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Which Subgroup of First-Episode Schizophrenia Patients Can Remit During the First Year of Antipsychotic Treatment?

OBJECTIVE: To investigate the persistent remission rate (PRR) and its predictors within the first year of antipsychotic treatment in first-episode schizophrenia (FES) patients. METHODS: In a sample of 301 FES patients who remained in antipsychotic treatment for 1 year, we assessed symptoms with the...

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Detalles Bibliográficos
Autores principales: Cheng, Zhang, Yuan, Yanbo, Han, Xue, Yang, Lei, Zeng, Xin, Yang, Fude, Lu, Zheng, Wang, Chuanyue, Deng, Hong, Zhao, Jingping, Yu, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318109/
https://www.ncbi.nlm.nih.gov/pubmed/32636771
http://dx.doi.org/10.3389/fpsyt.2020.00566
Descripción
Sumario:OBJECTIVE: To investigate the persistent remission rate (PRR) and its predictors within the first year of antipsychotic treatment in first-episode schizophrenia (FES) patients. METHODS: In a sample of 301 FES patients who remained in antipsychotic treatment for 1 year, we assessed symptoms with the Positive and Negative Syndrome Scale (PANSS), cognition in six domains and functioning with the Personal and Social Performance Scale (PSP). RESULTS: In total, 75.4% (227/301) of FES patients remaining in antipsychotic treatment reached persistent remission (PR) in one year. The PSP score was higher in remitters than non-remitters at the endpoint of the 1-year follow-up (P <0.0001). The PANSS negative score—but not the PANSS total score, positive score or general psychopathological score; PSP score; or cognitive performance at baseline—was negatively associated with PR. Lower scores for “abstract thinking” and “stereotyped thinking” were independent predictors of PR. CONCLUSIONS: In FES, nearly 3/4 patients could achieve PR with 1 year of antipsychotic treatment, and having fewer negative symptoms, especially thinking and volition symptoms, can predict PR. CLINICAL TRIAL REGISTRATION: www.ClinicalTrials.gov, identifier NCT01057849.