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. 2025 Mar 12:rapm-2024-105656.
doi: 10.1136/rapm-2024-105656. Online ahead of print.

Use and safety of corticosteroid injections in joints and musculoskeletal soft tissue: guidelines from the American Society of Regional Anesthesia and Pain Medicine, the American Academy of Pain Medicine, the American Society of Interventional Pain Physicians, and the International Pain and Spine Intervention Society

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Use and safety of corticosteroid injections in joints and musculoskeletal soft tissue: guidelines from the American Society of Regional Anesthesia and Pain Medicine, the American Academy of Pain Medicine, the American Society of Interventional Pain Physicians, and the International Pain and Spine Intervention Society

Honorio T Benzon et al. Reg Anesth Pain Med. .

Abstract

Background: Intra-articular corticosteroid (IACS) injection and peri-articular corticosteroid injection are commonly used to treat musculoskeletal conditions. Results vary by musculoskeletal region, but most studies report short-term benefit with mixed results on long-term relief. Publications showed adverse events from single corticosteroid injections. Recommended effective doses were lower than those currently used by clinicians.

Methods: Development of the practice guideline for joint injections was approved by the Board of Directors of the American Society of Regional Anesthesia and Pain Medicine and the participating societies. A Corticosteroid Safety Work Group coordinated the development of three guidelines: peripheral nerve blocks and trigger points; joints; and neuraxial, facet, and sacroiliac joint injections. The topics included safety of the technique in relation to landmark-guided, ultrasound-guided, or radiology-aided injections; effect of the addition of the corticosteroid on the efficacy of the injectate; and adverse events related to the injection. Experts on the topics were assigned to extensively review the literature and initially develop consensus statements and recommendations. A modified version of the US Preventive Services Task Force grading of evidence and strength of recommendation was followed. A modified Delphi process was adhered to in arriving at a consensus.

Results: This guideline focuses on the safety and efficacy of corticosteroid joint injections for managing joint chronic pain in adults. The joints that were addressed included the shoulder, elbow, hand, wrist, hip, knee, and small joints of the hands and feet. All the statements and recommendations were approved by all participants and the Board of Directors of the participating societies after four rounds of discussion. There is little evidence to guide the selection of one corticosteroid over another. Ultrasound guidance increases the accuracy of injections and reduces procedural pain. A dose of 20 mg triamcinolone is as effective as 40 mg for both shoulder IACS and subacromial subdeltoid bursa corticosteroid injections. The commonly used dose for hip IACS is 40 mg triamcinolone or methylprednisolone. Triamcinolone 40 mg is as effective as 80 mg for knee IACS. Overall, IACS injections result in short-term pain relief from a few weeks to a few months. The adverse events include an increase in blood glucose, adrenal suppression, detrimental effect on cartilage lining the joint, reduction of bone mineral density, and postoperative joint infection.

Conclusions: In this practice guideline, we provided specific recommendations on the role of corticosteroids in joint, bursa, and peritendon injections for musculoskeletal pain.

Keywords: chronic pain; outcomes; pain management.

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Conflict of interest statement

Competing interests: HTB: NIH NIAMS P30AR072579; DAP: consulting: Avanos, Boston Scientific, Medtronic, Nevro, and SI Bone; Research support: Avanos, Boston Scientific, Medtronic, Nevro; AN: speaker: Averitas Pharmaceuticals; Research: Saol Therapeutics; DS: Advisory Board, funded research: Scilex; speaker: AbbVie; MSE: funded research: SPR Therapeutics; consultant: Avanos, Abbott; MM: consultant: Juris Medicus; AA-E: consultant: Curonix; AC: research funding: NIH RM1NS128956; consultant: Swing Therapeutics, Scilex Pharmaceuticals; TLD: research support: Biohaven, NIH; consultant: Guidepoint Global; speaker honorarium: Remedy Health Media; CP: consulting: Mainstay Medical; royalties, UpToDate; SS: consultant: SPR Therapeutics, Allergan; AS: NIH R34AR080279; SPC: consulting (past 2 years): Avanos, Scilex, SPR, SWORD, Releviate (ended), Clearing (ended), Persica (inactive); research funds paid to institution: Scilex, Avanos; JAH: grants: Neiman Health Policy Institute (no number associated with this foundation grant); consulting (last 12 months): Medtronic, Relievant, Persica; DMC Chair: Balt, Rapid Medical, Arsenal; BS: consultant: State Farm, Carelon; TM: consultant, Interventional AnalgesiX; SN: consultant, Shiratonics; AW: investigator-initiated grant, Goodblends; TH: Acella: Advisory Board, speaker: Acella; CH: research grant: Nevro. The remaining authors declare no competing interests.

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