Noninferiority of ultrasound-guided lumbar disc block versus fluoroscopy-controlled lumbar discography for diagnosis of discogenic low back pain.

IF 1.7 Q2 ANESTHESIOLOGY
Wenxing Zhao, Liangliang He, Zhi Dou, Hongyan Wang, Liqiang Yang
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Abstract

Introduction: Evaluation of ultrasound (US)-guided disc block used to diagnose discogenic pain, as described in case reports. The study aimed to ascertain the noninferiority of US-guided lumbar disc block to conventional discography in the diagnosis of discogenic low back pain (DLBP).

Material and methods: The reports of 418 patients undergoing lumbar fusion for DLBP were stratified into a US group receiving US-guided lumbar disc block and a control group receiving fluoroscopy (FL)-assistant discography via a propensity-score matched method in a 1 : 1 ratio. The primary endpoint was the confirmatory rate defined as the rate of clinical success following surgery measured by a numerical pain rating scale score ≤ 2 and an Oswestry Disability Index score ≤ 15 at the 1-month follow-up point. Secondary outcomes included needle insertions until contrast given, procedure time, radiation dosages and adverse events.

Results: The confirmatory rates for disc block and discography were 71.8% and 73.2% (difference = -1.3%, 95% confidence interval [CI]: -9.9%, 7.2%, P = 0.353). The lower bound of 95% CI did not cross the noninferiority margin of 10%. There were fewer needle insertions (median 2, IQR: 1-3 vs. 5, IQR: 4-6, P < 0.001), shorter procedure times (8.94 ± 2.28 vs. 16.13 ± 3.39 min, P < 0.001) and lower radiation dosage (1689.56 ± 898.54 vs. 8293.50 ± 1039.09 μGy m2 , P < 0.001) in the US group than the control group. No serious adverse events were observed.

Conclusions: US-guided lumbar disc block was not inferior to conventional discography as a diagnostic modality in the evaluation of DLBP being considered for surgery. Given that the sonographic method provided advantages in terms of facilitation of needle insertion, reduced procedure time, and attenuated radiation exposure, it might be an alternative option for surgery decision making.

超声引导下的腰椎间盘阻断与透视控制下的腰椎间盘造影术诊断椎间盘源性腰痛的非劣效性。
简介:评估超声(US)引导椎间盘阻滞用于诊断椎间盘源性疼痛,如病例报告所述。该研究旨在确定us引导下的腰椎间盘阻滞在诊断椎间盘源性腰痛(DLBP)方面优于传统的椎间盘造影术。材料和方法:报告418例DLBP腰椎融合术患者,采用倾向-评分匹配方法,按1:1比例将其分层为接受US引导腰椎间盘阻滞的US组和接受透视(FL)辅助椎间盘造影术的对照组。主要终点是确定率,定义为手术后临床成功率,在1个月的随访点通过数值疼痛评定量表评分≤2和Oswestry残疾指数评分≤15来衡量。次要结局包括注射针到造影剂,手术时间,辐射剂量和不良事件。结果:椎间盘阻滞和椎间盘造影术的确诊率分别为71.8%和73.2%(差异= -1.3%,95%可信区间[CI]: -9.9%, 7.2%, P = 0.353)。95% CI的下限没有超过10%的非劣效性界限。与对照组相比,美国组针头插入次数较少(中位数2次,IQR: 1-3比5,IQR: 4-6, P < 0.001),手术时间较短(8.94±2.28比16.13±3.39 min, P < 0.001),放射剂量较低(1689.56±898.54比8293.50±1039.09 μGy m2, P < 0.001)。未观察到严重不良事件。结论:在考虑进行手术的DLBP评估中,us引导的腰椎间盘阻滞作为一种诊断方式并不亚于传统的椎间盘造影术。鉴于超声方法在针入方便、缩短手术时间和减少辐射暴露方面具有优势,它可能是手术决策的另一种选择。
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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来源期刊
CiteScore
3.00
自引率
5.90%
发文量
48
审稿时长
25 weeks
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