Frontiers in Pediatrics (Feb 2022)

Exercise-induced Laryngeal Obstruction: Protocol for a Randomized Controlled Treatment Trial

  • Hege Clemm,
  • Hege Clemm,
  • Ola D. Røksund,
  • Ola D. Røksund,
  • Ola D. Røksund,
  • Tiina Andersen,
  • Tiina Andersen,
  • Tiina Andersen,
  • John-Helge Heimdal,
  • John-Helge Heimdal,
  • John-Helge Heimdal,
  • Tom Karlsen,
  • Magnus Hilland,
  • Zoe Fretheim-Kelly,
  • Zoe Fretheim-Kelly,
  • Karl Ove Hufthammer,
  • Astrid Sandnes,
  • Sigrun Hjelle,
  • Maria Vollsæter,
  • Maria Vollsæter,
  • Thomas Halvorsen,
  • Thomas Halvorsen,
  • Thomas Halvorsen,
  • Bergen ILO-group,
  • Haakon Kvidaland,
  • Petrine Solli,
  • Petter Carlsen,
  • Praveen Muralitharan,
  • Mette Engan,
  • Lorentz Sandvik,
  • Ole C.O. Gamlemshaug

DOI
https://doi.org/10.3389/fped.2022.817003
Journal volume & issue
Vol. 10

Abstract

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BackgroundExercise-induced laryngeal obstruction (EILO) is a common cause of exertional breathing problems in young individuals, caused by paradoxical inspiratory adduction of laryngeal structures, and diagnosed by continuous visualization of the larynx during high-intensity exercise. Empirical data suggest that EILO consists of different subtypes, possibly requiring different therapeutic approaches. Currently applied treatments do not rest on randomized controlled trials, and international guidelines based on good evidence can therefore not be established. This study aims to provide evidence-based information on treatment schemes commonly applied in patients with EILO.Methods and AnalysisConsenting patients consecutively diagnosed with EILO at Haukeland University Hospital will be randomized into four non-invasive treatment arms, based on promising reports from non-randomized studies: (A) standardized information and breathing advice only (IBA), (B) IBA plus inspiratory muscle training, (C) IBA plus speech therapy, and (D) IBA plus inspiratory muscle training and speech therapy. Differential effects in predefined EILO subtypes will be addressed. Patients failing the non-invasive approach and otherwise qualifying for surgical treatment by current department policy will be considered for randomization into (E) standard or (F) minimally invasive laser supraglottoplasty or (G) no surgery. Power calculations are based on the main outcomes, laryngeal adduction during peak exercise, rated by a validated scoring system before and after the interventions.Ethics and DisseminationThe study will assess approaches to EILO treatments that despite widespread use, are insufficiently tested in structured, verifiable, randomized, controlled studies, and is therefore considered ethically sound. The study will provide knowledge listed as a priority in a recent statement issued by the European Respiratory Society, requested by clinicians and researchers engaged in this area, and relevant to 5–7% of young people. Dissemination will occur in peer-reviewed journals, at relevant media platforms and conferences, and by engaging with patient organizations and the healthcare bureaucracy.

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