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Transoral robotic‐assisted laryngeal cleft repair in the pediatric patient
Author(s) -
Leonardis Rachel L.,
Duvvuri Umamaheswar,
Mehta Deepak
Publication year - 2014
Publication title -
the laryngoscope
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.181
H-Index - 148
eISSN - 1531-4995
pISSN - 0023-852X
DOI - 10.1002/lary.24680
Subject(s) - medicine , swallowing , dysphagia , surgery , larynx , choking , demographics , demography , sociology , anatomy
Objectives/Hypothesis To assess the feasibility of performing robotic‐assisted laryngeal cleft repair in the pediatric population. Study Design Retrospective chart review at a tertiary academic children's hospital. Methods All patients underwent transoral robotic‐assisted laryngeal cleft repair from March 2011 to June 2013. Demographics, robotic docking time, operative time, and postoperative course and swallowing function were collected and analyzed. Results Five children, three male and two female, underwent successful transoral robotic‐assisted laryngeal cleft repair for closure of a type I laryngeal cleft. Mean age at time of surgery was 21.6 months (standard deviation 6.1 months; range, 15–29 months). From case 1 to case 5, robotic docking time (18–10 minutes), robotic operative time (102–36 minutes), and total operating room time (173–105 minutes) decreased. There were no complications with time until extubation (range, 2–3 days), length of intensive care unit stay (range, 3–4 days), and total hospital stay (range, 3–5 days) within acceptable range following laryngeal cleft repair. Modified barium swallow (two patients) or fiberoptic endoscopic evaluation of swallowing (three patients) was performed postoperatively, with all patients showing complete resolution of penetration and aspiration. In addition, all patients experienced subjective resolution of dysphagia and/or choking with feeds postoperatively. Conclusions Transoral robotic‐assisted laryngeal cleft repair may offer specific advantages over a traditional endoscopic approach. In our experience, the procedure was well tolerated and associated with definitive surgical cure in all patients. The scope of robotic technology continually expands and should be considered a feasible tool at an institution‐based level. Level of Evidence 4 Laryngoscope , 124:2167–2169, 2014

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