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抗血友病因子并非所有VIII因子缺乏症的唯一解决方案。一名甲型血友病患者发生牙源性感染的病例报告,该患者并发VIII因子抑制剂,并通过输注抗血友病因子和VIII因子抑制剂旁路活性进行治疗。

"Antihemophilic factor is not the only answer for all factor VIII deficiencies." Case report of odontogenic infection in a patient with hemophilia A, complicated by factor VIII inhibitors, and managed by transfusion of antihemophilic factor and factor VIII inhibitor bypass activity.

作者信息

Sudheesh K M, Bharani K S N Siva, Kiran H Y, Hanagavadi Suresh

机构信息

Department of Oral and Maxillofacial Surgery, College of Dental Sciences, Davangere, Karnataka, India.

Department of Pathology, J J M Medical College, Davangere, Karnataka, India.

出版信息

Indian J Dent. 2016 Sep;7(3):149-152. doi: 10.4103/0975-962X.186700.

Abstract

Dental extraction in hemophiliacs with acquired inhibitors is always a risky procedure, which often presents a lot of problems associated with bleeding. A known case of hemophilia A complicated with factor VIII inhibitors and having odontogenic infection was successfully managed by transfusion of factor VIII inhibitor bypass activity (FEIBA) and antihemophilic factor. Past medical history was significant for multiple factor VIII transfusions. Bethesda assay done to identify inhibitors revealed low titer factor VIII inhibitors. Extraction of the involved tooth was done after transfusion of FEIBA with low-dose protocols. Minimal bleeding was noted after extraction which was controlled by local measures. FEIBA was proven to be highly effective, and no side effects of the product were observed.

摘要

患有获得性抑制剂的血友病患者进行拔牙始终是一项有风险的操作,常常会出现许多与出血相关的问题。一名已知的甲型血友病合并因子VIII抑制剂且患有牙源性感染的病例,通过输注因子VIII抑制剂旁路活性制剂(FEIBA)和抗血友病因子成功得到治疗。既往病史显示有多次输注因子VIII的情况。为确定抑制剂而进行的贝塞斯达检测显示因子VIII抑制剂滴度较低。在按照低剂量方案输注FEIBA后拔除了患牙。拔牙后出血极少,通过局部措施得以控制。事实证明FEIBA非常有效,且未观察到该产品的副作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d712/5015568/e87797cade8d/IJDENT-7-149-g001.jpg

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