Department of Dermatology and Cutaneous Surgery, Itch Center, University of Miami Miller School of Medicine, Miami, FL, USA.
Division of Hepatology, Schiff Center for Liver Diseases, University of Miami Miller School of Medicine, 1500 NW 12th Ave Ste 1101, Miami, FL, USA.
Dig Dis Sci. 2021 May;66(5):1693-1699. doi: 10.1007/s10620-020-06392-2. Epub 2020 Jun 18.
Pruritus is a debilitating symptom of cholestatic diseases such as primary biliary cholangitis and primary sclerosing cholangitis and often results in major reduction in quality of life for afflicted patients. Classic treatment options for the treatment of cholestatic pruritus include antihistamines, bile acid resins, serotonin reuptake inhibitors, and mu-opioid antagonists. Unfortunately, these drugs are not always successful in treating pruritus of cholestasis and may be associated with adverse effects. Recent advances in our understanding of itch pathophysiology have led to the use of butorphanol, a kappa-opioid agonist and mu-opioid antagonist, for the treatment of various forms of pruritus. Reports of butorphanol to treat cholestatic itch specifically are rare.
To better understand the role of butorphanol in the treatment of cholestatic pruritus, including characterization of its side effect profile.
We present a case series of eight adult patients with cholestatic disease who were treated with butorphanol in hopes of alleviating intractable pruritus. Patients were identified through a clinical data request form serviced by University of Miami Information Technology.
Five out of eight patients (62.5%) reported successful reductions in itch severity after treatment with butorphanol, two patients reported no (or transient) change in itch severity, and one patient reported a paradoxical increase in itching. Side effects included somnolence, sedation, nausea, vomiting, and dizziness.
Butorphanol was safe and leads to clinically significant symptomatic improvement. Clinicians should be aware of butorphanol as an off-label treatment option for pruritus of cholestasis. Further studies are needed to better characterize the effect of butorphanol on cholestatic itch.
瘙痒是原发性胆汁性胆管炎和原发性硬化性胆管炎等胆汁淤积性疾病的一种使人虚弱的症状,常导致受影响患者的生活质量大幅下降。治疗胆汁淤积性瘙痒的经典治疗选择包括抗组胺药、胆汁酸树脂、5-羟色胺再摄取抑制剂和μ-阿片受体拮抗剂。不幸的是,这些药物并不总是能成功治疗胆汁淤积性瘙痒,并且可能伴有不良反应。我们对瘙痒病理生理学的理解的最新进展导致了使用丁丙诺啡,一种κ-阿片受体激动剂和μ-阿片受体拮抗剂,来治疗各种形式的瘙痒。关于丁丙诺啡专门用于治疗胆汁淤积性瘙痒的报告很少。
更好地了解丁丙诺啡在治疗胆汁淤积性瘙痒中的作用,包括其副作用特征。
我们报告了 8 例成年胆汁淤积性疾病患者的病例系列,他们接受了丁丙诺啡治疗,以期缓解顽固性瘙痒。通过迈阿密大学信息技术提供的临床数据请求表识别患者。
8 例患者中有 5 例(62.5%)报告丁丙诺啡治疗后瘙痒严重程度降低,2 例患者报告瘙痒严重程度无(或短暂)变化,1 例患者报告瘙痒程度反而增加。副作用包括嗜睡、镇静、恶心、呕吐和头晕。
丁丙诺啡是安全的,并导致临床显著的症状改善。临床医生应意识到丁丙诺啡是胆汁淤积性瘙痒的一种非标签治疗选择。需要进一步的研究来更好地描述丁丙诺啡对胆汁淤积性瘙痒的影响。