Patel Ashwin, Kalmus Grace, Dampier Carlton, Osunkwo Ifeyinwa, New Tamara, Gee Beatrice, Saah Elna
Emory University School of Medicine, Atlanta, Georgia, USA.
Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, Georgia, USA.
Pediatr Blood Cancer. 2025 Aug;72(8):e31731. doi: 10.1002/pbc.31731. Epub 2025 May 24.
Patients with sickle cell disease (SCD) experience painful vaso-occlusive episodes that increase with age; a subset develops chronic pain (CP). CP is usually managed with acute pain management guidelines despite evidence of ineffectiveness. Buprenorphine (BUP), a partial opioid agonist, is a potent analgesic with less euphoric effect and a respiratory "ceiling effect." BUP therefore provides an alternative "harm reduction" approach for CP management in pediatric SCD patients.
This single urban center retrospective study assessed the feasibility of inpatient transition to BUP-containing analgesics in adolescents with SCD and CP. Patients aged 12-20 years who transitioned from full opioid agonists (FOA) to BUP between December 2020 and September 2022 were included. Acute care utilization, hospital length of stay, and FOA use in both inpatient and outpatient settings were compared pre- and post-BUP induction for up to a year.
Fourteen adolescents with SCD underwent inpatient BUP induction and maintenance therapy. Inpatient transition using a micro-induction approach was feasible and well tolerated in this population. There were low rates of adverse events, such as opioid withdrawal signs. Maintenance on BUP products was sustainable over the 1-year post-induction period. Three patients (21%) discontinued BUP during maintenance therapy. There was a significant reduction (p < 0.05) in acute care utilization, length of stay, and FOA use (both inpatient and outpatient).
Inpatient micro-induction to BUP from FOA in adolescent SCD patients with CP is feasible with minimal signs of opioid withdrawal. This study suggests decreased acute care utilization with BUP.
镰状细胞病(SCD)患者会经历疼痛性血管闭塞发作,且发作频率随年龄增长而增加;一部分患者会发展为慢性疼痛(CP)。尽管有证据表明无效,但CP通常仍按照急性疼痛管理指南进行治疗。丁丙诺啡(BUP)是一种部分阿片类激动剂,是一种强效镇痛药,欣快感作用较小且有呼吸“封顶效应”。因此,BUP为小儿SCD患者的CP管理提供了一种替代性的“减少伤害”方法。
这项单中心回顾性研究评估了患有SCD和CP的青少年住院患者转换为含BUP镇痛药的可行性。纳入了2020年12月至2022年9月期间从完全阿片类激动剂(FOA)转换为BUP的12 - 20岁患者。比较了BUP诱导前后长达一年的急性护理利用率、住院时间以及住院和门诊环境中FOA的使用情况。
14名患有SCD的青少年接受了住院BUP诱导和维持治疗。在该人群中,使用微诱导方法进行住院转换是可行的,且耐受性良好。不良事件发生率较低,如阿片类药物戒断症状。BUP产品维持治疗在诱导后1年内是可持续的。3名患者(21%)在维持治疗期间停用了BUP。急性护理利用率、住院时间和FOA使用(住院和门诊)均显著降低(p < 0.05)。
患有CP的青少年SCD患者从FOA住院微诱导转换为BUP是可行的,阿片类药物戒断迹象 minimal。本研究表明BUP可降低急性护理利用率。 (注:原文中“minimal signs of opioid withdrawal”表述似乎不完整,可能存在遗漏信息,但按照要求直接翻译。)