Using Chronic Pain Outcomes Data to Improve Outcomes - 20/05/16
Résumé |
Standardization of care that is derived from analysis of outcomes data can lead to improvements in quality and efficiency of care. The outcomes data should be validated, standardized, and integrated into ongoing patient care with minimal burden on the patient and health care team. This article describes the organization and workflow of a chronic pain clinic registry designed to collect and analyze patient data for quality improvement and dissemination. Future efforts in using mobile technology and integrating patient-reported outcome data in the electronic health records have the potential to offer new and improved models of comprehensive pain management.
Le texte complet de cet article est disponible en PDF.Keywords : Practice-based evidence, Patient-reported outcomes, Outcomes data collection, Analysis of patient data, Quality improvement, Mobile health, Electronic health record integration
Plan
| Disclosures: The Tri-Institutional Pain Registry was developed with the support of grant RC2 DA028928 from NIDA and is currently supported in part by a grant from Purdue Pharm, Ltd. No authors have any other conflicts of interest/disclosures to report. |
Vol 34 - N° 2
P. 395-408 - juin 2016 Retour au numéro
Article précédent
- Assessing and Managing Sleep Disturbance in Patients with Chronic Pain
- Martin D. Cheatle, Simmie Foster, Aaron Pinkett, Matthew Lesneski, David Qu, Lara Dhingra
- State Policies Regulating the Practice of Pain Management : Statutes, Rules, and Guidelines That Shape Pain Care
- Robert K. Twillman, Aaron M. Gilson, Kathryn N. Duensing
Bienvenue sur EM-consulte, la référence des professionnels de santé.
L’accès au texte intégral de cet article nécessite un abonnement.
Déjà abonné à cette revue ?