Division of Otolaryngology, Department of Surgery, Yale University School of Medicine, New Haven, CT, United States of America.
Division of Otolaryngology, Department of Surgery, Yale University School of Medicine, New Haven, CT, United States of America; School of Medicine, Universidad Central del Caribe, Bayamon, Puerto Rico.
Am J Otolaryngol. 2024 May-Jun;45(3):104233. doi: 10.1016/j.amjoto.2024.104233. Epub 2024 Feb 24.
Neural integrity monitoring (NIM) endotracheal tubes are widely used to provide intraoperative monitoring of the recurrent laryngeal nerve during certain neck surgeries, especially thyroidectomy, in order to reduce the risk of nerve injury and subsequent vocal fold paralysis. The unique design of NIM tubes and the increased technical skill required for correct placement compared to standard endotracheal tubes may increase the risk of upper aerodigestive tract soft tissue injury. This study aims to describe adverse events related to NIM endotracheal tubes.
Retrospective cross-sectional study.
The US Food and Drug Administration's MAUDE database (2010-2022); (Manufacturer and User Facility Device Experience).
The MAUDE database was queried for reports of adverse events that resulted in patient soft tissue injury involving the use of endotracheal tubes approved by the Food and Drug Administration.
There were 28 reported soft tissue injuries, with all events being related to the NIM EMG family of endotracheal tubes manufactured by Medtronic Xomed, Inc. Overall, 24 were categorized as device-related adverse events, and 4 were unspecified in the event description. The most common soft tissue injuries were edema (n = 7) and perforation (n = 7), each accounting for 25 % of adverse events. The second most common injury type was laceration (n = 4), representing 14 % of all adverse events. Overall, 9 patients (32 %) in our cohort required a surgical intervention to treat their injuries, which consisted of 6 tracheotomies and 3 instances of suture repair.
The most commonly reported types of soft tissue injury included edema and perforation, followed by laceration. Increased awareness of device-related patient injuries associated with NIM endotracheal tubes can be used to better inform surgeons and anesthesiologists during the process of intubation and surgical decision-making.
神经完整性监测(NIM)气管插管广泛应用于某些颈部手术(尤其是甲状腺切除术)中,以提供术中对喉返神经的监测,从而降低神经损伤和随后声带麻痹的风险。与标准气管插管相比,NIM 插管的独特设计和正确放置所需的更高技术技能可能会增加上呼吸道软组织损伤的风险。本研究旨在描述与 NIM 气管插管相关的不良事件。
回顾性横断面研究。
美国食品和药物管理局的 MAUDE 数据库(2010-2022 年);(制造商和用户设施设备经验)。
在 MAUDE 数据库中查询因使用经食品和药物管理局批准的气管插管而导致患者软组织损伤的不良事件报告。
报告了 28 例软组织损伤,所有事件均与 Medtronic Xomed, Inc. 制造的 NIM EMG 系列气管插管有关。总体而言,24 例被归类为与器械相关的不良事件,4 例在事件描述中未具体说明。最常见的软组织损伤是水肿(n=7)和穿孔(n=7),各占不良事件的 25%。第二常见的损伤类型是撕裂伤(n=4),占所有不良事件的 14%。总体而言,我们队列中的 9 名患者(32%)需要手术干预来治疗他们的损伤,其中包括 6 例气管切开术和 3 例缝合修复。
报告的最常见类型的软组织损伤包括水肿和穿孔,其次是撕裂伤。提高对与 NIM 气管插管相关的与器械相关的患者损伤的认识,可以帮助外科医生和麻醉师在插管和手术决策过程中更好地了解情况。