在学龄前儿童进行手术前镇静时使用鼻内雷米马佐拉姆的有效剂量:使用迪克森的上下方法进行了一项剂量确定研究
Ming-Jie Ni1, Yu-Ting Jin2, Qian-Lin Wu1
1Department of Anesthesiology and Perioperative Medicine, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Key Laboratory of Pediatric Anesthesiology, Ministry of Education, Wenzhou Medical University, Key Laboratory of Anesthesiology of Zhejiang Province, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Frontiers in pharmacology
|April 4, 2024
概括
鼻内雷米马佐拉姆在麻醉之前有效地镇静学龄前儿童,显示出迅速发作. 该研究确定了这种有前途的诱导前镇静方法在儿科患者中的有效剂量.
科学领域:
- 麻醉学 麻醉学
- 儿科药理学 儿科药理学
背景情况:
- 幼儿园儿童在麻醉诱导过程中经常经历痛苦.
- 目前的药理方法需要优化,以实现理想的诱导前镇静.
- 鼻内雷米马佐拉姆为儿科患者的诱导前镇静提供了一个潜在的解决方案.
研究的目的:
- 评估效果并确定内鼻式雷米马佐拉姆在学龄前儿童的诱导前镇静的有效剂量.
- 为了评估鼻内雷米马佐拉姆镇静的开始时间和成功率.
主要方法:
- 一项涉及32名接受小手术的学龄前儿童的研究.
- 在利多卡因预治疗后,注射鼻内雷米马佐拉姆.
- 使用密歇根大学镇静分数 (UMSS) 评估镇静.
- 迪克森的上下方法和探针/同位素回归计算ED50和ED95.5.
主要成果:
- 50%的有效剂量 (ED50) 为0.65 mg/kg,而95%的有效剂量 (ED95) 为0.78 mg/kg.
- 在81.2%的参与者中,在6分钟内成功实现了镇静 (UMSS ≥ 1).
- 所有成功服用镇静剂的参与者都在9分钟内达到目标得分.
结论:
- 鼻内雷米马佐拉姆是一种可行的和有效的选择,用于在学龄前儿童的诱导前镇静.
- 这种药物表现出迅速开始起作用.
- 已确定的ED50和ED95值为临床使用提供了指导.
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