Recombinant factor VIIa to prevent surgical bleeding in factor XI deficiency

被引:43
作者
O'Connell, N. M. [1 ]
Riddell, A. F. [1 ]
Pascoe, G. [1 ]
Perry, D. J. [1 ]
Lee, C. A. [1 ]
机构
[1] UCL Royal Free & Univ Coll Med Sch, Katharine Dormandy Haemophilia Ctr & Haemostasis, London WC1E 6BT, England
关键词
factor XI deficiency; recombinant factor VIIa; surgery; thrombin generation; thromboelastography;
D O I
10.1111/j.1365-2516.2008.01663.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Factor XI (FXI) deficiency is associated with bleeding after invasive Procedures. Risks of human plasma-derived FXI replacement products include transfusion transmitted infection, thrombosis and fluid overload. This study was designed to test the hypothesis that recombinant factor VIIa (rFVIIa) is an effective haemostatic agent in patients with FXI deficiency undergoing surgery. Fourteen FXI deficient patients [five severely deficient (FXI:C < 20 U dL(-1)) and nine partially deficient (FXI:C 20-70 U dL(-1)] received rFVIIa to prevent surgical bleeding during five major, four minor and six dental procedures. Minor surgical and dental procedures were covered with two doses of rFVIIa (90 mu g kg(-1) iv.), the first pre-operatively and the second 4 h postoperatively. Major surgery was covered with 90 mu g kg(-1) i.v. two hourly for the first 24 h and four hourly for the second 24 h. Oral tranexamic acid was given for 7 days Postoperatively. Effective haemostasis was observed in all cases avid no alternative haemostatic agents or blood transfusions were required. Three adverse events were recorded; an acute cerebrovascular accident in a patient with a history of cardiovascular disease, ail allergic reaction and local phlebitis. In this study, rFVIIa Was an effective alternative to plasma-derived FXI replacement for the prevention of surgical bleeding in FXI deficient patients but rFVIIa may not be suitable for patients with pre-existing risk factors for thrombosis.
引用
收藏
页码:775 / 781
页数:7
相关论文
共 43 条
[1]   Comparative thrombotic event incidence after infusion of recombinant factor VIIa versus factor VII inhibitor bypass activity [J].
Aledort, LM .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2004, 2 (10) :1700-1708
[2]   DENTAL SURGERY IN PATIENTS WITH SEVERE FACTOR-XI DEFICIENCY WITHOUT PLASMA REPLACEMENT [J].
BERLINER, S ;
HOROWITZ, I ;
MARTINOWITZ, U ;
BRENNER, B ;
SELIGSOHN, U .
BLOOD COAGULATION & FIBRINOLYSIS, 1992, 3 (04) :465-468
[3]   The use of recombinant factor VIIa (NovoSeven®) in a patient with a factor XI deficiency and a circulating anticoagulant [J].
Billon, S ;
Le Niger, C ;
Escoffre-Barbe, M ;
Vicariot, M ;
Abgrall, JF .
BLOOD COAGULATION & FIBRINOLYSIS, 2001, 12 (07) :551-553
[4]   The management of factor XI deficiency [J].
Bolton-Maggs, PHB .
HAEMOPHILIA, 1998, 4 (04) :683-688
[5]  
BOLTONMAGGS PHB, 1995, THROMB HAEMOSTASIS, V73, P194
[6]   INHERITANCE AND BLEEDING IN FACTOR-XI DEFICIENCY [J].
BOLTONMAGGS, PHB ;
WANYIN, BY ;
MCCRAW, AH ;
SLACK, J ;
KERNOFF, PBA .
BRITISH JOURNAL OF HAEMATOLOGY, 1988, 69 (04) :521-528
[7]   THROMBOGENIC POTENTIAL OF FACTOR-XI CONCENTRATE [J].
BOLTONMAGGS, PHB ;
COLVIN, BT ;
SATCHI, G ;
LEE, CA ;
LUCAS, GS .
LANCET, 1994, 344 (8924) :748-749
[8]  
BOLTONMAGGS PHB, 1992, THROMB HAEMOSTASIS, V67, P314
[9]   Role of blood coagulation factor XI in downregulation of fibrinolysis [J].
Bouma, BN ;
Meijers, JCM .
CURRENT OPINION IN HEMATOLOGY, 2000, 7 (05) :266-272
[10]   Bleeding predictors in factor-XI-deficient patients [J].
Brenner, B ;
Laor, A ;
Lupo, H ;
Zivelin, A ;
Lanir, N ;
Seligsohn, U .
BLOOD COAGULATION & FIBRINOLYSIS, 1997, 8 (08) :511-515