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Epidural Needle Extension through the Ligamentum Flavum Using the Standard versus the CompuFlo®-Assisted Loss of Resistance to Saline Technique: A Simulation Study

机译:通过Ligamentum Flavum使用标准对韧带耐受耐盐性耐药性的硬膜外针延伸:仿真研究

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摘要

Background. The CompuFlo® epidural system has been recently introduced and validated as an objective and sensible tool to detect the epidural space. We aimed to verify whether the high sensitivity of the instrument may help the anesthesiologist to identify the epidural space very early, limiting the extension of the Tuohy needle into the epidural space. Methods. In this prospective, simulation study, we evaluated the Tuohy needle extension through a simulated ligamentum flavum during the epidural procedure performed by 52 expert anesthesiologists by using the CompuFlo® epidural instrument or their standard loss of resistance to saline technique (LORT). Results. The mean (SD) needle extension length was 3.90 (3.71) mm in the standard technique group and 0.68 (0.46) mm in the CompuFlo® group (P<000001). The extremely reduced variability of the data in the CompuFlo® group (F test 0.01) made the results obtained with this instrument highly predictable. Conclusions. Puncturing high-resistance material that simulated the ligamentum flavum, the use of CompuFlo® has determined the arrest of the needle more precociously when compared with the traditional LORT.
机译:背景。该CompuFlo®硬膜外系统是最近引入的,验证是否客观和合理的工具来检测硬膜外腔。我们的目的是验证仪器的高灵敏度是否可以帮助麻醉师很早就确定硬膜外腔,限制了扩展的Tuohy针进入硬膜外腔。方法。在这项前瞻性,模拟研究中,我们通过52名专家麻醉师通过使用CompuFlo®硬膜外仪器或它们的电阻的标准损失盐水技术(LORT)执行的硬膜外过程期间评估通过模拟黄韧带的的Tuohy针延伸。结果。的平均(SD)针头伸展长度为3.90(3.71)毫米的标准技术组和CompuFlo®组0.68(0.46)毫米(P <000001)。该CompuFlo®组(F检验0.01)中的数据的极度降低可变性由用该仪器高度可预测的结果。结论。该穿刺模拟黄韧带,与传统相比LORT使用CompuFlo®已经确定针的被捕更早熟高电阻材料。

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