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Efficacy of once-daily tiotropium Respimat in adults with asthma at GINA Steps 2-5.
Buhl, Roland; FitzGerald, J M; Meltzer, Eli O; de la Hoz, Alberto; Sigmund, Ralf; Kerstjens, Huib A M; Bleecker, Eugene R.
Afiliação
  • Buhl R; Johannes Gutenberg University Mainz, Mainz, Germany. Electronic address: Roland.Buhl@unimedizin-mainz.de.
  • FitzGerald JM; Centre for Heart and Lung Health, Vancouver, Canada. Electronic address: Mark.Fitzgerald@vch.ca.
  • Meltzer EO; University of California, San Diego, La Jolla, CA, USA. Electronic address: eliomeltzer@gmail.com.
  • de la Hoz A; Boehringer Ingelheim International GmbH, Ingelheim Am Rhein, Germany. Electronic address: alberto.de_la_hoz@boehringer-ingelheim.com.
  • Sigmund R; Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach an der Riss, Germany. Electronic address: ralf.sigmund@boehringer-ingelheim.com.
  • Kerstjens HAM; University of Groningen, University Medical Center Groningen, And Groningen Research Institute for Asthma and COPD GRAIC, Groningen, the Netherlands. Electronic address: h.a.m.kerstjens@umcg.nl.
  • Bleecker ER; Genomics and Precision Medicine, University of Arizona College of Medicine, Tucson, AZ, USA. Electronic address: erbleecker@email.arizona.edu.
Pulm Pharmacol Ther ; 60: 101881, 2020 02.
Article em En | MEDLINE | ID: mdl-31874283
Tiotropium Respimat is an efficacious add-on to maintenance treatment in patients with symptomatic asthma. Currently, the Global Initiative for Asthma (GINA) strategy recommends tiotropium for patients at Steps 4-5. To assess the clinical benefits of tiotropium Respimat across asthma severities, GINA Steps 2-5, a post hoc analysis of five double-blind trials (12-48-weeks; patients aged 18-75 years) investigated the effect of tiotropium Respimat, 5 µg or 2.5 µg, versus placebo, on peak forced expiratory volume in 1 s (FEV1) within 3 h post-dose (FEV1(0-3h)) response, and Asthma Control Questionnaire-7 (ACQ-7) responder rate. GINA step grouping was based on patients' background treatment regimen. Baseline characteristics of patients (N = 2926) were balanced between treatments. Tiotropium Respimat showed consistent improvements in lung function across GINA steps; placebo-corrected peak FEV1(0-3h) improvements after tiotropium Respimat 5 µg and 2.5 µg were: Step 2 (Week 8), 135 mL (95% confidence interval: 84, 187) and 155 mL (103, 206); Step 3 (Week 24), 187 mL (139, 235) and 235 mL (187, 283); Step 4 (Week 24), 111 mL (63, 159) and 181 mL (35, 326); Step 5 (Week 24; 5 µg only), 164 mL (5, 323). Asthma control improved with tiotropium Respimat versus placebo, showing statistical significance (nominal P value) with tiotropium Respimat 5 µg at Step 4 (odds ratio 1.36 [1.03, 1.78]). Safety profiles were similar between treatments. In conclusion, tiotropium Respimat add-on therapy improves lung function, and may improve asthma control, in adults across disease severities.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Broncodilatadores / Brometo de Tiotrópio Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Pulm Pharmacol Ther Assunto da revista: FARMACOLOGIA Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Broncodilatadores / Brometo de Tiotrópio Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Pulm Pharmacol Ther Assunto da revista: FARMACOLOGIA Ano de publicação: 2020 Tipo de documento: Article