Comparison of the efficacy of amisulpride and risperidone in the treatment of patients with first-episode schizophrenia
Tongbao Zhan
Abstract
Tongbao Zhan
Abstract
Objective To compare and analyze the efficacy and safety of amisulpride and risperidone in the treatment of patients with first-episode schizophrenia(FES). Methods 80 patients with FES were randomly divided into the observation group (n=40, orally given amisulpride) and the control group (n=40, orally given risperidone) according to random number table.The total effective rate, positive and negative symptoms scale (PANSS), adverse reaction rate of two groups were compared. Results 1 week after treatment, the negative symptoms score of the observation group was significantly lower than that of the control group[(20.89±3.07)points vs.(18.15±3.64)points, t=3.639, P=0.001].8 weeks after treatment, the PANSS scores and factor score of the two groups had no significant differences(all P>0.05). The total effective rate and adverse reaction rate of the observation group were 90.00%, 17.50% respectively, which of the control group were 82.50%, 27.50% respectively, there were no statistically significant differences (χ2=0.949, P=0.330; χ2=1.147, P=0.284). Conclusion Amisulpride and risperidone has similar efficacy and safety in the treatment of patients with FES, but amisulpride has better early effect in improving negative symptoms. Key words: Schizophrenia; Amisulpride; Risperidone
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To compare and analyze the efficacy and safety of amisulpride and risperidone in the treatment of patients with first-episode schizophrenia(FES). Methods 80 patients with FES were randomly divided into the observation group (n=40, orally given amisulpride) and the control group (n=40, orally given risperidone) according to random number table.The total effective rate, positive and negative symptoms scale (PANSS), adverse reaction rate of two groups were compared. Results 1 week after treatment, the negative symptoms score of the observation group was significantly lower than that of the control group[(20.89±3.07)points vs.(18.15±3.64)points, t=3.639, P=0.001].8 weeks after treatment, the PANSS scores and factor score of the two groups had no significant differences(all P>0.05). The total effective rate and adverse reaction rate of the observation group were 90.00%, 17.50% respectively, which of the control group were 82.50%, 27.50% respectively, there were no statistically significant differences (χ2=0.949, P=0.330; χ2=1.147, P=0.284). Conclusion Amisulpride and risperidone has similar efficacy and safety in the treatment of patients with FES, but amisulpride has better early effect in improving negative symptoms. Key words: Schizophrenia; Amisulpride; Risperidone
Key concepts: Amisulpride, Risperidone, Medicine, Schizophrenia (object-oriented programming), Internal medicine, Adverse effect, Positive and Negative Syndrome Scale, Clinical efficacy