Ultrasound‐Guided Neuromodulation Is Non‐inferior to Fluoroscopy Approach for Painful Diabetic Neuropathy

OBJECTIVES: To evaluate the efficacy and safety of ultrasound (US)-guided pulsed radiofrequency (PRF) on the lumbar sympathetic ganglion (LSG) for treating painful diabetic neuropathy (PDN). METHODS: A total of 228 patients were retrospectively included. Patients undergoing PRF under US guidance were identified as US cohort. A 1:1 propensity-score matching was performed to select controls that received FL-guided procedures. Primary endpoint was the proportion of patients experiencing at least a 50% reduction in pain at 1 week after treatment. Noninferiority margin was set as 10%. Secondary outcomes included procedure outcomes, lower limb temperature, and scores of numerical rating scale (NRS) pain, neuropathy impairment score-lower limbs (NIS-LL), medical outcomes study sleep scale (MOS-SS), hospital anxiety and depression scale (HADS), and Norfolk quality of life-diabetic neuropathy (Norfolk QoL-DN). RESULTS: In US cohort, 67.8% of patients reported ≥50% pain relief at 1 week, with a mean difference of -0.9% (95% CI: -9.5%, 7.8%) between the 2 cohorts, exceeding the non-inferiority margin. The proportion of patients achieving ≥50% pain relief remained at 65.6% in US cohort versus 66.7% in FL cohort at 4 weeks post-treatment, and 63.3% in US cohort versus 64.0% in FL cohort at 12 weeks post-treatment, with no significant inter-cohort differences at all follow-up time points. Temperature was immediately increased by 5°C in both cohorts. Significant improvements were observed in NRS pain, NIS-LSS, MOS-SS, HADS, and Norfolk QoL-DN scores across the entire 12-week follow-up, with no significant differences between the cohorts (all p > .05). US cohort was associated with fewer number of needle insertions, shorter performance times, less radiation dosages, and a lower incidence of intravascular puncture (all p < .05). CONCLUSIONS: US-guided PRF on the LSG was shown to be non-inferior to procedures under conventional FL guidance for treating PDN. Its unique advantages supported its application in clinical settings.

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Journal
Journal of Ultrasound in Medicine
Published
2026-09-11
DOI
https://doi.org/10.1002/jum.70442
Primary Topic
Pain Management and Treatment
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article
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article

Ultrasound‐Guided Neuromodulation Is Non‐inferior to Fluoroscopy Approach for Painful Diabetic Neuropathy

Ling Wang, Jing Dong, Hong Liu, Wenxing Zhao et al.
Journal of Ultrasound in Medicine
Pain Management and Treatment
article

Ultrasound‐Guided Neuromodulation Is Non‐inferior to Fluoroscopy Approach for Painful Diabetic Neuropathy

Ling Wang, Jing Dong, Hong Liu, Wenxing Zhao, Rui Qin
article en

Abstract

OBJECTIVES: To evaluate the efficacy and safety of ultrasound (US)-guided pulsed radiofrequency (PRF) on the lumbar sympathetic ganglion (LSG) for treating painful diabetic neuropathy (PDN). METHODS: A total of 228 patients were retrospectively included. Patients undergoing PRF under US guidance were identified as US cohort. A 1:1 propensity-score matching was performed to select controls that received FL-guided procedures. Primary endpoint was the proportion of patients experiencing at least a 50% reduction in pain at 1 week after treatment. Noninferiority margin was set as 10%. Secondary outcomes included procedure outcomes, lower limb temperature, and scores of numerical rating scale (NRS) pain, neuropathy impairment score-lower limbs (NIS-LL), medical outcomes study sleep scale (MOS-SS), hospital anxiety and depression scale (HADS), and Norfolk quality of life-diabetic neuropathy (Norfolk QoL-DN). RESULTS: In US cohort, 67.8% of patients reported ≥50% pain relief at 1 week, with a mean difference of -0.9% (95% CI: -9.5%, 7.8%) between the 2 cohorts, exceeding the non-inferiority margin. The proportion of patients achieving ≥50% pain relief remained at 65.6% in US cohort versus 66.7% in FL cohort at 4 weeks post-treatment, and 63.3% in US cohort versus 64.0% in FL cohort at 12 weeks post-treatment, with no significant inter-cohort differences at all follow-up time points. Temperature was immediately increased by 5°C in both cohorts. Significant improvements were observed in NRS pain, NIS-LSS, MOS-SS, HADS, and Norfolk QoL-DN scores across the entire 12-week follow-up, with no significant differences between the cohorts (all p > .05). US cohort was associated with fewer number of needle insertions, shorter performance times, less radiation dosages, and a lower incidence of intravascular puncture (all p < .05). CONCLUSIONS: US-guided PRF on the LSG was shown to be non-inferior to procedures under conventional FL guidance for treating PDN. Its unique advantages supported its application in clinical settings.

Journal of Ultrasound in Medicine
Capital Medical University (CN), Chinese PLA General Hospital (CN), Chinese People's Armed Police General Hospital (CN)
Good health and well-being
Openalex Percentile: Top 8%
Pain Management and Treatment
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