Kim Kyung-Mi, Lee Ki-Hwa, Park Jae-Hong
Department of Anesthesiology and Pain Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea.
Department of Anesthesiology and Pain Medicine, Haeundae Paik Hospital, Inje University School of Medicine, Busan 47392, Korea.
Medicina (Kaunas). 2021 Sep 28;57(10):1034. doi: 10.3390/medicina57101034.
: Phase lag entropy, an electroencephalographic monitor, evaluates the variety in temporal patterns of phase relationship between frontal and prefrontal brain region. Phase lag entropy can reflect the depth of anesthesia induced by propofol, but the association between sevoflurane and phase lag entropy has not been elucidated. This study examined the effect of sevoflurane on phase lag entropy during induction of general anesthesia. We also explored the pharmacodynamic model between end-tidal anesthetic concentration and electroencephalographic monitor. : A total of 20 patients were enrolled. General anesthesia was produced by escalating the sevoflurane (1 vol% up to 8 vol%). The relationship between phase lag entropy and end-tidal anesthetic concentration was analyzed. A non-linear mixed-effects model was used to get the relationship of pharmacodynamics between the end-tidal sevoflurane concentration and phase lag entropy. Mean blood pressure, heart rate, and the modified observer's assessment of alertness/sedation scale were also recorded during sevoflurane anesthesia. : As level of sedation increased, phase lag entropy decreased. A significant correlation was showed between phase lag entropy and end-tidal sevoflurane concentration (r = -0.759, < 0.001). The correlation coefficient between the modified observer's assessment of alertness/sedation scale and phase lag entropy was 0.731 ( < 0.001). The pharmacodynamic factors assessed by the sigmoid model were = 84.9, = 42, = 1.81, γ = 4.78, and = 0.692. The prediction probability of phase-lag entropy for measuring the modified observer's assessment of alertness/sedation scale and end-tidal sevoflurane concentration were 0.764 and 0.789, respectively. With the increasing concentration of sevoflurane, mean blood pressure decreased, but heart rate did not change. : The continuing escalation in end-tidal sevoflurane concentration caused a decline in phase lag entropy. Phase lag entropy can serve as an indicator of hypnotic depth in patients receiving sevoflurane anesthesia.
相位滞后熵是一种脑电图监测指标,用于评估额叶和前额叶脑区之间相位关系的时间模式变化。相位滞后熵可反映丙泊酚诱导的麻醉深度,但七氟醚与相位滞后熵之间的关系尚未阐明。本研究探讨了七氟醚在全身麻醉诱导过程中对相位滞后熵的影响。我们还探索了呼气末麻醉药浓度与脑电图监测指标之间的药效学模型。
共纳入20例患者。通过逐步增加七氟醚浓度(从1%到8%)来实施全身麻醉。分析了相位滞后熵与呼气末麻醉药浓度之间的关系。采用非线性混合效应模型来获取呼气末七氟醚浓度与相位滞后熵之间的药效学关系。在七氟醚麻醉期间还记录了平均血压、心率以及改良的警觉/镇静评分。
随着镇静程度的增加,相位滞后熵降低。相位滞后熵与呼气末七氟醚浓度之间存在显著相关性(r = -0.759,P < 0.001)。改良的警觉/镇静评分与相位滞后熵之间的相关系数为0.731(P < 0.001)。用Sigmoid模型评估的药效学参数为:EC50 = 84.9,γ = 42,γinf = ∞,γ1 = 1.81,γ2 = 4.78,S = 0.692。相位滞后熵用于测量改良的警觉/镇静评分和呼气末七氟醚浓度的预测概率分别为0.764和0.789。随着七氟醚浓度的增加,平均血压下降,但心率未改变。
呼气末七氟醚浓度的持续升高导致相位滞后熵下降。相位滞后熵可作为接受七氟醚麻醉患者催眠深度的指标。