Elevating the role of carers in rheumatoid arthritis management in the Asia-Pacific region.
Adaptation, Psychological
Adult
Aged
Arthritis, Rheumatoid
/ diagnosis
Attitude of Health Personnel
Australia
Caregivers
/ psychology
China
Clinical Decision-Making
Cost of Illness
Emotions
Female
Health Knowledge, Attitudes, Practice
Health Status
Humans
Japan
Male
Mental Health
Middle Aged
Patient-Centered Care
Patients
/ psychology
Qualitative Research
Rheumatologists
/ psychology
Severity of Illness Index
Social Support
Stakeholder Participation
carer reported
holistic
patient centred
qualitative
Journal
International journal of rheumatic diseases
ISSN: 1756-185X
Titre abrégé: Int J Rheum Dis
Pays: England
ID NLM: 101474930
Informations de publication
Date de publication:
Jul 2020
Jul 2020
Historique:
received:
19
09
2019
revised:
01
03
2020
accepted:
27
05
2020
pubmed:
3
7
2020
medline:
9
6
2021
entrez:
3
7
2020
Statut:
ppublish
Résumé
Carers may offer valuable insight into the true health status of patients with rheumatoid arthritis (RA). This multinational, multi-stakeholder, exploratory study in Australia, China and Japan aimed to enrich our understanding of the role and potential impact of carers on RA management. This study used a 2-phase sequential mixed methods approach involving 3 key stakeholder groups: rheumatologists, RA patients and carers. The first phase involved an in-depth qualitative exploratory survey (n = 30), which informed the development of the subsequent quantitative validation survey (n = 908). In both phases, patients and carers provided self-assessments of disease and support parameters. In the qualitative phase, patients usually understated the amount of physical support required, compared to carers. Rheumatologists underestimated the amount of physical and emotional care required, compared to carers and patients; however, in the quantitative phase, rheumatologists overestimated the level of support provided by carers. Levels of support provided by carers increased as disease severity increased. Active participation of carers in clinical consultations and treatment decision-making was deemed important by 55% of all patients and 82% of all carers. All stakeholders believed carers' insights into the physical and emotional conditions of patients were useful and should be considered in clinical decision-making. Over 95% of rheumatologists reported soliciting input from the carer. Carers provide valuable input that can give clinicians greater insight into the patients' physical and emotional states, and treatment adherence. Development of standardized carer-reported outcomes that correlate with patient-reported outcomes and clinical parameters will ensure clinical meaningfulness and external validity.
Identifiants
pubmed: 32613764
doi: 10.1111/1756-185X.13893
pmc: PMC7496573
doi:
Types de publication
Comparative Study
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
898-910Subventions
Organisme : Janssen Pharmaceuticals
Informations de copyright
© 2020 The Authors. International Journal of Rheumatic Diseases published by Asia Pacific League of Associations for Rheumatology and John Wiley & Sons Australia, Ltd.
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