Tiotropium add-on therapy is safe and reduces seasonal worsening in paediatric asthma patients
Year: 2019
Type: article
Abstract: There remains an unmet need for effective, well-tolerated therapeutic options in paediatric patients with not fully controlled asthma, for whom safety is of paramount importance. Data were pooled from five randomised, double-blind, placebo-controlled studies evaluating tiotropium 5 or 2.5 µgversusplacebo add-on therapy in patients with symptomatic asthma aged 1–17 years. Analysis included adverse events (AEs) and serious AEs (SAEs) reported throughout and for 30 days following treatment. Of 1691 patients treated, 1119 received tiotropium. Reporting of AEs was low and comparable across all groups: tiotropium 5 µg (51%), tiotropium 2.5 µg (51%) and placebo (54%). Reporting of drug-related AEs, those leading to discontinuation and SAEs was also low and balanced between treatment groups, irrespective of age, disease severity or sex. The number of AEs related to asthma symptoms and exacerbations was lower with tiotropium (5 µg) than with placebo, particularly during the seasonal peaks of these AEs. This comprehensive analysis of a large safety database allowed subgroup analyses that are often impractical with individual trials and provides further support for the safety of once-daily tiotropium Respimat add-on therapy in paediatric patients with symptomatic asthma.
Source: European Respiratory Journal
Institutions: University Hospital Carl Gustav Carus, Technische Universität Dresden, Children's Hospital Colorado, University of Colorado Anschutz, University of Colorado Denver, University Medical Center Groningen, University of Groningen, University of Verona, Boehringer Ingelheim (Germany), Boehringer Ingelheim (Australia), Goethe University Frankfurt, Ruhr University Bochum
Language: English
Subfield: Physiology
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
OpenAlex ID: W2945173237
