Factor XI deficiency and orthognathic surgery: a case report on anesthesia management
Journal of Dental Anesthesia and Pain Medicine
;
: 25-29, 2015.
Artículo
en Inglés
| WPRIM
| ID: wpr-95438
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 (ROTEM™) and noninvasive measurements of total hemoglobin (SpHb) using Masimo Radical 7 (Masimo Co. CA, USA).
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Osteotomía
/
Tromboelastografía
/
Factor XI
/
Deficiencia del Factor XI
/
Cirugía Ortognática
/
Hemorragia
/
Anestesia
Tipo de estudio:
Estudio pronóstico
Límite:
Humanos
Idioma:
Inglés
Revista:
Journal of Dental Anesthesia and Pain Medicine
Año:
2015
Tipo del documento:
Artículo
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