Division of General Internal Medicine, Department of Medicine, University of Colorado School of Medicine, Mail Stop B180, 12631 E. 17Th Ave, Aurora, CO, 80045, USA.
Division of General Internal Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Addict Sci Clin Pract. 2023 Sep 2;18(1):51. doi: 10.1186/s13722-023-00408-8.
We use a novel, longitudinal approach to describe average time spent in opioid use disorder (OUD) cascade of care stages for people with HIV (PWH) and with OUD, incorporating four definitions of treatment retention. Using this approach, we describe the impact of cocaine or hazardous alcohol use on time spent retained on buprenorphine.
We followed PWH with OUD enrolled in the Johns Hopkins HIV Clinical Cohort from their first buprenorphine treatment episode between 2013 and 2020. We estimated 4-year restricted mean time spent on buprenorphine below buprenorphine retention threshold, on buprenorphine above retention threshold, off buprenorphine and in HIV care, loss to follow-up, and death. Retention definitions were based on retention threshold (180 vs 90 days) and allowable treatment gap (7 vs 30 days). Differences in 2-year restricted mean time spent retained on buprenorphine were estimated for patients with and without cocaine or hazardous alcohol use.
The study sample (N = 179) was 63% male, 82% non-Hispanic Black, and mean age was 53 (SD 8) years. Patients spent on average 13.9 months (95% CI 11.4, 16.4) on buprenorphine over 4 years. There were differences in time spent retained on buprenorphine based on the retention definition, ranging from 6.5 months (95% CI 4.6, 8.5) to 9.6 months (95% CI 7.4, 11.8). Patients with cocaine use spent fewer months retained on buprenorphine. There were no differences for patients with hazardous alcohol use.
PWH with OUD spend relatively little time receiving buprenorphine in their HIV primary care clinic. Concurrent cocaine use at buprenorphine initiation negatively impact time on buprenorphine.
我们采用一种新颖的纵向方法来描述艾滋病毒感染者(HIV)和阿片类药物使用障碍(OUD)患者在 OUD 治疗连续体各阶段的平均治疗时间,其中包含四种治疗保留定义。使用这种方法,我们描述了可卡因或有害酒精使用对丁丙诺啡保留时间的影响。
我们对 2013 年至 2020 年期间在约翰霍普金斯 HIV 临床队列中首次接受丁丙诺啡治疗的 OUD 合并 HIV 的患者进行了随访。我们估计了 4 年内患者处于丁丙诺啡保留阈值以下、保留阈值以上、停止丁丙诺啡治疗和 HIV 护理、失访和死亡的时间。保留定义基于保留阈值(180 天与 90 天)和允许的治疗间隙(7 天与 30 天)。我们评估了有无可卡因或有害酒精使用的患者在 2 年内保留丁丙诺啡的平均时间的差异。
研究样本(N=179)中 63%为男性,82%为非西班牙裔黑人,平均年龄为 53(8)岁。患者在 4 年内平均接受丁丙诺啡治疗 13.9 个月(95%CI 11.4-16.4)。根据保留定义,患者保留丁丙诺啡的时间存在差异,范围从 6.5 个月(95%CI 4.6-8.5)到 9.6 个月(95%CI 7.4-11.8)。在开始丁丙诺啡治疗时同时使用可卡因的患者保留丁丙诺啡的时间更少。在开始丁丙诺啡治疗时同时使用有害酒精的患者保留丁丙诺啡的时间没有差异。
OUD 合并 HIV 的患者在其 HIV 初级保健诊所接受丁丙诺啡治疗的时间相对较短。在开始丁丙诺啡治疗时同时使用可卡因会对丁丙诺啡的使用时间产生负面影响。