Naloxone Dosing and Hospitalization for Nitazene Overdose: A Scoping Review.

IF 2.6 4区 医学 Q3 TOXICOLOGY Journal of Medical Toxicology Pub Date : 2025-04-01 Epub Date: 2025-02-04 DOI:10.1007/s13181-025-01059-8
Jonathan C Berger, Alec D Severe, Mohamed S Jalloh, Alex F Manini
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引用次数: 0

Abstract

Introduction: Nitazene compounds are high potency, synthetic opioids, recently detected in the United States illicit opioid supply. This is a scoping review to summarize the available body of literature on naloxone and hospitalization reports in response to nitazene compound overdose.

Methods: This review adhered to the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) extension for Scoping Reviews. PubMed, ProQuest, and Google Scholar were accessed. Articles were limited to full-text peer-reviewed publications appearing in scholarly journals between January 2018 and December 2024. Total naloxone dose (in mg, primary outcome) and total length of stay (LOS, in hours, secondary outcome) were recorded.

Results: Of 109 articles screened, 103 were excluded (44 non-human; 35 no nitazene exposure, 9 no naloxone administered, 9 post-mortem data only, 3 non-overdose, 2 non-English, and 1 full text unavailable), leaving 6 articles included. Data were described on 19 distinct patients with nitazene compound overdose (meto-, isoto-, proto-, and eto-nitazene), all of whom had naloxone data, and 10 of whom had LOS data. Median total naloxone doses were the following: metonitazene 6.00mg; etonitazene 3.06mg; isotonitazene 3.00mg; protonitazene 1mg (p=0.4). Mean hospital LOS were the following: metonitazene 360 hours; etonitazene 122.25 hrs; isotonitazene 32.67 hrs; protonitazene 20 hrs.

Conclusion: This scoping review reveals a paucity of data on nitazene compound overdoses and identifies a gap in our current opioid crisis response. Most nitazene cases reviewed involved hospitalization, had high naloxone dosing, and relatively long LOS. Differences in naloxone dose and hospital LOS could underscore the unpredictable and potent nature of these substances.

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纳洛酮剂量与尼他嗪过量住院治疗:范围审查。
Nitazene化合物是一种高效的合成阿片类药物,最近在美国发现了非法供应的阿片类药物。这是一篇范围综述,总结了纳洛酮和nitazene化合物过量的住院报告的现有文献。方法:本综述遵循系统评价和荟萃分析首选报告项目(PRISMA)扩展范围评价。PubMed, ProQuest和谷歌Scholar被访问。文章仅限于2018年1月至2024年12月期间发表在学术期刊上的全文同行评审出版物。记录纳洛酮总剂量(mg,主要转归)和总住院时间(LOS,小时,次要转归)。结果:在筛选的109篇文章中,103篇被排除(44篇非人类;35篇未接触nitazene, 9篇未使用纳洛酮,9篇仅提供尸检数据,3篇非过量,2篇非英文,1篇无法获得全文),共纳入6篇文章。数据描述了19例不同的nitazene化合物过量患者(meto-、isoto-、原nitazene和eto-nitazene),所有患者都有纳洛酮数据,其中10例有LOS数据。纳洛酮总剂量中位数如下:甲硝唑6.00mg;etonitazene 3.06毫克;isotonitazene 3.00毫克;原硝泽烯1mg (p=0.4)。平均住院时间如下:甲硝唑360小时;乙硝唑122.25小时;异烟肼32.67小时;原硝唑20小时。结论:本综述揭示了nitazene化合物过量数据的缺乏,并确定了我们目前阿片类药物危机应对的差距。大多数尼硝唑病例涉及住院、高纳洛酮剂量和相对较长的LOS。纳洛酮剂量和医院LOS的差异可能强调了这些物质的不可预测性和强效性。
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来源期刊
CiteScore
5.40
自引率
10.30%
发文量
46
期刊介绍: Journal of Medical Toxicology (JMT) is a peer-reviewed medical journal dedicated to advances in clinical toxicology, focusing on the diagnosis, management, and prevention of poisoning and other adverse health effects resulting from medications, chemicals, occupational and environmental substances, and biological hazards. As the official journal of the American College of Medical Toxicology (ACMT), JMT is managed by an editorial board of clinicians as well as scientists and thus publishes research that is relevant to medical toxicologists, emergency physicians, critical care specialists, pediatricians, pre-hospital providers, occupational physicians, substance abuse experts, veterinary toxicologists, and policy makers.       JMT articles generate considerable interest in the lay media, with 2016 JMT articles cited by various social media sites, the Boston Globe, and the Washington Post among others.     For questions or comments about the journal, please contact jmtinfo@acmt.net.    For questions or comments about the journal, please contact jmtinfo@acmt.net.
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