Combination of FVIII and by-passing agent potentiates in vitro thrombin production in haemophilia A inhibitor plasma

被引:26
作者
Klintman, Jenny [1 ]
Astermark, Jan [1 ]
Berntorp, Erik [1 ]
机构
[1] Lund Univ, Skane Univ Hosp, Dept Coagulat Disorders, SE-20502 Malmo, Sweden
关键词
thrombin generation; inhibitors; haemophilia A; factor VIII concentrates; by passing agents; RECOMBINANT FACTOR VIIA; VON-WILLEBRAND-FACTOR; PROTHROMBIN COMPLEX CONCENTRATE; TISSUE FACTOR; SEQUENTIAL THERAPY; GENERATION ASSAY; PATIENT; FEIBA; MANAGEMENT; EXPERIENCE;
D O I
10.1111/j.1365-2141.2010.08378.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
P>The by-passing agents, recombinant activated factor VII (rFVIIa) and activated prothrombin complex concentrate (APCC), are important tools in the treatment of patients with haemophilia A and high-responding inhibitory antibodies. It has been observed clinically that in some patients undergoing immune tolerance induction the bleeding frequency decreases, hypothetically caused by a transient haemostatic effect of infused FVIII not measurable ex vivo. We evaluated how by-passing agents and factor VIII (FVIII) affect thrombin generation (TG) in vitro using plasma from 11 patients with severe haemophilia A and high titre inhibitors. Samples were spiked with combinations of APCC, rFVIIa and five different FVIII products. Combination of APCC and FVIII showed a synergistic effect in eliciting TG (P < 0 center dot 005) for four FVIII products. When rFVIIa and FVIII were combined the interaction between the preparations was found to be additive. APCC and rFVIIa were then combined without FVIII, resulting in an additive effect on thrombin production. Each product separately increased TG above baseline. In conclusion, the amount of thrombin formed in vitro by adding a by-passing agent, was higher in the presence of FVIII. Our findings support the use of FVIII in by-passing therapy to optimize the haemostatic effect.
引用
收藏
页码:381 / 386
页数:6
相关论文
共 30 条
[1]   Treatment of the bleeding inhibitor patient [J].
Astermark, J .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2003, 29 (01) :77-85
[2]   VWF/FVIII complex and the management of patient with inhibitors: from laboratory to clinical practice [J].
Berntorp, E. .
HAEMOPHILIA, 2007, 13 :69-72
[3]   Haemate P/Humate-P: a systematic review [J].
Berntorp, Erik .
THROMBOSIS RESEARCH, 2009, 124 :S11-S14
[4]   Major surgery in a severe haemophilia A patient with high titre inhibitor: use of the thrombin generation test in the therapeutic decision [J].
Dargaud, Y ;
Lienhart, A ;
Meunier, S ;
Hequet, O ;
Chavanne, H ;
Chamouard, V ;
Marin, S ;
Negrier, C .
HAEMOPHILIA, 2005, 11 (05) :552-558
[5]   Sequential therapy with activated prothrombin complex concentrate (FEIBA) and recombinant factor VIIa in a patient with severe haemophilia A, inhibitor presence and refractory bleeding [J].
Economou, M. ;
Teli, A. ;
Tzantzaroudi, A. ;
Tsatra, I. ;
Zavitsanakis, A. ;
Athanassiou-Metaxa, M. .
HAEMOPHILIA, 2008, 14 (02) :390-391
[6]   Influence of von Willebrand factor on the reactivity of human factor VIII inhibitors with factor VIII [J].
Gensana, M ;
Altisent, C ;
Aznar, JA ;
Casaña, P ;
Hernández, F ;
Jorquera, JI ;
Magallón, M ;
Massot, M ;
Puig, L .
HAEMOPHILIA, 2001, 7 (04) :369-374
[7]   From theory to practice: Applying current clinical knowledge and treatment strategies to the care of hemophilia A patients with inhibitors [J].
Gomperts, Edward D. ;
Astermark, Jan ;
Gringeri, Alessandro ;
Teitel, Jerome .
BLOOD REVIEWS, 2008, 22 :S1-S11
[8]   Influence of the type of factor VIII concentrate on the incidence of factor VIII inhibitors in previously untreated patients with severe hemophilia A [J].
Goudemand, J ;
Rothschild, C ;
Demiguel, V ;
Vinciguerrat, C ;
Lambert, T ;
Chambost, H ;
Borel-Derlon, A ;
Claeyssens, S ;
Laurian, Y ;
Calvez, T .
BLOOD, 2006, 107 (01) :46-51
[9]   Management of haemophilic patients with inhibitors in major orthopaedic surgery by immunadsorption, substitution of factor VIII and recombinant factor VIIa (NovoSeven®):: a single centre experience [J].
Habermann, B ;
Hochmuth, K ;
Hovy, L ;
Scharrer, I ;
Kurth, AHA .
HAEMOPHILIA, 2004, 10 (06) :705-712
[10]   von Willebrand factor in factor VIII concentrates protects against neutralization by factor VIII antibodies of haemophilia A patients [J].
Kallas, A ;
Talpsep, T .
HAEMOPHILIA, 2001, 7 (04) :375-380