Intranasal midazolam for procedural distress in children in the emergency department: a systematic review and meta-analysis.

IF 2.4 CJEM Pub Date : 2024-09-01 Epub Date: 2024-08-28 DOI:10.1007/s43678-024-00731-2
Jie Yi Wang, Kathy Speechley, Kelly K Anderson, George Gainham, Samina Ali, Evelyn D Trottier, Vikram Sabhaney, Anna Heath, Christy Sich, Arielle Forbes, Naveen Poonai
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Abstract

Objectives: 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.

Methods: 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.

Results: 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; I2 = 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; I2 = 53%), IN ketamine (RR = 1.1; 95% CI: 0.91, 1.25; 6 trials; I2 = 0%), or IN dexmedetomidine (RR = 0.4; 95% CI: 0.17, 1.05; 3 trials; I2 = 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; I2 = 0%) (Fig. 3E) [64,65]. Using validated instruments, IN midazolam was "unfavorable" versus IN dexmedetomidine but "favorable" versus oral diazepam and placebo.

Conclusions: 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.

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在急诊科使用咪达唑仑治疗儿童手术中的痛苦:系统回顾和荟萃分析。
目的:咪达唑仑(IN)是急诊科(ED)儿童最常用的抗焦虑药物,但有关其益处的证据并不一致。我们综合了有关IN咪达唑仑治疗接受急诊室疼痛手术的儿童的手术痛苦的证据:我们纳入了涉及 0-18 岁儿童接受急诊室疼痛手术并使用 IN 咪达唑仑的试验。主要结果为手术痛苦。我们采用 Tricco 等人的 "中性"(p ≥ 0.05)、"有利 "和 "不利"(p 结果)分类法对结果进行了总结:我们纳入了 41 项试验(n = 2973 名参与者)。其中 30 项试验涉及静脉注射。静脉注射咪达唑仑优于安慰剂(RR = 7.2;95% CI:3.43, 15.25;3 项试验;I2 = 0%)。然而,56%-90%的咪达唑仑IN组患者对手术有抵触情绪。从三项使用有效测量方法的试验来看,IN咪达唑仑与IN氯胺酮相比呈 "中性",与IN右美托咪定相比呈 "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;I2=53%)、IN氯胺酮(RR=1.1;95% CI:0.91,1.25;6项试验;I2=0%)或IN右美托咪定(RR=0.4;95% CI:0.17,1.05;3项试验;I2=84%)相比,患儿痛苦评分达到满意的比例没有差异。10项试验涉及裂伤修复。咪达唑仑IN与安慰剂相比效果 "良好";但是,两组患者的评分都在焦虑范围内。IN 咪达唑仑和口服咪达唑仑在焦虑方面没有差异(SMD = 0.01;95% CI:-0.32,0.34;2 项试验;I2 = 0%)(图 3E)[64,65]。使用经过验证的工具,IN咪达唑仑与IN右美托咪定相比 "不利",但与口服地西泮和安慰剂相比 "有利":在静脉注射和裂伤修补方面,只有有限的严格方法学证据表明 IN 咪达唑仑优于安慰剂。在所研究的剂量下,初步证据表明,在静脉插入和裂伤修补方面,IN 右美托咪定可能优于 IN 咪达唑仑。
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