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Low-Dose Ziprasidone in Combination with Sertraline for First-Episode Drug-Naïve Patients with Schizophrenia: a Randomized Controlled Trial.
Zhu, Cheng; Guan, Xiaoni; Wang, Yuechan; Liu, Jiahong; Kosten, Thomas R; Xiu, Meihong; Wu, Fengchun; Zhang, Xiangyang.
Afiliação
  • Zhu C; The Second Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, China.
  • Guan X; The Affiliated Kangning Hospital of Wenzhou Medical University, Wenzhou, China.
  • Wang Y; Peking University HuiLongGuan Clinical Medical School, Beijing HuiLongGuan Hospital, Beijing, China.
  • Liu J; Peking University HuiLongGuan Clinical Medical School, Beijing HuiLongGuan Hospital, Beijing, China.
  • Kosten TR; The Second Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, China.
  • Xiu M; The Affiliated Kangning Hospital of Wenzhou Medical University, Wenzhou, China.
  • Wu F; Department of Psychology, University of Houston, Houston, TX, USA.
  • Zhang X; Texas Institute of Measurement Evaluation and Statistics, University of Houston, Houston, TX, USA.
Neurotherapeutics ; 19(3): 1037-1046, 2022 04.
Article em En | MEDLINE | ID: mdl-35467271
ABSTRACT
Many patients with schizophrenia (SCZ) discontinue antipsychotics, frequently due to dose-related multiple and severe adverse effects. We hypothesized that a low-dose ziprasidone plus sertraline would reduce serious side effects without affecting treatment efficacy. Therefore, this clinical trial was designed to investigate the efficacy, safety, and tolerability of adding sertraline to ziprasidone in order to substantially reduce ziprasidone dose and potential side effects in first-episode and drug-naive (FEDN) patients with SCZ. This 24-week randomized, double-blinded, controlled clinical trial randomly allocated 452 FEDN SCZ patients to receive a usual dose of ziprasidone (control group) or half the dose of ziprasidone in combination with sertraline (ZS group). Treatment outcome included the Positive and Negative Syndrome Scale (PANSS), the Hamilton Depression Rating Scale (HAMD), CGI-Severity (CGI-S) and the Personal and Social Performance Scale (PSP) at baseline and weeks 2, 4, 8, 12, and 24. Repeated measures ANCOVA showed significant treatment by time interactions on the PANSS general psychopathology and total scores, as well as CGI-S, HAMD, and PSP scores (all p < 0.05). Furthermore, the ZS group had greater reductions in PANSS general psychopathology, total scores, HAMD, and CGI-S (all p < 0.05) and greater increases in the PSP total score (p < 0.01) than the control group. Importantly, adverse effects were lower in the ZS than control group. The reduction in PANSS, CGI-S, or HAMD scores was not correlated with the increase in PSP. Sex and duration of disease predicted PSP improvement from baseline to week 24 in the ZS group. Our FEDN patients with SCZ were effectively treated for their psychotic and depressive symptoms while experiencing significantly fewer adverse effects using half the usual ziprasidone dose when combined with sertraline. ClinicalTrials.gov, NCT04076371.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 1_ASSA2030 Problema de saúde: 1_doencas_nao_transmissiveis Assunto principal: Esquizofrenia / Antipsicóticos Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Neurotherapeutics Assunto da revista: NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 1_ASSA2030 Problema de saúde: 1_doencas_nao_transmissiveis Assunto principal: Esquizofrenia / Antipsicóticos Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Neurotherapeutics Assunto da revista: NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China
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