Acquired hemophilia A: Diagnosis, aetiology, clinical spectrum and treatment options

被引:84
作者
Shetty, Shrimati [1 ]
Bhave, Manali [2 ]
Ghosh, Kanjaksha [1 ]
机构
[1] King Edward Mem Hosp, Natl Inst Immunohematol ICMR, Bombay 400012, Maharashtra, India
[2] Northwestern Univ, Feinberg Sch Med, Evanston, IL 60208 USA
关键词
Acquired hemophilia A; Autoantibodies; Immunosuppressive therapy; Factor VIII; Inhibitors; FACTOR-VIII INHIBITORS; RECOMBINANT FACTOR-VIIA; PORCINE FACTOR-VIII; CENTER DOCTORS ORGANIZATION; CRITICAL-APPRAISAL; BETHESDA ASSAY; UNITED-KINGDOM; ANTIBODIES; EXPERIENCE; RITUXIMAB;
D O I
10.1016/j.autrev.2010.11.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Acquired hemophilia A (AHA) is a rare disorder with an incidence of approximately 1 per million/year with a high mortality rate of more than 20%. The disease occurs due to autoantibodies against coagulation factor VIII (FVIII) which neutralize its procoagulant function and result in severe, often life-threatening bleeding. The antibodies arise in individuals with no prior history of hemophilia A. AHA may be associated with pregnancy, autoimmune diseases, malignancy, infections or medication and occurs most commonly in the elderly. Approximately 50% of the patients remain idiopathic with no known underlying pathological condition. Clinical manifestations include spontaneous hemorrhages into the skin, muscles or soft tissues or excessive bleeding during surgery. Hemarthrosis which is the hallmark of congenital severe hemophilia A seldom occurs in AHA. The diagnosis of AHA is based on the isolated prolongation of activated partial thromboplastin time (APTT) which does not normalize after the addition of normal plasma along with reduced FVIII levels. The treatment involves two aspects eradication of antibodies and maintaining effective hemostasis during a bleeding episode. The protocols for eradication of antibodies include immunoadsorption, immunosuppression or immune tolerance induction (ITI). The treatment of acute bleeding episodes involves use of different bypassing agents like recombinant activated factor Vila (rFVIIa, NovoSeven (R)) and activated prothrombin complex concentrate (aPCC, (FEIBA (R)) in case of patients with high titer inhibitors or with antifibrinolytics, 1-deamino-8-D-arginine vasopressin (DDAVP) or FVIII concentrates in low titer inhibitor patients. The anti CD20 monoclonal antibody, rituximab, has shown very good results either singly or in combination with immunosuppressive regimens in patients who do not respond to standard immunosuppressors. The present review summarizes the diagnostic, aetiological, clinical and treatment aspects of AHA focusing on the recent advances in this area. (c) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:311 / 316
页数:6
相关论文
共 72 条
[1]
Rituximab for autoimmune haemophilia: a proposed treatment algorithm [J].
Aggarwal, A ;
Grewal, R ;
Green, RJ ;
Boggio, L ;
Green, D ;
Weksler, BB ;
Wiestner, A ;
Schechter, GP .
HAEMOPHILIA, 2005, 11 (01) :13-19
[2]
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
[3]
Angchaisuksiri P, 1993, Southeast Asian J Trop Med Public Health, V24 Suppl 1, P152
[4]
Successful treatment of acquired factor VIII inhibitor with cyclosporin [J].
Au, WY ;
Lam, CCK ;
Kwong, YL .
HAEMOPHILIA, 2004, 10 (01) :98-100
[5]
BAUDO F, 2007, ACQUIRED HAEMOPHILIA, P389
[6]
BROXSON EH, 1987, THROMB HAEMOSTASIS, V57, P126
[7]
Review of clinical experience of desmopressin in patients with congenital and acquired bleeding disorders [J].
Cattaneo, M .
EUROPEAN JOURNAL OF ANAESTHESIOLOGY, 1997, 14 :10-14
[8]
A population based, unselected, consecutive cohort of patients with acquired haemophilia A [J].
Collins, P ;
Macartney, N ;
Davies, R ;
Lees, S ;
Giddings, J ;
Majer, R .
BRITISH JOURNAL OF HAEMATOLOGY, 2004, 124 (01) :86-90
[9]
Consensus recommendations for the diagnosis and treatment of acquired hemophilia A [J].
Collins P. ;
Baudo F. ;
Huth-Kühne A. ;
Ingerslev J. ;
Kessler C.M. ;
Castellano M.E.M. ;
Shima M. ;
St-Louis J. ;
Lévesque H. .
BMC Research Notes, 3 (1)
[10]
Acquired hemophilia A in the United Kingdom: a 2-year national surveillance study by the United Kingdom Haemophilia Centre Doctors' Organisation [J].
Collins, Peter W. ;
Hirsch, Sybil ;
Baglin, Trevor P. ;
Dolan, Gerard ;
Hanley, John ;
Makris, Michael ;
Keeling, David M. ;
Liesner, Ri ;
Brown, Simon A. ;
Hay, Charles R. M. .
BLOOD, 2007, 109 (05) :1870-1877