椎体神经消融治疗骨质疏松和骨质减少患者的安全性和有效性:一项真实世界的研究

Emily Bellow, Derek Johnson, Sandi Bajrami, William Caldwell
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引用次数: 0

摘要

背景:该手术是首个获得fda批准的椎体神经消融技术,是一种治疗椎体源性慢性腰痛的微创治疗方法。虽然先前的研究支持其有效性,但骨质疏松症和骨质减少患者的数据仍然有限。目的评价基椎神经消融术的安全性和有效性,特别关注疼痛减轻、功能改善和术后椎体压缩性骨折的发生率。方法回顾性分析2019年11月至2025年1月在我院行内置管术的患者。使用DEXA扫描对骨密度状态进行分类。将患者分层分为骨密度降低组(N = 32),其中骨质减少组23例,骨质疏松组9例,整体队列(N = 134)。在基线和术后4 - 6周随访时使用视觉模拟量表(VAS)评估疼痛严重程度,并根据患者报告的同一时间点的结果确定功能改善情况。术后并发症,包括椎体压缩性骨折,一直监测到最近的随访。结果整个队列的VAS评分显著下降(7.04 vs. 3.78, p <;0.001)和骨密度降低组(6.75 vs. 4.13, p <;0.001)。总体研究人群中79.1%的患者和骨密度降低组中78.1%的患者报告功能改善。整个队列中未观察到术后椎体压缩性骨折,平均随访时间为18.07个月。结论:在整个队列和骨密度降低的患者中,截骨术显示出明显的疼痛减轻和功能改善。值得注意的是,即使在骨质疏松和骨质减少的患者中,也没有观察到术后椎体压缩性骨折。这些发现有助于越来越多的独立文献支持内截骨术的安全性和有效性,并为其在骨密度降低患者中的应用提供了真实的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Safety and effectiveness of basivertebral nerve ablation in patients with osteoporosis and osteopenia: A real-world study

Background

The Intracept procedure was the first FDA-cleared technique for basivertebral nerve ablation, a minimally invasive treatment for vertebrogenic chronic low back pain. While prior studies support its effectiveness, data in patients with osteoporosis and osteopenia remains limited.

Objective

To evaluate the safety and effectiveness of basivertebral nerve ablation with a specific focus on pain reduction, functional improvement, and the incidence of post-procedure vertebral compression fractures.

Methods

A retrospective chart review was conducted on patients who underwent the Intracept procedure at our institution from November 2019 to January 2025. Bone density status was categorized using available DEXA scans. Patients were stratified into a Reduced Bone Density group (N = 32), consisting of 23 patients with osteopenia and 9 with osteoporosis, and the overall cohort (N = 134). Pain severity was assessed using the Visual Analog Scale (VAS) at baseline and at the 4–6-week post-procedure follow-up visit, and functional improvement was determined based on patient-reported outcomes at the same time point. Post-procedure complications, including vertebral compression fractures, were monitored until the most recent available follow-up.

Results

A significant decrease in VAS was observed for the overall cohort (7.04 vs. 3.78, p < 0.001) and the Reduced Bone Density group (6.75 vs. 4.13, p < 0.001). Functional improvement was reported by 79.1 % of patients in the overall study population and 78.1 % of patients in the Reduced Bone Density group. No post-procedure vertebral compression fractures were observed in the entire cohort, with a mean follow-up length of 18.07 months.

Conclusion

The Intracept procedure demonstrated significant pain reduction and functional improvement in the overall cohort and in patients with reduced bone density. Notably, no post-procedure vertebral compression fractures were observed, even in patients with osteoporosis and osteopenia. These findings contribute to the growing body of independent literature supporting the safety and effectiveness of the Intracept procedure and offer real-world insight into its use in patients with reduced bone density.
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