The effectiveness of fluoroscopically guided lumbar facet steroid joint injections: A systematic review

Alexandra E. Fogarty , Jordan A. Buttner , Belinda Duszynski , Michael J. McKenna , David C. Miller , Alan Gonzalez-Cota , Arsenio Avila , Eduard Vaynberg , Samir Sheth , Aaron Conger , Lisa V. Doan , Reza Ehsanian
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Abstract

Summary of background data

Facet joint degeneration is a known source of chronic axial low back pain, and intra-articular steroid injections (IASI) have been used as a treatment.

Objectives

To systematically review the evidence of the effectiveness of fluoroscopically guided lumbar IASI for the treatment of lumbar facet joint pain.

Methods

The primary outcome was ≥50 % pain reduction at ≥ 1 month, measured by Visual Analog Scale and/or Numeric Rating Scale. Secondary outcomes included ≥30 % functional improvement on a validated functional scale. Studies including group mean improvements in pain/function without categorical reporting were also considered. Two reviewers independently screened Embase, Cochrane, PubMed Medline, Ovid Medline, Web of Knowledge, and Google Scholar. The risk of bias was assessed using the Cochrane Risk of Bias Tool, and evidence quality was evaluated using Grades of Recommendation, Assessment, Development, and Evaluation (GRADE).

Results

Of the 701 publications screened, 21 met the inclusion criteria. Success rates for clinically significant pain reduction (≥50 % pain relief) ranged from 13 to 74 %, and functional improvement (≥30 % improvement) was 29 % at ≥ 1 month, based on only one study. Overall, mean improvement ranged from 11 to 59 % for pain relief and 8–58 % for function at ≥ 1 month. In the seven studies selecting patients with facet or medial branch blocks, success rates for clinically significant pain reduction (≥50 % pain relief) are reported as 13–74 % at ≥ 1 month. In this subgroup, mean pain improvement rates ranged from 23 to 67 % and functional improvement from 15 to 58 % at ≥ 1 month. According to GRADE, the overall quality of the evidence is very low due to the high risk of bias, study heterogeneity, and inconsistent methodologies.

Discussion/conclusion

Pragmatic and observational studies suggest IASI may reduce pain and disability, while sham-controlled trials have not demonstrated efficacy. Given the very low quality of evidence, the true effect of IASI is highly uncertain. Further high-quality, placebo-controlled studies using standardized diagnostic criteria are needed.
透视引导下腰椎关节突类固醇关节注射的有效性:一项系统综述
背景资料概述:髋突关节退变是慢性轴性腰痛的已知来源,关节内类固醇注射(IASI)已被用作治疗方法。目的系统回顾透视引导下腰椎IASI治疗腰椎小关节痛的有效性证据。方法主要终点为≥1个月疼痛减轻≥50%,通过视觉模拟量表和/或数值评定量表测量。次要结果包括经验证的功能量表上≥30%的功能改善。包括疼痛/功能无分类报告的组平均改善的研究也被考虑。两位审稿人独立筛选了Embase、Cochrane、PubMed Medline、Ovid Medline、Web of Knowledge和谷歌Scholar。使用Cochrane偏倚风险工具评估偏倚风险,使用推荐、评估、发展和评价等级(GRADE)评估证据质量。结果701篇文献中,21篇符合纳入标准。仅基于一项研究,临床显著疼痛减轻(≥50%疼痛缓解)的成功率为13%至74%,≥1个月的功能改善(≥30%改善)为29%。总体而言,≥1个月时,疼痛缓解的平均改善幅度为11%至59%,功能改善的平均改善幅度为8 - 58%。在7项选择关节突或内侧分支阻滞患者的研究中,在≥1个月时,临床显着疼痛减轻(≥50%疼痛缓解)的成功率为13 - 74%。在该亚组中,≥1个月的平均疼痛改善率为23%至67%,功能改善率为15%至58%。根据GRADE,由于高偏倚风险、研究异质性和方法不一致,证据的总体质量非常低。讨论/结论实用和观察性研究表明IASI可以减轻疼痛和残疾,而假对照试验尚未证明其有效性。鉴于证据质量非常低,IASI的真正效果是高度不确定的。需要进一步采用标准化诊断标准的高质量安慰剂对照研究。
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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