Efficacy of Rivastigmine Augmentation on Positive and Negative Symptoms, General Psychopathology, and Quality of Life in Patients with Chronic Schizophrenia: A Randomized Controlled Trial.

Psychopharmacology bulletin Pub Date : 2024-04-04
Sepideh Herizchi, Ali Reza Shafiee-Kandjani, Mostafa Farahbakhsh, Zahra Jahangiri, Shahriyar Ghanbarzadeh Javid, Hosein Azizi
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Abstract

The study aimed to assess Rivastigmine augmentation on positive and negative symptoms (PNSs), general psychopathology, and quality of life in patients with chronic Schizophrenia. A double-blind, parallel-design, randomized, placebo-controlled trial of 60 schizophrenia patients was conducted. Intervention group received rivastigmine 3 mg/day + Treatment as Usual (TAU) and the control group: TAU + placebo. Negative and positive symptoms, general psychopathology; and quality of life were measured using Positive and Negative Symptom Scale (PANSS) and Manchester Short Assessment of Quality of Life (MANSA). T-test, ANOVA, and the general univariate linear model tests were used for the analyses. Out of 60 participants, 52 (86.6%) were male. At baseline, no significant relationship was found for demographic and clinical characteristics between intervention and control groups. Between-group analysis indicated that all outcome measures PNSs, general psychopathology symptoms, and QoL score in rivastigmine group was significantly improved (p = 0.001). According to within-group analysis, a significant association was found between Rivastigmine and placebo groups in PNSs (p < 0.05). Rivastigmine augmentation improved PNSs and psychopathology in schizophrenia patients. However, no significant association found for improving the life quality after 8 weeks treatment.

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利伐斯的明对慢性精神分裂症患者的阳性和阴性症状、一般精神病理学和生活质量的疗效:随机对照试验
这项研究旨在评估利伐斯的明对慢性精神分裂症患者的阳性和阴性症状(PNSs)、一般精神病理学和生活质量的影响。该研究对 60 名精神分裂症患者进行了双盲、平行设计、随机、安慰剂对照试验。干预组接受利伐斯的明3毫克/天+常规治疗(TAU),对照组接受TAU+安慰剂:TAU+安慰剂。采用阳性和阴性症状量表(PANSS)和曼彻斯特生活质量简短评估(MANSA)测量阴性和阳性症状、一般精神病理学和生活质量。分析采用了 T 检验、方差分析和一般单变量线性模型检验。在 60 名参与者中,52 人(86.6%)为男性。基线分析显示,干预组和对照组的人口统计学特征和临床特征之间没有明显关系。组间分析表明,利伐斯的明组的所有结果指标PNSs、一般精神病理症状和QoL评分均有显著改善(P = 0.001)。组内分析显示,利伐斯的明组和安慰剂组在 PNSs 方面有明显的相关性(P < 0.05)。利伐斯的明增效剂改善了精神分裂症患者的 PNS 和精神病理学。然而,8周治疗后,在改善生活质量方面没有发现明显的关联。
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