Investigation of dynamic hyperinflation and its relationship with exercise capacity in children with bronchiectasis

Beyza Nur Caglar Tosun1, Melih Zeren2, Meral Barlik3

  • 1Department of Physiotherapy and Rehabilitation, Graduate Education Institute, Izmir Bakircay University, Izmir, Turkey.

Insights

Dynamic hyperinflation (DH) is common in children with bronchiectasis (BE), but its severity is low and does not significantly impact exercise capacity. Peripheral muscle strength is a key factor in functional exercise capacity for these children.

Area of Science:

  • Pediatric Pulmonology
  • Respiratory Physiology
  • Exercise Medicine

Background:

  • Dynamic hyperinflation (DH) significantly limits exercise in obstructive lung diseases.
  • DH has not been previously studied in pediatric bronchiectasis (BE).

Purpose of the Study:

  • To investigate dynamic ventilatory responses during exercise in children with BE.
  • To determine the influence of DH on functional exercise capacity in pediatric BE.

Main Methods:

  • Forty children with BE underwent a 6-minute walk test (6MWT) with Spiropalm 6MWT® to assess dynamic ventilatory responses (inspiratory capacity, minute ventilation, breathing reserve, respiratory rate).
  • DH was defined as a ≥100 ml decrease in inspiratory capacity during exertion. Spirometry and peripheral muscle strength were also measured.

Main Results:

  • 50% of children with BE developed DH during the 6MWT, with a mean decrease in inspiratory capacity of 176 ml.
  • DH severity was generally low and did not correlate with clinical indicators or 6MWT distance, except for an increased respiratory rate.
  • Peripheral muscle strength (quadriceps and handgrip) and FEV1% were the primary predictors of 6MWT distance.

Conclusions:

  • Dynamic hyperinflation is prevalent but mild in children with bronchiectasis.
  • The severity of DH in this cohort did not significantly impair functional exercise capacity.
  • Peripheral muscle strength is a critical determinant of exercise performance in children with BE.
Abstract

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