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Patient-Identified Quality Measures
Patient–Identified Indicators of High Quality Epilepsy Care Most quality indicators are based on published evidence, or experts’ opinion of what constitutes high quality of care. In order to assure that the patients’ perspective was also included during the development of these CDC quality indicators, we also asked patients to identify specific situations where they received what they thought was high quality of care and poor quality of care. After reviewing transcripts from six focus groups we found that patients in all groups reported similar themes. These patient identified quality indicators represent a number of the themes. Interestingly, several of the patient identified themes were also represented in the literature review and are included in the evidence based indicators. The links at the bottom of this page will help you provide information to your patients for each of these quality indicators such as how to obtain psychosocial support and details about the social effects of epilepsy.
For more information: Literature: Webpages:
Topic Editor: Mary Jo V. Pugh, PhD, RN and Steven C. Schachter, MD. |
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