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首页> 外文期刊>Pediatric allergy and immunology: official publication of the European Society of Pediatric Allergy and Immunology >Ding Chuan Tang, a Chinese herb decoction, could improve airway hyper-responsiveness in stabilized asthmatic children: a randomized, double-blind clinical trial*.
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Ding Chuan Tang, a Chinese herb decoction, could improve airway hyper-responsiveness in stabilized asthmatic children: a randomized, double-blind clinical trial*.

机译:中药汤鼎川堂可改善稳定型哮喘儿童的气道高反应性:一项随机,双盲临床试验*。

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摘要

Traditional Chinese medicine has a long history of application in the treatment of bronchial asthma. Solid scientific evidence, however, is not available despite its widespread use among patients worldwide and in Taiwan. To assess the effect of Ding Chuan Tang (DCT) in airway hyper-responsiveness (AHR) on asthmatic children via randomized, double blind, placebo-controlled clinical trial. This study enrolled children who were aged 8-15 and diagnosed as mild to moderate persistent asthma patients. They were randomly allocated to receive 6.0 g DCT or placebo daily for 12 wk. Self-recorded daily symptom scores, medication scores, and morning and evening peak expiratory flow rates were returned at the monthly clinic. Pulmonary function test, methacholine challenge test, and serum inflammatory mediators were measured before and at the end of the trial. Fifty-two asthmatic children completed the clinical study. Twenty-eight patients were assigned to the treatment group and 24 to the placebo group. At the end of the treatment period, AHR determined by log PC(20) was significantly improved in the DCT group (0.51 +/- 1.05 mg/ml vs. 0.26 +/- 0.84 mg/ml, p = 0.034). The total clinical and medication reduced parameters showed improvement in the DCT group (p = 0.004). The AHR, symptom and medication scores in children with persistent asthma were significantly improved with DCT treat for 12 wk. The results suggested more stable airways achieved with such an add-on complementary therapy.
机译:中药在支气管哮喘的治疗中有着悠久的应用历史。尽管在全球和台湾患者中广泛使用,但尚无可靠的科学证据。通过随机,双盲,安慰剂对照的临床试验,评估丁喘汤(DCT)对哮喘儿童的气道高反应性(AHR)的影响。该研究纳入了8-15岁并被诊断为轻度至中度持续性哮喘患者的儿童。他们被随机分配每天接受6.0克DCT或安慰剂,连续12周。在每月的诊所返回自我记录的每日症状评分,药物评分以及早晚高峰呼气流速。在试验之前和试验结束时分别进行肺功能检查,乙酰甲胆碱激发试验和血清炎症介质。 52名哮喘儿童完成了临床研究。 28名患者被分配到治疗组,24名患者被分配到安慰剂组。在治疗期结束时,DCT组通过log PC(20)测定的AHR显着改善(0.51 +/- 1.05 mg / ml对0.26 +/- 0.84 mg / ml,p = 0.034)。总体临床和用药减少的参数显示DCT组有所改善(p = 0.004)。持续性哮喘患儿的AHR,症状和用药评分通过DCT治疗12周显着改善。结果表明,使用这种补充性补充疗法可获得更稳定的气道。

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