The Beneficial Effects of the Herbal Medicine Free and Easy Wanderer Plus (FEWP) and Fluoxetine on Post-Stroke Depression

氟西汀 医学 安慰剂 耐受性 萧条(经济学) 脑卒中后抑郁 冲程(发动机) 内科学 随机对照试验 巴氏指数 麻醉 日常生活活动 物理疗法 不利影响 治疗组和对照组 血清素 病理 经济 宏观经济学 受体 替代医学 工程类 机械工程
作者
Liantao Li,Shuhua Wang,Hong-You Ge,Jing Chen,Shouwei Yue,Mei Yu
出处
期刊:Journal of Alternative and Complementary Medicine [Mary Ann Liebert]
卷期号:14 (7): 841-846 被引量:43
标识
DOI:10.1089/acm.2008.0010
摘要

Depression occurs frequently in post-stroke patients and appears to be associated with impairment of their rehabilitation and functional recovery. In this study, we evaluated the efficacy and tolerability of the herbal drug, Free and Easy Wanderer Plus (FEWP), in patients affected by post-stroke depression (PSD).One hundred fifty (150) moderately to severely depressed patients as determined by a score >20 on the Hamilton Depression Scale (HDS) after a single ischemic or hemorrhagic stroke were randomly divided into the FEWP group (n = 60), the fluoxetine group (n = 60), and the placebo group (n = 30). The FEWP, fluoxetine, and placebo were administered to the patients over a period of 8 weeks. Depression was evaluated by HDS and the Barthel Index (BI) before, during, and after the treatment.Significantly higher clinical response rates were observed in both the FEWP and fluoxetine groups compared to the placebo group (60% and 65.5% versus 21.4%, chi(2) = 15.9, p < 0.01) and there was no difference in the response rates between the FEWP group and the fluoxetine group at the end of this study (60% versus 65.5%, chi(2) = 0.38, p > 0.05). Compared to fluoxetine, FEWP produced significantly greater improvement in depression at week 2 (15% versus 3.3%, chi(2) = 4.9, p < 0.05). Furthermore, FEWP produced significantly greater improvement in the activities of daily living (ADL) than fluoxetine at the end of this trial (BI: 43.8 +/- 5.6 versus 40.7 +/- 3.7, p < 0.01).FEWP showed good efficacy, safety, and tolerability in PSD patients. We conclude that FEWP is well tolerated and may be a useful therapeutic option in patients with PSD.

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