Patel D K, Keeling P A, Newman G B, Radford P
Queen Mary's Hospital for Children, Carshalton, Surrey.
Anaesthesia. 1988 Nov;43(11):949-52. doi: 10.1111/j.1365-2044.1988.tb05659.x.
In a study of 144 children aged 1-12 years, attempts were made to assess the ED50 and ED90 of the intravenous induction agent, propofol. The doses required for loss of eyelash reflex and tolerance of facemask, in 50% of unpremedicated children, were 1.6 mg/kg and 2.5 mg/kg respectively. In children premedicated with oral trimeprazine the corresponding values of ED50 were 1.1 mg/kg and 2.0 mg/kg. Doses of 2.8 mg/kg in unpremedicated and 2.0 mg/kg for those who received trimeprazine were required for loss of eyelash reflex in 90% of children. This probably corresponds to an effective induction dose. Pain and movement on induction were common; the incidence was 27% and 21.5% respectively.
在一项针对144名1至12岁儿童的研究中,研究人员尝试评估静脉诱导剂丙泊酚的半数有效剂量(ED50)和90%有效剂量(ED90)。对于50%未使用术前药的儿童,睫毛反射消失和能耐受面罩所需的剂量分别为1.6毫克/千克和2.5毫克/千克。对于术前口服三甲丙嗪的儿童,ED50的相应值分别为1.1毫克/千克和2.0毫克/千克。对于90%的儿童,未使用术前药的儿童睫毛反射消失所需剂量为2.8毫克/千克,接受三甲丙嗪的儿童为2.0毫克/千克。这可能对应于有效的诱导剂量。诱导时疼痛和肢体活动很常见;发生率分别为27%和21.5%。