Neurophysiological outcomes that sustained clinically significant improvements over 3 years of physiologic ECAP-controlled closed-loop spinal cord stimulation for the treatment of chronic pain

Author:

Mekhail Nagy AORCID,Levy Robert M,Deer Timothy RORCID,Kapural Leonardo,Li Sean,Amirdelfan Kasra,Hunter Corey W,Rosen Steven M,Costandi Shrif JORCID,Falowski Steven M,Burgher Abram H,Pope Jason E,Gilmore Christopher A,Qureshi Farooq A,Staats Peter S,Scowcroft James,McJunkin Tory,Kim Christopher K,Yang Michael I,Stauss Thomas,Rauck Richard,Duarte Rui VORCID,Soliday Nicole,Leitner Angela,Hanson Erin,Ouyang Zhonghua,Mugan Dave,Poree Lawrence

Abstract

IntroductionA novel, spinal cord stimulation (SCS) system with a physiologic closed-loop (CL) feedback mechanism controlled by evoked compound action potentials (ECAPs) enables the optimization of physiologic neural dose and the accuracy of the stimulation, not possible with any other commercially available SCS systems. The report of objective spinal cord measurements is essential to increase the transparency and reproducibility of SCS therapy. Here, we report a cohort of the EVOKE double-blind randomized controlled trial treated with CL-SCS for 36 months to evaluate the ECAP dose and accuracy that sustained the durability of clinical improvements.Methods41 patients randomized to CL-SCS remained in their treatment allocation and were followed up through 36 months. Objective neurophysiological data, including measures of spinal cord activation, were analyzed. Pain relief was assessed by determining the proportion of patients with ≥50% and ≥80% reduction in overall back and leg pain.ResultsThe performance of the feedback loop resulted in high-dose accuracy by keeping the elicited ECAP within 4µV of the target ECAP set on the system across all timepoints. Percent time stimulating above the ECAP threshold was >98%, and the ECAP dose was ≥19.3µV. Most patients obtained ≥50% reduction (83%) and ≥80% reduction (59%) in overall back and leg pain with a sustained response observed in the rates between 3-month and 36-month follow-up (p=0.083 and p=0.405, respectively).ConclusionThe results suggest that a physiological adherence to supra-ECAP threshold therapy that generates pain inhibition provided by ECAP-controlled CL-SCS leads to durable improvements in pain intensity with no evidence of loss of therapeutic effect through 36-month follow-up.

Funder

Saluda Medical

Publisher

BMJ

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