Effect of intravenous lidocaine on the ED50 of propofol induction dose in elderly patients undergoing painless gastroscopy: a prospective, randomized, double-blinded, controlled study

IF 2 3区 医学 Q2 ANESTHESIOLOGY Perioperative Medicine Pub Date : 2024-03-05 DOI:10.1186/s13741-024-00370-2
Lili Tang, Wenhui Lv, Jingjing Sun, Lijian Chen
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Abstract

Intravenous lidocaine could be a potential alternative adjuvant to propofol-based sedation for gastroscopy in elderly patients. This study aimed to evaluate the effect of intravenous lidocaine on the median effective dose (ED50) of propofol induction dose in elderly patients undergoing painless gastroscopy. The study included 70 patients aged ≥ 60 years undergoing painless gastroscopy with 64 randomly assigned to either group L (2% lidocaine 1.5 mg/kg, n = 31) or group N (equal volume normal saline, n = 33). All patients received propofol induction following 0.1 μg/kg intravenous sufentanil. The Dixon “up-and-down” sequential method was used, with a 1.5 mg/kg initial induction dose of propofol followed by a 0.1 mg/kg sequential variable dose. The primary endpoint was the ED50 of the propofol induction dose. The total propofol dose, recovery time, adverse events, and local anesthetic intoxication reactions were also recorded. The ED50 of propofol induction dose was 0.670 (95% confidence interval [CI] 0.216–0.827) mg/kg in group L and 1.118 (95% CI 0.803–1.232) mg/kg in group N. There was a statistically significant difference between the two groups (p < 0.001). The incidence of hypotension and propofol injection pain were lower in group L than in group N (p < 0.05). Furthermore, the orientation recovery time in group L was shorter compared to group N (p < 0.05). None of the participants in group L observed local anesthetic intoxication reactions after receiving lidocaine. The administration of intravenous lidocaine to elderly patients undergoing painless gastroscopy resulted in a significant 40% reduction in the ED50 of propofol induction dose, which may be related to the decreased incidence of hypotension and injection pain, as well as the improved post-gastroscopy orientation recovery. ChiCTR, ChiCTR2200065530. Registered on 08 November 2022.
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静脉注射利多卡因对接受无痛胃镜检查的老年患者异丙酚诱导剂量 ED50 的影响:一项前瞻性、随机、双盲对照研究
静脉注射利多卡因可能是老年患者接受胃镜检查时使用异丙酚镇静剂的潜在替代辅助药物。本研究旨在评估静脉注射利多卡因对接受无痛胃镜检查的老年患者异丙酚诱导剂量中位有效剂量(ED50)的影响。研究纳入了70名年龄≥60岁接受无痛胃镜检查的患者,其中64人被随机分配到L组(2%利多卡因1.5 mg/kg,n = 31)或N组(等体积生理盐水,n = 33)。所有患者在接受异丙酚诱导后,静脉注射 0.1 μg/kg 舒芬太尼。采用的是迪克森 "上下 "顺序法,初始异丙酚诱导剂量为 1.5 毫克/千克,然后是 0.1 毫克/千克的顺序可变剂量。主要终点是异丙酚诱导剂量的 ED50。此外,还记录了异丙酚的总剂量、恢复时间、不良反应和局麻药中毒反应。L 组的异丙酚诱导剂量 ED50 为 0.670(95% 置信区间 [CI] 0.216-0.827)毫克/公斤,N 组为 1.118(95% 置信区间 [CI] 0.803-1.232)毫克/公斤。L 组低血压和异丙酚注射疼痛的发生率低于 N 组(P < 0.05)。此外,与 N 组相比,L 组的定向恢复时间更短(P < 0.05)。L 组的参与者在接受利多卡因注射后均没有出现局麻药中毒反应。给接受无痛胃镜检查的老年患者静脉注射利多卡因可使异丙酚诱导剂量的ED50显著降低40%,这可能与低血压和注射疼痛发生率降低以及胃镜检查后定向力恢复改善有关。ChiCTR,ChiCTR2200065530。注册日期:2022年11月8日。
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3.80%
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审稿时长
10 weeks
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