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首页> 外文期刊>Egyptian Journal of Anaesthesia >Comparative study between prophylactic single dose of fentanyl and dexmedetomidine in the management of agitation after sevoflurane anesthesia in children
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Comparative study between prophylactic single dose of fentanyl and dexmedetomidine in the management of agitation after sevoflurane anesthesia in children

机译:预防性单剂量芬太尼和右美托咪定在儿童七氟醚麻醉后控制躁动的比较研究

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Objective The higher incidence of post sevoflurane agitation presents a great dilemma. This controlled study was performed to test the hypothesis that the prophylactic single dose of either dexmedetomidine or fentanyl reduces the incidence of emergence agitation post sevoflurane anesthesia in children. Patients and methods Ninety pediatric patients were scheduled for elective surgical procedures under general anesthesia and caudal block. They were randomized to one of three groups (each one is 30 patients); fentanyl group (1 μg/kg), dexmedetomidine (DEX) group (0.15 μg/kg), and control group. Recovery was assessed by time until eye opening on command, pain was evaluated by the children’s and infants’ postoperative pain scale (CHIPPS) and adequacy of recovery was assessed using a Modified Aldert score. Both were recorded every 15 min. Behavior score was recorded in the pre- and postoperative periods. Main results Patients in control group obtained higher values (9.65 ± 0.34) in the modified Aldert score than patients who received fentanyl (9.58 ± 0.30) and dexmedetomidine (9.37 ± 0.37). There was significant difference between dexmedetomidine and fentanyl groups For pain assessment, patients in control group suffered from pain when measured by CHIPPS (0.93 ± 0.56) more than patients in dexmedetomidine group (0.48 ± 0.45) and fentanyl group (0.13 ± 0.35), with more significant pain in dexmedetomidine group when compared to fentanyl group ( p 0.05). As regard behavior during emergence, there were significant differences between the placebo with 40% agitation and both fentanyl group with 21.4% agitation ( p = 0.002) and dexmedetomidine group with 16.7% agitation ( p = 0.001), while there were no significant differences between fentanyl and dexmedetomidine group. Conclusions Incidence of postoperative agitation in pediatric patients receiving sevoflurane was decreased from 40% with placebo to 16.7% with dexmedetomidine and 21.4% with fentanyl with no significant differences between dexmedetomidine and fentanyl groups.
机译:目的七氟醚后躁动发生率较高,这是一个巨大的难题。进行了这项对照研究以检验以下假说:预防性单剂量右美托咪定或芬太尼可降低儿童七氟醚麻醉后出现躁动的发生率。患者和方法90名儿科患者计划在全身麻醉和尾巴阻滞下进行择期外科手术。他们被随机分为三组之一(每组为30名患者)。芬太尼基(1μg/ kg),右美托咪定(DEX)组(0.15μg/ kg)和对照组。直到命令时睁开眼睛为止的时间评估恢复情况,通过儿童和婴儿的术后疼痛量表(CHIPPS)评估疼痛,​​并使用改良的Aldert评分评估恢复的充分性。两者均每15分钟记录一次。在手术前后记录行为评分。主要结果对照组患者的改良Aldert评分值高于接受芬太尼(9.58±0.30)和右美托咪定(9.37±0.37)的患者(9.65±0.34)。右美托咪定组与芬太尼组之间存在显着差异。对于疼痛评估,对照组患者通过CHIPPS测量的疼痛程度(0.93±0.56)比右美托咪定组(0.48±0.45)和芬太尼组(0.13±0.35)的疼痛程度更大。与芬太尼组相比,右美托咪定组的疼痛更明显(p <0.05)。关于出苗期间的行为,40%搅拌的安慰剂与21.4%搅拌的芬太尼组(p = 0.002)和右美托咪定组搅拌16.7%(p = 0.001)均存在显着差异,而两者之间无显着差异。芬太尼和右美托咪定基团。结论接受七氟醚治疗的小儿术后躁动发生率从使用安慰剂的40%降至使用右美托咪定的16.7%和使用芬太尼的21.4%,右美托咪定和芬太尼组之间无显着差异。

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