Safety and efficacy of continuous infusion of a combined factor VIII -: von Willebrand factor (vWF) concentrate (Haemate-P™) in patients with von Willebrand disease

被引:37
作者
Lubetsky, A
Schulman, S
Varon, D
Martinowitz, U
Kenet, G
Gitel, S
Inbal, A [1 ]
机构
[1] Chaim Sheba Med Ctr, Inst Thrombosis & Hemostasis, IL-52621 Tel Hashomer, Israel
[2] Chaim Sheba Med Ctr, Sackler Sch Med, IL-52621 Tel Hashomer, Israel
[3] Karolinska Hosp, Dept Med, Haemophilia Ctr, S-10401 Stockholm, Sweden
关键词
D O I
10.1055/s-0037-1614448
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:229 / 233
页数:5
相关论文
共 20 条
[1]  
AUERSWALD G, 1995, THROMB HAEMOSTASIS, V73, P1024
[2]   USE OF A HIGH-PURITY FACTOR-VIII CONCENTRATE (HEMATE-P) IN VONWILLEBRANDS DISEASE [J].
BERNTORP, E ;
NILSSON, IM .
VOX SANGUINIS, 1989, 56 (04) :212-217
[3]  
BOWIE EJW, 1980, SCAND J HAEMATOL, V25, P87
[4]   ASSAY OF RISTOCETIN COFACTOR USING FIXED PLATELETS AND A PLATELET COUNTING TECHNIQUE [J].
EVANS, RJ ;
AUSTEN, DEG .
BRITISH JOURNAL OF HAEMATOLOGY, 1977, 37 (02) :289-294
[5]   HEMOSTATIC EFFECT OF A HEAT-TREATED FACTOR-VIII CONCENTRATE (HEMATE-P) IN VON-WILLEBRANDS DISEASE [J].
FUKUI, H ;
NISHINO, M ;
TERADA, S ;
NISHIKUBO, T ;
YOSHIOKA, A ;
KINOSHITA, S ;
NIINOMI, K ;
YOSHIOKA, K .
BLUT, 1988, 56 (04) :171-178
[6]  
HARDISTY RM, 1962, THROMB DIATH HAEMOST, V7, P215
[7]  
KREUZ W, 1994, HAEMOSTASIS, V24, P304
[8]   PHARMACOKINETICS OF A NEW HEAT-TREATED CONCENTRATE OF FACTOR-VIII ESTIMATED BY MODEL-INDEPENDENT METHODS [J].
LONGO, G ;
MATUCCI, M ;
MESSORI, A ;
MORFINI, M ;
ROSSIFERRINI, P .
THROMBOSIS RESEARCH, 1986, 42 (04) :471-476
[9]   Coagulation factor concentrates by continuous infusion [J].
Martinowitz, U ;
Schulman, S .
TRANSFUSION MEDICINE REVIEWS, 1997, 11 (01) :56-63
[10]  
Martinowitz U, 1994, INT J PEDIAT HEMATOL, V1, P471