Cardiopulmonary exercise testing to indicate increased ventilatory variability in subjects with dysfunctional breathing.

dysfunctional breathing dyspnoea exercise test hyperventilation respiration

Journal

Clinical physiology and functional imaging
ISSN: 1475-097X
Titre abrégé: Clin Physiol Funct Imaging
Pays: England
ID NLM: 101137604

Informations de publication

Date de publication:
Sep 2023
Historique:
revised: 01 03 2023
received: 21 11 2022
accepted: 30 03 2023
medline: 8 8 2023
pubmed: 1 4 2023
entrez: 31 3 2023
Statut: ppublish

Résumé

Dysfunctional breathing (DB) is a common, but largely underappreciated, cause of chronic dyspnoea. Under visual inspection, most subjects with DB present with larger sequential changes in ventilation (V̇E) and breathing pattern (tidal volume (VT) and breathing frequency (f)) before and/or during incremental cardiopulmonary exercise testing (CPET). Currently, however, there are no objective criteria to indicate increased ventilatory variability in these subjects. Twenty chronically dyspnoeic subjects with DB and 10 age- and sex-matched controls performed CPET on a cycle ergometer. Cut-offs to indicate increased V̇E, VT, f, and f/VT ratio variability (Δ = highest-lowest 20 s arithmetic mean) over the last resting minute ( Subjects with DB presented with increased V̇E, higher ventilatory variability, higher dyspnoea burden, and lower exercise capacity compared to controls (p < 0.05). ΔV̇E This study provides objective criteria to indicate increased ventilatory variability during incremental CPET in dyspnoeic subjects with DB. Large variability in breathing frequency seems particularly useful in this context, a finding that should be prospectively confirmed in larger studies.

Sections du résumé

BACKGROUND BACKGROUND
Dysfunctional breathing (DB) is a common, but largely underappreciated, cause of chronic dyspnoea. Under visual inspection, most subjects with DB present with larger sequential changes in ventilation (V̇E) and breathing pattern (tidal volume (VT) and breathing frequency (f)) before and/or during incremental cardiopulmonary exercise testing (CPET). Currently, however, there are no objective criteria to indicate increased ventilatory variability in these subjects.
METHODS METHODS
Twenty chronically dyspnoeic subjects with DB and 10 age- and sex-matched controls performed CPET on a cycle ergometer. Cut-offs to indicate increased V̇E, VT, f, and f/VT ratio variability (Δ = highest-lowest 20 s arithmetic mean) over the last resting minute (
RESULTS RESULTS
Subjects with DB presented with increased V̇E, higher ventilatory variability, higher dyspnoea burden, and lower exercise capacity compared to controls (p < 0.05). ΔV̇E
CONCLUSIONS CONCLUSIONS
This study provides objective criteria to indicate increased ventilatory variability during incremental CPET in dyspnoeic subjects with DB. Large variability in breathing frequency seems particularly useful in this context, a finding that should be prospectively confirmed in larger studies.

Identifiants

pubmed: 36998164
doi: 10.1111/cpf.12820
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

305-312

Subventions

Organisme : Conselho Nacional de Desenvolvimento Científico e Tecnológico
ID : 304061/2019-0
Organisme : Incentive Fund of Research (FIPE; Brazil) of Hospital de Clinicas de Porto Alegre
ID : 2018-0586

Informations de copyright

© 2023 Scandinavian Society of Clinical Physiology and Nuclear Medicine.

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Auteurs

Nathalia B S Mendes (NBS)

Hospital de Clínicas de Porto Alegre; Rio Grande do Sul, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.

Franciele Plachi (F)

Hospital de Clínicas de Porto Alegre; Rio Grande do Sul, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.

Amanda Guimarães (A)

Hospital de Clínicas de Porto Alegre; Rio Grande do Sul, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.

Talmir Nolasco (T)

Hospital de Clínicas de Porto Alegre; Rio Grande do Sul, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.

Ricardo Gass (R)

Hospital de Clínicas de Porto Alegre; Rio Grande do Sul, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.

Marcelo Nogueira (M)

Santa Casa de Porto Alegre, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, Brazil.

Paulo J Z Teixeira (PJZ)

Santa Casa de Porto Alegre, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, Brazil.

Marcelo B Gazzana (MB)

Hospital de Clínicas de Porto Alegre; Rio Grande do Sul, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.

J Alberto Neder (JA)

Kingston Health Science Center, Division of Respirology and Sleep Medicine, Queen's University, Kingston, Ontario, Canada.

Danilo C Berton (DC)

Hospital de Clínicas de Porto Alegre; Rio Grande do Sul, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.

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