Dexmedetomidine reduced the severity of emergence delirium and respiratory complications, but increased intraoperative hypotension in children underwent tonsillectomy: a retrospective analysis.

IF 1 Q3 PEDIATRICS Minerva Pediatrics Pub Date : 2024-10-01 Epub Date: 2021-09-13 DOI:10.23736/S2724-5276.21.06330-8
Alessandro Simonini, Etrusca Brogi, Giorgio Conti, Alessandro Vittori, Marco Cascella, Maria G Calevo
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Abstract

Background: Intraoperative dexmedetomidine can be useful for its sedative and analgesic sparing effects, and for the prevention of emergence delirium. Conversely, it can cause hypotension and bradycardia. The aim of this study was to assess the safety and efficacy of dexmedetomidine in pediatric anesthesia.

Methods: This is a retrospective cohort study in children who received intravenous dexmedetomidine (Dex group) or opioids (No-Dex group) during general anesthesia for tonsillectomy, between November 2014 and November 2016. From the medical records, data on the intraoperative phase (hemodynamic adverse events, respiratory failure at the emergence, awakening and extubation times, emergence delirium), recovery room (pain, hemodynamic parameters, and desaturation), and ward stay (pain, and nausea and vomiting) were investigated. Time of hospital discharge was calculated.

Results: Three hundred twenty-eight (Dex group 183; No-Dex group 145) children ranging from 1.5 to 10 years were included. The percentage of intraoperative hypotension was significantly higher in the Dex group (P=0.01). The extubation times were significantly higher in No-Dex group (P=0.0001), although the awakening times were significantly longer with dexmedetomidine (P=0.0001). Desaturation episodes were higher in the Dex group (P=0.0001). The incidence of emergence delirium was similar in the two groups, but of greater intensity in the No-Dex group. While in the immediate postoperative period there was no difference in pain, after 24 hours, the incidence of pain and vomiting was significantly higher (P=0.003; P=0.0001) in the No-Dex group.

Conclusions: Although several outcome parameters showed important advantages of dexmedetomidine over opioid-based regimens in terms of safety and efficacy, issues such as the increased intraoperative hypotension, indicated that it is not possible to draw any definitive conclusions.

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右美托咪定可降低扁桃体切除术患儿术后谵妄和呼吸系统并发症的严重程度,但会增加术中低血压。回顾性分析。
背景:术中使用右美托咪定可以起到镇静和镇痛的作用,还可以预防术后谵妄。相反,它可能会导致低血压和心动过缓。本研究旨在评估右美托咪定在小儿麻醉中的安全性和有效性:这是一项回顾性队列研究,研究对象是2014年11月至2016年11月期间在扁桃体切除术全身麻醉中接受静脉注射右美托咪定(右美托咪定组)或阿片类药物(无右美托咪定组)的儿童。从病历中调查了术中阶段(血流动力学不良事件、苏醒时呼吸衰竭、苏醒和拔管时间、苏醒谵妄)、恢复室(疼痛、血流动力学参数和饱和度降低)和病房留观(疼痛、恶心和呕吐)的数据。计算出院时间:共纳入 328 名(地塞米松组 183 名;无地塞米松组 145 名)1.5 至 10 岁的儿童。地塞米松组术中出现低血压的比例明显更高(P=0.01)。尽管右美托咪定的唤醒时间明显更长(p= 0.0001),但无右旋咪定组的拔管时间明显更长(p= 0.0001)。右美托咪定组的饱和度降低率更高(p=0.0001)。两组术后谵妄发生率相似,但无右旋美托咪定组的谵妄发生率更高。虽然在术后初期疼痛没有差异,但在24小时后,无地塞米松组的疼痛和呕吐发生率明显更高(P=0.003;P=0.0001):尽管多项结果参数显示右美托咪定在安全性和有效性方面比阿片类药物治疗方案更具优势,但术中低血压增加等问题表明目前还无法得出任何明确的结论。
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