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首页> 外文期刊>Pragmatic and Observational Research >A multicenter, open-label, noninterventional study to evaluate the impact on clinical effects, user-friendliness and patients’ acceptance of AirFluSal Forspiro in the treatment of asthma under real-life conditions (ASSURE)
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A multicenter, open-label, noninterventional study to evaluate the impact on clinical effects, user-friendliness and patients’ acceptance of AirFluSal Forspiro in the treatment of asthma under real-life conditions (ASSURE)

机译:一项多中心,开放性,非介入性研究,评估在现实生活条件下哮喘对临床效果,用户友好性和患者接受AirFluSal Forspiro的接受程度的影响(ASSURE)

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Background: The design of inhaler devices may potentially influence adherence/persistence and outcomes in asthma. Objective: The primary objective was to assess asthma control and any change in the quality of life in patients using an intuitive dry powder inhaler containing fluticasone propionate/salmeterol (AirFluSalsup?,/sup Forspirosup?,/sup) for the treatment of asthma in everyday practice. Methods: ASSURE was a multicenter, noninterventional, open-label, prospective study in patients with asthma, aged ≥12 years and treated with the Forspiro device in Denmark, Sweden and Norway. Patients’ opinions of their asthma control were assessed by the Asthma Control Test (ACT) questionnaire and asthma-related quality of life by the Mini Asthma Quality of Life Questionnaire (miniAQLQ) at baseline and at two follow-up visits (approximately 4–8-week intervals). Results: Of 321 patients enrolled in the study, 299 received at least one dose of fluticasone propionate/salmeterol via the Forspiro device and 204 had evaluable data at the baseline visit and at least one later visit. Patients showed improvements in asthma control and quality of life during the study. The mean sum score of ACT increased from 18.0 (SD 4.5) at visit 1 to 19.9 (4.2) at visit 2 and 20.5 (4.3) at visit 3. Overall, 38.2% of patients improved by the minimal clinically important difference (MCID) of ≥3 points (45.6% among those with a baseline score below 23 [ie, not already well controlled]). The mean score on the miniAQLQ increased from 5.16 (SD 1.24) at visit 1 to 5.58 (SD 1.20) at visit 2 and 5.82 (SD 1.04) at visit 3. Overall, 42.6% of patients improved by the MCID of ≥0.5. Conclusion: This real-life study suggests that treatment with fluticasone propionate/salmeterol via the Forspiro device can improve asthma symptom control and quality of life.
机译:背景:吸入器的设计可能会影响哮喘的依从性/持久性和预后。目的:主要目的是使用含有丙酸氟替卡松/沙美特罗(AirFluSal ?, Forspiro ?,)在日常实践中用于治疗哮喘。方法:ASSURE是一项针对多于12岁且在丹麦,瑞典和挪威使用Forspiro装置治疗的哮喘患者的多中心,非介入,开放标签的前瞻性研究。在基线和两次随访中(约4–8),通过哮喘控制测试(ACT)调查表评估患者对哮喘控制的意见,并通过迷你哮喘生活质量问卷(miniAQLQ)评估与哮喘相关的生活质量。 -周间隔)。结果:参与研究的321名患者中,有299名通过Forspiro装置接受了至少一剂丙酸氟替卡松/沙美特罗,并且204名在基线访视时和以后至少访视中具有可评估的数据。在研究期间,患者表现出哮喘控制和生活质量的改善。 ACT的平均总分从访视1的18.0(SD 4.5)增加到访视2的19.9(4.2)和访视3的20.5(4.3)。总体上,38.2%的患者通过临床上的最小临床重要差异(MCID)得到改善≥3分(基线得分低于23(即尚未得到良好控制)的患者中为45.6%)。 miniAQLQ的平均评分从第一次就诊时的5.16(SD 1.24)增加到了第二次就诊时的5.58(SD 1.20)和第三次就诊时的5.82(SD 1.04)。总体而言,42.6%的患者的MCID≥0.5有改善。结论:这项现实生活研究表明,通过Forspiro装置使用丙酸氟替卡松/沙美特罗治疗可以改善哮喘症状的控制和生活质量。

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