# Clinical effectiveness of spinal cord stimulation in managing refractory upper-extremity pain

**Authors:** Yanisa Ingkapassakorn, Songrit Vuttipongkul, Bunpot Sitthinamsuwan, Sukunya Jirachaipitak, Pramote Euasobhon, Nantthasorn Zinboonyahgoon, Sarun Nunta-aree

PMC · DOI: 10.1007/s10143-025-04123-7 · 2026-02-20

## TL;DR

Spinal cord stimulation (SCS) can effectively reduce severe upper body pain that doesn't respond to other treatments, with benefits seen across different pain causes.

## Contribution

Demonstrates SCS efficacy for refractory upper extremity pain without preference for specific pain etiologies like CRPS.

## Key findings

- SCS reduced average pain scores from 9.5 to 3.6 in implanted patients.
- Pain improvement was consistent across neural/non-neural and CRPS/non-CRPS subgroups.
- Most patients maintained pain relief at last follow-up.

## Abstract

Spinal cord stimulation (SCS) is an effective therapy for intractable pain, but it is used less frequently for upper extremity than for lower limb pain. Evidence supporting SCS for the upper extremity remains limited. This study evaluated the efficacy of SCS for severe refractory upper extremity pain. Thirteen patients with refractory upper extremity pain underwent a trial of SCS. Eleven patients, who achieved marked pain relief during the trial, proceeded to permanent implantation. We collected clinical characteristics and outcomes, including numeric pain rating scale (NPRS) measurements. We then compared pain reduction among subgroups: neural versus non-neural lesions, and complex regional pain syndrome (CRPS) versus non-CRPS. In the 11 implanted patients, the mean NPRS score decreased from 9.5 of 10 preoperatively to 3.6 of 10 postoperatively (p < 0.001). Analysis showed significant pain improvement in each subgroup (p < 0.05). At last follow-up, the NPRS scores remained below baseline levels in 10 of 11 patients. However, the magnitude of the NPRS score reduction did not differ significantly between neural and non-neural lesions (p = 0.350), or CRPS and non-CRPS (p = 0.245). One participant with CRPS type 2 experienced treatment failure during long-term follow-up. This study demonstrated that SCS effectively alleviates refractory upper extremity pain caused by various etiologies. No single pain etiology, including CRPS, conferred a superior response, suggesting broad potential benefits of SCS in these patients.

## Linked entities

- **Diseases:** complex regional pain syndrome (MONDO:0019369), CRPS (MONDO:0019369)

## Full-text entities

- **Diseases:** Traumatic (MESH:D014947), inflammation (MESH:D007249), peripheral vascular disease (MESH:D016491), fibrosis (MESH:D005355), Pain (MESH:D010146), Churg-Strauss syndrome (MESH:D015267), Brachial plexus avulsion (MESH:D020516), disturbances (MESH:D014832), avulsion injuries (MESH:D000069836), back surgery syndrome (MESH:D055111), psychiatric (MESH:D001523), sensory disturbances (MESH:D012678), muscle weakness (MESH:D018908), ischemic (MESH:D002545), idiopathic axonal polyneuropathy (MESH:D011115), postoperative pain (MESH:D010149), neoplasms (MESH:D009369), intramedullary or nerve root lesions (MESH:D011843), neck surgery (MESH:D006258), headache disorders (MESH:D020773), spinal stenosis (MESH:D013130), vasomotor dysfunction (MESH:D012223), -lesion (MESH:D009059), peripheral arterial occlusive disease (MESH:C564658), postherpetic neuralgia (MESH:D051474), ischemia (MESH:D007511), ependymoma (MESH:D004806), neurological deficits (MESH:D009461), compressive myelopathy (MESH:D013117), spinal cord injury (MESH:D013119), Chiari I malformation (MESH:D001139), facial pain (MESH:D005157), SCS (MESH:D013118), back and lower limb pain (MESH:D017116), CRPS (MESH:D020918), phantom limb pain (MESH:D010591), neck and upper extremity pain (MESH:D019547), cervical spondylotic myelopathy (MESH:D002575), inflammatory arthritis (MESH:D001168), arterial occlusion (MESH:D001157), painful neuropathy (MESH:C564945), neurologic injury (MESH:D020196), ischemic discoloration (MESH:D014075), myoclonus (MESH:D009207), eosinophilic granulomatosis with polyangiitis (MESH:D014890), infections (MESH:D007239), fibromyalgia (MESH:D005356), myocardial ischemia (MESH:D017202), numbness (MESH:D006987), avulsion (MESH:D000071562), cervical syringomyelia (MESH:D013595), deafferentation pain (MESH:D002422), impaired social cognition (OMIM:300082), neuropathic pain (MESH:D009437), Chronic pain (MESH:D059350), pain syndromes (MESH:C538101), paresthesia (MESH:D010292), Peripheral neuropathy (MESH:D010523), immune dysregulation (OMIM:614878), impaired voluntary motor function (MESH:D009155)
- **Chemicals:** acetylcholine (MESH:D000109), gamma-aminobutyric acid (MESH:D005680), glutamate (MESH:D018698), nitric oxide (MESH:D009569), glycine (MESH:D005998), BPA (-), amino acids (MESH:D000596), steroid (MESH:D013256)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12923450/full.md

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Source: https://tomesphere.com/paper/PMC12923450