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亚分离剂量鼻内氯胺酮治疗急诊科儿童肢体损伤疼痛:一项初步研究。

Sub-dissociative dose intranasal ketamine for limb injury pain in children in the emergency department: a pilot study.

机构信息

Southern Health Emergency Medicine Research Group, Southern Clinical School, Faculty of Medicine, Nursing and Health Sciences, Monash University, Clayton, VIC 3168, Australia.

出版信息

Emerg Med Australas. 2013 Apr;25(2):161-7. doi: 10.1111/1742-6723.12059. Epub 2013 Mar 20.

DOI:10.1111/1742-6723.12059
PMID:23560967
Abstract

OBJECTIVE

The present study aims to conduct a pilot study examining the effectiveness of intranasal (IN) ketamine as an analgesic for children in the ED.

METHODS

The present study used an observational study on a convenience sample of paediatric ED patients aged 3-13 years, with moderate to severe (≥6/10) pain from isolated limb injury. IN ketamine was administered at enrolment, with a supplementary dose after 15 min, if required. Primary outcome was change in median pain rating at 30 min. Secondary outcomes included change in median pain rating at 60 min, patient/parent satisfaction, need for additional analgesia and adverse events being reported.

RESULTS

For the 28 children included in the primary analysis, median age was 9 years (interquartile range [IQR] 6-10). Twenty-three (82.1%) were male. Eighteen (64%) received only one dose of IN ketamine (mean dose 0.84 mg/kg), whereas 10 (36%) required a second dose at 15 min (mean for second dose 0.54 mg/kg). The total mean dose for all patients was 1.0 mg/kg (95% CI: 0.92-1.14). The median pain rating decreased from 74.5 mm (IQR 60-85) to 30 mm (IQR 12-51.5) at 30 min (P < 0.001, Mann-Whitney). For the 24 children who contributed data at 60 min, the median pain rating was 25 mm (IQR 4-44). Twenty (83%) subjects were satisfied with their analgesia. Eight (33%) were given additional opioid analgesia and the 28 reported adverse events were all transient and mild.

CONCLUSIONS

In this population, an average dose of 1.0 mg/kg IN ketamine provided adequate analgesia by 30 min for most patients.

摘要

目的

本研究旨在进行一项试点研究,以检验鼻内(IN)氯胺酮作为急诊科儿童镇痛剂的效果。

方法

本研究采用便利抽样法对 3-13 岁的孤立性肢体损伤儿童进行观察性研究,这些儿童的疼痛为中度至重度(≥6/10)。在入组时给予 IN 氯胺酮,15 分钟后如果需要则给予补充剂量。主要结局为 30 分钟时中位数疼痛评分的变化。次要结局包括 60 分钟时中位数疼痛评分的变化、患者/家长满意度、需要额外镇痛以及报告的不良事件。

结果

在主要分析中,28 名儿童纳入研究,中位年龄为 9 岁(四分位距 [IQR] 6-10)。23 名(82.1%)为男性。18 名(64%)仅接受了一次 IN 氯胺酮剂量(平均剂量 0.84mg/kg),而 10 名(36%)在 15 分钟时需要第二次剂量(第二次剂量的平均剂量为 0.54mg/kg)。所有患者的总平均剂量为 1.0mg/kg(95%CI:0.92-1.14)。疼痛评分中位数从 74.5mm(IQR 60-85)下降到 30mm(IQR 12-51.5)(P<0.001,Mann-Whitney)。在 60 分钟时提供数据的 24 名儿童中,疼痛评分中位数为 25mm(IQR 4-44)。20 名(83%)患者对镇痛效果满意。8 名(33%)给予了额外的阿片类镇痛药,28 名报告了不良事件均为短暂和轻度的。

结论

在本研究人群中,平均剂量为 1.0mg/kg 的 IN 氯胺酮在 30 分钟内为大多数患者提供了足够的镇痛效果。

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