Laryngomalacia: disease presentation, spectrum, and management

April M Landry, Dana M Thompson, April M Landry, Dana M Thompson

Abstract

Laryngomalacia is the most common cause of stridor in newborns, affecting 45-75% of all infants with congenital stridor. The spectrum of disease presentation, progression, and outcomes is varied. Identifying symptoms and patient factors that influence disease severity helps predict outcomes. Findings. Infants with stridor who do not have significant feeding-related symptoms can be managed expectantly without intervention. Infants with stridor and feeding-related symptoms benefit from acid suppression treatment. Those with additional symptoms of aspiration, failure to thrive, and consequences of airway obstruction and hypoxia require surgical intervention. The presence of an additional level of airway obstruction worsens symptoms and has a 4.5x risk of requiring surgical intervention, usually supraglottoplasty. The presence of medical comorbidities predicts worse symptoms. Summary. Most with laryngomalacia will have mild-to-moderate symptoms and not require surgical intervention. Those with gastroesophageal reflux and/or laryngopharyngeal reflux have symptom improvement from acid suppression therapy. Those with severe enough disease to require supraglottoplasty will have minimal complications and good outcomes if multiple medical comorbidities are not present. Identifying patient factors that influence disease severity is an important aspect of care provided to infants with laryngomalacia.

Figures

Figure 1
Figure 1
(a) Omega-shaped epiglottis. (b) A tubular-shaped epiglottis along with redundant supra-arytenoid tissue which is obstructing the glottis during inspiration. (c) the site of redundant supra-arytenoid tissue after surgical removal.

References

    1. Richter GT, Thompson DM. The Surgical Management of Laryngomalacia. Otolaryngologic Clinics of North America. 2008;41(5):837–864.
    1. Thompson DM. Abnormal sensorimotor integrative function of the larynx in congenital laryngomalacia: a new theory of etiology. Laryngoscope. 2007;117(6, supplement):1–33.
    1. Richter GT, Wootten CT, Rutter MJ, Thompson DM. Impact of supraglottoplasty on aspiration in severe laryngomalacia. Annals of Otology, Rhinology and Laryngology. 2009;118(4):259–266.
    1. Thompson DM. Laryngomalacia: factors that influence disease severity and outcomes of management. Current Opinion in Otolaryngology and Head and Neck Surgery. 2010;18(6):564–570.
    1. Cohen SR, Desmond MS, Eavey RD, May BC. Endoscopy and tracheotomy in the neonatal period. A 10-year review. Annals of Otology, Rhinology and Laryngology. 1977;86(5):577–583.
    1. Dickson JM, Richter GT, Meinzen-Derr J, Rutter MJ, Thompson DM. Secondary airway lesions in infants with laryngomalacia. Annals of Otology, Rhinology and Laryngology. 2009;118(1):37–43.
    1. Schroeder JW, Bhandarkar ND, Holinger LD. Synchronous airway lesions and outcomes in infants with severe laryngomalacia requiring supraglottoplasty. Archives of Otolaryngology. 2009;135(7):647–651.
    1. Krashin E, Ben-Ari J, Springer C, DeRowe A, Avital A, Sivan Y. Synchronous airway lesions in laryngomalacia. International Journal of Pediatric Otorhinolaryngology. 2008;72(4):501–507.
    1. Yuen HW, Tan HKK, Balakrishnan A. Synchronous airway lesions and associated anomalies in children with laryngomalacia evaluated with rigid endoscopy. International Journal of Pediatric Otorhinolaryngology. 2006;70(10):1779–1784.
    1. Masters IB, Chang AB, Patterson L, et al. Series of laryngomalacia, tracheomalacia, and bronchomalacia disorders and their associations with other conditions in children. Pediatric Pulmonology. 2002;34(3):189–195.
    1. Olney DR, Greinwald JH, Smith RJH, Bauman NM. Laryngomalacia and its treatment. Laryngoscope. 1999;109(11):1770–1775.
    1. Hoff SR, Schroeder JW, Rastatter JC, Holinger LD. Supraglottoplasty outcomes in relation to age and comorbid conditions. International Journal of Pediatric Otorhinolaryngology. 2010;74(3):245–249.
    1. Bertrand P, Navarro H, Caussade S, Holmgren N, Sánchez I. Airway anomalies in children with Down syndrome: endoscopic findings. Pediatric Pulmonology. 2003;36(2):137–141.
    1. Mitchell RB, Call E, Kelly J. Diagnosis and therapy for airway obstruction in children with down syndrome. Archives of Otolaryngology. 2003;129(6):642–645.
    1. Mitchell RB, Call E, Kelly J. Ear, nose and throat disorders in children with Down syndrome. Laryngoscope. 2003;113(2):259–263.
    1. Naito Y, Higuchi M, Koinuma G, Aramaki M, Takahashi T, Kosaki K. Upper airway obstruction in neonates and infants with CHARGE sndrome. American Journal of Medical Genetics, Part A. 2007;143(16):1815–1820.
    1. Digilio MC, McDonald-McGinn DM, Heike C, et al. Three patients with oculo-auriculo-vertebral spectrum and microdeletion 22q11.2. American Journal of Medical Genetics, Part A. 2009;149(12):2860–2864.
    1. Yu S, Cox K, Friend K, et al. Familial 22q11.2 duplication: a three-generation family with a 3-Mb duplication and a familial 1.5-Mb duplication. Clinical Genetics. 2008;73(2):160–164.
    1. Petersson RS, Wetjen NM, Thompson DM. Neurologic variant laryngomalacia associated with Chiari malformation and cervicomedullary compression: case reports. Annals of Otology, Rhinology and Laryngology. 2011;120(2):99–103.

Source: PubMed

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