Ten kilohertz SCS for Treatment of Chronic Upper Extremity Pain (UEP): Results from Prospective Observational Study

被引:13
作者
Burgher, Abram [1 ]
Kosek, Peter [2 ]
Surrett, Steven [3 ]
Rosen, Steven M. [4 ]
Bromberg, Todd [4 ]
Gulve, Ashish [5 ]
Kansal, Anu [5 ]
Wu, Paul [6 ]
McRoberts, W. Porter [6 ]
Udeshi, Ashish [7 ]
Esposito, Michael [7 ]
Gliner, Bradford E. [8 ]
Maneshi, Mona [8 ]
Rotte, Anand [8 ]
Subbaroyan, Jeyakumar [8 ]
机构
[1] Hope Res Inst, Phoenix, AZ USA
[2] Oregon Neurosurg, Eugene, OR USA
[3] Oregon Med Grp, Eugene, OR USA
[4] Delaware Valley Spine & Pain, Trevose, PA USA
[5] James Cook Univ Hosp, Middlesbrough, Cleveland, England
[6] Holy Cross Hosp Inc, Ft Lauderdale, FL USA
[7] Florida Pain Inst, Merritt Isl, FL USA
[8] Nevro Corp, 1800 Bridge Pkwy, Redwood City, CA 94065 USA
关键词
10 kHz SCS; VAS; upper extremity pain; shoulder and upper limb pain; SPINAL-CORD STIMULATION; TISSUE TEMPERATURE INCREASES; 10-KHZ HIGH-FREQUENCY; LOW-BACK-PAIN; CLINICAL-TRIALS; SYSTEM PHANTOM; UPPER-LIMB; NECK PAIN; KHZ SCS; OUTCOMES;
D O I
10.2147/JPR.S278661
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Chronic upper extremity pain (UEP) has complex etiologies and is often disabling. It has been shown that 10 kHz SCS can provide paresthesia-free and durable pain relief in multiple pain types and improve the quality of life of patients. Objective: To gain additional evidence on the safety and effectiveness of 10 kHz SCS for the treatment of chronic UEP. Study Design: It was a prospective, multicenter, and observational study. The study was registered on ClinicalTrials.gov prospectively (clinical trial identifier: NCT02703818). Setting: Multicenter. Patients, Intervention and Main Outcomes: A total of 43 subjects with chronic UEP of >= 5 cm (on a 0-10 cm visual analog scale; VAS) underwent a trial of 10 kHz SCS, and subjects with >= 40% pain relief received a permanent implant. All subjects had upper limb pain at baseline, while some had concomitant shoulder or neck pain. Subject outcomes were assessed for 12 months, and the primary outcome was the responder rate (percentage of subjects experiencing >= 50% pain relief from baseline) at three months. Results: Thirty-eight subjects successfully completed the trial (88.3% success rate), 33 received permanent implants (five withdrew consent), and 32 had device activation (per protocol population). There were no paresthesias or uncomfortable changes in stimulation related to changes in posture during the study and there were no neurological deficits. Responder rates at 12 months for upper limb, shoulder, and neck pain in per protocol population (N=32) were 78.1%, 85.2%, and 75.0%, respectively. At 12 months, 84.4% of subjects were satisfied or very satisfied with 10 kHz SCS, and 38.7% either reduced or eliminated opioid usage. Conclusion: This study further supports the effectiveness of 10 kHz SCS for chronic UEP treatment and documents the safety profile of the therapy.
引用
收藏
页码:2837 / 2851
页数:15
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