Is preoperative genicular radiofrequency ablation effective for reducing pain following total knee arthroplasty? A pilot randomized clinical trial.

关节置换术 可视模拟标度 烧蚀 麻醉 布比卡因 膝关节痛 罗哌卡因
作者
Puneet Mishra,David A. Edwards,Marc A. Huntoon,Christopher Sobey,Gregory G. Polkowski,John M. Corey,Kelly Louise Mishra,Andrew A. Shinar,Stephen M. Engstrom,Cassandra J. Palmer,Stephen Bruehl
出处
期刊:Regional Anesthesia and Pain Medicine [BMJ]
卷期号:46 (9): 752-756 被引量:1
标识
DOI:10.1136/rapm-2021-102501
摘要

Background and objective Although total knee arthroplasty (TKA) is an effective treatment for severe knee osteoarthritis (OA), a subset of patients experience significant postoperative pain and dissatisfaction. Several clinical trials support the analgesic benefits of genicular nerve radiofrequency ablation (GN-RFA) for non-operative knee OA, but only one prior trial has examined the effects of this intervention given preoperatively on postoperative outcomes following TKA, showing no analgesic benefit of cooled GN-RFA. The current study evaluated whether conventional thermal GN-RFA performed preoperatively resulted in significant improvements in pain and function following TKA. Methods This was a single-center, prospective, randomized, sham-controlled, double-blinded pilot trial in which patients received either conventional GN-RFA (n=30) or sham (n=30) between 2 and 4 weeks prior to their TKA. Baseline measures were obtained preprocedurally on the day of intervention, with follow-up outcomes obtained preoperatively on the day of surgery, and at 2 and 6 weeks postoperatively. Results Patients receiving GN-RFA showed no significant improvements relative to sham controls in the primary outcome, pain intensity at rest at 6-week follow-up. Secondary outcomes, including pain with ambulation and physical function, also showed no significant differences between groups at any follow-up assessment. Conclusions Conventional GN-RFA of the superior lateral, superior medial, and inferior medial genicular nerves when performed prior to TKA did not provide clinically significant pain relief or improvement in functional status at 2 or 6 weeks postoperatively. Trial registration number NCT02947321.

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