首页> 外文期刊>Canadian journal of anesthesia: Journal canadien d'anesthesie >Variations in ILMA external diameters: another cause of device failure.
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Variations in ILMA external diameters: another cause of device failure.

机译:ILMA外径的变化:导致设备故障的另一个原因。

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摘要

PURPOSE: To report failure of insertion of #5 and #4 intubating laryngeal mask airways (ILMAs) in a patient with a mouth opening of just under 25 mm, and the variances among same-size ILMAs. CLINICAL FEATURES: A 53-yr-old man with obstructive sleep apnea underwent elective ENT surgical repair. His mouth opening was just under 25 mm. Ventilation by mask was easy. Direct laryngoscopy failed after induction of anesthesia and neuromuscular block. Neither a #5 nor a #4 ILMA could be passed between the patient's teeth, despite different twisting maneuvres. A #4 LMA was thus prepared as a conduit for fibreoptic intubation. Placement of the LMA was easy, as was fibreoptic-guided intubation. The LMA was removed over the tracheal tube (TT) to enable ENT surgery, and the further course was uneventful. Manual examination showed that, unlike others of the same type, the failed ILMAs were not sufficiently compressible either to allow insertion in this patient or to the 20 mm reported as the maximal outer dimension of the device. Radiological examination revealed that, at the point of the device where it is intended to be compressible, the silicone layer was thicker in the failed devices than in stock compressible ILMAs, and the end of the steel tube was not so sharply beveled. CONCLUSION: Our inability to insert an ILMA in a patient with an interdental distance of just under 25 mm was because the device was not sufficiently compressible although the manufacturer states the maximal outer dimension to be 20 mm.
机译:目的:报告在口径小于25 mm的患者中插入#5和#4插管喉罩气道(ILMA)失败,以及同尺寸ILMA之间的差异。临床特征:一名患有阻塞性睡眠呼吸暂停的53岁男性接受了选择性耳鼻喉外科手术修复。他的嘴张开不到25毫米。戴口罩通风很容易。诱导麻醉和神经肌肉阻滞后,直接喉镜检查失败。尽管扭曲方式不同,但#5 ILMA和#4 ILMA都不能在患者的牙齿之间通过。因此,制备了#4 LMA作为用于光纤插管的导管。 LMA的放置很容易,光纤引导的插管也很容易。在气管导管(TT)上切除LMA以进行耳鼻喉科手术,并且进一步的过程顺利进行。手动检查显示,与其他同类产品不同,失败的ILMA不能充分压缩,以致无法插入该患者或被报道为装置最大外部尺寸的20毫米。放射学检查表明,在设备打算可压缩的位置,失效设备中的有机硅层要比库存的可压缩ILMA厚,并且钢管的末端没有那么陡峭地倾斜。结论:我们无法将ILMA插入到齿间距离不到25毫米的患者体内,是因为尽管制造商规定最大外部尺寸为20毫米,但该装置不能充分压缩。

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