Surgery and inhibitor development in hemophilia A: a systematic review

被引:57
作者
Eckhardt, C. L. [1 ,2 ]
van der Bom, J. G. [3 ,4 ]
Van der Naald, M. [2 ]
Peters, M. [1 ]
Kamphuisen, P. W. [2 ]
Fijnvandraat, K. [1 ]
机构
[1] Emma Childrens Hosp, Acad Med Ctr, Dept Pediat Hematol, Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Vasc Med, NL-1105 AZ Amsterdam, Netherlands
[3] Leiden Univ, Med Ctr, Jon J van Rood Ctr Clin Transfus Res, Leiden, Netherlands
[4] Leiden Univ, Med Ctr, Dept Clin Epidemiol, Leiden, Netherlands
关键词
antibody; hemophilia A; intensive FVIII exposure; risk factor; surgery; systematic review; PREVIOUSLY UNTREATED PATIENTS; RECOMBINANT FACTOR-VIII; PREVIOUSLY TREATED PATIENTS; QUALITY-OF-LIFE; RISK-FACTORS; CLINICAL-EVALUATION; IMMUNE TOLERANCE; SAFETY; CHILDREN; EFFICACY;
D O I
10.1111/j.1538-7836.2011.04467.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Although the association between intensive treatment and the formation of inhibiting antibodies towards factor VIII (FVIII) in hemophilia A has been demonstrated, the contributing effect of surgery is presently unclear. The release of immunological danger signals resulting from tissue damage during surgery in the presence of a high FVIII antigen load may elicit the formation of FVIII antibodies. The aim of this systematic review was to investigate the role of surgery in the inhibitor risk associated with intensive treatment as compared with treatment for bleeding and prophylactic administration of FVIII. Methods: A comprehensive literature search was performed that identified four cohort studies and three case control studies, comprising 342 inhibitor patients among a total of 957 hemophilia A patients. Results: Intensive treatment increased the inhibitor risk, most pronounced with intensive treatment of >= 5 exposure days (EDs) compared with < 3 EDs (OR, 4.1; 95% confidence interval, 2.6-6.5). Pooled odds ratio for inhibitor development in severe hemophilia patients that received intensive treatment for surgery at first exposure was 4.1 (95% confidence interval, 2.0-8.4) compared with treatment for bleeding or prophylaxis. Information on continuous infusion, previously treated patients and non-severe hemophilia A was insufficient for valid meta-analyses. Conclusions: Intensive FVIII treatment for surgery at first exposure leads to a higher inhibitor risk in hemophilia A patients compared with intensive treatment for bleeding.
引用
收藏
页码:1948 / 1958
页数:11
相关论文
共 45 条
[1]   Non-genetic risk factors and the development of inhibitors in haemophilia: a comprehensive review and consensus report [J].
Astermark, J. ;
Altisent, C. ;
Batorova, A. ;
Diniz, M. J. ;
Gringeri, A. ;
Holme, P. A. ;
Karafoulidou, A. ;
Lopez-Fernandez, M. F. ;
Reipert, B. M. ;
Rocino, A. ;
Schiavoni, M. ;
von Depka, M. ;
Windyga, J. ;
Fijnvandraat, K. .
HAEMOPHILIA, 2010, 16 (05) :747-766
[2]   The orthopaedic status of severe haemophiliacs in Spain [J].
Aznar, JA ;
Magallón, M ;
Querol, F ;
Gorina, E ;
Tusell, JM .
HAEMOPHILIA, 2000, 6 (03) :170-176
[3]  
BRAY GL, 1994, BLOOD, V83, P2428
[4]   Understanding inhibitor development in haemophilia A: towards clinical prediction and prevention strategies [J].
Coppola, A. ;
Santoro, C. ;
Tagliaferri, A. ;
Franchini, M. ;
Di Minno, G. .
HAEMOPHILIA, 2010, 16 :13-19
[5]   Clinical evaluation of B-domain deleted recombinant factor VIII in previously untreated patients [J].
Courter, SG ;
Bedrosian, CL .
SEMINARS IN HEMATOLOGY, 2001, 38 (02) :52-59
[6]  
Courter SG, 2001, SEMIN HEMATOL, V38, P44, DOI 10.1053/shem.2001.25893
[7]   Mild/moderate haemophilia A: new insights into molecular mechanisms and inhibitor development [J].
d'Oiron, R. ;
Pipe, S. W. ;
Jacquemin, M. .
HAEMOPHILIA, 2008, 14 :138-146
[8]   The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977-99 [J].
Darby, SC ;
Keeling, DM ;
Spooner, RJD ;
Kan, SW ;
Giangrande, PLF ;
Collins, PW ;
Hill, FGH ;
Hay, CRM .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2004, 2 (07) :1047-1054
[9]   Immune response against therapeutic factor VIII in hemophilia A patients - A survey of probable risk factors [J].
Dasgupta, Suryasarathi ;
Navarrete, Ana-Maria ;
Delignat, Sandrine ;
Wootla, Bharath ;
Andre, Sebastien ;
Nagaraja, Valakunja ;
Lacroix-Desmazes, Sebastien ;
Kaveri, Srinivas V. .
IMMUNOLOGY LETTERS, 2007, 110 (01) :23-28
[10]   Intensive peri-operative use of factor VIII and the Arg593→Cys mutation are risk factors for inhibitor development in mild/moderate hemophilia A [J].
Eckhardt, C. L. ;
Menke, L. A. ;
van Ommen, C. H. ;
van der Lee, J. H. ;
Geskus, R. B. ;
Kamphuisen, P. W. ;
Peters, M. ;
Fijnvandraat, K. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2009, 7 (06) :930-937