Zick G, Eimer C, Renner J, Becher T, Kott M, Schädler D, Weiler N, Elke G
Klinik für Anästhesiologie und Operative Intensivmedizin, Universitätsklinikum Schleswig-Holstein, Campus Kiel, Arnold-Heller-Straße 3, Haus R3, 24105, Kiel, Deutschland.
Klinik für Anästhesiologie, Helios Kliniken Schwerin, Wismarsche Straße 393-397, 19049, Schwerin, Deutschland.
Anaesthesist. 2020 Jul;69(7):489-496. doi: 10.1007/s00101-020-00794-7. Epub 2020 May 14.
After insertion of a central venous catheter (CVC) the catheter position must be controlled and a pneumothorax ruled out.
The aim was to examine whether the use of two standard acoustic windows known from emergency sonography examination techniques is feasible to 1) verify the correct intravenous localization and direction of the guidewire before final CVC insertion and 2) correctly predict the required CVC length for positioning of the catheter tip in the lower third of the superior vena cava.
This single center prospective observational study included adult patients (age ≥18 years) with an indication for CVC insertion after institutional ethics approval was obtained. Puncture sites were restricted to bilateral internal jugular and subclavian veins and except for duplicate examinations no further exclusion criteria were defined. After vessel puncture and insertion of the guidewire, the vena cava was displayed by an additional ultrasound examiner (sector scanner 1.5-3.6 MHz) using the transhepatic or subcostal acoustic window to localize the guidewire. For positioning of the CVC tip, the required catheter length in relation to the cavoatrial junction was measured using the guidewire marks during slow retraction and consecutive disappearance of the J‑shaped guidewire tip from each acoustic window. From the resulting insertion length of the guidewire 4 cm was subtracted for the transhepatic and 2 cm for the subcostal window under the assumption that this length correlates to the distance from the cavoatrial junction. The CVC was finally inserted and a chest radiograph was performed for radiological verification of the CVC position.
Of 100 included patients, 94 could finally be analyzed. The guidewire could be identified in the vena cava in 91 patients (97%) within a time period of 2.2 ± 1.9 min. In three patients, the wire could not be visualized, although two catheters had the correct position, while one catheter was incorrectly positioned in the opposite axillary vein. In the second study part, positioning of the CVC was evaluated in 44 of the 94 patients. In 5 of these 44 patients, the correct direction and disappearance of the guidewire from the acoustic window could also be reliably visualized; however, with the left subclavian vein as the puncture site, the respective catheters were up to 6 cm too short for correct positioning. Thus, these 5 patients were excluded from this analysis. In the remaining 39 patients, the position of the CVC tip was optimally located in the lower third of the superior vena cava according to the chest radiograph in 20 patients (51%), while it was relatively too high in 5 patients (13%) and too low (entrance of the right atrium) in 9 patients. In the other 5 patients, disappearance of the guidewire from the acoustic window was not definitely detectable.
The presented intraprocedural ultrasound-based method using two standard acoustic windows is reliable for verification of the correct intravenous location and direction of the guidewire even before dilatation of the vessel puncture site for insertion of the catheter. Furthermore, the method allows the clinically acceptable measurement of the required length for catheter positioning. A chest radiograph can be waived provided the ultrasound examination (identification of the guidewire and exclusion of puncture-related complications such as pneumothorax) is unambiguous.
插入中心静脉导管(CVC)后,必须控制导管位置并排除气胸。
本研究旨在探讨采用急诊超声检查技术中两种标准声学窗,是否可行于:1)在最终插入CVC前,确认导丝在静脉内的正确位置及方向;2)准确预测将导管尖端置于上腔静脉下三分之一处所需的CVC长度。
本单中心前瞻性观察性研究纳入了在获得机构伦理批准后有CVC插入指征的成年患者(年龄≥18岁)。穿刺部位限于双侧颈内静脉和锁骨下静脉,除重复检查外,未定义其他排除标准。在血管穿刺并插入导丝后,另一名超声检查人员(1.5 - 3.6MHz扇形扫描仪)使用经肝或肋下声学窗显示腔静脉,以定位导丝。为了定位CVC尖端,在缓慢回撤导丝过程中,利用导丝标记测量相对于腔房交界处所需的导管长度,同时观察J形导丝尖端从每个声学窗连续消失的情况。假设该长度与距腔房交界处的距离相关,经肝声学窗从导丝插入长度结果中减去4cm,肋下声学窗减去2cm。最终插入CVC,并进行胸部X线检查以进行CVC位置的放射学验证。
100例纳入患者中,最终94例可进行分析。91例患者(97%)在2.2±1.9分钟内可在腔静脉中识别出导丝。3例患者尽管两根导管位置正确,但导丝未能可视化,而1例导管错误地置于对侧腋静脉。在第二项研究中,对94例患者中的44例评估了CVC的定位。在这44例患者中的5例中,导丝从声学窗的正确方向和消失情况也能可靠地观察到;然而,以左锁骨下静脉为穿刺部位时,相应导管短了6cm,无法正确定位。因此,这5例患者被排除在该分析之外。在其余39例患者中,根据胸部X线检查,20例患者(51%)的CVC尖端位置最佳,位于上腔静脉下三分之一处,5例患者(13%)相对过高,9例患者(23%)过低(进入右心房)。另外5例患者中,导丝从声学窗消失的情况无法明确检测到。
所提出的基于术中超声的方法,使用两个标准声学窗,即使在扩张血管穿刺部位以插入导管之前,也能可靠地验证导丝在静脉内的正确位置和方向。此外,该方法能够对导管定位所需长度进行临床可接受的测量。如果超声检查(导丝识别及排除穿刺相关并发症如气胸)明确无误,则可无需进行胸部X线检查。