151. Effects of short-term risedronate on bone resorption and patient satisfaction in postmenopausal osteoporosis patients.
- Author
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Fernandes CE, Zerbini C, Russo LA, Albernaz MA, Eis SR, Szejnfeld VL, and Pompei LM
- Subjects
- Aged, Biomarkers blood, Collagen Type I blood, Etidronic Acid administration & dosage, Humans, Middle Aged, Patient Satisfaction, Peptides blood, Prospective Studies, Risedronic Acid, Bone Density Conservation Agents administration & dosage, Bone Remodeling drug effects, Bone Resorption prevention & control, Etidronic Acid analogs & derivatives, Osteoporosis, Postmenopausal prevention & control
- Abstract
This multicenter, open-label study evaluated the effects of short-term risedronate on bone resorption and patient satisfaction in postmenopausal women with osteoporosis in Brazil. Entry requirements included: osteoporosis of the spine/femoral neck diagnosed by a bone mineral density (BMD) T-score
or=1 dose of study drug (intent-to-treat [ITT] population), and 390 completed treatment (81%). After 12 wk, CTX decreased in 94% of patients (from 0.419+/-0.234 to 0.158+/-0.171 microg/L, p<0.0001). Mean CTX reduction was 60.6%. Patient satisfaction was good/excellent in 91.7% of patients. A total of 156 adverse events (AEs) were reported by 113 (23.5%) patients in the ITT population. Digestive symptoms emerged or worsened in 7.1% and 3.5%, respectively. Five patients (1.0%) experienced serious AEs, not considered to be related to risedronate. In conclusion, risedronate significantly reduced serum CTX after 12-wk treatment. Almost all patients reported good/excellent satisfaction. - Published
- 2009
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