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Accidental esophageal intubation a large type C congenital tracheoesophageal fistula: A case report.
World J Clin Cases
October 2022
Department of Anesthesiology and Pain Medicine, School of Medicine, Kyungpook National University, Daegu 41944, South Korea.
Background: Tracheoesophageal fistula (TEF) is a congenital anomaly characterized by interruptions in esophageal continuity with or without fistulous communication to the trachea. Anesthetic management during TEF repair is challenging because of the difficulty of perioperative airway management. It is important to determine the appropriate position of the endotracheal tube (ETT) for proper ventilation and to prevent excessive gastric dilatation.
View Article and Find Full Text PDFA Rare Case of Ectopic Colonic Mucosa Presenting With Airway Compromise in a Neonate.
Cureus
July 2022
Otolaryngology, University of Florida College of Medicine, Gainesville, USA.
This case report documents a rare and unique presentation of an oropharyngeal duplication cyst and subsequent neonatal airway management. A one-day-old premature female presented with postpartum respiratory distress requiring emergent intubation secondary to an oropharyngeal mass of the left tongue. After being stabilized and transferred to an academic center, imaging revealed a cystic lesion that was then marsupialized and drained by the otolaryngology team.
View Article and Find Full Text PDFVerifying the placement and length of feeding tubes in canine and feline neonates.
BMC Vet Res
June 2021
Clinic of Reproductive Medicine, Vetsuisse Faculty, University of Zurich, Winterthurerstrasse 260, 8057, Zurich, Switzerland.
Background: Tube feeding is a common procedure in neonatology. In humans, tube misplacement reportedly occurs in up to 59% of all cases and may lead to perforation in 1.1% of preterm intubated neonates.
View Article and Find Full Text PDFUse of an Aortic Cannula for Tracheal Intubation in a Patient With Severe Tracheal Stenosis and Tracheoesophageal Fistula: A Case Report.
Cureus
July 2020
Anesthesia and Pain Medicine, Hospital for Sick Children, Toronto, CAN.
A one-day-old girl was brought to the OR for the repair of a type C esophageal atresia (EA) [EA with tracheoesophageal fistula (TEF)]. Rigid bronchoscopy was performed to locate the fistula, and it revealed a severe long-segment tracheal stenosis. Therefore, the airway could not have been secured past the fistula using normal-sized endotracheal tubes (ETTs).
View Article and Find Full Text PDFNovel mutation-deletion in the gene of the patient diagnosed with Neuroblastoma, Hirschsprung's Disease, and Congenital Central Hypoventilation Syndrome (NB-HSCR-CCHS) Cluster.
J Genet Syndr Gene Ther
December 2015
Phoenix Biomolecular Engineering Foundation, San Francisco, CA, USA; NMRFM, National Institutes of Health, Madison, WI, USA; University of Wisconsin, Madison, WI, USA.
Introduction: Neuroblastoma (NB), Hirschsprung disease (HSCR), Congenital Central Hypoventilation Syndrome (CCHS), clinically referred as the NB-HSCR-CCHS cluster, are genetic disorders linked to mutations in the gene on chromosome 4p12.
Specific Aim: The specific aim of this project is to define the gene mutations as the genomic basis for the clinical manifestations of the NB-HSCR-CCHS cluster.
Patient: A one day old male patient presented to the Jagiellonian University Medical College (JUMC), American Children Hospital, neonatal Intensive Care Unit (ICU) due to abdominal distention, vomiting, and severe apneic episodes.
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