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Comparative-effectiveness study evaluating outcomes for transforaminal epidural steroid injections performed with 3% hypertonic saline or normal saline in lumbosacral radicular pain.
Munjupong, Sithapan; Malaithong, Wanwipha; Chantrapannik, Ekasak; Ratchano, Poomin; Tontisirin, Nuj; Cohen, Steven P.
Afiliação
  • Munjupong S; Department of Anesthesiology, Phramongkutklao Hospital and Phramongkutklao College of Medicine, Bangkok, 10400, Thailand.
  • Malaithong W; Department of Anesthesiology, Phramongkutklao Hospital and Phramongkutklao College of Medicine, Bangkok, 10400, Thailand.
  • Chantrapannik E; Department of Anesthesiology, Phramongkutklao Hospital and Phramongkutklao College of Medicine, Bangkok, 10400, Thailand.
  • Ratchano P; Department of Anesthesiology, Phramongkutklao Hospital and Phramongkutklao College of Medicine, Bangkok, 10400, Thailand.
  • Tontisirin N; Department of Anaesthesiology, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, 10400, Thailand.
  • Cohen SP; Departments of Anesthesiology, Neurology, Physical Medicine & Rehabilitation, Psychiatry and Neurosurgery, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, United States.
Pain Med ; 25(7): 451-458, 2024 Jul 01.
Article em En | MEDLINE | ID: mdl-38514395
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Radiculopatia Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Pain Med Assunto da revista: NEUROLOGIA / PSICOFISIOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Tailândia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Radiculopatia Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Pain Med Assunto da revista: NEUROLOGIA / PSICOFISIOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Tailândia