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Paediatr Anaesth ; 17(2): 171-5, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17238890

ABSTRACT

Laryngotracheo-esophageal cleft is a rare congenital anomaly that results from complete or partial failure of the development of the tracheoesophageal septum. The presenting symptoms include stridor, respiratory distress, and coughing or cyanotic episodes with feeding. There are four classifications for laryngeal clefts; the severity depends on the type present. We discuss the anesthesia management of a neonate with a Type IV cleft who presented for an emergency gastric division to prevent pulmonary aspiration and later returned for final repair of the defect.


Subject(s)
Anesthesia/methods , Esophagus/abnormalities , Larynx/abnormalities , Anesthetics, Inhalation/administration & dosage , Anesthetics, Intravenous/administration & dosage , Cardiopulmonary Bypass/methods , Esophagus/surgery , Female , Gastrostomy/methods , Humans , Infant, Newborn , Intubation, Intratracheal/methods , Isoflurane/administration & dosage , Larynx/surgery , Neuromuscular Nondepolarizing Agents/administration & dosage , Pancuronium/administration & dosage , Piperidines/administration & dosage , Pneumonia, Aspiration/complications , Rare Diseases , Remifentanil , Severity of Illness Index , Tracheostomy , Treatment Outcome , Vecuronium Bromide/administration & dosage
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