Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

A 'real puzzle': the views of patients with epilepsy about the organisation of care

Elwyn, Glyn, Todd, Stuart Phlip, Hibbs, R., Thapar, Ajay Kumar, Edwards, P., Webb, A., Wilkinson, Clare Elizabeth and Kerr, Michael Patrick 2003. A 'real puzzle': the views of patients with epilepsy about the organisation of care. BMC Family Practice 4 , p. 4. 10.1186/1471-2296-4-4

[img]
Preview
PDF - Published Version
Available under License Creative Commons Attribution.

Download (235kB) | Preview

Abstract

Background Little is known about how individuals who have a diagnosis of epilepsy have experienced healthcare services or their views about how they should best be organised to meet their ongoing needs. Methods Focus group interviews. Individuals with epilepsy were identified in 5 practices in Wales: 90 were invited, 40 confirmed attendance and 19 individuals attended interviews in 5 groups of size 6, 5, 4, 3 and 1 (Table 2). Inclusion criteria: individuals with a confirmed diagnosis of epilepsy, aged between 18–65. The exclusion criteria were learning disability or an inability to travel to interview locations. Results The individuals in these group interviews were not 'epilepsy activists' yet they remained critical in extended discussions about the services encountered during their patient careers, wanting more information and advice about how to adapt to problems, particularly after initial diagnosis, more involvement in decision making, rapid access to expertise, preferably local, and improved communication between clinicians. A central concern was the tendency for concerns to be silenced, either overtly, or covertly by perceived haste, so that they felt marginalised, despite their own claims to own expert personal knowledge. Conclusions Users of existing services for epilepsy are critical of current systems, especially the lack of attention given to providing information, psychosocial support and the wishes of patients to participate in decision making. Any reorganisation of services for individuals with epilepsy should take into account these perceived problems as well as try to reconcile the tension between the distant and difficult to access expertise of specialists and the local but unconfident support of generalists. The potential benefit of harnessing information technology to allow better liaison should be investigated.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Medicine
MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG)
Subjects: R Medicine > R Medicine (General)
Uncontrolled Keywords: Delivery of Health Care/organization & administration, Delivery of Health Care/standards, Epilepsy/psychology, Female, Humans, Interviews as Topic, Male, Patient Participation, Patient Satisfaction, Quality of Health Care, Wales
Publisher: BioMed Central
ISSN: 1471-2296
Date of First Compliant Deposit: 30 March 2016
Last Modified: 13 Apr 2019 02:50
URI: http://orca.cf.ac.uk/id/eprint/65226

Citation Data

Cited 11 times in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item Edit Item

Downloads

Downloads per month over past year

View more statistics