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The use of heat-treated factor VIII-concentrates in von willebrand's disease

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Summary

In vitro investigations have demonstrated a high F VIII:Rcof potency and a high F VIII:Rcof/F VIII R:Ag ratio of two heat-treated F VIII concentrates. We therefore studied the in vivo effectiveness of these preparations (F VIII HSR, Behringwerke Marburg and F VIII HTR, Travenol) in five patients with von Willebrand's disease (vWd). In the steady state in vivo recoveries of F VIII:Rcof ranged from 73–153% after transfusion of F VIII HSR and from 11.5–17% after F VIII HTR respectively. The gain of F VIII-complex after F VIII HS was comparable to cryopecipitate (KryobulinR SP, Immuno AG Wien). All three products shortened the bleeding-time. Three of our five patients underwent surgery (Billroth I, papillotomy, laparatomy, open heart surgery) under F VIII HS cover without bleeding complications. The dose applied ranged from 20 to 40 U/kg at 8 or 12 h intervals for a period of approx. 14 days. Serum-transaminase elevations were observed in two of four patients after F VIII HT treatment. Although the risk of hepatitis of heat-treated F VIII concentrates remains to be determined, these products proved to be effective in vWd. The major advantages of these preparations are stability, rapid solubility, a low content of contaminating proteins, and a rapid, general availability.

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References

  1. Blatt PM, Brinkhous KM, Culp HR, Krauss JS, Roberts HR (1976) Antihemophilic factor concentrate therapy in von Willebrand disease. JAMA 236: 2770–2772

    Google Scholar 

  2. Chediak JR, Telfer MC, Green D (1977) Platelet function and immunologic parameters in von Willebrand's disease following cryoprecipitate and factor VIII concentrate infusion. Am J Med 62: 369–376

    Google Scholar 

  3. Green D, Potter EV (1976) Failure of AHF concentrate to control bleeding in von Willebrand's disease. Am J Med 60: 357–360

    Google Scholar 

  4. Holberg L, Borge L, Nilsson IM (1981) Factor VIII: C and factor VIII: CAg response in patients with hemophilia A and von Willebrand's disease after administration of different factor VIII concentrates or plasma. Br J Haematol 47: 587–596

    Google Scholar 

  5. Mielke CH, Kaneshiro MM, Maher IA, Weiner JM, Rapaport SI (1969) The standardized normal Ivy bleeding time and its prolongation by aspirin. Blood 34: 204–215

    Google Scholar 

  6. Miyashita C, Hellstern P, Köhler M, von Blohn G, Wenzel E (1984) In vitro characterization of commercial factor VIII concentrates. Blut 49: 53–59

    Google Scholar 

  7. Nilsson IM, Hedner U (1977) Characteristics of various factor VIII concentrates used in treatment of hemophilia A. Br J Haematol 37: 543–557

    Google Scholar 

  8. Perkins HA (1967) Correction of the hemostatic defects in von Willebrand's disease. Blood 30: 375–380

    Google Scholar 

  9. Schimpf K (1984) Hämophilie und Lebererkrankung. Hämostaseologie 4: 58–62

    Google Scholar 

  10. Weiss HJ (1974) Relation of von Willebrand factor to bleeding time. N Engl J Med 291: 420

    Google Scholar 

  11. Zimmermann TS, Ruggeri ZM (1982) Von Willebrand's disease. In: Spaet TH (ed) Progress in Hemostasis and Thrombosis. Grune and Stratton, pp 203–236

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Köhler, M., Hellstern, P. & Wenzel, E. The use of heat-treated factor VIII-concentrates in von willebrand's disease. Blut 50, 25–27 (1985). https://doi.org/10.1007/BF00319766

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