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

Puneet Mishra, David A. Edwards, Marc A. Huntoon, Christopher M. Sobey, Gregory G. Polkowski, John M. Corey, Kelly Mishra, Andrew A. Shinar, Stephen M. Engstrom, Cassandra Palmer, Stephen Bruehl

2021Regional Anesthesia & Pain Medicine23 citationsDOIOpen Access PDF

Abstract

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.

Topics & Concepts

MedicineRandomized controlled trialArthroplastyTotal knee arthroplastySurgeryOsteoarthritisRadiofrequency ablationPain managementClinical trialPhysical therapyAblationAlternative medicineInternal medicinePathologyAnesthesia and Pain ManagementTotal Knee Arthroplasty OutcomesSurgical Sutures and Adhesives