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

被引:27
|
作者
Wildman, Martin J. [1 ,2 ]
O'Cathain, Alicia [2 ]
Maguire, Chin [3 ]
Arden, Madelynne A. [4 ]
Hutchings, Marlene [1 ]
Bradley, Judy [5 ]
Walters, Stephen J. [2 ]
Whelan, Pauline [6 ]
Ainsworth, John [6 ]
Buchan, Iain [6 ,7 ]
Mandefield, Laura [2 ]
Sutton, Laura [2 ]
Tappenden, Paul [2 ]
Elliott, Rachel A. [8 ]
Hoo, Zhe Hui [1 ,2 ]
Drabble, Sarah J. [2 ]
Beever, Daniel [3 ]
机构
[1] Sheffield Teaching Hosp NHS Fdn Trust, Sheffield Adult Cyst Fibrosis Ctr, Sheffield, S Yorkshire, England
[2] Univ Sheffield, Sch Hlth & Related Res, Sheffield, S Yorkshire, England
[3] Univ Sheffield, Clin Trials Res Unit, Sheffield, S Yorkshire, England
[4] Sheffield Hallam Univ, Ctr Behav Sci & Appl Psychol, Sheffield, S Yorkshire, England
[5] Queens Univ Belfast, Sch Med Dent & Biomed Sci, Wellcome Wolfson Inst Expt Med, Belfast, Antrim, North Ireland
[6] Univ Manchester, Fac Biol Med & Hlth, Hlth eRes Ctr, Div Imaging Informat & Data Sci,Sch Hlth Sci, Manchester, Lancs, England
[7] Univ Liverpool, Inst Populat Hlth, Dept Publ Hlth & Policy, Liverpool, Merseyside, England
[8] Univ Manchester, Fac Biol Med & Hlth, Sch Hlth Sci, Div Populat Hlth Hlth Serv Res & Primary Care, Manchester, Lancs, England
关键词
cystic fibrosis; psychology; nebuliser therapy; MEDICATION ADHERENCE; CLINICAL-TRIALS; QUESTIONNAIRE; EXPLORATION; EFFICACY; HEALTH;
D O I
10.1136/thoraxjnl-2021-217594
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
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/m(2)), 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.
引用
收藏
页码:461 / 469
页数:9
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