Lee Soo Eon, Choi Yoon Ji, Chi Seong-In, Kim Hyun-Jeong, Seo Kwang-Suk
Department of Dental Anesthesiology, Seoul National University Dental Hospital, Seoul, Korea.
J Dent Anesth Pain Med. 2015 Mar;15(1):25-29. doi: 10.17245/jdapm.2015.15.1.25. Epub 2015 Mar 31.
Factor XI deficiency (Hemophilia C) is a very rare autosomal recessive bleeding disorder. Patients with factor XI deficiency do not typically show any spontaneous bleeding or specific symptoms. Sometimes those who have this disorder are identified during special situations such as trauma or surgery. Orthognathic surgery is particularly associated with a high bleeding risk. Therefore, great care must be taken when treating patients with bleeding disorders such as factor XI deficiency. There are a few reports that address the management of patients with bleeding disorders during orthognathic surgery. The current report describes a patient with factor XI deficiency who underwent Le Fort I osteotomy together with bilateral sagittal split osteotomy. The patient's condition was assessed using both rotation thromboelastometry (ROTEM™) and noninvasive measurements of total hemoglobin (SpHb) using Masimo Radical 7 (Masimo Co. CA, USA).
因子 XI 缺乏症(血友病 C)是一种非常罕见的常染色体隐性出血性疾病。因子 XI 缺乏症患者通常不会出现任何自发性出血或特定症状。有时,患有这种疾病的人是在创伤或手术等特殊情况下被发现的。正颌手术尤其具有较高的出血风险。因此,在治疗患有因子 XI 缺乏症等出血性疾病的患者时必须格外小心。有一些报告涉及正颌手术期间出血性疾病患者的管理。本报告描述了一名患有因子 XI 缺乏症的患者,该患者接受了 Le Fort I 截骨术和双侧矢状劈开截骨术。使用旋转血栓弹力图(ROTEM™)和使用 Masimo Radical 7(美国加利福尼亚州 Masimo 公司)对总血红蛋白(SpHb)进行无创测量来评估患者的病情。