Division of Paediatric Emergency Medicine, Department of Paediatrics, Western University, London, ON, Canada.
Department of Epidemiology & Biostatistics, Western University, London, ON, Canada.
CJEM. 2024 Sep;26(9):658-670. doi: 10.1007/s43678-024-00731-2. Epub 2024 Aug 28.
Intranasal (IN) midazolam is the most common anxiolytic for children in the emergency department (ED), but evidence of benefit is conflicting. We synthesized the evidence on IN midazolam for procedural distress in children undergoing ED painful procedures.
We included trials involving painful ED procedures in children 0-18 years involving IN midazolam. Primary outcome was procedural distress. We summarized results using Tricco et al.'s classification of "neutral" (p ≥ 0.05), "favorable," and "unfavorable" (p < 0.05), supporting IN midazolam or comparator, respectively, or "indeterminate" (unable to judge). Where possible, we pooled results using meta-analysis. Methodologic quality of evidence was evaluated using Cochrane Collaboration's risk of bias tool and GRADE system.
We included 41 trials (n = 2973 participants). Thirty trials involved intravenous insertion. IN midazolam was superior to placebo (RR = 7.2; 95% CI: 3.43, 15.25; 3 trials; I = 0%). However, 56-90% of the IN midazolam group resisted the procedure. Focusing on the three trials that used validated measures, IN midazolam was "neutral" versus IN ketamine and either "neutral" or "unfavorable" versus IN dexmedetomidine. There was no difference in the proportion of children with a satisfactory distress score between IN midazolam and oral midazolam (RR = 1.1; 95% CI: 0.74, 1.73; 2 trials; I = 53%), IN ketamine (RR = 1.1; 95% CI: 0.91, 1.25; 6 trials; I = 0%), or IN dexmedetomidine (RR = 0.4; 95% CI: 0.17, 1.05; 3 trials; I = 84%). Ten trials involved laceration repair. IN midazolam was "favorable" versus placebo; however, both groups scored in the anxious range. There was no difference in distress between IN midazolam and oral midazolam (SMD = 0.01; 95% CI:-0.32, 0.34; 2 trials; I = 0%) (Fig. 3E) [64,65]. Using validated instruments, IN midazolam was "unfavorable" versus IN dexmedetomidine but "favorable" versus oral diazepam and placebo.
There is limited methodologically rigorous evidence that IN midazolam is better than placebo for IV insertion and laceration repair. At the doses studied, preliminary evidence suggests that IN dexmedetomidine may be superior to IN midazolam for both IV insertion and laceration repair.
鼻内(IN)咪达唑仑是急诊科(ED)儿童最常用的镇静剂,但获益的证据存在冲突。我们综合了 IN 咪达唑仑在 ED 行疼痛操作的儿童中减轻操作痛苦的证据。
我们纳入了 0-18 岁儿童行 ED 疼痛操作的涉及 IN 咪达唑仑的试验。主要结局为操作痛苦。我们使用 Triceo 等人的分类总结结果,分别为“中性”(p≥0.05)、“有利”和“不利”(p<0.05),分别支持 IN 咪达唑仑或比较剂,或“不确定”(无法判断)。在可能的情况下,我们使用荟萃分析汇总结果。使用 Cochrane 协作组的偏倚风险工具和 GRADE 系统评估证据的方法学质量。
我们纳入了 41 项试验(n=2973 名参与者)。30 项试验涉及静脉插入。IN 咪达唑仑优于安慰剂(RR=7.2;95%CI:3.43,15.25;3 项试验;I=0%)。然而,IN 咪达唑仑组有 56-90%的儿童抗拒该操作。关注使用验证措施的三项试验,IN 咪达唑仑与 IN 氯胺酮相比为“中性”,与 IN 右美托咪定相比为“中性”或“不利”。IN 咪达唑仑与口服咪达唑仑(RR=1.1;95%CI:0.74,1.73;2 项试验;I=53%)、IN 氯胺酮(RR=1.1;95%CI:0.91,1.25;6 项试验;I=0%)或 IN 右美托咪定(RR=0.4;95%CI:0.17,1.05;3 项试验;I=84%)相比,儿童有满意痛苦评分的比例无差异。10 项试验涉及裂伤修复。IN 咪达唑仑优于安慰剂;然而,两组的评分都处于焦虑范围内。IN 咪达唑仑与口服咪达唑仑(SMD=0.01;95%CI:-0.32,0.34;2 项试验;I=0%)之间的痛苦无差异(图 3E)[64,65]。使用验证工具,IN 咪达唑仑与 IN 右美托咪定相比为“不利”,但与口服地西泮和安慰剂相比为“有利”。
有有限的方法学严谨证据表明 IN 咪达唑仑在静脉插入和裂伤修复方面优于安慰剂。在研究剂量下,初步证据表明,与 IN 咪达唑仑相比,IN 右美托咪定可能更有利于静脉插入和裂伤修复。