Patient and Caregiver Perceptions of Airway Clearance Methods Used for Cystic Fibrosis.


Journal

Canadian respiratory journal
ISSN: 1916-7245
Titre abrégé: Can Respir J
Pays: Egypt
ID NLM: 9433332

Informations de publication

Date de publication:
2023
Historique:
received: 12 01 2023
revised: 06 03 2023
accepted: 24 06 2023
medline: 8 8 2023
pubmed: 7 8 2023
entrez: 7 8 2023
Statut: epublish

Résumé

Cystic Fibrosis Foundation guidelines recommend people with CF perform daily airway clearance. This can be difficult for patients, as some find it time consuming or uncomfortable. Data comparing airway clearance methods are limited. We surveyed patients and their families to understand which methods are preferred and identify obstacles to performing airway clearance. We designed a REDCap survey and enrolled participants in 2021. Respondents reported information on airway clearance usage, time commitment, and medication use. They rated airway clearance methods for effectiveness, comfort, time commitment, importance, and compatibility with other treatments. The analysis included descriptive statistics and clustering. 60 respondents started and 52 completed the survey. The median patient age was 20 years. Respondents experienced a median of four airway clearance methods in their lifetime, including chest wall oscillation (vest, 92%), manual chest physical therapy (CPT, 88%), forced expiration technique (huff or cough, 77%), and exercise (75%). Past 30-day use was highest for exercise (62%) and vest (57%). The time commitment was generally less than 2 hours daily. Of those eligible for CFTR modulators, 53% reported decreased time commitment to airway clearance after starting treatment. On a scale of 0-100, respondents rated CFTR modulators as their most important treatment (median 99.5), followed by exercise (88).

Identifiants

pubmed: 37547298
doi: 10.1155/2023/1422319
pmc: PMC10403321
doi:

Substances chimiques

Cystic Fibrosis Transmembrane Conductance Regulator 126880-72-6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1422319

Informations de copyright

Copyright © 2023 Zoe E. Kienenberger et al.

Déclaration de conflit d'intérêts

Dr. Singh is now an employee of Johnson & Johnson. Dr. Singh's spouse is now an employee of Vertex Pharmaceuticals. Dr. Larson Ode has received an honorarium from Vertex Pharmaceuticals for participating in an advisory panel. Dr. Fischer and Dr. Larson Ode have received grant funding from the Cystic Fibrosis Foundation.

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Auteurs

Zoe E Kienenberger (ZE)

Pediatrics, University of Iowa, Iowa City, IA, USA.
Department of Physical Therapy and Rehabilitation Science, University of Iowa, Iowa City, IA, USA.

Tyler O Farber (TO)

Pediatrics, University of Iowa, Iowa City, IA, USA.

Mary E Teresi (ME)

Pediatrics, University of Iowa, Iowa City, IA, USA.

Francesca Milavetz (F)

Pediatrics, University of Iowa, Iowa City, IA, USA.

Sachinkumar B Singh (SB)

Pediatrics, University of Iowa, Iowa City, IA, USA.

Katie Larson Ode (K)

Pediatrics, University of Iowa, Iowa City, IA, USA.

Theodosia Thoma (T)

Pediatrics, University of Iowa, Iowa City, IA, USA.

Rebecca L Weiner (RL)

Pediatrics, University of Iowa, Iowa City, IA, USA.

Kathryn R Burlage (KR)

Department of Physical Therapy and Rehabilitation Science, University of Iowa, Iowa City, IA, USA.

Anthony J Fischer (AJ)

Pediatrics, University of Iowa, Iowa City, IA, USA.

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