对于甲用于阿片类药物使用障碍治疗的州特定障碍
Kellen Russoniello1, Cailin Harrington2, Sarah Beydoun3
1DRUG POLICY ALLIANCE, NEW YORK, NY, USA.
概括
用甲治疗阿片类激素治疗是治疗阿片类药物使用障碍和预防过量死亡的最有效方法. 然而,州级的法规对获得这种救命药物造成了重大障碍.
科学领域:
- 成 药物 药物 药物 药物
- 公共卫生政策 公共卫生政策
- 药理学 药理学是指药理学的学科.
背景情况:
- 阿片类药物使用障碍 (OUD) 是一个主要的公共卫生危机.
- 片激动剂治疗 (OAT) 是OUD管理的黄金标准.
- 甲是OAT的关键药物,已被证明可以降低死亡率.
研究的目的:
- 检查国家特定法规对甲获取的影响.
- 为了突出不同州OAT可用性的差异.
- 为旨在改善治疗可访问性的政策变化提供信息.
主要方法:
- 分析与甲分发有关的联邦和州法规.
- 对OUD治疗障碍的现有文献的审查.
- 国家级OAT可访问性指标的比较评估.
主要成果:
- 联邦法规规管甲的使用,但许多州实施了额外的,更严格的要求.
- 这些国家强加的障碍限制了患者获得基本的OUD治疗的机会.
- 甲的可用性存在显著的地理和监管差异.
结论:
- 国家法规为甲治疗创造了不必要的障碍,与公共卫生目标相矛盾.
- 政策改革是必要的,以减少国家层面的障碍,并扩大获得OAT的机会.
- 改善对美沙的获取对于打击阿片类药物过量流行病至关重要.
更多相关视频
09:29Investigating Drivers of Antireward in Addiction Behavior with Anatomically Specific Single-Cell Gene Expression Methods
Published on: August 4, 2022
2.2K
09:16A General Method for Evaluating Deep Brain Stimulation Effects on Intravenous Methamphetamine Self-Administration
Published on: January 22, 2016
15.3K
相关概念视频
Opioid Analgesics: Synthetic and Semisynthetic Opioids
333
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...
333
Drug Abuse and Addiction: Pharmacological Phenomena
508
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...
508
Analgesia and Pain Management
654
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...
654
Prescription, Nonprescription and Orphan Drugs
764
Prescription drugs require a prescription from a medical practitioner and can only be obtained from a pharmacy. They have many applications, including treating pain, anxiety, and hypertension.
The misuse and addiction to prescription drugs is a growing problem that can affect people of all age groups, specifically teenagers. This can happen when prescription medications are used in ways not intended by the prescriber, such as taking someone else's prescription or using medication for...
The misuse and addiction to prescription drugs is a growing problem that can affect people of all age groups, specifically teenagers. This can happen when prescription medications are used in ways not intended by the prescriber, such as taking someone else's prescription or using medication for...
764
Opioid Analgesics: Morphine and Other Natural Cogeners
287
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...
287
Opioid Receptors: Overview
1.0K
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,...
1.0K
