aronson DL. New treatments of von Willebrand disease: plasma derived von Willebrand factor concentrates. Thromb Haemost 1997;78:566-570
    • (1997) Thromb Haemost , vol.78 , pp. 566-570
    • Menache, D.1    Aronson, D.L.2
  • 23
    • 3543046522 scopus 로고    scopus 로고
    • Comparison von Willebrand factor activities measured by ristocetin cofactor assay and two different VWF-collagen-binding-assays in VWF/FVIII-concentrates
    • abst
    • Suiter P, Budde U, Metzner HJ, et al. Comparison von Willebrand factor activities measured by ristocetin cofactor assay and two different VWF-collagen-binding-assays in VWF/FVIII-concentrates. J Thromb Haemost 2003:(suppl; abst):1667
    • (2003) J Thromb Haemost , vol.1667 , Issue.SUPPL.
    • Suiter, P.1    Budde, U.2    Metzner, H.J.3
  • 24
    • 0033985083 scopus 로고    scopus 로고
    • Collagen binding assay for von Willebrand factor (VWF: CBA): Detection of von Willebrand Disease (VWD), and discrimination of VWD subtypes, depends on collagen source
    • Favaloro EJ. Collagen binding assay for von Willebrand factor (VWF: CBA): detection of von Willebrand Disease (VWD), and discrimination of VWD subtypes, depends on collagen source. Thromb Haemost 2000;83:127-135
    • (2000) Thromb Haemost , vol.83 , pp. 127-135
    • Favaloro, E.J.1
  • 25
    • 0036853012 scopus 로고    scopus 로고
    • A collagen binding assay, an additional method for von Willebrand factor activity in therapeutic concentrates
    • Neugebauer BM, Goy C, Seitz R. A collagen binding assay, an additional method for von Willebrand factor activity in therapeutic concentrates. Thromb Haemost 2002;88:871-872
    • (2002) Thromb Haemost , vol.88 , pp. 871-872
    • Neugebauer, B.M.1    Goy, C.2    Seitz, R.3
  • 26
    • 0036713328 scopus 로고    scopus 로고
    • Standardisation of von Willebrand factor in therapeutic concentrates: Calibration of the 1st International standard for von Willebrand factor concentrate (00/514)
    • Hubbard AR, Dands D, Chang AC, et al. Standardisation of von Willebrand factor in therapeutic concentrates: calibration of the 1st International standard for von Willebrand factor concentrate (00/514). Thromb Haemost 2002;88: 380-386
    • (2002) Thromb Haemost , vol.88 , pp. 380-386
    • Hubbard, A.R.1    Dands, D.2    Chang, A.C.3
  • 27
    • 0023226902 scopus 로고
    • 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
    • Mannucci PM, Moia M, Rebulla P, et al. 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
    • (1987) Am J Hematol , vol.25 , pp. 55-65
    • Mannucci, P.M.1    Moia, M.2    Rebulla, P.3
  • 28
    • 25344445472 scopus 로고    scopus 로고
    • Determination of high-molecular-weight von Willebrand factor multimers and their impact on specific VWF-activities in VWF/FVIII concentrates
    • abst
    • Walter O, Budde U, Muysers C, et al. Determination of high-molecular-weight von Willebrand factor multimers and their impact on specific VWF-activities in VWF/FVIII concentrates. J Thromb Haemost 2003(suppl: abst):1673
    • (2003) J Thromb Haemost , Issue.SUPPL. , pp. 1673
    • Walter, O.1    Budde, U.2    Muysers, C.3
  • 29
    • 27844521329 scopus 로고    scopus 로고
    • Characterization, classification, and treatment of von Willebrand diseases: A critical appraisal of the literature and personal experiences
    • Michiels JJ, Gadisseur A, Budde U, et al. Characterization, classification, and treatment of von Willebrand diseases: a critical appraisal of the literature and personal experiences. Semin Thromb Hemost 2005;31:577-601
    • (2005) Semin Thromb Hemost , vol.31 , pp. 577-601
    • Michiels, J.J.1    Gadisseur, A.2    Budde, U.3
  • 30
    • 0030841895 scopus 로고    scopus 로고
    • Plasma derived von Willebrand factor preparations: Collagen binding and ristocetin cofactor activities
    • Chang P, Aronson DL. Plasma derived von Willebrand factor preparations: collagen binding and ristocetin cofactor activities. Thromb Haemost 1997;78:930-933
    • (1997) Thromb Haemost , vol.78 , pp. 930-933
    • Chang, P.1    Aronson, D.L.2
  • 31
    • 33746593234 scopus 로고    scopus 로고
    • Project on the von Willebrand factor monograph
    • 17.1
    • European Directorate for the Quality of Medicines. Project on the von Willebrand factor monograph. Pharmeuropa 2005; 17.1:90-92
    • (2005) Pharmeuropa , pp. 90-92
  • 32
    • 22244493905 scopus 로고    scopus 로고
    • Haemostatic management of intraoral bleeding in patients with von Willebrand disease
    • Morimoto Y, Yoshioka A, Sugimoto M, et al. Haemostatic management of intraoral bleeding in patients with von Willebrand disease. Oral Dis 2005;11:243-248
    • (2005) Oral Dis , vol.11 , pp. 243-248
    • Morimoto, Y.1    Yoshioka, A.2    Sugimoto, M.3
  • 33
    • 0032860887 scopus 로고    scopus 로고
    • Laboratory testing for von Willebrand's disease: An assessment of current diagnostic practice and efficacy by means of a multi-laboratory survey
    • Favaloro EJ, Smith J, Petinos Pet al., on behalf of the RCPA Quality Assurance Program (QAP) in Hematology Scientific Hemostasis Advisory Panel.. Laboratory testing for von Willebrand's disease: an assessment of current diagnostic practice and efficacy by means of a multi-laboratory survey. Thromb Haemost 1999;82:1276-1282
    • (1999) Thromb Haemost , vol.82 , pp. 1276-1282
    • Favaloro, E.J.1    Smith, J.2    Petinos, P.3


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