Sullivan Cornelius A, Egbuta Chinyere, Park Raymond S, Lukovits Karina, Cavanaugh David, Mason Keira P
Department of Anesthesiology, Critical Care and Pain Medicine, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Department of Anesthesiology, Critical Care and Pain Medicine, Boston Children's Hospital, Boston, MA 02115, USA.
J Clin Med. 2020 Jul 30;9(8):2437. doi: 10.3390/jcm9082437.
The exposure of infants and children to volatile anesthetics, such as sevoflurane, has been a topic of concern with respect to the potential risk for long term neurocognitive effects. The primary objective of this study was to determine whether the perioperative utilization of Bispectral Index (BIS) monitoring alters the sevoflurane delivery and exposure to children. This is a prospective randomized trial of two groups of healthy ambulatory day surgery patients (2 to 12 years). The patients in both groups had the BIS applied soon after the induction of general anesthesia, but only the anesthesiologists in the group randomized to BIS visible were able to see the BIS values. All of the patients received general anesthesia with sevoflurane. This study found no difference in the overall exposure to sevoflurane between both groups (mean end-tidal sevoflurane level of 1.8 in both groups, = 084). The duration of time in the recovery room, the time to meet discharge criteria, the Pediatric Agitation Emergence Delirium (PAED) scores and the Face, Legs, Activity, Cry, Consolability (FLACC) scores were not statistically different between the groups. The application and utilization of intraoperative BIS monitoring does not alter the sevoflurane administration nor the discharge readiness nor the recovery profile in healthy ambulatory children.
婴幼儿接触挥发性麻醉剂,如七氟醚,就其对长期神经认知影响的潜在风险而言,一直是一个备受关注的话题。本研究的主要目的是确定围手术期使用脑电双频指数(BIS)监测是否会改变七氟醚的给药情况以及儿童对其的接触程度。这是一项针对两组健康门诊日间手术患者(2至12岁)的前瞻性随机试验。两组患者在全身麻醉诱导后不久均应用了BIS,但只有随机分配到可见BIS组的麻醉医生能够看到BIS值。所有患者均接受七氟醚全身麻醉。本研究发现两组之间七氟醚的总体接触情况无差异(两组的平均呼气末七氟醚水平均为1.8,P = 0.84)。恢复室停留时间、达到出院标准的时间、小儿躁动谵妄(PAED)评分以及面部、腿部、活动、哭闹、安慰(FLACC)评分在两组之间无统计学差异。术中BIS监测的应用和使用不会改变健康门诊儿童的七氟醚给药情况、出院准备情况或恢复情况。