BPRS

Stepwise multiple regression analysis suggested that the major factors related to compliance were as following: BPRS ( ACTV), duration of hospitalization, family members' age, premorbid character.

逐步回归分析提示，影响服药依从性的因素依次为BPRS激活性、留医时间、家属年龄、病前性格。

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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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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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The patients were assessed by brief psychiatric rating scale ( BPRS), inpatient psychiatric rehabilitation outcome scale ( IPROS) and general self-efficacy scale ( GESE).

评定工具用简明精神病评定量表（BPRS）、住院精神病人康复疗效评定量表（IPROS）和自我效能感量表（GESE）进行对照评定分析。

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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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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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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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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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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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The response to clozapine was rated within BPRS. According to the reducing rate of BPRS ≥ 20% and < 20%, the patients were divided into two group effective group and ineffective group.

治疗前后用简明精神病评定量表（BPRS）评定氯氮平疗效，按BPRS减分率≥20%和

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BPRS including anxiety-depression factor, lacking in activity factor, thinking disturbance factor, reaction factor and hostile factor;

简明精神病评定量表包含焦虑抑郁因子、缺乏活力因子、思维障碍因子、活动性因子和敌对态度因子；

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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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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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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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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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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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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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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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Efficacy and safety of the treatment were assessed respectively by Brief Psychiatric Rating Scale ( BPRS), treatment-emergent signs and symptoms ( TESS), ECG, liver renal function.

以治疗前后简明精神病量表（BPRS）激越分的减分率评定疗效，以副反应量表（TESS）及心电图及肝肾功能评价安全性。

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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).

结果出院6、12个月时家访组病人BPRS评分明显低于对照组（P

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Both were double-blindly assessed with the SAPS, SANS, BPRS and TESS, before and after treatment, to evaluate the effects on positive and negative symptoms.

两组均以阴性症状量表（SANS）、阳性症状量表（SAPS）、简明精神病症状量表（BPRS）和副反应量表（TESS）进行盲式评分。

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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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Method: 146 first-episode schizophrenic patients were evaluated with BPRS before and after treatment, then 18 items of BPRS were conducted factor analysis, item analysis and computed Cronbach alpha.

方法：对首发精神分裂症患者在治疗前后分别评定BPRS，然后对其18个项目进行因子分析、项目分析和计算Cronbachα值。

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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 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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The total scores of the BPRS 、 SAPS 、 and SANS in clozapine group at endpoint were significantly smaller than that of chlorpromazine group ( P < 0.01);

疗后氯氮平组的BPRS、SAPS、SANS总分均明显低于氯丙嗪组（P＜0.01）；

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Insights and treatment compliance were assessed with the Brief Psychiatric Rating Scale ( BPRS) and Insight and Treatment Attitude Questionnaire ( ITAQ) in 1 st week of admission.

两组在入院1w内和出院时采用简明精神病评定量表、自知力与治疗态度问卷及服药依从性进行评定和对比分析。

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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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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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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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