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1.
奎硫平治疗老年期精神分裂症对照研究   总被引:4,自引:0,他引:4  
目的:比较奎硫平与奋乃静治疗老年期精神分裂症的疗效与不良反应。方法:对72例老年期精神分裂症患者分别以奎硫平和奋乃静治疗。疗程8周。采用阳性与阴性症状量表(PANSS)及副反应量表(TESS)评定疗效及不良反应。结果:治疗8周后PANSS评分较治疗前显著下降。奎硫平组有效率77.8%,显效率61.1%,奋乃静组分别为75.0%和58.3%,两组差异无显著性(P〉0.05),奎硫平组不良反应少而轻。结论:奎硫平与奋乃静治疗老年期精神分裂症患者疗效相当,奎硫平不良反应较轻,安全性好。  相似文献   

2.
奎硫平治疗老年精神分裂症对照研究   总被引:6,自引:0,他引:6  
目的:对比奎硫平和奋乃静的疗效和安全性。方法:对96例老年精神分裂症患者随机平分为两组,分别给予奎硫平及奋乃静。疗程8周。在治疗前和治疗第1、2、4、8周末,采用阳性与阴性症状量表(PANSS)、临床疗效总评量表(CGI)、副反应量表(TESS)评估疗效及不良反应。结果:奎硫平与奋乃静对老年精神分裂症疗效相似,但不良反应以前者显著较少。结论:奎硫平治疗老年精神分裂症安全,疗效确切,不良反应少。  相似文献   

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目的比较奎硫平与氯丙嗪治疗女性精神分裂症的临床疗效及安全性。方法将68例住院女性精神分裂症患者分为奎硫平组与氯丙嗪组各34例进行临床比较分析。奎硫平剂量为500—800mg,/d,氯丙嗪为250~600mg/d,共治疗8周。分别采用PANSS、CGI及TESS评定疗效及安全性。结果治疗8周后,两组患者的PANSS、CGI评分均明显下降,差异有显著性(P〈0.01),两组间比较PANSS、CGI评分差异无显著性(P〉0.05)。奎硫平组不良反应发生率低于氯丙嗪组,差异有显著性(P〈0.05)。结论奎硫平治疗女性精神分裂症的精神病性症状有效,安全性、依从性好。  相似文献   

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奎硫平与氯氮平治疗精神分裂症的比较研究   总被引:21,自引:2,他引:19  
目的 探索奎硫平治疗精神分裂症的疗效及安全性。方法 对 6 3例精神分裂症患者分别给予奎硫平、氯氮平治疗 ,其中奎硫平组 32例 ,剂量为 (330± 5 8)mg d ;氯氮平组 31例 ,剂量 (30 0±4 3)mg d ;疗程共 8周。采用阳性和阴性症状量表 (PANSS)及副反应量表 (TESS)在治疗前及治疗后 1、2、4、8周末分别评定疗效和副反应。结果  (1)两组治疗后第 1,2 ,4 ,8周的PANSS分与治疗前比较 ,差异具有显著性 (P <0 0 1)。 (2 )奎硫平与氯氮平有效率分别为 83 3%和 85 7% ,两者有效治疗剂量分别为 2 75~ 4 5 0mg d ,2 5 0~ 4 0 0mg d。 (3)TESS评定奎硫平组副作用少于氯氮平组 (P <0 0 1)。 结论 奎硫平治疗精神分裂症阳性、阴性症状与氯氮平同样有效 ,但不良反应更少。  相似文献   

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目的比较国产奎硫平与奋乃静治疗老年精神分裂症的临床疗效及安全性。方法将66例老年精神分裂症患者随机分为两组,分别服用国产奎硫平和奋乃静,疗程8周。采用阳性和阴性症状量表(PANSS)评定疗效,治疗时出现的症状量表(TESS)评定不良反应。结果国产奎硫平与奋乃静疗效相当,前者对阴性症状起效更快。结论国产奎硫平与奋乃静治疗老年精神分裂症患者疗效相当,前者不良反应少而轻。  相似文献   

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奎硫平与奋乃静治疗老年期精神分裂症对照观察   总被引:2,自引:0,他引:2  
目的:探讨奎硫平对老年期精神分裂症的疗效及依从性。方法:将61例老年期精神分裂症住院患者随机分为两组,分别予以奎硫平与奋乃静治疗,疗程10周。以阳性与阴性症状量表(PANSS)评定疗效,以治疗中出现的症状量表(TESS)评定不良反应。结果:两组疗效无显著差异,奎硫平组依从性显著好于奋乃静组。结论:奎硫平与奋乃静对老年期精神分裂症患者皆有较好的疗效,奎硫平治疗的依从性更高。  相似文献   

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奎硫平治疗老年期首发精神分裂症患者对照研究   总被引:6,自引:0,他引:6  
目的:研究奎硫平治疗老年期首发精神分裂症患者的疗效和不良反应。方法:将61例老年期首发精神分裂症住院患者随机分为两组,分别给予奎硫平和奋乃静治疗,疗程8周。以阳性与阴性症状量表(PANSS)评定疗效,以副反应量表(TESS)评定药物不良反应。结果:奎硫平与奋乃静疗效相仿,不良反应相似。结论:奎硫平、奋乃静对老年期首发精神分裂症均有较好疗效。  相似文献   

8.
国产奎硫平与利培酮治疗精神分裂症对照研究   总被引:12,自引:1,他引:11  
目的 探讨国产奎硫平治疗精神分裂症的疗效及副反应。方法 将 10 0例精神分裂症患者随机分为奎硫平组 (5 0例 )和利培酮组 (5 0例 ) ,进行临床对照试验 ,两组药物治疗剂量分别为 4 0 0~ 6 0 0mg/d和 4~8mg/d ,疗程 8周。疗效指标包括阳性和阴性症状量表 (PANSS)及临床总体印象量表 (CGI) ,不良反应指标为不良反应症状量表 (TESS)及有关实验室检查。结果 治疗结束时 ,两组PANSS评分较入组时均显著减低 (P <0 .0 1)。PANSS总减分率 :奎硫平组为 (5 2 .6± 10 .2 ) % ,利培酮组为 (71.8± 11.6 ) % ;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 )。奎硫平组的不良反应较利培酮组少 ,其中静坐不能和肌强直等EPS发生率显著少于利培酮组 (P <0 .0 1) ,未出现月经失调 (闭经、经期过长或过短 ) ,泌乳、男性乳房发育、性欲减退、勃起障碍等副作用。结论 国产奎硫平治疗精神分裂症是一种有效、安全、经济的药物 ,虽然疗效稍逊于利培酮 ,但不良反应比利培酮轻微 ,尤其适合对锥外反应和催乳素敏感者使用  相似文献   

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国产奎硫平与氯丙嗪治疗精神分裂症的多中心双盲对照研究   总被引:35,自引:0,他引:35  
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。  相似文献   

10.
奎硫平和利培酮治疗精神分裂症的比较研究   总被引:11,自引:0,他引:11  
目的 以利培酮为对照 ,探讨奎硫平治疗精神分裂症的疗效和副作用。方法 将 79例符合CCMD 3诊断标准的精神分裂症病人随机分为两组 ,分别给予奎硫平和利培酮治疗 8周。采用阳性症状和阴性症状量表 (PANSS)评定临床疗效 ,副反应量表 (TESS)评定副反应。结果 治疗 8周后的疗效近似 (P >0 0 5 ) ;奎硫平组和利培酮组的显效率差异无显著性 (P >0 0 5 ) ;奎硫平组的副反应发生率低于利培酮组 ,但差异无显著性 (P >0 0 5 )。利培酮组锥体外系副反应和内分泌改变的发生均明显高于奎硫平组 (P <0 0 5 )。结论 奎硫平和利培酮对精神分裂症的疗效相当 ,副作用较小。  相似文献   

11.
OBJECTIVE: The purpose of the work described here was to determine those variables associated with satisfaction with care among patients with epilepsy. METHODS: We interviewed patients followed at a tertiary epilepsy center. Predictor variables included age, gender, race, education, income, insurance, seizure frequency, and Quality of Life in Epilepsy-10 inventory (QOLIE-10) results. Target variables were the subscales of the Short Form Patient Satisfaction Questionnaire (PSQ-18). We used univariate analysis to identify those variables significantly associated with the subscales and multiple linear regression to determine those independently significant. RESULTS: The study population comprised 193 patients. Lower education and better QOLIE-10 scores were independently associated with general satisfaction with care. The mental health scale was associated with general satisfaction with care. Lower educational level was the only variable independently associated with patient satisfaction with communication, the financial aspect of care, and time spent with physician. CONCLUSION: Lower educational level and better quality of life are the main variables associated with higher general satisfaction with care among patients with epilepsy.  相似文献   

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Summary: Purpose: This retrospective study reports the long-term surgical outcome of patients with medically refractory epilepsy and vascular malformations who were treated with lesionectomy. A detailed analysis of surgical failures had been performed in an attempt to define predictors of surgical success and failure.
Methods: Fifteen patients with medically intractable epilepsy and angiographically occult vascular malformations (AOVMs) were treated surgically with lesionectomy at Duke University Medical Center. Lesionectomy consisted of removal of the AOVM and surrounding hemosiderin-stained brain only, without the use of electrocorticography (ECoG) to guide resection.
Results: Eleven (73%) patients are seizure free after lesionectomy. Three showed no significant improvement, and one patient died, presumably after a seizure. Age of onset, duration of seizures, age at resection, and gender did not affect outcome. All patients with neocortical AOVMs in whom EEG findings correlated with the site of the lesion were seizure free after lesional resection. Treatment failures were associated with the presence of multiple intracranial lesions, poorly localized or diffuse EEG findings, discordant positron emission tomography (PET) imaging, or with a lesion in close proximity to the limbic system.
Conclusions: Lesionectomy, with removal of surrounding hemosiderin-stained brain, can be considered the procedure of choice in carefully selected patients with epilepsy with occult vascular malformations.  相似文献   

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The purpose of this study was to identify group differences in children with attention-deficit-hyperactivity disorder and motor dysfunction (ADHD-MD) and ADHD only, and to evaluate the medication responsiveness of ADHD-MD. Sixty-three children (49 males and 14 females; mean age 9 years 10 months, SD 2 years 10 months) underwent a triple blind, placebo-controlled crossover study evaluating two dose levels of methylphenidate (0.3 mg/kg and 0.5 mg/kg [corrected], twice daily) and placebo. Forty-nine trials were completed. Nineteen were children with ADHD-MD, 44 had ADHD only. Behavior and functioning were assessed at home and at school. Treatment effects were assessed using the Abbreviated Symptom Questionnaire for Parents and Teachers. Children with ADHD-MD were more likely to have severe ADHD-combined type and other neurodevelopmental and behavioral problems. Both groups of children had a linear dose response to medication (placebo, low, high) and there was no evidence of a group by dose interaction or an overall group effect at home or school. The lack of group effect suggests that these children responded to medication like the other subgroups.  相似文献   

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