Comparative-effectiveness study evaluating outcomes for transforaminal epidural steroid injections performed with 3% hypertonic saline or normal saline in lumbosacral radicular pain

Author:

Munjupong Sithapan1ORCID,Malaithong Wanwipha1,Chantrapannik Ekasak1,Ratchano Poomin1,Tontisirin Nuj2,Cohen Steven P345

Affiliation:

1. Department of Anesthesiology, Phramongkutklao Hospital and Phramongkutklao College of Medicine , Bangkok, 10400, Thailand

2. Department of Anaesthesiology, Faculty of Medicine, Ramathibodi Hospital, Mahidol University , Bangkok, 10400, Thailand

3. Northwestern University Feinberg School of Medicine Departments of Anesthesiology, Neurology, Physical Medicine & Rehabilitation, Psychiatry and Neurosurgery, , Chicago, IL 60611, United States

4. Johns Hopkins School of Medicine Departments of Anesthesiology, Neurology, Physical Medicine & Rehabilitation and Psychiatry and Behavioral Sciences, , Baltimore, MD, United States

5. Walter Reed National Military Medical Center Departments of Physical Medicine & Rehabilitation and Anesthesiology, , Uniformed Services University of the Health Sciences, Bethesda, MD 20889, United States

Abstract

Abstract Background Transforaminal epidural steroid injections (TFESI) are commonly employed to treat lumbosacral radiculopathy. Despite anti-inflammatory properties, the addition of 3% hypertonic saline has not been studied. Objective Compare the effectiveness of adding 0.9% NaCl (N-group) vs. 3% NaCl (H-group) in TFESI performed for lumbosacral radiculopathy. Methods This retrospective study compared TFESI performed with lidocaine, triamcinolone and 0.9% NaCl vs. lidocaine, triamcinolone and 3% NaCl. The primary outcome was the proportion of patients who experienced a ≥ 30% reduction in pain on a verbal rating scale (VRS; 0–100) at 3 months. Secondary outcome measures included the proportion of patients who improved by at least 30% for pain at 1 and 6 months, and who experienced ≥15% from baseline on the Oswestry disability index (ODI) at follow-up. Results The H-group experienced more successful pain outcomes than the N-group at 3 months (59.09% vs. 41.51%; P = .002) but not at 1 month (67.53% vs. 64.78%; P = .61) or 6 months (27.13% vs 21.55%: P = .31). For functional outcome, there was a higher proportion of responders in the H-group than the N-group at 3 months (70.31% vs. 53.46%; P = .002). Female, age ≤ 60 years, and duration of pain ≤ 6 months were associated with superior outcomes at the 3-month endpoint. Although those with a herniated disc experienced better outcomes in general with TFESI, the only difference favoring the H-group was for spondylolisthesis patients. Conclusions 3% hypertonic saline is a viable alternative to normal saline as an adjunct for TFESI, with randomized studies needed to compare its effectiveness to steroids as a possible alternative. Registration Thai Clinical Trials Registry ID TCTR 20231110006

Funder

Uniformed Services University

Publisher

Oxford University Press (OUP)

Reference38 articles.

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