JOURNAL ARTICLE
OBSERVATIONAL STUDY
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Efficacy of a new dual channel laryngeal mask airway, the LMA ® Gastro™ Airway, for upper gastrointestinal endoscopy: a prospective observational study.

BACKGROUND: Significant cardiorespiratory events are frequent in patients undergoing gastrointestinal endoscopy. Central to the occurrence of respiratory events is an unsecured airway. This study sought to determine the efficacy of a new laryngeal mask airway, the LMA® GastroTM Airway (Teleflex Medical, Athlone, Ireland), in patients undergoing upper gastrointestinal endoscopy. New design features include a dedicated channel for oesophageal intubation and separate channel with terminal cuff for lung ventilation.

METHODS: In a prospective, open label, observational study, 292 ASA physical status classification 1 and 2 patients at low risk of pulmonary aspiration undergoing upper gastrointestinal endoscopy received i.v. propofol anaesthesia and standardized insertion of the LMA® GastroTM Airway. Endoscopy outcomes included insertion success, first attempt success, and ease of endoscope insertion. LMA® GastroTM Airway outcomes included insertion success, first attempt success, ease of insertion, lowest oxygen saturation, airway compromise, laryngospasm, bloodstained device, and sore throat.

RESULTS: Per protocol analysis (n=290), the endoscopy success rate amongst the cohort with successful LMA® GastroTM Airway insertion was 99% [95% confidence interval (CI): 98, 100]. LMA® GastroTM Airway insertion success rate (n=292) was 99% (95% CI: 98, 100). For endoscopy and LMA® GastroTM Airway insertion success, the lower limit of the 95% CIs was at least 98%, indicating LMA® GastroTM Airway efficacy. Median (inter-quartile range) lowest intraoperative oxygen saturation was 98% (98, 99). Only one serious adverse event occurred (re-admission for sore throat and inability to tolerate fluids) and was reported to the Tasmanian Health and Medical Human Research Ethics Committee.

CONCLUSIONS: The LMA® GastroTM Airway appears effective for clinical use in upper gastrointestinal endoscopy.

CLINICAL TRIAL REGISTRATION: ACTRN12616001464459.

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