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Self-management intervention to reduce pulmonary exacerbations by supporting treatment adherence in adults with cystic fibrosis: a randomised controlled trial.
Wildman, Martin J; O'Cathain, Alicia; Maguire, Chin; Arden, Madelynne A; Hutchings, Marlene; Bradley, Judy; Walters, Stephen J; Whelan, Pauline; Ainsworth, John; Buchan, Iain; Mandefield, Laura; Sutton, Laura; Tappenden, Paul; Elliott, Rachel A; Hoo, Zhe Hui; Drabble, Sarah J; Beever, Daniel.
Afiliação
  • Wildman MJ; Sheffield Adult Cystic Fibrosis Centre, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK martin.wildman3@nhs.net.
  • O'Cathain A; School of Health and Related Research, University of Sheffield, Sheffield, UK.
  • Maguire C; School of Health and Related Research, University of Sheffield, Sheffield, UK.
  • Arden MA; Clinical Trials Research Unit, University of Sheffield, Sheffield, UK.
  • Hutchings M; Centre for Behavioural Science and Applied Psychology, Sheffield Hallam University, Sheffield, UK.
  • Bradley J; Sheffield Adult Cystic Fibrosis Centre, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
  • Walters SJ; Wellcome-Wolfson Institute for Experimental Medicine, School of Medicine Dentistry and Biomedical Sciences, Queen's University Belfast, Belfast, UK.
  • Whelan P; School of Health and Related Research, University of Sheffield, Sheffield, UK.
  • Ainsworth J; Health eResearch Centre - Division of Imaging, Informatics and Data Sciences, Faculty of Biology, Medicine and Health, The University of Manchester School of Health Sciences, Manchester, UK.
  • Buchan I; Health eResearch Centre - Division of Imaging, Informatics and Data Sciences, Faculty of Biology, Medicine and Health, The University of Manchester School of Health Sciences, Manchester, UK.
  • Mandefield L; Health eResearch Centre - Division of Imaging, Informatics and Data Sciences, Faculty of Biology, Medicine and Health, The University of Manchester School of Health Sciences, Manchester, UK.
  • Sutton L; Department of Public Health and Policy, Institute of Population Health, University of Liverpool, Liverpool, UK.
  • Tappenden P; School of Health and Related Research, University of Sheffield, Sheffield, UK.
  • Elliott RA; School of Health and Related Research, University of Sheffield, Sheffield, UK.
  • Hoo ZH; School of Health and Related Research, University of Sheffield, Sheffield, UK.
  • Drabble SJ; Division of Population Health, Health Services Research and Primary Care, Faculty of Biology, Medicine and Health, The University of Manchester School of Health Sciences, Manchester, UK.
  • Beever D; Sheffield Adult Cystic Fibrosis Centre, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
Thorax ; 77(5): 461-469, 2022 05.
Article em En | MEDLINE | ID: mdl-34556552
ABSTRACT

INTRODUCTION:

Recurrent pulmonary exacerbations lead to progressive lung damage in cystic fibrosis (CF). Inhaled medications (mucoactive agents and antibiotics) help prevent exacerbations, but objectively measured adherence is low. We investigated whether a multi-component (complex) self-management intervention to support adherence would reduce exacerbation rates over 12 months.

METHODS:

Between October 2017 and May 2018, adults with CF (aged ≥16 years; 19 UK centres) were randomised to the intervention (data-logging nebulisers, a digital platform and behavioural change sessions with trained clinical interventionists) or usual care (data-logging nebulisers). Outcomes included pulmonary exacerbations (primary outcome), objectively measured adherence, body mass index (BMI), lung function (FEV1) and Cystic Fibrosis Questionnaire-Revised (CFQ-R). Analyses were by intent to treat over 12 months.

RESULTS:

Among intervention (n=304) and usual care (n=303) participants (51% female, median age 31 years), 88% completed 12-month follow-up. Mean exacerbation rate was 1.63/year with intervention and 1.77/year with usual care (adjusted ratio 0.96; 95% CI 0.83 to 1.12; p=0.64). Adjusted mean differences (95% CI) were in favour of the intervention versus usual care for objectively measured adherence (9.5% (8.6% to 10.4%)) and BMI (0.3 (0.1 to 0.6) kg/m2), with no difference for %FEV1 (1.4 (-0.2 to 3.0)). Seven CFQ-R subscales showed no between-group difference, but treatment burden reduced for the intervention (3.9 (1.2 to 6.7) points). No intervention-related serious adverse events occurred.

CONCLUSIONS:

While pulmonary exacerbations and FEV1 did not show statistically significant differences, the intervention achieved higher objectively measured adherence versus usual care. The adherence difference might be inadequate to influence exacerbations, though higher BMI and lower perceived CF treatment burden were observed.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrose Cística / Autogestão Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male Idioma: En Revista: Thorax Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrose Cística / Autogestão Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male Idioma: En Revista: Thorax Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido