Improving the wellbeing of caregivers of patients with COPD using a home-based pulmonary rehabilitation programme

被引:10
作者
Grosbois, Jean-Marie [1 ]
Gephine, Sarah [2 ]
Kyheng, Maeva [3 ]
Le Rouzic, Olivier [4 ,5 ]
Chenivesse, Cecile [4 ,5 ]
机构
[1] FormAct Sante, Perenchies, France
[2] Univ Lille, Univ Artois, Univ Littoral Cote Dopale, ULR 7369 URePSSS Unite Rech Pluridisciplinaire Sp, Lille, France
[3] Univ Lille, CHU Lille, Dept Biostat, EA Sante Publ Epidemiol & Qualite Soins 2694, Lille, France
[4] CHU Lille, Serv Pneumol & Immunoallergol, Ctr Reference Constitutif Malad Pulm Rares, Lille, France
[5] Univ Lille, Lille, France
关键词
QUALITY-OF-LIFE; INFORMAL CAREGIVERS; DISEASE; BURDEN; HEALTH; DEPRESSION; DIFFERENCE; ANXIETY; CARERS; IMPACT;
D O I
10.1183/23120541.00255-2022
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Objectives The aim of this study was to evaluate the effects of a home-based pulmonary rehabilitation (PR) programme on anxiety and depressive symptoms, general fatigue and burden in informal caregivers of patients with COPD. We also evaluated the baseline characteristics of both patients and caregivers that contributed to the change in caregiver's outcomes after PR. Methods In this retrospective study, patients with COPD were referred to an 8-week home-based PR programme consisting of a weekly supervised 90-min session. Informal caregivers were invited to participate in PR according to the patient's preference and its availability. Caregivers received educational support, behavioural therapies and self-management strategies using the same methods as for patients. Burden, anxiety and depressive symptoms, and general fatigue of caregivers were assessed at baseline and at the end of PR. Results 241 patients with COPD and 138 (57.3%) caregivers were included. The majority of the caregivers were women (70.5%) and spouses (90.3%) and had at least three comorbidities (57.3%). A large proportion of caregivers showed baseline high burden, anxiety symptoms and abnormal fatigue (40%, 40% and 45%, respectively). Burden, anxiety and depressive symptoms, and general fatigue of informal caregivers were all improved after PR (p<0.05). Long-term oxygen therapy and/or noninvasive ventilation, coronaropathy and/or peripheral arterial disease and a higher baseline modified Medical Research Council Dyspnoea scale score in patients with COPD were associated with a decrease in caregiver's burden after PR. Conclusion A large proportion of caregivers of patients with COPD showed anxiety symptoms, fatigue and a high burden. These outcomes were improved by integrating the caregiver into a home-based PR programme.
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页数:10
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共 45 条
[1]   Using the Standardized Difference to Compare the Prevalence of a Binary Variable Between Two Groups in Observational Research [J].
Austin, Peter C. .
COMMUNICATIONS IN STATISTICS-SIMULATION AND COMPUTATION, 2009, 38 (06) :1228-1234
[2]   Usefulness of the Medical Research Council (MRC) dyspnoea scale as a measure of disability in patients with chronic obstructive pulmonary disease [J].
Bestall, JC ;
Paul, EA ;
Garrod, R ;
Garnham, R ;
Jones, PW ;
Wedzicha, JA .
THORAX, 1999, 54 (07) :581-586
[3]   A longitudinal study looking at and beyond care recipient health as a predictor of long term care home admission [J].
Betini, Raquel S. D. ;
Hirdes, John P. ;
Lero, Donna S. ;
Cadell, Susan ;
Poss, Jeff ;
Heckman, George .
BMC HEALTH SERVICES RESEARCH, 2017, 17
[4]   Involvement of informal caregivers in supporting patients with COPD: a review of intervention studies [J].
Bryant, Jamie ;
Mansfield, Elise ;
Boyes, Allison W. ;
Waller, Amy ;
Sanson-Fisher, Rob ;
Regan, Timothy .
INTERNATIONAL JOURNAL OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE, 2016, 11 :1587-1596
[5]   Informal caregiving in COPD: A systematic review of instruments and their measurement properties [J].
Cruz, Joana ;
Marques, Alda ;
Machado, Ana ;
O'Hoski, Sachi ;
Goldstein, Roger ;
Brooks, Dina .
RESPIRATORY MEDICINE, 2017, 128 :13-27
[6]   Minimal (clinically) important differences for the Fatigue Assessment Scale in sarcoidosis [J].
de Kleijn, Willemien P. E. ;
De Vries, Jolanda ;
Wijnen, Petal A. H. M. ;
Drent, Marjolein .
RESPIRATORY MEDICINE, 2011, 105 (09) :1388-1395
[7]   Postintensive care unit psychological burden in patients with chronic obstructive pulmonary disease and informal caregivers: A multicenter study [J].
de Miranda, Sandra ;
Pochard, Frederic ;
Chaize, Marine ;
Megarbane, Bruno ;
Cuvelier, Antoine ;
Bele, Nicolas ;
Gonzalez-Bermejo, Jesus ;
Aboab, Jerome ;
Lautrette, Alexandre ;
Lemiale, Virginie ;
Roche, Nicolas ;
Thirion, Marina ;
Chevret, Sylvie ;
Schlemmer, Benoit ;
Similowski, Thomas ;
Azoulay, Elie .
CRITICAL CARE MEDICINE, 2011, 39 (01) :112-118
[8]   Definition of a COPD self-management intervention: International Expert Group consensus [J].
Effing, Tanja W. ;
Vercoulen, Jan H. ;
Bourbeau, Jean ;
Trappenburg, Jaap ;
Lenferink, Anke ;
Cafarella, Paul ;
Coultas, David ;
Meek, Paula ;
van der Valk, Paul ;
Bischoff, Erik W. M. A. ;
Bucknall, Christine ;
Dewan, Naresh A. ;
Early, Frances ;
Fan, Vincent ;
Frith, Peter ;
Janssen, Daisy J. A. ;
Mitchell, Katy ;
Morgan, Mike ;
Nici, Linda ;
Patel, Irem ;
Walters, Haydn ;
Rice, Kathryn L. ;
Singh, Sally ;
Zuwallack, Richard ;
Benzo, Roberto ;
Goldstein, Roger ;
Partridge, Martyn R. ;
van der Palen, Job .
EUROPEAN RESPIRATORY JOURNAL, 2016, 48 (01) :46-54
[9]   Clinicians' Views of Educational Interventions for Carers of Patients With Breathlessness Due to Advanced Disease: Findings From an Online Survey [J].
Ewing, Gail ;
Penfold, Clarissa ;
Benson, John A. ;
Mahadeva, Ravi ;
Howson, Sophie ;
Burkin, Julie ;
Booth, Sara ;
Lovick, Roberta ;
Gilligan, David ;
Todd, Christopher ;
Farquhar, Morag .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2017, 53 (02) :265-271
[10]   Assessing carer needs in chronic obstructive pulmonary disease [J].
Farquhar, Morag .
CHRONIC RESPIRATORY DISEASE, 2018, 15 (01) :26-35