Department of Psychiatry, Faculty of Medicine, University of Turku, Turku, Finland.
Addiction Psychiatry Unit, Department of Psychiatry, Turku University Hospital, The Wellbeing Services County of Southwest Finland, Turku, Finland.
Schizophr Bull. 2024 Nov 8;50(6):1287-1294. doi: 10.1093/schbul/sbae034.
There is a paucity of research on treatment outcomes of patients with psychosis and cannabis use disorder (CUD). We aimed to compare the effectiveness of antipsychotics in reducing the risk of hospitalization in patients with first-episode psychosis (FEP) and co-occurring CUD.
We utilized a nationwide Swedish cohort of patients with longitudinal register data from the year 2006 to 2021. Participants were patients with FEP and co-occurring CUD (n = 1820, 84.73% men, mean age 26.80 years, SD 8.25 years). The main outcome was hospitalization due to psychotic relapse. Hospitalization due to any psychiatric disorder or substance use disorder (SUD) were examined as secondary outcomes. Within-individual Cox regression models were used to study these associations.
Use of any antipsychotic was associated with a 33% risk reduction of psychotic relapse (aHR = 0.67; 95% CI 0.60-0.75). Clozapine (0.43; 0.29-0.64), long-acting injectable (LAI) formulations of risperidone (0.40; 0.22-0.71), aripiprazole (0.42; 0.27-0.65), and paliperidone (0.46; 0.30-0.69) were associated with the lowest risk of relapse. The association between the LAI formulation of olanzapine and hospitalization due to psychosis was statistically non-significant (0.61; 0.35-1.05). Clozapine was associated with an 86% risk reduction of hospitalization due to SUD (0.14; 0.05-0.44). Of oral non-clozapine antipsychotics, aripiprazole was associated with the lowest risk of hospitalization due to psychotic relapse (0.61; 0.45-0.83).
These findings support the use of clozapine, LAI formulations of second-generation antipsychotics other than olanzapine, or oral aripiprazole to prevent hospitalization in FEP and co-occurring CUD.
目前,针对精神分裂症合并大麻使用障碍(CUD)患者的治疗结果研究较为匮乏。本研究旨在比较第一代抗精神病药物治疗首发精神分裂症(FEP)合并 CUD 患者的疗效,评估其降低住院风险的效果。
本研究使用了来自瑞典全国纵向登记数据的队列研究,纳入了 2006 年至 2021 年期间的患者。参与者为 FEP 合并 CUD 患者(n=1820,84.73%为男性,平均年龄 26.80 岁,标准差 8.25 岁)。主要结局为因精神病复发导致的住院。因任何精神障碍或物质使用障碍(SUD)导致的住院被作为次要结局进行评估。采用个体内 Cox 回归模型来研究这些关联。
使用任何一种抗精神病药物均可降低 33%的精神病复发风险(aHR=0.67;95%CI 0.60-0.75)。氯氮平(0.43;0.29-0.64)、利培酮长效注射剂(0.40;0.22-0.71)、阿立哌唑(0.42;0.27-0.65)和帕利哌酮(0.46;0.30-0.69)与复发风险最低相关。奥氮平长效注射剂与精神病住院之间的关联无统计学意义(0.61;0.35-1.05)。氯氮平与 SUD 导致的住院风险降低 86%相关(0.14;0.05-0.44)。在非氯氮平的口服抗精神病药物中,阿立哌唑与精神病复发导致的住院风险最低相关(0.61;0.45-0.83)。
这些发现支持使用氯氮平、除奥氮平之外的第二代抗精神病药物长效注射剂或口服阿立哌唑,以预防 FEP 合并 CUD 患者的住院。