使用因果框架评估缓释羟考酮对现实世界环境中篡改的滥用威慑特性的影响。

IF 2.4 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pharmacoepidemiology and Drug Safety Pub Date : 2025-01-01 DOI:10.1002/pds.70085
Karilynn M Rockhill, Hannah Burkett, Richard Dart, Joshua C Black
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引用次数: 0

摘要

目的:评估暴露于具有滥用威慑特性(ADF)的缓释(ER)羟考酮是否在现实世界中减少了羟考酮的篡改,以解决FDA第4类标签背后的想法。方法:在一个因果框架下,使用一项针对普通成年人的观察性横断面研究(2022年)的数据,估计暴露于两种ADF ER羟考酮后,经混杂校正后羟考酮被篡改的几率。以单一实体速释氧可酮(SE-IR)组的篡改行为为对照。篡改结果定义为通过鼻吸、吸烟或注射任何羟考酮(ER或SE-IR)使用。用有向无环图识别协变量。使用逆倾向评分加权结合回归中的调查权重来估计被治疗者的平均治疗效果。结果:2022年,普通人群中分别有0.14%和3.0%报告使用两组ER羟考酮,2.4%报告使用SE-IR羟考酮。两个比较国的倾向评分分析(共同支持度为98%)平衡了人口统计学、健康和药物使用协变量。在对选择和混杂偏倚进行调整后,在使用ER羟考酮组1中,篡改任何形式羟考酮的优势比升高,但无统计学意义(2.25;95% ci: 0.94, 5.39)。ER羟考酮2组使用者篡改的优势比显著升高(1.90;95% ci: 1.08, 3.19)。结论:雌激素受体羟考酮产品的个人篡改是罕见的。我们发现有证据表明,使用ADF ER羟考酮会增加篡改行为的几率。
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Use of Causal Framework to Evaluate Effect of Abuse Deterrent Properties of Extended-Release Oxycodone on Tampering in a Real-World Settings.

Purpose: To assess whether exposure to an extended-release (ER) oxycodone with abuse deterrent properties (ADF) reduced tampering of oxycodone in a real-world, postmarket setting to address the thinking behind Category 4 labeling by the FDA.

Methods: Data from an observational cross-sectional study of the general adult population (2022) was used under a causal framework to estimate the confounding-adjusted odds of tampering oxycodone after exposure to two types of ADF ER oxycodone. The tampering behaviors of those who used only single entity immediate-release (SE-IR) oxycodone was used as a comparison. The tampering outcome was defined as use by snorting, smoking, or injecting any oxycodone (ER or SE-IR). A directed acyclic graph was used to identify covariates. Average treatment effect among the treated was estimated using inverse propensity score weighting combined with survey weights in a regression.

Results: In 2022, 0.14% and 3.0% among the general population reported using the two ER oxycodone groups, while 2.4% used SE-IR oxycodone. Propensity score analyses with both comparators (common support > 98%) balanced demographic, health, and drug use covariates. After adjustment for selection and confounding bias, among those who used ER oxycodone group 1 the odds ratio of tampering with any form of oxycodone was elevated but not statistically significant (2.25; 95% CI: 0.94, 5.39). The odds ratio of tampering by users of ER oxycodone group 2 was significantly elevated (1.90; 95% CI: 1.08, 3.19).

Conclusions: Tampering of ER oxycodone products by individuals was rare. We found evidence suggestive of elevated odds of tampering behaviors with use of an ADF ER oxycodone.

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来源期刊
CiteScore
4.80
自引率
7.70%
发文量
173
审稿时长
3 months
期刊介绍: The aim of Pharmacoepidemiology and Drug Safety is to provide an international forum for the communication and evaluation of data, methods and opinion in the discipline of pharmacoepidemiology. The Journal publishes peer-reviewed reports of original research, invited reviews and a variety of guest editorials and commentaries embracing scientific, medical, statistical, legal and economic aspects of pharmacoepidemiology and post-marketing surveillance of drug safety. Appropriate material in these categories may also be considered for publication as a Brief Report. Particular areas of interest include: design, analysis, results, and interpretation of studies looking at the benefit or safety of specific pharmaceuticals, biologics, or medical devices, including studies in pharmacovigilance, postmarketing surveillance, pharmacoeconomics, patient safety, molecular pharmacoepidemiology, or any other study within the broad field of pharmacoepidemiology; comparative effectiveness research relating to pharmaceuticals, biologics, and medical devices. Comparative effectiveness research is the generation and synthesis of evidence that compares the benefits and harms of alternative methods to prevent, diagnose, treat, and monitor a clinical condition, as these methods are truly used in the real world; methodologic contributions of relevance to pharmacoepidemiology, whether original contributions, reviews of existing methods, or tutorials for how to apply the methods of pharmacoepidemiology; assessments of harm versus benefit in drug therapy; patterns of drug utilization; relationships between pharmacoepidemiology and the formulation and interpretation of regulatory guidelines; evaluations of risk management plans and programmes relating to pharmaceuticals, biologics and medical devices.
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