Reza Hashemian Seyed Mohammad, Nouraei Navid, Razavi Seyed Sadjad, Zaker Ebrahim, Jafari Alireza, Eftekhari Parivash, Radmand Golnar, Mohajerani Seyed Amir, Radpay Badiozzaman
Clinical Tuberculosis and Epidemiology Research Center, National Research Institute of Tuberculosis and Lung Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Anesthesiology Research Center, National Research Institute of Tuberculosis and Lung Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Int J Crit Illn Inj Sci. 2014 Oct-Dec;4(4):288-92. doi: 10.4103/2229-5151.147520.
The i-gel™ is a new device introduced recently. It differs from other supraglottic airway devices. It has a non-inflatable, gel-made cuff. Previously used devices, have some disadvantages which are claimed to be absent in i-gel™. In this study we aimed to compare the performance of the laryngeal mask airway (LMA)-Classic™ and i-gel™ during anesthesia in paralyzed patients.
A total of 64 anaesthetized patients with paralysis were enrolled in a single-blind, randomized control trial to be intubated with one of the devices. We compared the device insertion parameters, some ventilatory parameters, and adverse effects after device insertion.
Vital signs were not significantly different between groups. Regarding duration of insertion attempts, the difference between groups was significant (P < 0.05); while the number of insertion attempts was insignificant (P = 0.265). There was no significant difference between both groups regarding postoperative complications (cough, sore throat, and blood on the cuff) (P > 0.05). Airway leak was assessed in both groups and data showed no significant difference (P = 0.662). Additionally, end-tidal CO2 change regarding the baseline value was significantly different after 10 and 15 min of anesthesia (P < 0.05).
Successful insertion time was shorter significantly for i-gel™. As i-gel™ has easy application, it is advantageous to be used during cardiopulmonary resuscitation by non-anesthetists in which time is very important. We concluded that i-gel™ can be an alternative to LMA-Classic™ for controlled ventilation during anesthesia as it is easier to be placed.
i-gel™是最近推出的一种新型设备。它与其他声门上气道设备不同。它有一个不可充气的凝胶制成的套囊。先前使用的设备存在一些缺点,而i-gel™据称没有这些缺点。在本研究中,我们旨在比较喉罩气道(LMA)-Classic™和i-gel™在麻痹患者麻醉期间的性能。
总共64例麻痹的麻醉患者参加了一项单盲、随机对照试验,用其中一种设备进行插管。我们比较了设备插入参数、一些通气参数以及设备插入后的不良反应。
两组之间的生命体征无显著差异。关于插入尝试的持续时间,组间差异显著(P < 0.05);而插入尝试的次数无显著差异(P = 0.265)。两组之间在术后并发症(咳嗽、喉咙痛和套囊上有血)方面无显著差异(P > 0.05)。对两组均评估了气道漏气情况,数据显示无显著差异(P = 0.662)。此外,麻醉10分钟和15分钟后,呼气末二氧化碳相对于基线值的变化有显著差异(P < 0.05)。
i-gel™的成功插入时间明显更短。由于i-gel™应用简便,对于非麻醉医生进行心肺复苏时非常有利,因为时间非常重要。我们得出结论,i-gel™在麻醉期间控制通气时可作为LMA-Classic™的替代品,因为它更容易放置。