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Association between intraoperative hypotension and motor evoked potential change in ossification of posterior longitudinal ligament and/or ossification of ligamentum flavum surgery 术中低血压与后纵韧带骨化和/或黄韧带骨化手术中运动诱发电位变化的关系
IF 2.5 Q3 Medicine Pub Date : 2025-12-01 DOI: 10.1016/j.xnsj.2025.100820
Tun Liu MD, PhD , Wentao Wang MD, PhD , Huaguang Qi MD , Jia Li MD, PhD , Bin Guo MD , Kuo Jiang MD, PhD , Songchuan Zhao MD , Ruiguo Wang MD, PhD , Jitao Zhang MD , Gang Wu MD, PhD , Gang Wang MD, PhD

Background

Intraoperative hypotension (IOH) is a recognized contributor to changes in motor evoked potential (MEP) during spinal surgeries. Additionally, it is essential to precisely define IOH across different surgical phases. However, there is limited data on optimal IOH thresholds for predicting MEP changes in thoracic ossification of the posterior longitudinal ligament (OPLL) and/or ossification of the ligamentum flavum (OLF) surgery. We aim to determine the IOH thresholds for predicting MEP changes during surgical treatment for OPLL and/or OLF based on different surgical phase.

Methods

Data collected included demographic information, surgical details, mean arterial pressure (MAP) values, and MEP signals. A receiver operating characteristic (ROC) curve was employed to determine the MAP thresholds. A comparative analysis was performed to evaluate IOH episodes occurring during predecompression versus postdecompression surgical phases, specifically in the early and later stages. Additionally, a multivariate logistic regression analysis was conducted to assess the association between surgical variables and MEP change.

Results

The MAP thresholds for predicting changes in MEP at the early surgical stage were determined as follows: 70 mmHg for patients with combined OPLL and OLF, 66 mmHg for OPLL patients, and 65 mmHg for OLF patients. However, it is recommended that MAP at the later surgical stage should be elevated to exceed 75 mmHg, 73 mmHg, and 71 mmHg in patients diagnosed with combined OPLL and OLF, OPLL, and OLF, respectively. A stronger correlation was observed between MAP variability ratio and MEP amplitude reduction ratio (ARR) during postdecompression surgical phase. At the early surgical stage, the administration of ephedrine bolus was identified as a risk factor for predicting MEP change (odds ratio [OR]=1.13, p<.01). At the later stage, the risk-factors included ephedrine bolus (OR=1.09, p<.01), estimated blood loss (per 100 mL) (OR=1.23, p=.02), and patients with combined OPLL and OLF (OR=12.12, p<.01).

Conclusions

We determined cutoff values for MAP to predict changes in MEP in patients undergoing surgical treatment for OPLL and/or OLF based on different surgical phases. Compared to the early surgical stage, patients exhibit less tolerance to IOH at the later surgical stage. A stronger correlation was observed between the MAP variability ratio and MEP ARR at the later surgical stage. Additionally, we identified surgical factors that are associated with a higher probability of MEP change.
背景:术中低血压(IOH)是脊柱手术中运动诱发电位(MEP)变化的公认因素。此外,在不同手术阶段精确定义IOH是必要的。然而,关于预测胸后纵韧带骨化(OPLL)和/或黄韧带骨化(OLF)手术中MEP变化的最佳IOH阈值的数据有限。我们的目的是根据不同手术阶段确定IOH阈值,以预测OPLL和/或OLF手术治疗期间MEP的变化。方法收集患者的人口学资料、手术细节、平均动脉压(MAP)值和MEP信号。采用受试者工作特征(ROC)曲线确定MAP阈值。我们进行了一项比较分析,以评估在减压前和减压后手术阶段,特别是在早期和晚期发生的IOH发作。此外,进行了多变量logistic回归分析,以评估手术变量与MEP变化之间的关系。结果预测手术早期MEP变化的MAP阈值为:OPLL合并黄韧带骨化患者70 mmHg, OPLL患者66 mmHg,黄韧带骨化患者65 mmHg。然而,对于诊断为OPLL合并黄韧带骨化、OPLL合并黄韧带骨化的患者,建议在手术后期将MAP分别升高至75 mmHg、73 mmHg和71 mmHg以上。在减压手术后阶段,MAP变异性比与MEP减幅比(ARR)之间存在较强的相关性。在手术早期,麻黄碱丸的使用被认为是预测MEP变化的危险因素(优势比[OR]=1.13, p< 0.01)。在晚期,危险因素包括麻黄碱丸(OR=1.09, p= 0.01)、估计失血量(每100 mL) (OR=1.23, p= 0.02)和OPLL和OLF合并患者(OR=12.12, p= 0.01)。我们确定了MAP的临界值,以预测手术治疗OPLL和/或OLF患者MEP的变化。与手术早期相比,手术后期患者对IOH的耐受性较差。在手术后期,MAP变异性比与MEP ARR之间存在更强的相关性。此外,我们还确定了与MEP改变可能性较高相关的手术因素。
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引用次数: 0
The future is now: How AI is reshaping spine care 未来就是现在:人工智能如何重塑脊柱护理
IF 2.5 Q3 Medicine Pub Date : 2025-12-01 DOI: 10.1016/j.xnsj.2025.100825
Eric J. Muelbauer , Mohammed Ali Alvi MD, MS , David J. Kennedy , Michael G. Fehlings MD, PhD

Introduction

Artificial intelligence (AI) is rapidly reshaping spinal care, transitioning from experimental algorithms to operational tools embedded in clinical workflows. This narrative review explores the evolving role of AI across the spine care continuum, including diagnostic imaging, surgical planning, intraoperative navigation, predictive analytics, and digital therapeutics.

Methods

Using a mixed-methods approach, we synthesized insights from peer-reviewed literature, regulatory documents, press releases, and grey sources published between 2017 and 2025.

Results

AI-enabled imaging platforms now assist in detecting spinal pathologies and extracting quantitative metrics such as disc heights and Cobb angles, improving diagnostic consistency and reducing inter-rater variability. In surgical planning, decision-support systems and robotics-integrated platforms offer personalized guidance and enhanced precision. Intraoperative tools using 2D–3D fusion and volumetric reconstruction are enabling hardware-light navigation, particularly in ambulatory settings. Predictive models for survival, reoperation risk, and patient-reported outcomes are emerging, though external validation remains limited.
Digital therapeutics and wearable technologies are expanding the reach of spine care beyond the clinic, offering scalable solutions for rehabilitation and postoperative monitoring. Meanwhile, regulatory and legal frameworks are evolving to address transparency, data governance, and intellectual property concerns. Recent FDA guidance and landmark legal cases underscore the need for disciplined collaboration and responsible deployment.

Conclusions

AI in spine care is no longer theoretical and is operational. Its integration promises enhanced precision, efficiency, and personalization, but also demands rigorous validation and ethical oversight. This review highlights the multifaceted impact of AI and calls for continued alignment between clinicians, developers, and regulators to ensure safe, equitable, and sustainable innovation.
人工智能(AI)正在迅速重塑脊柱护理,从实验算法过渡到嵌入临床工作流程的操作工具。这篇叙述性综述探讨了人工智能在脊柱护理连续体中的不断发展的作用,包括诊断成像、手术计划、术中导航、预测分析和数字治疗。方法采用混合方法,综合2017年至2025年间发表的同行评议文献、监管文件、新闻稿和灰色来源的见解。基于ai的成像平台现在可以帮助检测脊柱病变并提取定量指标,如椎间盘高度和Cobb角,从而提高诊断一致性并减少内部变异性。在手术计划中,决策支持系统和机器人集成平台提供个性化指导和更高的精度。术中使用2D-3D融合和体积重建的工具使硬件轻导航成为可能,特别是在门诊环境中。生存、再手术风险和患者报告结果的预测模型正在出现,尽管外部验证仍然有限。数字治疗和可穿戴技术正在将脊柱护理的范围扩展到诊所之外,为康复和术后监测提供可扩展的解决方案。与此同时,监管和法律框架也在不断发展,以解决透明度、数据治理和知识产权问题。最近的FDA指南和具有里程碑意义的法律案例强调了有纪律的合作和负责任的部署的必要性。结论sai在脊柱护理中不再是理论的,而是可操作的。它的集成承诺提高精度、效率和个性化,但也需要严格的验证和道德监督。本综述强调了人工智能的多方面影响,并呼吁临床医生、开发人员和监管机构继续保持一致,以确保安全、公平和可持续的创新。
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引用次数: 0
Anterior cement augmentation technique for correction of kyphotic deformity in the lumbar spine using an anterior-to-Psoas approach 前路骨水泥增强技术用于前路-腰大肌入路腰椎后凸畸形矫正
IF 2.5 Q3 Medicine Pub Date : 2025-12-01 DOI: 10.1016/j.xnsj.2025.100818
David Shin BS , David Cheng BS, MPH , Debra Cheng BS , Carson Cummings BS , Jacob Razzouk BS , Olumide Danisa MD , Wayne Cheng MD

Background

Posterior kyphotic deformity correction in patients with osteoporosis carries a significant risk of instrumentation cut-out. Anterior approaches allow direct distraction at the center of the deformity, yet reduction devices or instrumentation may telescope into vertebral endplates. This study proposes an anterior cementing augmentation technique for correction of kyphotic deformity involving a less invasive oblique lateral interbody fusion (OLIF) approach.

Case description

Patient 1 had a previous compression fracture at L2 above prior instrumented fusion, with kyphotic deformity, and underwent a stage-one anterior lateral L2 corpectomy via an (OLIF) approach. Cement was placed centrally at L1 and L3, followed by an expandable cage and a stage-two posterior T11-to-pelvis instrumented fusion with prophylactic cement augmentation at T10–T12. Patient 2 had a previous remote L5–S1 anterior lumbar interbody fusion and underwent a posterior C4–S1 osteotomy and instrumented fusion for kyphoscoliosis deformity. The patient developed immediate postoperative instrumentation failure with kyphosis at L4–L5 and instrumentation loosening and migration at L4–S1 within 2 weeks of surgery. They then underwent (OLIF) at L4–L5 with anterior cement augmentation at L4–L5, followed by a revision lumbar-pelvic instrumented fusion.

Outcome

A step-by-step technique was described for anterior corpectomy and cement augmentation via an anterior lateral approach, presenting an alternative for correction of kyphotic deformity and restoration of sagittal alignment in the lumbar spine of patients with poor-bone density.

Conclusions

A minimally invasive, anterior-to- psoas approach may decrease morbidity of approach related complications. Both patients demonstrated kyphotic deformity correction with follow-up records suggesting favorable outcomes.
背景:骨质疏松症患者后路后凸畸形矫形术存在器械切除的显著风险。前路入路可以在畸形中心直接撑开,但复位装置或内固定可能会进入椎体终板。本研究提出了一种前路骨水泥增强技术,采用侵入性较小的斜侧体间融合(OLIF)入路矫正后凸畸形。病例描述:患者1在之前的内固定融合术中曾发生L2压缩性骨折,伴后凸畸形,并通过OLIF入路行一期L2前外侧椎体切除术。在L1和L3中央放置水泥,随后在T10-T12进行可伸缩笼和二期后路t11 -骨盆内固定融合,预防性水泥增强。患者2既往行L5-S1前路腰椎椎间融合术,后凸侧凸畸形行后路C4-S1截骨和固定式融合术。患者术后立即出现内固定失败,L4-L5后凸,手术2周内L4-S1内固定松动和移位。然后他们在L4-L5行OLIF手术,在L4-L5行前路骨水泥增强,随后进行腰椎-骨盆内固定融合翻修。结果:通过前外侧入路进行前椎体切除术和骨水泥增强的一步一步技术,为骨密度低的患者腰椎后凸畸形的矫正和矢状位的恢复提供了一种替代方法。结论微创前腰肌入路可降低入路并发症的发生率。两名患者均表现出后凸畸形矫正,随访记录显示预后良好。
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引用次数: 0
Letter to the editor regarding chemical prophylaxis and venous thromboembolism following elective spinal surgery: a systematic review and meta-analysis 致编辑的信--关于脊柱择期手术后的化学药物预防和静脉血栓栓塞症:系统回顾和荟萃分析
IF 2.5 Q3 Medicine Pub Date : 2025-12-01 DOI: 10.1016/j.xnsj.2024.100311
Zahra Ramezani MD, Seyed Danial Alizadeh MD, Vafa Rahimi-Movaghar MD
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引用次数: 0
Development and reliability of a systematic method to evaluate lumbar paraspinal muscle size and quality in computed tomography images 一种在计算机断层图像中评估腰椎棘旁肌大小和质量的系统方法的发展和可靠性
IF 2.5 Q3 Medicine Pub Date : 2025-12-01 DOI: 10.1016/j.xnsj.2025.100822
Cristiane R. Carlesso PT, PhD , Jaclyn M. Sions PT, DPT, PhD , William J. Anderst PhD , Charity G. Patterson PhD , Rafaela M. Barbosa PT , Luiza P. Weissmann , Tom Gale MS , Michael J. Schneider DC, PhD , Sara R. Piva PT, PhD

Background

Lumbar paraspinal muscles (LPMs) are critical for spinal stability, and their morphological alterations are associated with chronic low back pain (cLBP). Computed tomography (CT) offers a feasible alternative to magnetic resonance imaging for assessing LPM morphology; however, its broader use has been hindered by inconsistent measurement methods and limited reliability data. This study aimed to describe a systematic CT-based method for evaluating LPM cross-sectional area (CSA) and attenuation (MA) in adults with cLBP and to determine its intra and inter-examiner procedural reliability.

Methods

High-resolution CT images were used to analyze bilateral LPMs: erector spinae (L1–L5), multifidi (L1–S1), psoas (L3), and quadratus lumborum (L3). Two trained examiners independently performed image selection and analysis, blinded to subject identity and prior results. Procedural reliability was quantified using intraclass correlation coefficients (ICC2,1) with 95% confidence intervals (CI). Mean ICCs<0.50 indicated poor, 0.50–0.74 moderate, 0.75–0.90 good, and >0.90 excellent procedural reliability.

Results

Thirty-six participants (40% female; age 48±15 years; BMI 27.2±4.3 kg/m²) with moderate disability were included. Intraexaminer procedural reliability was excellent for CSA of the erector spinae, psoas, and quadratus lumborum (ICC point estimates >0.916, >0.959, and >0.962, respectively); and good to excellent for multifidi CSA (ICC point estimates: 0.770–0.916), with greater variability at L1 and L2. Inter-examiner procedural reliability was excellent for CSA of the erector spinae, psoas, and quadratum lumborum (ICC point estimates >0.916, >0.946, and >0.941, respectively); and moderate to excellent for multifidi CSA (ICC point estimates: 0.593–0.945), with lower reliability at upper lumbar levels. Intra and inter-examiner procedural reliability for MA was excellent across all LPMs.

Conclusions

The presented CT-based protocol provides a standardized and reproducible method for assessing LPM CSA and MA in adults with cLBP. Demonstrated high procedural reliability—including image selection and analysis—supports its use for consistent evaluation of LPM morphology in both clinical and research contexts, particularly where muscle degeneration complicates image-based assessment.
腰椎棘旁肌(lpm)对脊柱稳定性至关重要,其形态改变与慢性腰痛(cLBP)有关。计算机断层扫描(CT)为评估LPM形态提供了一种可行的替代磁共振成像;然而,由于测量方法不一致和可靠性数据有限,阻碍了其广泛应用。本研究旨在描述一种系统的基于ct的方法来评估成人cLBP患者的LPM横截面积(CSA)和衰减(MA),并确定其内部和内部检查程序的可靠性。方法采用高分辨率CT图像分析双侧lvm:竖脊肌(L1-L5)、多裂肌(L1-S1)、腰肌(L3)和腰方肌(L3)。两名训练有素的审查员独立进行图像选择和分析,不知道受试者身份和先前的结果。程序信度采用类内相关系数(ICC2,1)和95%置信区间(CI)进行量化。平均ICCs<;0.50表示程序可靠性差,0.50 - 0.74表示中等,0.75-0.90表示良好,>;0.90表示极好。结果纳入36例中度残疾患者,其中女性占40%,年龄48±15岁,BMI 27.2±4.3 kg/m²。对竖脊肌、腰大肌和腰方肌的CSA,检查员的程序可靠性非常好(ICC点估计值分别为>;0.916, >;0.959和>;0.962);对于多分辨率CSA (ICC点估计值:0.77 - 0.916),具有较大的L1和L2变异性。竖脊肌、腰肌和腰方肌CSA的检查者间程序可靠性极好(ICC点估计值分别为>;0.916、>;0.946和>;0.941);多椎体CSA为中等至优异(ICC点估计值:0.593-0.945),上腰椎水平的可靠性较低。在所有lpm中,MA的内部和内部程序可靠性都很好。结论本文提出的基于ct的方案为评估成人cLBP患者的LPM CSA和MA提供了一种标准化和可重复的方法。具有较高的程序可靠性,包括图像选择和分析,支持其在临床和研究背景下用于一致的LPM形态学评估,特别是在肌肉变性使基于图像的评估复杂化的情况下。
{"title":"Development and reliability of a systematic method to evaluate lumbar paraspinal muscle size and quality in computed tomography images","authors":"Cristiane R. Carlesso PT, PhD ,&nbsp;Jaclyn M. Sions PT, DPT, PhD ,&nbsp;William J. Anderst PhD ,&nbsp;Charity G. Patterson PhD ,&nbsp;Rafaela M. Barbosa PT ,&nbsp;Luiza P. Weissmann ,&nbsp;Tom Gale MS ,&nbsp;Michael J. Schneider DC, PhD ,&nbsp;Sara R. Piva PT, PhD","doi":"10.1016/j.xnsj.2025.100822","DOIUrl":"10.1016/j.xnsj.2025.100822","url":null,"abstract":"<div><h3>Background</h3><div>Lumbar paraspinal muscles (LPMs) are critical for spinal stability, and their morphological alterations are associated with chronic low back pain (cLBP). Computed tomography (CT) offers a feasible alternative to magnetic resonance imaging for assessing LPM morphology; however, its broader use has been hindered by inconsistent measurement methods and limited reliability data. This study aimed to describe a systematic CT-based method for evaluating LPM cross-sectional area (CSA) and attenuation (MA) in adults with cLBP and to determine its intra and inter-examiner procedural reliability.</div></div><div><h3>Methods</h3><div>High-resolution CT images were used to analyze bilateral LPMs: erector spinae (L1–L5), multifidi (L1–S1), psoas (L3), and quadratus lumborum (L3). Two trained examiners independently performed image selection and analysis, blinded to subject identity and prior results. Procedural reliability was quantified using intraclass correlation coefficients (ICC<sub>2,1</sub>) with 95% confidence intervals (CI). Mean ICCs&lt;0.50 indicated poor, 0.50–0.74 moderate, 0.75–0.90 good, and &gt;0.90 excellent procedural reliability.</div></div><div><h3>Results</h3><div>Thirty-six participants (40% female; age 48±15 years; BMI 27.2±4.3 kg/m²) with moderate disability were included. Intraexaminer procedural reliability was excellent for CSA of the erector spinae, psoas, and quadratus lumborum (ICC point estimates &gt;0.916, &gt;0.959, and &gt;0.962, respectively); and good to excellent for multifidi CSA (ICC point estimates: 0.770–0.916), with greater variability at L1 and L2. Inter-examiner procedural reliability was excellent for CSA of the erector spinae, psoas, and quadratum lumborum (ICC point estimates &gt;0.916, &gt;0.946, and &gt;0.941, respectively); and moderate to excellent for multifidi CSA (ICC point estimates: 0.593–0.945), with lower reliability at upper lumbar levels. Intra and inter-examiner procedural reliability for MA was excellent across all LPMs.</div></div><div><h3>Conclusions</h3><div>The presented CT-based protocol provides a standardized and reproducible method for assessing LPM CSA and MA in adults with cLBP. Demonstrated high procedural reliability—including image selection and analysis—supports its use for consistent evaluation of LPM morphology in both clinical and research contexts, particularly where muscle degeneration complicates image-based assessment.</div></div>","PeriodicalId":34622,"journal":{"name":"North American Spine Society Journal","volume":"24 ","pages":"Article 100822"},"PeriodicalIF":2.5,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145736472","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Robotic-assisted bilateral lumbar pars fracture endoscopic debridement and direct repair as treatment for lumbar radiculopathy: A case report 机器人辅助双侧腰椎部骨折内镜清创和直接修复治疗腰椎神经根病1例报告
IF 2.5 Q3 Medicine Pub Date : 2025-12-01 DOI: 10.1016/j.xnsj.2025.100823
S. Garg BS , Y. Wang MD , N. Lehman MSPA , M. Gallizzi MD, MS

Background

Management of lumbar spondylolysis in the athletic population can be successful with conservative means, however surgical intervention may be required for fractures presenting with radiculopathy. Direct repair with intralaminar screws is a commonly used technique which has been described previously with various rates of success. Technological advancements now allow minimally invasive direct pars repair with robotic assistance as a viable option. Robotic assistance for instrumentation and stabilization of the fracture can also be combined with endoscopic spine techniques, to debride the fracture site, to effectively treat this issue.

Methods

A 16-year-old giant slalom skier presented with low back pain and associated bilateral L5 radiculopathy to our facility. Using MRI and CT, they were diagnosed with bilateral L5 pars interarticularis fractures with bony edema and with subtle hypermobile retrolisthesis in combination with bilateral foraminal stenosis at the L5-S1 disc space. Due to patient’s active sports participation and continued symptoms despite rest, physical therapy, chiropractic therapy, and bracing, the patient decided to undergo elective, outpatient, bilateral robotic-assisted percutaneous endoscopic debridement of the pars fractures through 7-mm skin incisions, and bilateral percutaneous intralaminar fixation of the pars fractures with pedicle screws through 1.5-cm skin incisions.

Results

In the immediate postoperative period, the patient reported complete resolution of mechanical low back pain and associated bilateral radiculopathy. The patient had resolution of incisional low back pain by 6 weeks postoperatively and demonstrated stable healing with no evidence of hardware failure radiographically through their 6-month postoperative x-rays. This 16-year-old was able to return to prior level of sport and competition at 3-months postoperatively.

Conclusions

This novel minimally invasive robotic-assisted percutaneous approach for lumbar spondylolysis fracture debridement and direct repair is a suitable option for nonhealing pars fracture with radiculopathy in high performing active adolescent patients.
背景:运动人群腰椎峡部裂的保守治疗是成功的,但是对于伴有神经根病的骨折可能需要手术治疗。椎板内螺钉直接修复是一种常用的技术,先前已描述过成功率不同的技术。技术的进步使得机器人辅助下的微创直接局部修复成为一种可行的选择。机器人辅助骨折的固定和稳定也可以与内窥镜脊柱技术相结合,对骨折部位进行清创,有效地治疗这一问题。方法一名16岁的大回转滑雪运动员以腰痛和双侧L5神经根病来我院就诊。通过MRI和CT,他们被诊断为双侧L5关节间部骨折伴骨水肿和轻度过度活动后滑脱合并双侧L5- s1椎间盘间隙椎间孔狭窄。由于患者积极参与运动,尽管休息、物理治疗、整脊治疗和支具仍持续出现症状,因此患者决定选择门诊、门诊、双侧机器人辅助下通过7mm皮肤切口经皮腔镜清创术,并通过1.5 cm皮肤切口用椎弓根螺钉经皮双侧椎板内固定。结果患者术后立即报告机械性腰痛和相关双侧神经根病完全缓解。患者术后6周切口腰痛消退,术后6个月x光片显示愈合稳定,无硬体失效迹象。术后3个月,这名16岁的患者能够恢复到以前的运动和比赛水平。结论:这种新型的微创机器人辅助经皮入路治疗腰椎峡部裂骨折清创和直接修复是一种适合于高性能活跃青少年患者伴有神经根病的未愈合部骨折的选择。
{"title":"Robotic-assisted bilateral lumbar pars fracture endoscopic debridement and direct repair as treatment for lumbar radiculopathy: A case report","authors":"S. Garg BS ,&nbsp;Y. Wang MD ,&nbsp;N. Lehman MSPA ,&nbsp;M. Gallizzi MD, MS","doi":"10.1016/j.xnsj.2025.100823","DOIUrl":"10.1016/j.xnsj.2025.100823","url":null,"abstract":"<div><h3>Background</h3><div>Management of lumbar spondylolysis in the athletic population can be successful with conservative means, however surgical intervention may be required for fractures presenting with radiculopathy. Direct repair with intralaminar screws is a commonly used technique which has been described previously with various rates of success. Technological advancements now allow minimally invasive direct pars repair with robotic assistance as a viable option. Robotic assistance for instrumentation and stabilization of the fracture can also be combined with endoscopic spine techniques, to debride the fracture site, to effectively treat this issue<em>.</em></div></div><div><h3>Methods</h3><div>A 16-year-old giant slalom skier presented with low back pain and associated bilateral L5 radiculopathy to our facility. Using MRI and CT, they were diagnosed with bilateral L5 pars interarticularis fractures with bony edema and with subtle hypermobile retrolisthesis in combination with bilateral foraminal stenosis at the L5-S1 disc space. Due to patient’s active sports participation and continued symptoms despite rest, physical therapy, chiropractic therapy, and bracing, the patient decided to undergo elective, outpatient, bilateral robotic-assisted percutaneous endoscopic debridement of the pars fractures through 7-mm skin incisions, and bilateral percutaneous intralaminar fixation of the pars fractures with pedicle screws through 1.5-cm skin incisions.</div></div><div><h3>Results</h3><div>In the immediate postoperative period, the patient reported complete resolution of mechanical low back pain and associated bilateral radiculopathy. The patient had resolution of incisional low back pain by 6 weeks postoperatively and demonstrated stable healing with no evidence of hardware failure radiographically through their 6-month postoperative x-rays. This 16-year-old was able to return to prior level of sport and competition at 3-months postoperatively.</div></div><div><h3>Conclusions</h3><div>This novel minimally invasive robotic-assisted percutaneous approach for lumbar spondylolysis fracture debridement and direct repair is a suitable option for nonhealing pars fracture with radiculopathy in high performing active adolescent patients.</div></div>","PeriodicalId":34622,"journal":{"name":"North American Spine Society Journal","volume":"24 ","pages":"Article 100823"},"PeriodicalIF":2.5,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145681369","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Proton pump inhibitors are associated with increased risk of pseudoarthrosis after lumbar fusion 质子泵抑制剂与腰椎融合术后假关节风险增加有关
IF 2.5 Q3 Medicine Pub Date : 2025-11-29 DOI: 10.1016/j.xnsj.2025.100829
Melissa Romoff BA, Michael S. Kim MD, Courtney Spitzer BA, Andy Ton MD, Vivian Chen MD, Ryan Le MD, Abhinav Sharma MD, Emily Mills MD, Hao-Hua Wu MD, Don Young Park MD, Yu-Po Lee MD, Nitin Bhatia MD, Sohaib Hashmi MD

Background

Pseudoarthrosis is a major complication following lumbar spine fusion, leading to revision surgery, increased disability, and substantial economic burden. Proton pump inhibitors (PPIs) are commonly used in the perioperative period, but their impact on fusion success remains poorly defined.

Methods

This retrospective cohort study utilized the TriNetX research database to identify adult patients undergoing lumbar spine fusion. Patients were divided into 2 cohorts based on documented PPI use within 30 days postoperatively and underwent 1:1 propensity score matching based on demographic and clinical characteristics. The incidence of pseudoarthrosis was assessed using diagnostic coding, and risk was compared using risk ratios and Kaplan-Meier survival analysis. An age-stratified analysis was also performed.

Results

A total of 122,584 matched pairs were analyzed. Pseudoarthrosis occurred in 7.38% of PPI users compared to 3.98% of nonusers (RR: 1.88; p < .0001). Kaplan-Meier survival analysis revealed early separation of pseudoarthrosis-free survival curves by postoperative day 60, persisting through 1-year follow-up. Age-stratified analysis showed consistently higher pseudoarthrosis risk among PPI users across all age groups, with the largest relative impact observed in patients under 55 years old.

Conclusions

Postoperative PPI use is associated with a significantly increased risk of pseudoarthrosis following lumbar spine fusion. These findings suggest careful consideration of the necessity of PPI therapy in the perioperative period, particularly in younger patients where the relative impact appears the greatest.
背景:假关节是腰椎融合术后的主要并发症,导致翻修手术、残疾增加和巨大的经济负担。质子泵抑制剂(PPIs)通常用于围手术期,但其对融合成功的影响仍不明确。方法本回顾性队列研究利用TriNetX研究数据库识别接受腰椎融合术的成年患者。根据术后30天内PPI使用记录将患者分为2组,并根据人口学和临床特征进行1:1倾向评分匹配。使用诊断编码评估假关节的发生率,并使用风险比和Kaplan-Meier生存分析比较风险。还进行了年龄分层分析。结果共分析配对对122584对。7.38%的PPI使用者发生假关节,而非PPI使用者发生假关节的比例为3.98% (RR: 1.88; p < 0.0001)。Kaplan-Meier生存分析显示,术后60天无假关节生存曲线早期分离,持续1年随访。年龄分层分析显示,在所有年龄组PPI使用者中,假关节风险始终较高,55岁以下患者的相对影响最大。结论:术后使用PPI与腰椎融合术后假关节的风险显著增加相关。这些发现提示在围手术期仔细考虑PPI治疗的必要性,特别是在相对影响最大的年轻患者中。
{"title":"Proton pump inhibitors are associated with increased risk of pseudoarthrosis after lumbar fusion","authors":"Melissa Romoff BA,&nbsp;Michael S. Kim MD,&nbsp;Courtney Spitzer BA,&nbsp;Andy Ton MD,&nbsp;Vivian Chen MD,&nbsp;Ryan Le MD,&nbsp;Abhinav Sharma MD,&nbsp;Emily Mills MD,&nbsp;Hao-Hua Wu MD,&nbsp;Don Young Park MD,&nbsp;Yu-Po Lee MD,&nbsp;Nitin Bhatia MD,&nbsp;Sohaib Hashmi MD","doi":"10.1016/j.xnsj.2025.100829","DOIUrl":"10.1016/j.xnsj.2025.100829","url":null,"abstract":"<div><h3>Background</h3><div>Pseudoarthrosis is a major complication following lumbar spine fusion, leading to revision surgery, increased disability, and substantial economic burden. Proton pump inhibitors (PPIs) are commonly used in the perioperative period, but their impact on fusion success remains poorly defined.</div></div><div><h3>Methods</h3><div>This retrospective cohort study utilized the TriNetX research database to identify adult patients undergoing lumbar spine fusion. Patients were divided into 2 cohorts based on documented PPI use within 30 days postoperatively and underwent 1:1 propensity score matching based on demographic and clinical characteristics. The incidence of pseudoarthrosis was assessed using diagnostic coding, and risk was compared using risk ratios and Kaplan-Meier survival analysis. An age-stratified analysis was also performed.</div></div><div><h3>Results</h3><div>A total of 122,584 matched pairs were analyzed. Pseudoarthrosis occurred in 7.38% of PPI users compared to 3.98% of nonusers (RR: 1.88; p &lt; .0001). Kaplan-Meier survival analysis revealed early separation of pseudoarthrosis-free survival curves by postoperative day 60, persisting through 1-year follow-up. Age-stratified analysis showed consistently higher pseudoarthrosis risk among PPI users across all age groups, with the largest relative impact observed in patients under 55 years old.</div></div><div><h3>Conclusions</h3><div>Postoperative PPI use is associated with a significantly increased risk of pseudoarthrosis following lumbar spine fusion. These findings suggest careful consideration of the necessity of PPI therapy in the perioperative period, particularly in younger patients where the relative impact appears the greatest.</div></div>","PeriodicalId":34622,"journal":{"name":"North American Spine Society Journal","volume":"25 ","pages":"Article 100829"},"PeriodicalIF":2.5,"publicationDate":"2025-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145840985","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Extraforaminal lumbar interbody fusion: A systematic review of clinical outcomes, fusion rates, and safety profile 椎间孔外腰椎椎体间融合术:临床结果、融合率和安全性的系统综述
IF 2.5 Q3 Medicine Pub Date : 2025-11-29 DOI: 10.1016/j.xnsj.2025.100830
Michael K. Coffin BS, Kyle A. McGrath DO, Rebecca M. Garner MD, Christiana M. Cornea MD, Joseph S. Cheng MD, Justin N. Virojanapa DO

Background

Extraforaminal lumbar interbody fusion (ELIF) accesses the disc through a posterolateral extraforaminal corridor that preserves the posterior ligamentous complex and avoids abdominal exposure. The objective of this systematic review is to synthesize the clinical outcomes, fusion rates, complications, and surgical indications for ELIF.

Methods

PRISMA 2020–conformant review registered in PROSPERO (ID: 1111090). Eligible studies reported clinical or radiographic outcomes of ELIF performed via the posterolateral extraforaminal approach. Extracted variables included indications, operative time, patient-reported outcomes, fusion, and complications. Risk of bias was assessed with the Newcastle–Ottawa Scale (NOS).

Results

Thirteen retrospective studies (n=518) met inclusion. The quality of studies included was generally fair, as graded by Newcastle–Ottawa Scale (NOS). The most common indication was degenerative disc disease. Mean operative time was 168.7 minutes. Fusion by technique: open pooled mean 98%, minimally invasive pooled mean 84%, and endoscopic 100% in a single series. Pooled VAS back improved as follows: open 6.27 to 2.80 (Δ 3.47; mean follow-up 12.8 months), minimally invasive 8.16 to 3.52 (Δ 4.64; 18.8 months), endoscopic 6.49 to 1.66 (Δ 4.83; 13.2 months). Pooled VAS leg improved: open 6.66 to 2.35 (Δ 4.31, 13.3 months), minimally invasive 8.66 to 2.17 (Δ 6.49; 15.5 months), endoscopic 6.60 to 1.50 (Δ 5.10; 14.2 months). Pooled Oswestry disability index (ODI) improved: open 60.17 to 26.25 (Δ 33.92; 9.5 months), minimally invasive 56.02 to 21.46 (Δ 34.56; 18.8 months), endoscopic 34.59 to 12.19 (Δ 22.40; 13.2 months). Transient radiculopathy was reported at 9.5% and dural tear at 0.5%.

Conclusions

As the first systematic review on ELIF, findings indicate it is a safe, effective alternative for lumbar fusion in select patients. Success necessitates favorable extraforaminal anatomy and intraoperative nerve monitoring to minimize complications. Future prospective trials are essential to validate these outcomes and standardize patient selection criteria.
椎间孔下腰椎椎体间融合术(ELIF)通过后外侧椎间孔外通道进入椎间盘,保留了后韧带复合体,避免了腹部暴露。本系统综述的目的是综合ELIF的临床结果、融合率、并发症和手术指征。方法sprisma 2020 -符合性审查已在普洛斯彼罗注册(ID: 1111090)。符合条件的研究报告了经后外侧椎间孔外入路行ELIF的临床或影像学结果。提取的变量包括适应证、手术时间、患者报告的结果、融合和并发症。偏倚风险采用纽卡斯尔-渥太华量表(NOS)进行评估。结果13项回顾性研究(n=518)符合纳入标准。根据纽卡斯尔-渥太华量表(NOS)的评分,纳入的研究质量总体上是公平的。最常见的适应症是椎间盘退行性病变。平均手术时间168.7分钟。技术融合:开放合池平均98%,微创合池平均84%,内镜下100%。合并VAS back改善情况如下:开放6.27 ~ 2.80 (Δ 3.47,平均随访12.8个月),微创8.16 ~ 3.52 (Δ 4.64,平均随访18.8个月),内镜6.49 ~ 1.66 (Δ 4.83,平均随访13.2个月)。合并VAS腿改善:开放6.66 ~ 2.35 (Δ 4.31, 13.3个月),微创8.66 ~ 2.17 (Δ 6.49; 15.5个月),内窥镜6.60 ~ 1.50 (Δ 5.10; 14.2个月)。综合Oswestry残疾指数(ODI)改善:开放60.17 ~ 26.25 (Δ 33.92; 9.5个月),微创56.02 ~ 21.46 (Δ 34.56; 18.8个月),内镜34.59 ~ 12.19 (Δ 22.40; 13.2个月)。短暂性神经根病占9.5%,硬脑膜撕裂占0.5%。结论作为首个关于ELIF的系统综述,研究结果表明,在特定患者中,ELIF是一种安全、有效的腰椎融合术替代方案。手术成功需要良好的椎间孔外解剖和术中神经监测以减少并发症。未来的前瞻性试验对于验证这些结果和标准化患者选择标准至关重要。
{"title":"Extraforaminal lumbar interbody fusion: A systematic review of clinical outcomes, fusion rates, and safety profile","authors":"Michael K. Coffin BS,&nbsp;Kyle A. McGrath DO,&nbsp;Rebecca M. Garner MD,&nbsp;Christiana M. Cornea MD,&nbsp;Joseph S. Cheng MD,&nbsp;Justin N. Virojanapa DO","doi":"10.1016/j.xnsj.2025.100830","DOIUrl":"10.1016/j.xnsj.2025.100830","url":null,"abstract":"<div><h3>Background</h3><div>Extraforaminal lumbar interbody fusion (ELIF) accesses the disc through a posterolateral extraforaminal corridor that preserves the posterior ligamentous complex and avoids abdominal exposure. The objective of this systematic review is to synthesize the clinical outcomes, fusion rates, complications, and surgical indications for ELIF.</div></div><div><h3>Methods</h3><div>PRISMA 2020–conformant review registered in PROSPERO (ID: 1111090). Eligible studies reported clinical or radiographic outcomes of ELIF performed via the posterolateral extraforaminal approach. Extracted variables included indications, operative time, patient-reported outcomes, fusion, and complications. Risk of bias was assessed with the Newcastle–Ottawa Scale (NOS).</div></div><div><h3>Results</h3><div>Thirteen retrospective studies (n=518) met inclusion. The quality of studies included was generally fair, as graded by Newcastle–Ottawa Scale (NOS). The most common indication was degenerative disc disease. Mean operative time was 168.7 minutes. Fusion by technique: open pooled mean 98%, minimally invasive pooled mean 84%, and endoscopic 100% in a single series. Pooled VAS back improved as follows: open 6.27 to 2.80 (Δ 3.47; mean follow-up 12.8 months), minimally invasive 8.16 to 3.52 (Δ 4.64; 18.8 months), endoscopic 6.49 to 1.66 (Δ 4.83; 13.2 months). Pooled VAS leg improved: open 6.66 to 2.35 (Δ 4.31, 13.3 months), minimally invasive 8.66 to 2.17 (Δ 6.49; 15.5 months), endoscopic 6.60 to 1.50 (Δ 5.10; 14.2 months). Pooled Oswestry disability index (ODI) improved: open 60.17 to 26.25 (Δ 33.92; 9.5 months), minimally invasive 56.02 to 21.46 (Δ 34.56; 18.8 months), endoscopic 34.59 to 12.19 (Δ 22.40; 13.2 months). Transient radiculopathy was reported at 9.5% and dural tear at 0.5%.</div></div><div><h3>Conclusions</h3><div>As the first systematic review on ELIF, findings indicate it is a safe, effective alternative for lumbar fusion in select patients. Success necessitates favorable extraforaminal anatomy and intraoperative nerve monitoring to minimize complications. Future prospective trials are essential to validate these outcomes and standardize patient selection criteria.</div></div>","PeriodicalId":34622,"journal":{"name":"North American Spine Society Journal","volume":"25 ","pages":"Article 100830"},"PeriodicalIF":2.5,"publicationDate":"2025-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145840986","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Artificial intelligence in spine care: A scoping review of treatment applications 人工智能在脊柱护理:治疗应用的范围综述
IF 2.5 Q3 Medicine Pub Date : 2025-11-20 DOI: 10.1016/j.xnsj.2025.100827
Victoria A. Bensel DC, MS, MPH , Anne Habeck MPH , Marcda Hilaire Brunot DC, MPH , Eleni-James Becton DC , Monika Ray PhD , Alexandria L. Brackett , Anthony J. Lisi DC

Background

Artificial intelligence (AI) is increasingly applied in healthcare to support decision-making, personalize treatment, and improve outcomes. In spine care, AI has been used for both operative and nonoperative interventions, including surgical planning, outcome prediction, and digital tools for chronic low back pain (cLBP). However, evidence remains fragmented and variable in quality, limiting its utility for clinicians and researchers. This review maps the current literature on AI in spinal disorder treatment and highlights gaps for future research.

Methods

This scoping review followed Joanna Briggs Institute (JBI) and PRISMA-ScR guidelines. Ovid MEDLINE, AMED, Embase, Cochrane CENTRAL, Web of Science, and Scopus were searched from January 2019 to December 2024. Eligible studies were English-language, peer-reviewed, involved AI applied to treatment interventions in human participants, included a comparison group, and provided sufficient methodological detail. No geographic restrictions were applied. Studies were evaluated by AI technology, treatment modality, outcomes, and quality. Methodological quality was assessed using a 19-point scoring system covering study design, reporting clarity, data validation, and feature selection.

Results

The search yielded 1,782 manuscripts; 16 met inclusion criteria. Of these, 3 originated from the United States, 8 were single-country studies, and 5 were international collaborations. Fourteen studies focused on nonoperative management of musculoskeletal pain, particularly cLBP, using chatbots, AI-driven exercise platforms, and decision-support systems. These demonstrated modest improvements in pain, disability, and quality of life, with high adherence and satisfaction. Two studies investigated operative applications, reporting favorable results. Methodological scores ranged from 8.5 to 17/19, with common limitations in data validation and feature selection.

Conclusions

Current literature demonstrates AI applications in nonoperative management of cLBP and in operative contexts such as surgical planning and outcome prediction. Most studies addressed cLBP, with limited exploration of neck pain, highlighting an area for future investigation.
人工智能(AI)越来越多地应用于医疗保健,以支持决策,个性化治疗和改善结果。在脊柱护理中,人工智能已被用于手术和非手术干预,包括手术计划、结果预测和慢性腰痛(cLBP)的数字工具。然而,证据仍然是碎片化的,质量参差不齐,限制了临床医生和研究人员的效用。本文综述了人工智能在脊柱疾病治疗中的现有文献,并指出了未来研究的空白。方法本综述遵循乔安娜布里格斯研究所(JBI)和PRISMA-ScR指南。检索了2019年1月至2024年12月的Ovid MEDLINE、AMED、Embase、Cochrane CENTRAL、Web of Science和Scopus。符合条件的研究是英语的,同行评审的,涉及人工智能应用于人类参与者的治疗干预,包括一个对照组,并提供足够的方法细节。没有地域限制。研究通过人工智能技术、治疗方式、结果和质量进行评估。方法学质量采用19分评分系统评估,包括研究设计、报告清晰度、数据验证和特征选择。结果共检索到1782篇论文;16例符合纳入标准。其中,3个来自美国,8个是单一国家的研究,5个是国际合作的。14项研究集中于肌肉骨骼疼痛的非手术治疗,特别是cLBP,使用聊天机器人、人工智能驱动的运动平台和决策支持系统。这些都显示出疼痛、残疾和生活质量的适度改善,具有很高的依从性和满意度。两项研究调查了手术应用,报告了良好的结果。方法学评分范围从8.5到17/19,在数据验证和特征选择方面存在常见局限性。目前的文献证实了人工智能在cLBP的非手术治疗以及手术计划和预后预测等手术环境中的应用。大多数研究涉及cLBP,对颈部疼痛的探索有限,强调了未来研究的领域。
{"title":"Artificial intelligence in spine care: A scoping review of treatment applications","authors":"Victoria A. Bensel DC, MS, MPH ,&nbsp;Anne Habeck MPH ,&nbsp;Marcda Hilaire Brunot DC, MPH ,&nbsp;Eleni-James Becton DC ,&nbsp;Monika Ray PhD ,&nbsp;Alexandria L. Brackett ,&nbsp;Anthony J. Lisi DC","doi":"10.1016/j.xnsj.2025.100827","DOIUrl":"10.1016/j.xnsj.2025.100827","url":null,"abstract":"<div><h3>Background</h3><div>Artificial intelligence (AI) is increasingly applied in healthcare to support decision-making, personalize treatment, and improve outcomes. In spine care, AI has been used for both operative and nonoperative interventions, including surgical planning, outcome prediction, and digital tools for chronic low back pain (cLBP). However, evidence remains fragmented and variable in quality, limiting its utility for clinicians and researchers. This review maps the current literature on AI in spinal disorder treatment and highlights gaps for future research.</div></div><div><h3>Methods</h3><div>This scoping review followed Joanna Briggs Institute (JBI) and PRISMA-ScR guidelines. Ovid MEDLINE, AMED, Embase, Cochrane CENTRAL, Web of Science, and Scopus were searched from January 2019 to December 2024. Eligible studies were English-language, peer-reviewed, involved AI applied to treatment interventions in human participants, included a comparison group, and provided sufficient methodological detail. No geographic restrictions were applied. Studies were evaluated by AI technology, treatment modality, outcomes, and quality. Methodological quality was assessed using a 19-point scoring system covering study design, reporting clarity, data validation, and feature selection.</div></div><div><h3>Results</h3><div>The search yielded 1,782 manuscripts; 16 met inclusion criteria. Of these, 3 originated from the United States, 8 were single-country studies, and 5 were international collaborations. Fourteen studies focused on nonoperative management of musculoskeletal pain, particularly cLBP, using chatbots, AI-driven exercise platforms, and decision-support systems. These demonstrated modest improvements in pain, disability, and quality of life, with high adherence and satisfaction. Two studies investigated operative applications, reporting favorable results. Methodological scores ranged from 8.5 to 17/19, with common limitations in data validation and feature selection.</div></div><div><h3>Conclusions</h3><div>Current literature demonstrates AI applications in nonoperative management of cLBP and in operative contexts such as surgical planning and outcome prediction. Most studies addressed cLBP, with limited exploration of neck pain, highlighting an area for future investigation.</div></div>","PeriodicalId":34622,"journal":{"name":"North American Spine Society Journal","volume":"25 ","pages":"Article 100827"},"PeriodicalIF":2.5,"publicationDate":"2025-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145798463","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Impact of sarcopenia and multifidus atrophy on outcomes from minimally invasive decompression surgery for lumbar spinal stenosis 肌少症和多裂肌萎缩对腰椎管狭窄微创减压手术疗效的影响
IF 2.5 Q3 Medicine Pub Date : 2025-11-17 DOI: 10.1016/j.xnsj.2025.100828
Gilad J. Regev MD , Uri Hochberg MD , Dror Ofir MD , Khalil Salame MD , Zvi Lidar MD , Morsi Khashan MD

Background

In order to improve outcomes for patients with lumbar spinal stenosis, identification of better prognostic factors is necessary to guide patient selection for surgery. The purpose of this study was to investigate the prognostic value of multifidus atrophy and sarcopenia on postoperative pain and disability following minimally invasive decompression for lumbar spinal stenosis.

Methods

We retrospectively reviewed medical records and imaging studies for patients with lumbar spinal stenosis who underwent minimally invasive tubular decompression. Multifidus total cross sectional area (tCSA), multifidus functional cross sectional area (fnCSA), multifidus fatty infiltration (FI), psoas tCSA, and psoas relative cross sectional area (rCSA) were evaluated by univariable and multivariable regression to identify predictors of postoperative improvement in visual analogue scores for back pain (VASB) and leg pain (VASL) and Oswestry disability index (ODI) scores for disability.

Results

Minimally invasive decompression was performed at 75 spinal levels in 64 patients with an average age of 70.1±10.0 years. In multivariable analysis, lower multifidus FI was significantly associated with 5 point improvement in ODI (p=.002), 10 point improvement in ODI (p=.017), and 17 point improvement in ODI (p=.044). Only male gender (p=.030), lower preoperative VASB (p=.001), and lower preoperative VASL (p=.015) were independently predictive of postoperative deterioration in ODI, VASB, and VASL, respectively.

Conclusions

Multifidus FI predicts postoperative improvement in disability following minimally invasive decompression for lumbar spinal stenosis with high accuracy. Minimally invasive decompression surgery is effective for elderly patients and sarcopenic patients, who are not at risk for poorer postoperative outcomes. Male gender and lower preoperative pain or disability are risk factors for postoperative deterioration in patient-reported outcomes.
背景:为了改善腰椎管狭窄患者的预后,有必要确定更好的预后因素来指导患者选择手术。本研究的目的是探讨多裂肌萎缩和肌少症对腰椎管狭窄微创减压术后疼痛和残疾的预后价值。方法回顾性分析腰椎管狭窄患者行微创管状减压术的医疗记录和影像学研究。通过单变量和多变量回归评估多裂肌总横截面积(tCSA)、多裂肌功能横截面积(fnCSA)、多裂肌脂肪浸润(FI)、腰肌tCSA和腰肌相对横截面积(rCSA),以确定背部疼痛(VASB)和腿部疼痛(VASL)视觉模拟评分和Oswestry残疾指数(ODI)残疾评分术后改善的预测因素。结果64例患者在75个脊柱节段行微创减压术,平均年龄70.1±10.0岁。在多变量分析中,较低的多裂肌FI与ODI改善5点(p= 0.002)、ODI改善10点(p= 0.017)和ODI改善17点(p= 0.044)显著相关。只有男性(p= 0.030)、术前VASB较低(p= 0.001)和术前VASL较低(p= 0.015)分别是ODI、VASB和VASL术后恶化的独立预测因素。结论多裂肌FI预测腰椎管狭窄症微创减压术后残疾改善的准确性高。微创减压手术对老年患者和肌肉减少症患者是有效的,他们没有术后预后较差的风险。男性和术前较低的疼痛或残疾是术后患者报告结果恶化的危险因素。
{"title":"Impact of sarcopenia and multifidus atrophy on outcomes from minimally invasive decompression surgery for lumbar spinal stenosis","authors":"Gilad J. Regev MD ,&nbsp;Uri Hochberg MD ,&nbsp;Dror Ofir MD ,&nbsp;Khalil Salame MD ,&nbsp;Zvi Lidar MD ,&nbsp;Morsi Khashan MD","doi":"10.1016/j.xnsj.2025.100828","DOIUrl":"10.1016/j.xnsj.2025.100828","url":null,"abstract":"<div><h3>Background</h3><div>In order to improve outcomes for patients with lumbar spinal stenosis, identification of better prognostic factors is necessary to guide patient selection for surgery. The purpose of this study was to investigate the prognostic value of multifidus atrophy and sarcopenia on postoperative pain and disability following minimally invasive decompression for lumbar spinal stenosis.</div></div><div><h3>Methods</h3><div>We retrospectively reviewed medical records and imaging studies for patients with lumbar spinal stenosis who underwent minimally invasive tubular decompression. Multifidus total cross sectional area (tCSA), multifidus functional cross sectional area (fnCSA), multifidus fatty infiltration (FI), psoas tCSA, and psoas relative cross sectional area (rCSA) were evaluated by univariable and multivariable regression to identify predictors of postoperative improvement in visual analogue scores for back pain (VASB) and leg pain (VASL) and Oswestry disability index (ODI) scores for disability.</div></div><div><h3>Results</h3><div>Minimally invasive decompression was performed at 75 spinal levels in 64 patients with an average age of 70.1±10.0 years. In multivariable analysis, lower multifidus FI was significantly associated with 5 point improvement in ODI (p=.002), 10 point improvement in ODI (p=.017), and 17 point improvement in ODI (p=.044). Only male gender (p=.030), lower preoperative VASB (p=.001), and lower preoperative VASL (p=.015) were independently predictive of postoperative deterioration in ODI, VASB, and VASL, respectively.</div></div><div><h3>Conclusions</h3><div>Multifidus FI predicts postoperative improvement in disability following minimally invasive decompression for lumbar spinal stenosis with high accuracy. Minimally invasive decompression surgery is effective for elderly patients and sarcopenic patients, who are not at risk for poorer postoperative outcomes. Male gender and lower preoperative pain or disability are risk factors for postoperative deterioration in patient-reported outcomes.</div></div>","PeriodicalId":34622,"journal":{"name":"North American Spine Society Journal","volume":"25 ","pages":"Article 100828"},"PeriodicalIF":2.5,"publicationDate":"2025-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145798543","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
North American Spine Society Journal
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