首页> 外文期刊>Drug Design, Development and Therapy >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
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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

机译:咪达唑仑预防七氟醚麻醉下极度恐惧和不配合牙科治疗的儿科患者出现躁动的效果,一项双盲,随机研究

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Background: 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. Patients and methods: 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. Results: 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 ( p =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. Conclusion: 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.
机译:背景:七氟醚由于其快速的诱导和恢复特性,通常是儿科患者全身麻醉的首选麻醉剂。但是,已经认识到,从全身麻醉中苏醒后,主要的并发症是出现躁动。这项研究的目的是评估在全麻情况下给小儿患者术中给予咪达唑仑后在手术室和术后恢复区出现躁动的发生率。患者和方法:本研究纳入了120名在七氟醚麻醉下接受牙科治疗的儿科患者。将患者分为三组(0.1 mg / kg咪达唑仑,0.05 mg / kg咪达唑仑和生理盐水对照组各40例)。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)评估手术室出现阶段的镇静和困倦程度。我们还使用了小儿麻醉性Deli妄量表(PAED)来评估恢复区麻醉后完全恢复阶段的躁动和del妄水平。结果:在出苗阶段,咪达唑仑0.1 mg / kg组的出院躁动发生率显着低于其他组(p = 0.0010)。在恢复阶段,三组之间没有显着差异。使用逻辑回归分析,PAED评分和RASS评分之间的优势比为4.0。 PAED得分与残障率的比值为2.5。结论:服用0.1 mg / kg咪达唑仑单剂量显着降低了七氟醚麻醉后出现严重剧烈躁动的发生率,但未恢复到恢复期。此外,麻醉后使用RASS评分对镇静和躁动状况的评估有助于预测恢复期躁动的发生。

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