Brain A I, Verghese C, Addy E V, Kapila A, Brimacombe J
Royal Berkshire Hospital, Reading.
Br J Anaesth. 1997 Dec;79(6):704-9. doi: 10.1093/bja/79.6.704.
We have assessed the efficacy of a new laryngeal mask prototype, the intubating laryngeal mask airway (ILMA), as a ventilatory device and blind intubation guide. The ILMA consists of an anatomically curved, short, wide bore, stainless steel tube sheathed in silicone which is bonded to a laryngeal mask and a guiding handle. It has a single moveable aperture bar, a guiding ramp and can accommodate an 8 mm tracheal tube (TT). After induction of anaesthesia with propofol 2.5 mg kg-1 and fentanyl 2.5 micrograms kg-1, the device was inserted successfully at the first attempt in all 150 (100%) patients and adequate ventilation achieved in all, with minor adjustments required in four patients. Placement did not require movement of the head and neck or insertion of the fingers in the patient's mouth. Blind tracheal intubation using a straight silicone cuffed TT was attempted after administration of atracurium 0.5 mg kg-1. If resistance was felt during intubation, a sequence of adjusting manoeuvres was used based on the depth at which resistance occurred. Tracheal intubation was possible in 149 of 150 (99.3%) patients. In 75 (50%) patients no resistance was encountered and the trachea was intubated at the first attempt, 28 (19%) patients required one adjusting manoeuvre and 46 (31%) patients required 2-4 adjusting manoeuvres before intubation was successful. There were 13 patients with potential or known airway problems. The lungs of all of these patients were ventilated easily and the trachea intubated using the ILMA. In 10 of 13 (77%) of these patients, no resistance was encountered and the trachea was intubated at the first attempt; three of 13 (23%) patients required one adjusting manoeuvre. Tracheal intubation required significantly fewer adjusting manoeuvres in patients with a predicted or known difficult airway (P < 0.05). We conclude that the ILMA appeared on initial assessment to be an effective ventilatory device and intubation guide for routine and difficult airway patients not at risk of gastric aspiration.
我们评估了一种新型喉罩原型——插管型喉罩气道(ILMA)作为通气装置和盲插引导工具的效果。ILMA由一根解剖学弯曲、短而宽孔的不锈钢管组成,该管套在硅胶中,硅胶与喉罩和引导手柄相连。它有一个可移动的单孔杆、一个引导斜面,并且能够容纳一根8毫米的气管导管(TT)。在用2.5毫克/千克丙泊酚和2.5微克/千克芬太尼诱导麻醉后,该装置在所有150例(100%)患者中首次尝试均成功插入,所有患者均实现了充分通气,4例患者需要进行轻微调整。放置时不需要移动头颈部或将手指插入患者口腔。在给予0.5毫克/千克阿曲库铵后,尝试使用直的硅胶带囊TT进行盲法气管插管。如果插管过程中感觉到阻力,则根据阻力出现的深度采用一系列调整操作。150例患者中有149例(99.3%)成功进行了气管插管。75例(50%)患者未遇到阻力,首次尝试即成功插入气管;28例(19%)患者需要进行一次调整操作,46例(31%)患者在插管成功前需要进行2 - 4次调整操作。有13例患者存在潜在或已知的气道问题。所有这些患者的肺部均易于通气,并且使用ILMA成功进行了气管插管。在这些患者中,13例中有10例(77%)未遇到阻力,首次尝试即成功插入气管;13例中有3例(23%)患者需要进行一次调整操作。对于预计或已知气道困难的患者,气管插管所需的调整操作明显较少(P < 0.05)。我们得出结论,初步评估显示ILMA对于无胃内容物误吸风险的常规和困难气道患者似乎是一种有效的通气装置和插管引导工具。