Choi Jung Ju, Kim Ji Young, Lee Dongchul, Chang Young Jin, Cho Noo Ree, Kwak Hyun Jeong
Department of Anesthesiology and Pain Medicine, Gachon University, Gil Medical Center, 1198 Guwol-dong, Namdong-gu, Incheon, 405-760, Republic of Korea.
Department of Anesthesiology and Pain Medicine, Anesthesiology and Pain Research Institute, Yonsei University College of Medicine, Seoul, South Korea.
BMC Anesthesiol. 2016 Mar 22;16:20. doi: 10.1186/s12871-016-0186-1.
The pharmacokinetics and pharmacodynamics of an anesthetic drug may be influenced by gender. The purpose of this study was to compare effect-site half maximal effective concentrations (EC50) of propofol in male and female patients during i-gel insertion with dexmedetomidine 0.5 μg/kg without muscle relaxants.
Forty patients, aged 20-46 years of ASA physical status I or II, were allocated to one of two groups by gender (20 patients per group). After the infusion of dexmedetomidine 0.5 μg/kg over 2 min, anesthesia was induced with a pre-determined effect-site concentration of propofol by target controlled infusion. Effect-site EC50 values of propofol for successful i-gel insertion were determined using the modified Dixon's up-and-down method.
Mean effect-site EC50 ± SD of propofol for successful i-gel insertion was significantly higher for men than women (5.46 ± 0.26 μg/ml vs. 3.82 ± 0.34 μg/ml, p < 0.01). The EC50 of propofol in men was approximately 40% higher than in women. Using isotonic regression with a bootstrapping approach, the estimated EC50 (95% confidence interval) of propofol was also higher in men [5.32 (4.45-6.20) μg/ml vs. 3.75 (3.05-4.43) μg/ml]. The estimated EC95 (95% confidence interval) of propofol in men and women were 5.93 (4.72-6.88) μg/ml and 4.52 (3.02-5.70) μg/ml, respectively.
During i-gel insertion with dexmedetomidine 0.5 μg/kg without muscle relaxant, male patients had higher effect-site EC50 for propofol using Schnider's model. Based on the results of this study, patient gender should be considered when determining the optimal dose of propofol during supraglottic airway insertion.
ClinicalTrials.gov identifier: NCT02268656. Registered August 26, 2014.
麻醉药物的药代动力学和药效动力学可能受性别影响。本研究旨在比较在未使用肌肉松弛剂的情况下,给予0.5μg/kg右美托咪定期间,男性和女性患者在插入i-gel喉罩时丙泊酚的效应室半数有效浓度(EC50)。
40例年龄在20 - 46岁、美国麻醉医师协会(ASA)身体状况分级为I或II级的患者,按性别分为两组(每组20例)。在2分钟内输注0.5μg/kg右美托咪定后,通过靶控输注以预定的效应室浓度诱导麻醉。使用改良的Dixon上下法确定丙泊酚用于成功插入i-gel喉罩的效应室EC50值。
成功插入i-gel喉罩时,丙泊酚的平均效应室EC50±标准差在男性中显著高于女性(5.46±0.26μg/ml对3.82±0.34μg/ml,p<0.01)。男性丙泊酚的EC50比女性高约40%。采用自抽样方法进行等渗回归分析,丙泊酚的估计EC50(95%置信区间)在男性中也更高[5.32(4.45 - 6.20)μg/ml对3.75(3.05 - 4.43)μg/ml]。男性和女性丙泊酚的估计EC95(95%置信区间)分别为5.93(4.72 - 6.88)μg/ml和4.52(3.02 - 5.70)μg/ml。
在未使用肌肉松弛剂、给予0.5μg/kg右美托咪定的情况下插入i-gel喉罩时,使用Schnider模型,男性患者丙泊酚的效应室EC50更高。基于本研究结果,在确定声门上气道插入时丙泊酚的最佳剂量时应考虑患者性别。
ClinicalTrials.gov标识符:NCT02268656。于2014年8月26日注册。