Literature DB >> 35896902

Psychological/social factors associated with transfer readiness in young people with juvenile idiopathic arthritis.

Philippa Howsley1, Lisa Dunkley2, Rachel Calvert3, Samuel Hawley4, Rachel Tattersall2,5, Anne-Marie McMahon5, Daniel Hawley6.   

Abstract

The aim of this study is to investigate the relationships between psychological/social factors and transfer readiness from paediatric to adult rheumatology services in pre- and post-transfer young people (YP) with juvenile idiopathic arthritis (JIA). Participants completed questionnaires measuring a broad range of psychological/social factors (generalised anxiety, pain-specific anxiety, pain-related thoughts, depression, prosocial behaviours, problem behaviours, arthritis-related quality of life (QoL), social support, family functioning) and transfer readiness (transfer-related knowledge and skills, health-related self-efficacy). JIA disease activity was measured on the same day as the questionnaires. This study received all relevant ethical and regulatory approvals, and informed consent was received from or on behalf of all participants. In total, 40 pre-transfer YP with JIA aged 10-16 years (M = 13.54 years, 26 females) and their parents/guardians participated at Sheffield Children's NHS Foundation Trust, and 40 post-transfer YP with JIA aged 16-24 years (M = 20.16 years, 26 females) participated at Sheffield Teaching Hospitals NHS Foundation Trust. For both pre- and post-transfer YP, greater transfer readiness was associated with lower generalised anxiety levels, lower pain-specific anxiety levels, fewer pain-related thoughts, lower depression levels, fewer problem behaviours, better arthritis-related QoL, better social support, and better family functioning. Greater transfer readiness was also associated with less JIA disease activity for post-transfer YP only. A broad range of psychological/social factors were associated with transfer readiness in pre- and post-transfer YP with JIA. This highlights the importance of assessing and addressing YP's psychological/social well-being during their transition to adult services. Key Points • A wide range of psychological and social factors may be associated with how ready young people with juvenile idiopathic arthritis feel to move from paediatric to adult rheumatology services. • Transition outcomes may be improved by comprehensively assessing and addressing young people's psychological and social well-being.
© 2022. The Author(s), under exclusive licence to International League of Associations for Rheumatology (ILAR).

Entities:  

Keywords:  Adolescence; Juvenile idiopathic arthritis; Psychology; Social; Transfer; Transition

Year:  2022        PMID: 35896902     DOI: 10.1007/s10067-022-06237-5

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   3.650


  18 in total

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Authors:  Christopher Eccleston; Lance M McCracken; Abbie Jordan; Michelle Sleed
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2.  The Bath Adolescent Pain Questionnaire (BAPQ): development and preliminary psychometric evaluation of an instrument to assess the impact of chronic pain on adolescents.

Authors:  Christopher Eccleston; Abbie Jordan; Lance M McCracken; Michelle Sleed; Hannah Connell; Jacqui Clinch
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3.  Pediatric rheumatology in the United Kingdom: data from the British Pediatric Rheumatology Group National Diagnostic Register.

Authors:  D P Symmons; M Jones; J Osborne; J Sills; T R Southwood; P Woo
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4.  Outcome of transition phase patients with juvenile idiopathic arthritis.

Authors:  Heikki Relas; Riitta Luosujärvi; Silja Kosola
Journal:  Mod Rheumatol       Date:  2018-01-08       Impact factor: 3.023

Review 5.  Factors influencing the transition from pediatric to adult care: A scoping review of the literature to conceptualize a relevant education program.

Authors:  Maxime Morsa; Rémi Gagnayre; Carole Deccache; Pierre Lombrail
Journal:  Patient Educ Couns       Date:  2017-05-15

6.  A brief measure for assessing generalized anxiety disorder: the GAD-7.

Authors:  Robert L Spitzer; Kurt Kroenke; Janet B W Williams; Bernd Löwe
Journal:  Arch Intern Med       Date:  2006-05-22

7.  EULAR/PReS standards and recommendations for the transitional care of young people with juvenile-onset rheumatic diseases.

Authors:  Helen E Foster; Kirsten Minden; Daniel Clemente; Leticia Leon; Janet E McDonagh; Sylvia Kamphuis; Karin Berggren; Philomine van Pelt; Carine Wouters; Jennifer Waite-Jones; Rachel Tattersall; Ruth Wyllie; Simon R Stones; Alberto Martini; Tamas Constantin; Susanne Schalm; Berna Fidanci; Burak Erer; Erkan Demirkaya; Seza Ozen; Loreto Carmona
Journal:  Ann Rheum Dis       Date:  2016-11-01       Impact factor: 19.103

8.  High rates of unsuccessful transfer to adult care among young adults with juvenile idiopathic arthritis.

Authors:  Elizabeth Hazel; Xun Zhang; Ciarán M Duffy; Sarah Campillo
Journal:  Pediatr Rheumatol Online J       Date:  2010-01-11       Impact factor: 3.054

9.  The challenges of transferring chronic illness patients to adult care: reflections from pediatric and adult rheumatology at a US academic center.

Authors:  Aimee O Hersh; Shirley Pang; Megan L Curran; Diana S Milojevic; Emily von Scheven
Journal:  Pediatr Rheumatol Online J       Date:  2009-06-08       Impact factor: 3.054

10.  The Experience of Cognitive Intrusion of Pain: scale development and validation.

Authors:  Nina Attridge; Geert Crombez; Dimitri Van Ryckeghem; Edmund Keogh; Christopher Eccleston
Journal:  Pain       Date:  2015-10       Impact factor: 7.926

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