脉冲射频治疗时间对腰根性疼痛腰背根神经节的疗效:一项双盲随机对照试验。

IF 3.5 2区 医学 Q1 ANESTHESIOLOGY
Jae Ni Jang, Soyoon Park, Ji-Hoon Park, Young-Soon Choi, Sukhee Park
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引用次数: 0

摘要

背景:背根神经节(DRG)脉冲射频(PRF)是治疗腰根性疼痛(LRP)的一种微创治疗方法,但最佳刺激时间仍不确定。临床前证据表明,延长PRF可能增强神经调节,但比较临床数据有限。这项随机、双盲对照试验旨在比较LRP患者PRF和DRG持续时间的疗效。方法:60例慢性单侧LRP患者分别接受4 min (A组)、6 min (B组)和8 min (C组)的DRG PRF治疗。主要结局是疼痛强度,通过数值评定量表(NRS)在1周、2周、1个月、3个月和6个月进行评估。次要结局包括功能残疾(Oswestry残疾指数,ODI)和患者满意度(全球感知效应,GPE),分别在1个月、3个月和6个月进行评估。初步分析采用意向治疗(ITT)方法,最后一次观察继续进行。每个方案(PP)分析也进行了验证结果。结果:随着时间的推移,所有组的NRS和ODI均有显著改善(结论:6分钟PRF持续时间在疼痛和功能方面提供了最一致和统计学上显著的改善,支持将其作为临床标准。在特定的患者中,8分钟的持续时间可能会产生额外的主观和功能益处。PRF在所有组中都是安全且耐受性良好的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of pulsed radiofrequency treatment duration to the lumbar dorsal root ganglion in lumbar radicular pain: a double-blind randomized controlled trial.

Background: Pulsed radiofrequency (PRF) of the dorsal root ganglion (DRG) is a minimally invasive treatment for lumbar radicular pain (LRP), but the optimal stimulation duration remains uncertain. Preclinical evidence suggests that extended PRF may enhance neuromodulation, yet comparative clinical data are limited. This randomized, double-blind controlled trial aimed to compare the efficacy according to duration of PRF of DRG in patients with LRP.

Methods: A total of 60 patients with chronic unilateral LRP were allocated to receive PRF of the DRG for 4 min (group A), 6 min (group B) or 8 min (group C). The primary outcome was pain intensity, measured by the Numeric Rating Scale (NRS) assessed at 1 week, 2 weeks, 1 month, 3 months, and 6 months. Secondary outcomes included functional disability (Oswestry Disability Index, ODI) and patient satisfaction (Global Perceived Effect, GPE) assessed at 1 month, 3 months and 6 months. The primary analysis followed an intention-to-treat (ITT) approach with the last observation carried forward. A per-protocol (PP) analysis was also conducted to validate results.

Results: All groups demonstrated significant improvement in NRS and ODI over time (p<0.001). At 6 months, group B showed significantly greater pain reduction compared with group A (mean difference=-1.35, SE=0.69, p=0.031). Group C also showed improved NRS and the lowest ODI scores, though not statistically significant in the ITT analysis. However, PP analysis revealed statistically significant NRS reduction in both groups B and C compared with group A. Group C was the only group to demonstrate significant within-group improvement in GPE over time.

Conclusions: A 6 min PRF duration provided the most consistent and statistically significant improvement in pain and function, supporting its use as a clinical standard. The 8 min duration may yield additional subjective and functional benefits in selected patients. PRF was safe and well tolerated across all groups.

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来源期刊
CiteScore
8.50
自引率
11.80%
发文量
175
审稿时长
6-12 weeks
期刊介绍: Regional Anesthesia & Pain Medicine, the official publication of the American Society of Regional Anesthesia and Pain Medicine (ASRA), is a monthly journal that publishes peer-reviewed scientific and clinical studies to advance the understanding and clinical application of regional techniques for surgical anesthesia and postoperative analgesia. Coverage includes intraoperative regional techniques, perioperative pain, chronic pain, obstetric anesthesia, pediatric anesthesia, outcome studies, and complications. Published for over thirty years, this respected journal also serves as the official publication of the European Society of Regional Anaesthesia and Pain Therapy (ESRA), the Asian and Oceanic Society of Regional Anesthesia (AOSRA), the Latin American Society of Regional Anesthesia (LASRA), the African Society for Regional Anesthesia (AFSRA), and the Academy of Regional Anaesthesia of India (AORA).
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