Cuomo Ilaria, Kotzalidis Georgios D, de Persis Simone, Piacentino Daria, Perrini Filippo, Amici Emanuela, De Filippis Sergio
Department of Neurosciences, Mental Health, and Sensory Organs (NESMOS), Sapienza School of Medicine and Psychology, Sant'Andrea Hospital, Rome, Italy.
Department of Neuropsychiatry, Villa von Siebenthal Neuropsychiatric Hospital and Clinic, Genzano di Roma, Rome, Italy.
Neuropsychiatr Dis Treat. 2018 Jun 21;14:1645-1656. doi: 10.2147/NDT.S171002. eCollection 2018.
To overcome nonadherence in patients with psychosis switch to long-acting injectable (LAI) antipsychotic formulations is adopted. Most oral versus LAI comparisons showed similar antipsychotic responses. Psychoses often overlap with substance use disorder (SUD). Head-to-head LAI comparisons have hitherto focused only on non-comorbid populations.
The objective of this study was to compare two LAIs, administered for 12 months, in initially hospitalized patients with psychosis comorbid with SUD in their clinical and quality of life (QoL) outcomes.
Inpatients were recruited during 2016 and switched randomly to 400 mg intramuscular aripiprazole monohydrate (AM) (N=50) or to 100 mg intramuscular paliperidone palmitate (PP) once-monthly (N=51); patients were discharged and followed up for 12 months. Patients were rated at baseline and after 1 year through the Clinical Global Impression scale - severity (CGIs), substance craving intensity was rated through a visual analog scale for substance craving, and QoL through the World Health Organization (WHOQOL-BREF) scale. We addressed confounders with backward stepwise logistic regression and three-way analysis of variance.
PP were older and had more cases of schizophrenia spectrum and less bipolar disorders than AM, but AM had a stronger craving for substances at baseline. Both LAIs were associated with significant improvements in all outcomes, with AM displaying stronger effect sizes than PP. The two groups did not differ on baseline WHOQOL-BREF scores in any domain, but at the 1-year follow-up, AM fared better on all domains. The two groups did not differ in final severity, but PP scored higher than AM in craving at the 1-year endpoint. The CGIs is not a refined tool for severity and the substance craving may be subject to recall bias.
1-year AM and PP was followed by improved clinical status and QoL and reduced substance craving in a population with psychosis and SUD comorbidity. AM, compared to PP, improved craving and QoL at the 1-year follow-up.
为克服精神病患者的不依从性,采用了长效注射(LAI)抗精神病药物制剂。大多数口服与LAI的比较显示出相似的抗精神病反应。精神病常与物质使用障碍(SUD)重叠。迄今为止,LAI的直接比较仅集中在非共病人群。
本研究的目的是比较两种在最初住院的合并SUD的精神病患者中使用12个月的LAI药物,在临床和生活质量(QoL)结果方面的差异。
在2016年招募住院患者,并随机转换为每月一次肌肉注射400mg阿立哌唑一水合物(AM)(N = 50)或100mg棕榈酸帕利哌酮(PP)(N = 51);患者出院并随访12个月。在基线和1年后通过临床总体印象量表-严重程度(CGIs)对患者进行评分,通过物质渴望视觉模拟量表对物质渴望强度进行评分,并通过世界卫生组织(WHOQOL-BREF)量表对生活质量进行评分。我们使用向后逐步逻辑回归和三因素方差分析来处理混杂因素。
与AM组相比,PP组患者年龄更大,精神分裂症谱系病例更多,双相情感障碍病例更少,但AM组在基线时对物质的渴望更强。两种LAI药物均与所有结果的显著改善相关,AM组的效应量比PP组更强。两组在任何领域的基线WHOQOL-BREF评分均无差异,但在1年随访时,AM组在所有领域的表现更好。两组的最终严重程度无差异,但在1年终点时,PP组在渴望方面的得分高于AM组。CGIs不是一个用于评估严重程度的精细工具,物质渴望可能存在回忆偏差。
在合并精神病和SUD的人群中,使用1年的AM和PP后,临床状况和生活质量得到改善,物质渴望减少。与PP相比,AM在1年随访时改善了渴望和生活质量。