在行政数据中识别阿片类药物使用障碍的基于证据的框架:系统审查和方法发展研究
Robert W Hurley1,2,3,4, Khadijah T Bland5, Mira D Chaskes6
1Department of Anesthesiology, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC, 27157, United States.
Pain medicine (Malden, Mass.)
|August 25, 2025
概括
在行政数据中识别阿片类药物使用障碍 (OUD) 的标准化方法至关重要. 本审查提出了基于证据的框架,使用诊断代码,时间要求和治疗数据来准确识别OUD.
科学领域:
- 医疗服务研究
- 公共卫生
- 数据科学
背景情况:
- 片使用障碍 (OUD) 是一个重大的公共卫生危机.
- 在行政数据集中准确识别OUD对于监测,研究和干预至关重要.
- 在行政数据中识别OUD的现有方法缺乏标准化,导致不一致.
研究的目的:
- 系统地评估目前在行政数据集中识别OUD的方法.
- 为标准化OUD识别方法制定基于证据的建议.
- 提出一个框架来提高OUD识别的准确性和一致性.
主要方法:
- 按照PRISMA范围审查指南进行系统审查.
- 在EMBASE,MEDLINE,Google Scholar和PubMed中进行全面的文献搜索.
- 综合证据和框架开发,整合来自169项研究的组成部分.
主要成果:
- 确定了OUD识别的四种主要方法:直接诊断代码,复合定义,过量使用代码和药物辅助治疗代码.
- 商业索赔数据是最常用的,其次是医疗补助索赔和电子健康记录.
- 结合诊断和治疗规范的多模式策略显示出比单一方法更强大的理论基础.
结论:
- 提出一个基于证据的框架,包括诊断代码,时间要求,间接指标和治疗证据.
- 该框架旨在标准化OUD识别协议并解决错误分类问题.
- 该框架强调临床诊断对齐和系统验证以提高特异性.
相关概念视频
Opioid Analgesics: Synthetic and Semisynthetic Opioids
426
Synthetic and semisynthetic opioids are pivotal in pain management and tackling opioid addiction. Semisynthetic opioids, including morphinans (morphine derivatives), oxycodone, oxymorphone, hydrocodone, and hydromorphone, have improved pharmacokinetic profiles compared to morphine. Additionally, heroin and 6-MAM (6-Monoacetylmorphine) show better CNS penetration than morphine due to heightened lipid solubility. Hydromorphone, a potent opioid, undergoes hepatic metabolism to form the active...
426
Analgesia and Pain Management
788
Pain is critical to various clinical pathologies, provoking an urgent need for effective management. Pain, whether acute or chronic, is a complex neurochemical process. Its alleviation depends on the type, with nonopioid analgesics effective for mild to moderate pain, such as musculoskeletal or inflammatory pain, while neuropathic pain responds best to anticonvulsants, tricyclic antidepressants, or serotonin/norepinephrine reuptake inhibitors. For severe acute or chronic pain, opioids may be...
788
Opioid Analgesics: Morphine and Other Natural Cogeners
361
Opioids are a class of drugs that mimic endogenous opioid peptides and act on opioid receptors, and help in pain relief. These compounds are classified as natural, synthetic, or semi-synthetic. Natural opioids, like morphine, codeine, and thebaine, are derived from the opium poppy plant (Papaver somniferum or Papaver album) and are termed opiates. Synthetic opioids are artificial, while semi-synthetic opioids combine natural and synthetic compounds. Morphine, a prototypical opioid, possesses a...
361
Substance Use Disorders Affecting Sleep
217
Substance use disorders involve a pattern of using drugs more extensively than intended and continuing use despite harmful consequences. This includes legal substances like alcohol and nicotine, as well as illegal drugs. These disorders often involve both physical and psychological dependence, reflecting compulsive use of substances that significantly alter thoughts, feelings, and behaviors, contributing to a major public health issue.
Understanding the concepts of physical dependence,...
Understanding the concepts of physical dependence,...
217
Drug Abuse and Addiction: Pharmacological Phenomena
655
Drug dependence, abuse, and addiction are complex phenomena that can precipitate various abnormal states. Physical dependence refers to a state of pharmacological adaptation to a drug. This adaptation often results in tolerance—a reduced response to the drug after repeated administrations. When the drug use is abruptly stopped, withdrawal symptoms occur due to the body's need to readjust from the pharmacologically induced imbalance. However, tolerance and withdrawal symptoms do not...
655
Opioid Receptors: Overview
1.8K
Opioid receptors, including the mu (μ, MOR), delta (δ, DOR), and kappa (κ, KOR) types, belong to the rhodopsin family of G protein-coupled receptors. These receptors are located throughout the central and peripheral nervous systems and in non-neuronal tissues such as macrophages and astrocytes. Opioid receptor ligands can be categorized into agonists or antagonists. Highly selective agonists include [d-Ala2, MePhe4, Gly(ol)5]-enkephalin or DAMGO for MOR, [D-Pen2,...
1.8K


