Leanne K Jackson, I. O. Poon, Mary A Garcia, Syed N Imam, Ursula K Braun
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引用次数: 0
Abstract
Buprenorphine is a semi-synthetic long-acting partial µ-opioid receptor (MOR) agonist that can be used for chronic pain as a sublingual tablet, transdermal patch (Butrans®), or a buccal film (Belbuca®). Buprenorphine’s unique high receptor binding affinity and slow dissociation at the MOR allow for effective analgesia while offering less adverse effects compared to a full agonist opioid, in particular, less concern for respiratory depression and constipation. It is underused in chronic pain and palliative care due to misconceptions and stigma from its use in opioid use disorder (OUD). This case report discusses the unique pharmacology of buprenorphine, including its advantages, disadvantages, available formulations, drug–drug interactions, initiation and conversion strategies, and identifies ideal populations for use, especially within the palliative care patient population.
丁丙诺啡是一种半合成长效部分μ-阿片受体(MOR)激动剂,可作为舌下片剂、透皮贴剂(Butrans®)或口腔膜剂(Belbuca®)用于慢性疼痛。丁丙诺啡独特的高受体结合亲和力和在 MOR 的缓慢解离使其能够有效镇痛,同时与完全激动剂阿片类药物相比,其不良反应较少,特别是呼吸抑制和便秘问题较少。由于对阿片类药物使用障碍(OUD)的误解和偏见,该药物在慢性疼痛和姑息治疗中使用不足。本病例报告讨论了丁丙诺啡的独特药理学,包括其优点、缺点、可用制剂、药物间相互作用、起始和转换策略,并确定了理想的使用人群,尤其是姑息治疗患者人群。