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本文引用的文献

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Drug and Opioid-Involved Overdose Deaths - United States, 2013-2017.药物和阿片类药物滥用相关的过量死亡-美国,2013-2017 年。
MMWR Morb Mortal Wkly Rep. 2018 Jan 4;67(5152):1419-1427. doi: 10.15585/mmwr.mm675152e1.
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Overdose Deaths Involving Opioids, Cocaine, and Psychostimulants - United States, 2015-2016.2015 - 2016年美国涉及阿片类药物、可卡因和精神兴奋剂的过量用药死亡情况
MMWR Morb Mortal Wkly Rep. 2018 Mar 30;67(12):349-358. doi: 10.15585/mmwr.mm6712a1.
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Fentanyl, fentanyl analogs and novel synthetic opioids: A comprehensive review.芬太尼、芬太尼类似物和新型合成阿片类药物:全面综述。
Neuropharmacology. 2018 May 15;134(Pt A):121-132. doi: 10.1016/j.neuropharm.2017.10.016. Epub 2017 Oct 14.
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Fentanyl Formulations in the Management of Pain: An Update.芬太尼制剂在疼痛管理中的应用:更新。
Drugs. 2017 May;77(7):747-763. doi: 10.1007/s40265-017-0727-z.
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Sustained-Release Buprenorphine (RBP-6000) Blocks the Effects of Opioid Challenge With Hydromorphone in Subjects With Opioid Use Disorder.缓释丁丙诺啡(RBP-6000)可阻断阿片类物质使用障碍患者中氢吗啡酮激发试验的阿片类效应。
J Clin Psychopharmacol. 2016 Feb;36(1):18-26. doi: 10.1097/JCP.0000000000000434.
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Population Pharmacokinetic Modeling After Repeated Administrations of RBP-6000, a New, Subcutaneously Injectable, Long-Acting, Sustained-Release Formulation of Buprenorphine, for the Treatment of Opioid Use Disorder.重复给予RBP-6000(一种新型皮下注射长效缓释丁丙诺啡制剂,用于治疗阿片类物质使用障碍)后的群体药代动力学建模
J Clin Pharmacol. 2016 Jul;56(7):806-15. doi: 10.1002/jcph.665. Epub 2016 Mar 11.
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The fentanyl story.芬太尼的故事。
J Pain. 2014 Dec;15(12):1215-26. doi: 10.1016/j.jpain.2014.08.010.
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Intravenous fentanyl kinetics.静脉注射芬太尼的动力学
Clin Pharmacol Ther. 1980 Jul;28(1):106-14. doi: 10.1038/clpt.1980.138.
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Pharmacological profiles of fentanyl analogs at mu, delta and kappa opiate receptors.芬太尼类似物在μ、δ和κ阿片受体上的药理学特征。
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病例系列:高效合成阿片类药物使用者快速诱导长效丁丙诺啡注射。

Case Series: Rapid Induction Onto Long Acting Buprenorphine Injection for High Potency Synthetic Opioid Users.

机构信息

Division on Substance Use Disorders, New York State Psychiatric Institute, New York, New York.

Department of Psychiatry, Columbia University Vagelos College of Physicians and Surgeons, New York, New York.

出版信息

Am J Addict. 2020 Jul;29(4):345-348. doi: 10.1111/ajad.13018. Epub 2020 Mar 13.

DOI:10.1111/ajad.13018
PMID:32167629
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7383940/
Abstract

BACKGROUND AND OBJECTIVES

Highly potent synthetic opioids (HPSO) are increasingly responsible for opioid overdose deaths in the United States.

METHODS

In an open-label, uncontrolled trial to test the feasibility of extended-release buprenorphine (BXR) injection treatment of heroin-using individuals with opioid use disorder testing positive for HPSO, participants were enrolled and began an induction with sublingual BXR (n = 5). During the induction, ancillary medications (clonidine, clonazepam, zolpidem, and prochlorperazine) were provided for breakthrough opioid withdrawal symptoms.

RESULTS

Two participants received the BXR injection on the second day of the induction and three participants on the third day.

DISCUSSION AND CONCLUSION

All five participants were retained at least 1-month postinduction.

SCIENTIFIC SIGNIFICANCE

It may be feasible to provide BXR treatment to HPSO-positive heroin users rapidly to achieve clinical stabilization. (Am J Addict 2020;00:00-00).

摘要

背景与目的

在美国,高活性合成阿片类药物(HPSO)越来越多地导致阿片类药物过量死亡。

方法

在一项开放性、非对照试验中,我们测试了使用经 HPSO 检测呈阳性的海洛因使用者的延长释放丁丙诺啡(BXR)注射治疗的可行性,招募了参与者并开始使用舌下 BXR 诱导(n=5)。在诱导过程中,提供了辅助药物(可乐定、氯硝西泮、唑吡坦和丙氯拉嗪)来缓解突破性阿片类戒断症状。

结果

两名参与者在诱导的第二天接受了 BXR 注射,三名参与者在第三天接受了 BXR 注射。

讨论与结论

所有五名参与者在诱导后至少 1 个月内都被保留下来。

科学意义

快速向 HPSO 阳性的海洛因使用者提供 BXR 治疗以实现临床稳定可能是可行的。