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Träfflista för sökning "WFRF:(Varon D) srt2:(1995-1999)"

Sökning: WFRF:(Varon D) > (1995-1999)

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  • BARZILAI, A, et al. (författare)
  • Hepatitis E virus infection in hemophiliacs
  • 1995
  • Ingår i: Journal of medical virology. - : Wiley. - 0146-6615 .- 1096-9071. ; 46:2, s. 153-156
  • Tidskriftsartikel (refereegranskat)
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  • Heim, M, et al. (författare)
  • Multifocal pseudotumour in a single limb
  • 1997
  • Ingår i: Haemophilia : the official journal of the World Federation of Hemophilia. - : Wiley. - 1351-8216. ; 3:1, s. 50-53
  • Tidskriftsartikel (refereegranskat)
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  • Lee, C A, et al. (författare)
  • Prophylactic treatment in Sweden - Overtreatment or optimal model?
  • 1998
  • Ingår i: Haemophilia. - : Wiley. - 1351-8216. ; 4:4, s. 409-412
  • Tidskriftsartikel (refereegranskat)abstract
    • At the haemophilia centre in Malmo, Sweden, regular prophylactic treatment is begun at 1-1 1/4 years of age, before the onset of joint bleeds. The dose and dose interval are optimised by means of pharmacokinetic studies to determine the individual patient's FVIII or IX metabolism, the goal of maintaining a level > 1% of normal being taken as a guideline which experience has shown to yield satisfactory control of bleeding diathesis. An optimal model for prophylactic treatment needs to be applicable to haemophiliacs and acceptable to health authorities in a majority of the countries in the world. To fulfill these criteria, the Swedish model, which has been shown to yield most satisfactory outcome, can hopefully be further refined in the future. Were continuous infusion, using a recombinate concentrate with a prolonged half-life, technically feasible and socially acceptable to the child, we would probably have attained the optimal model of prophylactic treatment.
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  • Lubetsky, A, et al. (författare)
  • Safety and efficacy of continuous infusion of a combined factor VIII-von Willebrand factor (vWF) concentrate (Haemate-P) in patients with von Willebrand disease
  • 1999
  • Ingår i: Thrombosis and haemostasis. - : Georg Thieme Verlag KG. - 0340-6245 .- 2567-689X. ; 81:2, s. 229-233
  • Tidskriftsartikel (refereegranskat)abstract
    • We studied the safety and efficacy of treatment with continuous infusion of a von Willebrand factor (vWF) concentrate Haemate-P in patients with von Willebrand disease (vWD). Three patients with mild and 5 patients with severe forms of vWD, were treated with continuous infusion of Haemate-P by minipump. The indications for treatment were: to prevent bleeding during 9 surgical procedures or 1 vaginal delivery in 6 patients and to treat 2 bleeding episodes in 2 patients. The patients were monitored daily for factor VIII (FVIII:C) and ristocetin cofactor (vWF:RCo) levels and the infusion rate was adjusted to maintain the desired therapeutic level of vWF:RCo. The treatment was effective in preventing surgical bleeding and controlling bleeding episodes. All factor VIII:C and most of the vWF:RCo levels measured during the study period were above the target therapeutic levels. A significant decrease in clearance of FVIII:C and vWF:RCo was observed over the treatment period. Haemate-P consumption averaged 24.3 ± 7.9 vWF:RCo U/kg/day which is approximately half the expected dose had intermittent bolus injections been used. We suggest that continuous Haemate-P infusion is superior to intermittent bolus injections for the treatment of vWD patients by virtue of its efficiency, simplicity and considerable savings.
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