Hospital Álvaro Cunqueiro, Complejo Hospitalario Universitario de Vigo, Vigo, Spain.
Hospital Universitario de Álava, Álava, Spain.
Eur Psychiatry. 2021 Apr 12;64(1):e40. doi: 10.1192/j.eurpsy.2021.23.
Poor adherence to antipsychotic drugs is a major problem in schizophrenia management and one of the most important risk factors for relapse and hospitalization. To date, there is little evidence on persistence predictors with long-acting injectable antipsychotics, especially with aripiprazole once-monthly (AOM). This study (NCT03130478) aimed to describe the impact of demographic and clinical characteristics on persistence with AOM treatment in real-world setting.
This was an observational, retrospective, non-interventional study that included adult patients with schizophrenia who were initiated on AOM during a schizophrenia-related hospitalization. Data were retrospectively collected from patients' medical records. The primary variable was persistence with AOM, measured as the number of days from AOM initiation up to all-cause AOM discontinuation during the first six months after treatment index.
140 patients were enrolled and 91 fulfilled the selection criteria. Six months after AOM initiation, 65 (71.4%) patients were still receiving AOM treatment, whereas 26 (28.6%) were not. The mean (standard deviation) time to AOM treatment discontinuation in the first six months was 138.1 (6.8) days, with most of the patients discontinuing at the first 28 days. The risk of AOM discontinuation in the first six months increases 1.05-fold annually since schizophrenia diagnosis (p=0.003); moreover, this risk increases 2.86-fold in patients with concomitant schizophrenia medication at AOM initiation compared to patients without concomitant schizophrenia treatments (p=0.02).
Main factors predicting persistence with AOM treatment at six months in clinical practice are fewer years since schizophrenia diagnosis and not receiving concomitant schizophrenia treatments at AOM initiation.
抗精神病药物治疗依从性差是精神分裂症管理中的一个主要问题,也是复发和住院的最重要危险因素之一。迄今为止,长效注射用抗精神病药物(尤其是阿立哌唑一月一次)的持续存在预测因素的证据很少。本研究(NCT03130478)旨在描述人口统计学和临床特征对现实环境中阿立哌唑治疗持续时间的影响。
这是一项观察性、回顾性、非干预性研究,纳入了在与精神分裂症相关的住院期间开始接受阿立哌唑治疗的成年精神分裂症患者。数据从患者的病历中回顾性收集。主要变量是阿立哌唑的持续使用,测量方法是从阿立哌唑开始治疗到治疗索引后 6 个月内因任何原因停用阿立哌唑的天数。
共纳入 140 例患者,其中 91 例符合入选标准。在阿立哌唑开始治疗后的 6 个月时,65 例(71.4%)患者仍在接受阿立哌唑治疗,26 例(28.6%)患者未接受治疗。在头 6 个月内停用阿立哌唑治疗的平均(标准差)时间为 138.1(6.8)天,大多数患者在头 28 天停药。自精神分裂症诊断以来,阿立哌唑停用风险每年增加 1.05 倍(p=0.003);此外,与未同时接受精神分裂症治疗的患者相比,在开始使用阿立哌唑时同时接受精神分裂症药物治疗的患者的阿立哌唑停用风险增加 2.86 倍(p=0.02)。
在临床实践中,预测阿立哌唑治疗持续时间达到 6 个月的主要因素是精神分裂症诊断后的时间较短,以及在开始使用阿立哌唑时未同时接受精神分裂症治疗。