使用速效亚知觉治疗脊髓刺激的两年结果:美国一项真实世界多中心研究的结果。

Expert review of medical devices Pub Date : 2025-01-01 Epub Date: 2025-01-16 DOI:10.1080/17434440.2025.2453554
Clark Metzger, Blake Hammond, Richard Ferro, James North, Stephen Pyles, Andy Kranenburg, Edward Washabaugh, Edward Goldberg
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引用次数: 0

摘要

背景:速效亚知觉疗法(FAST)是一种新型的脊髓刺激(SCS)治疗方式,可缓解无感觉异常的疼痛。我们的研究评估了FAST对慢性疼痛的长期影响。研究设计和方法:作为多中心、真实世界、连续病例系列的一部分,我们回顾性地确定了使用FAST-SCS的患者并分析了他们的数据。采用数值评定量表(NRS)对疼痛进行评定。结果:315例患者在基线和最后一次随访(SCS植入后中位6.8个月)时的数据进行了分析。在分析时,分别有112例、86例和50例患者的12个月、18个月和24个月的数据。最后一次随访时,NRS疼痛评分较基线降低5.5±2.5分(从7.8±1.7分降至2.3±2.0分;结论:这项正在进行的、真实世界的、多中心的研究表明,FAST-SCS实现了显著的无感觉异常疼痛缓解,而长期中期分析表明,结果可持续长达2年。我们的数据为使用双相主动充电脉冲形状的低频亚感知SCS范式的潜在效用提供了初步的见解。试验注册:ClinicalTrials.gov (CT.gov标识符:NCT01550575)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Two-year outcomes using fast-acting sub-perception therapy for spinal cord stimulation: results of a real-world multicenter study in the United States.

Background: Fast-acting Sub-perception Therapy (FAST) is a novel spinal cord stimulation (SCS) modality delivering paresthesia-free pain relief. Our study evaluated the longer-term, real-world impact of FAST on chronic pain.

Research design and methods: As part of a multicenter, real-world, consecutive case series, we retrospectively identified patients who used FAST-SCS and analyzed their data. The numerical rating scale (NRS) was used to evaluate the overall pain.

Results: Data from 315 patients were analyzed at baseline and their last available follow-up (median 6.8 months after SCS implantation). At the time of the analysis, 12-, 18-, and 24-month data were available for 112, 86, and 50 patients, respectively. At the last follow-up, NRS pain score was reduced by 5.5 ± 2.5 compared to baseline (from 7.8 ± 1.7 to 2.3 ± 2.0; p < 0.0001). Interim long-term analysis showed that results were sustained for up to 2 years, with 64% of patients reporting a minimal overall pain score (NRS ≤2/10).

Conclusion: This ongoing, real-world, multicenter study showed that FAST-SCS achieved significant paresthesia-free pain relief, while long-term interim analysis suggests that outcomes could be sustained for up to 2 years. Our data provide preliminary insights into the potential utility of this low-frequency sub-perception SCS paradigm using a biphasic active recharge pulse shape.

Trial registration: ClinicalTrials.gov (CT.gov identifier: NCT01550575).

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