Experiences of coordinated care for people in the UK affected by rare diseases: cross-sectional survey of patients, carers, and healthcare professionals

Walton, Holly; Ng, Pei Li; Simpson, Amy; Bloom, Lara; Chitty, Lyn S.; Fulop, Naomi J.; Hunter, Amy; Jones, Jennifer; Kai, Joe; Kerecuk, Larissa; Kokocinska, Maria; Leeson-Beevers, Kerry; Parkes, Sharon; Ramsay, Angus I.G.; Sutcliffe, Alastair; Taylor, Christine; Morris, Stephen

Abstract

Background
Poorly coordinated care can have major impacts on patients and families affected by rare conditions, with negative physical health, psychosocial and financial consequences. This study aimed to understand how care is coordinated for rare diseases in the United Kingdom.

Methods
We undertook a national survey in the UK involving 760 adults affected by rare diseases, 446 parents/carers of people affected by rare diseases, and 251 healthcare professionals who care for people affected by rare diseases.

Results
Findings suggested that a wide range of patients, parents and carers do not have coordinated care. For example, few participants reported having a care coordinator (12% patients, 14% parents/carers), attending a specialist centre (32% patients, 33% parents/carers) or having a care plan (10% patients, 44% parents/carers). A very small number of patients (2%) and parents/carers (5%) had access to all three—a care coordinator, specialist centre and care plan. Fifty four percent of patients and 33% of parents/carers reported access to none of these. On the other hand, a higher proportion of healthcare professionals reported that families with rare conditions had access to care coordinators (35%), specialist centres (60%) and care plans (40%).

Conclusions
Care for families with rare conditions is generally not well coordinated in the UK, with findings indicating limited access to care coordinators, specialist centres and care plans. Better understanding of these issues can inform how care coordination might be improved and embrace the needs and preferences of patients and families affected by rare conditions.

Citation

Walton, H., Ng, P. L., Simpson, A., Bloom, L., Chitty, L. S., Fulop, N. J., Hunter, A., Jones, J., Kai, J., Kerecuk, L., Kokocinska, M., Leeson-Beevers, K., Parkes, S., Ramsay, A. I., Sutcliffe, A., Taylor, C., & Morris, S. (2023). Experiences of coordinated care for people in the UK affected by rare diseases: cross-sectional survey of patients, carers, and healthcare professionals. Orphanet Journal of Rare Diseases, 18(1), Article 364. https://doi.org/10.1186/s13023-023-02934-9

• Journal Article Type: Article
• Acceptance Date: Sep 25, 2023
• Online Publication Date: Nov 23, 2023
• Publication Date: Nov 23, 2023
• Deposit Date: Nov 27, 2023
• Publicly Available Date: Nov 27, 2023
• Journal: Orphanet Journal of Rare Diseases
• Electronic ISSN: 1750-1172
• Publisher: Springer Verlag
• Peer Reviewed: Peer Reviewed
• Volume: 18
• Issue: 1
• Article Number: 364
• DOI: https://doi.org/10.1186/s13023-023-02934-9
• Keywords: Rare conditions, Rare diseases, Care coordination, Survey, Care plan, Care coordinator, Specialist centre
• Public URL: https://nottingham-repository.worktribe.com/output/27599648
• Publisher URL: https://ojrd.biomedcentral.com/articles/10.1186/s13023-023-02934-9