Department of Pediatrics, Internal Medicine, Epidemiology and Biostatistics, Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada.
Department of Pediatrics, BC Children's Hospital, University of British Columbia, Vancouver, British Columbia, Canada.
Ann Emerg Med. 2023 Aug;82(2):179-190. doi: 10.1016/j.annemergmed.2023.01.023. Epub 2023 Mar 3.
To determine the optimal sedative dose of intranasal dexmedetomidine for children undergoing laceration repair.
This dose-ranging study employing the Bayesian Continual Reassessment Method enrolled children aged 0 to 10 years with a single laceration (<5 cm), requiring single-layer closure, who received topical anesthetic. Children were administered 1, 2, 3, or 4 mcg/kg intranasal dexmedetomidine. The primary outcome was the proportion with adequate sedation (Pediatric Sedation State Scale score of 2 or 3 for ≥90% of the time from sterile preparation to tying of the last suture). Secondary outcomes included the Observational Scale of Behavior Distress-Revised (range: 0 [no distress] to 23.5 [maximal distress]), postprocedure length of stay, and adverse events.
We enrolled 55 children (35/55 [64%] males; median [interquartile range {IQR}] age 4 [2, 6] years). At 1, 2, 3, and 4 mcg/kg intranasal dexmedetomidine, respectively, the proportion of participants "adequately" sedated was 1/3 (33%), 2/9 (22%), 13/21 (62%), and 12/21 (57%); the posterior mean (95% equitailed credible intervals) for the probability of adequate sedation was 0.38 (0.04, 0.82), 0.25 (0.05, 0.54), 0.61 (0.41, 0.80), and 0.57 (0.36, 0.76); the median (IQR) Observational Scale of Behavior Distress-Revised scores during suturing was 2.7 (0.3, 3), 0 (0, 3.8), 0.6 (0, 5), and 0 (0, 3.7); the median (IQR) postprocedure length of stay was 67 (60, 78), 76 (60, 100), 89 (76, 109), and 113 (76, 150) minutes. There was 1 adverse event, a decrease in oxygen saturation at 4 mcg/kg, which resolved with head repositioning.
Despite limitations, such as our limited sample size and subjectivity in Pediatric Sedation State Scale scoring, sedation efficacy for 3 and 4 mcg/kg were similarly based on equitailed credible intervals suggesting either could be considered optimal.
确定经鼻给予右美托咪定用于儿童裂伤修复术的最佳镇静剂量。
本剂量范围研究采用贝叶斯连续再评估法,纳入年龄 0 至 10 岁、有单个裂伤(<5cm)、需要单层缝合、接受局部麻醉的儿童。儿童接受 1、2、3 或 4μg/kg 经鼻给予右美托咪定。主要结局是 90%以上时间(从无菌准备到最后缝线打结)镇静评分达到 2 或 3(小儿镇静状态评分)的患儿比例。次要结局包括改良观察行为困扰评分(范围:0 [无困扰]至 23.5 [最大困扰])、术后留观时间和不良事件。
共纳入 55 例患儿(35/55 [64%]为男性;中位[四分位间距 {IQR}]年龄 4[2,6]岁)。在 1、2、3 和 4μg/kg 经鼻给予右美托咪定后,分别有 1/3(33%)、2/9(22%)、13/21(62%)和 12/21(57%)的患儿“充分”镇静;充分镇静概率的后验均值(95%相等可信区间)分别为 0.38(0.04,0.82)、0.25(0.05,0.54)、0.61(0.41,0.80)和 0.57(0.36,0.76);缝皮期间改良观察行为困扰评分的中位数(IQR)分别为 2.7(0.3,3)、0(0,3.8)、0.6(0,5)和 0(0,3.7);术后留观时间的中位数(IQR)分别为 67(60,78)、76(60,100)、89(76,109)和 113(76,150)分钟。发生 1 例不良事件,4μg/kg 时出现氧饱和度下降,经头部重新定位后缓解。
尽管存在一些局限性,如样本量有限和小儿镇静状态评分的主观性,但 3 和 4μg/kg 右美托咪定的镇静效果基于相等可信区间相似,这表明两者都可被视为最佳剂量。