Tieppo Francio Vinicius, Leavitt Logan, Radlicz Christopher, Gill Benjamin, Sayed Dawood
Division of Pain Medicine, Department of Anesthesiology, Washington University School of Medicine in St. Louis, St. Louis, MO, USA.
Department of Physical Medicine and Rehabilitation, The University of Kansas Medical Center, Kansas City, KS, USA.
Curr Pain Headache Rep. 2025 Jun 25;29(1):98. doi: 10.1007/s11916-025-01413-z.
Lumbar radiofrequency ablation (LRFA) is an interventional procedure that utilizes thermal energy to selectively ablate the lumbar medial branch nerves (LMBN) to provide relief from facet-mediated chronic axial low back pain. While LRFA is widely performed, considerable variability exists in its technical execution. This review aims to synthesize the current literature on key device- and procedure-related factors that influence radiofrequency lesioning and to clarify common misconceptions regarding LRFA.
Emerging evidence suggests that several device-related parameters-including cannula and needle size, active tip length, temperature settings, lesioning duration, and needle angulation-affect lesion size and clinical outcomes. However, the impact of adjunctive steroid administration on lesion characteristics and therapeutic efficacy remains inconclusive. Furthermore, while some concerns have been raised regarding the potential for LRFA to accelerate spinal degeneration, definitive evidence is lacking. There is, however, a plausible association between LRFA and multifidus atrophy. The use of motor testing prior to ablation is warranted. Current data support the safety of LRFA in patients with posterior spinal instrumentation and implantable devices. Device- and procedure-specific variables may significantly influence LRFA lesion characteristics and clinical outcomes. While the safety profile of LRFA is generally favorable, potential complications exist, underscoring the need for a nuanced understanding of optimal procedural techniques. Despite its widespread adoption, misconceptions persist regarding optimal approaches, safety considerations, and determinants of efficacy. This review critically evaluates the existing literature to address these controversies and provide an evidence-based perspective on LRFA.
腰椎射频消融术(LRFA)是一种介入手术,利用热能选择性地消融腰内侧支神经(LMBN),以缓解小关节介导的慢性轴性下腰痛。虽然LRFA被广泛应用,但其技术操作存在很大差异。本综述旨在综合当前关于影响射频损伤的关键设备和手术相关因素的文献,并澄清关于LRFA的常见误解。
新出现的证据表明,几个与设备相关的参数,包括套管和针的尺寸、有效尖端长度、温度设置、损伤持续时间和针的角度,都会影响损伤大小和临床结果。然而,辅助使用类固醇对损伤特征和治疗效果的影响仍无定论。此外,虽然有人担心LRFA可能会加速脊柱退变,但缺乏确凿证据。然而,LRFA与多裂肌萎缩之间存在合理的关联。消融前进行运动测试是有必要的。目前的数据支持LRFA在有后路脊柱内固定和植入式设备的患者中的安全性。特定于设备和手术的变量可能会显著影响LRFA的损伤特征和临床结果。虽然LRFA的安全性总体良好,但仍存在潜在并发症,这凸显了对最佳手术技术进行细致了解的必要性。尽管LRFA已被广泛采用,但关于最佳方法、安全考虑和疗效决定因素的误解仍然存在。本综述批判性地评估了现有文献,以解决这些争议,并为LRFA提供基于证据的观点。