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Editorial review of the validation of thoracolumbar injury classification and severity score in the management of acute and subacute osteoporotic vertebral compression fractures 胸腰椎损伤分类和严重程度评分在急性和亚急性骨质疏松性椎体压缩骨折治疗中的验证编辑综述
Pub Date : 2024-10-15 DOI: 10.1016/j.inpm.2024.100441
Alexander R. Vaccaro
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引用次数: 0
Preoperative abdominal wall Botulinum A toxin in the outpatient pain clinic prior to complex abdominal wall repair: A letter to the editor 在门诊疼痛诊所进行复杂腹壁修复术前腹壁 A 型肉毒杆菌毒素注射:致编辑的信
Pub Date : 2024-10-04 DOI: 10.1016/j.inpm.2024.100440
Kimberly Youngren, Armando Alvarez, Mikayleigh Pearson, Sarah E. Billmeier, Marissa Mendez, Brent White
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引用次数: 0
Letter to the editor: The use of XperGuide® needle guidance software for CT guided thoracic sympathetic block 致编辑的信:在 CT 引导下使用 XperGuide® 针引导软件进行胸交感神经阻滞
Pub Date : 2024-09-20 DOI: 10.1016/j.inpm.2024.100439
Christiaan SJ. Hammerstein , Sjoerd Servaas , Erik GJ. Vermeulen , Oscar BHAM. van Haagen

With the introduction of modern cone beam computed tomography in the operating room, the benefits of imaging modalities in daily practice are recognized by an increasing number of clinicians. Newer generation imaging modalities include CT needle guidance software, which can aid the operator place the needle correctly during percutaneous intervention. This technique has several advantages over traditional percutaneous interventions, especially for high risk procedures like thoracic sympathectomy.

We describe and discuss outcomes and possible advantages of applying CT guided needle placement using needle guidance software (XperGuide®) for percutaneous thoracic sympathetic blockade in 8 patients. Based on our findings, we conclude that the use of high quality imaging and needle guidance software such as XperGuide® may improve patient outcomes, and reduce the risk of adverse effects, providing a relatively easy, safe, and valuable alternative treatment strategy for thoracic sympathectomies.

随着现代锥形束计算机断层扫描被引入手术室,越来越多的临床医生认识到成像模式在日常实践中的好处。新一代成像模式包括 CT 针引导软件,它可以帮助操作员在经皮介入治疗过程中正确放置穿刺针。与传统的经皮介入相比,这种技术有很多优势,尤其是在胸交感神经切除术等高风险手术中。我们描述并讨论了在 8 名患者中使用 CT 引导针引导软件(XperGuide®)进行经皮胸交感神经阻滞的结果和可能的优势。根据我们的研究结果,我们得出结论:使用 XperGuide® 等高质量成像和针引导软件可改善患者的治疗效果,降低不良反应的风险,为胸交感神经切除术提供了一种相对简单、安全且有价值的替代治疗策略。
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引用次数: 0
Validation of thoracolumbar injury classification and Severity Score in the management of acute and subacute Osteoporotic vertebral compression fractures – A pilot study and a suggested modification 胸腰椎损伤分类和严重程度评分在急性和亚急性骨质疏松性椎体压缩骨折治疗中的验证--一项试点研究和一项修改建议
Pub Date : 2024-09-01 DOI: 10.1016/j.inpm.2024.100438
Jatinder S. Gill , Martina Stippler , Qing Ruan , Nasir Hussain , Andrew P. White , Vwaire Oruhurhu , Obaid Malik , Thomas Simopoulos , Ivan Urits , Ryan S. D'Souza , Sanjeet Narang , Joshua A. Hirsch

Objective

To retrospectively assess the Thoracolumbar Injury Classification and Severity Score (TLICS) in patients with osteoporotic vertebral compression fractures (OVCF) and compare the treatment given with that predicted by the TLICS score.

Methods

All medical records of patients presenting from January 2014 to November 2017 for acute atraumatic or low impact OVCF were screened, and eligible patients were retrospectively reviewed. The TLICS score was determined based upon magnetic resonance imaging (MRI) findings and clinical records. Clinical records (including pain score data), imaging data, operative procedures, and stability of neurological examination were tracked over three months for each patient.

Results

Of the 56 patients included, 36 patients had a TLICS score of 1, 18 had a TLICS score of 2, and two had a TLICS score of 4. Only one patient with a TLICS score of 4 underwent surgical stabilization, while the rest of the cohort was managed non-operatively, with or without kyphoplasty. TLICS score 1 corresponded to simple compression and TLICS score 2 corresponded to burst morphology with retropulsion and without neurological deficits. Of the patients with a TLICS score of 1 and 2 who underwent kyphoplasty, there was a statistically significant improvement in pain scores in both groups; however no significant difference was observed, between each TLICS score (i.e., 1 or 2). None of the patients developed instability or neurological decline.

Conclusion

TLICS score correctly predicted operative versus non-operative management in all patients with OVCF. TLICS may be used in making management decisions, and in the triage of these patients for operative versus non-operative evaluations. Our study suggests that patients with TLICS score of 4 or higher require surgical evaluation, while those with TLICS of 1 or 2 are likely to have satisfactory non-surgical management with augmentation or conservative care. In general, patients with OVCF typically present with low TLICS score. Kyphoplasty appears to be similarly beneficial in patients with a TLICS score of 1 or a TLICS score of 2. A modification of the TLICS score by adding TLICS Zero to include uncompressed OVCF with edema is suggested. The limitations of this study include a small size; a larger study is needed to confirm these findings.

目的回顾性评估骨质疏松性椎体压缩骨折(OVCF)患者的胸腰椎损伤分类和严重程度评分(TLICS),并比较所给予的治疗与TLICS评分预测的治疗。方法筛选2014年1月至2017年11月期间因急性非创伤性或低冲击性OVCF就诊的所有患者的医疗记录,并对符合条件的患者进行回顾性审查。根据磁共振成像(MRI)结果和临床记录确定TLICS评分。结果 在纳入的 56 名患者中,36 名患者的 TLICS 评分为 1 分,18 名患者的 TLICS 评分为 2 分,2 名患者的 TLICS 评分为 4 分。只有一名 TLICS 评分为 4 分的患者接受了手术稳定治疗,其余患者均接受了非手术治疗,无论是否进行了椎体成形术。TLICS 评分 1 分的患者为单纯压迫,TLICS 评分 2 分的患者为爆裂形态伴有后推,且无神经功能障碍。在 TLICS 评分为 1 分和 2 分并接受了椎体成形术的患者中,两组患者的疼痛评分均有明显改善,但在每个 TLICS 评分(即 1 分或 2 分)之间未观察到明显差异。结论 TLICS 评分能正确预测所有 OVCF 患者的手术与非手术治疗方案。TLICS可用于管理决策,以及对这些患者进行手术与非手术评估的分流。我们的研究表明,TLICS 评分为 4 分或更高的患者需要进行手术评估,而 TLICS 评分为 1 分或 2 分的患者则有可能通过增强或保守治疗获得满意的非手术治疗效果。一般来说,OVCF 患者的 TLICS 评分通常较低。建议对 TLICS 评分进行修改,增加 TLICS Zero 分值,以纳入未受压且伴有水肿的 OVCF。这项研究的局限性包括规模较小;需要更大规模的研究来证实这些发现。
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引用次数: 0
Superior Cluneal neuralgia—An underappreciated cause of low back pain? 上楔神经痛--腰痛的一个未被重视的原因?
Pub Date : 2024-09-01 DOI: 10.1016/j.inpm.2024.100436
Einar Ottestad, Anthony Machi
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引用次数: 0
Clinical history correlates with lateral atlantoaxial (C1-2) joint edema. A pilot study 临床病史与寰枢椎(C1-2)外侧关节水肿的相关性。试点研究
Pub Date : 2024-09-01 DOI: 10.1016/j.inpm.2024.100434
Joshua Levin , Matthew Kaufman , Gerald Yeung

Background

Clinical evaluation in the determination of the etiology of axial spine pain is limited.

Objective

To determine if a set of three features of the clinical history are indicative of C1-2 joint edema on MRI.

Methods

All patients from one physician's practice who had axial cervical spine pain from 2021 to 2023 were evaluated. Cases were defined as those with all 3 of the ASL criteria, defined as Age >65, Superior cervical/suboccipital pain, and exacerbation of pain primarily by Lateral cervical spine rotation. Age-matched controls had axial cervical spine pain without meeting the ASL criteria. Edema around the atlantoaxial joint and/or odontoid was evaluated by STIR MR sequences.

Results

The ASL criteria had a sensitivity of 82 % [95 % CI: 64–100 %], specificity of 79 %, [95 % CI: 63–95 %], positive predictive value of 74 % [95 % CI: 54–94 %], and negative predictive value of 86 % [95 % CI: 72–100 %] in diagnosing C1-2 joint edema.

Conclusion

A positive ASL criteria is sensitive and specific in the diagnosis of C1-2 joint edema, which may have clinical implications.

背景临床评估在确定轴椎疼痛的病因方面存在局限性。目的确定临床病史中的三组特征是否可指示 MRI 上的 C1-2 关节水肿。方法对一名医生诊所中 2021 年至 2023 年期间出现轴椎颈椎疼痛的所有患者进行评估。病例被定义为符合 ASL 全部 3 项标准的患者,即年龄 65 岁、颈椎/枕骨下上部疼痛、主要通过颈椎外侧旋转加剧疼痛。年龄相匹配的对照组有轴颈椎疼痛,但不符合 ASL 标准。结果 ASL标准在诊断C1-2关节水肿方面的灵敏度为82% [95 % CI: 64-100%],特异度为79% [95 % CI: 63-95%],阳性预测值为74% [95 % CI: 54-94%],阴性预测值为86% [95 % CI: 72-100%]。结论 ASL 阳性标准对诊断 C1-2 关节水肿具有敏感性和特异性,可能具有临床意义。
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引用次数: 0
How soon after an epidural steroid injection can you predict the patient's response? 硬膜外类固醇注射后多久可以预测患者的反应?
Pub Date : 2024-09-01 DOI: 10.1016/j.inpm.2024.100435
Byron J. Schneider, Valentine U. Chukwuma, Blake M. Fechtel, David J. Kennedy

Background

Epidural steroid injections (ESI) are utilized for the management of radicular pain, but there are no previous published studies that detail the specific timeline of patient response to an ESI.

Purpose

To describe patients’ temporal response in pain relief following an ESI.

Study design/setting

Prospective in vivo study of consecutive patients at an outpatient physical medicine and rehabilitation clinic at a single academic spine center.

Patient sample

134 consecutive patients who received an ESI between January 2020 through June 2020.

Methods

Patients were contacted every 3 days ± 1 day for 21 days post ESI to assess pain as measured via 11-point numeric pain score and subjective percentage pain relief question.

Results

134 consecutive patients were enrolled, with 108 (80.6 %) having follow-up data through 3 weeks post ESI. At 3 weeks, 51/108 patients (47.2 %) had reported a successful response as defined by at least 50 % reduction of their pain index. Of these 51 patients, 37 (72.5 %) reported >50 % relief on day 1, a further 11 (21.6 %) first reported >50 % relief on day 4, and the remaining 3 (5.9 %) successes first reported >50 % relief on days 13, 16, and 22. 57/108 patients (52.8 %) were non-responders, most of whom never reached the 50 % threshold at any time point. Of these non-responders, 19/57 (33.3 %) did report >50 % relief on day 1. Those patient's pain relief fell below 50 % on day 4 (12/19 patients, 63.2 %), day 7 (5/19 patients, 26.3 %), day 13 (1 patient, 5.3 %), and day 16 (1 patient, 5.3 %). A positive response or negative response at each follow up point was looked at as a predictor of a concordant three-week outcome for the population. The positive likelihood ratio at follow-up day 1, day 4, day 7, and day 10, was 2.14, 6.12, 7.97, and 40 respectively. The negative likelihood ratio at follow-up day 1, day 4, day 7, and day 10 was 0.42, 0.15, 0.16, and 0.24 respectively.

Discussion/conclusion

This is the first study to meticulously follow up patients every 72 h after ESI. A patient's response on day 4, either positive or negative, is predictive of their 3-week outcome. Sustained relief at day 7 or 10 further increases the likelihood of a positive 3-week outcome.

背景硬膜外类固醇注射(ESI)是治疗根性疼痛的一种方法,但目前还没有公开发表的研究报告详细说明患者对ESI反应的具体时间表。目的描述患者在ESI后疼痛缓解的时间反应。患者样本134名在2020年1月至2020年6月期间接受ESI治疗的连续患者。方法在ESI治疗后的21天内,每3天±1天与患者联系一次,通过11点数字疼痛评分和主观疼痛缓解百分比问题来评估疼痛情况。结果134名连续患者被纳入研究,其中108名(80.6%)在ESI治疗后3周内有随访数据。3 周后,51/108 名患者(47.2%)报告了成功的反应,即疼痛指数至少降低了 50%。在这 51 名患者中,37 人(72.5%)在第 1 天报告疼痛缓解 50%,另有 11 人(21.6%)在第 4 天首次报告疼痛缓解 50%,其余 3 人(5.9%)在第 13、16 和 22 天首次报告疼痛缓解 50%。57/108(52.8%)名患者为无应答者,其中大多数在任何时间点都没有达到 50% 的阈值。在这些无应答患者中,有 19/57 人(33.3%)在第 1 天的疼痛缓解率达到了 50%。这些患者在第 4 天(12/19 名患者,63.2%)、第 7 天(5/19 名患者,26.3%)、第 13 天(1 名患者,5.3%)和第 16 天(1 名患者,5.3%)的疼痛缓解率均低于 50%。每个随访点的阳性反应或阴性反应被视为人群三周结果一致的预测因素。随访第 1 天、第 4 天、第 7 天和第 10 天的阳性似然比分别为 2.14、6.12、7.97 和 40。随访第 1 天、第 4 天、第 7 天和第 10 天的阴性似然比分别为 0.42、0.15、0.16 和 0.24。患者在第 4 天的反应,无论是阳性还是阴性,都能预测其 3 周后的结果。第 7 天或第 10 天的持续缓解进一步增加了 3 周结果为阳性的可能性。
{"title":"How soon after an epidural steroid injection can you predict the patient's response?","authors":"Byron J. Schneider,&nbsp;Valentine U. Chukwuma,&nbsp;Blake M. Fechtel,&nbsp;David J. Kennedy","doi":"10.1016/j.inpm.2024.100435","DOIUrl":"10.1016/j.inpm.2024.100435","url":null,"abstract":"<div><h3>Background</h3><p>Epidural steroid injections (ESI) are utilized for the management of radicular pain, but there are no previous published studies that detail the specific timeline of patient response to an ESI.</p></div><div><h3>Purpose</h3><p>To describe patients’ temporal response in pain relief following an ESI.</p></div><div><h3>Study design/setting</h3><p>Prospective in vivo study of consecutive patients at an outpatient physical medicine and rehabilitation clinic at a single academic spine center.</p></div><div><h3>Patient sample</h3><p>134 consecutive patients who received an ESI between January 2020 through June 2020.</p></div><div><h3>Methods</h3><p>Patients were contacted every 3 days ± 1 day for 21 days post ESI to assess pain as measured via 11-point numeric pain score and subjective percentage pain relief question.</p></div><div><h3>Results</h3><p>134 consecutive patients were enrolled, with 108 (80.6 %) having follow-up data through 3 weeks post ESI. At 3 weeks, 51/108 patients (47.2 %) had reported a successful response as defined by at least 50 % reduction of their pain index. Of these 51 patients, 37 (72.5 %) reported &gt;50 % relief on day 1, a further 11 (21.6 %) first reported &gt;50 % relief on day 4, and the remaining 3 (5.9 %) successes first reported &gt;50 % relief on days 13, 16, and 22. 57/108 patients (52.8 %) were non-responders, most of whom never reached the 50 % threshold at any time point. Of these non-responders, 19/57 (33.3 %) did report &gt;50 % relief on day 1. Those patient's pain relief fell below 50 % on day 4 (12/19 patients, 63.2 %), day 7 (5/19 patients, 26.3 %), day 13 (1 patient, 5.3 %), and day 16 (1 patient, 5.3 %). A positive response or negative response at each follow up point was looked at as a predictor of a concordant three-week outcome for the population. The positive likelihood ratio at follow-up day 1, day 4, day 7, and day 10, was 2.14, 6.12, 7.97, and 40 respectively. The negative likelihood ratio at follow-up day 1, day 4, day 7, and day 10 was 0.42, 0.15, 0.16, and 0.24 respectively.</p></div><div><h3>Discussion/conclusion</h3><p>This is the first study to meticulously follow up patients every 72 h after ESI. A patient's response on day 4, either positive or negative, is predictive of their 3-week outcome. Sustained relief at day 7 or 10 further increases the likelihood of a positive 3-week outcome.</p></div>","PeriodicalId":100727,"journal":{"name":"Interventional Pain Medicine","volume":"3 3","pages":"Article 100435"},"PeriodicalIF":0.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772594424000566/pdfft?md5=ffc2602657847a0a2edffbfd98051934&pid=1-s2.0-S2772594424000566-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142150255","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Posterior internal vertebral venous plexus, the “Black Ice” of epidural hematoma: A letter to the editor 椎体后内部静脉丛--硬膜外血肿的 "黑冰":致编辑的一封信
Pub Date : 2024-09-01 DOI: 10.1016/j.inpm.2024.100437
Christopher Amen, Zirong Zhao
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引用次数: 0
FACTFINDERS FOR PATIENT SAFETY: Minimizing risks with cervical epidural injections 患者安全实况调查:将颈椎硬膜外注射的风险降至最低
Pub Date : 2024-08-27 DOI: 10.1016/j.inpm.2024.100430
Eric K. Holder , Haewon Lee , Aditya Raghunandan , Benjamin Marshall , Adam Michalik , Minh Nguyen , Mathew Saffarian , Byron J. Schneider , Clark C. Smith , Christin A. Tiegs-Heiden , Patricia Zheng , Jaymin Patel , David Levi , International Pain and Spine Intervention Society's Patient Safety Committee
<div><p>This series of FactFinders presents a brief summary of the evidence and outlines recommendations to minimize risks associated with cervical epidural injections.</p><p>Evidence in support of the following facts is presented.</p><p><em>Minimizing Risks with Cervical Interlaminar Epidural Steroid Injections</em> – 1) CILESIs should be performed at C6-C7 or below, with C7-T1 as the preferred access point due to the more generous dorsal epidural space at this level compared to the more cephalad interlaminar segments. This reduces the risk of the minor complication of dural puncture and the major complication of spinal cord injury due to inadvertent needle placement. 2) LF gaps are most prevalent in the midline cervical spine. This can result in diminished tactile feedback with loss of resistance (LOR), increasing the risk for inadvertent dural puncture or spinal cord injury. Based on current evidence, needle placement in the paramedian portion of the interlaminar space is safest to avoid LF gaps. 3) An optimal AP trajectory view and the physician's ability to discern engagement in the LF and subsequent LOR are crucial. Confirmation of minimal needle insertion depth relative to the ventral margin of the lamina with either a lateral or contralateral oblique (CLO) safety view is critical to minimize the risk of inadvertently inserting the needle too ventral. 4) There have been closed claims and case reports of patients who have suffered catastrophic neurologic injuries while receiving CILESIs under deep sedation. If sedation is administered, the least amount necessary should be utilized to ensure the patient can provide verbal feedback during the procedure. 5) CILESIs are an elective procedure; therefore, necessity and likelihood of benefit must be foremost considerations. Current guidelines recommend holding ACAP therapy before CILESIs due to the potentially catastrophic complications associated with epidural hematoma (EH) formation. However, there is also a risk of severe systemic complications with ceasing ACAP in specific clinical scenarios. The treating physician is obligated to determine if the procedure is indicated and can ultimately decide to delay the intervention or not perform the procedure if the benefit does not outweigh the risks.</p><p><em>Minimizing Risks with Cervical Transforaminal Epidural Steroid Injections – the Role of Preprocedural Review of Advanced Imaging</em> -- Variations in vascular anatomy may warrant a modified approach to CTFESI. Preprocedural review of cross-sectional imaging can provide critical information for safe injection angle planning specific to individual patients and may help to decrease the risk of unintended vascular events with potentially catastrophic outcomes.</p><p><em>Safety of Multi-level or Bilateral Fluoroscopically-Guided Cervical Transforaminal Epidural Steroid Injections --</em> Safe performance of a CTFESI procedure requires the ability to detect inadvertent arterial injection. Contrast me
1) 颈椎层间硬膜外类固醇注射的风险最小化 - 1) 颈椎层间硬膜外类固醇注射应在 C6-C7 或以下进行,C7-T1 为首选进针点,因为该水平的背侧硬膜外腔比头侧的层间节段更宽敞。这降低了硬膜穿刺这一轻微并发症的风险,以及因进针不慎而导致脊髓损伤这一主要并发症的风险。2) LF间隙在颈椎中线最为普遍。这可能会导致阻力损失(LOR)时触觉反馈减弱,增加意外硬膜穿刺或脊髓损伤的风险。根据目前的证据,将针头放置在层间间隙的旁侧部分是最安全的,可避免 LF 间隙。3) 最佳的 AP 轨迹视图以及医生辨别 LF 和随后 LOR 啮合的能力至关重要。通过侧位或对侧斜位(CLO)安全视图确认相对于椎板腹缘的最小进针深度,对于最大限度地降低因疏忽而将针插入过腹侧的风险至关重要。4) 有已结案的索赔和病例报告显示,有患者在深度镇静的情况下接受 CILESI 时遭受了灾难性的神经损伤。如果使用镇静剂,应尽量少用,以确保患者能在手术过程中提供言语反馈。5) CILESI 是一种选择性手术;因此,必须首先考虑手术的必要性和获益的可能性。由于硬膜外血肿(EH)的形成可能带来灾难性的并发症,目前的指南建议在进行 CILESIs 之前暂停 ACAP 治疗。然而,在特定的临床情况下,停止 ACAP 也有可能导致严重的全身并发症。主治医生有责任确定手术是否适用,如果收益不能抵消风险,最终可以决定推迟干预或不实施手术。最大限度降低颈椎经硬膜外腔注射类固醇的风险--先进成像术前审查的作用 -- 血管解剖结构的变化可能会导致 CTFESI 的方法有所改变。多层次或双侧透视引导的颈椎经硬膜外类固醇注射的安全性 -- CTFESI手术的安全实施要求能够检测到意外的动脉注射。在最初的 CTFESI 中向硬膜外腔和/或沿脊神经出口注射造影剂,可能会使随后的 CTFESI 无法检测到无意中插入的髓桡动脉。虽然没有文献直接论述多层次或双侧 CTFESI 的潜在风险,但仍需谨慎。
{"title":"FACTFINDERS FOR PATIENT SAFETY: Minimizing risks with cervical epidural injections","authors":"Eric K. Holder ,&nbsp;Haewon Lee ,&nbsp;Aditya Raghunandan ,&nbsp;Benjamin Marshall ,&nbsp;Adam Michalik ,&nbsp;Minh Nguyen ,&nbsp;Mathew Saffarian ,&nbsp;Byron J. Schneider ,&nbsp;Clark C. Smith ,&nbsp;Christin A. Tiegs-Heiden ,&nbsp;Patricia Zheng ,&nbsp;Jaymin Patel ,&nbsp;David Levi ,&nbsp;International Pain and Spine Intervention Society's Patient Safety Committee","doi":"10.1016/j.inpm.2024.100430","DOIUrl":"10.1016/j.inpm.2024.100430","url":null,"abstract":"&lt;div&gt;&lt;p&gt;This series of FactFinders presents a brief summary of the evidence and outlines recommendations to minimize risks associated with cervical epidural injections.&lt;/p&gt;&lt;p&gt;Evidence in support of the following facts is presented.&lt;/p&gt;&lt;p&gt;&lt;em&gt;Minimizing Risks with Cervical Interlaminar Epidural Steroid Injections&lt;/em&gt; – 1) CILESIs should be performed at C6-C7 or below, with C7-T1 as the preferred access point due to the more generous dorsal epidural space at this level compared to the more cephalad interlaminar segments. This reduces the risk of the minor complication of dural puncture and the major complication of spinal cord injury due to inadvertent needle placement. 2) LF gaps are most prevalent in the midline cervical spine. This can result in diminished tactile feedback with loss of resistance (LOR), increasing the risk for inadvertent dural puncture or spinal cord injury. Based on current evidence, needle placement in the paramedian portion of the interlaminar space is safest to avoid LF gaps. 3) An optimal AP trajectory view and the physician's ability to discern engagement in the LF and subsequent LOR are crucial. Confirmation of minimal needle insertion depth relative to the ventral margin of the lamina with either a lateral or contralateral oblique (CLO) safety view is critical to minimize the risk of inadvertently inserting the needle too ventral. 4) There have been closed claims and case reports of patients who have suffered catastrophic neurologic injuries while receiving CILESIs under deep sedation. If sedation is administered, the least amount necessary should be utilized to ensure the patient can provide verbal feedback during the procedure. 5) CILESIs are an elective procedure; therefore, necessity and likelihood of benefit must be foremost considerations. Current guidelines recommend holding ACAP therapy before CILESIs due to the potentially catastrophic complications associated with epidural hematoma (EH) formation. However, there is also a risk of severe systemic complications with ceasing ACAP in specific clinical scenarios. The treating physician is obligated to determine if the procedure is indicated and can ultimately decide to delay the intervention or not perform the procedure if the benefit does not outweigh the risks.&lt;/p&gt;&lt;p&gt;&lt;em&gt;Minimizing Risks with Cervical Transforaminal Epidural Steroid Injections – the Role of Preprocedural Review of Advanced Imaging&lt;/em&gt; -- Variations in vascular anatomy may warrant a modified approach to CTFESI. Preprocedural review of cross-sectional imaging can provide critical information for safe injection angle planning specific to individual patients and may help to decrease the risk of unintended vascular events with potentially catastrophic outcomes.&lt;/p&gt;&lt;p&gt;&lt;em&gt;Safety of Multi-level or Bilateral Fluoroscopically-Guided Cervical Transforaminal Epidural Steroid Injections --&lt;/em&gt; Safe performance of a CTFESI procedure requires the ability to detect inadvertent arterial injection. Contrast me","PeriodicalId":100727,"journal":{"name":"Interventional Pain Medicine","volume":"3 3","pages":"Article 100430"},"PeriodicalIF":0.0,"publicationDate":"2024-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772594424000517/pdfft?md5=5f30e10e1c04a17ffd6649f739cd145f&pid=1-s2.0-S2772594424000517-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142084131","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Optimal caudal needle angulation for lumbar medial branch denervation: A 3D cadaveric and clinical imaging comparison study 腰椎内侧支神经支配的最佳尾针角度:三维尸体和临床成像对比研究
Pub Date : 2024-08-19 DOI: 10.1016/j.inpm.2024.100433
John Tran , Abdulrahman Alboog , Ujjoyinee Barua , Nicole Billias , Eldon Loh

Background

Lumbar medial branch (MB) radiofrequency ablation is a common intervention to treat facetogenic low back pain. The consensus among spine pain interventionalists is that capturing a greater length of the MB correlates with a longer duration of pain relief. Therefore, there has been interest in defining optimal needle angles to achieve parallel cannula placement. Presently, there is inconsistency regarding the optimal caudal needle angles.

Objectives

The objectives of this study were to: 1) use a dissection-based 3D modelling methodology to quantify optimal caudal needle angles from cadaveric models; and 2) compare optimal cadaver-derived caudal needle angles with real-world patient-derived needle angles.

Methods

Eighteen formalin embalmed lumbosacral spine specimens were dissected, digitized, and modelled in 3D. Virtual needles were simulated and placed parallel with the L1-L5 MBs. Cadaver-derived caudal needle angles were measured from the high-fidelity 3D models with optimally placed virtual needles. Lateral fluoroscopic images of patients (n = 200) that received lumbar MB denervation were reviewed to measure patient-derived caudal needle angles (L3-L5 MB levels). Descriptive statistics were used to analyze the cadaver (L1-L5 MB levels) and patient-derived (L3-L5 MB levels) caudal needle angles. The cadaver and patient-derived mean caudal needle angles for L3-L5 MB levels were compared.

Results

There was variability in the cadaver-derived mean caudal needle angles. The lowest mean caudal needle angle was the L1 MB level measured at 41.57 ± 8.56° (range: 27.14° - 53.96°). The highest was the L5 MB level with a mean caudal needle angle of 60.79 ± 8.55° (range: 46.97° - 79.74°). A total of 123 patients were included and 369 caudal needle angles (L3-L5 MB levels) were measured and analyzed. There was variability in the patient-derived mean caudal needle angles. The patient-derived mean caudal needle angles were 29.18 ± 8.77° (range: 11.80° - 61.31°), 33.34 ± 7.23° (range: 16.40° - 54.15°), and 49.08 ± 8.87° (range: 26.45° - 76.95°) for the L3, L4, and L5 MB levels, respectively. There was a significant difference in mean caudal needle angle between cadaver and patient-derived needle angles at the L3, L4, and L5 MB levels.

Conclusions

Analysis of cadaver-derived needle angles versus patient-derived data suggests optimization of lumbar MB denervation requires greater caudal angulation to achieve parallel needle placement. Further research is required to assess the clinical implications.

背景腰椎内侧支(MB)射频消融术是治疗面源性腰痛的常见干预方法。脊柱疼痛介入专家的共识是,捕捉到的内侧支长度越长,疼痛缓解的时间就越长。因此,人们对确定最佳针角度以实现平行套管置入很感兴趣。目前,关于尾椎针的最佳角度还不一致:1) 使用基于解剖的三维建模方法,从尸体模型中量化最佳尾椎针角度;以及 2) 将尸体得出的最佳尾椎针角度与真实世界中患者得出的针角度进行比较。方法对 18 个福尔马林防腐腰骶椎标本进行解剖、数字化和三维建模。模拟虚拟针,并将其与 L1-L5 MBs 平行放置。根据高保真三维模型和最佳放置的虚拟针测量尸体衍生的尾椎针角度。对接受腰椎 MB 神经支配的患者(n = 200)的侧向透视图像进行审查,以测量患者衍生的尾椎针角度(L3-L5 MB 水平)。描述性统计用于分析尸体(L1-L5 MB 水平)和患者衍生(L3-L5 MB 水平)尾针角度。结果尸体得出的平均尾针角度存在差异。L1 MB 水平的平均尾针角度最低,为 41.57 ± 8.56°(范围:27.14° - 53.96°)。最高的是 L5 MB 水平,平均尾针角度为 60.79 ± 8.55°(范围:46.97° - 79.74°)。共纳入 123 名患者,测量并分析了 369 个尾针角(L3-L5 MB 水平)。患者得出的平均尾针角度存在差异。患者得出的 L3、L4 和 L5 MB 水平平均尾针角度分别为 29.18 ± 8.77°(范围:11.80° - 61.31°)、33.34 ± 7.23°(范围:16.40° - 54.15°)和 49.08 ± 8.87°(范围:26.45° - 76.95°)。在 L3、L4 和 L5 MB 水平,尸体和患者得出的针角度在平均尾针角度上存在明显差异。需要进一步研究以评估其临床意义。
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引用次数: 0
期刊
Interventional Pain Medicine
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