Weldon B C, Watcha M F, White P F
Department of Anesthesiology, Washington University School of Medicine, St. Louis, Missouri.
Anesth Analg. 1992 Jul;75(1):51-5. doi: 10.1213/00000539-199207000-00010.
The purpose of this study was to determine the influence of timing and concomitant administration of atropine and/or meperidine on the perioperative effects of oral midazolam in children. In 154 healthy children, 1-8 yr old, we studied six oral preanesthetic medication regimens according to a randomized, double-blind protocol. Group A (placebo) received 5 mL of apple juice. The other five groups received medication with apple juice to a total volume of 5 mL, 20-60 min before induction of anesthesia. Group B received atropine (0.02 mg/kg); group C received midazolam (0.5 mg/kg); group D received midazolam (0.5 mg/kg) and atropine (0.02 mg/kg); group E received meperidine (1.5 mg/kg) and atropine (0.02 mg/kg); and group F received meperidine (1.5 mg/kg), atropine (0.02 mg/kg), and midazolam (0.5 mg/kg). The sedative effect of midazolam was maximal 30 min after oral administration. Ninety-five percent of the children who were separated from their parents within 45 min after oral midazolam administration (with or without atropine) had satisfactory separation scores (vs 66% of those separated after 45 min; P less than 0.02). Midazolam-treated patients were more cooperative with a mask induction of anesthesia compared with non-midazolam-treated children (83% vs 56%). Neither atropine nor meperidine appeared to significantly improve the effectiveness of oral midazolam. No preoperative changes in heart rate, respiratory rate, or hemoglobin oxygen saturation were noted in any of the treatment groups. Finally, oral midazolam did not prolong recovery even after outpatient procedures lasting less than 30 min. In conclusion, midazolam (0.5 mg/kg) given orally 30-45 min before induction of anesthesia is safe and effective without delaying recovery after ambulatory surgery.
本研究的目的是确定阿托品和/或哌替啶的给药时间及联合使用对儿童口服咪达唑仑围手术期效果的影响。在154名1至8岁的健康儿童中,我们按照随机、双盲方案研究了六种口服麻醉前用药方案。A组(安慰剂组)接受5毫升苹果汁。其他五组在麻醉诱导前20至60分钟,用苹果汁冲服药物,总量为5毫升。B组接受阿托品(0.02毫克/千克);C组接受咪达唑仑(0.5毫克/千克);D组接受咪达唑仑(0.5毫克/千克)和阿托品(0.02毫克/千克);E组接受哌替啶(1.5毫克/千克)和阿托品(0.02毫克/千克);F组接受哌替啶(1.5毫克/千克)、阿托品(0.02毫克/千克)和咪达唑仑(0.5毫克/千克)。咪达唑仑的镇静作用在口服后30分钟达到最大。口服咪达唑仑(无论是否联用阿托品)后45分钟内与父母分离的儿童中,95%的分离评分令人满意(而45分钟后分离的儿童中这一比例为66%;P<0.02)。与未接受咪达唑仑治疗的儿童相比,接受咪达唑仑治疗的患者在面罩诱导麻醉时更配合(83%对56%)。阿托品和哌替啶似乎均未显著提高口服咪达唑仑的有效性。各治疗组术前心率、呼吸频率或血红蛋白氧饱和度均无变化。最后,即使是持续时间不到30分钟的门诊手术,口服咪达唑仑也不会延长恢复时间。总之,麻醉诱导前30至45分钟口服咪达唑仑(0.5毫克/千克)是安全有效的,且不会延迟门诊手术后的恢复。