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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...
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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...
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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...
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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,...
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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.
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在整形手术中改变阿片类药物处方算法

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整形外科医生可以通过实施新的算法来减少阿片类药物处方. 这种变化显著减少了未使用的阿片类药丸,但没有影响患者的疼痛管理.

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科学领域:

  • 整形外科 整形外科 整形外科
  • 疼痛管理 疼痛管理
  • 阿片类药物处方的做法

背景情况:

  • 外科手术中的阿片类药物处方做法缺乏标准化,造成了整形外科医生之间的犹.
  • 减少阿片类药物使用已经证明了好处,但实施仍然是一个挑战.
  • 介绍了一种新的处方算法,以指导实践修改和减少阿片类药物处方.

研究的目的:

  • 为乳腺手术患者实施和评估一种新的阿片类药物处方算法.
  • 为了减少处方手术后阿片类药丸的数量.
  • 分析算法对阿片类药物消费和过量药物的影响.

主要方法:

  • 在2023年10月,为乳腺手术患者实施了阿片类算法.
  • 干预前组接受了30片阿片类药丸;干预后组最多接受了10片药丸.
  • 术后止痛药的使用和药丸的消费被记录在两个队列中.

主要成果:

  • 中位数未使用的阿片类药丸显著下降,从干预后的24小时降至0.5小时 (P < 0.000).
  • 在各组之间,中位数阿片类药物消费仍然相似 (干预前6粒药和干预后5.5粒药).
  • 两组之间在补充需求或止痛药使用方面没有发现显著差异.

结论:

  • 在整形外科手术中建立了一条更新阿片类药物处方算法的途径.
  • 该干预措施显著减少了过量的阿片类药物使用,降低了滥用风险.
  • 外科医生可以自信地采用这项改革来有效监管阿片类药物处方.