Dysfunctional breathing diagnosed by cardiopulmonary exercise testing in 'long COVID' patients with persistent dyspnoea.


Journal

BMJ open respiratory research
ISSN: 2052-4439
Titre abrégé: BMJ Open Respir Res
Pays: England
ID NLM: 101638061

Informations de publication

Date de publication:
03 2022
Historique:
received: 14 10 2021
accepted: 16 03 2022
entrez: 31 3 2022
pubmed: 1 4 2022
medline: 2 4 2022
Statut: ppublish

Résumé

'Long COVID'-associated dyspnoea may persist for months after SARS-CoV-2 infection. Among the causes of persistent dyspnoea, dysfunctional breathing (DB), defined as an erratic or inappropriate ventilation at rest or exercise, has been observed, but little is known about its occurrence and pathophysiology among individuals with 'long COVID'. We aimed to describe the occurrence and identify clinical predictors of DB among patients following SARS-CoV-2 infection. Cardiopulmonary exercise testing (CPET) was performed in 51 SARS-CoV-2 patients (median age, 64 years (IQR, 15)); male, 66.7%) living with 'long COVID' and persistent dyspnoea. CPET was classified into three dominant patterns: respiratory limitation with gas exchange abnormalities (RL); normal CPET or O Among 51 patients, DB mostly without hyperventilation was found in 29.4% (n=15), RL in 54.9% (n=28) and D in 15.7% (n=8). When compared with RL individuals, patients with DB were younger, had significantly less severe initial infection, a better transfer capacity for carbon monoxide (median 85% (IQR, 28)), higher oxygen consumption (22.9 mL/min/kg (IQR, 5.5)), a better ventilatory efficiency slope (31.6 (IQR, 12.8)), and a higher SpO Our findings suggest that DB without hyperventilation could be an important pathophysiological mechanism of disabling dyspnoea in younger outpatients following SARS-CoV-2 infection, which appears to be a feature of COVID-19 not described in other viral diseases.

Sections du résumé

BACKGROUND
'Long COVID'-associated dyspnoea may persist for months after SARS-CoV-2 infection. Among the causes of persistent dyspnoea, dysfunctional breathing (DB), defined as an erratic or inappropriate ventilation at rest or exercise, has been observed, but little is known about its occurrence and pathophysiology among individuals with 'long COVID'. We aimed to describe the occurrence and identify clinical predictors of DB among patients following SARS-CoV-2 infection.
METHODS
Cardiopulmonary exercise testing (CPET) was performed in 51 SARS-CoV-2 patients (median age, 64 years (IQR, 15)); male, 66.7%) living with 'long COVID' and persistent dyspnoea. CPET was classified into three dominant patterns: respiratory limitation with gas exchange abnormalities (RL); normal CPET or O
RESULTS
Among 51 patients, DB mostly without hyperventilation was found in 29.4% (n=15), RL in 54.9% (n=28) and D in 15.7% (n=8). When compared with RL individuals, patients with DB were younger, had significantly less severe initial infection, a better transfer capacity for carbon monoxide (median 85% (IQR, 28)), higher oxygen consumption (22.9 mL/min/kg (IQR, 5.5)), a better ventilatory efficiency slope (31.6 (IQR, 12.8)), and a higher SpO
CONCLUSIONS
Our findings suggest that DB without hyperventilation could be an important pathophysiological mechanism of disabling dyspnoea in younger outpatients following SARS-CoV-2 infection, which appears to be a feature of COVID-19 not described in other viral diseases.

Identifiants

pubmed: 35354589
pii: 9/1/e001126
doi: 10.1136/bmjresp-2021-001126
pmc: PMC8968537
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Isabelle Frésard (I)

Service de pneumologie, Hôpital de Sion Centre Hospitalier du Valais Romand, Sion, Switzerland Isabelle.Fresard@hopitalvs.ch.
Service de pneumologie, Hôpital Riviera-Chablais, Rennaz, Switzerland.

Léon Genecand (L)

Service de pneumologie, Hôpital de Sion Centre Hospitalier du Valais Romand, Sion, Switzerland.
Faculté de médecine, Université de Genève, Geneva, Switzerland.

Marco Altarelli (M)

Service de pneumologie, Hôpital de Sion Centre Hospitalier du Valais Romand, Sion, Switzerland.
Service de pneumologie, Hôpital Riviera-Chablais, Rennaz, Switzerland.

Grégoire Gex (G)

Service de pneumologie, Hôpital de Sion Centre Hospitalier du Valais Romand, Sion, Switzerland.
Service de pneumologie, Hôpital Riviera-Chablais, Rennaz, Switzerland.

Petrut Vremaroiu (P)

Service de pneumologie, Hôpital de Sion Centre Hospitalier du Valais Romand, Sion, Switzerland.

Andreea Vremaroiu-Coman (A)

Service de pneumologie, Hôpital de Sion Centre Hospitalier du Valais Romand, Sion, Switzerland.
Service de pneumologie, Hôpital Riviera-Chablais, Rennaz, Switzerland.

David Lawi (D)

Service de pneumologie, Hôpital de Sion Centre Hospitalier du Valais Romand, Sion, Switzerland.

Pierre-Olivier Bridevaux (PO)

Service de pneumologie, Hôpital de Sion Centre Hospitalier du Valais Romand, Sion, Switzerland.
Service de pneumologie, Hôpital Riviera-Chablais, Rennaz, Switzerland.
Faculté de médecine, Université de Genève, Geneva, Switzerland.

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