Mason Keira P, Zgleszewski Steven E, Dearden Jennifer L, Dumont Raymond S, Pirich Michele A, Stark Cynthia D, D'Angelo Peggy, Macpherson Shann, Fontaine Paulette J, Connor Linda, Zurakowski David
Department of Anesthesia, Children's Hospital Boston and Harvard Medical School, 300 Longwood Avenue, Boston, Massachusetts 02115, USA.
Anesth Analg. 2006 Jul;103(1):57-62, table of contents. doi: 10.1213/01.ane.0000216293.16613.15.
Dexmedetomidine is a sedative with limited experience in the pediatric population. This is the first study that prospectively evaluates the sedation profile of a dexmedetomidine pilot program for pediatric sedation for radiological imaging studies. In March 2005, our hospital sedation committee approved the replacement of IV pentobarbital with dexmedetomidine as the standard of care for CT imaging. Detailed Quality Assurance (QA) data sheets collect relevant information on each patient, which is then logged into a computerized sedation database. After IRB approval, all QA data was accessed. Sixty-two patients with a mean age of 2.8 years (SD = 1.8, range 0.5-9.7) received IV (IV) dexmedetomidine administered as a 2 mcg/kg loading dose over 10 minutes, followed by repeat boluses of 2 mcg/kg over 10 minutes until target of Ramsay Sedation Score 4 (RSS) achieved. Patients were then maintained on 1 mcg/kg/hr infusion until imaging is completed. Repeated-measures ANOVA indicated that compared to pre-sedation values, the heart rate and mean arterial blood pressure decreased an average of 15% during bolus, infusion and recovery (P < 0.01). No significant changes were observed in respiratory rate or end-tidal CO2. Mean recovery time was 32 +/- 18 minutes. Based on our pilot results, dexmedetomidine may provide a reliable and effective method of providing sedation.
右美托咪定是一种在儿科人群中应用经验有限的镇静剂。这是第一项前瞻性评估右美托咪定用于儿科放射影像学检查镇静试验项目镇静情况的研究。2005年3月,我院镇静委员会批准用右美托咪定替代静脉注射戊巴比妥作为CT成像的标准护理药物。详细的质量保证(QA)数据表收集每位患者的相关信息,然后记录到计算机化的镇静数据库中。经机构审查委员会(IRB)批准后,获取了所有QA数据。62名平均年龄为2.8岁(标准差=1.8,范围0.5 - 9.7岁)的患者接受静脉注射(IV)右美托咪定,以2 mcg/kg的负荷剂量在10分钟内给药,随后在10分钟内重复推注2 mcg/kg,直至达到拉姆齐镇静评分4分(RSS)的目标。然后患者以1 mcg/kg/小时的速度持续输注,直至成像完成。重复测量方差分析表明,与镇静前的值相比,在推注、输注和恢复过程中心率和平均动脉血压平均下降了15%(P < 0.01)。呼吸频率或呼气末二氧化碳未观察到显著变化。平均恢复时间为32±18分钟。根据我们的试验结果,右美托咪定可能提供一种可靠且有效的镇静方法。