Literature DB >> 22213280

Everyday life with rheumatoid arthritis and implications for patient education and clinical practice: a focus group study.

Tine Mechlenborg Kristiansen1, Jette Primdahl, Rasmus Antoft, Kim Hørslev-Petersen.   

Abstract

OBJECTIVES: This study aimed to explore how everyday life is affected by rheumatoid arthritis (RA), in order to inform patient education and clinical practice and generate further research.
METHODS: Six focus group interviews were conducted with, in total, 32 participants. Interview data were analysed using content analysis methods.
RESULTS: The study showed that RA affected almost every aspect of participants' everyday lives, particularly self-identity, social relationships, work and relationships with health and social care professionals. A small number of the participants did not have these experiences, due to receiving fast diagnosis and effective medical treatment.
CONCLUSION: The findings point to a need to increase knowledge about RA, support symptom management and reduce the physical, social and psychological challenges posed by RA in everyday life. An individualized and engaged approach to patient education, taking the individual experiences as the point of departure, is suggested. The results indicate directions for further research. The general implications for patient education that emerge from this study might not address the support needs of those who did not experience significant changes in everyday life. A more detailed and in-depth understanding about living with RA in the first years after diagnosis would provide a valuable supplement to the many retrospective studies, and useful knowledge in the design of patient education tailored to those who are newly diagnosed with RA.
Copyright © 2011 John Wiley & Sons, Ltd.

Entities:  

Mesh:

Year:  2011        PMID: 22213280     DOI: 10.1002/msc.224

Source DB:  PubMed          Journal:  Musculoskeletal Care        ISSN: 1478-2189


  23 in total

1.  Towards a better quality of life (QoL) for patients with pituitary diseases: results from a focus group study exploring QoL.

Authors:  Cornelie D Andela; Nicolasine D Niemeijer; Margreet Scharloo; Jitske Tiemensma; Shaaji Kanagasabapathy; Alberto M Pereira; Noëlle G A Kamminga; Ad A Kaptein; Nienke R Biermasz
Journal:  Pituitary       Date:  2015-02       Impact factor: 4.107

Review 2.  Patient goals in rheumatoid arthritis care: A systematic review and qualitative synthesis.

Authors:  Elizabeth Hulen; Ayla Ervin; Allison Schue; Gina Evans-Young; Somnath Saha; Edward H Yelin; Jennifer L Barton
Journal:  Musculoskeletal Care       Date:  2016-12-14

3.  [EULAR recommendations for patient education of people with inflammatory arthritis. Translation and evaluation in Germany].

Authors:  J Patermann; I Ehlebracht-König; G Lind-Albrecht; E Genth; A Reusch; R Küffner; U Müller-Ladner; J Braun
Journal:  Z Rheumatol       Date:  2016-03       Impact factor: 1.372

4.  (In)Visible illness: A photovoice study of the lived experience of self-managing rheumatoid arthritis.

Authors:  Susie Donnelly; Anthony G Wilson; Hasheem Mannan; Claire Dix; Laura Whitehill; Thilo Kroll
Journal:  PLoS One       Date:  2021-03-08       Impact factor: 3.240

5.  The motherhood choices decision aid for women with rheumatoid arthritis increases knowledge and reduces decisional conflict: a randomized controlled trial.

Authors:  T Meade; E Dowswell; N Manolios; L Sharpe
Journal:  BMC Musculoskelet Disord       Date:  2015-09-22       Impact factor: 2.362

6.  Sedentary behaviour in patients with rheumatoid arthritis: A qualitative study.

Authors:  Tanja Thomsen; Nina Beyer; Mette Aadahl; Merete L Hetland; Katrine Løppenthin; Julie Midtgaard; Bente A Esbensen
Journal:  Int J Qual Stud Health Well-being       Date:  2015-10-12

7.  Value-Based Health Care for Chronic Care: Aligning Outcomes Measurement with the Patient Perspective.

Authors:  David Ebbevi; Helena Hvitfeldt Forsberg; Anna Essén; Sofia Ernestam
Journal:  Qual Manag Health Care       Date:  2016 Oct/Dec       Impact factor: 0.926

8.  Psychometric properties of the single-item measure, severity of worst tiredness, in patients with moderately to severely active rheumatoid arthritis.

Authors:  Elizabeth D Bacci; Amy M DeLozier; Chen-Yen Lin; Carol L Gaich; Xiang Zhang; Terence Rooney; Stephanie de Bono; Richard Hoffman; Kathleen W Wyrwich
Journal:  Health Qual Life Outcomes       Date:  2017-12-06       Impact factor: 3.186

9.  Readability of patient information and consent documents in rheumatological studies.

Authors:  Bente Hamnes; Yvonne van Eijk-Hustings; Jette Primdahl
Journal:  BMC Med Ethics       Date:  2016-07-16       Impact factor: 2.652

10.  Building a Tailored, Patient-Guided, Web-Based Self-Management Intervention 'ReumaUitgedaagd!' for Adults With a Rheumatic Disease: Results of a Usability Study and Design for a Randomized Control Trail.

Authors:  Judy W Ammerlaan; Olga K Mulder; Nienke C de Boer-Nijhof; Bertha Maat; Aike A Kruize; Jaap van Laar; Harmieke van Os-Medendorp; Rinie Geenen
Journal:  JMIR Res Protoc       Date:  2016-06-23
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.