Narrative review of the advances in the pharmacotherapeutic management of juvenile-onset schizophrenia

被引:2
作者
Crump, Chesika J. J. [1 ]
Good, Megan E. E. [1 ]
Abuelazm, Hagar [1 ]
El-Mallakh, Rif S. S. [1 ]
机构
[1] Univ Louisville, Sch Med, Dept Psychiat & Behav Sci, Louisville, KY 40202 USA
关键词
Adolescent schizophrenia; aripiprazole; asenapine; brexpiprazole; lurasidone; negative symptoms; olanzapine; quetiapine; paliperidone; psychosis; risperidone; ziprasidone; CARD SORTING TEST; PALIPERIDONE EXTENDED-RELEASE; CLINICAL HIGH-RISK; DOUBLE-BLIND; NEGATIVE SYMPTOMS; 1ST-EPISODE SCHIZOPHRENIA; ANTIPSYCHOTIC MEDICATION; PSYCHOTIC DISORDERS; SPECTRUM DISORDERS; RECEPTOR OCCUPANCY;
D O I
10.1080/14656566.2023.2208269
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionSchizophrenia usually begins with prodromal symptoms in adolescence. In 39% of patients, onset of psychotic symptoms occurs prior to age 19. Advances in the treatment of psychosis with medications over the last decade are reviewed in this paper.Areas coveredUnderstanding how to prescribe antipsychotics early in schizophrenia requires an understanding of the pathophysiology of the disease. The current structure of the dopamine hypothesis is reviewed. Risperidone, paliperidone, olanzapine, quetiapine, and aripiprazole have become established treatments prior to 2012. Since 2012, lurasidone (2017) and brexpiprazole (2022) have also been approved. Lurasidone was approved based on placebo-controlled studies, but brexpiprazole has been approved on the bases of open safety trials. In comparative trials, aripiprazole was better tolerated and less likely to cause hyperprolactinemia and metabolic abnormalities.Expert opinionAntipsychotics can induce adaptive changes in the brain that predispose patients to future problems such as tardive dyskinesia and supersensitivity psychosis. When pathophysiology of schizophrenia, and a clear understanding of the pharmacology of existing antipsychotics are included in the evidence-based analysis, use of partial agonists, which are less likely to induce adaptive changes in the brain and less likely to induce metabolic and prolactin side effects, become the preferred agents.
引用
收藏
页码:1039 / 1052
页数:14
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