首页> 外文期刊>Kobe journal of medical sciences >An Open-Label, Multi-Institutional, Randomized Study to Evaluate the Additive Effect of a Leukotriene Receptor Antagonist on Cough Score in Patients with Cough-Variant Asthma Being Treated with Inhaled Corticosteroids
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An Open-Label, Multi-Institutional, Randomized Study to Evaluate the Additive Effect of a Leukotriene Receptor Antagonist on Cough Score in Patients with Cough-Variant Asthma Being Treated with Inhaled Corticosteroids

机译:一项开放性,多机构,随机研究,评估白三烯受体拮抗剂对吸入性糖皮质激素治疗的咳嗽变异性哮喘患者咳嗽评分的加和作用

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Cough-variant asthma is one of the most common reasons for chronic cough. It is important to treat appropriately cough-variant asthma because 30% to 40% of cough-variant asthma becomes a typical asthma. However, little is known about the treatment of cough-variant asthma except for inhaled corticosteroid (ICS). The aim of this study was to validate the additive efficacy of a leukotriene receptor antagonist (LTRA) on cough score and respiratory function in patients with cough-variant asthma being treated with ICS. A total 28 patients were randomly assigned to either an ICS + LTRA group or an ICS group. There were statistically significant improvements in cough scores in the ICS + LTRA group from 0 weeks (6.7 ? 4.4) to 2 weeks (2.9 ? 3.2) (P 0.05), 4 weeks (0.7 ? 1.1) (P 0.001), and 8 weeks (0.8 ? 1.2) (P 0.001). However similar improvements were not evident in the ICS group from 0 weeks (6.7 ? 4.4) to 2 weeks (5.6 ? 10.0) (P = 0.59), 4 weeks (4.6 ? 7.6) (P = 0.32), and 8 weeks (2.9 ? 5.2) (P = 0.08). On the other hand, no significant changes were evident in the forced expiratory volume in 1 s (FEV1) and FEV1/forced vital capacity (FVC). In conclusion, the LTRA was useful in improving cough in patients with cough-variant asthma, even though it appeared to be ineffective in improving respiratory function.
机译:咳嗽变异性哮喘是慢性咳嗽的最常见原因之一。适当治疗咳嗽变异性哮喘很重要,因为30%至40%的咳嗽变异性哮喘会成为典型的哮喘。但是,除吸入糖皮质激素(ICS)外,关于咳嗽变异性哮喘的治疗知之甚少。这项研究的目的是验证白三烯受体拮抗剂(LTRA)对接受ICS治疗的咳嗽变异型哮喘患者的咳嗽评分和呼吸功能的累加效果。共有28例患者随机分为ICS + LTRA组或ICS组。 ICS + LTRA组的咳嗽评分从0周(6.7?4.4)到2周(2.9?3.2)(P <0.05),4周(0.7?1.1)(P <0.001)和8周(0.8?1.2)(P <0.001)。然而,ICS组从0周(6.7?4.4)到2周(5.6?10.0)(P = 0.59),4周(4.6?7.6)(P = 0.32)和8周(2.9)均未见类似的改善。 5.2)(P = 0.08)。另一方面,在1 s内的呼气量(FEV1)和FEV1 /强迫肺活量(FVC)没有明显变化。总之,LTRA在改善咳嗽变异性哮喘患者的咳嗽中是有用的,尽管它在改善呼吸功能方面似乎无效。

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