Locatelli Bruno G, Ingelmo Pablo M, Emre Sahillioğlu, Meroni Veronica, Minardi Carmelo, Frawley Geoff, Benigni Alberto, Di Marco Salvatore, Spotti Angelica, Busi Ilaria, Sonzogni Valter
1st Service of Anesthesia and Intensive Care, Ospedali Riuniti di Bergamo, Bergamo, Italy.
Paediatr Anaesth. 2013 Apr;23(4):301-8. doi: 10.1111/pan.12038. Epub 2012 Oct 9.
OBJECTIVES/AIM: This randomized control trial was designed to evaluate the incidence of emergence delirium (ED) in preschool children receiving sevoflurane or desflurane anesthesia combined with an effective caudal block.
While ED has been described in children receiving sevoflurane or desflurane anesthesia, a direct comparison between the two agents using a validated ED assessment tool has not been reported previously.
METHODS/MATERIALS: Two hundred and sixty preschool children scheduled for elective sub-umbilical surgery were randomized to receive sevoflurane or desflurane anesthesia combined with a caudal block. ED was defined as a Paediatric Anesthesia Emergence Delirium scale (PAED) ≥ 10 points. A delirium-specific score (ED I) was calculated from the first three items of the PAED score (eye contact, purposeful actions, awareness of the surroundings) and a nonspecific score (ED II) from the last two items on the PAED score (restlessness and inconsolability) to test the hypothesis that some items of the PAED scale may better reflect clinical ED than others.
Thirty-one (25%) children in each group demonstrated ED after awakening with ED being of shorter duration in the desflurane group than the sevoflurane group. An ED I score of nine points had a sensitivity of 0.93 and a specificity of 0.94 for ED. An ED II score of five points had a sensitivity of 0.34 and specificity of 0.95 for ED.
Sevoflurane and desflurane anesthesia were associated with similar incidences of ED in children undergoing sub-umbilical surgery and receiving effective regional anesthesia. High scores on the first three items of the PAED scale were highly correlated with ED. The items restlessness and inconsolability had lower sensitivity for the diagnosis of ED.
本随机对照试验旨在评估接受七氟烷或地氟烷麻醉并联合有效的骶管阻滞的学龄前儿童出现苏醒期谵妄(ED)的发生率。
虽然已有关于接受七氟烷或地氟烷麻醉的儿童出现ED的报道,但此前尚未有使用经过验证的ED评估工具对这两种药物进行直接比较的报道。
方法/材料:260例计划接受择期脐下手术的学龄前儿童被随机分为两组,分别接受七氟烷或地氟烷麻醉并联合骶管阻滞。ED定义为小儿麻醉苏醒期谵妄量表(PAED)评分≥10分。从PAED评分的前三项(眼神接触、有目的的动作、对周围环境的意识)计算出谵妄特异性评分(ED I),从PAED评分的后两项(烦躁不安和无法安抚)计算出非特异性评分(ED II),以检验PAED量表的某些项目可能比其他项目更能反映临床ED的假设。
每组各有31例(25%)儿童在苏醒后出现ED,地氟烷组ED的持续时间短于七氟烷组。ED I评分为9分时,对ED的敏感度为0.93,特异度为0.94。ED II评分为5分时,对ED的敏感度为0.34,特异度为0.95。
在接受脐下手术并接受有效区域麻醉的儿童中,七氟烷和地氟烷麻醉与ED的发生率相似。PAED量表前三项的高分与ED高度相关。烦躁不安和无法安抚这两项对ED诊断的敏感度较低。