首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >Efficacy and Safety of a Traditional Herbal Medicine Hochu-ekki-to in the Long-term Management of Kikyo (Delicate Constitution) Patients with Atopic Dermatitis: A 6-month Multicenter Double-blind Randomized Placebo-controlled Study
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Efficacy and Safety of a Traditional Herbal Medicine Hochu-ekki-to in the Long-term Management of Kikyo (Delicate Constitution) Patients with Atopic Dermatitis: A 6-month Multicenter Double-blind Randomized Placebo-controlled Study

机译:传统草药Hochu-ekki-to在异位性皮炎患者Kikyo(体质良好)患者的长期管理中的功效和安全性:一项为期6个月的多中心双盲随机安慰剂对照研究

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摘要

Hochu-ekki-to is a traditional herbal (Kampo) medicine that has been shown to be effective for patients with Kikyo (delicate, easily fatigable, or hypersensitive) constitution. Previous case reports have suggested that this herbal drug was effective for a certain subgroup of patients with atopic dermatitis (AD). We aimed to evaluate the efficacy and safety of Hochu-ekki-to in the long-term management of Kikyo patients with AD. In this multicenter, double blind, randomized, placebo-controlled study, 91 Kikyo patients with AD were enrolled. Kikyo condition was evaluated by a questionnaire scoring system. All patients continued their ordinary treatments (topical steroids, topical tacrolimus, emollients or oral antihistamines) before and after their protocol entry. Hochu-ekki-to or placebo was orally administered twice daily for 24 weeks. The skin severity scores, total equivalent amount (TEA) of topical agents used for AD treatment, prominent efficacy (cases with skin severity score = 0 at the end of the study) rate and aggravated rate (more than 50% increase of TEA of topical agents from the beginning of the study) were monitored and evaluated. Seventy-seven out of 91 enrolled patients completed the 24-week treatment course (Hochu-ekki-to: n = 37, placebo: n = 40). The TEA of topical agents (steroids and/or tacrolimus) was significantly (P < 0.05) lower in the Hochu-ekki-to group than in the placebo group, although the overall skin severity scores were not statistically different. The prominent efficacy rate was 19% (7 of 37) in the Hochu-ekki-to group and 5% (2 of 40) in the placebo group (P = 0.06). The aggravated rate was significantly (P < 0.05) lower in the Hochu-ekki-to group (3%; 1 of 37) than in the placebo group (18%; 7 of 39). Only mild adverse events such as nausea and diarrhea were noted in both groups without statistical difference. This placebo-controlled study demonstrates that Hochu-ekki-to is a useful adjunct to conventional treatments for AD patients with Kikyo constitution. Use of Hochu-ekki-to significantly reduces the dose of topical steroids and/or tacrolimus used for AD treatment without aggravating AD.
机译:Hochu-ekki-to是一种传统的草药(Kampo),已被证明对具有Kikyo(微妙,易肥胖或过敏)体质的患者有效。以前的病例报告表明,该草药对特应性皮炎(AD)的某些亚组患者有效。我们旨在评估Hochu-ekki-to在Kikyo AD患者的长期治疗中的疗效和安全性。在这项多中心,双盲,随机,安慰剂对照研究中,纳入了91名Kikyo AD患者。通过问卷评分系统评估Kikyo状况。所有患者在进入治疗方案之前和之后均继续常规治疗(局部类固醇,局部他克莫司,润肤剂或口服抗组胺药)。每天两次口服Hochu-ekki-to或安慰剂,持续24周。皮肤严重程度评分,用于AD治疗的局部用药总当量(TEA),显着疗效(研究结束时皮肤严重程度评分= 0的病例)发生率和加重率(局部使用TEA增加超过50%)从研究开始就对药物进行监测和评估。 91名入组患者中有77名完成了为期24周的治疗过程(Hochu-ekki-to:n = 37,安慰剂:n = 40)。尽管总体皮肤严重程度评分无统计学差异,但在Hochu-ekki-to组中,局部用药(类固醇和/或他克莫司)的TEA明显低于(P <0.05)安慰剂组。 Hochu-ekki-to组的显着疗效为19%(37个中的7个),安慰剂组为5%(40个中的2个)(P = 0.06)。 Hochu-ekki-to组(3%; 37分之一)的加重率显着低于安慰剂组(18%; 39分之7)(P <0.05)。两组仅注意到轻度不良事件,如恶心和腹泻,无统计学差异。这项安慰剂对照研究表明, Hochu-ekki-to 是对具有 Kikyo 体质的AD患者常规治疗的有用辅助手段。 Hochu-ekki-to 的使用可显着减少用于AD治疗的局部类固醇和/或他克莫司的剂量,而不会加重AD。

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