Wat L I, Brimacombe J R, White P F, Templin P A, Lynch M E, Hammamura R K
Department of Anesthesiology, Loma Linda University, CA, USA.
J Clin Anesth. 1998 Aug;10(5):386-8. doi: 10.1016/s0952-8180(98)00050-6.
To determine the utility of the laryngeal mask airway (LMA) in an ambulatory surgery practice.
Prospective, longitudinal device (survival) study.
University-based ambulatory surgery center.
1,831 ASA physical status I, II, and III outpatients undergoing superficial ambulatory surgery procedures.
Twenty LMA devices were entered into service over a 2-year period and the number of uses, as well as the structural integrity, were assessed at the end of this study period. The serial number on each LMA device was used to track the number of times it was autoclaved, as well as the date that the device failed any of the standardized pre-use tests or was lost.
During the 2-year survey, 6,430 general anesthetics were administered at the ambulatory surgery center, with 1,831 (28%) using an LMA device for airway management. At the end of the study period, nine devices were still in use, three had been withdrawn for structural analysis by the manufacturer (after > 100 uses), three failed the pre-use test (after 38-82 uses), and five devices were lost (after 21-162 uses). The structural examination revealed that the tubes were 50% weaker; however, the cuffs, pilot balloons, and values were functioning normally. The median (range) number of uses was 92 (21-195). Thus, the 20 LMA devices evaluated tolerated an average of 92 autoclave cycles each over the 2-year observation period.
To optimize the use of the LMA device in the ambulatory setting, it is necessary to increase awareness that it is a nondisposable piece of equipment and to adhere to the manufacturer's instructions for cleaning, sterilization, and insertion.
确定喉罩气道(LMA)在门诊手术中的效用。
前瞻性纵向设备(存活)研究。
大学附属门诊手术中心。
1831例美国麻醉医师协会(ASA)身体状况为I、II和III级的门诊患者,接受浅表门诊手术。
在两年期间投入使用了20个LMA设备,在研究期结束时评估使用次数以及结构完整性。每个LMA设备上的序列号用于追踪其高压灭菌次数,以及该设备未能通过任何标准化使用前测试或丢失的日期。
在为期两年的调查期间,门诊手术中心实施了6430例全身麻醉,其中1831例(28%)使用LMA设备进行气道管理。在研究期结束时,9个设备仍在使用,3个已被制造商撤回进行结构分析(使用超过100次后),3个未通过使用前测试(使用38 - 82次后),5个设备丢失(使用21 - 162次后)。结构检查显示管道强度减弱了50%;然而,袖带、指示球囊和阀门功能正常。使用次数的中位数(范围)为92次(21 - 195次)。因此,在两年观察期内,所评估的20个LMA设备平均每个耐受92次高压灭菌循环。
为了在门诊环境中优化LMA设备的使用,有必要提高认识,即它是一种非一次性设备,并遵守制造商关于清洁、消毒和插入的说明。