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首页> 外文期刊>Journal of Acupuncture and Meridian Studies >Acupuncture Improves Symptoms in Patients with Mild to Moderate Atopic Dermatitis: A Randomized, Sham-Controlled Preliminary Trial
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Acupuncture Improves Symptoms in Patients with Mild to Moderate Atopic Dermatitis: A Randomized, Sham-Controlled Preliminary Trial

机译:针灸可改善轻度至中度特应性皮炎患者的症状:一项随机,假手术控制的初步试验

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Objectives: To assess the feasibility of a definitive trial investigating the effects of acupuncture on atopic dermatitissymptoms including itching.Design: A randomized, sham-controlled preliminary trial with three arms with a 4-week intervention period and a 4-weekfollow-up.Interventions: Thirty participants were allocated to three arms (the verum acupuncture group 1 [VA1, 3 times weekly for 4weeks], the verum acupuncture group 2 [VA2, twice weekly for 4 weeks], and the sham acupuncture group [SA, twiceweekly for 4 weeks]) at a 1:1:1 ratio.Main outcome measures: We determined the visual analogue scale (VAS) for itching and insomnia, SCORing AtopicDermatitis (SCORAD), Eczema Area and Severity Index (EASI), Patient Oriented Eczema Measure (POEM), and DermatologyLife Quality Index (DLQI) scores over the course of the study. Baseline index score (BIS) comparison according to generalsymptom was performed.Results: The SCORAD, VAS (Pruritus), VAS (Insomnia), POEM, DLQI, and EASI were significantly improved in the VA groups.Significant BIS mean differences were observed most predominantly in epigastric tenderness and dyspepsia. There was nosignificant difference between VA1 and VA2 groups in all the main evaluation indices.Conclusions: For the following research, the authors suggest SCORAD (Total) as primary outcome and SCORAD (objective),VAS (Itch), VAS (insomnia), EASI, POEM, and DLQI as secondary outcomes. Thirty six participants should be conducted a 4-week acupuncture period (twice weekly) and a 4-week follow-up. It is necessary to compare the differences of generalsymptoms according to presence of epigastric tenderness or dyspepsia at the screening level.
机译:目的:评估一项针对针刺对特应性皮炎症状(包括瘙痒)影响进行研究的确定性试验的可行性设计:一项由假肢控制的随机随机初步试验,分为三组,干预时间为4周,随访时间为4周。 :30名参与者被分配给三个组(Verum针刺组1 [VA1,每周3次,共4周],Verum针刺组2 [VA2,每周两次,共4周]和假针刺组[SA,每周两次,共4周]主要结果:我们确定了瘙痒和失眠的视觉模拟量表(VAS),SCORing特应性皮炎(SCORAD),湿疹面积和严重程度指数(EASI),以患者为导向的湿疹量度( POEM)和皮肤病生活质量指数(DLQI)在研究过程中的得分。结果:VA组的SCORAD,VAS(Pruritus),VAS(失眠),POEM,DLQI和EASI均得到了明显改善,其中BIS的平均差异最显着在上腹压痛和消化不良。结论:对于以下研究,作者建议以SCORAD(总)为主要结果,以SCORAD(客观),VAS(瘙痒),VAS(失眠),EASI为主要结果。 ,POEM和DLQI作为次要结果。应对36名参与者进行为期4周的针灸(每周两次)和4周的随访。有必要在筛查水平上根据上腹部压痛或消化不良的存在比较一般症状的差异。

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