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首页> 外文期刊>Canadian journal of anesthesia: Journal canadien d'anesthesie >The PAxpress(TM) is an effective ventilatory device but has an 18% failure rate for flexible lightwand-guided tracheal intubation in anesthetized paralyzed patients: (Le PAxpress(TM) est un appareil de ventilation efficace, mais presente un taux d'ec
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The PAxpress(TM) is an effective ventilatory device but has an 18% failure rate for flexible lightwand-guided tracheal intubation in anesthetized paralyzed patients: (Le PAxpress(TM) est un appareil de ventilation efficace, mais presente un taux d'ec

机译:PAxpress™是一种有效的通气设备,但在麻痹的瘫痪患者中进行轻柔引导的气管插管失败率高达18%:(Le PAxpressTM的通气效率不高,可能出现呼吸困难

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摘要

PURPOSE: The PAxpress(TM) is a new, single-use, extraglottic airway device. We evaluate: 1) insertion success rates; 2) airway sealing pressure, ventilatory capability and calculated mucosal pressures (in vitro minus in vivo intracuff pressure) at 30-60 mL cuff inflation volume; 3) the feasibility of lightwand-guided tracheal intubation; and 4) the incidence of mucosal trauma. METHODS: Ninety anesthetized, paralyzed adults were studied. Airway management was by senior anesthesiologists with no prior experience with the PAX, but considerable experience with extraglottic airway devices and the flexible-lightwand. RESULTS: Insertion was successful at the first attempt in 95.5% (86/90) and at the second attempt in 4.5% (4/90). Mean +/- SD airway sealing pressure at 30, 40, 50 and 60 mL cuff inflation volume was 27 +/- 8, 29 +/- 9, 32 +/- 9 and 35 +/- 7 cm H(2)O respectively; expired tidal volume at airway sealing pressure was 16 +/- 6, 18 +/- 6, 19 +/- 5 and 19 +/- 6 mL*kg(-1); and calculated mucosal pressure was 38 +/- 14, 55 +/- 20, 56 +/- 19 and 57 +/- 20 cm H(2)O. Airway sealing pressure, expired tidal volume at airway sealing pressure and calculated mucosal pressures increased with cuff inflation volume (all: P /= 35 cm H(2)O and cuff inflation volumes >/= 40 mL. Lightwand-guided intubation was successful in 82% (74/90) of patients. Mild, moderate and severe blood staining was detected in 40% (36/90), 15% (13/90) and 1% (1/90) respectively. Blood staining was more frequent after adjusting maneuvers (22/54 vs 32/36, P = 0.002). CONCLUSION: The PAX has a high insertion success rate and is an effective ventilatory device with a low risk of gastric insufflation, but has a moderately high failure rate for lightwand-guided intubation and is associated with a relatively high incidence of mucosal trauma. Mucosal pressures may exceed pharyngeal perfusion pressure.
机译:目的:PAxpress(TM)是一种新型的一次性使用的声门外气道设备。我们评估:1)插入成功率; 2)30-60 mL袖带充气量时的气道密封压力,通气能力和计算出的粘膜压力(体外减去体内袖带内压力); 3)光导气管插管的可行性; 4)粘膜创伤的发生率。方法:对90名麻醉,瘫痪的成年人进行了研究。气道管理是由高级麻醉师进行的,他们以前没有使用PAX的经验,但是在声门外气道装置和柔光管方面有相当的经验。结果:第一次插入成功率为95.5%(86/90),第二次插入成功为4.5%(4/90)。在30、40、50和60 mL袖带充气量下的平均+/- SD气道密封压力为27 +/- 8、29 +/- 9、32 +/- 9和35 +/- 7 cm H(2)O分别;气道密封压力下的潮气量为16 +/- 6、18 +/- 6、19 +/- 5和19 +/- 6 mL * kg(-1);和计算的粘膜压力为38 +/- 14、55 +/- 20、56 +/- 19和57 +/- 20 cm H(2)O。气道密封压力,在气道密封压力下的潮气量和计算的粘膜压力随袖带充气量而增加(所有:P / = 35 cm H(2)O和袖带充气量> / = 40 mL时才发现。 Lightwand引导的插管在82%(74/90)的患者中成功。分别在40%(36/90),15%(13/90)和1%(1/90)中检测到轻度,中度和重度血迹。调整操作后,血液染色更为频繁(22/54对32/36,P = 0.002)。结论:PAX插入成功率高,是一种有效的通气设备,具有较低的胃气管插管风险,但对于轻度引导的插管失败率较高,并且与粘膜创伤的发生率相对较高有关。粘膜压力可能超过咽部灌注压力。

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