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通过直肠给予咪达唑仑对儿童进行麻醉诱导前准备。

Preinduction of anesthesia in children with rectally administered midazolam.

作者信息

Spear R M, Yaster M, Berkowitz I D, Maxwell L G, Bender K S, Naclerio R, Manolio T A, Nichols D G

机构信息

Children's Hospital of San Diego, California.

出版信息

Anesthesiology. 1991 Apr;74(4):670-4. doi: 10.1097/00000542-199104000-00009.

DOI:10.1097/00000542-199104000-00009
PMID:2008948
Abstract

The authors evaluated the efficacy of rectally administered midazolam for preinduction (i.e., premedication/induction) of anesthesia in 67 pediatric patients, ASA physical status 1 or 2, undergoing a variety of elective surgical procedures. In phase 1, 41 children weighing 12 +/- 3 kg (range 7-20 kg) and 31 +/- 16 months (range 8-67 months) of age (mean +/- SD) received midazolam, 0.4-5.0 mg.kg-1, in an attempt to produce unconsciousness. Only one child lost consciousness (4.5 mg.kg-1). However, at all doses, inhalational induction of anesthesia was facilitated because children were tranquil and calmly separated from their parent(s). There were no clinically significant changes in arterial blood pressure, heart rate, oxyhemoglobin saturation, and end-tidal carbon dioxide concentration, 10 min after drug administration. In phase 2, 26 children weighing 17 +/- 4 kg (range 10-26 kg) and 44 +/- 19 months (range 17-84 months) months of age undergoing tonsil and/or adenoid surgery were studied to determine the optimal sedative dose of rectally administered midazolam. Patients received 0.3, 1.0, 2.0, or 3.0 mg.kg-1 of midazolam in a randomized, double-blind fashion. One third (3 of 9) of patients receiving 0.3 mg.kg-1 struggled during mask induction. All patients receiving greater than or equal to 1.0 mg.kg-1 were adequately sedated (P less than 0.008). Discharge from the postanesthesia care unit (PACU), however, was delayed (greater than 60 min) in children receiving greater than or equal to 2.0 mg.kg-1 (P less than 0.03).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

作者评估了直肠给予咪达唑仑用于67例ASA身体状况为1或2级、正在接受各种择期外科手术的儿科患者麻醉诱导前(即术前用药/诱导)的效果。在第一阶段,41名年龄为31±16个月(范围8 - 67个月)、体重12±3 kg(范围7 - 20 kg)(均值±标准差)的儿童接受了0.4 - 5.0 mg·kg⁻¹的咪达唑仑,试图使其失去意识。只有一名儿童失去意识(4.5 mg·kg⁻¹)。然而,在所有剂量下,由于儿童安静且能平静地与父母分开,吸入麻醉诱导变得更容易。给药10分钟后,动脉血压、心率、氧合血红蛋白饱和度和呼气末二氧化碳浓度均无临床显著变化。在第二阶段,对26名年龄为44±19个月(范围17 - 84个月)、体重17±4 kg(范围10 - 26 kg)、正在接受扁桃体和/或腺样体手术的儿童进行研究,以确定直肠给予咪达唑仑的最佳镇静剂量。患者以随机、双盲方式接受0.3、1.0、2.0或3.0 mg·kg⁻¹的咪达唑仑。接受0.3 mg·kg⁻¹的患者中有三分之一(9例中的3例)在面罩诱导期间挣扎。所有接受大于或等于1.0 mg·kg⁻¹的患者均得到充分镇静(P<0.008)。然而,接受大于或等于2.0 mg·kg⁻¹的儿童从麻醉后恢复室(PACU)出院延迟(大于60分钟)(P<0.03)。(摘要截短至250字)

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