Management of laryngomalacia in children with congenital syndrome: the role of supraglottoplasty.

Abstract

BACKGROUND/IMPORTANCE:

Supraglottoplasty is the surgical procedure of choice for severe laryngomalacia and has shown to be successful in most cases; however, patients with medical comorbidities present a higher rate of failure. To date, the best management of laryngomalacia in children with congenital syndrome remains unclear.

PURPOSE:

To study the outcome of supraglottoplasty in children with severe laryngomalacia, and to analyze the management and outcome in infants with a congenital syndrome.

METHODS:

Retrospective medical records review from January 2003 to October 2012 of all patients who underwent laser supraglottoplasty for severe laryngomalacia at the University Children's Hospital Zurich, Switzerland.

RESULTS:

Thirty-one patients were included; median age at time of surgery was 3.5 months. Three patients (10%) had a genetically proven congenital syndrome with associated neurologic anomalies. Overall success rate was 87%. Failures were observed in four (13%) of 31 cases; including all three patients presenting a congenital syndrome.

CONCLUSIONS:

Supraglottoplasty is an effective and safe treatment for laryngomalacia in otherwise healthy children. Signs of a possible underlying predominant neurologic origin and discrepancy between the clinical presentation and the endoscopic findings have to be taken into account, as in children with congenital syndrome with neurologic anomalies the risk of failure is higher.

• Authors: Anette Escher, Rudolf Probst, Claudine Gysin
• Journal: Journal of pediatric surgery (J Pediatr Surg) Vol. 50 Issue 4 Pg. 519-23 (Apr 2015) ISSN: 1531-5037 [Electronic] United States
• PMID: 25840054 (Publication Type: Journal Article)
• Copyright: Copyright © 2015 Elsevier Inc. All rights reserved.

Topics

• Child
• Child, Preschool
• Congenital Abnormalities
• Endoscopy (methods)
• Female
• Glottis (surgery)
• Humans
• Infant
• Laryngomalacia (surgery)
• Laryngoplasty (methods)
• Male
• Retrospective Studies
• Syndrome