Yang Ge, Liu Jinfeng, Ma Liangjuan, Cai Zhenhua, Meng Chao, Qi Sihua, Zhou Huacheng
*Department of Anesthesiology, The Fourth Affiliated Hospital, Harbin Medical University Departments of †Anesthesiology §Dermatology, The Second Affiliated Hospital, Harbin Medical University, Harbin, China ‡The Hei Long Jiang Province Key Lab of Research on Anesthesiology and Critical Care Medicine, Harbin, China.
Clin J Pain. 2016 Feb;32(2):103-8. doi: 10.1097/AJP.0000000000000237.
Recently, most lumbar spine injections have been administered under ultrasound (US) guidance; however, there is no standard method for US-guided lumbar transforaminal epidural injection (TFEI). In this study, we evaluated the accuracy, effect on pain relief, and safety of US-guided lumbar TFEI.
A total of 80 patients with low back pain and radicular pain were enrolled. The patients were randomly assigned to either the fluoroscopy (FL) group or the US group. The FL-guided approaches were performed under standardized procedures using the C-arm, whereas the US-guided injections were performed with an US device with a linear probe, and were verified by FL. The needle tip reached the lateral side of the lamina in the axis view and the middle of the adjacent facet joints in the parasagittal view. Afterward, the needle was advanced slightly deeper until the loss-of-resistance test was positive.
The success ratio of the US-guided interventions was 85%. The operation time in the US group (518±103 s) was shorter than the FL group (929±228 s) (P<0.05). In addition, the radiation dosage in the US group (2640±906 μGy m²) was lower than in the FL group (8992±2132 μGy m²). There was no significant difference in pain relief between the US and FL groups. No serious complication was observed in any of the patients in either group.
Lumbar TFEI under US guidance was feasible, safe, and required less radiation to achieve the same benefit as the FL-guided interventions.
最近,大多数腰椎注射是在超声(US)引导下进行的;然而,超声引导下腰椎经椎间孔硬膜外注射(TFEI)尚无标准方法。在本研究中,我们评估了超声引导下腰椎TFEI的准确性、疼痛缓解效果及安全性。
共纳入80例腰痛伴根性痛患者。患者被随机分为荧光透视(FL)组或超声组。FL引导的方法按照标准化程序使用C形臂进行,而超声引导的注射使用带有线性探头的超声设备进行,并通过FL进行验证。针尖在轴位视图中到达椎板外侧,在矢状旁视图中到达相邻小关节中部。之后,将针稍向深处推进,直到阻力消失试验呈阳性。
超声引导干预的成功率为85%。超声组的手术时间(518±103秒)短于FL组(929±228秒)(P<0.05)。此外,超声组的辐射剂量(2640±906μGy m²)低于FL组(8992±2132μGy m²)。超声组和FL组在疼痛缓解方面无显著差异。两组患者均未观察到严重并发症。
超声引导下的腰椎TFEI是可行、安全的,且与FL引导的干预相比,在获得相同益处的情况下所需辐射更少。