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咪达唑仑用于预防在七氟醚麻醉下接受牙科治疗的极度恐惧和不合作儿科患者出现苏醒期躁动的效果,一项双盲随机研究。

The effect of midazolam administration for the prevention of emergence agitation in pediatric patients with extreme fear and non-cooperation undergoing dental treatment under sevoflurane anesthesia, a double-blind, randomized study.

作者信息

Kawai Mari, Kurata Shinji, Sanuki Takuro, Mishima Gaku, Kiriishi Kensuke, Watanabe Toshihiro, Ozaki-Honda Yu, Yoshida Mizuki, Okayasu Ichiro, Ayuse Terumi, Tanoue Naomi, Ayuse Takao

机构信息

Department of Dental Anesthesia, Nagasaki University Hospital, Nagasaki, Japan.

Nagasaki University Institute of Biomedical Sciences, Course of Medical and Dental Sciences, Dental Anesthesiology, Nagasaki, Japan.

出版信息

Drug Des Devel Ther. 2019 May 17;13:1729-1737. doi: 10.2147/DDDT.S198123. eCollection 2019.

Abstract

Sevoflurane is generally the preferred anesthetic agent for general anesthesia in pediatric patients, due to its rapid induction and recovery characteristics. However, it has been recognized that a major complication is emergence agitation when awakening from general anesthesia. The aim of this study was to evaluate the occurrence rate of emergence agitation in the operating room and postoperative recovery area following intraoperative administration of midazolam to pediatric patients under general anesthesia. One hundred and twenty pediatric patients undergoing dental treatment under sevoflurane anesthesia were enrolled in this study. The patients were divided into three groups (n=40 each in the 0.1 mg/kg midazolam, 0.05 mg/kg midazolam, and control with saline groups). Midazolam or saline was injected intravenously approximately 30 minutes before the end of the dental treatment. We used the Richmond Agitation and Sedation Scale (RASS) to assess the level of sedation and drowsiness at emergence phase in the operating room. We also used the Pediatric Anesthesia Emergence Delirium Scale (PAED) to assess the level of agitation and delirium at the full recovery phase from anesthesia in the recovery area. At the emergence phase, the incidence of emergence agitation in the 0.1 mg/kg midazolam group was significantly lower than in the other groups (=0.0010). At the recovery phase, there was no significant difference among the three groups. The odds ratio between PAED score and RASS score was 4.0 using logistic regression analysis. The odds ratio between PAED score and Disability was 2.5. Administration of a single dose of 0.1 mg/kg midazolam dose significantly decreases the incidence of severe emergence agitation at the emergence after sevoflurane anesthesia, but not at the recovery phase. Furthermore, the evaluation of sedative and agitation condition using RASS score at emergence from anesthesia is useful to predict occurrence of agitation in the recovery phase.

摘要

由于七氟醚具有快速诱导和恢复的特性,它通常是小儿患者全身麻醉的首选麻醉剂。然而,人们已经认识到,全身麻醉苏醒时的一个主要并发症是苏醒期躁动。本研究的目的是评估在全身麻醉下向小儿患者术中给予咪达唑仑后,手术室和术后恢复区苏醒期躁动的发生率。本研究纳入了120例接受七氟醚麻醉下牙科治疗的小儿患者。患者被分为三组(咪达唑仑0.1mg/kg组、咪达唑仑0.05mg/kg组和生理盐水对照组,每组n = 40)。在牙科治疗结束前约30分钟静脉注射咪达唑仑或生理盐水。我们使用里士满躁动和镇静量表(RASS)评估手术室苏醒期的镇静和嗜睡程度。我们还使用小儿麻醉苏醒谵妄量表(PAED)评估恢复区麻醉完全恢复阶段的躁动和谵妄程度。在苏醒期,咪达唑仑0.1mg/kg组的苏醒期躁动发生率显著低于其他组(P = 0.0010)。在恢复阶段,三组之间没有显著差异。使用逻辑回归分析,PAED评分与RASS评分之间的优势比为4.0。PAED评分与残疾之间的优势比为2.5。单次给予0.1mg/kg咪达唑仑剂量可显著降低七氟醚麻醉后苏醒时严重苏醒期躁动的发生率,但在恢复阶段则不然。此外,在麻醉苏醒时使用RASS评分评估镇静和躁动情况有助于预测恢复阶段躁动的发生。

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