supraglottic airway devices

声门上气道装置
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    文章类型: Journal Article
    癌症患者不断升级的气道管理需求促使我们不断地管理气道设备,声门上气道装置(SAD)在这方面发挥着重要作用。SAD用作维持上气道开放的工具。自1980年代初最早的SAD成立以来,一系列先进和增强型的第二代器械已在临床应用.这些升级的SAD集成了特定功能,旨在增强正压通气并减轻误吸风险。如今,它们广泛用于全身麻醉程序,并在困难的气道管理中起关键作用,院前护理,和急诊医学。在某些情况下,SAD可被认为是优于气管内导管(ETT)的替代方案,并且可用于更广泛的外科手术和非手术病例。这篇综述概述了当前的证据,分类摘要,相关应用场景,以及未来SAD的开发或临床应用需要改进的领域。
    The escalating airway management demands of cancer patients have prompted us to continually curate airway devices, with supraglottic airway devices (SADs) playing a significant role in this regard. SADs serve as instrumental tools for maintaining an open upper airway. Since the inception of the earliest SADs in the early 1980s, an array of advanced and enhanced second-generation devices have been employed in clinical settings. These upgraded SADs integrate specific features designed to enhance positive-pressure ventilation and mitigate the risk of aspiration. Nowadays, they are extensively used in general anesthesia procedures and play a critical role in difficult airway management, pre-hospital care, and emergency medicine. In certain situations, SADs may be deemed a superior alternative to endotracheal tube (ETT) and can be employed in a broader spectrum of surgical and non-surgical cases. This review provides an overview of the current evidence, a summary of classifications, relevant application scenarios, and areas for improvement in the development or clinical application of future SADs.
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  • 文章类型: Journal Article
    已经描述了具有可变成功率的i-gel插入的不同技术。本研究旨在评估90°旋转儿童i-gel错位的发生率。180°旋转,下颌推力辅助和标准插入技术。
    这项研究纳入了132名接受择期手术的儿童,这些儿童在没有神经肌肉阻滞的情况下接受了全身麻醉,并获得了伦理委员会的批准。使用四种随机技术之一插入i-gel(90°旋转,180°旋转,下颌推力辅助插入或标准插入技术)由麻醉学员提供。这项研究的主要目的是通过柔性视频支气管镜检查与标准插入技术相比,使用三种替代技术评估设备错位。
    180°旋转技术组的错位发生率最低(27%),而标准和90°旋转技术组的错位发生率为39%,颌骨推力技术组的错位发生率为70%(P=0.004)。180°旋转技术组口咽部渗漏压力(OLP)最高,也就是说,180°旋转技术组中的27.1(5.3)cmH2O与23(4.3)相比,标准中的25.8(4.1)和24.7(5.6)cmH2O,90°旋转和辅助钳口推力组,分别为(P=0.006)。使用标准插入技术,插入i-gel的时间最少,也就是说,16.9(3.3)s,与90°旋转组中的18.4(3.1)s相比,180°旋转组19.5(3.2)s,辅助颌推力技术组20.1(3.4)s(P<0.001)。
    麻醉受训者在儿童中放置i-gel的180°旋转技术与其他技术相比,错位发生率最低,OLP最佳,但在临床表现和通气方面缺乏任何明显的优势。
    UNASSIGNED: Different techniques of i-gel insertion have been described with variable success rates. This study aimed to assess the incidence of malposition of i-gel in children with 90° rotation, 180° rotation, jaw thrust-assisted and standard insertion techniques.
    UNASSIGNED: The study included 132 children undergoing elective surgery under general anaesthesia without neuromuscular blockade after approval from the Institutional Ethics Committee. The i-gel was inserted using one of the four randomised techniques (90° rotation, 180° rotation, jaw thrust-assisted insertion or standard insertion technique) by anaesthesia trainees. The primary objective of this study was to assess device malposition using three alternative techniques compared to the standard insertion technique by flexible video bronchoscopy.
    UNASSIGNED: The incidence of malposition was the least in the 180° rotation technique group (27%) versus 39% in the standard and 90° rotation technique groups and 70% in the jaw thrust technique group (P = 0.004). Oropharyngeal leak pressure (OLP) was highest in the 180° rotation technique group, that is, 27.1 (5.3) cm H2O in the 180° rotation technique group versus 23 (4.3), 25.8 (4.1) and 24.7 (5.6) cm H2O in the standard, 90° rotation and assisted jaw thrust groups, respectively (P = 0.006). The time to i-gel insertion was the least with the standard insertion technique, that is, 16.9 (3.3) s, compared to 18.4 (3.1) s in the 90° rotation group, 19.5 (3.2) s in the180° rotation group and 20.1 (3.4) s in the assisted jaw thrust technique group (P < 0.001).
    UNASSIGNED: The 180° rotation technique for i-gel placement in children by anaesthesia trainees has the lowest incidence of malposition and the best OLP versus other techniques but lacks any clear advantage in clinical performance and ventilation.
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  • 文章类型: Journal Article
    Baska面膜(BM)和AmbuAuraGain(AAG)在最近的试验中显示出可喜的结果,但尚未进行比较。因此,我们的目的是比较BM和AAG用于成人患者气道管理的临床表现.
    在这项随机比较研究中,纳入年龄在18~60岁,预期手术时间少于2h的患者.患者被随机分配到AAG(A组,n=37)和BM(B组,n=37)用于气道管理。麻醉诱导后,插入分配的声门上气道装置(SAD)。口咽渗漏压力(OLP)插入SAD所需的时间,插入尝试次数,泄漏分数(LF),首次尝试成功率,总体成功率,易于插入,声门的光纤视图,并对并发症进行比较。数据采用学生t检验进行分析,Mann-WhitneyU测试,和费希尔的精确测试。
    基线和人口统计学特征具有可比性。OLP(31.32±2.59比27.54±1.32cmH2O)更高(P<0.001),BM组的LF(6.19%±1.20%对7.24%±1.72%)较低(P=0.003)。首次尝试和总体成功率,插入所需的时间,插入尝试次数,易于插入,两组之间通过SAD的声门的纤维视视图在统计学上相似。然而,AAG组喉咙痛(P=0.007)和咳嗽(P=0.028)的发生率较高。
    BM的临床表现优于AAG,因为前者具有较高的OLP,低LF和并发症。
    UNASSIGNED: The Baska mask (BM) and the Ambu AuraGain (AAG) have shown promising results in recent trials but have not been compared. Therefore, we aimed to compare the clinical performance of the BM and the AAG for airway management of adult patients.
    UNASSIGNED: In this randomised comparative study, patients aged 18-60 years and with an expected surgical duration of less than 2 h were enroled. Patients were randomly allocated to AAG (Group A, n = 37) and BM (Group B, n = 37) for airway management. After induction of anaesthesia, an allocated supraglottic airway device (SAD) was inserted. Oropharyngeal leak pressure (OLP), time taken to insert SAD, number of insertion attempts, leak fraction (LF), first-attempt success rate, overall success rate, ease of insertion, fiberoptic view of the glottis, and complications were compared. The data were analysed using Student\'s t-test, Mann-Whitney U test, and Fisher\'s exact tests.
    UNASSIGNED: Baseline and demographic characteristics were comparable. OLP (31.32 ± 2.59 versus 27.54 ± 1.32 cmH2O) was higher (P < 0.001), and LF (6.19% ± 1.20% versus 7.24% ± 1.72%) was lower (P = 0.003) in the BM group. First-attempt and overall success rate, time taken to insert, number of insertion attempts, ease of insertion, and fibreoptic view of glottis through the SADs were statistically similar between groups. However, the incidence of sore throat (P = 0.007) and cough (P = 0.028) was higher with AAG.
    UNASSIGNED: Clinical performance of BM was better than AAG as the former had higher OLP, lower LF and complications.
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  • 文章类型: Journal Article
    在本研究中,我们假设喉罩气道(LMA)保护器提供的口咽部渗漏压(OLP)高于LMAProSeal.因此,我们计划这项研究以OLP为主要目标,插入特征为次要目标,比较LMAProSeal和LMAProSeal的临床表现.
    90名男女患者,18-70岁,随机分为PS组(LMAProSeal)和P组(LMA保护者)。麻醉诱导后,设备是按照组分配插入的。将两种装置的OLP作为主要目标。次要目标,如插入时间,易于插入,所需的尝试次数,光纤视图分级,获得60cmH2O的袖带压力(CP)所需的空气量(mL),以及所需的CP调整和并发症,如果有的话,也注意到了。使用coGuide统计软件分析数据,版本1(BDSS公司班加罗尔,卡纳塔克邦,印度)。
    使用LMA保护剂的OLP中位数(四分位数间距)明显高于使用LMAProSeal的OLP[33.00(27.0,36.0)与[29.50(26.0,32.0)(P=0.009)]。PS组首次尝试成功率为95.4%(42/44),P组首次尝试成功率为93%(40/43)。易于插入,两组之间的光纤视图分级没有差异。PS组1例胃管放置失败,P组3例胃管放置失败(P=0.606)。获得60cmH2O的CP所需的空气(mL)的中位数在PS组为26.5(20,28),在P组为12(8,13)(95%置信区间[CI]=10.808-14.575)(P<0.001)。在所有时间点,CP明显增高,PS组比P组需要更多的CP调整(P<0.001)。两组之间在1和24小时的血液染色和术后咽喉痛的发生率没有差异。
    LMAProtector提供了明显更高的OLP和较少的CP调整要求,但可比较的首次尝试成功率,平均插入时间,光纤视图,与LMAProSeal相比,插入胃管。
    UNASSIGNED: In the present study, we hypothesised that the laryngeal mask airway (LMA) Protector would provide higher oropharyngeal leak pressure (OLP) than LMA ProSeal. Thus, we planned this study to compare the clinical performance of LMA Protector and LMA ProSeal in terms of OLP as a primary objective and insertion characteristics as secondary objectives.
    UNASSIGNED: Ninety patients of either gender, aged 18-70 years, were randomised into groups PS (LMA ProSeal) and P (LMA Protector). Following anaesthetic induction, the device was inserted as per group allocation. OLP of both devices was taken as a primary objective. Secondary objectives such as insertion time, ease of insertion, number of attempts required, fibre-optic view grading, amount of air (mL) required to get a cuff pressure (CP) of 60 cm H2O, and CP adjustment required and complications, if any, were also noted. Data were analysed using coGuide statistics software, Version 1 (BDSS Corp. Bangalore, Karnataka, India).
    UNASSIGNED: The median (interquartile range) OLP was significantly higher with LMA protector than with LMA ProSeal [33.00 (27.0, 36.0) versus [29.50 (26.0, 32.0) (P = 0.009)]. First-attempt success rate was 95.4% (42/44) in group PS and 93% (40/43) in group P. Insertion time, ease of insertion, and fibre-optic view grading were not different between the groups. Gastric tube placement failed in one patient in group PS and in three patients in group P (P = 0.606). The median amount of air (mL) required to get a CP of 60 cm H2O was 26.5 (20, 28) in group PS and 12 (8,13) in group P (95% confidence interval [CI] =10.808-14.575) (P < 0.001). At all time points, CP was significantly higher, and more CP adjustments were needed in group PS than in group P (P < 0.001). Incidence of blood staining and post-operative sore throat at 1 and 24 h were not different between the groups.
    UNASSIGNED: LMA Protector provided a significantly higher OLP and less requirement of CP adjustments but comparable first-attempt success rate, mean insertion time, fibre-optic view, and gastric tube insertion as compared to LMA ProSeal.
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  • 文章类型: Journal Article
    声门上气道装置目前广泛用于麻醉和急诊医学的气道管理。第一代SAD仅具有通气通道,如果发生反流,则无法防止可能吸入的胃内容物。第二代SAD配备有胃通道,以允许插入胃导管和抽吸胃内容物。此外,封口形状的改变改善了密封。一些第二代SAD也被设计为允许使用纤维镜通过管腔插管。尽管使用SAD的安全性和有效性非常高,在提供足够的密封和保护免受与SAD错位相关的可能并发症方面仍然存在一些问题。新的SAD允许用户选择插入范围并控制SAD的位置,可以克服这些问题。此外,可视喉罩气道可用作气管内插管装置,通过第二代SAD提供光纤插管的良好替代方案。在这篇叙述性评论中,我们提供了视频喉罩气道的使用知识,以及将其引入日常临床实践的可能优势。
    Supraglottic airway devices are currently widely used for airway management both for anaesthesia and emergency medicine. First-generation SADs only had a ventilation channel and did not provide protection from possible aspiration of gastric content if regurgitation occurred. Second-generation SADs are equipped with a gastric channel to allow the insertion of a gastric catheter and suctioning of gastric content. Additionally, the seal was improved by a change in the shape of the cuff. Some second-generation SADs were also designed to allow for intubation through the lumen using fiberscopes. Although the safety and efficacy of use of SADs are very high, there are still some issues in terms of providing an adequate seal and protection from possible complications related to misplacement of SAD. New SADs which allow users to choose the insertion scope and control the position of SAD can overcome those problems. Additionally, the Video Laryngeal Mask Airway may serve as an endotracheal intubation device, offering a good alternative to fibre-optic intubation through second-generation SADs. In this narrative review, we provide knowledge of the use of video laryngeal mask airways and the possible advantages of introducing them into daily clinical practice.
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  • 文章类型: Journal Article
    腹腔镜手术是全世界最常见的手术之一。从气管内插管到声门上气道装置(SAD)的气道固定方法逐渐转变。当前工作的目的是对已发表的关于SAD或气管插管(ETT)的腹腔镜手术中气道并发症的RCT进行系统回顾和荟萃分析。
    这项研究在PROSPERO注册,并在GoogleScholar和PubMed中进行了文献检索,直到2022年8月。在78项研究中,筛选了31项研究,其中21项用于分析。RevMan5.4用于分析喉咙痛的数据,声音嘶哑,恶心,呕吐,喘鸣和咳嗽。
    21项随机对照试验,共招募2213名成年患者,都包括在定量分析中。ETT组术后喉咙痛和声音嘶哑发生率显著,风险比(RR)为0.44,P<0.00001[0.30,0.65],i2=72%,RR0.38,P<0.001[0.21,0.69],i2=72%,分别。然而,恶心的发生率,呕吐和喘鸣不显著,RR为0.83,P=0.26[0.60,1.15],i2=52%的恶心和RR0.55,P=0.03[0.33,0.93],i2=14%的呕吐。ETT组咳嗽发生率较高,RR为0.11,P<0.00001[0.06,0.20],i2=42%,与SAD组相比。
    就声音嘶哑的发生率而言,SAD和ETT之间存在很大差异,喉咙痛,恶心和咳嗽。本更新的系统综述中发现的证据加强了现有文献。
    UNASSIGNED: Laparoscopic surgeries are among the most frequent procedures done worldwide. There is a gradual shift in the method of airway securement from endotracheal intubation to supraglottic airway devices (SAD). The objective of the current work was to perform a systematic review and meta-analysis of published RCTs on airway complications in laparoscopic surgery performed with a SAD or endotracheal intubation (ETT).
    UNASSIGNED: The research was registered in PROSPERO, and a literature search was conducted in Google Scholar and PubMed until August 2022. Out of 78 studies, 31 studies were screened and 21 were included for analysis. RevMan 5.4 was used to analyse data on sore throat, hoarseness, nausea, vomiting, stridor and cough.
    UNASSIGNED: Twenty-one randomised controlled trials, enrolling a total of 2213 adult patients, were included in the quantitative analysis. A significant incidence of sore throat and hoarseness was seen at post-operative period in ETT group with risk ratio (RR) 0.44, P < 0.00001 [0.30, 0.65], i2 = 72% and RR 0.38, P < 0.001 [0.21, 0.69], i2 = 72%, respectively. However, incidence of nausea, vomiting and stridor was not significant with RR 0.83, P = 0.26 [0.60, 1.15], i2 = 52% for nausea and RR 0.55, P = 0.03 [ 0.33, 0.93], i2 = 14% for vomiting. Incidence of cough was more in ETT group with RR 0.11, P < 0.00001 [ 0.06, 0.20], i2 = 42%, as compared to SAD group.
    UNASSIGNED: There was a substantial variation between SADs and ETTs with respect to the incidence of hoarseness, sore throat, nausea and cough. The existing literature is reinforced by the evidence uncovered in this updated systematic review.
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  • 文章类型: Journal Article
    各种各样的气道装置,技术,在过去的100年中,已经开发了认知工具来提高气道管理的安全性,并成为主要研究兴趣的话题。本文回顾了这一时期的主要发展,从1940年代的现代喉镜检查开始,1960年代的纤维喉镜检查,1980年代的声门上气道装置,20世纪90年代困难气道的算法,最后是2000年代的现代视频喉镜检查。
    A large variety of airway devices, techniques, and cognitive tools have been developed during the last 100 years to improve airway management safety and became a topic of major research interest. This article reviews the main developments in this period, starting with modern day laryngoscopy in the 1940s, fiberoptic laryngoscopy in the 1960s, supraglottic airway devices in the 1980s, algorithms for difficult airway in the 1990s, and finally modern video-laryngoscopy in the 2000s.
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  • 文章类型: Randomized Controlled Trial
    背景和目的:众所周知,声门上气道装置(SAD)可用于消除喉镜和气管插管的缺点,尤其是眼压和应激反应。视神经鞘直径(ONSD)的超声测量反映了颅内压(ICP)的升高。在我们的研究中,我们旨在比较SAD对血流动力学反应和ONSD的影响.材料和方法:我们的前瞻性研究包括90名年龄超过18岁的ASAI-II患者,他们没有困难插管或眼科病理学史。根据所使用的喉罩气道(LMA)装置,将患者随机分为三组:ProSealLMA(pLMA,n=30),LMA至尊(sLMA,n=30),和I-gel(n=30)。记录诱导前(T0)和1分钟(T1)接受标准麻醉诱导和监测的患者的双侧ONSD测量值和血流动力学数据,5分钟(T5),和SAD放置后10分钟(T10)。结果:在所有测量时间,两组的血流动力学反应和ONSD值相似.在所有三组中,T0和T1组间血流动力学变化相似,且高于其他测量时间(p<0.001).所有组的ONSD值均在T1时增加,之后趋于恢复到基线值(p<0.001)。结论:我们得出结论,所有三个SAD都可以安全使用,因为它们在放置过程中保留了血液动力学稳定性和ONSD变化。它们并未导致ONSD升高至导致ICP增加的程度。
    Background and Objectives: Supraglottic airway devices (SADs) are known to be useful in eliminating the drawbacks of laryngoscopy and tracheal intubation, especially ocular pressure and stress responses. The ultrasonographic measurement of optic nerve sheath diameter (ONSD) reflects increases in intracranial pressure (ICP). In our study, we aimed to compare the effects of SADs on hemodynamic response and ONSD. Materials and Methods: Our prospective study included 90 ASA I-II patients over the age of 18 who did not have a history of difficult intubation or ophthalmic pathology. The patients were randomly divided into three groups based on the laryngeal mask airway (LMA) devices used: ProSeal LMA (pLMA, n = 30), LMA Supreme (sLMA, n = 30), and I-gel (n = 30). The bilateral ONSD measurements and hemodynamic data of the patients who underwent standard anesthesia induction and monitoring were recorded before induction (T0) and 1 min (T1), 5 min (T5), and 10 min (T10) after SAD placement. Results: At all measurement times, the hemodynamic responses and ONSD values of the groups were similar. In all three groups, intergroup hemodynamic changes at T0 and T1 were similar and higher than those at other times of measurement (p < 0.001). The ONSD values of all groups increased at T1, and they tended to return to baseline values afterward (p < 0.001). Conclusions: We concluded that all three SADs could be used safely because they preserved both hemodynamic stability and ONSD changes in their placement processes, and they did not cause elevations in ONSD to an extent that would lead to increased ICP.
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  • 文章类型: Editorial
    这是对肯尼迪等人进行的研究的评论。来自维多利亚,澳大利亚,该研究分析了该地区所有成人EMS目击院外心脏骤停(OHCA)患者的队列,并将COVID-19期间接受治疗的患者与历史比较期进行了比较。评论总结了研究结果,并讨论了该研究在COVID-19大流行期间OHCA患者的生存链和气道管理变化的背景下的重要性。
    This is a commentary on the study conducted by Kennedy et al. from Victoria, Australia, that analyzed the cohort of all adult EMS-witnessed out-of-hospital cardiac arrest (OHCA) patients in the region and compared patients treated during the COVID-19 period to a historical comparator period. The commentary summarizes the study findings and discusses the importance of the study in the context of the chain of survival and changes in airway management for OHCA patients during the COVID-19 pandemic.
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  • 文章类型: Randomized Controlled Trial
    背景:AmbuAuraGain已被证明在较高的首次尝试插入成功率方面比其他声门上气道装置更好,插入的时间和便利性,口咽渗漏压高,儿童并发症少。尚未在儿童中评估BlockBuster喉罩的性能。
    目的:本研究的主要目的是比较BlockBuster喉罩与AmbuAuraGain在儿童受控通气期间的口咽渗漏压力。
    方法:将50名6个月至12岁气道正常的儿童随机分为A组(AmbuAuraGain)和B组(BlockBuster喉罩)。全身麻醉后,根据各组插入合适大小的声门上气道(大小1.5/2.0/2.5).口咽渗漏压力,成功和易于插入声门上气道,胃管插入,并记录了通气参数。声门视图通过纤维支气管镜进行分级。
    结果:人口统计学参数具有可比性。BlockBuster组的平均口咽渗漏压(24.72±6.81cmH2O)明显高于AmbuAuraGain组(17.20±4.28cmH2O)7.52cmH2O(95%CI4.27至10.76;p=0.001)。BlockBuster和AmbuAuraGain组的平均声门上气道插入时间为12.04±2.55s和13.64±2.76s,分别(平均差-1.6s,95%CI0.09-3.12;p=0.04)。通风参数,首次尝试声门上气道插入成功率,两组之间的胃管插入的难易程度相当。与AmbuAuraGain组相比,BlocktBuster组显示出容易的声门上气道插入。与AmbuAuraGain相比,BlockBuster组的声门视野更好,仅在25名儿童中的23名儿童中看到了喉部。两组均无并发症发生。
    结论:我们发现,在儿科人群中,与AmbuAuraGain相比,BlocktBuster喉罩具有更高的口咽渗漏压。
    Ambu AuraGain has proven to be better compared with other supraglottic airway devices in terms of higher first-attempt insertion success rate, time and ease of insertion, high oropharyngeal leak pressure, and fewer complications in children. The performance of the BlockBuster laryngeal mask has not been evaluated in children.
    The primary objective of this study was to compare the oropharyngeal leak pressure of the BlockBuster laryngeal mask with those of the Ambu AuraGain during controlled ventilation in children.
    Fifty children aged 6 months to 12 years with normal airways were randomized into group A (Ambu AuraGain) and group B (BlockBuster laryngeal mask). After administration of general anesthesia, an appropriate size supraglottic airway (size 1.5/2.0/2.5) was inserted according to the groups. Oropharyngeal leak pressure, success and ease of supraglottic airway insertion, gastric tube insertion, and ventilatory parameters were noted. The glottic view was graded by fiberoptic bronchoscopy.
    Demographic parameters were comparable. The mean oropharyngeal leak pressure in the BlockBuster group (24.72 ± 6.81 cm H2 O) was significantly higher than Ambu AuraGain group (17.20 ± 4.28 cm H2 O) by 7.52 cm H2 O (95% CI 4.27 to 10.76; p = 0.001). The mean time for supraglottic airway insertion in the BlockBuster and Ambu AuraGain group was 12.04 ± 2.55 s and 13.64 ± 2.76 s, respectively (mean difference- 1.6 s, 95% CI 0.09-3.12; p = 0.04). Ventilatory parameters, first-attempt supraglottic airway insertion success rate, and ease of gastric tube insertion were comparable between the groups. The BlockBuster group showed easy supraglottic airway insertion compared with the Ambu AuraGain group. The BlockBuster group had better glottic views with only the larynx seen in 23 out of 25 children compared to the Ambu AuraGain with only the larynx seen in 19 out of 25 children. No complication was noted in either group.
    We found that the BlockBuster laryngeal mask has higher oropharyngeal leak pressure compared with Ambu AuraGain in a pediatric population.
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