Aripiprazole vs Risperidone for the acute-phase treatment of first-episode psychosis: A 6-week randomized, flexible-dose, open-label clinical trial

被引:7
|
作者
Gomez-Revuelta, Marcos [1 ]
Pelayo-Teran, Jose Maria [1 ,2 ,3 ]
Vazquez-Bourgon, Javier [1 ,2 ]
de la Foz, Victor Ortiz-Garcia [1 ,2 ]
Mayoral-van Son, Jacqueline [1 ,2 ,4 ,5 ]
Ayesa-Arriola, Rosa [1 ,2 ]
Crespo-Facorro, Benedicto [1 ,2 ,4 ,5 ]
机构
[1] Univ Cantabria, Univ Hosp Marques Valdecilla, IDIVAL, Dept Psychiat,Sch Med, Avda Valdecilla 25, Santander 39008, Spain
[2] CIBERSAM, Ctr Invest Biomed Red Salud Mental, Madrid, Spain
[3] Hosp El Bierzo, GASBI, Serv Psiquiatria & Salud Mental, Serv Salud Castilla & Leon SACYL, Ponferrada, Leon, Spain
[4] Univ Seville, Hosp Univ Virgen Rocio, Dept Psychiat, Seville, Spain
[5] Inst Invest Sanitaria Sevilla, IBiS Spain, Seville, Spain
关键词
Schizophrenia; Antipsychotics; First-episode-psychosis; RATING-SCALE; NONAFFECTIVE PSYCHOSIS; ANTIPSYCHOTIC-DRUGS; 1ST EPISODE; SCHIZOPHRENIA; QUETIAPINE; AKATHISIA; DISORDERS; EFFICACY;
D O I
10.1016/j.euroneuro.2021.02.009
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Selecting the first antipsychotic agent for the acute phase of a first episode of psychosis (FEP) is a critical task that may impact on the long-term outcome. Despite that, there is a lack of research comparing head-to-head different second-generation antipsychotics at this stage. The aim of this study was to compare the effectiveness of aripiprazole and risperidone in the treatment of the acute phase after a FEP. For that purpose, from February 2011 to October 2018, a prospective, randomized, open-label study was undertaken. Two hundred-sixty-six first-episode, drug-na & iuml;ve patients were randomly assigned to aripiprazole ( n = 136), or risperidone ( n = 130) and followed-up for 6-weeks. The primary effectiveness measure was all-cause treatment discontinuation. In addition, an analysis based on intention-to-treat principle was conducted to assess clinical efficacy. The overall dropout rate at 6-week reached 19.5%. Effectiveness measures were similar between both treatment groups as treatment discontinuation rates (chi 2 = 1.863; p = 0.172) and mean time until all-cause discontinuation (log rank = 1.421; p = 0.233) showed no statistically significant differences. In terms of clinical efficacy, risperidone proved a statistically significant better performance according to BPRS mean change between baseline and 6-week total score ( t = 3.187; p = 0.002). Patients under risperidone treatment were significantly more likely to suffer sex-related adverse events. In conclusion, no differences regarding effectiveness were found between aripiprazole and risperidone for the acute-phase treatment of FEP. Despite the importance of efficacy during this phase of treatment, selecting the most effective treatment for the long-term outcome, requires addressing safety and patient s & acute; preferences. (c) 2021 Elsevier B.V. and ECNP. All rights reserved.
引用
收藏
页码:74 / 85
页数:12
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