Regional Anesthesia and Valproate Sodium for the Prevention of Chronic Post-Amputation Pain
Abstract
This research was designed to test the efficacy of valproic in reducing the incidence of chronic pain after amputation, and to elucidate the underlying epigenetic mechanisms. We have completed the randomized controlled trial at Duke University, WRNMMC, and the Durham VAMC. All patients received multimodal perioperative care including regional anesthesia and were randomized to valproic acid or placebo. Our data reveal an overall rate of chronic pain of 68.22 % without a significant effect of valproic acid. The incidence of chronic pain was 65.45 % in the treatment group and 71.15 % in the placebo group.
Document Details
- Document Type
- Technical Report
- Publication Date
- Jun 01, 2018
- Accession Number
- AD1060310
Entities
People
- Thomas E. Buchheit
Organizations
- Duke University