Anderson Carolyn, Cooley Rachel, Patil Dustin
From the Department of Psychiatry, Julian F. Keith Alcohol and Drug Abuse Treatment Center, North Carolina Department of Health and Human Services, Black Mountain, NC (CA, RC, DP); Department of Psychiatry, University of North Carolina School of Medicine, Asheville, NC (DP).
J Addict Med. 2023;17(2):241-244. doi: 10.1097/ADM.0000000000001085. Epub 2022 Sep 27.
Transitions from high-dose methadone to buprenorphine for treatment of opioid use disorder (OUD) present risk of precipitated withdrawal related to the introduction of a high-affinity partial agonist at the mu-opioid receptor after occupancy by a lower-affinity full agonist. Various strategies have been explored to maintain patient stability during this process, including microdosing buprenorphine. Current literature lacks consensus on an optimal setting and strategy for initiating a buprenorphine microdosing protocol and gives little detail on patients' conditions after the acute transition period. We report a 6-day microdosing transition from methadone 100 mg directly to sublingual buprenorphine, followed by a 20-day period of monitoring and additional treatment. This patient tolerated a sublingual buprenorphine microdosing protocol while using supportive medications with a peak Clinical Opiate Withdrawal Scale score of 6. The patient's most significant withdrawal symptoms occurred several days after completion of the microdosing process. This case demonstrates the feasibility of using a transmucosal buprenorphine formulation in microdosing transitions from high-dose methadone directly to buprenorphine, and highlights the utility of a medically monitored intensive inpatient setting (American Society of Addiction Medicine level 3.7) in providing appropriate monitoring and treatment during and after a microdosing transition.
从高剂量美沙酮转换为丁丙诺啡用于治疗阿片类物质使用障碍(OUD),存在因在低亲和力的完全激动剂占据μ-阿片受体后引入高亲和力的部分激动剂而引发戒断反应的风险。在此过程中,人们探索了各种策略来维持患者的稳定性,包括丁丙诺啡的微剂量给药。目前的文献对于启动丁丙诺啡微剂量给药方案的最佳设置和策略尚未达成共识,并且对于急性过渡期后患者的状况也鲜有详细描述。我们报告了一例从100毫克美沙酮直接转换为舌下含服丁丙诺啡的6天微剂量给药转换过程,随后进行了为期20天的监测和额外治疗。该患者在使用支持性药物的情况下耐受了舌下含服丁丙诺啡微剂量给药方案,临床阿片戒断量表最高评分为6分。患者最明显的戒断症状发生在微剂量给药过程完成后的几天。该病例证明了在从高剂量美沙酮直接转换为丁丙诺啡的微剂量给药转换中使用经粘膜丁丙诺啡制剂的可行性,并强调了在微剂量给药转换期间及之后,在医学监测的强化住院环境(美国成瘾医学协会3.7级)中提供适当监测和治疗的实用性。