Literature DB >> 22782067

Adherence to airway clearance therapies by adult cystic fibrosis patients.

Josani Silva Flores1, Fernanda Ângela Teixeira, Paula Maria Eidt Rovedder, Bruna Ziegler, Paulo de Tarso Roth Dalcin.   

Abstract

BACKGROUND: Airway clearance therapy (ACT) is critical in cystic fibrosis (CF).
OBJECTIVES: To determine rates of self-reported adherence to ACT by patients treated in an adult CF program, to identify patient characteristics associated with poor adherence, to typify adherence according to ACT technique, and to indicate reasons for poor adherence.
METHODS: Our cross-sectional study included CF subjects age 16 years and older. Enrollees were evaluated via general structured questionnaire, adherence questionnaire, clinical assessment, spirometry, and S(pO(2)) values. Each was stratified by self-reporting protocol as high, moderate, or poor adherence to ACT. Concordance between physiotherapist recommended ACT technique and self-reported subject adherence was subjected to agreement analysis.
RESULTS: Of the 63 subjects studied, 38 (60%) qualified as high adherence, 12 (19%) as moderate adherence, and 13 (21%) as poor adherence. Logistic regression identified education level (less than high school) as an independent factor associated with poor adherence (odds ratio 10.2, 95% CI 1.23-84.7, P = .03). Positive expiratory pressure (κ = 0.87) and flutter device (κ = 0.63) usage both corresponded with a high level of agreement, while active cycle of breathing technique (κ = 0.40) and autogenic drainage (κ = 0.39) each showed moderate agreement. Agreement was low for percussion and postural drainage (κ = 0.23). Reasons given most frequently for poor adherence to ACT were "not enough time to do ACT" (28%), "cannot be bothered" (16%), and "do not enjoy ACT technique" (8%). Many (32%) provided no reason.
CONCLUSIONS: Study outcomes showed a high rate of ACT adherence in adult CF subjects. Lower level of education was the most important factor in poor adherence to ACT. Self-reported adherence and treatment recommendations were in best agreement with positive expiratory pressure and flutter device techniques.
© 2013 Daedalus Enterprises.

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Year:  2013        PMID: 22782067     DOI: 10.4187/respcare.01389

Source DB:  PubMed          Journal:  Respir Care        ISSN: 0020-1324            Impact factor:   2.258


  7 in total

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Authors:  Mary Beth Happ; Leslie A Hoffman; Linda W Higgins; Dana Divirgilio; Dana DiVirgilio; David M Orenstein
Journal:  Nurs Res       Date:  2013 Sep-Oct       Impact factor: 2.381

2.  Respiratory therapy: a problem among children and adolescents with cystic fibrosis.

Authors:  Taiane Dos Santos Feiten; Josani Silva Flores; Bruna Luciano Farias; Paula Maria Eidt Rovedder; Eunice Gus Camargo; Paulo de Tarso Roth Dalcin; Bruna Ziegler
Journal:  J Bras Pneumol       Date:  2016 Jan-Feb       Impact factor: 2.624

3.  Benefit of educational feedback for the use of positive expiratory pressure device.

Authors:  Gregory Reychler; Manon Jacquemart; William Poncin; Anne-Sophie Aubriot; Giuseppe Liistro
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4.  Comparing airways clearance techniques in chronic obstructive pulmonary disease and bronchiectasis: positive expiratory pressure or temporary positive expiratory pressure? A retrospective study.

Authors:  Francesco D'Abrosca; Barbara Garabelli; Gloria Savio; Agnese Barison; Lorenzo Appendini; Luis V F Oliveira; Paola Baiardi; Bruno Balbi
Journal:  Braz J Phys Ther       Date:  2017-01-13       Impact factor: 3.377

5.  TREATMENT ADHERENCE AMONG CHILDREN AND ADOLESCENTS IN A CYSTIC FIBROSIS REFERENCE CENTER.

Authors:  Bianca Sampaio Bonfim; Valmir Machado de Melo Filho; Fernanda Matos Fontenelle; Edna Lúcia Souza
Journal:  Rev Paul Pediatr       Date:  2020-06-05

6.  Cleaning and infection control of airway clearance devices used by CF patients.

Authors:  Eynav Manor; Michal Gur; Yuval Geffen; Lea Bentur
Journal:  Chron Respir Dis       Date:  2017-05-17       Impact factor: 2.444

7.  Influence of the Vibralung Acoustical Percussor on pulmonary function and sputum expectoration in individuals with cystic fibrosis.

Authors:  Courtney M Wheatley; Sarah E Baker; Cori M Daines; Hanna Phan; Marina G Martinez; Wayne J Morgan; Eric M Snyder
Journal:  Ther Adv Respir Dis       Date:  2018 Jan-Dec       Impact factor: 4.031

  7 in total

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