首页> 美国卫生研究院文献>Current Controlled Trials in Cardiovascular Medicine >Inhaled methoxyflurane (Penthrox®) versus placebo for injury-associated analgesia in children—the MAGPIE trial (MEOF-002): study protocol for a randomised controlled trial
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Inhaled methoxyflurane (Penthrox®) versus placebo for injury-associated analgesia in children—the MAGPIE trial (MEOF-002): study protocol for a randomised controlled trial

机译:吸入甲氧氟烷(Penthrox®)与安慰剂进行儿童损伤相关镇痛的比较-MAGPIE试验(MEOF-002):一项随机对照试验的研究方案

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摘要

BackgroundPain from injuries is one of the commonest symptoms in children attending emergency departments (EDs), and this is often inadequately treated in both the pre-hospital and ED settings, in part due to challenges of continual assessment and availability of easily administered analgesic options. Pain practices are therefore a key research priority, including within the field of paediatric emergency medicine. Methoxyflurane, delivered via a self-administered Penthrox® inhaler, belongs to the fluorinated hydrocarbon group of volatile anaesthetics and is unique among the group in having analgesic properties at low doses. Despite over 30 years of clinical acute analgesia use, and a large volume of evidence supporting its safety and efficacy, there is a paucity of randomised controlled trial data for Penthrox®.
机译:背景受伤疼痛是上急诊室(ED)儿童的最常见症状之一,在院前和ED环境中常常没有得到足够的治疗,部分原因是持续评估的挑战以及易于使用的止痛药的挑战。因此,疼痛的实践是关键的研究重点,包括在儿科急诊医学领域。通过自行吸入的Penthrox®吸入器提供的甲氧基氟烷属于挥发性麻醉药的氟化烃基团,在低剂量下具有镇痛特性,在该组别中是独一无二的。尽管临床上使用了30多年的镇痛剂,并且有大量证据证明其安全性和有效性,但Penthrox®的随机对照试验数据很少。

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