Literature DB >> 25261572

Patient preferences for psychological support in inflammatory arthritis: a multicentre survey.

Emma Dures1, Celia Almeida1, Judy Caesley2, Alice Peterson2, Nicholas Ambler3, Marianne Morris1, Jon Pollock1, Sarah Hewlett1.   

Abstract

OBJECTIVES: Inflammatory arthritis (IA) can lead to anxiety, depression, pain and fatigue. Psychological support can improve quality of life and self-management; and European and American guidelines recommend support be offered. This study examined patient views on psychological support for their IA.
METHODS: A questionnaire designed by researchers, patient partners and clinicians was administered to 2280 patients with IA.
RESULTS: 1210 patients responded (53%): 74% women; mean age 59 years (SD 12.7); patient global 5 (2.3); disease duration <5 years (41%), 5-10 (20%), >10 (39%). Only 23% reported routinely being asked about social and emotional issues by a rheumatology professional, but 46% would like the opportunity to discuss psychological impact. If offered, 66% of patients reported they would use a self-management/coping clinic (63% pain management, 60% occupational therapy, 48% peer support groups, 46% patient education, 46% psychology/counselling). Patients want support with managing the impact of pain and fatigue (82%), managing emotions (57%), work and leisure (52%), relationships (37%) and depression (34%). Preferences are for support to be delivered by the rheumatology team (nurse 74%, doctor 55%) and general practitioners (GPs) (51%). Only 6% of patients stated that social and emotional issues were not relevant.
CONCLUSIONS: Demand for psychological support is high; however, less than a quarter of patients reported being asked about social and emotional issues, suggesting a gap between needs and provision. The preference is for delivery from rheumatology clinicians and GPs, and research should establish whether they have the skills and resources to meet patients' needs. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/

Entities:  

Keywords:  Health services research; Patient perspective; Psychology

Mesh:

Year:  2014        PMID: 25261572     DOI: 10.1136/annrheumdis-2014-205636

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  29 in total

1.  Improving recognition of anxiety and depression in rheumatoid arthritis: a qualitative study in a community clinic.

Authors:  Annabelle Machin; Samantha Hider; Nicky Dale; Carolyn Chew-Graham
Journal:  Br J Gen Pract       Date:  2017-07-17       Impact factor: 5.386

2.  Upswings in Cheerful Mood and Disease Activity in Patients with Rheumatoid Arthritis.

Authors:  Carlos Jesús Delgado-Domínguez; Alejandro Escudero-Contreras; Pilar Font-Ugalde; Desireé Ruiz-Vilchez; Eduardo Collantes-Estévez; Hugo Carretero-Dios
Journal:  Int J Behav Med       Date:  2016-10

Review 3.  Patient preferences for rheumatoid arthritis treatment.

Authors:  Betty Hsiao; Liana Fraenkel
Journal:  Curr Opin Rheumatol       Date:  2019-05       Impact factor: 5.006

Review 4.  Incorporating the patient's perspective in outcomes research.

Authors:  Betty Hsiao; Liana Fraenkel
Journal:  Curr Opin Rheumatol       Date:  2017-03       Impact factor: 5.006

5.  Lay Perspectives of Quality of Life in Rheumatoid Arthritis Patients: The Relevance of Autonomy and Psychological Distress.

Authors:  Isabel Santos; Natália Duarte; Oscar Ribeiro; Pedro Cantista; Carlos Vasconcelos
Journal:  Community Ment Health J       Date:  2019-03-29

Review 6.  Fatigue in inflammatory rheumatic diseases: current knowledge and areas for future research.

Authors:  Kristen Davies; Emma Dures; Wan-Fai Ng
Journal:  Nat Rev Rheumatol       Date:  2021-10-01       Impact factor: 20.543

7.  Brief intervention to reduce fatigue impact in patients with inflammatory arthritis: design and outcomes of a single-arm feasibility study.

Authors:  Emma Dures; Susan Bridgewater; Bryan Abbott; Jo Adams; Alice Berry; Lance M McCracken; Siobhan Creanor; Sarah Hewlett; Joe Lomax; Mwidimi Ndosi; Joanna Thorn; Marie Urban; Paul Ewings
Journal:  BMJ Open       Date:  2022-07-18       Impact factor: 3.006

8.  Remotely delivered cognitive-behavioural and personalized exercise interventions to lessen the impact of fatigue: a qualitative evaluation.

Authors:  Sarah E Bennett; Celia Almeida; Eva-Maria Bachmair; Stuart R Gray; Karina Lovell; Lorna Paul; Alison Wearden; Gary J Macfarlane; Neil Basu; Emma Dures
Journal:  Rheumatol Adv Pract       Date:  2022-06-25

9.  Agreement between Rheumatologist and Patient-reported Adherence to Methotrexate in a US Rheumatoid Arthritis Registry.

Authors:  Jeffrey R Curtis; Aseem Bharat; Lang Chen; Jeffrey D Greenberg; Leslie Harrold; Joel M Kremer; Tanya Sommers; Dimitrios Pappas
Journal:  J Rheumatol       Date:  2016-05-01       Impact factor: 4.666

10.  A qualitative study of patients' perspectives on collaboration to support self-management in routine rheumatology consultations.

Authors:  Emma Dures; Sarah Hewlett; Nicholas Ambler; Remona Jenkins; Joyce Clarke; Rachael Gooberman-Hill
Journal:  BMC Musculoskelet Disord       Date:  2016-03-15       Impact factor: 2.362

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