Ahmed Sheikh Sohail, Unland Tamara, Slaven James E, Nitu Mara E
Department of Pediatrics, Section of Pediatric Critical Care, Pediatric Sedation and Cardiovascular Intensive Care Unit, Riley Hospital for Children at Indiana University Health, Indiana University School of Medicine, 705 Riley Hospital Drive RI 4909 4B, Indianapolis, IN 46202, USA.
Department of Pediatrics, Pediatric Procedural Sedation, Riley Hospital for Children at IU Health North, 11700 N. Meridian Street, Carmel, IN 46032, USA.
Int J Pediatr. 2015;2015:397372. doi: 10.1155/2015/397372. Epub 2015 Jan 29.
Objective. To determine the efficacy and safety of high dose dexmedetomidine as a sole sedative agent for MRI. We report our institution's experience. Design. A retrospective institutional review of dexmedetomidine usage for pediatric MRI over 5.5 years. Protocol included a dexmedetomidine bolus of 2 μg/kg intravenously over ten minutes followed by 1 μg/kg/hr infusion. 544 patients received high dose dexmedetomidine for MRI. A second bolus was used in 103 (18.9%) patients. 117 (21.5%) required additional medications. Efficacy, side effects, and use of additional medicines to complete the MRI were reviewed. Data was analyzed using Student's t-test, Fisher's exact test, and Analysis of Variance (ANOVA). Main Results. Dexmedetomidine infusion was associated with bradycardia (3.9%) and hypotension (18.4%). None of the patients required any intervention. Vital signs were not significantly different among the subgroup of patients receiving one or two boluses of dexmedetomidine or additional medications. Procedure time was significantly shorter in the group receiving only one dexmedetomidine bolus and increased with second bolus or additional medications (P < 0.0001). Discharge time was longer for children experiencing bradycardia (P = 0.0012). Conclusion. High dose Dexmedetomidine was effective in 78.5% of cases; 21.5% of patients required additional medications. Side effects occurred in approximately 25% of cases, resolving spontaneously.
目的。确定高剂量右美托咪定作为磁共振成像(MRI)唯一镇静剂的有效性和安全性。我们报告我们机构的经验。设计。对5.5年期间儿科MRI使用右美托咪定的情况进行回顾性机构审查。方案包括在10分钟内静脉注射2μg/kg右美托咪定推注,随后以1μg/kg/小时的速度输注。544例患者接受高剂量右美托咪定进行MRI检查。103例(18.9%)患者使用了第二次推注。117例(21.5%)患者需要额外用药。对完成MRI检查的有效性、副作用及额外药物的使用情况进行了评估。使用学生t检验、Fisher精确检验和方差分析(ANOVA)对数据进行分析。主要结果。右美托咪定输注与心动过缓(3.9%)和低血压(18.4%)相关。无一例患者需要任何干预。接受一次或两次右美托咪定推注或额外用药的患者亚组之间生命体征无显著差异。仅接受一次右美托咪定推注的组检查时间显著更短,第二次推注或额外用药时检查时间增加(P<0.0001)。发生心动过缓的儿童出院时间更长(P = 0.0012)。结论。高剂量右美托咪定在78.5%的病例中有效;21.5%的患者需要额外用药。约25%的病例出现副作用,且可自行缓解。