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欧洲随机对照试验评估了差异靶向脊髓刺激和传统医学管理在不符合脊柱手术适应证的持续性背痛患者中的应用:24 个月的结果。

European randomized controlled trial evaluating differential target multiplexed spinal cord stimulation and conventional medical management in subjects with persistent back pain ineligible for spine surgery: 24-month results.

机构信息

Rijnstate, Elst, The Netherlands.

Amsterdam University Medical Centre, Amsterdam, The Netherlands.

出版信息

Eur J Pain. 2024 Nov;28(10):1745-1761. doi: 10.1002/ejp.2306. Epub 2024 Jun 28.

Abstract

BACKGROUND

Differential target multiplexed spinal cord stimulation (DTM SCS) was shown to be superior to conventional SCS for treating chronic low back pain (CLBP) in subjects with persistent spinal pain syndrome with previous spinal surgery (PSPS-T2) or ineligible for it (PSPS-T1). This study reports 24-month efficacy and safety of DTM SCS vs. conventional medical management (CMM) in PSPS-T1 subjects across four European countries.

METHODS

This is a prospective, multicenter, open-label, randomized, controlled trial with optional crossover. Subjects randomized 1:1 to DTM SCS or CMM. Primary endpoint was responder rate (% subjects reporting ≥50% CLBP relief) at 6 months. A superiority test compared responder rates between treatments. CLBP and leg pain levels, functional disability, quality of life (QoL), patient satisfaction and global impression of change were evaluated for 24 months. A Composite Responder Index (CRI) was obtained using CLBP relief, disability and QoL. Incidence of study-related adverse events evaluated safety.

RESULTS

A total of 55 and 57 subjects were randomized to DTM SCS and CMM respectively. DTM SCS was superior, with CLBP responder rates ≥80% and CLBP relief >5.6 cm (>70% reduction) through the 24-month follow-up. Improvements with DTM SCS in other outcomes were sustained. The CRI was >80% for DTM SCS through 24 months. Opioid medication intake decreased in subjects treated with DTM SCS. Most patients treated with DTM SCS felt satisfied and improved at the end of the study. Safety was congruent with other studies.

CONCLUSION

DTM SCS is efficacious and safe during 24 months for the treatment of CLBP and leg pain in PSPS-T1 patients ineligible for spine surgery.

SIGNIFICANCE STATEMENT

This randomized controlled trial shows that Differential Target Multiplexed SCS (DTM SCS) is an effective and safe long-term treatment for PSPS type 1 patients suffering from axial low back pain with or without leg pain and who are ineligible for spinal surgery. Currently, CMM treatments are their only option and provide limited benefits. Besides superior pain relief, DTM SCS provides significant improvements in functional disability, quality of life, high levels of satisfaction and perceived impression of change.

摘要

背景

对于有既往脊柱手术史(PSPS-T2)或不适合手术(PSPS-T1)的持续性脊柱疼痛综合征伴慢性下腰痛(CLBP)患者,与传统脊髓刺激(SCS)相比,差异靶向复用脊髓刺激(DTM SCS)显示出在治疗 CLBP 方面的优越性。本研究报告了在四个欧洲国家的 PSPS-T1 患者中,DTM SCS 与传统医学管理(CMM)相比 24 个月的疗效和安全性。

方法

这是一项前瞻性、多中心、开放标签、随机、对照试验,具有可选的交叉设计。将患者以 1:1 的比例随机分为 DTM SCS 或 CMM 组。主要终点是 6 个月时的应答率(%报告 CLBP 缓解≥50%的患者)。对治疗之间的应答率进行了优效性检验。对 24 个月的 CLBP 和腿痛水平、功能障碍、生活质量(QoL)、患者满意度和总体变化印象进行了评估。使用 CLBP 缓解、残疾和 QoL 获得复合应答指数(CRI)。评估研究相关不良事件的发生率以评估安全性。

结果

共有 55 名和 57 名患者分别随机分为 DTM SCS 和 CMM 组。DTM SCS 具有优越性,CLBP 应答率≥80%,CLBP 缓解>5.6cm(>70%减轻),随访 24 个月。其他结局的改善在 DTM SCS 治疗中也得到了维持。24 个月时,CRI>80%。接受 DTM SCS 治疗的患者阿片类药物的摄入量减少。大多数接受 DTM SCS 治疗的患者在研究结束时感到满意并有所改善。安全性与其他研究一致。

结论

在 24 个月的时间里,对于不适合脊柱手术的 PSPS-T1 患者,DTM SCS 治疗 CLBP 和腿部疼痛是有效且安全的。

意义

这项随机对照试验表明,对于患有轴向下腰痛伴或不伴腿部疼痛且不适合脊柱手术的 PSPS 型 1 患者,差异靶向复用脊髓刺激(DTM SCS)是一种有效且安全的长期治疗方法。目前,CMM 治疗是他们唯一的选择,提供的益处有限。除了更优越的疼痛缓解外,DTM SCS 还可显著改善功能障碍、生活质量、满意度和感知变化印象。

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