Biportal Endoscopic Spinal Cord Stimulation Paddle Lead Implantation: Technical Note and Preliminary Clinical Results.

Neuromodulation

Department of Pain Medicine, the Second Affiliated Hospital of Chongqing Medical University, Chongqing, China; Department of Spine Surgery, the Second Affiliated Hospital of Chongqing Medical University, Chongqing, China. Electronic address:

Published: August 2024

AI Article Synopsis

  • This study investigates a new, minimally invasive technique for implanting spinal cord stimulation (SCS) paddle leads using a biportal endoscope and shares early clinical results.
  • Six patients underwent the procedure from February 2022 to December 2023, showing low blood loss (30 mL on average) and a reasonably quick operative time (87.5 minutes).
  • Results indicated significant pain reduction post-surgery, with most patients experiencing minimal complications, and the technique demonstrates promise for safely implementing SCS systems.

Article Abstract

Objective: This study aims to elucidate a novel, minimally invasive surgical technique using a biportal endoscope for the implantation of spinal cord stimulation (SCS) paddle leads and to report the preliminary results of its clinical application.

Materials And Methods: The perioperative data of patients who underwent the biportal endoscopic SCS paddle lead implantation in our department were collected; the surgical procedure was delineated, and the clinical outcomes were assessed.

Results: From February 2022 to December 2023, six patients underwent biportal endoscopic SCS paddle lead implantation. The median follow-up time was nine months (range one to three months). The median intraoperative blood loss was 30 mL (range 25-50 mL), and the median operative time was 87.5 minutes (range 75-110 minutes). One patient experienced severe neck pain during the operation, whereas the other five patients experienced no surgical complications. One patient was found to have a slight lead migration three months after surgery, which did not affect the therapeutic effect. The median visual analogue scale (VAS) of the surgical area was 0.5 (range 0-2), 2.5 (range 1-4), and 0.5 (range 0-1) during the operation and one day and one week after the operation, respectively. The median VAS of the six patients' primary disease was 8 (range 7-9) before surgery and 2.5 (range 1-4) at the last postoperative follow-up (pain reduction ≥50%).

Conclusion: Paddle lead systems for SCS can be implanted successfully using a biportal endoscopic technique.

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Source
http://dx.doi.org/10.1016/j.neurom.2024.06.003DOI Listing

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