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Self-management intervention to reduce pulmonary exacerbations by supporting treatment adherence in adults with cystic fibrosis: a randomised controlled trial

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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016257/
https://www.ncbi.nlm.nih.gov/pubmed/34556552
http://dx.doi.org/10.1136/thoraxjnl-2021-217594
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author 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
author_facet 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
author_sort Wildman, Martin J
collection PubMed
description 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 (FEV(1)) 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/m(2)), with no difference for %FEV(1) (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 FEV(1) 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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spelling pubmed-90162572022-05-04 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 Thorax Cystic Fibrosis 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 (FEV(1)) 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/m(2)), with no difference for %FEV(1) (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 FEV(1) 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. BMJ Publishing Group 2022-05 2021-09-23 /pmc/articles/PMC9016257/ /pubmed/34556552 http://dx.doi.org/10.1136/thoraxjnl-2021-217594 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
spellingShingle Cystic Fibrosis
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
Self-management intervention to reduce pulmonary exacerbations by supporting treatment adherence in adults with cystic fibrosis: a randomised controlled trial
title Self-management intervention to reduce pulmonary exacerbations by supporting treatment adherence in adults with cystic fibrosis: a randomised controlled trial
title_full Self-management intervention to reduce pulmonary exacerbations by supporting treatment adherence in adults with cystic fibrosis: a randomised controlled trial
title_fullStr Self-management intervention to reduce pulmonary exacerbations by supporting treatment adherence in adults with cystic fibrosis: a randomised controlled trial
title_full_unstemmed Self-management intervention to reduce pulmonary exacerbations by supporting treatment adherence in adults with cystic fibrosis: a randomised controlled trial
title_short Self-management intervention to reduce pulmonary exacerbations by supporting treatment adherence in adults with cystic fibrosis: a randomised controlled trial
title_sort self-management intervention to reduce pulmonary exacerbations by supporting treatment adherence in adults with cystic fibrosis: a randomised controlled trial
topic Cystic Fibrosis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9016257/
https://www.ncbi.nlm.nih.gov/pubmed/34556552
http://dx.doi.org/10.1136/thoraxjnl-2021-217594
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