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Corticosteroid plus β2-agonist in a single inhaler as reliever therapy in intermittent and mild asthma: a proof-of-concept systematic review and meta-analysis.

机译:单一吸入器中的皮质类固醇加β2-激动剂作为间歇性和轻度哮喘的缓解剂治疗:概念验证系统评价和荟萃分析。

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摘要

BACKGROUND: Current guidelines recommend a single inhaler maintenance and reliever therapy (SMART) regimen for moderate to severe asthma. However, evidence for the inhaled corticosteroid plus fast-onset-acting β2-agonist (ICS/FABA) as reliever therapy in management of intermittent and mild asthma patients is lacking. OBJECTIVE: To systematically explore efficacy and safety of the proof-of-concept of the ICS plus FABA regimen in a single inhaler as reliever therapy across children and adults with intermittent and mild persistent asthma. METHODS: We searched online bibliographic databases for randomized controlled trials (RCTs) involving the as-needed use of ICS/FABA as monotherapy in intermittent or mild asthma patients. The primary outcomes were exacerbations and the hazard ratio (HR) of the time to first exacerbation. RESULTS: Six RCTs (n = 1300) met the inclusion criteria. Compared with the as-needed FABA regimen, the as-needed use of ICS/FABA as monotherapy statistically reduced exacerbations (RR = 0.56, P = 0.001). Compared with regular ICS regimen, the as-needed ICS/FABA therapy had slightly higher risk of exacerbations (RR = 1.39, P = 0.011). The HR for time to first exacerbations in the ICS/FABA regimen was significant lower when compared with FABA regimen (HR = 0.52, P = 0.002) but had no difference when compared with ICS regimen (HR = 1.30, P = 0.286). The corticosteroid exposure in the daily ICS regimen was 2- to 5-fold compared with as-needed use of ICS/FABA regimen. CONCLUSIONS: Our analysis shows that the ICS/FABA as a symptom-driven therapy may be a promising alternative regimen for the patients with intermittent or mild asthma, but it needs further real-world RCTs to confirm these findings.
机译:背景:目前的指南建议针对中度至重度哮喘的单一吸入器维持和缓解治疗(SMART)方案。但是,缺乏在间歇性和轻度哮喘患者中吸入皮质类固醇加速效β2-激动剂(ICS / FABA)作为缓解剂的证据。目的:系统研究单一吸入器中ICS + FABA方案的概念验证的有效性和安全性,以治疗间歇性和轻度持续性哮喘的儿童和成人。方法:我们在在线书目数据库中搜索了涉及随机或轻度哮喘患者按需使用ICS / FABA作为单药治疗的随机对照试验(RCT)。主要结果是病情加重和首次加重时间的风险比(HR)。结果:六个RCT(n = 1300)符合纳入标准。与需要的FABA方案相比,ICS / FABA作为单一疗法的需要在统计学上减少了病情加重(RR = 0.56,P =)0.001)。与常规ICS方案相比,按需ICS / FABA治疗的病情加重风险略高(RR = 1.39,P = 0.011)。与FABA方案相比(HR = 0.52,P = 0.002),ICS / FABA方案至首次加重时间的HR显着较低,但与ICS方案相比(HR = 1.30,P = 0.286)则无差异。与按需使用ICS / FABA方案相比,每日ICS方案中的皮质类固醇暴露量是2至5倍。结论:我们的分析表明,ICS / FABA作为一种症状驱动疗法可能是间歇性或轻度哮喘患者的有前途的替代治疗方案,但需要进一步的现实世界RCT来证实这些发现。

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