Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/8297
Full metadata record
DC FieldValueLanguage
dc.contributor.authorGEUSENS, Piet-
dc.contributor.authorRoux, CH-
dc.contributor.authorReid, DM-
dc.contributor.authorLems, WF-
dc.contributor.authorAdami, S.-
dc.contributor.authorAdachi, Jonathan D.-
dc.contributor.authorSambrook, PN-
dc.contributor.authorSaag, KG-
dc.contributor.authorLane, NE-
dc.contributor.authorHochberg, MC-
dc.date.accessioned2008-05-27T10:15:55Z-
dc.date.available2008-05-27T10:15:55Z-
dc.date.issued2008-
dc.identifier.citationNATURE CLINICAL PRACTICE RHEUMATOLOGY, 4(5). p. 240-248-
dc.identifier.issn1745-8382-
dc.identifier.urihttp://hdl.handle.net/1942/8297-
dc.description.abstractMany randomized controlled trials (RCTs) have investigated drug treatment for women at high risk of fracture, with a reduction in fracture risk as their end point. There has also been progress in identifying women at the highest risk of fractures. The most important clinical determinant contributing to the clinical decision of initiating and choosing drug therapy for fracture prevention is a woman's fracture risk, which, in RCTs, was determined by menopausal state, age, bone mineral density, fracture history, fall risks and glucocorticoid use. Women with secondary osteoporosis were excluded, except in studies of glucocorticoid use. A second determinant of drug therapy is the evidence for fracture prevention in terms of spectrum (vertebral, nonvertebral and/or hip fractures), size and speed of effect. In the absence of head-to-head RCTs with fracture risk as the end point, however, the efficacy of antifracture drugs cannot be directly compared. Other determinants include the potential extraskeletal benefits and safety concerns of the drug, patient preferences and reimbursement issues.-
dc.language.isoen-
dc.publisherNATURE PUBLISHING GROUP-
dc.subject.otherdrug safety; drug treatment; fracture risk; glucocorticoid osteoporosis; postmenopausal osteoporosis-
dc.titleDrug Insight: choosing a drug treatment strategy for women with osteoporosis - an evidence-based clinical perspective-
dc.typeJournal Contribution-
dc.identifier.epage248-
dc.identifier.issue5-
dc.identifier.spage240-
dc.identifier.volume4-
local.format.pages9-
local.bibliographicCitation.jcatA1-
dc.description.notesUniv Hasselt, Inst Biomed Res, Haselt, Belgium. Univ Paris, Bone Unit, Paris, France. Univ Aberdeen, Aberdeen AB9 1FX, Scotland. Vrije Univ Amsterdam Med Ctr, Amsterdam, Netherlands. Univ Verona, I-37100 Verona, Italy. McMaster Univ, Hamilton, ON L8S 4L8, Canada. Univ Sydney, Sydney, NSW 2006, Australia. Univ Alabama, Birmingham, AL USA. Univ Calif Davis, Med Ctr, Sacramento, CA 95817 USA. Univ Maryland, Sch Med, College Pk, MD 20742 USA.-
local.type.refereedRefereed-
local.type.specifiedReview-
dc.bibliographicCitation.oldjcatA1-
dc.identifier.doi10.1038/ncprheum0773-
dc.identifier.isi000255348000007-
item.fulltextWith Fulltext-
item.fullcitationGEUSENS, Piet; Roux, CH; Reid, DM; Lems, WF; Adami, S.; Adachi, Jonathan D.; Sambrook, PN; Saag, KG; Lane, NE & Hochberg, MC (2008) Drug Insight: choosing a drug treatment strategy for women with osteoporosis - an evidence-based clinical perspective. In: NATURE CLINICAL PRACTICE RHEUMATOLOGY, 4(5). p. 240-248.-
item.contributorGEUSENS, Piet-
item.contributorRoux, CH-
item.contributorReid, DM-
item.contributorLems, WF-
item.contributorAdami, S.-
item.contributorAdachi, Jonathan D.-
item.contributorSambrook, PN-
item.contributorSaag, KG-
item.contributorLane, NE-
item.contributorHochberg, MC-
item.accessRightsOpen Access-
item.validationecoom 2009-
crisitem.journal.issn1745-8382-
Appears in Collections:Research publications
Files in This Item:
File Description SizeFormat 
drug insight.pdf136.94 kBAdobe PDFView/Open
Show simple item record

SCOPUSTM   
Citations

29
checked on Sep 3, 2020

WEB OF SCIENCETM
Citations

21
checked on May 7, 2024

Page view(s)

72
checked on Nov 7, 2023

Download(s)

134
checked on Nov 7, 2023

Google ScholarTM

Check

Altmetric


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