CHARLOTTE HALL CHARLOTTE.HALL@NOTTINGHAM.AC.UK
Principal Research Fellow
Healthcare utilisation and costs associated with poor access to diagnosis and treatment for children and young people with tic disorders
Hall, Charlotte L; Le Novere, Marie; Murphy, Tara; McNally, Emma; Hollis, Christopher; Hunter, Rachael
Authors
Marie Le Novere
Tara Murphy
Emma McNally
CHRIS HOLLIS chris.hollis@nottingham.ac.uk
Professor of Child and Adolescent Psychiatry and Digital Mental Health
Rachael Hunter
Abstract
Background: There are no specific national guidelines in England to guide healthcare professionals in how to assess or treat young people with tic disorders. Access to evidence-based treatment, including behavioural therapy is of limited availability.
Objectives: This study examined the economic impact on services arising from a lack of access to appropriate healthcare services for young people with tic disorders, alongside the impact on school attendance.
Methods: This study used data from the randomised controlled trial “ORBIT” (online remote behavioural intervention for tics). ORBIT compared online exposure and response prevention behavioural therapy for tics with online psychoeducation and recruited 224 young people aged 9-17 years in England. Here, we explore costs of health service use and school absenteeism from children who participated in ORBIT and present these alongside the economic impact of including ORBIT within a tic service. We supplement ORBIT data with findings from two case studies.
Findings: The data showed that patients have care from several healthcare professionals and miss school due to accessing care for tics. The case studies suggest that most of these contacts with specialist services are unlikely to be supportive. However, adding ORBIT could save the National Healthcare Service £1million.
Conclusions: Young people with tic disorders are likely to engage in substantial use of healthcare resources because of inadequate care pathways. The availability of an evidence-based online therapy such as ORBIT could save money to the healthcare system.
Clinical implications: There is a need to improve service provision and develop national guidelines for tic disorders.
Citation
Hall, C. L., Le Novere, M., Murphy, T., McNally, E., Hollis, C., & Hunter, R. (2024). Healthcare utilisation and costs associated with poor access to diagnosis and treatment for children and young people with tic disorders. BMJ Mental Health, 27(1), Article e301241. https://doi.org/10.1136/bmjment-2024-301241
Journal Article Type | Article |
---|---|
Acceptance Date | Sep 20, 2024 |
Online Publication Date | Nov 7, 2024 |
Publication Date | 2024-11 |
Deposit Date | Sep 23, 2024 |
Publicly Available Date | Nov 7, 2024 |
Journal | BMJ Mental Health |
Electronic ISSN | 2755-9734 |
Publisher | BMJ Publishing Group |
Peer Reviewed | Peer Reviewed |
Volume | 27 |
Issue | 1 |
Article Number | e301241 |
DOI | https://doi.org/10.1136/bmjment-2024-301241 |
Public URL | https://nottingham-repository.worktribe.com/output/39982232 |
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Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
Copyright Statement
© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY. Published by BMJ.
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