Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/681
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dc.contributor.authorChampion, A. A.en
dc.contributor.authorPetsky, H. L.en
dc.contributor.authorSloots, T. P.en
dc.contributor.authorWheeler, C.en
dc.contributor.authorAcworth, J. P.en
dc.contributor.authorChang, A. B.en
dc.contributor.authorStone, D. G.en
dc.contributor.authorClark, R.en
dc.contributor.authorThearle, D.en
dc.date.accessioned2018-06-16T20:36:52Z-
dc.date.available2018-06-16T20:36:52Z-
dc.date.issued2008en
dc.identifier.citation15 Sep 189 (6) , 2008, p. 306-310en
dc.identifier.otherRISen
dc.identifier.urihttp://dora.health.qld.gov.au/qldresearchjspui/handle/1/681-
dc.description.abstractObjective: To determine whether a 5-day course of oral prednisolone is superior to a 3-day course in reducing the 2-week morbidity of children with asthma exacerbations who are not hospitalised. Design, setting and participants: Double-blind randomised controlled trial of as outcomes following a 5-day course of oral prednisolone (1 mg/ kg) compared with 3-day course of prednisolone plus placebo for 2 days. Participants were children aged 2-15 years who presented to the emergency departments of three Queensland hospitals between March 2004 and February 2007 with an acute exacerbation of asthma, but were not hospitalised. Sample size was defined a priori for a study power of 90%. Main outcome measures: Difference in proportion of children who were symptom-free at Day 7, as measured by intention-to-treat (ITT) and per-protocol analysis; quality of life (QOL) on Days 7 and 14. Results: 201 children were enrolled, and there was an 82% completion rate. There was no difference between groups in the proportion of children who were symptom-free (observed difference, 0.04 [95% Cl, -0.09 to 0.18] by ITT analysis; 0.04 [95% Cl, -0.17 to 0.09] by per-protocol analysis). There was also no difference between groups in QOL (P= 0.42). The difference between groups for the primary outcome was within the equivalence range calculated post priori. Conclusion: A 5-day course of oral prednisolone confers no advantage over a 3-day course for children with asthma exacerbations who are not hospitalised.<br />en
dc.languageenen
dc.relation.ispartofMedical Journal of Australiaen
dc.titleA 5- versus 3-day course of oral corticosteroids for children with asthma exacerbations who are not hospitalised: A randomised controlled trialen
dc.typeArticleen
dc.relation.urlhttp://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&D=emed8&AN=2008472361en
dc.identifier.risid359en
dc.description.pages306-310en
local.message.claim2024-06-20T15:52:49.661+1000|||rp06230|||submit_approve|||dc_contributor_author|||None*
item.openairetypeArticle-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
Appears in Sites:Sunshine Coast HHS Publications
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