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Evone? Flow-Controlled Ventilation During Upper Airway Surgery: A Clinical Feasibility Study and Safety Assessment

机译:vone? 上气道手术期间的流量控制通气:临床可行性研究和安全评估

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Introduction: During upper airway surgery in a narrowed airway due to tumor or stenosis, safe ventilation, good laryngotracheal exposure, and preservation of an adequate surgical working space are of paramount importance. This can be achieved by small-lumen ventilation such as High Frequency Jet Ventilation (HFJV). However, this technique has major drawbacks, such as air-trapping and desaturation in patients with poor pulmonary reserve. Recently, an innovative ventilating system with flow-controlled ventilation (FCV) and a small-lumen endotracheal tube, the Evone? (Ventinova, Eindhoven, The Netherlands), was introduced, claiming to counter the drawbacks of HFJV. Objectives: To evaluate feasibility and safety of the Evone? FCV system in difficult upper airway surgery and to critically appraise this novel ventilation method. Patients and methods: Evone? is a FCV-device using a small-bore cuffed tube (Tritube?). This ventilator actively sucks air out of the lungs, rather than relying on the passive backflow of air like in HFJV. Data related to the medical history, surgery, and anesthesia of all consecutive patients undergoing upper airway surgery with Evone? FCV ventilation were included in a tertiary center retrospective observational study. Results: Fifteen Patients, with a median age of 54 years, were included. Surgical procedures and indications included laser-assisted endoscopic treatment of idiopathic subglottic stenosis ( n = 3), tracheal stenosis ( n = 1), and posterior glottic stenosis ( n = 2), biopsy and/or Transoral Laser Microsurgery for laryngeal (pre)malignancy ( n = 7) and resection of benign lesions with posterior (supra)glottic location ( n = 2). Mean ventilation duration was 52.0 min (range 30–115 min, SD 19.6 min), mean surgery duration was 31.7 min (range 15–65 min, SD 13.2 min), mean minimal SaO 2 was 96.3% (range 89–100%, SD 4.0%) and mean peak pCO 2 was 41.4 mmHg (range 31–50 mmHg, SD = 5.5 mmHg). No anesthesia- or surgery-related complications, adverse events or intra-operative difficulties were reported during or after any of the 15 procedures. In all cases, compared to HFJV, Evone? FCV ventilation allowed a superior visualization and working space during the surgical procedure. Conclusion: The Evone? FCV ventilation system provides excellent conditions in patients undergoing upper airway surgery, as it combines excellent accessibility and visibility of the operation site with safe and stable ventilation.
机译:介绍:由于肿瘤或狭窄,安全通风,良好的喉部暴露和保护足够的手术工作空间,在狭窄的气道上进行上层手术期间。这可以通过诸如高频射流通风(HFJV)的小腔通气来实现。然而,这种技术具有主要的缺点,例如肺部损坏患者的空气捕获和去饱和度。最近,一种具有流量控制通气(FCV)和小腔内外伤管的创新通风系统,所以vonone? (Ventinova,Eindhoven,荷兰)被介绍,声称反驳了HFJV的缺点。目标:评估vone的可行性和安全性? FCV系统在困难的上气道手术中,并批判性地评估这种新型通风方法。患者和方法:求求吗?是一种使用小孔袖扣管(Tritube?)的FCV装置。该呼吸机主动吸出肺部的空气,而不是依赖于HFJV中的空气的被动回流。与vione voone vieNe上呼吸道手术的所有连续患者的病史,手术和麻醉有关的数据? FCV通风包括在三级中心回顾性观察研究中。结果:15名患者,包括54岁的中位数。外科手术和适应症包括激光辅助内窥镜治疗特发性脱墨狭窄(n = 3),气管狭窄(n = 1),和喉部后浊声狭窄(n = 2),活组织检查和/或传输激光显微外科(pre)恶性肿瘤(n = 7)和分解良性病变,后(同上)喇叭位置(n = 2)。平均通风持续时间为52.0分钟(范围30-115分钟,SD 19.6分钟),平均手术持续时间为31.7分钟(范围15-65分钟,SD 13.2分钟),平均SAO 2为96.3%(范围89-100%, SD 4.0%)和平均峰PCO 2为41.4 mmHg(范围31-50mmHg,SD = 5.5mmHg)。在15个程序中的任何一个程序期间或之后,报告了任何麻醉或手术相关的并发症,不良事件或术语术后困难。在所有情况下,与HFJV相比,vone?在外科手术过程中,FCV通风允许卓越的可视化和工作空间。结论:求求吗? FCV通风系统提供了患有高呼吸道手术的患者的优异条件,因为它结合了良好的可访问性和操作现场的通风了良好的可访问性和可见性。

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