Results In the 6th and 12th month after being discharged from hospital, the score of the BPRS of the follow-up group was lower than the control group ( P < 0.01).

The results showed that zuclopenthixol acetate can effectively control acute psychotic symptoms, BPRS amelioration expressed marked improvement rate of clinical symptoms is 30. 2%, improvement rate 62.3%.

结果显示：该药能有效地控制急性精神症状，BPRS减分率显示显好率是30.2%，好转率为62.3%；

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All cases were assessed by brief psychiatric rating scale ( BPRS), Hamilton anxiety scale ( HAMA), and Hamilton depression scale ( HAMD).

用简明精神病评定量表（BPRS）、Hamilton抑郁量表（HAMD）、Hamilton焦虑量表（HAMA）进行评定。

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Methods: 140 cases of psychiatric in-patients randomly arrange to painting therapy group and control group. BPRS and SFRS were applied to assess the effect before and after treatment.

方法：140例男性住院精神病患者随机分为绘画治疗组和对照组，采用症状评定（BPRS）量表和社会功能评定（SFRS）量表得分的变化评估治疗效果。

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Method: 32 patients with first episode schizophrenia were treated with olanzapine for 8 weeks, and assessed with BPRS and TESS for the efficacy and safety.

方法用奥氮平治疗首发精神分裂症32例，疗程8周；用简明精神病评定量表（BPRS）和副反应量表（TESS）评定疗效及副反应。

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Psychiatric interview and physical examination completely, assessment for BPRS, GAS, SDSS, making out psychiatric diagnosis and assessment disability rank of mental disease exactly.

全面精神及体格检查，BPRS、GAS、SDSS等量表评定，作出疾病诊断，对相关残情进行准确的等级评定。

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Results: The scores of BPRS of painting therapy group is better than control group. But there is no statistic difference between the scores of SFRS of two groups.

结果：绘画治疗组治疗后症状评定（BPRS）量表得分要优于对照组，差异有统计学意义，但两组社会功能评定量表得分差异无统计学意义。

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QOLS, IPROS, BPRS and SANS were used to evaluate the efficacy before treatment and 8 weeks after treatment and to analyze associated factors.

治疗8周。于治疗前后分别以QOLS、IPROS、BPRS、SANS量表进行疗效评定及相关因素分析。

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Results The reduction of scores of BPRS, SDSS, ADL and bone minerals test in Morita Therapy group were significantly more than that in controls.

结果森田疗法组的BPRS、SDSS、ADL评分和骨矿物质含量结果明显优于对照组。

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Method Patients with first-onset schizophrenia were treated with risperidone for 12 weeks, and assessed with BPRS and TESS for the efficacy and side effect.

方法单独使用维思通治疗连续住院的首发精神分裂症12周，用BPRS和TESS量表评定疗效和副反应。

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Result After the rehabilitation training, score of IPROS, BPRS and sub scale were decreased after treatment ( P < 0.05~ 0.01).

结果经康复训练后IPROS、BPRS总分及分量表分均低于治疗前（P

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Compared with baseline, the scores of PANSS and BPRS in endpoint were significantly reduced in both groups ( P < 0.05).

治疗结束时，2组PANSS和BPRS评分较入组时均显著减低（P＜0.05）；

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BPRS showing that the factor scores of lack vitality were obviously higher than those of activation and hostile suspicion ( P < 0 05);

BPRS示缺乏活力因子分明显高于激活性及敌对猜疑因子分（P均

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BPRS, CGI and TESS were adopted to evaluate the efficacy and side effects before and after 2,4 and 6 weeks of the treatment.

疗程6周，于治疗前及治疗第2、4、6周末进行简明精神病评定量表（BPRS）、临床疗效总评量表（CGI）评定疗效，用副反应量表（TESS）评定不良反应。

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All patients were assessed using BPRS in pre-treatment, post-treatment 1,2,4 and 8 week, and assessed using TESS after 8 week.

经8周治疗在治疗前、治疗后的1、2、4、8周应用简明精神病量表（BPRS）评定疗效，在8周后做副反应量表（TESS）评定不良反应。

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BPRS, SDSS, SANS scores decreased obviously after 2 years treatment in community rehabilitation ( P < 0 01).

通过2年的社区康复治疗后，BPRS、SDSS、SANS等量表总分明显降低（P

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Brief psychiatric Rating Scale ( BPRS) and Positive And Negative Syndrome Scale ( PANSS) were used to assess the effects.

采用简明精神病量表（BPRS）、阳性和阴性症状量表（PANSS）进行评价。

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Result: Thinking disorder factor and active factor of BPRS and P value of PANSS affect the competency to stand trial significantly;

结果：BPRS的思维障碍因子、激活性因子、PANSS的P分对受审能力具有显著影响；

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The clinical effects and adverse reactions were assessed by BPRS, TESS for 4 wk.

临床疗效和不良反应以BPRS，TESS评分观察4wk。

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Methods Making the guide and rating the symptoms and curative effect of the patients with BPRS.

方法对出院精神分裂症病人进行出院指导，并用BPRS、S DSS量表评定病人症状及疗效。

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Evaluation on each subscale of BPRS

简明精神病评定量表中各分量表的评价

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