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Factor XI deficiency and orthognathic surgery: a case report on anesthesia management

Journal of Dental Anesthesia and Pain Medicine 2015³â 15±Ç 1È£ p.25 ~ 29
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À̼ö¾ð ( Lee Soo-Eon ) - Seoul National University Dental Hospital Department of Dental Anesthesiology
ÃÖÀ±Áö ( Choi Yoon-Ji ) - Seoul National University Dental Hospital Department of Dental Anesthesiology
Áö¼ºÀΠ( Chi Seong-In ) - Seoul National University Dental Hospital Department of Dental Anesthesiology
±èÇöÁ¤ ( Kim Hyun-Jeong ) - Seoul National University Dental Hospital Department of Dental Anesthesiology
¼­±¤¼® ( Seo Kwang-Suk ) - Seoul National University Dental Hospital Department of Dental Anesthesiology

Abstract


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 (ROTEMTM) and noninvasive measurements of total hemoglobin (SpHb) using Masimo Radical 7 (Masimo Co. CA, USA).

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Continuous noninvasive hemoglobin monitoring; Factor XI deficiency; Orthognathic surgery; Rotation thromboelastometry

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