Department of Physical Medicine and Rehabilitation, University of Utah, Salt Lake City, UT 84108, United States.
Eccles Health Sciences Library, University of Utah, Salt Lake City, UT 84112, United States.
Pain Med. 2024 Jan 4;25(1):33-46. doi: 10.1093/pm/pnad127.
Determine the effectiveness of intradiscal corticosteroid injection (IDCI) for the treatment of discovertebral low back pain.
Systematic review.
Adults with chronic low back pain attributed to disc or vertebral end plate pain, as evidenced by positive provocation discography or Modic 1 or 2 changes on magnetic resonance imaging.
Fluoroscopically guided or computed tomography-guided IDCI.
Sham/placebo procedure including intradiscal saline, anesthetic, discography alone, or other active treatment.
Reduction in chronic low back pain reported on a visual analog scale or numeric rating scale and reduction in disability reported by a validated scale such as the Oswestry Disability Index.
Four reviewers independently assessed articles published before January 31, 2023, in Medline, Embase, CENTRAL, and CINAHL. The quality of evidence was evaluated with the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) framework. The risk of bias in randomized trials was evaluated with the Cochrane Risk of Bias tool (version 2).
Of the 7806 unique records screened, 6 randomized controlled trials featuring 603 total participants ultimately met the inclusion criteria. In multiple randomized controlled trials, IDCI was found to reduce pain and disability for 1-6 months in those with Modic 1 and 2 changes but not in those selected by provocation discography.
According to GRADE, there is low-quality evidence that IDCI reduces pain and disability for up to 6 months in individuals with chronic discovertebral low back pain as evidenced by Modic 1 and 2 changes but not in individuals selected by provocation discography.
PROSPERO (CRD42021287421).
评估椎间盘内皮质类固醇注射(IDCI)治疗椎间盘源性下腰痛的疗效。
系统评价。
患有慢性下腰痛的成年人,其腰痛归因于椎间盘或椎体终板疼痛,证据为阳性诱发性椎间盘造影或磁共振成像上的 Modic 1 或 2 改变。
荧光透视或计算机断层扫描引导下 IDCI。
假/安慰剂程序,包括椎间盘内盐水、麻醉、单独椎间盘造影或其他活性治疗。
视觉模拟评分或数字评分量表报告的慢性下腰痛减轻,以及 Oswestry 残疾指数等经过验证的量表报告的残疾减轻。
四位审查员独立评估了 2023 年 1 月 31 日前在 Medline、Embase、CENTRAL 和 CINAHL 上发表的文章。使用 Grading of Recommendations Assessment, Development, and Evaluation(GRADE)框架评估证据质量。使用 Cochrane 偏倚风险工具(版本 2)评估随机试验的偏倚风险。
在筛选的 7806 条独特记录中,最终有 6 项随机对照试验(共 603 名参与者)符合纳入标准。在多项随机对照试验中,IDCI 被发现可在 1-6 个月内减轻 Modic 1 和 2 改变患者的疼痛和残疾,但在诱发性椎间盘造影选择的患者中无效。
根据 GRADE,有低质量证据表明,IDCI 可在 6 个月内减轻慢性椎间盘源性下腰痛患者的疼痛和残疾,这些患者的证据为 Modic 1 和 2 改变,但在通过诱发性椎间盘造影选择的患者中无效。
PROSPERO(CRD42021287421)。