摘要
目的 评价利培酮与阿立哌唑治疗精神分裂症的临床疗效和安全性.方法 选择80例精神分裂症患者作为研究对象,随机分为利培酮组(40例)和阿立哌唑组(40例),按照随机双盲对照的原则进行8周治疗.在治疗前后分别应用阳性和阴性症状量表(PANSS)、临床疗效总评量表(CGI)和副反应量表(TESS)及有关实验室检查进行疗效和安全性评估.结果 治疗8周后,两组患者PANSS评分较治疗前均显著降低(P〈0.05),但是组间减分差异无统计学意义(P〉0.05).治疗后,利培酮组有效率90%,阿立哌唑组有效率80%,两组差异无统计学意义(P〉0.05).阿立哌唑组消化道反应发生率明显高于利培酮组(P〈0.05).结论 利培酮治疗精神分裂症的疗效较阿立哌唑略好,安全性高.
Objective To assess the efficacy and safety of aripiprazole and risperidone on the treatment of schizophrenia. Method 80 patients with schizophrenia were randomly divided into risperidone group ( n = 40) and aripiprazole group( n= 40). According to random, controlled principles, all patients were treated for 8 weeks. The positive and negative syndrome scale ( PANSS ), clinical global impression ( CGI ), treatment emergent symptom scale (TESS) and laboratory examinations were used to assess the effectiveness and the safety of the treatment. Results By the end of the 8 weeks treatment,the scores of PANSS in both groups decreased significantly compared to the baseline ( P 〈 0. 05 ) without statistica differences between groups ( P 〉 0. 05 ). Total clinical effective rates was 90% in risperidone group and 80% in aripiprazole group, without significant difference between two groups. Digestion adverse reactions in aripiprazole group were significantly more than in risperidone group (P 〈 0. 05). Conclusion Both aripiprazole and risperidone could treat schizophrenia effectively,and risperidone showed better results.
出处
《中国基层医药》
CAS
2010年第19期2643-2645,共3页
Chinese Journal of Primary Medicine and Pharmacy