A Retrospective Review of Real-world Outcomes Following 60-day Peripheral Nerve Stimulation for the Treatment of Chronic Pain

被引:2
作者
Huntoon, Marc A. [1 ,5 ]
Slavin, Konstantin, V [2 ,3 ]
Hagedorn, Jonathan M. [4 ]
Crosby, Nathan D. [5 ]
Boggs, Joseph W. [5 ]
机构
[1] Virginia Commonwealth Univ, Dept Anesthesiol, 1200 E Broad St, Richmond, VA 23298 USA
[2] Univ Illinois, Dept Neurosurg, Chicago, IL USA
[3] Jesse Brown Vet Adm Med Ctr, Neurol Sect, Chicago, IL USA
[4] Mayo Clin, Dept Anesthesiol & Perioperat Med, Div Pain Med, Rochester, MN USA
[5] SPR Therapeut, Cleveland, OH USA
关键词
Peripheral nerve stimulation; neuromodulation; 60-day PNS; nonopiod; real-world evidence; HEMIPLEGIC SHOULDER PAIN; CLINICAL-TRIALS; NEUROSTIMULATION; POINTS; RELIEF;
D O I
暂无
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: Real-world data can provide important insights into treatment effectiveness in routine clinical practice. Studies have demonstrated that in multiple different pain indications temporary (60-day) percutaneous peripheral nerve stimulation (PNS) treatment can produce significant relief, but few real-world studies have been published. The present study is the first real-world, retrospective review of a large database depicting outcomes at the end of a 60-day PNS treatment period. Objectives: Evaluate outcomes during a 60-day PNS treatment in routine clinical practice. Study Design: Secondary retrospective review. Methods: Anonymized records of 6,160 patients who were implanted with a SPRINT PNS System from August 2019 through August 2022 were retrospectively reviewed from a national real-world database. The percentage of patients with >= 50% pain relief and/or improvement in quality of life was evaluated and stratified by nerve target. Additional outcomes included average and worst pain score, patient-reported percentage of pain relief, and patient global impression of change. Results: Overall, 71% of patients (4,348/6,160) were responders with >= 50% pain relief and/ or improvement in quality of life; pain relief among responders averaged 63%. The responder rate was largely consistent across nerve targets throughout the back and trunk, upper and lower extremities, and posterior head and neck. Limitations: This study was limited by its retrospective nature and reliance on a device manufacturer's database. Additionally, detailed demographic information and measures for pain medication usage and physical function were not assessed. Conclusions: This retrospective analysis supports recent prospective studies demonstrating that 60-day percutaneous PNS can provide significant relief across a wide range of nerve targets. These data serve an important role in complementing the findings of published prospective clinical trials.
引用
收藏
页码:273 / 281
页数:9
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