2004
DOI: 10.1111/j.1365-2044.2004.03529.x
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Anaesthetic management in facial bipartition surgery: The experience of one centre

Abstract: SummaryFacial bipartition is amongst the most radical craniofacial surgery undertaken but is performed rarely. There is little published information on its anaesthetic management. We undertook a retrospective case-note review of 22 consecutive patients undergoing bipartition surgery by the same surgical team in one centre in the period 1993-2001. There were incomplete data for two cases and these were therefore excluded. Patients were aged 2 months to 19 years. Conditions treated were facial cleft (n = 5), fro… Show more

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Cited by 2 publications
(2 citation statements)
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“…This type of surgery is often performed at an early age and is associated with prolonged operating times, extensive operative exposure, and significant heat and blood loss (3,4). Estimation of intraoperative blood loss in patients undergoing craniosynostosis repair is often inaccurate and significantly underestimates actual blood loss (5,6). Almost all patients undergoing repair of craniofacial deformities will need a blood transfusion with potential for massive blood transfusion (4).…”
Section: Discussionmentioning
confidence: 99%
“…This type of surgery is often performed at an early age and is associated with prolonged operating times, extensive operative exposure, and significant heat and blood loss (3,4). Estimation of intraoperative blood loss in patients undergoing craniosynostosis repair is often inaccurate and significantly underestimates actual blood loss (5,6). Almost all patients undergoing repair of craniofacial deformities will need a blood transfusion with potential for massive blood transfusion (4).…”
Section: Discussionmentioning
confidence: 99%
“…There are very little published data looking specifically at perioperative outcomes in children with Apert syndrome. Reviews and reports tend to group them together with other craniofacial syndromes (11–13), so specific complications may be masked. Our institution has records of 71 children with Apert syndrome diagnosed clinically and genetically.…”
Section: Introductionmentioning
confidence: 99%