02510nas a2200325 4500000000100000008004100001653001100042653002200053653003000075653001700105653003900122653003100161653005100192653003800243653006700281653006800348653003000416653006400446100001500510700001300525700001200538700001200550245009500562250001500657300001000672490000700682050001600689520142800705020005102133 2016 d10aHumans10aTreatment Outcome10aDrug Therapy, Combination10aTime Factors10aLung/ drug effects/physiopathology10aAdministration, Inhalation10aAsthma/diagnosis/ drug therapy/physiopathology10aBronchoconstriction/ drug effects10aBronchodilator Agents/ administration & dosage/adverse effects10aMuscarinic Antagonists/ administration & dosage/adverse effects10aNebulizers and Vaporizers10aTiotropium Bromide/ administration & dosage/adverse effects1 aJenkins C.1 aBusse W.1 aDahl R.1 aCruz A.00aLong-acting muscarinic antagonists: a potential add-on therapy in the treatment of asthma? a2016/03/02 a54-640 v25 a[IF]: 0.0003 a

Asthma is a chronic inflammatory disorder of the airways that is a major global burden on both individuals and healthcare systems. Despite guideline-directed treatment, a significant proportion of patients with asthma do not achieve control. This review focuses on the potential use of long-acting anticholinergics as bronchodilators in the treatment of asthma, with results published from clinical trials of glycopyrrolate, umeclidinium and tiotropium. The tiotropium clinical trial programme is the most advanced, with data available from a number of phase II and III studies of tiotropium as an add-on to inhaled corticosteroid maintenance therapy, with or without a long-acting beta2-agonist, in patients across asthma severities. Recent studies using the Respimat Soft Mist inhaler have identified 5 microg once daily as the preferred dosing regimen, which has shown promising results in adults, adolescents and children with asthma. Tiotropium Respimat has recently been incorporated into the Global Initiative for Asthma 2015 treatment strategy as a recommended alternative therapy at steps 4 and 5 in adult patients with a history of exacerbations. The increasing availability of evidence from ongoing and future clinical trials will be beneficial in determining where long-acting anticholinergic agents fit in future treatment guidelines across a variety of patient populations and disease severities.

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