Journal
JOURNAL OF ORTHOPAEDIC RESEARCH
Volume 24, Issue 7, Pages 1336-1341Publisher
WILEY
DOI: 10.1002/jor.20162
Keywords
alendronate; bone loss; hip arthroplasty; DEXA; bone remodeling
Categories
Ask authors/readers for more resources
Following total hip arthroplasty (THA), femoral periprosthetic bone undergoes a remodeling process that results in bone loss in its proximal regions that may compromise the long-term outcome of THA. Periprosthetic bone loss mainly occurs during the first postoperative months. The question is whether a postoperative treatment with alendronate is effective in reducing periprosthetic bone loss and which doses and duration of treatment are required. In a 12-month prospective, randomized double-blind study, 51 patients undergoing cementless THA were treated postoperatively either with a daily dose of 20 mg alendronate for 2 months and 10 mg for 2 months thereafter (group 1), with 20 mg of alendronate for 2 months and 10 mg for 4 months thereafter (group 11), or treated with placebo (group III). Proximal femoral bone mineral density (BMD) was measured with dual-energy X-ray absorptiometry (DEXA) and serum biochemical markers of bone turnover bone specific alkaline phosphatase, osteocalcin, and C-terminal telopeptides (CTX-I) were assayed. Six months of alendronate treatment significantly reduced (p < 0.001) bone loss in proximal medial region (- 10%) compared with placebo (-26%). All biochemical markers of bone turnover were suppressed by alendronate. These data suggest that alendronate administered for the first 6 postoperative months following TRA was effective in preventing early periprosthetic bone loss. (c) 2006 Orthopaedic Research Society. Published by Wiley Periodicals, Inc.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available