Managing Osteoporosis in Patients on Long-Term Bisphosphonate Treatment: Report of a Task Force of the American Society for Bone and Mineral Research

dc.contributor.authorAdler, Robert A.
dc.contributor.authorEl-Hajj Fuleihan, Ghada A.
dc.contributor.authorBauer, Douglas C.
dc.contributor.authorCamacho, Pauline M.
dc.contributor.authorClarke, Bart Lyman
dc.contributor.authorClines, Gregory A.
dc.contributor.authorCompston, Juliette Elizabeth
dc.contributor.authorDrake, Matthew T.
dc.contributor.authorEdwards, Beatrice J.A.
dc.contributor.authorFavus, Murray J.
dc.contributor.authorGreenspan, Susan L.
dc.contributor.authorMcKinney, Ross E.
dc.contributor.authorPignolo, Robert J.
dc.contributor.authorSellmeyer, Deborah E.
dc.contributor.departmentInternal Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:47:38Z
dc.date.available2025-01-24T11:47:38Z
dc.date.issued2016
dc.description.abstractBisphosphonates (BPs) are the most commonly used medications for osteoporosis. This ASBMR report provides guidance on BP therapy duration with a risk-benefit perspective. Two trials provided evidence for long-term BP use. In the Fracture Intervention Trial Long-term Extension (FLEX), postmenopausal women receiving alendronate for 10 years had fewer clinical vertebral fractures than those switched to placebo after 5 years. In the HORIZON extension, women who received 6 annual infusions of zoledronic acid had fewer morphometric vertebral fractures compared with those switched to placebo after 3 years. Low hip T-score, between -2 and -2.5 in FLEX and below -2.5 in HORIZON extension, predicted a beneficial response to continued therapy. Hence, the Task Force suggests that after 5 years of oral BP or 3 years of intravenous BP, reassessment of risk should be considered. In women at high risk, for example, older women, those with a low hip T-score or high fracture risk score, those with previous major osteoporotic fracture, or who fracture on therapy, continuation of treatment for up to 10 years (oral) or 6 years (intravenous), with periodic evaluation, should be considered. The risk of atypical femoral fracture, but not osteonecrosis of the jaw, clearly increases with BP therapy duration, but such rare events are outweighed by vertebral fracture risk reduction in high-risk patients. For women not at high fracture risk after 3 to 5 years of BP treatment, a drug holiday of 2 to 3 years can be considered. The suggested approach for long-term BP use is based on limited evidence, only for vertebral fracture reduction, in mostly white postmenopausal women, and does not replace the need for clinical judgment. It may be applicable to men and patients with glucocorticoid-induced osteoporosis, with some adaptations. It is unlikely that future trials will provide data for formulating definitive recommendations. © 2015 American Society for Bone and Mineral Research.
dc.identifier.doihttps://doi.org/10.1002/jbmr.2708
dc.identifier.eid2-s2.0-84957609430
dc.identifier.pmid26350171
dc.identifier.urihttp://hdl.handle.net/10938/30755
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc.
dc.relation.ispartofJournal of Bone and Mineral Research
dc.sourceScopus
dc.subjectBisphosphonates
dc.subjectDrug holiday
dc.subjectLong term-bisphosphonate use
dc.subjectOther osteoporosis therapies
dc.subjectRisk benefit
dc.subjectAdvisory committees
dc.subjectAge factors
dc.subjectDiphosphonates
dc.subjectFemale
dc.subjectFemoral fractures
dc.subjectHumans
dc.subjectImidazoles
dc.subjectMale
dc.subjectOsteoporosis
dc.subjectRisk factors
dc.subjectSex factors
dc.subjectSpinal fractures
dc.subjectAlendronic acid
dc.subjectAngiogenesis inhibitor
dc.subjectBazedoxifene
dc.subjectBiological marker
dc.subjectBisphosphonic acid derivative
dc.subjectCalcitonin
dc.subjectCalcium
dc.subjectColecalciferol
dc.subjectConjugated estrogen
dc.subjectDenosumab
dc.subjectEstrogen
dc.subjectGlucocorticoid
dc.subjectIbandronic acid
dc.subjectLasofoxifene
dc.subjectParathyroid hormone[1-34]
dc.subjectPlacebo
dc.subjectRaloxifene
dc.subjectRisedronic acid
dc.subjectStrontium ranelate
dc.subjectTibolone
dc.subjectVitamin d
dc.subjectZoledronic acid
dc.subjectImidazole derivative
dc.subjectBody mass
dc.subjectBone density
dc.subjectBone turnover
dc.subjectClinical trial (topic)
dc.subjectCochrane library
dc.subjectDrug cost
dc.subjectDrug efficacy
dc.subjectDrug safety
dc.subjectDrug tolerability
dc.subjectDrug withdrawal
dc.subjectEmbase
dc.subjectFemur fracture
dc.subjectFragility fracture
dc.subjectHealth care cost
dc.subjectHigh risk patient
dc.subjectHip fracture
dc.subjectHuman
dc.subjectIncidence
dc.subjectJaw osteonecrosis
dc.subjectMedical society
dc.subjectMedication compliance
dc.subjectMedline
dc.subjectNursing home patient
dc.subjectPostmenopause
dc.subjectPostmenopause osteoporosis
dc.subjectPrevalence
dc.subjectRandomized controlled trial (topic)
dc.subjectReview
dc.subjectRisk assessment
dc.subjectRisk factor
dc.subjectRisk reduction
dc.subjectScoring system
dc.subjectSecondary osteoporosis
dc.subjectSpine fracture
dc.subjectSystematic review
dc.subjectTreatment duration
dc.subjectAdvisory committee
dc.subjectAge
dc.subjectChemically induced
dc.subjectMetabolism
dc.subjectSex difference
dc.titleManaging Osteoporosis in Patients on Long-Term Bisphosphonate Treatment: Report of a Task Force of the American Society for Bone and Mineral Research
dc.typeReview

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