Effectiveness of epidural amniotic fluid injection for low back pain

Glenn R. Buttermann , Matthew Thorson , Louis C. Saeger
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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.
硬膜外羊水注射治疗腰痛的疗效
长期以来,硬膜外皮质类固醇注射一直用于治疗与腰背部疾病相关的疼痛和炎症,包括腰椎间盘突出症、HNP;椎管狭窄症;以及椎间盘退行性疾病(DDD)羊水,AF,富含蛋白质和因子,被认为有助于减少炎症愈合。在非脊柱疾病中注射AF已被证明是安全的,并且避免了与类固醇相关的不良反应。目的探讨单次腰硬膜外腔注入羊水治疗腰痛的安全性和有效性。具体来说,这项试点研究是为了确定未来大规模比较研究的适应症。方法:本研究通过了IRB批准的前瞻性临床研究,包括3个队列,每个队列包括20例HNP、SS和DDD患者,随访1年。入选的患者均有腰痛±腿部症状,且持续2个月,临床和MRI表现为HNP、SS或DDD。纳入标准必须是研究患者对药物、物理治疗和/或脊椎指压疗法无反应。在获得同意后,每个诊断组(HNP, SS和DDD) 20例患者在主要症状水平通过透视注射2cc经椎间孔硬膜外房颤。在2-3周、6-8周、3-4个月、6-8个月和1年的随访期间测量术前和术后结果。结果测量是背部和腿部疼痛的视觉模拟量表(VAS)、Oswestry残疾量表(ODI)、患者报告的结果测量信息系统(PROMIS)评分和止痛药使用情况。使用VAS和ODI测量,得出最小临床重要差异(MCID)和成功率(50%改善)。结果HNP、狭窄和DDD患者的平均年龄分别为46岁、60岁和46岁。没有并发症或其他不良反应。HNP患者的症状减轻最大,平均LBP VAS改善从6.3到2.9,腿部VAS从5.9到2.2,ODI从37到19,PROMIS物理成分从13.1到14.7。SS患者的LBP VAS从6.8改善到5.3,腿部VAS从5.8改善到3.1,ODI从46改善到33,PROMIS Physical component从10.9改善到13.0。DDD患者的LBP VAS评分为7.0 ~ 4.8,腿部VAS评分为3.9 ~ 2.7,ODI评分为41 ~ 37,PROMIS Physical component评分为12.0 ~ 13.1。HNP患者的止痛药使用显著减少。在一年的随访中,HNP组达到MCID的比率最高(65% - 79%),成功率最高(47% - 60%)。SS治疗腿痛的成功率相似。与其他两组相比,HNP组的ODI、MCDI和成功率明显更高。总体而言,15%的患者接受了额外的注射,20%的患者接受了手术。结论AF硬膜外注射对腰椎HNP最有效,对SS效果中等,对DDD效果不一致。对于HNP和狭窄患者,特别是已知对类固醇有不良反应的患者,房颤与类固醇注射的前瞻性研究是有必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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