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Dr. V. Sankara Subramanian Consultant Anaesthesiologist Dr. Jeyasekharan Hospital Nagercoil.
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Anaesthetic Management of Interesting Case

Feb 13, 2016

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Dr. V. Sankara Subramanian Consultant Anaesthesiologist Dr. Jeyasekharan Hospital Nagercoil. Anaesthetic Management of Interesting Case. Case . Baby X a case of APERT SYNDROME with Incomplete cleft palate was posted for palatorplasty. Brief Summary. - PowerPoint PPT Presentation
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Page 1: Anaesthetic Management of   Interesting Case

Dr. V. Sankara SubramanianConsultant Anaesthesiologist

Dr. Jeyasekharan HospitalNagercoil.

Page 2: Anaesthetic Management of   Interesting Case

Case

Baby X a case of APERT SYNDROME with Incomplete cleft palate was posted for palatorplasty.

Page 3: Anaesthetic Management of   Interesting Case

Brief Summary

Baby was full term normal delivery baby No H/O of birth asphyxia H/o delayed milestones (+) H/o epilepsy (+) and was on medications Last episode of fits 4 months back Congenital hydrocephalus (+), VP shunt

procedure done at the age of 5 years Age 7 years, Weight – 12.5 Kgs

Page 4: Anaesthetic Management of   Interesting Case
Page 5: Anaesthetic Management of   Interesting Case

Pre op Assessment

No verbalisation Large Head + Syndactyly + Macroglossia + Micrognathia + Maxillary hyper plasia + CVS-RS – Clinically normal P/A – umbilical hernia +

Page 6: Anaesthetic Management of   Interesting Case

Anaesthetic Management

IV line secured with difficulty Pre oxygenation done Inhalation induction : 6% Sevoflurane+ N2O +

O2 Trial laryngoscopy done, epiglottis visualised Induced with PROPOFOL 45 mg, FENTANYL 25

mic Orally intubated with 5 size uncuffed RAE

tube Maintenance N2O + O2 + Atracurium + Sevo Intraop – uneventful baby Girl extubated on table, smooth postop

Page 7: Anaesthetic Management of   Interesting Case
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Discussion Anticipating airway difficulty in paediatric population Syndrome associated with cleft lip / palate Apert Syndrome 1906 French Neurologist first described Mutation in a gene located on Ch:10Q Incidence – 1:65000 Features

Hyper hidrosis Craniosynostosis Chiarri malformation, Frontal Bossing, Development delay Low set ears Mid face – development delay Associated ASD, VSD Syndactly

Page 13: Anaesthetic Management of   Interesting Case
Page 14: Anaesthetic Management of   Interesting Case