PMID- 31931792 OWN - NLM STAT- MEDLINE DCOM- 20201112 LR - 20201112 IS - 1465-993X (Electronic) IS - 1465-9921 (Print) IS - 1465-9921 (Linking) VI - 21 IP - 1 DP - 2020 Jan 13 TI - A comparison of tiotropium, long-acting beta(2)-agonists and leukotriene receptor antagonists on lung function and exacerbations in paediatric patients with asthma. PG - 19 LID - 10.1186/s12931-020-1282-9 [doi] LID - 19 AB - Diagnosing and treating asthma in paediatric patients remains challenging, with many children and adolescents remaining uncontrolled despite treatment. Selecting the most appropriate pharmacological treatment to add onto inhaled corticosteroids (ICS) in children and adolescents with asthma who remain symptomatic despite ICS can be difficult. This literature review compares the efficacy and safety of long-acting beta(2)-agonists (LABAs), leukotriene receptor antagonists (LTRAs) and long-acting muscarinic antagonists (LAMAs) as add-on treatment to ICS in children and adolescents aged 4-17 years.A literature search identified a total of 29 studies that met the inclusion criteria, including 21 randomised controlled trials (RCTs) of LABAs versus placebo, two RCTs of LAMAs (tiotropium) versus placebo, and four RCTs of LTRA (montelukast), all as add-on to ICS. In these studies, tiotropium and LABAs provided greater improvements in lung function than LTRAs, when compared with placebo as add-on to ICS. Although exacerbation data were difficult to interpret, tiotropium reduced the risk of exacerbations requiring oral corticosteroids when added to ICS, with or without additional controllers. LABAs and LTRAs had a comparable risk of asthma exacerbations with placebo when added to ICS. When adverse events (AEs) or serious AEs were analysed, LABAs, montelukast and tiotropium had a comparable safety profile with placebo.In conclusion, this literature review provides an up-to-date overview of the efficacy and safety of LABAs, LTRAs and LAMAs as add-on to ICS in children and adolescents with asthma. Overall, tiotropium and LABAs have similar efficacy, and provide greater improvements in lung function than montelukast as add-on to ICS. All three controller options have comparable safety profiles. FAU - Vogelberg, Christian AU - Vogelberg C AD - Department of Pediatric Pulmonology and Allergy, University Hospital Carl Gustav Carus, Technical University of Dresden, Dresden, Germany. christian.vogelberg@uniklinikum-dresden.de. FAU - Goldstein, Stanley AU - Goldstein S AD - Allergy and Asthma Care of Long Island, Rockville Centre, New York, USA. FAU - Graham, LeRoy AU - Graham L AD - Pediatric Pulmonology, Children's Healthcare of Atlanta, Atlanta, GA, USA. FAU - Kaplan, Alan AU - Kaplan A AD - Family Physician Airways Group of Canada, University of Toronto, Toronto, Ontario, Canada. FAU - de la Hoz, Alberto AU - de la Hoz A AD - TA Respiratory/Biosimilars Medicine, Boehringer Ingelheim International GmbH, Ingelheim am Rhein, Germany. FAU - Hamelmann, Eckard AU - Hamelmann E AD - Klinik fur Kinder und Jugendmedizin, Evangelisches Klinikum Bethel, Bielefeld, and Allergy Center of the Ruhr University, Bochum, Germany. LA - eng GR - N/A/Boehringer Ingelheim/ PT - Comparative Study PT - Journal Article PT - Review DEP - 20200113 PL - England TA - Respir Res JT - Respiratory research JID - 101090633 RN - 0 (Adrenergic beta-2 Receptor Agonists) RN - 0 (Anti-Asthmatic Agents) RN - 0 (Bronchodilator Agents) RN - 0 (Delayed-Action Preparations) RN - 0 (Leukotriene Antagonists) RN - XX112XZP0J (Tiotropium Bromide) SB - IM MH - Adolescent MH - Adrenergic beta-2 Receptor Agonists/*administration & dosage MH - Anti-Asthmatic Agents/administration & dosage MH - Asthma/diagnosis/*drug therapy/physiopathology MH - Bronchodilator Agents/administration & dosage MH - Child MH - Child, Preschool MH - Delayed-Action Preparations/administration & dosage MH - *Disease Progression MH - Humans MH - Leukotriene Antagonists/*administration & dosage MH - Lung/drug effects/*physiology MH - Randomized Controlled Trials as Topic/methods MH - Tiotropium Bromide/*administration & dosage PMC - PMC6958672 OTO - NOTNLM OT - Asthma OT - LABA OT - LAMA OT - LTRA OT - Paediatrics COIS- CV reports personal fees from Allergopharma, ALK, Bencard, Boehringer Ingelheim, Novartis, Stallergenes, Sanofi Avensis, Engelhard and DBV Technology, and grants from the German Society of Research (DFG), outside the submitted work. LG reports personal fees from Boehringer Ingelheim and serves as a speaker and member of the paediatric advisory board for Boehringer Ingelheim outside of the submitted work. AK reports personal fees from Boehringer Ingelheim, Covis, GlaxoSmithKline, Teva, Novartis, Pfizer, AstraZeneca, Purdue, Sanofi, Paladdin and Trudell outside the submitted work. AdlH is an employee of Boehringer Ingelheim. SG and EH have nothing to disclose. EDAT- 2020/01/15 06:00 MHDA- 2020/11/13 06:00 PMCR- 2020/01/13 CRDT- 2020/01/15 06:00 PHST- 2019/09/09 00:00 [received] PHST- 2020/01/05 00:00 [accepted] PHST- 2020/01/15 06:00 [entrez] PHST- 2020/01/15 06:00 [pubmed] PHST- 2020/11/13 06:00 [medline] PHST- 2020/01/13 00:00 [pmc-release] AID - 10.1186/s12931-020-1282-9 [pii] AID - 1282 [pii] AID - 10.1186/s12931-020-1282-9 [doi] PST - epublish SO - Respir Res. 2020 Jan 13;21(1):19. doi: 10.1186/s12931-020-1282-9.