No major complications seen in a retrospective review of 1,018 cervical transforaminal epidural steroid injections

Gabriella H. Wozniak, Anish A. Rana, Andrew R. Stephens, Ramzi El-Hassan, Ben L. Laplante, Rajeev K. Patel
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Abstract

Background

Cervical transforaminal epidural steroid injections (CTFESI) are commonly used to treat cervical radicular pain, but concerns remain about their safety due to case reports of complications such as stroke, spinal cord injury and death. These complications have been associated with use of particulate steroids causing embolic infarcts from inadvertent intra-arterial injection. With the use of non-particulate steroids these complications have never been reported. Additionally, recent cohort studies have demonstrated safety. Yet many providers still consider these procedures to be unsafe. Additional work is needed to further elucidate the risk of complications after CTFESI.

Objective

The goal of this study is to demonstrate the safety of CTFESI in a large retrospective cohort study using non-particulate steroids.

Methods

Medical records of all consecutive patients who underwent CFTESI within a tertiary academic multidisciplinary spine center from December 2002 through September 2024 were retrospectively reviewed. Data collected included vertebral level of injection, major (stroke, seizure, spinal cord injury, and death) and minor (headache, diaphoresis, syncope) complications, ED/urgent care visits within 2 weeks of procedure, and length of follow up within the performing PM&R department.

Results

A total of 1018 CTFESI procedures involving 558 patients were reviewed. There were no major complications in our study and no patients necessitated an ED or urgent care visit. Of 1018 total procedures, 16 (1.57 %) were attempted and aborted mid-procedure. Of these, 3 procedures were aborted due to inability to access the neuroforamen, 6 procedures were aborted due to signs of vascular uptake and/or subjective symptoms of vascular uptake, 3 procedures were aborted due to patient inability to tolerate the procedure, and 4 procedures were aborted due to vasovagal response. Only 1 (0.01 %) procedure resulted in a vasovagal response (hypotension, bradycardia, dizziness) following completion of the procedure.

Conclusion

This study demonstrated no major complications after fluoroscopy guided CTFESI with use of non-particulate steroids and standard safety techniques.
回顾性分析1018例经椎间孔硬膜外类固醇注射未见重大并发症
背景颈椎经椎间孔硬膜外类固醇注射(CTFESI)通常用于治疗颈椎神经根性疼痛,但由于卒中、脊髓损伤和死亡等并发症的病例报道,人们对其安全性仍然存在担忧。这些并发症与使用颗粒类固醇引起的动脉内意外注射栓塞性梗死有关。使用非颗粒类固醇后,这些并发症从未报道过。此外,最近的队列研究已经证明了安全性。然而,许多提供者仍然认为这些程序是不安全的。需要进一步的工作来进一步阐明CTFESI后并发症的风险。本研究的目的是在一项大型回顾性队列研究中证明CTFESI使用非颗粒类固醇的安全性。方法回顾性分析2002年12月至2024年9月在某三级学术多学科脊柱中心连续接受CFTESI治疗的所有患者的病历。收集的数据包括椎体注射水平、主要(中风、癫痫、脊髓损伤和死亡)和次要(头痛、出汗、晕厥)并发症、2周内急诊科/急诊就诊情况以及在执行pm&r科的随访时间。结果共回顾了1018例CTFESI手术,涉及558例患者。在我们的研究中没有重大并发症,没有患者需要急诊科或紧急护理。在总共1018例手术中,有16例(1.57%)尝试并中途流产。其中,3例手术因无法进入神经孔而流产,6例手术因血管摄取的迹象和/或血管摄取的主观症状而流产,3例手术因患者无法耐受手术而流产,4例手术因血管迷走神经反应而流产。只有1例(0.01%)手术后出现血管迷走神经反应(低血压、心动过缓、头晕)。结论:本研究显示,在使用非颗粒类固醇和标准安全技术的情况下,透视引导CTFESI无重大并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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