一种新的微创神经外科颅固定装置,用于提高脑室内导管放置的准确性:实验动物研究。

IF 2.6 Q1 SURGERY
Atai Daniel, Matan Coronel, Segev Peer, Ben Grinshpan, Soner Duru, Jose L Peiro, James L Leach, Elena Abellán, Carolyn M Doerning, David Zarrouk, Francesco T Mangano
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引用次数: 0

摘要

背景:外脑室引流(EVD)插入是最常用的神经外科手术之一。在此,我们介绍了一种用于evd插入的颅骨固定装置的新概念,该装置减少了对徒手放置和钻孔技术的依赖,并提供了一种简单、微创的方法,可以为最小厚度的颅骨提供牢固的固定。方法:设计一种导管插入固定的实验装置,并在离体和体内条件下进行测试,以评估脑室的准确插管,并测试固定到头骨的强度。离体实验在以色列贝尔舍瓦的内盖夫本古里安大学(BGU)进行。这些实验包括功能台架测试和球机构和导管固定的拉拔力测量。在体内实验中,固定装置最初在俄亥俄州辛辛那提儿童医院医学中心(CCHMC)对出生1日(DOL 1)的雄性对照羔羊进行了测试。在西班牙卡塞雷斯Jesús Usón微创手术中心(JUMISC)对3只DOL 0型脑积水羔羊(1公2母)进行了进一步的实验。本研究使用的脑积水动物模型是在胎儿羔羊子宫内腹腔内注射生物胶建立的。使用磁共振成像确定导管插入轨迹,以评估该装置对放置精度的影响。评估固定装置是否到达脑室,并对放置的所有7个固定装置进行CSF提取。对其中5个固定装置进行死后拔出力测量。该装置的一般功能也进行了评估。结果:在实验中,7/7(100%)的导管轨迹成功到达心室,没有任何与装置或手术相关的明显并发症。颅固定装置底座在不脱离受试者颅骨的情况下承受4.18kgf (STD[公式:见文本]0.72,N = 5)的平均拉拔力时显示出显著的强度。此外,在EVD导管拉拔试验中,增加了一个安全环,该安全环不允许EVD在3.6kgf的力下移动。在这个力下,导管撕裂但没有从固定点释放。结论:新设计的实验装置从离体和体内测试中证明了概念的初步证明。它似乎适合于精确的心室导管放置和颅固定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A novel minimally invasive neurosurgical cranial fixation device for improved accuracy of intraventricular catheter placement: an experimental animal study.

Background: External ventricular drain (EVD) insertion is one of the most commonly performed neurosurgical procedures. Herein, we introduce a new concept of a cranial fixation device for insertion of EVDs, that reduces reliance on freehand placement and drilling techniques and provides a simple, minimally invasive approach that provides strong fixation to minimal thickness skulls.

Methods: An experimental device for catheter insertion and fixation was designed and tested in both ex-vivo and in-vivo conditions to assess accurate cannulation of the ventricle and to test the strength of fixation to the skull. The ex-vivo experiments were conducted at Ben-Gurion University of the Negev (BGU) in Be'er Sheva, Israel. These experiments included functionality bench testing and pullout force measurements for the ball mechanism and catheter fixation. For the in-vivo experiments the fixation device was initially tested at the Cincinnati Children's Hospital Medical Center (CCHMC) in Cincinnati, Ohio on one day of life 1 (DOL 1) male control lamb. Additional experiments were conducted on 3 hydrocephalic DOL 0 lambs (1 male 2 female) at the Jesús Usón Minimally Invasive Surgery Centre (JUMISC) in Caceres, Spain. The hydrocephalic animal model used for this study was created with in utero intracisternal injection of BioGlue in fetal lambs. The catheter insertion trajectory was determined using MR imaging to assess the device's impact on the placement accuracy. The fixation device was evaluated on reaching the ventricle and enabling extraction of CSF for all 7 fixations placed. For 5 of the fixation devices, post-mortem pullout force was measured. The general functionality of the device was also evaluated.

Results: In the experiments, 7/7 (100%) catheter trajectories successfully reached the ventricle without any apparent complications related to the device or the procedure. The cranial fixation device base demonstrated significant strength in withstanding an average pull-out force of 4.18kgf (STD[Formula: see text]0.72, N = 5) without detachment from the subject's skull for all 5 devices included in this test. Additionally, the EVD catheter pull test was conducted with the addition of a safety loop which did not allow movement of the EVD to a force of 3.6kgf. At this force the catheter tore but did not release from its fixation point.

Conclusion: The newly designed experimental device demonstrates initial proof of concept from ex vivo and in vivo testing. It appears suitable for accurate ventricular catheter placement and cranial fixation.

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来源期刊
CiteScore
6.80
自引率
8.10%
发文量
37
审稿时长
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