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一项为期12周的随机平行组概念验证研究,比较妥洛特罗贴剂和沙美特罗吸入器作为成人起病的轻度至中度哮喘附加治疗的效果。

A 12-week, randomized, parallel-group, proof-of-concept study of tulobuterol patch and salmeterol inhaler as add-on therapy in adult-onset mild-to-moderate asthma.

作者信息

Inoue Hideki, Niimi Akio, Matsumoto Hisako, Ito Isao, Oguma Tsuyoshi, Otsuka Kojiro, Takeda Tomoshi, Nakaji Hitoshi, Tajiri Tomoko, Iwata Toshiyuki, Nagasaki Tadao, Mishima Michiaki

机构信息

Department of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Department of Respiratory Medicine, Allergy and Clinical Immunology, Graduate School of Medical Sciences, Nagoya City University, Nagoya, Aichi, Japan.

出版信息

Clin Exp Pharmacol Physiol. 2017 Jan;44(1):21-29. doi: 10.1111/1440-1681.12683.

DOI:10.1111/1440-1681.12683
PMID:27718262
Abstract

Patch formulation of tulobuterol has been used in asthma treatment as a long-acting β -agonist (LABA) through sustained skin absorption. Its treatment efficacy, especially in small airways, remains poorly understood. The study aim was to investigate LABA add-on effects of tulobuterol patch (TP) and salmeterol inhaler (SA) on pulmonary function, asthma control and health status. Patients who had adult-onset under-control asthma, despite taking inhaled corticosteroids, were enrolled in a randomized, open-label, parallel-group, proof-of-concept study of 12-week add-on treatment with TP (n=16) or SA (n=17). Spirometry, impulse oscillometry (IOS), exhaled nitric oxide levels, and clinical questionnaires of asthma control, health status (St. George's Respiratory Questionnaire: SGRQ), and symptoms were evaluated every 4 weeks. Add-on treatment of SA significantly improved the spirometric indices of small airway obstruction (forced expiratory flow between 25% and 75% of FVC: FEF , and maximum expiratory flow at 25% of FVC: MEF ) and IOS indices of whole respiratory resistance (resistance at 5 Hz) as compared to TP. In intra-group comparisons, add-on treatment of TP improved the scores of the asthma control test and the total SGRQ, as well as the symptom and impact components of the SGRQ. SA add-on treatment improved FEV and IOS parameters of resistance at 20 Hz and reactance at 5 Hz. Neither of the treatments improved exhaled nitric oxide levels. In conclusion, add-on treatment of TP improved asthma control and health status, whereas SA improved pulmonary function measures associated with large and small airway involvement among patients with adult-onset mild-to-moderate asthma.

摘要

妥洛特罗贴剂作为一种长效β受体激动剂(LABA),通过持续的皮肤吸收已被用于哮喘治疗。但其治疗效果,尤其是在小气道方面,仍知之甚少。本研究旨在探讨妥洛特罗贴剂(TP)和沙美特罗吸入器(SA)作为LABA的附加治疗对肺功能、哮喘控制和健康状况的影响。尽管使用了吸入性糖皮质激素,但仍患有成人起病且控制不佳的哮喘患者被纳入一项为期12周的附加治疗的随机、开放标签、平行组概念验证研究,分别接受TP(n = 16)或SA(n = 17)治疗。每4周评估一次肺活量测定、脉冲振荡法(IOS)、呼出一氧化氮水平以及哮喘控制、健康状况(圣乔治呼吸问卷:SGRQ)和症状的临床问卷。与TP相比,SA的附加治疗显著改善了小气道阻塞的肺活量测定指标(用力肺活量25%至75%之间的用力呼气流量:FEF ,以及用力肺活量25%时的最大呼气流量:MEF )和整个呼吸阻力的IOS指标(5赫兹时的阻力)。在组内比较中,TP的附加治疗改善了哮喘控制测试分数、SGRQ总分以及SGRQ的症状和影响部分。SA的附加治疗改善了第1秒用力呼气容积(FEV )以及20赫兹时的阻力和5赫兹时的电抗的IOS参数。两种治疗均未改善呼出一氧化氮水平。总之,TP的附加治疗改善了哮喘控制和健康状况,而SA改善了成人起病的轻度至中度哮喘患者与大气道和小气道受累相关的肺功能指标。

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