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治疗同时服用其他药物的患者的阿片类药物诱导性便秘:避免 CYP450 药物相互作用。

Treating opioid-induced constipation in patients taking other medications: Avoiding CYP450 drug interactions.

机构信息

University of Arizona College of Pharmacy, Tucson, Arizona.

Temple University School of Pharmacy, Philadelphia, Pennsylvania.

出版信息

J Clin Pharm Ther. 2019 Jun;44(3):361-371. doi: 10.1111/jcpt.12812. Epub 2019 Feb 21.

Abstract

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.

摘要

已知和目的

当患者在其他治疗方案失败后仍遭受严重疼痛时,阿片类镇痛药是适当且必需的。不幸的是,便秘是阿片类药物的常见不良反应。阿片类药物引起的便秘(OIC)可以用一种新的外周作用µ阿片受体拮抗剂(PAMORA)药物治疗。我们总结了这些药物的作用机制,重点比较了它们发生代谢药物相互作用的潜在可能性。

方法

搜索了与主题相关的英文摘要的互联网资源。重点放在 PAMORAs 的作用机制上,强调它们的代谢途径,与阿片类药物共同给药的药物以及潜在的药物-药物相互作用(特别是在 CYP450 同工酶药物代谢水平上)。对每个来源进行评估并综合到综述中。

结果与讨论

PAMORAs 剂量依赖性地拮抗激动剂分子与阿片受体的结合,从而直接消除或减少 OIC。但它们与其他阿片类拮抗剂不同,它们仅限于外周。因此,它们阻断便秘,但不减弱中枢阿片受体介导的疼痛缓解。PAMORAs 具有相似的疗效和安全性特征,但许多疼痛患者都有合并症,因此正在服用其他药物,这增加了发生代谢药物相互作用的潜在可能性。

新内容和结论

对于已经尝试过 OTC 或其他治疗方案而失败的 OIC 患者,可以使用 PAMORA 进行治疗,但医疗保健提供者必须做出谨慎的决策,以避免或至少减轻那些患有其他合并症的患者发生代谢药物相互作用的潜在风险,这些患者需要通过合理的多药物治疗策略来管理合并症。

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