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. 2021 Feb 23;67(2):598–605. doi: 10.1007/s10620-021-06896-5

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© The Author(s) 2021

Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.

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Fig. 3 — Percent change in reported pain compared with baseline for each patient in the case series is shown at approximately 6 months after implant (a) and during the most recent visit (b). Responders were defined by achievement of greater than 50% pain relief. Overall, 17 of 23 patients were responders. Of the six non-responders, four were low frequency spinal cord stimulators (Trad-SCS) and two were high frequency spinal cord stimulators (10 kHz SCS)