Regional Trends in the Opioid Epidemic Using Safety Signals of Drug Abuse and Dependence: A Disproportionality Analysis Using VigiBase.

IF 1.9 Q3 PHARMACOLOGY & PHARMACY
Bohyun Suh, Hyung Suk Oh, Ju-Young Shin, Ju Hwan Kim
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引用次数: 0

Abstract

Background: The opioid epidemic, once a major concern in the United States, has escalated worldwide through three waves driven by prescription and synthetic opioids like oxycodone and fentanyl. Regional patterns of misuse and dependence remain unclear due to data heterogeneity. To address this, we compared adverse events reporting for these opioids using VigiBase.

Methods: We analyzed "drug abuse and dependence" adverse events using VigiBase, a global pharmacovigilance database containing more than 40 million Individual Case Safety Reports (ICSRs). A regional comparison of opioid-related adverse event reporting was performed, with oxycodone and fentanyl as the primary drugs and morphine and tramadol as comparators. Adverse events were defined by Standardized MedDRA Query (SMQ) criteria and cases were stratified by three periods (1990-2009, 2010-2012, 2013-2024) and regions (Americas, Western Pacific, Europe). Opioid-related death was additionally assessed as a secondary outcome. Disproportionality analysis was conducted to identify safety signals, using the reporting odds ratio (ROR). Signals were considered significant if ROR > 2, χ2 > 4, and more than three reports were observed.

Results: Oxycodone-related reports peaked in 2005 (n = 8395), 2011 (n = 10,444), and 2021 (n = 45,025), while fentanyl peaked in 2011 (n = 11,451) and 2017 (n = 32,704). The safety signals for oxycodone were found across all predefined periods in the Americas (1990-2009: ROR 4.40, n = 9102; 2010-2012: ROR 2.13, n = 2299; 2013-2024: ROR 5.20, n = 108,068), and in two periods in the Western Pacific (2010-2012: ROR 6.53, n = 81; 2013-2024: ROR 5.94, n = 1066). No signals were detected for oxycodone in Europe, and fentanyl did not meet signal criteria in any region or period in the primary analyses.

Conclusions: Oxycodone showed consistent safety signals in the Americas and Western Pacific. The absence of signals for fentanyl and in Europe may reflect under-reporting, highlighting the need for improved surveillance of illicit opioid use.

使用药物滥用和依赖安全信号的阿片类药物流行的区域趋势:使用VigiBase进行歧化分析。
背景:阿片类药物流行曾经是美国的一个主要问题,在处方和合成阿片类药物如羟考酮和芬太尼的推动下,在全球范围内经历了三波升级。由于数据的异质性,滥用和依赖的区域模式仍然不清楚。为了解决这个问题,我们使用VigiBase比较了这些阿片类药物的不良事件报告。方法:我们使用全球药物警戒数据库VigiBase分析“药物滥用和依赖”不良事件,该数据库包含超过4000万例个体病例安全报告(ICSRs)。以羟考酮和芬太尼为主要药物,吗啡和曲马多为对照,对阿片类药物相关不良事件报告进行区域比较。不良事件按标准化MedDRA查询(SMQ)标准定义,病例按三个时期(1990-2009年、2010-2012年、2013-2024年)和地区(美洲、西太平洋、欧洲)分层。阿片类药物相关死亡也作为次要结局进行评估。使用报告优势比(ROR)进行歧化分析以识别安全信号。如果观察到ROR > 2、χ2 > 4和超过3个报告,则认为信号显著。结果:羟考酮相关报告高峰出现在2005年(n = 8395)、2011年(n = 10444)和2021年(n = 45025),芬太尼相关报告高峰出现在2011年(n = 11451)和2017年(n = 32704)。在美洲(1990-2009年:ROR 4.40, n = 9102; 2010-2012年:ROR 2.13, n = 2299; 2013-2024年:ROR 5.20, n = 108068)和西太平洋的两个时期(2010-2012年:ROR 6.53, n = 81; 2013-2024年:ROR 5.94, n = 1066)均发现了羟考酮的安全信号。在欧洲没有检测到羟考酮的信号,芬太尼在任何地区或时期的初步分析中都没有达到信号标准。结论:羟考酮在美洲和西太平洋地区表现出一致的安全性信号。芬太尼和欧洲缺乏信号可能反映了报告不足,突出表明需要改进对非法阿片类药物使用的监测。
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来源期刊
Drugs - Real World Outcomes
Drugs - Real World Outcomes PHARMACOLOGY & PHARMACY-
CiteScore
3.60
自引率
5.00%
发文量
49
审稿时长
8 weeks
期刊介绍: Drugs - Real World Outcomes targets original research and definitive reviews regarding the use of real-world data to evaluate health outcomes and inform healthcare decision-making on drugs, devices and other interventions in clinical practice. The journal includes, but is not limited to, the following research areas: Using registries/databases/health records and other non-selected observational datasets to investigate: drug use and treatment outcomes prescription patterns drug safety signals adherence to treatment guidelines benefit : risk profiles comparative effectiveness economic analyses including cost-of-illness Data-driven research methodologies, including the capture, curation, search, sharing, analysis and interpretation of ‘big data’ Techniques and approaches to optimise real-world modelling.
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