Oh Ju-Yeon, Park Sung-Yong, Moon Jung-Yoon, Park Ji-Hyun, Joe Han-Bum
Department of Anesthesiology and Pain Medicine, Ajou University School of Medicine, Suwon 16499, Republic of Korea.
Office of Biostatistics, Medical Research Collaborating Center, Ajou Research Institute for Innovative Medicine, Ajou University Medical Center, Suwon 16499, Republic of Korea.
J Clin Med. 2024 Jan 24;13(3):670. doi: 10.3390/jcm13030670.
The physiological and pharmacological variations between men and women are known to influence drug efficacy. The objective of this study was to determine the 50% and 95% effective doses (ED and ED) of remimazolam required for i-gel supraglottic airway (ISA) insertion under remifentanil infusion without neuromuscular blocking agents (NMBAs) in both males and females. Patients aged 19-65 years, scheduled for general anesthesia using ISA, were enrolled in this study. Patients were divided into two groups based on their sex. The anesthesia process began with a remifentanil infusion targeting an effect-site concentration of 3.0 ng/mL, accompanied by a remimazolam injection. The initial remimazolam dose was 0.25 mg/kg, and it was adjusted with a step size of 0.05 mg/kg based on the outcome of ISA insertion in the preceding patient. The ED of remimazolam (mean ± standard error) was 0.28 ± 0.02 mg/kg in the male group and 0.18 ± 0.02 mg/kg in the female group ( < 0.001). Additionally, ED, which was calculated using the isotonic regression method, was significantly comparable between the male and female groups (male: 0.35 mg/kg, 95% confidence interval [CI] = 0.34-0.35; female: 0.29 mg/kg, 95% CI = 0.25-0.30). This study showed that both the ED and the ED of remimazolam for successful ISA insertion was higher for men than that for women. Therefore, while using remimazolam alongside remifentanil infusion without NMBAs for ISA insertion, one should consider the patient's sex for appropriate dosing.
已知男性和女性之间的生理及药理差异会影响药物疗效。本研究的目的是确定在输注瑞芬太尼且无神经肌肉阻滞剂(NMBA)的情况下,男性和女性患者使用i-gel喉罩气道(ISA)时所需的瑞马唑仑50%和95%有效剂量(ED50和ED95)。本研究纳入了年龄在19至65岁、计划使用ISA进行全身麻醉的患者。根据性别将患者分为两组。麻醉过程开始时输注瑞芬太尼,目标效应室浓度为3.0 ng/mL,同时注射瑞马唑仑。瑞马唑仑初始剂量为0.25 mg/kg,并根据前一位患者ISA插入的结果以0.05 mg/kg的步长进行调整。瑞马唑仑的ED50(均值±标准误)在男性组中为0.28±0.02 mg/kg,在女性组中为0.18±0.02 mg/kg(P<0.001)。此外,使用等渗回归法计算的ED95在男性和女性组之间具有显著可比性(男性:0.35 mg/kg,95%置信区间[CI]=0.34 - 0.35;女性:0.29 mg/kg,95% CI = 0.25 - 0.30)。本研究表明,成功插入ISA时瑞马唑仑的ED50和ED95在男性中均高于女性。因此,在不使用NMBA的情况下,将瑞马唑仑与瑞芬太尼输注联合用于ISA插入时,应考虑患者性别以进行适当给药。