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本文引用的文献

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Inhaled methoxyflurane for the management of trauma related pain in patients admitted to hospital emergency departments: a randomised, double-blind placebo-controlled trial (PenASAP study).吸入甲氧氟烷治疗因创伤导致疼痛而收入医院急诊科的患者:一项随机、双盲、安慰剂对照试验(PenASAP 研究)。
Eur J Emerg Med. 2020 Dec;27(6):414-421. doi: 10.1097/MEJ.0000000000000686.
2
Methoxyflurane May Provide Faster Relief Than Suboptimal Treatment, but Not Better.甲氧氟烷可能比次优治疗提供更快的缓解,但效果并不更好。
Ann Emerg Med. 2020 Apr;75(4):550-551. doi: 10.1016/j.annemergmed.2019.12.007.
3
Non-interventional study evaluating exposure to inhaled, low-dose methoxyflurane experienced by hospital emergency department personnel in France.在法国,一项非干预性研究评估了医院急诊部门人员接触吸入性低剂量甲氧氟烷的情况。
BMJ Open. 2020 Feb 10;10(2):e034647. doi: 10.1136/bmjopen-2019-034647.
4
Synthesis without meta-analysis (SWiM) in systematic reviews: reporting guideline.系统评价中不进行荟萃分析的综合 (SWiM):报告指南。
BMJ. 2020 Jan 16;368:l6890. doi: 10.1136/bmj.l6890.
5
Inhaled Methoxyflurane Provides Greater Analgesia and Faster Onset of Action Versus Standard Analgesia in Patients With Trauma Pain: InMEDIATE: A Randomized Controlled Trial in Emergency Departments.吸入甲氧氟烷相较于标准镇痛在创伤疼痛患者中提供更强的镇痛效果和更快的起效时间:INMEDIATE:急诊科的一项随机对照试验。
Ann Emerg Med. 2020 Mar;75(3):315-328. doi: 10.1016/j.annemergmed.2019.07.028. Epub 2019 Oct 14.
6
Analgesic Efficacy, Practicality and Safety of Inhaled Methoxyflurane Versus Standard Analgesic Treatment for Acute Trauma Pain in the Emergency Setting: A Randomised, Open-Label, Active-Controlled, Multicentre Trial in Italy (MEDITA).吸入甲氧氟烷对急诊急性创伤疼痛的镇痛效果、实用性和安全性与标准镇痛治疗的比较:意大利一项随机、开放标签、阳性对照、多中心试验(MEDITA)。
Adv Ther. 2019 Nov;36(11):3030-3046. doi: 10.1007/s12325-019-01055-9. Epub 2019 Oct 12.
7
RoB 2: a revised tool for assessing risk of bias in randomised trials.《随机对照试验偏倚风险评估工具2:修订版》
BMJ. 2019 Aug 28;366:l4898. doi: 10.1136/bmj.l4898.
8
A Rigorous Evaluation of Methoxyflurane is Needed: Comment on "Methoxyflurane Versus Standard of Care for Acute Trauma-Related Pain in the Emergency Setting: Protocol for a Randomised, Controlled Study in Italy (MEDITA)".需要对甲氧氟烷进行严格评估:对“甲氧氟烷与急诊环境中急性创伤相关疼痛的护理标准:意大利一项随机对照研究的方案(MEDITA)”的评论
Adv Ther. 2019 Jun;36(6):1241-1242. doi: 10.1007/s12325-019-00936-3. Epub 2019 Mar 30.
9
Essential pharmacologic options for acute pain management in the emergency setting.急诊环境中急性疼痛管理的基本药物选择。
Turk J Emerg Med. 2018 Dec 10;19(1):1-11. doi: 10.1016/j.tjem.2018.11.003. eCollection 2019 Jan.
10
Penthrox: a breath of PHEC air for the military?喷他佐辛:军事领域的PHEC新风向?
BMJ Mil Health. 2020 Aug;166(4):257-260. doi: 10.1136/jramc-2018-001122. Epub 2019 Feb 6.

吸入甲氧氟烷(Penthrōx)用于创伤镇痛:系统评价方案。

Inhaled methoxyflurane (Penthrox) for analgesia in trauma: a systematic review protocol.

机构信息

Academic Department of Military General Practice & Primary Care, Research and Clinical Innovation, Royal Centre for Defence Medicine, HQ Joint Medical Group, ICT Centre, Vincent Drive, Edgbaston, Birmingham, B15 2SQ, UK.

Department of Anaesthetics and Critical Care, Queen Elizabeth Hospital, University Hospitals Birmingham NHS Trust, Mindelsohn Way, Edgbaston, B15 2TH, UK.

出版信息

Syst Rev. 2021 Feb 3;10(1):47. doi: 10.1186/s13643-021-01600-0.

DOI:10.1186/s13643-021-01600-0
PMID:33536052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7860209/
Abstract

BACKGROUND

More than 75% of patients presenting to the Emergency Department are suffering symptoms of pain. Despite this, 67% will not receive any analgesia. Methoxyflurane is a fluorinated hydrocarbon gas which has analgesic properties when inhaled. Penthrox is a methoxyflurane autoinhaler recently licenced in Europe. Its ease of administration, safety, and fast onset of action make it of particular relevance to emergency medicine. Additionally, outside the hospital, it has the advantage of increased temperature stability and portability over current standard care. New evidence of its efficacy is emerging; however, currently, its use in Europe is not widespread. The objective of this study will be to systematically evaluate the evidence on inhaled methoxyflurane to determine if it is a superior analgesia in the acute trauma setting.

METHODS

We designed and registered a study protocol for a systematic review and meta-analysis on randomised controlled trials, comparing inhaled methoxyflurane and either placebo or standard care. A comprehensive search will be conducted from database inception onwards in MEDLINE, Embase, and the Cochrane CENTRAL database, concurrent with a search of the grey literature for other relevant studies, including clinical trial databases. Only randomised controlled trials will be included. No limitations will be imposed on publication status or language of publication. The primary outcome will be mean difference in patient-reported pain at time points within the first 30 min of administration. Secondary outcomes will be mean difference in time to clinically significant pain relief and relative risk of adverse effects. Two reviewers will independently screen all returned studies and collect data. Disagreements will be resolved through discussion or referral to a third reviewer. Individual study methodological quality will be appraised using an appropriate tool. If feasible, we will conduct a random effects meta-analysis; if this is not possible, we will construct a narrative synthesis.

DISCUSSION

This systematic review will summarise the best available evidence and definitively establish if inhaled methoxyflurane is a superior analgesia to standard care in the acute trauma setting. This knowledge will directly impact emergency care in the UK and worldwide and may require amendments to European pain relief guidelines.

SYSTEMATIC REVIEW REGISTRATION

PROSPERO CRD42020189119 .

摘要

背景

超过 75%的急诊科就诊患者都有疼痛症状。尽管如此,仍有 67%的患者未接受任何镇痛治疗。甲氧氟烷是一种吸入时有镇痛作用的含氟碳氢化合物气体。戊烷脒是一种最近在欧洲获得许可的甲氧氟烷自动吸入器。它的给药简便、安全性高、起效迅速,这使其在急诊医学中具有特殊意义。此外,在医院外,它在温度稳定性和便携性方面优于目前的标准护理。新的证据表明其具有疗效;然而,目前在欧洲,它的使用并不广泛。本研究的目的是系统评估吸入甲氧氟烷的证据,以确定其在急性创伤环境中是否是一种更好的镇痛剂。

方法

我们设计并注册了一项关于随机对照试验的系统评价和荟萃分析的研究方案,比较吸入甲氧氟烷与安慰剂或标准护理的效果。我们将从数据库建立之初开始,在 MEDLINE、Embase 和 Cochrane CENTRAL 数据库中进行全面搜索,并同时在灰色文献中搜索其他相关研究,包括临床试验数据库。仅纳入随机对照试验。不限制发表状态或语言。主要结局是在给药后 30 分钟内患者报告的疼痛的平均差异。次要结局是临床显著疼痛缓解的平均差异和不良反应的相对风险。两位评审员将独立筛选所有返回的研究并收集数据。意见分歧将通过讨论或提交给第三位评审员解决。将使用适当的工具评估个别研究的方法学质量。如果可行,我们将进行随机效应荟萃分析;如果不可行,我们将进行叙述性综合。

讨论

这项系统评价将总结最佳现有证据,并明确确定在急性创伤环境中,吸入甲氧氟烷是否优于标准护理。这一知识将直接影响英国和全球的急诊护理,并可能需要对欧洲疼痛缓解指南进行修订。

系统评价注册

PROSPERO CRD42020189119。