Fluoroscopy-guided high-intensity focused ultrasound neurotomy of the lumbar zygapophyseal joints: a prospective, open-label study

Michael Gofeld, Kevin J Smith, Anuj Bhatia, Vladimir Djuric, Suzanne Leblang, Niv Rebhun, Ron Aginsky, Eric Miller, Brian Skoglind, Arik Hananel
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Abstract

Objective The objective of this study is to investigate safety and effectiveness of a fluoroscopy-guided high-intensity focused ultrasound (HIFU) system for thermal ablation of the lumbar medial branch nerves. Methods This dual center prospective cohort study enrolled 30 participants with lumbar zygapophyseal joint syndrome. Each participant previously had a positive response to either a single diagnostic analgesic block or radiofrequency ablation (RFA). The primary effectiveness outcome was individual responder rate, defined as a reduction of two points or more on the pain intensity numerical rating scale without an increase in opioid intake, or a reduction in opioid intake without an increase in pain at 6 months after the intervention. The primary safety outcome was procedure-related or device-related adverse events (AEs). Secondary outcome variables included MRI evidence of tissue ablation, Oswestry Disability Index, 12-Item Short Form Health Survey, Brief Pain Inventory, and Patient Global Impression of Change. Results The individual responder rate was 89.7% at 2 days, 89.7% at 7 days, 72.4% at 14 days, 82.1% at 30 days, 59.3% at 90 days and 82.6% at 180 days. The average Numeric Rating Scale for pain severity decreased from 7.1 at baseline to 3.0 (N=29) after 2 days, 3.0 (N=29) after 7 days, 3.1 (N=29) after 14 days, 3.2 (N=28) after 30 days, 4.3 (N=27) after 90 days, and 3.3 (N=23) after 180 days. All participants tolerated the procedure well with no significant side effects or complications. Conclusions Fluoroscopy-guided HIFU neurotomy achieved clinical responses comparable with RFA, and there were no significant device-related or procedure-related AEs. Trial registration number [NCT04129034][1]. Data are available on reasonable request. [1]: /lookup/external-ref?link_type=CLINTRIALGOV&access_num=NCT04129034&atom=%2Frapm%2Fearly%2F2024%2F04%2F04%2Frapm-2024-105345.atom
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透视引导下的腰椎颧骨关节高强度聚焦超声神经切除术:一项前瞻性开放标签研究
目的 本研究旨在探讨透视引导下的高强度聚焦超声(HIFU)系统用于腰椎内侧支神经热消融的安全性和有效性。方法 这项双中心前瞻性队列研究共招募了 30 名腰椎颧骨关节综合征患者。每位患者之前都对单次诊断性镇痛阻滞或射频消融术(RFA)有过积极反应。主要疗效指标是个体应答率,即在干预6个月后,疼痛强度数值评定量表降低两分或更多,而阿片类药物摄入量没有增加,或阿片类药物摄入量减少而疼痛没有增加。主要安全性结果是与手术或设备相关的不良事件(AEs)。次要结果变量包括核磁共振成像组织消融证据、Oswestry 残疾指数、12 项简表健康调查、简明疼痛量表和患者总体变化印象。结果 2 天、7 天、14 天、30 天、90 天和 180 天的个体应答率分别为 89.7%、89.7%、72.4%、82.1%、59.3% 和 82.6%。疼痛严重程度的平均数字评级量表从基线时的 7.1 分降至 2 天后的 3.0 分(29 人)、7 天后的 3.0 分(29 人)、14 天后的 3.1 分(29 人)、30 天后的 3.2 分(28 人)、90 天后的 4.3 分(27 人)和 180 天后的 3.3 分(23 人)。所有参与者都能很好地耐受手术,没有出现明显的副作用或并发症。结论 透视引导下 HIFU 神经切除术取得了与 RFA 相当的临床疗效,而且没有出现明显的设备相关或手术相关的 AEs。试验注册号[NCT04129034][1]。如有合理要求,可提供相关数据。[1]:/lookup/external-ref?link_type=CLINTRIALGOV&access_num=NCT04129034&atom=%2Frapm%2Fearly%2F2024%2F04%2F04%2Frapm-2024-105345.atom
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