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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

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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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