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Published online before print September 28, 2005, 10.1148/radiol.2372041406
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(Radiology 2005;237:738-741.)
© RSNA, 2005


Vascular and Interventional Radiology

Lumbar Radiculopathy: Treatment with Selective Lumbar Nerve Blocks—Comparison of Effectiveness of Triamcinolone and Betamethasone Injectable Suspensions1

Donna G. Blankenbaker, MD, Arthur A. De Smet, MD, Jeffrey D. Stanczak, MD and Jason P. Fine, ScD

1 From the Department of Radiology, Division of Musculoskeletal Imaging, University of Wisconsin Medical School, Clinical Science Center-E3/311, 600 Highland Ave, Madison, WI 53792-3252 (D.G.B., A.A.D.S.); Charlottesville Radiology Ltd, Charlottesville, Va (J.D.S.); and Departments of Statistics and Biostatistics and Informatics, University of Wisconsin, Madison, Wis (J.P.F.). Received August 11, 2004; revision requested October 27; revision received November 22; accepted December 27. Address correspondence to D.G.B. (e-mail: dg.blankenbaker{at}hosp.wisc.edu).

PURPOSE: To retrospectively determine if there is a difference in the effectiveness of triamcinolone acetonide injectable suspension versus betamethasone sodium phosphate and betamethasone acetate injectable suspension in the treatment of radiculopathy and low back pain with selective lumbar nerve blocks.

MATERIALS AND METHODS: This retrospective study was approved by the institutional review board and was HIPAA compliant; informed consent was not required. Charts and self-reported pain score evaluations were retrospectively reviewed in 114 patients (56 men, 58 women; age range, 36–84 years; mean age, 60 years) treated for radiculopathy from 1997 to 2003 with 130 selective lumbar nerve blocks with triamcinolone or betamethasone. Perineural location was confirmed with fluoroscopic guidance. Forty-nine patients received a mixture of 1 mL of the triamcinolone, 40 mg/mL, and 1 mL of 0.5% bupivacaine hydrochloride. Eighty-one patients received a mixture of 1 mL of the betamethasone, 6 mg/mL, and 1 mL of 0.5% bupivacaine hydrochloride. Patients completed standardized pain evaluation sheets and compared their pain with baseline levels during 14 days after injection. Fisher exact test was used for data analysis.

RESULTS: From day 0 to 1 after the procedure, there was no statistically significant difference in improvement in low back pain and lower extremity pain between groups. On day 3, 42% of triamcinolone recipients and 58% of betamethasone recipients demonstrated improvement in low back pain (P = .04, Fisher exact test), whereas 55% of triamcinolone recipients and 57% of betamethasone recipients had lower extremity pain improvement (P = .33). On day 7, 45% of triamcinolone recipients and 58% of betamethasone recipients had improvement in low back pain (P = .38), whereas 52% of triamcinolone recipients and 57% of betamethasone recipients had improvement in lower extremity pain (P = .69). On day 14, 42% of triamcinolone recipients and 53% of betamethasone recipients had improvement in low back pain (P = .26), whereas 49% of triamcinolone recipients and 55% of betamethasone recipients had improvement in lower extremity pain (P = .69).

CONCLUSION: Selective nerve root blocks with betamethasone and triamcinolone reduced low back pain and lower extremity pain, although there was no significant difference in effectiveness between the two.

© RSNA, 2005




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