右美托咪定输注与芬太尼对腺扁桃体切除术儿童镇痛和预防出现性躁动和谵妄的影响

S. Elfawal, Abeer M. Eldeek, M. Kamal
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The patients were randomly assigned to two groups: group D (dexmedetomidine infusion group; 35 patients) received intravenous dexmedetomidine (2 μg/kg) over 10 min, followed by 0.7 μg/kg/h until 5 min before the end of the surgery, and group F (intravenous fentanyl group; 35 patients) received intravenous fentanyl 1 μg/kg as a bolus. No premedication was given to any of the patients. The number of patients in each group who needed intraoperative fentanyl, the fentanyl dose, time of administration of fentanyl, duration of surgery and anesthesia, and the time to awakening were recorded. Pain was evaluated using the objective pain scale score in the postanesthesia care unit (PACU), which was managed with rescue intravenous pethidine. Emergence agitation was evaluated in the PACU using two scales: the Pediatric Anesthesia Emergence Delirium scale and the five-point agitation scale described by Cole. 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引用次数: 2

摘要

本随机对照研究旨在评估术中输注右美托咪定是否可以安全有效地替代芬太尼,以及是否可以有效降低儿童腺扁桃体切除术后出现的焦虑和谵妄的发生率和严重程度。患者和方法本研究纳入70例年龄为3-7岁,男女均为ASA I型和II型患儿,计划择期行腺扁桃体切除术。患者随机分为两组:D组(右美托咪定输注组;35例患者)术后10 min静脉注射右美托咪定(2 μg/kg),术后5 min静脉注射0.7 μg/kg/h, F组(芬太尼静脉注射组;35例患者)静脉注射芬太尼1 μg/kg。所有的病人都没有预先用药。记录各组术中需要芬太尼的患者人数、芬太尼剂量、芬太尼给药时间、手术麻醉时间、苏醒时间。在麻醉后护理单位(PACU)使用客观疼痛量表评分评估疼痛,并给予急救静脉注射哌替啶。在PACU中使用两种量表来评估出现时的躁动:儿科麻醉出现时谵妄量表和Cole描述的5分躁动量表。结果D组苏醒时间明显短于F组(P<0.05)。与F组相比,D组到达PACU时最大客观疼痛评分、小儿麻醉出现谵妄评分和出现躁动评分均有统计学意义显著降低。两组术前心率差异无统计学意义,但诱导后D组心率明显低于F组(P<0.05)。两组患者术后24小时内均未见不良反应。结论右美托咪定是术中芬太尼安全有效的镇痛替代品,可降低术后镇痛需求。它也有效地降低发生率和严重程度出现躁动和谵妄的儿童接受腺扁桃体切除术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dexmedetomidine infusion versus fentanyl for analgesia and prevention of emergence agitation and delirium in children undergoing adenotonsillectomy
Background This randomized controlled study aimed to evaluate whether an intraoperative infusion of dexmedetomidine would be a safe and effective substitute to fentanyl intraoperatively, and whether it would be effective in reducing the incidence and severity of emergence agitation and delirium in children undergoing adenotonsillectomy. Patients and methods This study was conducted on 70 pediatric patients, aged 3–7 years, of both sexes, of ASA I and II, who were scheduled for elective adenotonsillectomy. The patients were randomly assigned to two groups: group D (dexmedetomidine infusion group; 35 patients) received intravenous dexmedetomidine (2 μg/kg) over 10 min, followed by 0.7 μg/kg/h until 5 min before the end of the surgery, and group F (intravenous fentanyl group; 35 patients) received intravenous fentanyl 1 μg/kg as a bolus. No premedication was given to any of the patients. The number of patients in each group who needed intraoperative fentanyl, the fentanyl dose, time of administration of fentanyl, duration of surgery and anesthesia, and the time to awakening were recorded. Pain was evaluated using the objective pain scale score in the postanesthesia care unit (PACU), which was managed with rescue intravenous pethidine. Emergence agitation was evaluated in the PACU using two scales: the Pediatric Anesthesia Emergence Delirium scale and the five-point agitation scale described by Cole. Results The time to awakening in group D was significantly shorter compared with that in group F (P<0.05). Group D showed a statistically significantly lower maximum objective pain scale score, lower Pediatric Anesthesia Emergence Delirium score, and lower emergence agitation score compared with group F at arrival at the PACU. There was no statistically significant difference between the two groups as regards preoperative heart rate, but there was significantly lower heart rate in group D than in group F after induction (P<0.05). No side effects were observed during the first 24 h postoperatively in the two groups. Conclusion Dexmedetomidine is a safe and effective analgesic substitute to fentanyl intraoperatively and reduces analgesic requirements postoperatively. It is also effective in reducing the incidence and severity of emergence agitation and delirium in children undergoing adenotonsillectomy.
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