A comparison of sevoflurane with halothane in outpatient adenotomy in children with mild upper respiratory tract infections

被引:19
作者
Rieger, A
Schroter, G
Philippi, W
Hass, I
Eyrich, K
机构
[1] Dept. Anesth. Oper. Intensive C., Benjamin Franklin Medical Center, Free University of Berlin, Berlin
[2] Dept. Anesth. Oper. Intensive C., Benjamin Franklin Medical Center, Free University of Berlin, 12200 Berlin
关键词
airway infections; pediatric; anesthesia; induction; recovery; halothane; pediatrics; sevoflurane; surgery; outpatient;
D O I
10.1016/0952-8180(95)00227-8
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Study Objective: To investigate the efficacy and safety of sevoflurane compared with halothane in pediatric outpatient ear-nose-throat (ENT) surgery during the induction, maintenance emergence, and recovery of anesthesia. Design: Prospective, randomized, comparative, open-label study. Setting: ENT operating room and postoperative recovery room at a university medical center. Patients: 41 ASA status I and II children between the ages of 2 to 10 years, with mild upper respiratory tract infection (URI). Interventions: Induction and maintenance of anesthesia with either sevoflurane or halothane for outpatient adenotomy, otomicroscopy, and myringotomy. Measurements and Main Results: Induction (mean +/- SEM) was significantly shorter the sevoflurane group (2.6 +/- 0.2 minutes) than in the halothane group (3.2 +/- 0.2 minutes). There was no difference between the two groups with regard to complications that occurred during the induction and maintenance period. The time to emergence and recovery was significantly shorter with sevoflurane than with halothane (means +/- SEM; time to extubation 9.9 +/- 0.98 minutes vs. 13.4 +/- 1.06 minutes, time to eye opening 12.9 +/- 1.6 minutes vs. 24.5 +/- 1.8 minutes, command response time 20.7 +/- 2.5 minutes vs. 36.4 +/- 2.8 minutes). No difference in the incidence of complications during emergence and recovery was found. Evaluation of recovery as assessed by a modified Aldrete score showed that children who had received sevoflurane reached higher scores in the first 30 minutes following the discontinuation of the anesthetic. The Pain/Discomfort Scale demonstrated a difference in the sevoflurane group, with more children being agitated and restless. Conclusion: Sevoflurane provides a safe and rapid anesthetic induction with no differences in complications during the induction, maintenance, and emergence period. With sevoflurane, the time of emergence and recovery was significantly shorter. The characteristics of sevoflurane as evaluated in the present study make it a suitable anesthetic in pediatric outpatient surgery even in the presence of mile URI.
引用
收藏
页码:188 / 193
页数:6
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