Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/10005
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSeeman, Egoen
dc.contributor.authorCrans, Gerald Gen
dc.contributor.authorDiez-Perez, Adolfoen
dc.contributor.authorPinette, Karen Ven
dc.contributor.authorDelmas, Pierre Den
dc.date.accessioned2015-05-15T23:18:55Z
dc.date.available2015-05-15T23:18:55Z
dc.date.issued2005-10-11en
dc.identifier.citationOsteoporosis International : A Journal Established As Result of Cooperation Between the European Foundation For Osteoporosis and the National Osteoporosis Foundation of The Usa 2005; 17(2): 313-6en
dc.identifier.govdoc16217588en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/10005en
dc.description.abstractIn the Multiple Outcomes of Raloxifene Evaluation (MORE) trial, raloxifene reduced the risk of vertebral fracture. However, a systematic analysis of the anti-vertebral fracture efficacy of raloxifene, which includes the results of newly reported studies, has not been performed. A meta-analysis was carried out using all randomized, double-blind, placebo-controlled trials to determine whether the reduction in the risk for vertebral fracture, reported with raloxifene, was consistent among studies, and to define more accurately the point estimate of the odds ratio. Three prevention studies, two arms of the MORE trial, and three additional treatment studies in which fracture data were available from prospectively scheduled spinal radiographs were included in the analysis. A systematic review of the literature (MedLine, EMBASE) confirmed that no studies with raloxifene had been excluded from this analysis. The effects of raloxifene 60 mg/day (RLX60) and 120 mg/day pooled with 150 mg/day (RLX120/150) were analyzed by intention to treat. There was no significant heterogeneity among the studies included in the meta-analysis. Odds ratio estimates (95% CI) were 0.60 (0.49, 0.74) for RLX60 and 0.51 (0.41, 0.64) for RLX120/150. From these data we infer that raloxifene consistently reduces the risk of vertebral fracture in postmenopausal women.en
dc.language.isoenen
dc.subject.otherBone Density Conservation Agents.therapeutic useen
dc.subject.otherDouble-Blind Methoden
dc.subject.otherFemaleen
dc.subject.otherHumansen
dc.subject.otherOdds Ratioen
dc.subject.otherOsteoporosis, Postmenopausal.complications.drug therapyen
dc.subject.otherRaloxifene.therapeutic useen
dc.subject.otherRandomized Controlled Trials as Topicen
dc.subject.otherRisk Factorsen
dc.subject.otherSpinal Fractures.prevention & controlen
dc.titleAnti-vertebral fracture efficacy of raloxifene: a meta-analysis.en
dc.typeJournal Articleen
dc.identifier.journaltitleOsteoporosis Internationalen
dc.identifier.affiliationDepartment of Endocrinology, University of Melbourne, Austin Hospital, Heidelberg, 3084, Melbourne, Victoria, Australiaen
dc.identifier.doi10.1007/s00198-005-2030-1en
dc.description.pages313-6en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/16217588en
dc.type.austinJournal Articleen
local.name.researcherSeeman, Ego
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextopen-
crisitem.author.deptEndocrinology-
Appears in Collections:Journal articles
Files in This Item:
File SizeFormat 
16217588.pdf43.66 kBAdobe PDFView/Open
Show simple item record

Page view(s)

22
checked on Jul 21, 2024

Download(s)

64
checked on Jul 21, 2024

Google ScholarTM

Check


Items in AHRO are protected by copyright, with all rights reserved, unless otherwise indicated.