Li Bing-Bing, Yan Jie, Zhou Hong-Gang, Hao Jing, Liu Ai-Jia, Ma Zheng-Liang
Department of Anesthesiology, The Affiliated Drum Tower Hospital, Nanjing University School of Medicine, Nanjing, Jiangsu 210008, China.
Chin Med J (Engl). 2015 Oct 5;128(19):2570-6. doi: 10.4103/0366-6999.166034.
High intracuff pressure can cause severe pharyngeal complications including sore throat or hoarseness after laryngeal mask airway (LMA) removal postoperatively. Though the application of minimum effective cuff inflating volume is suggested to maintain airway sealing and adequacy of ventilation for patients receiving general anesthesia with LMA at lower level of the intracuff pressure, it is currently not a standard care in most of the anesthetic departments. In this study, the minimum effective cuff inflating volume was determined for classic LMA Well Lead™ (Well Lead Medical Co., Ltd., China) and its impact on postoperative pharyngeal complications was also explored.
Patients with American Society of Anesthesiologists physical status (I-III) undergoing the short-duration urological surgery were recruited in this trial. First, the minimum effective cuff inflating volume was determined for size 4 or 5 LMA Well Lead in the study 1. Immediately following placement and confirmation of ideal LMA position, the cuff was inflated with 5, 7, 10 ml of air and up to 30 ml at 5 ml increment. The intracuff pressure, oropharyngeal leak pressure (OLP), and inspiratory peak airway pressure under positive pressure ventilation at the corresponding cuff volume as indicated above were recorded. Second, the enrolled patients were randomly allocated into minimum effective cuff inflating volume group (MC) and routine care (RC) group in the study 2. The minimum effective cuff inflating volume was applied and maintained in MC group, whereas the cuff volume was inflated with half of the maximum cuff inflating volume recommended by manufacturer in RC group throughout the surgical procedure and stay in postanesthesia care unit prior to LMA removal. The incidence of pharyngeal complications at 0, 2, 24, and 48 h after removal of LMA and other intra-operative adverse events were also documented.
The intracuff pressure varied with the cuff inflating volume in a positive linear correlation manner (Y = 11.68X - 42.1, r(2) = 0.9191) under the range of 5-30 ml for size 4 LMA. In similar with size 4 LMA, the data were also showed the linear relationship between the intracuff pressure and the cuff inflating volume (Y = 7.39X - 10.9, r(2) = 0.8855) for size 5 LMA. The minimal effective cuff inflating volume for size 4 or 5 LMA was 7-9 ml in combination of considering OLP needed to maintain airway sealing during intermittently positive pressure ventilation. The intracuff pressure in MC group was lower compared with RC group (63.0 ± 3.7 vs. 126.4 ± 24.0 cmH2O for size 4 LMA; 55.6 ± 2.4 vs. 138.5± 26.8 cmH2O for size 5 LMA; P < 0.0001). The incidence of pharyngeal adverse events was lower in MC group versus the RC group at 2, 24 h after LMA removal.
The relationship between the cuff inflating volume and the intracuff pressure for size 4 or 5 LMA Well Lead(TM) is in a linear correlation manner at the range of 5-30 ml. The minimal cuff inflating volume is adequate for satisfactory airway sealing and consequently associated with lower incidence of postoperative pharyngeal complications for LMA Well Lead.™.
喉罩气道(LMA)术后拔除时,高套囊压力可导致包括咽痛或声音嘶哑在内的严重咽部并发症。尽管建议应用最小有效套囊充气量,以在较低套囊压力水平下维持接受LMA全身麻醉患者的气道密封和通气充分性,但目前在大多数麻醉科室这并非标准护理措施。在本研究中,确定了经典LMA Well Lead™(中国威利多医疗器械有限公司)的最小有效套囊充气量,并探讨了其对术后咽部并发症的影响。
本试验招募了美国麻醉医师协会身体状况分级(I-III级)的短期泌尿外科手术患者。首先,在研究1中确定4号或5号LMA Well Lead的最小有效套囊充气量。在放置并确认LMA位置理想后,立即分别向套囊内充入5、7、10 ml空气,然后以5 ml增量充至30 ml。记录上述相应套囊容积下的套囊压力、口咽漏气压(OLP)和正压通气时的吸气峰气道压。其次,在研究2中,将入选患者随机分为最小有效套囊充气量组(MC)和常规护理组(RC)。MC组应用并维持最小有效套囊充气量,而RC组在整个手术过程中及LMA拔除前在麻醉后护理单元将套囊充入制造商推荐的最大套囊充气量的一半。记录LMA拔除后0、2、24和48小时咽部并发症的发生率以及其他术中不良事件。
对于4号LMA,在5 - 30 ml范围内,套囊压力与套囊充气量呈正线性相关(Y = 11.68X - 42.1,r² = 0.9191)。与4号LMA类似,对于5号LMA,套囊压力与套囊充气量之间也呈线性关系(Y = 7.39X - 10.9,r² = 0.8855)。考虑到间歇正压通气期间维持气道密封所需的OLP,4号或5号LMA的最小有效套囊充气量为7 - 9 ml。MC组的套囊压力低于RC组(4号LMA:63.0 ± 3.7 vs. 126.4 ± 24.0 cmH₂O;5号LMA:55.6 ± 2.4 vs. 138.5 ± 26.8 cmH₂O;P < 0.0001)。LMA拔除后2、24小时,MC组咽部不良事件的发生率低于RC组。
在5 - 30 ml范围内,4号或5号LMA Well Lead™的套囊充气量与套囊压力呈线性相关。最小套囊充气量足以实现满意的气道密封,因此与LMA Well Lead™术后咽部并发症的较低发生率相关。