Relapse in patients with schizophrenia and amisulpride-induced hyperprolactinemia or olanzapine-induced metabolic disturbance after switching to other antipsychotics

阿米必利 奥氮平 阿立哌唑 精神分裂症(面向对象编程) 阳性与阴性症状量表 利培酮 内科学 抗精神病药 非定型抗精神病薬 医学 心理学 静坐不能 奎硫平 精神科 精神病
作者
Jingda Cai,Li Li,Tiannan Shao,Mengxi Sun,Weiyan Wang,Peng Xie,Xiaoyi Wang,Ye Yang,Yujun Long,Dongyu Kang,Jingmei Xiao,Yu‐Han Su,Xingjie Peng,Yuyan Huang,Menghui Gao,Qiongqiong Wu,Chuhan Song,Furu Liu,Ping Shao,Jianjun Ou
出处
期刊:Psychiatry Research-neuroimaging [Elsevier BV]
卷期号:322: 115138-115138 被引量:2
标识
DOI:10.1016/j.psychres.2023.115138
摘要

Hyperprolactinemia and metabolic disturbance are common side effects of antipsychotics that cause intolerance. Despite its potential influence on relapse, there are no established guidelines for antipsychotic switching. This naturalistic study explored the association between antipsychotic switching, baseline clinical status, metabolic changes, and relapse in patients with schizophrenia. In total, 177 patients with amisulpride-induced hyperprolactinemia and 274 with olanzapine-induced metabolic disturbance were enrolled. Relapse was determined by assessing changes in Positive and Negative Syndrome Scale (PANSS) total scores from baseline to 6 months (increased over 20% or 10% reaching 70). Metabolic indices were measured at baseline and 3 months. Patients with baseline PANSS >60 were more likely to relapse. Further, patients switching to aripiprazole had a higher risk of relapse regardless of their original medication. Participants who originally used amisulpride had reduced prolactin levels following medication change, while switching to olanzapine caused increased weight and blood glucose levels. In patients originally using olanzapine, only switching to aripiprazole reduced insulin resistance. Adverse effects on weight and lipid metabolism were observed in patients who switched to risperidone, while amisulpride improved lipid profiles. Changing schizophrenia treatment requires careful consideration of multiple variables, particularly the choice of substituted drug and the patient's baseline symptoms.
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