Smuck Matthew, Truumees Eeric, Macadaeg Kevin, Jaini Ashwin M, Chatterjee Susmita, Levin Joshua
Department of Orthopaedic Surgery, Division of Physical Medicine & Rehabilitation, Stanford University, 430 Broadway Street, Pavilion C 4th For, Redwood City, CA, 94063, USA.
Ascension Texas Spine & Scoliosis, 1004 W 32nd St Suite 200, TX, 78705, USA.
Interv Pain Med. 2023 Jun 10;2(2):100256. doi: 10.1016/j.inpm.2023.100256. eCollection 2023 Jun.
Vertebrogenic pain is an established source of anterior column chronic low back pain (CLBP) resulting from damaged vertebral endplates with pain signals transmitted by the basivertebral nerve (BVN). Type 1 or Type 2 Modic changes on magnetic resonance imaging (MRI) are objective biomarkers for vertebrogenic pain. Radiofrequency ablation of the BVN (BVNA) has demonstrated both efficacy and effectiveness for the treatment of vertebrogenic pain in two randomized trials. Here, we report 3-year aggregate results from two prospective studies of BVNA-treated patients.
Pooled results at 3 years post-BVNA are reported for two studies with similar inclusion/exclusion criteria and outcomes measurements: 1) a prospective, open label, single-arm follow-up of the treatment arm of a randomized controlled trial (RCT) comparing BVNA to standard care (INTRACEPT Trial), and 2) a prospective, open label, single cohort long-term follow-up study of BVNA-treated patients. Paired datasets (baseline and 3-years) for mean changes in Oswestry disability index (ODI) and numeric pain scores (NPS) were analyzed using a two-sided -test with a 0.05 level of significance.
There were 95/113 (84%) BVNA patients who completed a 3-year visit across 22 study sites. At baseline, 71% of patients reported back pain for ≥5 years, 28% were taking opioids, 34% had spinal injections in the prior 12 months, and 14% had prior low back surgery. Pain and functional improvements were significant at 3 years with a mean reduction in NPS of 4.3 points from 6.7 at baseline (95% CI 3.8, 4.8; p<0.0001) and a mean reduction in ODI of 31.2 points from 46.1 at baseline (95% CI 28.4, 34.0; p<0.0001). Responder rates, using minimal clinically important differences of ≥15-points for ODI and ≥50% reduction in NPS from baseline to three years, were 85.3% and 72.6%, respectively (combined response 69.5%), with 26.3% of patients reporting 100% pain relief at 3 years. There was a 74% reduction in the use of opioids and 84% reduction in the use of therapeutic spinal interventions from baseline to 3 years. There were no serious device or device-procedure related adverse events reported through three years.
Intraosseous BVNA demonstrates statistically significant, clinically meaningful, and durable improvements in pain and function through 3 years in patients with primary vertebrogenic low back pain. BVNA-treated patients significantly reduced opioid use and interventions for low back pain.
椎体源性疼痛是前柱慢性下腰痛(CLBP)的一个既定来源,它由受损的椎体终板引起,疼痛信号通过椎基底神经(BVN)传导。磁共振成像(MRI)上的1型或2型Modic改变是椎体源性疼痛的客观生物标志物。在两项随机试验中,BVN射频消融术(BVNA)已证明对治疗椎体源性疼痛有效且有效果。在此,我们报告两项对接受BVNA治疗患者的前瞻性研究的3年汇总结果。
报告了BVNA术后3年的汇总结果,这两项研究具有相似的纳入/排除标准和结局测量:1)一项随机对照试验(RCT)治疗组的前瞻性、开放标签、单臂随访,将BVNA与标准治疗进行比较(INTRACEPT试验),以及2)一项对接受BVNA治疗患者的前瞻性、开放标签、单队列长期随访研究。使用双侧检验分析配对数据集(基线和3年)的Oswestry功能障碍指数(ODI)和数字疼痛评分(NPS)的平均变化,显著性水平为0.05。
在22个研究地点,95/113(84%)的BVNA患者完成了3年随访。基线时,71%的患者报告背痛≥5年,28%的患者正在服用阿片类药物,34%的患者在过去12个月内接受过脊柱注射,14%的患者曾接受过腰椎手术。3年时疼痛和功能有显著改善,NPS从基线时的6.7分平均降低4.3分(95%CI 3.8,4.8;p<0.0001),ODI从基线时的46.1分平均降低31.2分(95%CI 28.4,34.0;p<0.0001)。使用ODI最小临床重要差异≥15分以及NPS从基线到3年降低≥50%作为标准,缓解率分别为85.3%和72.6%(综合缓解率69.5%),26.3%的患者在3年时报告疼痛完全缓解。从基线到3年,阿片类药物的使用减少了74%,治疗性脊柱干预的使用减少了84%。在3年期间,未报告严重的器械或与器械 - 操作相关的不良事件。
对于原发性椎体源性下腰痛患者,骨内BVNA在3年内显示出疼痛和功能方面具有统计学显著、临床有意义且持久的改善。接受BVNA治疗的患者显著减少了阿片类药物的使用以及针对下腰痛的干预措施。