Deer Timothy Ray, Pope Jason E, Petersen Erika A, Abdallah Rany T, Amirdelfan Kasra, Azeem Nomen, Bansal Vishal, Barkoh Kaku, Chapman Kenneth B, Denis Daniel R, Dorsi Michael J, Escobar Alexander, Falowski Steven Michael, Garcia Rosa Amelia, Hagedorn Jonathan M, Heros Robert D, James Whitney S, Kalia Hemant, Lansford Todd, Malinowski Mark N, Manzi Suzanne Marie, Mehta Pankaj, Moghim Robert Z, Moore Gregory Anthony, Motivala Soriaya Lizette, Navalgund Yeshvant A, Patel Raj G, Pilitsis Julie G, Schatman Michael E, Shumsky Philip Michael, Strand Natalie Holmes, Tomycz Nestor D, Yue James J, Sayed Dawood
Pain Services, Spine and Nerve Center of the Virginias, Charleston, WV, USA.
Evolve Restorative Center, Santa Rosa, CA, USA.
J Pain Res. 2025 Mar 14;18:1247-1274. doi: 10.2147/JPR.S500342. eCollection 2025.
The use of electrical neuromodulation has often been limited to those with previous back surgery, peripheral neuropathy, and complex regional pain syndrome. Many patients with severe intractable low back pain were thought to be candidates for spinal cord stimulation (SCS), dorsal root ganglion stimulation, or peripheral nerve stimulation but did not meet the criteria. Recently, additional high-level data has supported the use of SCS in non-surgical low back pain (NSLBP), and United States Food and Drug Administration approval has been granted. The American Society of Pain and Neuroscience (ASPN) executive committee realized an unmet need to develop criteria for patient selection for this specific patient population. This is a NEURON project (neuroscience, education, utilization, risk mitigation, optimal outcomes, and neuromodulation), a living guideline for evolving therapies and indications, and is focused on the use of neuraxial stimulation for the treatment of refractory pain.
After board approval, the society accepted nominees for the project, with an emphasis on experience, publication, research, and diversity. The team created an outline for discussion, chose a grading system based on published guidelines, and created consensus points.
The evidence led to several consensus points to best guide patient selection based on the level of evidence and expert opinion. The results will lead to improved safety and efficacy in implanted patients, and to a new standard for best practices.
The selection of patients for implantation in those who have NSLBP should be based on published literature, best practice, and expert opinion. This NEURON project will allow for regular updates to create a living guideline that will allow for better assimilation of information to improve safety and efficacy going forward.
电神经调节的应用通常局限于曾接受过背部手术、患有周围神经病变和复杂性区域疼痛综合征的患者。许多患有严重顽固性腰痛的患者被认为是脊髓刺激(SCS)、背根神经节刺激或周围神经刺激的候选对象,但不符合标准。最近,更多的高级别数据支持了SCS在非手术性腰痛(NSLBP)中的应用,并且美国食品药品监督管理局已批准该应用。美国疼痛与神经科学学会(ASPN)执行委员会意识到有必要为这一特定患者群体制定患者选择标准。这是一个NEURON项目(神经科学、教育、应用、风险缓解、最佳结果和神经调节),是一个关于不断发展的治疗方法和适应症的实用指南,重点是使用神经轴刺激来治疗难治性疼痛。
经委员会批准后,该学会接受了该项目的提名者,提名重点在于经验、发表的文章、研究成果和多样性。该团队制定了讨论大纲,根据已发表的指南选择了分级系统,并确定了共识点。
基于证据水平和专家意见,这些证据得出了几个共识点,以最佳地指导患者选择。这些结果将提高植入患者的安全性和疗效,并形成最佳实践的新标准。
对于NSLBP患者,植入手术的患者选择应基于已发表的文献、最佳实践和专家意见。这个NEURON项目将允许定期更新,以创建一个实用指南,从而更好地吸收信息,提高未来的安全性和疗效。