Patients' perspectives on services for epilepsy: a survey of patient satisfaction, preferences and information provision in 2394 people with epilepsy

K Poole, N Moran, G Bell, J Solomon, S. Kendall, M McCarthy, D McCormick, L Nashef, A Johnson, J Sander, S Shorvon

Research output: Contribution to journalArticlepeer-review

71 Citations (Scopus)

Abstract

The objectives of this study were to provide a comprehensive survey of satisfaction with care, care preferences and information provision for patients with epilepsy, and to formulate recommendations for the development of epilepsy services based on the findings. A questionnaire was distributed to 4620 patients who were currently receiving antiepileptic drugs for epilepsy, regardless of aetiology, duration or severity. Two different samples of patients with epilepsy were questioned: the first an unselected sample drawn from primary care, and the second consisting of consecutive patients drawn from hospital clinics. There were 2394 responses to the questionnaire. Satisfaction with primary and hospital care was high, both overall and for specific aspects. However, two major shortcomings were identified. First, few respondents felt that their care was shared between hospital and GP. Secondly, provision of information about epilepsy was perceived to be poor, particularly by the elderly. Younger patients and patients with severe epilepsy had a higher satisfaction with and preference for hospital care, whereas older age groups were more satisfied with and preferred primary care. Patients' main reasons for preferring primary care were that it was more personal and the GP was more familiar with them, and secondary care was preferred because the hospital doctor knew more about epilepsy. In conclusion, we have conducted the largest representative UK survey of patients' perceptions and views of the care available for epilepsy. Although patient satisfaction was high, information provision is poor and the shared care model is not operating effectively. We recommend that an emphasis be placed on methods for improving the interface between primary and secondary care. The setting up of hospital epilepsy centres, as recommended by the recently published Clinical Standards Advisory Group report on epilepsy, would provide a focus for these efforts and for information provision.
Original languageEnglish
Pages (from-to)551-8
Number of pages8
JournalSeizure
Volume9
Issue number8
DOIs
Publication statusPublished - 2000

Keywords

  • Adolescent
  • Adult
  • Aged
  • Epilepsy
  • Female
  • Health Services Research
  • Hospitalization
  • Humans
  • Male
  • Middle Aged
  • Patient Admission
  • Patient Education as Topic
  • Patient Satisfaction

Fingerprint

Dive into the research topics of 'Patients' perspectives on services for epilepsy: a survey of patient satisfaction, preferences and information provision in 2394 people with epilepsy'. Together they form a unique fingerprint.

Cite this