Putri, Kassie Gracella, Sampath, Sunil, Richardson, Charlotte Lucy, McCloskey, Alice and Rathbone, Adam Pattison (2025) A qualitative study exploring experiences of treatment in paediatric rheumatology - children’s, young people’s, parents’ and carers’ perspectives. Pediatric Rheumatology, 23 (7). pp. 1-12. ISSN 1546-0096
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Abstract
Background: There is limited literature in paediatric rheumatology describing holistic lived experiences of medical treatment from perspectives of children and young people (CYP) and their parents or carers (PC). This is important as it could have implications for adherence. This study aimed to explore treatment experiences of CYP and PC in a paediatric rheumatology service. Methods: Participants were recruited at a day-case unit for intravenous infusions at a tertiary paediatric rheumatology centre. Joint qualitative semi-structured interviews with CYP and PC were used to collect data. Data were transcribed, quality checked and thematically analysed using NVivo 12.4 to identify findings. Results: Thirty-two participants (15 CYP between the ages of 6 and 16 years, 17 PC) took part in interviews lasting 41 min and 43 s, on average. Participants described experiences using infliximab, followed by tocilizumab and abatacept. Participants experienced a wave, oscillating between positive and negative trajectories. Experiences of medical treatments were described as temporary, eventually changing and leading to treatment changes or cessation. Behaviours were influenced through somatic factors (pain, function), social factors (advice from health professionals, encouragement from friends, family and teachers, practicality of using treatment in relation to school, work and finance) and cognitive factors (fear of needles, fear of specific medications, beliefs about necessity). Conclusions: Collectively, findings demonstrate experiences of medical treatment reflect the nature of many paediatric rheumatology conditions, oscillating between periods of positive and negative trajectories. Somatic, social and cognitive experiences can be positive, when treatment is considered ‘successful’. Negative somatic, social or cognitive experiences led to behaviours such as treatment non-adherence. A limitation of the study is interviews were conducted jointly with CYP and PC, which may have influenced what participants were willing to say in front of one another however this does mean findings relate to both CYP and PC and so could be suitable targets for interventions to improve adherence.
Item Type: | Article |
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Uncontrolled Keywords: | Patient lived experiences, Qualitative research, Children and young people, Behavioural science, Treatment adherence, Medicines use, Carer experiences |
Subjects: | B Philosophy. Psychology. Religion > BF Psychology R Medicine > RA Public aspects of medicine > RA0421 Public health. Hygiene. Preventive Medicine R Medicine > RJ Pediatrics |
Divisions: | Pharmacy and Biomolecular Sciences |
Publisher: | BioMed Central |
SWORD Depositor: | Publications Router |
Date Deposited: | 24 Jan 2025 15:59 |
Last Modified: | 24 Jan 2025 16:00 |
DOI or ID number: | 10.1186/s12969-025-01063-w |
URI: | https://researchonline.ljmu.ac.uk/id/eprint/25390 |
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