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舒肝解郁胶囊治疗帕金森病合并抑郁的临床观察 被引量:11

Clinical research on Shugan-jieyu capsule in the treatment of Parkinson's disease combined with depression
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摘要 目的评价舒肝解郁胶囊治疗帕金森病(PD)合并抑郁的疗效及安全性。方法随机将70例帕金森病合并抑郁患者分成治疗组(舒肝解郁胶囊,n=36)及对照组(舍曲林,n=34),记录治疗前及治疗2、4、8和12周两组汉密顿抑郁量表(HAMD)及帕金森病综合评价量表(UPDRS)评分,并观察与用药相关的不良反应。结果治疗12周,治疗组总有效率达83.33%,与对照组(85.29%)相比,差异无统计学意义(P>0.05)。治疗组HAMD评分及UPDRSⅡ、UPDRSⅢ评分较治疗前均降低(P<0.05)。与同一时点对照组相比,两组HAMD评分及UPDRSⅡ、UPDRSⅢ评分差异无统计学意义(P>0.05)。结论对于PD合并抑郁患者的抑郁症状,舒肝解郁胶囊疗效与舍曲林相当,同时不加重PD患者的运动症状,不良反应少。 Objective To investigate the efficacy and safety of Shugan-jieyu capsule in the treatment of Parkinson,sdisease (PD) combined with depression. Methods A total of 70 patients were randomly divided into treatment group(Shugan-jieyu capsule) and control group (sertraline). Efficacy was measured by Hamilton Depression Scale (HAMD,17-item) and Unified Parkinson’s Disease Rating Scale (UPDRS) before and after treatments of 2, 4, 8 and 12 weeks.The adverse drug reactions related to medication was observed. Results After 12 weeks, compared with the control group(85.29%) the total effective rate of treatment group (83.33%) had no statistically significant difference (P 〉 0.05).Compared with before treatment, the scores of HAMD and UPDRS Ⅱ and UPDRS Ⅲ in the treatment group weredecreased (P 〈 0.05). Compared with the control group, there was no significant difference in HAMD, UPDRSⅡandUPDRS Ⅲ at the same time between two groups. Conclusion Shugan-jieyu capsule in the treatment of PD combined withdepression is safe and effective.
出处 《世界临床药物》 CAS 2015年第7期480-483,共4页 World Clinical Drug
关键词 帕金森病(PD) 抑郁症 舒肝解郁胶囊 舍曲林 Parkinson's disease(PD) depression Shugan-jieyu capsule sertraline
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参考文献16

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