Fast-Acting Subperception Spinal Cord Stimulation for Persistent Spinal Pain Syndromes: Real-World Outcomes for up to 3 Years in an “As-Treated” Cohort from a Global Observational Study
13 affiliations
- 1Orthopedic Surgery Department, HCA Florida West Orthopedic Specialists, Pensacola, FL 32514, USA
- 2Interventional Pain Management Department, Multidisciplinary Pain Management Services, Okemos, MI 48864, USA
- 3Department of Neurosurgery, Hospital Universitario La Paz, 28046 Madrid, Spain
- 4Johanniter-Kliniken Hamm, 59063 Hamm, Germany
- 5Department of Neuro-Spine and Neuromodulation, Poitiers University Hospital, 86021 Poitiers, France
- 6Department of Anesthesiology and Pain Management, James Cook University Hospital, Middlesbrough TS4 3BW, UK
- 7Department of Anesthesiology and Pain Management, Hospital de la Ribera, 46600 Valencia, Spain
- 8Department of Stereotactic and Functional Neurosurgery, University Hospital Cologne, 50937 Cologne, Germany
- 9Department of Anesthesiology and Pain Management, Southmead Hospital, Bristol BS10 5NB, UK
- 10Department of Anesthesiology and Pain Management, Rijnstate Hospital, 6815 AD Arnhem, The Netherlands
- 11Department of Stereotactic and Functional Neurosurgery, Heinrich Heine University, 40225 Düsseldorf, Germany
- 12Interventional Pain Management Department, Florida Pain Clinic, Ocala, FL 34471, USA
- 13Department of Neurosurgery, Inter Neuro, 10629 Berlin, Germany
Abstract
Background/Objectives: Evidence on the effectiveness of spinal cord stimulation using fast-acting subperception therapy (FAST-SCS) in patients with persistent spinal pain syndrome (PSPS) remains limited. We evaluated clinical outcomes of FAST-SCS in patients with PSPS types 1 (i.e., non-surgical back pain) and 2 (i.e., failed back surgery syndrome). Methods: Our global, multicenter, retrospective, observational chart review included all consecutive adults with chronic low back and/or leg pain due to PSPS who received SCS with a multimodal device and reported using FAST-SCS at their latest follow-up. Available data from the patients’ medical files, documented by site personnel per their standard of care, were collected and analyzed. Pain intensity was assessed using the numerical rating scale (NRS); percent pain relief (PPR) was recorded where available. Main outcomes included changes in overall pain (NRS) compared to baseline, proportion of patients with ≥50% reduction in overall pain (NRS), proportion of patients with minimal pain (NRS ≤ 2), and high responder rates (PPR ≥ 80%). Data was analyzed for all PSPS patients at the last follow-up, with preliminary analysis of patients who completed 3-year assessments. Results in PSPS type 1 and 2 patients at the last follow-up are also presented. Results: In total, 424 patients (mean age 61.6 ± 13.5 years; 57% female; 61% PSPS type 2) were included. Mean baseline NRS was 8.0 ± 1.4. At the last follow-up (mean 1.6 ± 1.5 years post-implantation), NRS decreased by 5.3 points to 2.7 ± 2.3 (p < 0.0001), 77% of patients achieved ≥50% reduction in pain, 56% reported minimal pain, and 62% were high responders. Similar improvements were observed in the preliminary analysis of 104 PSPS patients who completed the 3-year follow-up, with ≥5-point reduction in the NRS, 77% responder rate, 60% patients with minimal pain, and 70% high responders. The analysis of PSPS type 1 and 2 populations, adjusted for baseline NRS and follow-up durations, showed comparable outcomes. Conclusions: In this global, observational, “as-treated” cohort, favorable real-world outcomes were observed in PSPS patients using FAST-SCS, supporting its use as an effective treatment option in chronic spinal pain management.
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BibTeX
@article{metzger2026fastacting,
title = {{Fast-Acting Subperception Spinal Cord Stimulation for Persistent Spinal Pain Syndromes: Real-World Outcomes for up to 3 Years in an “As-Treated” Cohort from a Global Observational Study}},
author = {Clark Metzger and Blake Hammond and Richard Ferro and Jose Paz-Solis and Georgios Kyriakopoulos and Philippe Rigoard and Ashish Gulve and Jose Emilio Llopis and Pablo Andrade and Sarah Love-Jones and Jan Willem Kallewaard and Jan Vesper and Stephen Pyles and Simon Bayerl},
journal = {Journal of clinical medicine},
year = {2026},
month = oct,
doi = {10.3390/jcm15197640},
url = {https://europepmc.org/article/PMC/PMC13666453},
note = {CC BY},
}
RIS
TY - JOUR
TI - Fast-Acting Subperception Spinal Cord Stimulation for Persistent Spinal Pain Syndromes: Real-World Outcomes for up to 3 Years in an “As-Treated” Cohort from a Global Observational Study
AU - Clark Metzger
AU - Blake Hammond
AU - Richard Ferro
AU - Jose Paz-Solis
AU - Georgios Kyriakopoulos
AU - Philippe Rigoard
AU - Ashish Gulve
AU - Jose Emilio Llopis
AU - Pablo Andrade
AU - Sarah Love-Jones
AU - Jan Willem Kallewaard
AU - Jan Vesper
AU - Stephen Pyles
AU - Simon Bayerl
PY - 2026
DA - 2026/10/01
JO - Journal of clinical medicine
DO - 10.3390/jcm15197640
UR - https://europepmc.org/article/PMC/PMC13666453
AB - Background/Objectives: Evidence on the effectiveness of spinal cord stimulation using fast-acting subperception therapy (FAST-SCS) in patients with persistent spinal pain syndrome (PSPS) remains limited. We evaluated clinical outcomes of FAST-SCS in patients with PSPS types 1 (i.e., non-surgical back pain) and 2 (i.e., failed back surgery syndrome). Methods: Our global, multicenter, retrospective, observational chart review included all consecutive adults with chronic low back and/or leg pain due to PSPS who received SCS with a multimodal device and reported using FAST-SCS at their latest follow-up. Available data from the patients’ medical files, documented by site personnel per their standard of care, were collected and analyzed. Pain intensity was assessed using the numerical rating scale (NRS); percent pain relief (PPR) was recorded where available. Main outcomes included changes in overall pain (NRS) compared to baseline, proportion of patients with ≥50% reduction in overall pain (NRS), proportion of patients with minimal pain (NRS ≤ 2), and high responder rates (PPR ≥ 80%). Data was analyzed for all PSPS patients at the last follow-up, with preliminary analysis of patients who completed 3-year assessments. Results in PSPS type 1 and 2 patients at the last follow-up are also presented. Results: In total, 424 patients (mean age 61.6 ± 13.5 years; 57% female; 61% PSPS type 2) were included. Mean baseline NRS was 8.0 ± 1.4. At the last follow-up (mean 1.6 ± 1.5 years post-implantation), NRS decreased by 5.3 points to 2.7 ± 2.3 (p < 0.0001), 77% of patients achieved ≥50% reduction in pain, 56% reported minimal pain, and 62% were high responders. Similar improvements were observed in the preliminary analysis of 104 PSPS patients who completed the 3-year follow-up, with ≥5-point reduction in the NRS, 77% responder rate, 60% patients with minimal pain, and 70% high responders. The analysis of PSPS type 1 and 2 populations, adjusted for baseline NRS and follow-up durations, showed comparable outcomes. Conclusions: In this global, observational, “as-treated” cohort, favorable real-world outcomes were observed in PSPS patients using FAST-SCS, supporting its use as an effective treatment option in chronic spinal pain management.
SN - 2077-0383
ER -