AI Article Synopsis

  • The study aimed to evaluate how effective intradiscal corticosteroid injections (IDCI) are for treating low back pain linked to disc issues.
  • It involved adults with chronic pain, using either real injections or placebo treatments for comparison, assessing outcomes like pain reduction and disability.
  • The review found that IDCI can reduce pain for 1-6 months in certain patients (with Modic 1 and 2 changes), but overall, the evidence quality is low.

Article Abstract

Objective: Determine the effectiveness of intradiscal corticosteroid injection (IDCI) for the treatment of discovertebral low back pain.

Design: Systematic review.

Population: 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.

Intervention: Fluoroscopically guided or computed tomography-guided IDCI.

Comparison: Sham/placebo procedure including intradiscal saline, anesthetic, discography alone, or other active treatment.

Outcomes: 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.

Methods: 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).

Results: 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.

Conclusion: 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.

Study Registration: PROSPERO (CRD42021287421).

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11494378PMC
http://dx.doi.org/10.1093/pm/pnad127DOI Listing

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