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National Institute on Drug Abuse Clinical Trials Network Meeting Report: Managing Patients Exposed to Xylazine-Adulterated Opioids in Emergency, Hospital and Addiction Care Settings
Annals of Emergency Medicine ( IF 5.0 ) Pub Date : 2024-03-16 , DOI: 10.1016/j.annemergmed.2024.01.041 Jeanmarie Perrone 1 , Rachel Haroz 2 , Joseph D'Orazio 2 , Giacomo Gianotti 3 , Jennifer Love 4 , Matthew Salzman 5 , Margaret Lowenstein 6 , Ashish Thakrar 7 , Stephanie Klipp 8 , Lisa Rae 9 , Megan K Reed 10 , Edward Sisco 11 , Rachel Wightman 12 , Lewis S Nelson 13
Annals of Emergency Medicine ( IF 5.0 ) Pub Date : 2024-03-16 , DOI: 10.1016/j.annemergmed.2024.01.041 Jeanmarie Perrone 1 , Rachel Haroz 2 , Joseph D'Orazio 2 , Giacomo Gianotti 3 , Jennifer Love 4 , Matthew Salzman 5 , Margaret Lowenstein 6 , Ashish Thakrar 7 , Stephanie Klipp 8 , Lisa Rae 9 , Megan K Reed 10 , Edward Sisco 11 , Rachel Wightman 12 , Lewis S Nelson 13
Affiliation
Used as a veterinary sedative and not approved for human use, xylazine has been increasingly linked with opioid overdose deaths in the United States. A growing number of people have been exposed to xylazine in the illicit opioid supply (especially fentanyl) or in other drugs, particularly in some areas of the Northeast. Xylazine is an α-2 adrenergic agonist that decreases sympathetic nervous system activity. When combined with fentanyl or heroin, it is purported to extend the duration of the opioid’s sedative effect and to cause dependence and an associated withdrawal syndrome; however, data to support these concerns are limited. Despite the escalating frequency of detection of xylazine in people with nonfatal and fatal opioid overdose, direct links to these outcomes have not been identified. Because the strongest causal link is to fentanyl coexposure, ventilatory support and naloxone remain the cornerstones of overdose management. Xylazine is also associated with severe tissue injury, including skin ulcers and tissue loss, but little is known about the underlying mechanisms. Nonetheless, strategies for prevention and treatment are emerging. The significance and clinical effects of xylazine as an adulterant is focused on 4 domains that merit further evaluation: fentanyl-xylazine overdose, xylazine dependence and withdrawal, xylazine-associated dermal manifestations, and xylazine surveillance and detection in clinical and nonclinical settings.
中文翻译:
国家药物滥用临床试验研究所网络会议报告:在急诊、医院和成瘾护理环境中管理暴露于甲苯噻嗪掺假阿片类药物的患者
甲苯噻嗪用作兽用镇静剂,未获准用于人类,在美国,甲苯噻嗪与阿片类药物过量死亡的联系越来越紧密。越来越多的人在非法阿片类药物供应(尤其是芬太尼)或其他药物中接触过甲苯噻嗪,尤其是在东北部的一些地区。甲苯噻嗪是一种 α-2 肾上腺素能激动剂,可降低交感神经系统活动。当与芬太尼或海洛因联合使用时,据称它会延长阿片类药物的镇静作用的持续时间,并导致依赖性和相关的戒断综合征;然而,支持这些担忧的数据是有限的。尽管在非致命性和致命性阿片类药物过量患者中检测到甲苯噻嗪的频率不断增加,但尚未确定与这些结果的直接联系。因为最强的因果关系是芬太尼共同暴露,所以通气支持和纳洛酮仍然是过量管理的基石。甲苯噻嗪还与严重的组织损伤有关,包括皮肤溃疡和组织损失,但对其潜在机制知之甚少。尽管如此,预防和治疗策略正在出现。甲苯噻嗪作为掺杂物的意义和临床影响集中在值得进一步评估的 4 个领域:芬太尼-甲苯噻嗪过量、甲苯噻嗪依赖和戒断、甲苯噻嗪相关皮肤表现以及临床和非临床环境中的甲苯噻嗪监测和检测。
更新日期:2024-03-16
中文翻译:
国家药物滥用临床试验研究所网络会议报告:在急诊、医院和成瘾护理环境中管理暴露于甲苯噻嗪掺假阿片类药物的患者
甲苯噻嗪用作兽用镇静剂,未获准用于人类,在美国,甲苯噻嗪与阿片类药物过量死亡的联系越来越紧密。越来越多的人在非法阿片类药物供应(尤其是芬太尼)或其他药物中接触过甲苯噻嗪,尤其是在东北部的一些地区。甲苯噻嗪是一种 α-2 肾上腺素能激动剂,可降低交感神经系统活动。当与芬太尼或海洛因联合使用时,据称它会延长阿片类药物的镇静作用的持续时间,并导致依赖性和相关的戒断综合征;然而,支持这些担忧的数据是有限的。尽管在非致命性和致命性阿片类药物过量患者中检测到甲苯噻嗪的频率不断增加,但尚未确定与这些结果的直接联系。因为最强的因果关系是芬太尼共同暴露,所以通气支持和纳洛酮仍然是过量管理的基石。甲苯噻嗪还与严重的组织损伤有关,包括皮肤溃疡和组织损失,但对其潜在机制知之甚少。尽管如此,预防和治疗策略正在出现。甲苯噻嗪作为掺杂物的意义和临床影响集中在值得进一步评估的 4 个领域:芬太尼-甲苯噻嗪过量、甲苯噻嗪依赖和戒断、甲苯噻嗪相关皮肤表现以及临床和非临床环境中的甲苯噻嗪监测和检测。