A systematic overview - A decade of research'. The information and counselling needs of people with epilepsy

Seizure

Volumn 10, Issue 8, 2001, Pages 605-614

  Couldridge, L ^a   Kendall, S ^b   March, A ^a  

^a EPILEPSY SOCIETY   (United Kingdom)

^b UNIVERSITY OF HERTFORDSHIRE   (United Kingdom)

Author keywords

Counselling; Epilepsy; Epilepsy clinics; Information; Specialist epilepsy nurses

Indexed keywords

ARTICLE; CONTROLLED STUDY; EPILEPSY; HEALTH CARE NEED; HEALTH SERVICE; HUMAN; INTERPERSONAL COMMUNICATION; MEDICAL RESEARCH; MEDICAL SPECIALIST; OUTCOMES RESEARCH; PATIENT COUNSELING; PATIENT EDUCATION; PATIENT INFORMATION; PRIORITY JOURNAL; QUALITY OF LIFE; SOCIAL PSYCHOLOGY;

EID: 0035697353     PISSN: 10591311     EISSN: None     Source Type: Journal    
DOI: 10.1053/seiz.2001.0652     Document Type: Article

References (63)

1. Epilepsy and society
2. Epilepsy services, what people need, what they want, what they get
3. Explaining epilepsy
4. The cost of epilepsy in the United Kingdom: An estimation based on the results of two population-based studies
5. Bringing epilepsy out of the shadows
6. A review on psychosocial adjustment to impairment among persons with epilepsy
7. General practice based nurse specialists-taking a lead in improving the care of people with epilepsy
8. Services for patients with epilepsy
9. Existing care for epilepsy
10. Psychosocial aspects of epilepsy: Education and counselling for patients and families
11. Clinical review, an epilepsy needs document
12. Medical and sociological typologies: The case of Epilepsy
13. Being epileptic: Coming to terms with stigma
14. Effectiveness of coping strategies employed by people with chronic epilepsy
15. A study into life with epilepsy
16. Information seeking: A component of client decisions and health behaviour
17. Measuring attitudes toward chronic illness
18. Investigating the Information Needs of Carers of People with Epilepsy
19. Lifestyle advice in general practice: Rates recalled by patients
20. Verbal consultation regarding prescription drugs: Findings from a statewide study
21. Routine communication in sexually transmitted disease clinics: An observational study
22. Epilepsy: Patient views on their condition and treatment
23. Patient views on primary care services for epilepsy and areas where additional professional knowledge would be welcome
24. Are what people know about their epilepsy and what they want from an epilepsy service related?
25. Information exchange in an epilepsy forum on the World Wide Web
26. What people with epilepsy want from a hospital clinic
27. Epilepsy: Patient perceptions of their condition
28. An assessment of epilepsy patients' knowledge of their disorder
29. Learning needs of persons with epilepsy a comparison of perceptions of persons with epilepsy, nurses and physicians
30. Towards an evaluation of the effectiveness of an epilepsy nurse in primary care
31. Promoting self-care in epilepsy: The views of patients on the advice they had received from specialists, family doctors and an epilepsy nurse
32. Epilepsy care evaluation group
33. The role of counselling in an out-patient epilepsy clinic: A three year study
34. Effect of a primary care-based epilepsy specialist nurse service on quality of care from the patients perspective: Quasi-experimental evaluation
35. Do patients know enough about epilepsy?
36. Knowledge of epilepsy among relatives of the epilepsy sufferer
37. Patients' experiences of and satisfaction with care for their epilepsy
38. Epilepsy: A general practice study of knowledge and attitudes among sufferers and non-sufferers
39. Importance of health and family variables related to quality of life in individuals with uncontrolled seizures
40. The nature of epilepsy in the general population. II. Medical care
41. Relationships among epilepsy, social stigma, self esteem and social support
42. A survey of epilepsy-patient perceptions of video-game material/electronic screens and other factors as seizure precipitants
43. Patients' experience of epilepsy and health care
44. Epilepsy monitoring and advice recorded: General practitioners' views, current practice and patients' preferences
45. Patient expectations of epilepsy and of doctors who manage epilepsy
46. Care of patients with epilepsy in the community: Will new initiatives address old problems?
47. Living with epilepsy: A qualitative study investigating the experiences of young people attending outpatients clinics in leicester
48. Patients' opinions: Having a say in epilepsy service provision down under
49. The development of a questionnaire to assess knowledge of epilepsy: Knowledge of own condition
50. Development of a scale to measure core beliefs and perceived self-efficacy in adults with epilepsy
51. Feasibility and effects of nurse run clinics for patients with epilepsy in general practice: Randomised controlled trial
52. A district epilepsy service, with community based specialist liaison nurses and guidelines for shared care
53. An assessment of an epilepsy clinic
54. An audit of the organization of adult epilepsy services in the UK: A comparative review of epilepsy and general neurology clinics
55. Sepulveda epilepsy education: The efficacy of a psychoeducational treatment program in treating medical and psychosocial aspects of epilepsy
56. Psychosocial well-being and epilepsy: An empirical study