Literature DB >> 3917697

The use of heat-treated Factor VIII-concentrates in von Willebrand's disease.

M Köhler, P Hellstern, E Wenzel.   

Abstract

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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Year:  1985        PMID: 3917697     DOI: 10.1007/bf00319766

Source DB:  PubMed          Journal:  Blut        ISSN: 0006-5242


  9 in total

1.  Failure of AHF concentration to control bleeding in von Willebrand's disease.

Authors:  D Green; E V Potter
Journal:  Am J Med       Date:  1976-03       Impact factor: 4.965

2.  Characteristics of various factor VIII concentrates used in treatment of haemophilia A.

Authors:  I M Nilsson; U Hedner
Journal:  Br J Haematol       Date:  1977-12       Impact factor: 6.998

3.  Platelet function and immunologic parameters in von Willebrand's disease following cryoprecipitate and factor VIII concentrate infusion.

Authors:  J R Chediak; M C Telfer; D Green
Journal:  Am J Med       Date:  1977-03       Impact factor: 4.965

4.  Letter: Relation of the von Willebrand factor to the bleeding time.

Authors:  H J Weiss
Journal:  N Engl J Med       Date:  1974-08-22       Impact factor: 91.245

5.  Correction of the hemostatic defects in Von Willebrand's disease.

Authors:  H A Perkins
Journal:  Blood       Date:  1967-09       Impact factor: 22.113

6.  The standardized normal Ivy bleeding time and its prolongation by aspirin.

Authors:  C H Mielke; M M Kaneshiro; I A Maher; J M Weiner; S I Rapaport
Journal:  Blood       Date:  1969-08       Impact factor: 22.113

7.  In vitro characterization of commercial Factor VIII concentrates: long-term follow-up.

Authors:  C Miyashita; P Hellstern; M Köhler; G von Blohn; E Wenzel
Journal:  Blut       Date:  1984-07

8.  Antihemophilic factor concentrate therapy in von Willebrand disease. Dissociation of bleeding-time factor and ristocetin-cofactor activities.

Authors:  P M Blatt; K M Brinkhous; H R Culp; J S Krauss; H R Roberts
Journal:  JAMA       Date:  1976-12-13       Impact factor: 56.272

9.  Factor VIII:C and VIII:CAg response in patients with haemophilia A and von Willebrand's disease after administration of different factor VIII concentrates or plasma.

Authors:  L Holmberg; L Borge; I M Nilsson
Journal:  Br J Haematol       Date:  1981-04       Impact factor: 6.998

  9 in total
  1 in total

1.  Hemostatic effect of a heat-treated factor VIII concentrate (Haemate P) in von Willebrand's disease.

Authors:  H Fukui; M Nishino; S Terada; T Nishikubo; A Yoshioka; S Kinoshita; K Niinomi; K Yoshioka
Journal:  Blut       Date:  1988-04
  1 in total

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