2007
DOI: 10.1185/030079908x253717
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Ibandronate and the risk of non-vertebral and clinical fractures in women with postmenopausal osteoporosis: results of a meta-analysis of phase III studies

Abstract: Ibandronate at dose levels of ACE > or = 10.8 mg, which includes the marketed 150 mg once-monthly oral and 3 mg quarterly IV injection regimens, may provide significant non-vertebral and clinical fracture efficacy.

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Cited by 127 publications
(74 citation statements)
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“…Age is the primary determinant in osteoporosis. A majority of the studies indicate that advancing age is associated with increased fracture risk and low BMD (Harris, Blumentals & Miller, 2007). Siris (2001) conducted a longitudinal observational study in USA.…”
Section: Discussionmentioning
confidence: 99%
“…Age is the primary determinant in osteoporosis. A majority of the studies indicate that advancing age is associated with increased fracture risk and low BMD (Harris, Blumentals & Miller, 2007). Siris (2001) conducted a longitudinal observational study in USA.…”
Section: Discussionmentioning
confidence: 99%
“…29 Tedavinin kemik yoğunluğuna ve kemik dönüşümüne etkisi yedi yıla kadar sürmektedir. 30 Erkeklerde kırık riskini azaltmaktadır. Glukokortikoide bağlı osteoporoz hastalarının tamanında 5-10 mg/gün tedavi dozu ile iki yıl sonunda yeni kırık oluşumu-nun engellenebildiği gösterilmiştir.…”
Section: Farmakoloji̇k Tedavi̇unclassified
“…34 Bazı meta-analizlerde her iki-üç ayda bir 2 mg ya da 3 mg kullanımın vertebral kı-rıkları azalttığı saptanmıştır. 30,35 Z Zo ol le ed dr ro on ni ik k a as si it t: : Zoledronik asit postmenopozal osteoporoz tedavisinde onay almıştır. Postmenopozal osteoporozlu kadınlarda vertebral, nonvertebral ve kalça kırıklarının engellenmesinde etkinliği gösterilmiştir.…”
Section: Farmakoloji̇k Tedavi̇unclassified
“…Тем не менее, два независимых мета-анализа показали эффективность ибандроната для предупреждения внепоз-воночных переломов, в том числе переломов бедра, при ус-ловии использования достаточной дозы препарата [32,33]. Определенные сложности были связаны с недостаточным количеством пациентов группы плацебо, так как подавляю-щее большинство исследований ибандроната, особенно те, в которые были включены пациенты с более высоким риском переломов, не были плацебо-контролируемыми.…”
Section: эффективность ибандроната для предупреждения низкотравматичнunclassified