RETRACTED: Risedronate sodium therapy for prevention of hip fracture in men 65 years or older after stroke (Retracted Article. See vol. 176, pg. 1256, 2016)

被引:106
作者
Sato, Y
Iwamoto, J
Kanoko, T
Satoh, K
机构
[1] Mitate Hosp, Dept Neurol, Tagawa 8260041, Japan
[2] Keio Univ, Sch Med, Dept Sport Med, Tokyo, Japan
[3] Hirosaki Univ, Sch Med, Dept Rehabil Med, Hirosaki, Aomori 036, Japan
[4] Hirosaki Univ, Sch Med, Dept Vasc Biol, Hirosaki, Aomori 036, Japan
关键词
D O I
10.1001/archinte.165.15.1743
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background: There is a high incidence of hip fractures in patients after hemiplegic stroke. Bone mineral density is decreased on the hemiplegic side in patients after stroke, correlating with the immobilization-induced bone resorption, the degree of paralysis, and hypovitaminosis D. The purpose of this study is to evaluate the effectiveness of risedronate sodium, an inhibitor of bone resorption, on osteoporosis and the risk of hip fractures in men 65 years or older after stroke. Methods: We conducted an 18-month randomized double-blind trial. Of 280 male patients 65 years or older who were poststroke, 140 received a daily dose of 2.5 mg risedronate sodium and the other 140 received placebo. incidence of hip fractures in the 2 groups was compared. Results: Ten patients sustained hip fractures in the placebo group, and 2 hip fractures occurred in the risedronate group. The relative risk of a hip fracture was 0.19 (95% confidence interval, 0.04-0.89). The number of patients needing the treatment was 16 (95% confidence interval, 9-32). Bone mineral density increased by 2.5% in the risedronate group and decreased by 3.5% in the placebo group (P < .001). Urinary deoxypyridinoline, a bone resorption marker, decreased by 58.7% in the risedronate group and by 37.2% in the placebo group. Conclusion: Treatment with risedronate increases bone mineral density and reduces hip fractures in elderly men who are poststroke.
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收藏
页码:1743 / 1748
页数:6
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