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

机译:获得性血友病:诊断,病因,临床范围和治疗选择。

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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(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.
机译:获得性血友病A(AHA)是一种罕见疾病,发病率约为百万分之一/年,死亡率高出20%以上。该疾病的发生是由于抗凝血因子VIII(FVIII)的自身抗体引起的,该抗体中和了其促凝血功能,并导致严重的,常常危及生命的出血。该抗体在没有血友病A病史的个体中出现。AHA可能与怀孕,自身免疫性疾病,恶性肿瘤,感染或药物治疗相关,并且最常见于老年人。大约50%的患者保持特发性,没有已知的潜在病理状况。临床表现包括手术中皮肤,肌肉或软组织自发性出血或大量出血。先天性严重血友病的标志性血友病AHA中很少发生。 AHA的诊断基于活化的部分凝血活酶时间(APTT)的孤立延长,该时间在添加正常血浆和降低的FVIII水平后无法正常化。治疗涉及两个方面:消除抗体和在出血发作期间维持有效止血。消除抗体的方案包括免疫吸附,免疫抑制或免疫耐受诱导(ITI)。急性出血发作的治疗涉及使用不同的绕过剂,例如重组滴定的激活因子VIIa(rFVIIa,NovoSeven)和激活的凝血酶原复合物浓缩物(aPCC(FEIBA)),如果患者使用高滴度抑制剂或抗纤溶蛋白,1-deamino-8-D-精氨酸加压素(DDAVP)或FVIII集中在低滴度抑制剂患者中,抗CD20单克隆抗体利妥昔单抗在无反应的患者中单独或联合免疫抑制方案均显示出良好的效果本综述总结了AHA的诊断,病因,临床和治疗方面,重点是该领域的最新进展。

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