Advances in methods for assessing the impact of epilepsy and antiepileptic drug therapy on patients' health-related quality of life

Author:

Wagner A. K.,Keller S. D.,Kosinski M.,Baker G. A.,Jacoby A.,Hsu M. -A.,Chadwick D. W.,Ware J. E.

Publisher

Springer Science and Business Media LLC

Subject

Public Health, Environmental and Occupational Health

Reference62 articles.

1. Livingston S. Psychosocial aspects of epilepsy. In: British Epilepsy Association, ed.Perspectives on Epilepsy 80/81. Berkshire: British Epilepsy Association 1981: 17–27.

2. The Roper Organization.Living with Epilepsy: Report of a Roper Poll of Patients on Quality of Life. New York, 1992.

3. Hermann BP. Quality of life in epilepsy.J Epilepsy 1992;5: 153–165.

4. Ellwood PM. Outcomes management: A technology of patient experience (Shattuck Lecture).New Engl J Med 1988;318: 1549–1556.

5. Slevin ML, Plant H, Lynch D, et al. Who should measure quality of life, the doctor or the patient?Br J Cancer 1988;57: 109–112.

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