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Feasibility and safety of a novel electrosurgery device as part of multi-modal bronchoscopic therapy for malignant central airway lesions

机译:一种新型电外科设备的可行性和安全性作为恶性中央气道病变的多模态支气管镜治疗的一部分

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摘要

Bronchoscopic interventions for restoring airway patency in patients with malignant central airway obstruction (CAO) have been proven to improve quality of life and lung function. Observational studies also suggest improvement in survival and successful weaning off mechanical ventilation in patients with CAO and respiratory failure (1-4). Patients with tracheal and mainstem bronchial obstruction and those with a high baseline dyspnea score are likely to have the greatest benefit from therapeutic bronchoscopic procedures (5). Studies show that survival in patients with malignant CAO that undergo successful recanalization is similar to those patients without CAO despite greater morbidity and lesser use of chemotherapy (6). Thermal ablative modalities consisting of contact electrosurgery (ES), argon plasma coagulation (APC) and laser-assisted debulking are the most commonly used modalities for immediate relief of airway obstruction. In contact ES, due to a voltage difference between the delivering probe and the target tissue, the electrons flow through the body and return to the grounding plate. Tissue resistance to flow generates heat that results in different effects depending on the temperature: coagulation (>60–80 °C), desiccation (>100 °C), carbonization (>200 °C) and vaporization (>300 °C) (7-10). CoreCath 2.7S (Medtronic Advanced Energy LLC, Portsmouth, NH, USA) is a relatively new FDA-approved, commercially available, single-use contact ES catheter specifically designed for airway use which enables coagulation and cut functions with an integrated suction port to evacuate carbonized tissue and smoke (11). This instrument can be used through the 2.8-mm working channel of a bronchoscope or inserted through the rigid bronchoscope. The aim of this study is to report the feasibility, safety and short-term outcomes of applying this technology in patients who undergo interventional bronchoscopic procedures for malignant CAO.
机译:已经证明了用于恢复恶性中央气道阻塞(CAO)患者气道通畅的支气管镜介入,以提高生活质量和肺功能。观察性研究还表明CAO和呼吸衰竭患者的生存和成功断奶机械通风(1-4)。气管和主干支气管梗阻的患者和具有高基线呼吸困难评分的人可能具有从治疗性支气管镜手术(5)的最大益处。研究表明,尽管更多的发病率和化疗使用较少(6),但经历成功的重新定量的恶性Cao患者的存活率类似于没有CAO的患者。由接触电外科(ES)组成的热烧蚀模式,氩等离子体凝固(APC)和激光辅助DEBULKING是最常用的呼吸道阻塞的宽度易用的方式。在接触ES中,由于输送探针和目标组织之间的电压差,电子通过主体流过并返回到接地板。组织抵抗流动产生的热量,这取决于温度:凝结(> 60-80℃),干燥(> 100℃),碳化(> 200℃)和蒸发(> 300℃)( 7-10)。 Corecath 2.7s(Medtronic Advanced Energy LLC,Portsmouth,NH,USA)是一个相对较新的FDA批准的,市售的单用的触点ES导管,专门为气道使用设计,可使凝固和切割功能与疏散的集成吸入口。碳化组织和烟雾(11)。该仪器可以通过支气管镜的2.8mm工作通道使用或通过刚性支气管镜插入。本研究的目的是举报在接受恶性曹操介入支气管镜手术的患者中应用该技术的可行性,安全性和短期结果。

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