Brown Patrick, Ryder Alexa, Robinson Christopher, Valenti Kayla, Phung Katie, Hasoon Jamal
Department of Neurology University of Texas Health Science Center at Houston, Houston, TX, USA.
Department of Physical Medicine and Rehabilitation University of Texas Health Science Center at Houston, Houston, TX, USA.
Health Psychol Res. 2025 Mar 2;13:129552. doi: 10.52965/001c.129552. eCollection 2025.
Methadone is a synthetic opioid extensively used in opioid use disorder management but is gaining recognition for its unique pharmacological properties that make it a viable alternative for chronic pain management. This review aims to explore methadone's pharmacokinetics, pharmacodynamics, efficacy, and safety profile to assess its potential role in managing chronic pain conditions.
Methadone's dual action as a mu-opioid receptor agonist and NMDA receptor antagonist positions it as an effective option for managing both nociceptive and neuropathic pain. It has shown promising results in cancer pain management, refractory pain, and opioid rotation strategies. Despite its therapeutic advantages, concerns regarding its narrow therapeutic window, variable pharmacokinetics, QT interval prolongation, and risk of respiratory depression highlight the need for careful patient selection and monitoring. New evidence also sheds light on its affordability and efficacy in low-resource settings, as well as its controversial role in mitigating opioid-induced hyperalgesia.
Methadone offers a unique therapeutic option in chronic pain management due to its multifaceted pharmacological properties. While it provides significant benefits for patients with complex pain syndromes, clinicians must exercise caution due to its safety concerns and variability in individual metabolism. A personalized approach, combined with rigorous monitoring, is essential to optimize its benefits while minimizing risks. Further research is needed to better define its role in chronic pain treatment and address unresolved safety concerns.
美沙酮是一种合成阿片类药物,广泛用于阿片类物质使用障碍的管理,但因其独特的药理特性而日益受到认可,这些特性使其成为慢性疼痛管理的可行替代方案。本综述旨在探讨美沙酮的药代动力学、药效学、疗效和安全性,以评估其在慢性疼痛病症管理中的潜在作用。
美沙酮作为μ-阿片受体激动剂和N-甲基-D-天冬氨酸(NMDA)受体拮抗剂的双重作用,使其成为管理伤害性疼痛和神经性疼痛的有效选择。它在癌症疼痛管理、难治性疼痛和阿片类药物轮换策略方面已显示出有前景的结果。尽管具有治疗优势,但对其治疗窗窄、药代动力学可变、QT间期延长以及呼吸抑制风险的担忧凸显了谨慎选择患者并进行监测的必要性。新证据还揭示了其在资源匮乏环境中的可负担性和疗效,以及其在减轻阿片类药物诱导的痛觉过敏方面的争议性作用。
由于其多方面的药理特性,美沙酮在慢性疼痛管理中提供了一种独特的治疗选择。虽然它为患有复杂疼痛综合征的患者带来显著益处,但由于其安全性问题和个体代谢的变异性,临床医生必须谨慎行事。个性化方法与严格监测相结合,对于优化其益处同时最小化风险至关重要。需要进一步研究以更好地界定其在慢性疼痛治疗中的作用并解决未解决的安全问题。