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超声引导锁骨下入路腋静脉平面内置管时使用超声显影针与非超声显影针的随机对照试验。

Echogenic needles versus non-echogenic needles for in-plane ultrasound-guided infraclavicular axillary vein cannulation, a randomized controlled trial.

机构信息

Division of Emergencies and Critical Care, Department of Anesthesiology, Oslo University Hospital, Nydalen, P.O. Box 4850, 0424, Oslo, Norway.

Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.

出版信息

Sci Rep. 2024 Sep 27;14(1):22258. doi: 10.1038/s41598-024-72620-8.

Abstract

Echogenic needles improve the reflection of the ultrasound beam. The aim of the study was to compare needle performance during ultrasound-guided cannulation of the infraclavicular axillary vein with an in-plane needle approach, using echogenic needles or non-echogenic standard needles. One hundred adult patients undergoing surgical procedures that required a central venous catheter were randomized for either echogenic or non-echogenic needles. The primary outcome was access time. Secondary outcomes encompassed total procedure time, success in first attempt, number of attempts, number of skin punctures, change of site for vascular access, catheter placement, subjective experience with needle visualization and needle procedure, and adverse events. Median (IQR) [range] venous access time was 21 (15-56) [6-440] in echogenic needle group and 26 (14-91) [6-925] in the non-echogenic needle group (p = 0.40). No statistically significant differences were found in the secondary outcome measures. One patient (non-echogenic needle group) experienced pneumothorax. In three patients in each group (6%) arterial puncture occurred. Echogenic needles did not significantly improve needle control or safety when used for infraclavicular axillary vein cannulation with an in-plane needle approach. The results indicate that standard needles are appropriate for ultrasound guided subclavian vascular access in a perioperative situation.

摘要

超声增强针可改善超声束的反射。本研究旨在比较平面内进针入路法超声引导下锁骨下腋静脉置管时使用超声增强针与非超声增强标准针的针具性能。100 例需行中心静脉置管的成年手术患者被随机分为超声增强针组或非超声增强标准针组。主要结局为置管时间。次要结局包括总操作时间、首次尝试成功率、尝试次数、皮肤穿刺次数、血管入路部位改变、导管放置、针具可视化和进针过程的主观体验,以及不良事件。超声增强针组的中位(IQR)[范围]静脉置管时间为 21(15-56)[6-440],非超声增强标准针组为 26(14-91)[6-925](p=0.40)。次要结局指标无统计学差异。1 例(非超声增强标准针组)患者发生气胸。两组各有 3 例(6%)患者发生动脉穿刺。在平面内进针入路法超声引导锁骨下腋静脉置管时,超声增强针并未显著改善针具控制或安全性。结果表明,在围手术期,标准针适用于超声引导下锁骨下血管入路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f494/11437108/11bb2eb48185/41598_2024_72620_Fig1_HTML.jpg

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