National Clinician Scholars Program, Yale School of Medicine, New Haven, CT, United States of America; Department of Medicine, Yale School of Medicine, New Haven, CT, United States of America; Department of Pediatrics, Yale School of Medicine, New Haven, CT, United States of America.
Department of Medicine, VA Connecticut Healthcare System, West Haven, CT, United States of America.
J Subst Abuse Treat. 2020 Feb;109:14-22. doi: 10.1016/j.jsat.2019.11.002. Epub 2019 Nov 6.
Infrequent use of and poor retention on evidence-based medications for alcohol use disorder (MAUD) represent a treatment gap, particularly among people living with HIV (PLWH). We examined predictors of MAUD initiation and retention across HIV status.
From Veterans Aging Cohort Study (VACS) data, we identified new alcohol use disorder (AUD) diagnoses from 1998 to 2015 among 163,339 individuals (50,826 PLWH and 112,573 uninfected, matched by age, sex, and facility). MAUD initiation was defined as a prescription fill for naltrexone, acamprosate or disulfiram within 30 days of a new diagnosis. Among those who initiated, retention was defined as filling medication for ≥80% of days over the following six months. We used multivariable logistic regression to assess patient- and facility-level predictors of AUD medication initiation across HIV status.
Among 10,603 PLWH and 24,424 uninfected individuals with at least one AUD episode, 359 (1.0%) initiated MAUD and 49 (0.14%) were retained. The prevalence of initiation was lower among PLWH than those without HIV (adjusted odds ratio [AOR] 0.66, 95% confidence interval [CI] 0.51-0.85). Older age (for PLWH: AOR 0.78, 95% CI 0.61-0.99; for uninfected: AOR 0.70, 95% CI 0.61-0.80) and black race (for PLWH: AOR 0.63, 95% CI 0.0.49-0.1.00; for uninfected: AOR 0.63, 95% CI 0.48-0.83), were associated with decreased odds of initiation for both groups. The low frequency of retention precluded multivariable analyses for retention.
For PLWH and uninfected individuals, targeted implementation strategies to expand MAUD are needed, particularly for specific subpopulations (e.g. black PLWH).
在酒精使用障碍(MAUD)的证据基础药物的使用频率低且保留率差,这代表了治疗差距,尤其是在感染艾滋病毒的人群(PLWH)中。我们研究了不同 HIV 状态下 MAUD 起始和保留的预测因素。
我们从退伍军人老龄化队列研究(VACS)数据中,确定了 1998 年至 2015 年间 163339 人中的新酒精使用障碍(AUD)诊断(50826 名 PLWH 和 112573 名未感染,按年龄、性别和机构匹配)。MAUD 的起始定义为在新诊断后 30 天内开出纳曲酮、安非他酮或双硫仑的处方。在那些开始治疗的人中,保留定义为在接下来的六个月内至少 80%的天数服用药物。我们使用多变量逻辑回归评估了 HIV 状态下患者和机构层面的 AUD 药物起始的预测因素。
在至少有一次 AUD 发作的 10603 名 PLWH 和 24424 名未感染个体中,有 359 名(1.0%)开始使用 MAUD,49 名(0.14%)保留。PLWH 中的起始率低于未感染 HIV 的人(调整后的优势比 [AOR] 0.66,95%置信区间 [CI] 0.51-0.85)。年龄较大(对于 PLWH:AOR 0.78,95%CI 0.61-0.99;对于未感染:AOR 0.70,95%CI 0.61-0.80)和黑种人(对于 PLWH:AOR 0.63,95%CI 0.49-0.83;对于未感染:AOR 0.63,95%CI 0.48-0.83)与两组的起始几率降低有关。保留的低频率使得保留的多变量分析变得不可能。
对于 PLWH 和未感染的个体,需要针对特定亚人群(例如黑人 PLWH)实施扩大 MAUD 的针对性实施策略。