Average Daily Dose Trajectories for Episodes of Buprenorphine Treatment for Opioid Use Disorder.

Substance use & addiction journal Pub Date : 2024-10-01 Epub Date: 2024-07-28 DOI:10.1177/29767342241263161
Corey J Hayes, Bradley C Martin, Katherine J Hoggatt, Michael A Cucciare, Teresa J Hudson, Adam J Gordon
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Abstract

Background: High-dose (≥24 mg) buprenorphine daily doses (BDD) may be important in treating patients with opioid use disorder (OUD) to improve retention and prevent overdose, particularly in the context of increased illicit fentanyl use. This study sought to: (1) identify trajectories for average BDD among patients initiating buprenorphine treatment for OUD and (2) assess patient characteristics associated with these identified trajectories.

Methods: Buprenorphine treatment episodes among patients in the US Veterans Healthcare Administration (VHA) from federal fiscal years 2006 to 2020 were identified. Group-based trajectory modeling (GBTM) was used to identify BDD trajectories based on weekly averages of BDD over the 180 days after buprenorphine episode initiation.

Results: A total of 79 303 buprenorphine treatment episodes among 44 583 patients were included in the analytic sample. GBTM identified 9 latent trajectories for BDD: (1) moderate dose, early discontinuation (10.1%), (2) moderate dose, delayed discontinuation (4.5%), (3) moderate dose, moderate-paced discontinuation (5.2%), (4) low-moderate dose, delayed discontinuation (7.0%), and (5) low-moderate dose, early discontinuation (21.1%), (6) low dose retention (9.6%), (7) low-moderate dose retention (16.7%), (8) moderate dose retention (18.6%), and (9) high dose retention (7.4%). Patient BDD can broadly be characterized as low [2-4 mg/day], low-moderate (6-8 mg/day), moderate (12-18 mg/day), and high dose (≥ 24 mg/day). Patients with episodes in the high BDD trajectory have the lowest social risk (eg, lowest rate of past-year history of homelessness) and the lowest diagnosed rate of physical and mental health-related comorbidities compared to those following other trajectories.

Conclusions: BDD ranges widely and patient characteristics are significantly different between those episodes following differing BDD trajectories. Future research on the association between BDD and subsequent patient outcomes (eg, overdose) needs to carefully consider these differences in baseline characteristics.

丁丙诺啡治疗阿片类药物使用障碍发作的日均剂量轨迹。
背景:大剂量(≥24 毫克)丁丙诺啡日剂量(BDD)对于治疗阿片类药物使用障碍(OUD)患者可能非常重要,可提高患者的保留率并防止用药过量,尤其是在非法芬太尼使用增加的情况下。本研究旨在(方法:方法:确定了美国退伍军人医疗保健管理局(VHA)2006 至 2020 联邦财政年度患者的丁丙诺啡治疗发作。根据丁丙诺啡治疗发作开始后 180 天内每周 BDD 的平均值,使用基于群体的轨迹建模(GBTM)来识别 BDD 轨迹:分析样本共包括 44 583 名患者的 79 303 次丁丙诺啡治疗。GBTM 确定了 9 种 BDD 的潜在轨迹:(1)中等剂量,早期停药(10.1%);(2)中等剂量,延迟停药(4.5%);(3)中等剂量,中速停药(5.2%);(4)低中等剂量,延迟停药(7.0%),(5)低中等剂量,提前停药(21.1%),(6)低剂量保留(9.6%),(7)低中等剂量保留(16.7%),(8)中等剂量保留(18.6%),(9)高剂量保留(7.4%)。患者的 BDD 大致可分为低剂量[2-4 毫克/天]、低-中剂量(6-8 毫克/天)、中剂量(12-18 毫克/天)和高剂量(≥ 24 毫克/天)。与其他轨迹的患者相比,BDD高发患者的社会风险最低(例如,过去一年无家可归史的比例最低),身体和精神健康相关合并症的诊断率也最低:结论:BDD 的范围很广,在遵循不同 BDD 发展轨迹的病例中,患者特征存在显著差异。未来有关 BDD 与患者后续结果(如用药过量)之间关系的研究需要仔细考虑这些基线特征的差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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