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硬膜外注射羊水治疗腰痛的有效性。

Effectiveness of epidural amniotic fluid injection for low back pain.

作者信息

Buttermann Glenn R, Thorson Matthew, Saeger Louis C

机构信息

Midwest Spine & Brain Institute, Stillwater, MN, USA.

Interventional Pain Specialists of Wisconsin, Rice Lake, WI, USA.

出版信息

Interv Pain Med. 2025 May 30;4(2):100598. doi: 10.1016/j.inpm.2025.100598. eCollection 2025 Jun.

DOI:10.1016/j.inpm.2025.100598
PMID:40519791
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12166700/
Abstract

BACKGROUND

Epidural corticosteroid injections have long been used to treat pain and inflammation associated with low back conditions including symptoms due to lumbar herniated disc, HNP; spinal stenosis, SS; and degenerative disc disease, DDD. Amniotic fluid, AF, is rich in the proteins and factors that are believed to contribute to healing by minimizing inflammation. AF injections in non-spinal conditions have been shown to be safe and avoid adverse effects related to steroids.

OBJECTIVES

To investigate the safety and efficacy of a single amniotic fluid injection into the lumbar epidural space for the treatment of low back pain. Specifically, this pilot study was to define indications for future large scale comparative studies.

METHODS

This IRB approved prospective clinical study of 3 cohorts included 20 patients each with HNP, SS, and DDD with a 1-year follow-up. Patients were enrolled who had LBP ± leg symptoms for >2 months, with clinical and MRI findings for HNP, SS, or DDD. Inclusion criteria necessitated that study patients had not responded to medications, physical therapy, and/or chiropractic. After obtaining consent, 20 patients in each diagnostic group (HNP, SS, and DDD) had 2 cc's transforaminal epidural AF injected at the primary symptomatic level using fluoroscopy. Pre- and post-procedure outcomes measurements were obtained at follow-up periods of 2-3 weeks, 6-8 weeks, 3-4 months, 6-8 months and 1 year. Outcome measures were Visual Analog Scale (VAS) for back and leg pain, Oswestry Disability Scale (ODI), Patient-Reported Outcomes Measurement Information System (PROMIS) scores, and pain medication usage. Using the VAS and ODI measurements, Minimal Clinical Important Difference (MCID) and Success (50 % improvement) rates were derived.

RESULTS

The average age (years) of HNP, stenosis, and DDD patients was 46, 60, and 46 respectively. There were no complications or other adverse effects. HNP patients had the greatest reduction in symptoms with average LBP VAS improvement from 6.3 to 2.9, leg VAS from 5.9 to 2.2, ODI from 37 to 19, and PROMIS Physical component 13.1 to 14.7. SS patients had LBP VAS improvement from 6.8 to 5.3, leg VAS from 5.8 to 3.1, ODI from 46 to 33 and PROMIS Physical component 10.9 to 13.0. DDD patients had LBP VAS from 7.0 to 4.8, leg VAS from 3.9 to 2.7, ODI from 41 to 37 and PROMIS Physical component 12.0 to 13.1. HNP patients had a significant reduction in pain medication use. Over the one year follow-up, the HNP group had the greatest rate of attaining MCID (65 %-79 %) and Success (47 %-60 %). SS had a similar rate of Success for leg pain. ODI MCDI and Success rates were significantly greater for HNP vs the other 2 groups. Overall, 15 % of patients had additional injections and 20 % went on to surgery.

CONCLUSIONS

AF epidural injections are most effective for patients with lumbar HNP and moderately effective for those with SS. AF injections for DDD patients gave inconsistent results. Future prospective studies of AF vs steroid injections are warranted for HNP and stenosis patients, particularly in patients with known adverse reactions to steroids.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5ab/12166700/0e29c1b0ef5f/gr12.jpg
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摘要

背景

硬膜外皮质类固醇注射长期以来一直用于治疗与下背部疾病相关的疼痛和炎症,包括腰椎间盘突出症(HNP)、腰椎管狭窄症(SS)和椎间盘退变疾病(DDD)引起的症状。羊水(AF)富含蛋白质和因子,据信这些物质通过减轻炎症有助于愈合。在非脊柱疾病中,羊水注射已被证明是安全的,且可避免与类固醇相关的不良反应。

目的

研究单次腰椎硬膜外腔注射羊水治疗腰痛的安全性和有效性。具体而言,这项初步研究旨在为未来的大规模对比研究确定适应症。

方法

这项经机构审查委员会批准的前瞻性临床研究共纳入3组队列,每组20例HNP、SS和DDD患者,并进行为期1年的随访。纳入的患者有持续超过2个月的腰痛及/或腿部症状,且有HNP、SS或DDD的临床及磁共振成像(MRI)表现。纳入标准要求研究患者对药物、物理治疗和/或整脊治疗无反应。获得患者同意后,在透视引导下,为每个诊断组(HNP、SS和DDD)的20例患者在主要症状水平经椎间孔硬膜外注射2毫升羊水。在2 - 3周、6 - 8周、3 - 4个月、6 - 8个月和1年的随访期进行术前和术后结果测量。结果测量指标包括背部和腿部疼痛的视觉模拟评分(VAS)、Oswestry功能障碍指数(ODI)、患者报告结局测量信息系统(PROMIS)评分以及止痛药物使用情况。利用VAS和ODI测量结果,得出最小临床重要差异(MCID)和成功率(改善50%)。

结果

HNP、腰椎管狭窄症和DDD患者的平均年龄(岁)分别为46、60和46。未出现并发症或其他不良反应。HNP患者症状改善最为显著,平均腰痛VAS从6.3降至2.9,腿痛VAS从5.9降至2.2,ODI从37降至19,PROMIS身体成分评分从13.1升至14.7。SS患者腰痛VAS从6.8降至5.3,腿痛VAS从5.8降至3.1,ODI从46降至33,PROMIS身体成分评分从10.9升至13.0。DDD患者腰痛VAS从7.0降至4.8,腿痛VAS从3.9降至2.7,ODI从41降至37,PROMIS身体成分评分从12.0升至13.1。HNP患者的止痛药物使用显著减少。在一年的随访中,HNP组达到MCID(65% - 79%)和成功率(47% - 60%)的比例最高。SS患者腿痛的成功率与之相似。与其他两组相比,HNP组的ODI最小临床重要差异和成功率显著更高。总体而言,15%的患者接受了额外注射,20%的患者接受了手术。

结论

羊水硬膜外注射对腰椎HNP患者最有效,对SS患者中度有效。对DDD患者进行羊水注射的结果不一致。对于HNP和腰椎管狭窄症患者,尤其是对类固醇有已知不良反应的患者,有必要开展未来羊水与类固醇注射对比的前瞻性研究。

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