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首页> 外文期刊>Journal of Clinical Pharmacy and Therapeutics >Treating opioid‐induced constipation in patients taking other medications: Avoiding CYP450 drug interactions
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Treating opioid‐induced constipation in patients taking other medications: Avoiding CYP450 drug interactions

机译:治疗其他药物患者的阿片类药物诱导的便秘:避免CYP450药物相互作用

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Summary What is known and objective When patients fail other treatment regimens and still suffer from pain sufficiently severe, opioid analgesics are appropriate and required. Unfortunately, constipation is a common adverse effect of opioids. Opioid‐induced constipation (OIC) can be treated with one of the new peripherally acting μ‐opioid receptor antagonist (PAMORA) agents. We summarize the mechanism of action of these drugs, with an emphasis on comparison of their potential for metabolic drug interactions. Methods Internet sources were searched for English‐language abstracts related to the topic. Emphasis was placed on the mechanism of the PAMORAs, their metabolic pathways, drugs co‐administered with opioids and potential drug‐drug interactions (particularly at the level of CYP450 isozyme drug metabolism). Each source was evaluated and synthesized into the review. Results and discussion PAMORAs dose‐dependently antagonize the access of agonist molecules to opioid receptors, thereby directly eliminating or reducing OIC. But they differ from other opioid antagonists in that they are restricted to the periphery. Hence, they block constipation, but leave central opioid receptor‐mediated pain relief undiminished. The PAMORAs have similar efficacy and safety profiles, but many pain patients have comorbidities and thus are taking other medications, which increases the potential for metabolic drug interactions. What is new and conclusion Managing OIC in patients who have failed OTC or other therapies can be accomplished using a PAMORA, but healthcare providers must make prudent decisions that avoid or at least mitigate the potential for metabolic drug interactions in those patients with other comorbidities being managed medically by rational polypharmacy strategies.
机译:发明内容患者未通过其他治疗方案而仍然患有足够严重的疼痛的患者,阿片类镇痛药是合适的,需要的。不幸的是,便秘是阿片类药物的常见不良影响。 Apioid诱导的便秘(OIC)可以用新的外周作用的μ-ApiOID受体拮抗剂(Pamora)试剂治疗。我们总结了这些药物的作用机制,重点是它们对代谢药物相互作用的潜力的比较。方法搜索互联网源与主题相关的英语摘要。重点是pamoras的机制,它们的代谢途径,药物与阿片类药物和潜在的药物 - 药物相互作用(特别是在CYP450同工酶代谢水平上)。每个来源都被评估并合成审查。结果与讨论Pamoras剂量依赖性地拮抗激动剂分子对阿片类受体的进入,从而直接消除或减少OIC。但它们与其他阿片类药物的不同之处在于它们仅限于周边。因此,它们阻止了便秘,但留下了中枢阿片受体介导的疼痛缓解规定。 Pamoras具有相似的功效和安全性曲线,但许多疼痛患者具有可血糖性,因此采取其他药物,这增加了代谢药物相互作用的可能性。可以使用Pamora完成失败或其他疗法的患者的新和结论管理,但医疗保健提供者必须做出谨慎的决定,以避免或至少减轻那些患有管理的其他合并症患者的代谢药物相互作用的可能性通过合理的多药物策略在医学上。

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