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首页> 外文期刊>Clinical and experimental pharmacology & physiology >Comparison of the effects of tulobuterol patch and salmeterol in moderate to severe asthma.
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Comparison of the effects of tulobuterol patch and salmeterol in moderate to severe asthma.

机译:妥布特罗贴剂和沙美特罗在中度至重度哮喘中的作用比较。

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1. Although the clinical effects of the tulobuterol patch have been reported to include an increase in morning peak expiratory flow (PEF) values and a decrease of symptoms and the frequency of the rescue use of inhaled short-acting beta2-adrenoceptor agonists, no trials comparing the efficacy of the tulobuterol patch to other standard inhaled long-acting beta2-adrenoceptor agonists have yet been conducted. The aim of the present study was to compare the clinical effects of the patch formulation of tulobuterol with those of inhaled salmeterol in moderate to severe asthma. 2. Fifty-four patients with moderate to severe asthma, whose conditions were suboptimally controlled despite receiving inhaled corticosteroids, were recruited. The study was a prospective, randomized trial of cross-over design comparing the effects of 4 weeks treatment with tulobuterol patch, 2 mg once daily, and salmeterol, 50 mg twice daily. The mean prebronchodilator morning PEF during the last 14 days of each treatment period and health-related quality of life (HRQoL) were the primary outcome variables. The HRQoL was assessed using the St George's Respiratory Questionnaire. 3. Forty-four patients (81.5%) completed the trial and were included in the analysis. The mean morning PEF and HRQoL score were significantly improved in both the salmeterol (P < 0.0001 and P < 0.05, respectively) and the tulobuterol patch (P < 0.01 and P < 0.05, respectively) treatment periods compared with the run-in period. Although the mean morning PEF was significantly higher in the salmeterol-treated group than in the tulobuterol-treated group (P < 0.001), the HRQoL scores were comparable. 4. The tulobuterol patch may be useful as a controller medication in addition to inhaled corticosteroids in moderate to severe asthma.
机译:1.尽管已报道妥洛特罗贴剂的临床效果包括早晨峰值呼气流量(PEF)值增加,症状和吸入性短效β2-肾上腺素受体激动剂的抢救使用频率降低,但尚无试验尚未将妥洛特罗贴剂与其他标准吸入长效β2-肾上腺素受体激动剂的功效进行比较。本研究的目的是比较妥洛特罗贴剂与吸入沙美特罗在中度至重度哮喘中的临床效果。 2.招募了54例中度至重度哮喘患者,尽管接受了糖皮质激素的吸入,但其病情仍未达到最佳状态。这项研究是一项交叉设计的前瞻性,随机试验,比较了每天2 mg的妥洛特罗贴剂和每天两次50 mg的沙美特罗治疗4周的效果。每个治疗期最后14天的平均支气管扩张剂前期PEF和健康相关的生活质量(HRQoL)是主要的结局变量。使用圣乔治呼吸调查问卷对HRQoL进行评估。 3.四十四名患者(81.5%)完成了试验并被纳入分析。与磨合期相比,沙美特罗(分别为P <0.0001和P <0.05)和妥洛特罗贴片(分别为P <0.01和P <0.05)治疗期的早晨PEF和HRQoL均值均得到了显着改善。尽管沙美特罗治疗组的早晨平均PEF显着高于妥洛特罗治疗组(P <0.001),但HRQoL评分是可比的。 4.除中度至重度哮喘患者吸入皮质类固醇激素外,妥洛特罗贴片还可用作控制药物。

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