Clinical and radiographic predictive factors for the favorable outcome of lumbar epidural steroid injection in lumbosacral radiculopathy: a prospective analytical study from Thailand

被引:0
作者
Chalermkitpanit, Pornpan [1 ,2 ]
Yingsakmongkol, Wicharn [2 ,3 ,4 ]
Singhatanadgige, Weerasak [2 ,3 ,4 ]
Tanasansomboon, Teerachat [5 ]
Pannangpetch, Patt [1 ,2 ]
Honsawek, Sittisak [2 ,6 ]
机构
[1] Chulalongkorn Univ, Dept Anesthesiol, Fac Med, Pain Management Res Unit, Bangkok, Thailand
[2] King Chulalongkorn Mem Hosp, Bangkok, Thailand
[3] Chulalongkorn Univ, Fac Med, Dept Orthopaed, Bangkok, Thailand
[4] Chulalongkorn Univ, Fac Med, Ctr Excellence Biomech & Innovat Spine Surg, Dept Orthopaed, Bangkok, Thailand
[5] Samut Sakhon Hosp, Dept Orthoped, Samut Sakhon, Thailand
[6] Chulalongkorn Univ, Dept Biochem, Fac Med, Ctr Excellence Osteoarthritis & Musculoskeleton, Bangkok, Thailand
关键词
Epidural analgesia; Corticosteroids; Sciatica; Radiculopathy; Spinal stenosis; DISC; EFFICACY; PAIN; INTERLAMINAR; HERNIATION;
D O I
10.31616/asj.2024.0412
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Study Design: A prospective analytic study. Purpose: To investigate the clinical factors and magnetic resonance imaging (MRI) findings that can predict a favorable outcome following transforaminal epidural steroid injection (TFESI) in patients with lumbosacral radiculopathy. Overview of Literature: The efficacy of lumbar epidural steroid injection varies, and no clinical parameters have been established to predict a favorable response to TFESI reliably. Methods: In total, 120 patients diagnosed with lumbosacral radiculopathy underwent TFESI. At each index spinal level, 5.0 mg of a dexamethasone mixture in 2.0% lidocaine and 0.5% bupivacaine was injected. At the 2-week follow-up, a favorable response to TFESI was defined as pain reduction upon movement of >50.0%. Pain manifestation and MRI findings were evaluated. Results: A favorable response was observed in 60.8% of the patients 2 weeks post-TFESI. In the multivariate analysis, patients with mild central canal stenosis had 4.8 times higher odds of a favorable response to TFESI than those with severe central canal stenosis (adjusted odds ratio, 4.8; 95% confidence interval [CI], 1.2-18.8; p=0.023). Favorable responders experienced a notable 29-week period of pain reduction (95% CI, 10.3-47.8), along with a significantly lower incidence of surgery at 12 months (13.7%) (p<0.01). The mean pain score differences of 3.5 out of 10 observed 2 weeks and 1 month post-TFESI represented the optimal sensitivity and specificity in forecasting favorable responder status. Conclusions: A pain reduction of 3.5 out of 10 within 1 month is considered a clinical benchmark for predicting long-term positive outcomes after TFESI. The presence of severe central canal stenosis is significantly associated with an unfavorable response to TFESI.
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页数:9
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