Tilhou Alyssa Shell, Grucza Richard A, Xu Kevin Y
Department of Family Medicine, Dowling Building, Boston Medical Center, 850 Harrison Ave, Boston, MA 02118, USA.
Advanced Health Data (AHEAD) Institute, Department of Family and Community Medicine, Saint Louis University, 3545 Lafayette Ave., 4th Floor, St. Louis, MO 63104, USA.
Drug Alcohol Depend. 2025 Jul 1;272:112685. doi: 10.1016/j.drugalcdep.2025.112685. Epub 2025 Apr 22.
People with opioid use disorder (OUD) often exhibit psychiatric symptoms representing primary (PMD) and substance induced mental disorders (SIMD). PMD are associated with increased discontinuation of medications for OUD (MOUD). It is unknown if this relationship holds for SIMD.
To examine the association between SIMD and time to MOUD discontinuation.
In this retrospective cohort study using the Merative™ MarketScan® Commercial and Multi-State Medicaid insurance claims Databases (2015-2019), we identified individuals initiating MOUD (buprenorphine, methadone, and extended-release naltrexone) following a 180-day pre-period of continuous enrollment without MOUD. Episodes were classified based on > 1 SIMD diagnosis in this pre-period. We estimated days to MOUD discontinuation using stepwise multivariable Cox regression, adjusting for age, sex, insurance type (Medicaid or Commercial), Charlson Comorbidity Index, MOUD at initiation, co-occurring substance use disorders (SUD), and PMD.
Of 31,134 MOUD initiation episodes, 3.5 % exhibited SIMD. Episodes with SIMD demonstrated a higher prevalence (p < .001 for all) of mood and psychotic disorders (42.8 vs 16.4 %; 4.0 % vs 0.7 % respectively) but lower prevalence of anxiety-related disorders (51.3 % vs 59.9 %) relative to episodes without SIMD. Unadjusted models illustrated a 44 % (95 %CI:1.34-1.55) increased hazard of MOUD discontinuation associated with SIMD. After adjusting for all covariates but PMD, SIMD retained a 13 % increased hazard of MOUD discontinuation (95 %CI:1.05-1.21). Adjusting for PMD eliminated this association.
SIMD is associated with reduced time to MOUD discontinuation, which may be accounted for by PMD. Further research on SIMD treatment among individuals with OUD is needed to improve OUD treatment outcomes.
患有阿片类物质使用障碍(OUD)的人常常表现出代表原发性精神障碍(PMD)和物质所致精神障碍(SIMD)的精神症状。PMD与OUD药物治疗(MOUD)停药率增加有关。尚不清楚这种关系是否适用于SIMD。
研究SIMD与MOUD停药时间之间的关联。
在这项回顾性队列研究中,我们使用了默克公司的MarketScan®商业保险和多州医疗补助保险理赔数据库(2015 - 2019年),确定了在连续180天未接受MOUD治疗的预观察期后开始接受MOUD治疗(丁丙诺啡、美沙酮和长效纳曲酮)的个体。根据该预观察期内是否有超过1次SIMD诊断对病例进行分类。我们使用逐步多变量Cox回归估计MOUD停药天数,并对年龄、性别、保险类型(医疗补助或商业保险)、查尔森合并症指数、起始MOUD治疗、同时存在的物质使用障碍(SUD)和PMD进行了调整。
在31,134例MOUD起始病例中,3.5%表现出SIMD。与无SIMD的病例相比,有SIMD的病例中情绪障碍和精神障碍的患病率更高(分别为42.8%对16.4%;4.0%对0.7%),但焦虑相关障碍的患病率较低(51.3%对59.9%)(所有p值均<0.001)。未调整模型显示,与SIMD相关的MOUD停药风险增加44%(95%CI:1.34 - 1.55)。在对除PMD外的所有协变量进行调整后,SIMD导致的MOUD停药风险仍增加了13%(95%CI:1.05 - 1.21)。对PMD进行调整后消除了这种关联。
SIMD与MOUD停药时间缩短有关,这可能是由PMD引起的。需要对患有OUD的个体中SIMD的治疗进行进一步研究,以改善OUD的治疗效果。