Shim Yon Hee, Shin Cheung Soo, Chang Chul Ho, Shin Yang-Sik
Department of Anesthesiology and Pain Medicine and Anesthesia and Pain Research Institute, Yonsei University College of Medicine, Seoul, Korea.
Anesth Analg. 2005 Oct;101(4):1034-1037. doi: 10.1213/01.ane.0000166977.17442.63.
Sevoflurane provides smooth and rapid emergence from anesthesia and can be used when the removal of a laryngeal mask airway (LMA) is required in anesthetized patients. We sought to determine the optimal end-tidal concentrations of sevoflurane required for the removal of LMA in anesthetized adults. We studied 35 adults, aged 22-64 years old with an ASA physical status I or II, who were undergoing perineal surgery. General anesthesia was induced with thiopental, and the LMA was then inserted. Anesthesia was maintained with sevoflurane, oxygen, and air. After the surgery, the target concentration was maintained for at least 10 min, and then the LMA was removed. Each target concentration at the time of removal was predetermined by the Dixon up-down method (with 0.1% as a step size) starting at 1.7% end-tidal concentration of sevoflurane. The LMA removal was considered successful when there was no coughing, clenching of teeth, or gross purposeful movements during or within 1 min after removal and also if there was no breath holding, laryngospasm, or desaturation after removal. The end-tidal concentration of sevoflurane to achieve successful LMA removal in 50% of adults was 0.99% +/- 0.09% (mean +/- SD) and in 95% of adults was 1.18% (95% confidence limits, 1.07%-1.79%). In conclusion, we have determined that LMA removal in 50% and 95% of anesthetized adults can be safely accomplished without coughing, moving, or any other airway complications at 0.99% and 1.18% end-tidal concentrations of sevoflurane.
Because the removal of the laryngeal mask airway (LMA) in the anesthetized state is required in some clinical situations, we sought to determine the end-tidal concentration of sevoflurane to safely remove the LMA in anesthetized adults.
七氟醚可使患者平稳、快速地从麻醉状态苏醒,可用于需要在麻醉患者中拔除喉罩气道(LMA)的情况。我们试图确定麻醉成年患者拔除LMA所需的七氟醚最佳呼气末浓度。我们研究了35例年龄在22 - 64岁、ASA身体状况为I或II级、正在接受会阴手术的成年患者。采用硫喷妥钠诱导全身麻醉,然后插入LMA。用七氟醚、氧气和空气维持麻醉。手术结束后,将目标浓度维持至少10分钟,然后拔除LMA。拔除时的每个目标浓度通过Dixon上下法预先确定(步长为0.1%),起始呼气末七氟醚浓度为1.7%。当拔除过程中及拔除后1分钟内无咳嗽、牙关紧闭或明显的有意识动作,且拔除后无屏气、喉痉挛或血氧饱和度下降时,LMA拔除被认为成功。在50%的成年患者中成功拔除LMA的七氟醚呼气末浓度为0.99%±0.09%(平均值±标准差),在95%的成年患者中为1.18%(95%置信区间,1.07% - 1.79%)。总之,我们已经确定,七氟醚呼气末浓度分别为0.99%和1.18%时,50%和95%的麻醉成年患者可以安全地拔除LMA,且无咳嗽、动作或任何其他气道并发症。
由于在某些临床情况下需要在麻醉状态下拔除喉罩气道(LMA),我们试图确定七氟醚的呼气末浓度,以安全地在麻醉成年患者中拔除LMA。