A Participatory Approach Involving Patients with Cystic Fibrosis and Healthcare Professionals for the Co-Design of an Adherence-Enhancing Intervention Toolkit
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I. Durieu | H. Rouzé | S. Touzet | J. Haesebaert | A. Dima | P. Occelli | M. Viprey | Q. Reynaud | F. Mougeot
[1] R. Fischer,et al. A multi-centre, randomized, controlled trial on coaching and telemonitoring in patients with cystic fibrosis: conneCT CF , 2021, BMC Pulmonary Medicine.
[2] E. Naureckas,et al. Patient and Family Participation in Clinical Guidelines Development: The Cystic Fibrosis Foundation Experience , 2020, Journal of participatory medicine.
[3] Alexander K. Saeri,et al. Research co-design in health: a rapid overview of reviews , 2020, Health Research Policy and Systems.
[4] J. Ainsworth,et al. Development of an intervention to increase adherence to nebuliser treatment in adults with cystic fibrosis: CFHealthHub , 2020, Pilot and Feasibility Studies.
[5] K. Riekert,et al. Clustered randomized controlled trial of a clinic-based problem-solving intervention to improve adherence in adolescents with cystic fibrosis. , 2019, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[6] Samuel S Allemann,et al. Adherence to long-term therapies in cystic fibrosis: a French cross-sectional study linking prescribing, dispensing, and hospitalization data , 2019, Patient preference and adherence.
[7] S. Donaldson,et al. Beyond the expected: Identifying broad research priorities of researchers and the cystic fibrosis community. , 2019, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[8] G. Bellis,et al. French Cystic Fibrosis Registry. Annual data report 2017 , 2019 .
[9] J. Ainsworth,et al. Supporting medication adherence for adults with cystic fibrosis: a randomised feasibility study , 2019, BMC Pulmonary Medicine.
[10] N. Kaciroti,et al. Impact of home spirometry on medication adherence among adolescents with cystic fibrosis , 2018, Pediatric pulmonology.
[11] P. Lombrail,et al. Lessons from patient and parent involvement (P&PI) in a quality improvement program in cystic fibrosis care in France , 2018, Orphanet Journal of Rare Diseases.
[12] E. Hatziagorou,et al. Telephone monitoring and home visits significantly improved the quality of life, treatment adherence and lung function in children with cystic fibrosis , 2017, Acta paediatrica.
[13] K. Boisen,et al. Coach to cope: feasibility of a life coaching program for young adults with cystic fibrosis , 2017, Patient preference and adherence.
[14] E. Nash,et al. The top 10 research priorities in cystic fibrosis developed by a partnership between people with CF and healthcare providers , 2017, Thorax.
[15] D. G. Altman,et al. GRIPP2 reporting checklists: tools to improve reporting of patient and public involvement in research , 2017, Research Involvement and Engagement.
[16] H. Elphick,et al. Investigating the feasibility of text message reminders to improve adherence to nebulized medication in children and adolescents with cystic fibrosis , 2017, Patient preference and adherence.
[17] L. Bentur,et al. The use of telehealth (text messaging and video communications) in patients with cystic fibrosis: A pilot study , 2017, Journal of telemedicine and telecare.
[18] C. Duncan,et al. A Quality Improvement Initiative to Improve Patient Adherence to Vitamin Supplementation in Cystic Fibrosis , 2017, Journal of pediatric gastroenterology and nutrition.
[19] J. Mainz,et al. Adherence to therapies in cystic fibrosis: a targeted literature review , 2017, Expert review of respiratory medicine.
[20] Z. Hoo,et al. Promoting adherence to nebulized therapy in cystic fibrosis: poster development and a qualitative exploration of adherence , 2015, Patient preference and adherence.
[21] B. Fullen,et al. Adherence of Subjects With Cystic Fibrosis to Their Home Program: A Systematic Review , 2014, Respiratory Care.
[22] Colin Tysall,et al. A Systematic Review of the Impact of Patient and Public Involvement on Service Users, Researchers and Communities , 2014, The Patient - Patient-Centered Outcomes Research.
[23] K. Riekert,et al. Pulmonary medication adherence and health-care use in cystic fibrosis. , 2014, Chest.
[24] Z. Hoo,et al. Moving cystic fibrosis care from rescue to prevention by embedding adherence measurement in routine care. , 2014, Paediatric respiratory reviews.
[25] Paul B Batalden,et al. The interdependent roles of patients, families and professionals in cystic fibrosis: a system for the coproduction of healthcare and its improvement , 2014, BMJ quality & safety.
[26] J. Sloan,et al. Patient engagement in research: a systematic review , 2014, BMC Health Services Research.
[27] K. Riekert,et al. The impact of medication adherence on lung health outcomes in cystic fibrosis , 2013, Current opinion in pulmonary medicine.
[28] G. Sawicki,et al. Treatment complexity in cystic fibrosis: trends over time and associations with site-specific outcomes. , 2013, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[29] F. Godlee,et al. Let the patient revolution begin , 2013, BMJ.
[30] M. Broder,et al. Adherence to dornase alfa treatment among commercially insured patients with cystic fibrosis , 2013, Journal of medical economics.
[31] J. Sweeney,et al. Patient and family engagement: a framework for understanding the elements and developing interventions and policies. , 2013, Health affairs.
[32] S. Madge,et al. Technological and behavioral strategies to reduce treatment burden and improve adherence to inhaled antibiotics in cystic fibrosis. , 2011, Respiratory medicine.
[33] K. Riekert,et al. Perceptions of barriers and facilitators: self-management decisions by older adolescents and adults with CF. , 2010, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[34] Olivier Las Vergnas,et al. Construction et reconnaissance des savoirs expérientiels des patients , 2010 .
[35] G. Latchford,et al. Motivational interviewing for adherence problems in cystic fibrosis , 2010, Pediatric pulmonology.
[36] Lisa Saiman,et al. Cell phone intervention to improve adherence: Cystic fibrosis care team, patient, and parent perspectives , 2010, Pediatric pulmonology.
[37] J. Gustafson,et al. Cystic Fibrosis , 2009, Journal of the Iowa Medical Society.
[38] G. Sawicki,et al. High treatment burden in adults with cystic fibrosis: challenges to disease self-management. , 2009, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[39] R. Gagnayre,et al. Le conducteur pédagogique : une aide pour mener des séances d’éducation thérapeutique , 2008 .
[40] P. L. Le Souëf,et al. Benefits of an education programme on the self-management of aerosol and airway clearance treatments for children with cystic fibrosis , 2006, Chronic respiratory disease.
[41] Richard A. Krueger,et al. Moderating Focus Groups , 1997 .
[42] L. Wirth. Clinical Sociology , 1931, American Journal of Sociology.
[43] K. Riekert,et al. Opportunities for cystic fibrosis care teams to support treatment adherence. , 2015, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[44] W. Lenney,et al. Developing a handheld record for patients with cystic fibrosis , 2015 .
[45] J. Rhéaume. Community Development and Empowerment: A Clinical Sociology Perspective , 2014 .
[46] P. Beirne,et al. Self-management education for cystic fibrosis. , 2011, Cochrane Database of Systematic Reviews.
[47] Paul Turner,et al. Enhancing Self-Efficacy for Self-Management in People with Cystic Fibrosis , 2011, MIE.
[48] V. D. Gaulejac. On the Origins of Clinical Sociology in France: Some Milestones , 2008 .
[49] J. Kitzinger. The methodology of focus groups: the importance of interaction between research participants , 1994 .
[50] P. Lazarsfeld,et al. Section: Overview of the Field: Definitions and History , 1989 .