A randomized clinical trial of intranasal dexmedetomidine versus inhaled nitrous oxide for procedural sedation and analgesia in children.

IF 3 2区 医学 Q1 EMERGENCY MEDICINE
Anna Nikula, Malin Ryd Rinder, Stefan Lundeberg, Mitja Lääperi, Katri Sandholm, Maaret Castrén, Lisa Kurland
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引用次数: 0

Abstract

Background: Procedural sedation and analgesia is an important part of pediatric emergency care, safe and clinically useful alternatives for adequate management are necessary. The objective of this clinical trial was to evaluate the non-inferiority of intranasal dexmedetomidine to nitrous oxide with respect to analgesia for a painful procedure in children 3-15 years of age.

Methods: This prospective, equally randomized, open-label, non-inferiority trial was conducted at a Pediatric Emergency Department. Previously healthy children 3-15 years of age, with an extremity fracture or luxation or a burn and requiring procedural sedation and analgesia were eligible. Patients were randomized to receive either intranasal dexmedetomidine or inhaled nitrous oxide. The primary outcome measure was highest pain level during the procedure, assessed with Face, Legs, Activity, Cry, Consolability scale (FLACC). Mann-Whitney U test (continuous variables) and Fisher's test (categorical variables) were used for statistical analysis.

Results: The highest FLACC was median 4 (IQR 3-6) with intranasal dexmedetomidine and median 4 (IQR 2-6) with nitrous oxide. The median of the difference between samples from each group for FLACC was 0 with 95%CI (0-1), thus intranasal dexmedetomidine was not inferior to nitrous oxide with respect to the level of pain during the procedure. The same method for procedural sedation and analgesia would be accepted by 52/74 (82.5%) children and 65/74 (91.5%) parents in the intranasal dexmedetomidine group respectively 59/74 (88.1%) versus 70/74 (94.6%) with nitrous oxide. No serious adverse events were reported.

Conclusions: The results of this trial support that intranasal dexmedetomidine is not inferior to 50% nitrous oxide in providing analgesia for a painful procedure in children 3-15 years of age and can be considered as an alternative to 50% nitrous oxide for procedural sedation and analgesia.

Trial registration: EudraCT 201,600,377,317, April 20, 2017. https://eudract.ema.europa.eu/ .

鼻内右美托咪定与吸入氧化亚氮用于儿童手术镇静和镇痛的随机临床试验。
背景:手术镇静和镇痛是儿科急诊护理的重要组成部分,因此有必要采用安全且对临床有用的替代方法进行适当管理。本临床试验的目的是评估在对 3-15 岁儿童进行疼痛手术时,鼻内右美托咪定镇痛效果是否优于氧化亚氮:这项前瞻性、平等随机、开放标签、非劣效试验在儿科急诊室进行。3-15岁的健康儿童均符合条件,他们患有四肢骨折、关节脱位或烧伤,需要手术镇静和镇痛。患者被随机分配接受鼻内右美托咪定或吸入氧化亚氮。主要结果指标为手术过程中的最高疼痛程度,采用脸部、腿部、活动、哭泣、安慰量表(FLACC)进行评估。统计分析采用 Mann-Whitney U 检验(连续变量)和费雪检验(分类变量):使用鼻内右美托咪定时,FLACC 的最高值中位数为 4(IQR 3-6),使用氧化亚氮时,FLACC 的最高值中位数为 4(IQR 2-6)。各组样本的 FLACC 差异中位数为 0,95%CI (0-1),因此就手术过程中的疼痛程度而言,鼻内右美托咪定并不比氧化亚氮差。52/74(82.5%)名儿童和65/74(91.5%)名家长接受相同的手术镇静和镇痛方法,鼻内右美托咪定组分别为59/74(88.1%)名和70/74(94.6%)名,氧化亚氮组分别为59/74(88.1%)名和70/74(94.6%)名。无严重不良事件报告:该试验结果表明,鼻内右美托咪定在为3-15岁儿童的疼痛手术提供镇痛方面并不逊色于50%的氧化亚氮,可作为50%氧化亚氮的替代品用于手术镇静和镇痛:EudraCT 201,600,377,317, April 20, 2017. https://eudract.ema.europa.eu/ 。
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来源期刊
CiteScore
6.10
自引率
6.10%
发文量
57
审稿时长
6-12 weeks
期刊介绍: The primary topics of interest in Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine (SJTREM) are the pre-hospital and early in-hospital diagnostic and therapeutic aspects of emergency medicine, trauma, and resuscitation. Contributions focusing on dispatch, major incidents, etiology, pathophysiology, rehabilitation, epidemiology, prevention, education, training, implementation, work environment, as well as ethical and socio-economic aspects may also be assessed for publication.
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