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   临床总 在 精神病学 分类中 的翻译结果: 查询用时:0.065秒
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临床总
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  the total
    Results The total effective rate was 93% and effectual rate 78%.
    结果利培酮治疗首发精神分裂症的临床总有效率为93%,显效率78%。
    RESULTS: At end of the treatment, the total effective rate of risperidon for SC was 91 % and remarkable effective rate was 78 %.
    结果 :利培酮治疗SC的临床总有效率为 91 % ,显效率 78%。
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    There were insignificant differences in the decreasing rate of HAMA score and the total clinical effective rate between the study group [(59.03±24.78)%and 72%] and the control group [(57.30±25.33)%and 67%] (P >0.05).
    对照组HAMA减分率为(57.30±25.33)%,临床总有效率为67%,两组比较差异无显著性意义艹卓艹卓艹卓艹卓艹卓(P>0.05)。
短句来源
    Results The total effective rate was 93% and effectual rate 78%.
    结果 利培酮治疗首发精神分裂症的临床总有效率为 93% ,显效率 78%。
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    The total rate of clinical therapeutic response was 70%.
    临床总有效率为 70 %。
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  “临床总”译为未确定词的双语例句
    RESULTS: The response rates were 68.6% and 60.0% for risperidone and haloperidol, respectively (P>0.05).
    结果:利培酮和氟哌啶醇的临床总有效率分别是68.6%和60.0%(P>0.05)。
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    Results The rate of patients with re- admission was 78.79%(26/33) and the responded rate to clozapine was 84.84%. But side effects rate and serious adverse were more and worse.
    结果  33例精神分裂症患者的再入院率为 78.79% (2 6 /33) ,临床总有效率为84 .84 % ,但临床副作用多而严重。
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    By the PANSS score reduction rate, the clinical effectiveness rate is: quetiapine was 61.61% and chlorpromazine was 64.81%.
    根据PANSS减分率评定临床总有效率,奎硫平组的有效率为61.61%,氯丙嗪组的有效率为64.81%,两组之间无显著性差异;
短句来源
    Total clinical effective rates were 73.9% in quetiapine group and 91.8% in risperidone group,and there was significant difference between two groups.
    临床总有效率 :奎硫平组 73.9% ,利培酮组 91.8% ,两组间疗效有显著性差异 (P <0 .0 5 )。
短句来源
    The efficacy rates were 77.0 % in experimental group and 79.2 % in the control group,there was no significant difference between two group(P>(0.05)).
    临床总有效率:阿立哌唑组为77.0%,利司哌酮组为79.2%,2组比较差异无显著意义(P>0.05)。
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Equivalently, ifCn, is the total space for a principalGa-bundle over some open subset ofCn-1 then the bundle is trivial.
      
This has brought the total of licensed anti-HIV drugs to nineteen.
      
Furthermore, it is proved that the minimum of the total number of bends in an at most single-bend embedding of a cubic graph of ordern is less than or equal to 0.5n+1.
      
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The total chromatic number of pseudo-outerplanar graphs
      
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The punpose of this study is to assess the efffectiveness of sodium valproate in the treatment of mental illness. One hundrad and fifty five psychiatric patients were treated openly by sodium valproate for 8 weeks, with 800-3000 mg/day. All of patients were rated blindly on CGI, TESS by two trained poychiatrists before the treatment, and in the first, second, fourth, sixth and eighth weeks after the tratment. The total improvement rate is 60%. Sodium valproate was found to be more effective in the treatment...

The punpose of this study is to assess the efffectiveness of sodium valproate in the treatment of mental illness. One hundrad and fifty five psychiatric patients were treated openly by sodium valproate for 8 weeks, with 800-3000 mg/day. All of patients were rated blindly on CGI, TESS by two trained poychiatrists before the treatment, and in the first, second, fourth, sixth and eighth weeks after the tratment. The total improvement rate is 60%. Sodium valproate was found to be more effective in the treatment of elation irritability, insomnia and auditory hallucination and delusion, but to be less effective in the treatment of thought disturbance, apathy, social withdrawal. No serious further comprehensive study is required to verify the effectiveness of sodium valproate in the treatment of mental illness adverse effects in observed.

用丙戊酸钠治疗155例精神病人,疗程8周,临床总有效率60%。对情感高涨、易激惹、失眠疗效较好;对幻听、妄想有一定的疗效;对思维联想障碍、情感淡漠、生活懒散疗效欠佳。使用中未见严重不良反应。

Objective To confirm the effect of nicergoline in treating patients with vascular dementa (VD).Method It was designed as a randomized ,double blind ,multi center trial .Patients enered the two groups randomized ,treated with either nicergoline (60mg/day )or aniracetam (400mg/day )for 12 weeks. MMSE,WMS ADL ,CGL and TESS were performed in this study .Result After 12 weeks of treatment there are signif icant effect on the two drugs The effect of group A on MMSE ADL and CGI sore was superior tothat of group...

Objective To confirm the effect of nicergoline in treating patients with vascular dementa (VD).Method It was designed as a randomized ,double blind ,multi center trial .Patients enered the two groups randomized ,treated with either nicergoline (60mg/day )or aniracetam (400mg/day )for 12 weeks. MMSE,WMS ADL ,CGL and TESS were performed in this study .Result After 12 weeks of treatment there are signif icant effect on the two drugs The effect of group A on MMSE ADL and CGI sore was superior tothat of group B Conclusion In our study ,nicergoline was found to have superior effects to VAD patients on improving the dysfunction of cognition ,memory and usual life Aniracetam also do some good to memory and usual life.

目的 验证尼麦角林对血管性痴呆 (VD)的治疗效果。方法 本试验为随机、双盲、双模拟多中心研究。研究组 (A组 )用尼麦角林,对照组 (B组 )用阿尼西坦治疗 VD。治疗前后应用相应的量表进行评估。结果 治疗 12周后,两者均有疗效,但 A组在智力、日常生活活动能力 (ADL)及临床总疗效方面均优于 B组。结论 尼麦角林能较快速改善轻中度 VD的认知功能、记忆力和生活功能,阿尼西坦对改善记忆和智力水平也有一定的作用。两药均具有较好的治疗安全性。

Objective To verify the efficacy and side effects of domestic manufactured quetiapine on schizophrenia Methods Patients who met CCMD 2 R criteria for schizophrenia were randomized into two groups: quetiapine group ( n =114) and chlorpromazine (CPZ) group ( n =107) in a double blind, double dummy study The range of dosage for the two experiment drugs was 200 800 mg/d, the treatment duration was 8 weeks The PANSS, BPRS, CGI, TESS and related lab tests were employed for assessing the treatment effectiveness...

Objective To verify the efficacy and side effects of domestic manufactured quetiapine on schizophrenia Methods Patients who met CCMD 2 R criteria for schizophrenia were randomized into two groups: quetiapine group ( n =114) and chlorpromazine (CPZ) group ( n =107) in a double blind, double dummy study The range of dosage for the two experiment drugs was 200 800 mg/d, the treatment duration was 8 weeks The PANSS, BPRS, CGI, TESS and related lab tests were employed for assessing the treatment effectiveness and side effects Results At the end of treatments, the scores of PANSS and BPRS in both treatment groups decreased significantly compared with baseline ( P <0 01), and the decreasing rates on PANSS were (65 9±27 8)% in quetiapine group and (66 5±26 4)% in CPZ group Total clinical effective rates were 68 1% in quetiapine group and 69 6% in CPZ group, which was no significant difference between two groups However, patients in quetiapine group reported much fewer side effects than those in CPZ group, especially in the items of reduced activities, tremor, akathisia, acute dystonia, dry month, blur sight, constipation, and dizziness on TESS ( P <0 05) Conclusion Quetiapine has similar efficacy to CPZ, but has less side effects Quetiapine is an effective antipsychotic drug with fewer side effects

目的 验证奎硫平治疗精神分裂症的疗效及安全性。方法 将 2 2 1例精神分裂症患者随机分为奎硫平组 ( 1 1 4例 )和氯丙嗪组 ( 1 0 7例 ) ,进行多中心双盲双模拟对照研究 ,两药治疗剂量均为 2 0 0~ 80 0mg d ,疗程 8周。疗效指标包括阳性和阴性症状量表 (PANSS)、简明精神病评定量表(BPRS)、临床总体印象量表 (CGI)。不良反应指标为不良反应量表 (TESS)及有关实验室检查。结果治疗结束时 ,两组PANSS和BPRS评分较入组时均显著减低 (P <0 0 1 ) ;PANSS减分率 :奎硫平组为( 65 9± 2 7 8) % ,氯丙嗪组为 ( 66 5± 2 6 4 ) % ;临床总有效率 :奎硫平组 68 1 % ,氯丙嗪组 69 6% ;两组疗效差异无显著性。奎硫平组的不良反应较氯丙嗪组少 ,其中活动减少、震颤、扭转痉挛、静坐不能、口干、视物模糊、便秘、头晕的发生率显著少于氯丙嗪组 (P <0 0 1或 0 0 5)。结论 国产奎硫平治疗精神分裂症的疗效与氯丙嗪相似 ,某些不良反应较氯丙嗪轻而少 ;是一种有效、耐受性好的抗精神病药。

 
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