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

Overview
Journal Can Respir J
Publisher Wiley
Specialty Pulmonary Medicine
Date 2023 Aug 7
PMID 37547298
Authors
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Abstract

Introduction: 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.

Methods: 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.

Results: 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). . Patients and caregivers are familiar with several methods of airway clearance for CF. They report distinct strengths and limitations of each method. Exercise and vest are the most common methods of airway clearance. The use of CFTR modulators may reduce patient-reported time commitment to airway clearance.

Citing Articles

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

Kienenberger Z, Farber T, Teresi M, Milavetz F, Singh S, Ode K Can Respir J. 2023; 2023:1422319.

PMID: 37547298 PMC: 10403321. DOI: 10.1155/2023/1422319.

References
1.
Mikesell C, Kempainen R, Laguna T, Menk J, Wey A, Gaillard P . Objective Measurement of Adherence to Out-Patient Airway Clearance Therapy by High-Frequency Chest Wall Compression in Cystic Fibrosis. Respir Care. 2017; 62(7):920-927. PMC: 6373861. DOI: 10.4187/respcare.05349. View

2.
Doull I . Cystic fibrosis 2019: Year in review. Paediatr Respir Rev. 2020; 35:95-98. DOI: 10.1016/j.prrv.2020.04.001. View

3.
Hoegger M, Fischer A, McMenimen J, Ostedgaard L, Tucker A, Awadalla M . Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis. Science. 2014; 345(6198):818-22. PMC: 4346163. DOI: 10.1126/science.1255825. View

4.
Morrison L, Milroy S . Oscillating devices for airway clearance in people with cystic fibrosis. Cochrane Database Syst Rev. 2020; 4:CD006842. PMC: 7197699. DOI: 10.1002/14651858.CD006842.pub5. View

5.
Flume P, Robinson K, OSullivan B, Finder J, Vender R, Willey-Courand D . Cystic fibrosis pulmonary guidelines: airway clearance therapies. Respir Care. 2009; 54(4):522-37. View