Short course montelukast for intermittent asthma in children: a randomised controlled trial

dc.contributor.authorRobertson, Colin Fen_AU
dc.contributor.authorPrice, Daviden_AU
dc.contributor.authorHenry, Richarden_AU
dc.contributor.authorMellis, Craig Men_AU
dc.contributor.authorGlasgow, Nicholasen_AU
dc.contributor.authorFitzgerald, Dominicen_AU
dc.contributor.authorLee, Amandaen_AU
dc.contributor.authorTurner, Jenniferen_AU
dc.contributor.authorSant, Melissaen_AU
dc.date.accessioned2015-12-07T22:16:19Z
dc.date.issued2007
dc.date.updated2015-12-07T07:48:56Z
dc.description.abstractRationale: In children, intermittent asthma is the most common pattern and is responsible for the majority of exacerbations. Montelukast has a rapid onset of action and may be effective if used intermittently. Objectives: To determine whether a short course of montelukast in children with intermittent asthma would modify the severity of an asthma episode. Methods: Children, aged 2-14 years with intermittent asthma participated in this multicenter, randomized, double-blind, placebo-controlled clinical trial over a 12-month period. Treatment with montelukast or placebo was initiated by parents at the onset of each upper respiratory tract infection or asthma symptoms and continued for a minimum of 7 days or until symptoms had resolved for 48 hours. Measurements and Main Results: A total of 220 children were randomized, 107 to montelukast and 113 to placebo. There were 681 treated episodes (345 montelukast, 336 placebo) provided by 202 patients. The montelukast group had 163 unscheduled health care resource utilizations for asthma compared with 228 in the placebo group (odds ratio, 0.65; 95% confidence interval, 0.47-0.89). There was a nonsignificant reduction in specialist attendances and hospitalizations, duration of episode, and β-agonist and prednisolone use. Symptomswere reduced by 14% and nights awakened by 8.6% (p = 0.043), and days off from school or childcare by 37% and parent time off from work by 33% (p < 0.0001 for both). Conclusions: A short course of montelukast, introduced at the first signs of an asthma episode, results in a modest reduction in acute health care resource utilization, symptoms, time off from school, and parental time off from work in children with intermittent asthma.
dc.identifier.issn1073-449X
dc.identifier.urihttp://hdl.handle.net/1885/17968
dc.publisherAmerican Thoracic Society
dc.sourceAmerican Journal of Respiratory and Critical Care Medicine
dc.subjectKeywords: beta adrenergic receptor stimulating agent; montelukast; placebo; prednisolone; adolescent; article; asthma; child; child care; child parent relation; clinical trial; confidence interval; controlled clinical trial; controlled study; double blind procedure Asthma; Montelukast; Pediatric
dc.titleShort course montelukast for intermittent asthma in children: a randomised controlled trial
dc.typeJournal article
local.bibliographicCitation.lastpage329
local.bibliographicCitation.startpage323
local.contributor.affiliationRobertson, Colin F, Royal Children's Hospital Melbourne
local.contributor.affiliationPrice, David, University of Aberdeen
local.contributor.affiliationHenry, Richard, University of New South Wales
local.contributor.affiliationMellis, Craig M, University of Sydney
local.contributor.affiliationGlasgow, Nicholas, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationFitzgerald, Dominic, University of Sydney
local.contributor.affiliationLee, Amanda, University of Aberdeen
local.contributor.affiliationTurner, Jennifer, St Vincent's Hospital Sydney
local.contributor.affiliationSant, Melissa, Merck Sharp and Dohme (Australia) Pty. Ltd
local.contributor.authoruidGlasgow, Nicholas, u4240990
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor111717 - Primary Health Care
local.identifier.absfor111499 - Paediatrics and Reproductive Medicine not elsewhere classified
local.identifier.ariespublicationu3961986xPUB3
local.identifier.citationvolume175
local.identifier.doi10.1164/rccm.200510-1546OC
local.identifier.scopusID2-s2.0-33847056975
local.type.statusPublished Version

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