Single-Lead Percutaneous Peripheral Nerve Stimulation for the Treatment of Hemiplegic Shoulder Pain: A Case Series

被引:46
作者
Chae, John [1 ,2 ,3 ,4 ]
Wilson, Richard D. [2 ,3 ]
Bennett, Maria E. [5 ]
Lechman, Tina E. [5 ]
Stager, Kathryn W. [6 ]
机构
[1] Case Western Reserve Univ, MetroHlth Med Ctr, Dept Phys Med & Rehabil, Cleveland, OH 44109 USA
[2] Case Western Reserve Univ, Cleveland Funct Elect Stimulat Ctr, Cleveland, OH 44109 USA
[3] MetroHlth Rehabil Inst Ohio, Cleveland, OH USA
[4] Case Western Reserve Univ, Dept Biomed Engn, Cleveland, OH 44109 USA
[5] SPR Therapeut, Cleveland, OH USA
[6] NDI Med, Cleveland, OH USA
关键词
electric stimulation therapy; shoulder pain; peripheral nerve stimulation; hemiplegia; CVA; stroke; NEUROMUSCULAR ELECTRICAL-STIMULATION; INTRAMUSCULAR ELECTRODES; UPPER EXTREMITY; STROKE PATIENT; REHABILITATION; RELIABILITY; SONOGRAPHY; MANAGEMENT; COHORT;
D O I
10.1111/j.1533-2500.2012.00541.x
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Objective: Previous studies demonstrated the efficacy of Intramuscular Nerve (IMN) therapy with a 4-lead percutaneous, peripheral nerve stimulation (PNS) system in reducing hemiplegic shoulder pain (HSP). This case series investigates the feasibility of a less complex, single-lead approach in reducing HSP. Methods: Eight participants received one percutaneous intramuscular lead in the hemiparetic deltoid muscle and were then treated 6 hours/day for 3 weeks. The primary outcome measure was the Brief Pain Inventory (Short-Form) Question 3 (BPI3), which queries worst pain in the last week on a 0 to 10 numeric rating scale. Secondary outcomes included pain interference (BPI9) and Medical Outcomes Study Short-Form 36 (SF-36v2). Primary and secondary outcomes were assessed at the end of treatment (EOT) and 1 and 4 weeks after the EOT. Results: All participants tolerated the treatment well with 96% compliance. All leads remained infection-free and were removed intact at the EOT. On average, participants exhibited 70% reduction in BPI3 at the EOT and 61% reduction at 4 weeks after the EOT. All participants satisfied the success criterion of at least a 2-point reduction in BPI3 at the EOT. Longitudinal analysis revealed significant treatment effect for BPI3 (F = 14.0, P < 0.001), BPI9 (F = 5.9, P < 0.01), and the bodily pain domain of SF-36v2 (F = 12.8, P < 0.001). Conclusion: This case series demonstrates the feasibility of a single-lead, 3-week IMN therapy for the treatment of chronic HSP. Additional studies are needed to further demonstrate safety, efficacy, and long-term benefit, define optimal prescriptive parameters and dose, and expand clinical indications.
引用
收藏
页码:59 / 67
页数:9
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