Literature DB >> 21115138

Acquired hemophilia a: diagnosis, aetiology, clinical spectrum and treatment options.

Shrimati Shetty1, Manali Bhave, Kanjaksha Ghosh.   

Abstract

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 VIIa (rFVIIa, NovoSeven®) and activated prothrombin complex concentrate (aPCC, (FEIBA®) 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.
Copyright © 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 21115138     DOI: 10.1016/j.autrev.2010.11.005

Source DB:  PubMed          Journal:  Autoimmun Rev        ISSN: 1568-9972            Impact factor:   9.754


  32 in total

Review 1.  Protective role of anti-idiotypic antibodies in autoimmunity--lessons for type 1 diabetes.

Authors:  Christiane S Hampe
Journal:  Autoimmunity       Date:  2012-02-23       Impact factor: 2.815

2.  Acquired haemophilia A with a recalcitrant high-titre factor VIII inhibitor in the setting of interstitial lung disease.

Authors:  Lova Sun; David B Sykes
Journal:  BMJ Case Rep       Date:  2017-07-28

3.  A bispecific antibody to factors IXa and X restores factor VIII hemostatic activity in a hemophilia A model.

Authors:  Takehisa Kitazawa; Tomoyuki Igawa; Zenjiro Sampei; Atsushi Muto; Tetsuo Kojima; Tetsuhiro Soeda; Kazutaka Yoshihashi; Yukiko Okuyama-Nishida; Hiroyuki Saito; Hiroyuki Tsunoda; Tsukasa Suzuki; Hideki Adachi; Taro Miyazaki; Shinya Ishii; Mika Kamata-Sakurai; Takeo Iida; Aya Harada; Keiko Esaki; Miho Funaki; Chifumi Moriyama; Eriko Tanaka; Yasufumi Kikuchi; Tetsuya Wakabayashi; Manabu Wada; Masaaki Goto; Takeshi Toyoda; Atsunori Ueyama; Sachiyo Suzuki; Kenta Haraya; Tatsuhiko Tachibana; Yoshiki Kawabe; Midori Shima; Akira Yoshioka; Kunihiro Hattori
Journal:  Nat Med       Date:  2012-09-30       Impact factor: 53.440

4.  Acquired haemophilia A: the importance of early recognition in cases of spontaneous bleeding in the elderly.

Authors:  Neeral Patel; Zoe Wyrko; Syeda Naqvi; Adam P Croft
Journal:  BMJ Case Rep       Date:  2014-11-20

Review 5.  Spontaneous multilevel airway haemorrhage in acquired haemophilia A.

Authors:  Anna See; Siti Radhziah Sudirman; Xin Yong Huang
Journal:  Eur Arch Otorhinolaryngol       Date:  2016-08-30       Impact factor: 2.503

6.  Rhesus monkeys and baboons develop clotting factor VIII inhibitors in response to porcine endothelial cells or islets.

Authors:  John M Stewart; Alice F Tarantal; Wayne J Hawthorne; Evelyn J Salvaris; Philip J O'Connell; Mark B Nottle; Anthony J F d'Apice; Peter J Cowan; Mary Kearns-Jonker
Journal:  Xenotransplantation       Date:  2014-05-08       Impact factor: 3.907

7.  Acquired hemophilia A associated with autoimmune pancreatitis with serum IgG4 elevation.

Authors:  Taisuke Narazaki; Shojiro Haji; Yasuhiro Nakashima; Yasuhiro Tsukamoto; Mariko Tsuda; Akiko Takamatsu; Hirofumi Ohno; Takamitsu Matsushima; Tomoko Matsumoto; Keiji Nogami; Midori Shima; Motoaki Shiratsuchi; Yoshihiro Ogawa
Journal:  Int J Hematol       Date:  2018-03-26       Impact factor: 2.490

8.  Treatment of chronic lymphocytic leukemia/small lymphocytic lymphoma presenting simultaneously with acquired hemophilia and warm autoimmune hemolytic anemia.

Authors:  Chelsea Williams; Christian Cable; Julia Choi
Journal:  Proc (Bayl Univ Med Cent)       Date:  2017-07

9.  [Spontaneous hematoma and hip pain in a 65-year old patient].

Authors:  C Sucker; S Korfmacher; M Papp-Váry; C Grieser; H Riess
Journal:  Internist (Berl)       Date:  2012-10       Impact factor: 0.743

10.  Acquired inhibitors: a special case of bleeding in older adults.

Authors:  Richard G Stefanacci
Journal:  Curr Gerontol Geriatr Res       Date:  2012-11-29
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