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dc.contributor.authorGreenspan, Susan L.
dc.contributor.authorWyman, Allison
dc.contributor.authorHooven, Frederick H.
dc.contributor.authorAdami, Silvano
dc.contributor.authorGehlbach, Stephen H.
dc.contributor.authorBoonen, Steven
dc.contributor.authorLaCroix, Andrea Z.
dc.contributor.authorLindsay, Robert
dc.contributor.authorNetelenbos, J. Coen
dc.contributor.authorPfeilschifter, Johannes
dc.contributor.authorSilverman, Stuart
dc.contributor.authorSiris, Ethel S.
dc.contributor.authorWatts, Nelson B.
dc.date2022-08-11T08:08:08.000
dc.date.accessioned2022-08-23T15:43:39Z
dc.date.available2022-08-23T15:43:39Z
dc.date.issued2012-03-01
dc.date.submitted2012-08-24
dc.identifier.citationJ Am Geriatr Soc. 2012 Mar;60(3):455-61. doi: 10.1111/j.1532-5415.2011.03854.x. Epub 2012 Feb 8. <a href="http://dx.doi.org/10.1111/j.1532-5415.2011.03854.x">Link to article on publisher's site</a>
dc.identifier.issn0002-8614 (Linking)
dc.identifier.doi10.1111/j.1532-5415.2011.03854.x
dc.identifier.pmid22316070
dc.identifier.urihttp://hdl.handle.net/20.500.14038/27143
dc.description.abstractOBJECTIVES: To determine the proportion of untreated women who reported receiving treatment after incident fracture and to identify factors that predict treatment across an international spectrum of individuals. DESIGN: Prospective observational study. Self-administered questionnaires were mailed at baseline and 1 year. SETTING: Multinational cohort of noninstitutionalized women recruited from 723 primary physician practices in 10 countries. PARTICIPANTS: Sixty thousand three hundred ninety-three postmenopausal women aged 55 and older were recruited with a 2:1 oversampling of women aged 65 and older. MEASUREMENTS: Data collected included participant demographics, medical history, fracture occurrence, medications, and risk factors for fracture. Anti-osteoporosis medications (AOMs) included estrogen, selective estrogen receptor modulators, bisphosphonates, calcitonin, parathyroid hormone, and strontium. RESULTS: After the first year of follow-up, 1,075 women reported an incident fracture. Of these, 17% had started AOM, including 15% of those with a single fracture and 35% with multiple fractures. Predictors of treatment included baseline calcium use (P = .01), baseline diagnosis of osteoporosis (P < .001), and fracture type (P < .001). In multivariable analysis, women taking calcium supplements at baseline (odds ratio (OR) = 1.67) and with a baseline diagnosis of osteoporosis (OR = 2.55) were more likely to be taking AOM. Hip fracture (OR = 2.61), spine fracture (OR = 6.61), and multiple fractures (OR = 3.79) were associated with AOM treatment. Age, global region, and use of high-risk medications were not associated with treatment. CONCLUSION: More than 80% of older women with new fractures were not treated, despite the availability of AOM. Important factors associated with treatment in this international cohort included diagnosis of osteoporosis before the incident fracture, spine fracture, and to a lesser degree, hip fracture. Geriatrics Society.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=22316070&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1111/j.1532-5415.2011.03854.x
dc.subjectAged
dc.subjectChi-Square Distribution
dc.subjectFemale
dc.subjectFollow-Up Studies
dc.subjectFractures, Bone
dc.subjectHumans
dc.subjectMiddle Aged
dc.subjectOsteoporosis, Postmenopausal
dc.subjectProspective Studies
dc.subjectQuestionnaires
dc.subjectRegression Analysis
dc.subjectRisk Factors
dc.subjectHealth Services Research
dc.subjectMusculoskeletal Diseases
dc.titlePredictors of treatment with osteoporosis medications after recent fragility fractures in a multinational cohort of postmenopausal women
dc.typeJournal Article
dc.source.journaltitleJournal of the American Geriatrics Society
dc.source.volume60
dc.source.issue3
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/cor_glow/10
dc.identifier.contextkey3257194
html.description.abstract<p>OBJECTIVES: To determine the proportion of untreated women who reported receiving treatment after incident fracture and to identify factors that predict treatment across an international spectrum of individuals.</p> <p>DESIGN: Prospective observational study. Self-administered questionnaires were mailed at baseline and 1 year.</p> <p>SETTING: Multinational cohort of noninstitutionalized women recruited from 723 primary physician practices in 10 countries.</p> <p>PARTICIPANTS: Sixty thousand three hundred ninety-three postmenopausal women aged 55 and older were recruited with a 2:1 oversampling of women aged 65 and older.</p> <p>MEASUREMENTS: Data collected included participant demographics, medical history, fracture occurrence, medications, and risk factors for fracture. Anti-osteoporosis medications (AOMs) included estrogen, selective estrogen receptor modulators, bisphosphonates, calcitonin, parathyroid hormone, and strontium.</p> <p>RESULTS: After the first year of follow-up, 1,075 women reported an incident fracture. Of these, 17% had started AOM, including 15% of those with a single fracture and 35% with multiple fractures. Predictors of treatment included baseline calcium use (P = .01), baseline diagnosis of osteoporosis (P < .001), and fracture type (P < .001). In multivariable analysis, women taking calcium supplements at baseline (odds ratio (OR) = 1.67) and with a baseline diagnosis of osteoporosis (OR = 2.55) were more likely to be taking AOM. Hip fracture (OR = 2.61), spine fracture (OR = 6.61), and multiple fractures (OR = 3.79) were associated with AOM treatment. Age, global region, and use of high-risk medications were not associated with treatment.</p> <p>CONCLUSION: More than 80% of older women with new fractures were not treated, despite the availability of AOM. Important factors associated with treatment in this international cohort included diagnosis of osteoporosis before the incident fracture, spine fracture, and to a lesser degree, hip fracture. Geriatrics Society.</p>
dc.identifier.submissionpathcor_glow/10
dc.contributor.departmentCenter for Outcomes Research
dc.source.pages455-61


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