Kaur Sukhdeep, Gupta Ruchi, Singh Saru, Kumar Raj, Singh Kulvinder
Department of Anesthesia, Government Multi Specialty Hospital, Chandigarh, Punjab, India.
Department of Anesthesia, Shri Guru Ram Das Institute of Medical Sciences and Research, Amritsar, Punjab, India.
Anesth Essays Res. 2017 Jul-Sep;11(3):697-701. doi: 10.4103/0259-1162.204205.
The objective of this study was to evaluate the clinical efficacy of epidural steroid injections through different approaches using pain relief and improvement in functional capacity as outcome measures.
Sixty patients with low backache and unilateral radiculopathy were randomly assigned to three groups of twenty patients each, for undergoing lumbar epidural steroid injection (LESI) through midline, transforaminal, and paramedian approaches under fluoroscopic guidance. All the patients were assessed at 1 week, 1 month and 3 months postintervention using visual analog scale (VAS) score, Quebec disability score, and depression score.
The primary and secondary outcome measured in terms of improvement of VAS showed statistically significant reduction ( < 0.05) when compared to preprocedure baseline readings on both intragroup analysis (Groups I, II and III) at 1-week, 1-month, and 3-month follow-up. However, on intergroup comparison, the difference in improvement of VAS score noted was statistically insignificant with value of 0.07 (Group I/II), 0.19 (Group II/III), 0.85 (Group I/III) at final 3 month follow-up. In addition, intergroup comparison for secondary outcome showed statistically insignificant improvement ( value for Quebec score 0.73 [Group I/II], 0.34 [Group II/III], 0.79 [Group I/III] and depression score 0.78 [Group I/II], 0.67 [Group II/III], 0.98 [Group I/III]) at final 3 month follow-up.
All three LESI approaches proved highly effective individually in terms of short-term pain relief, improvement in the quality of life, and depression; however, none proved to be better than the other.
本研究的目的是通过不同途径进行硬膜外类固醇注射,以疼痛缓解和功能能力改善作为结局指标,评估其临床疗效。
60例腰痛伴单侧神经根病患者被随机分为三组,每组20例,在透视引导下分别通过中线、经椎间孔和旁正中途径进行腰椎硬膜外类固醇注射(LESI)。所有患者在干预后1周、1个月和3个月时使用视觉模拟量表(VAS)评分、魁北克残疾评分和抑郁评分进行评估。
在组内分析(I组、II组和III组)中,在1周、1个月和3个月随访时,与术前基线读数相比,以VAS改善情况衡量的主要和次要结局均显示出统计学上的显著降低(<0.05)。然而,在组间比较中,在最终3个月随访时,VAS评分改善的差异在统计学上不显著,I/II组的P值为0.07,II/III组为0.19,I/III组为0.85。此外,次要结局的组间比较显示,在最终3个月随访时,改善在统计学上不显著(魁北克评分的P值:I/II组为0.73,II/III组为0.34,I/III组为0.79;抑郁评分的P值:I/II组为0.78,II/III组为0.67,I/III组为0.98)。
就短期疼痛缓解、生活质量改善和抑郁而言,所有三种LESI途径各自都被证明非常有效;然而,没有一种途径被证明比其他途径更好。