scholarly journals Ventilation Difficulty after Intubation Due to Tracheal Diverticulum Caused by Esophageal Atresia/Tracheoesophageal Fistula Repair

2019 ◽  
Vol 39 (3) ◽  
pp. 253-256
Author(s):  
Akihiro YAMADA ◽  
Tomoko OKUMURA ◽  
Noriyuki MORIMOTO ◽  
Kazuko HASEGAWA ◽  
Yoko ARAKAWA ◽  
...  
2020 ◽  
Vol 58 (3) ◽  
pp. 601-609
Author(s):  
Ashton A. Moorhead ◽  
David Nair ◽  
Chris Morison ◽  
Nicholas J. Cook ◽  
Spencer W. Beasley ◽  
...  

2009 ◽  
Vol 44 (7) ◽  
pp. e15-e17 ◽  
Author(s):  
Emmanuel Le Bret ◽  
François Roubertie ◽  
Gilles Roger ◽  
Anne Sigal-Cinqualbre ◽  
Mathieu Coblence ◽  
...  

2014 ◽  
Vol 49 (1) ◽  
pp. 29-33 ◽  
Author(s):  
Katherine A. Barsness ◽  
Deborah M. Rooney ◽  
Lauren M. Davis ◽  
Anthony C. Chin

2017 ◽  
Vol 9 (1) ◽  
pp. 28-30 ◽  
Author(s):  
Joanna M. Dion ◽  
Anthony M.-H. Ho ◽  
Andrea Winthrop ◽  
Michael P. Flavin

2012 ◽  
Vol 22 (06) ◽  
pp. 415-419 ◽  
Author(s):  
Pietro Impellizzeri ◽  
Angela Montalto ◽  
Pietro Antonuccio ◽  
Emanuela Santacaterina ◽  
Gianfranco Scalfari ◽  
...  

2018 ◽  
Vol 53 (5) ◽  
pp. 925-928 ◽  
Author(s):  
Damian Dylkowski ◽  
Sumit Dave ◽  
J. Andrew McClure ◽  
Blayne Welk ◽  
Jennifer Winick-Ng ◽  
...  

2018 ◽  
Vol 7 (4) ◽  
pp. 44
Author(s):  
Alessandra Glover Williams ◽  
Janet McNally ◽  
Julian Gaskin ◽  
Ela Chakkarapani

A 32+4-week-preterm neonate was operated on day 1 for esophageal atresia with tracheoesophageal fistula with a tight primary anastomosis and closure of a tracheoesophageal fistula. Postoperatively, he needed ventilation for 6 days. Post-extubation, he needed continuous positive airway pressure support for increased work of breathing, increasing oxygen requirement, and respiratory acidosis when respiratory support was weaned. Further, during the post-operative period, he had right hemidiaphragmatic paresis and acute lifethreatening events requiring manual high-pressure, non-invasive positive pressure ventilation resuscitation. These complications were considered, and a computed tomography assisted by three-dimensional reconstruction was performed. This revealed a congenital tracheal diverticulum and severe tracheomalacia which was confirmed with microlaryngoscopy and bronchoscopy. The presentation and the diagnostic dilemma surrounding this rare diagnosis are discussed in this case report.


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