打字猴:1.700632861e+09
1700632861
1700632862 表5-5 ADFR治疗方案
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1700632867 四、总 结
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1700632869 OP的预防可通过筛查高危人群、改善饮食结构、适当运动等方式实现。在OP临床治疗中,补充钙和维生素D是基本措施,在用其他药物治疗同时更需要注意钙和维生素D的补充。二膦酸盐、SERMs、降钙素都被临床资料证明能够降低OP骨折发生率(各种防治OP药物的适应证、常规推荐剂量具体见表5-6)。二膦酸盐是防治OP的一线药物,每周1次、每月1次或静脉给药方法可以减少上消化道反应、增加了依从性和耐受性,用二膦酸盐治疗OP还需要注意下颌骨坏死问题;SERMs减少PMOP骨折的同时降低了乳腺癌风险,却提高了静脉栓塞的风险,所以近期有血栓栓塞病史者禁用。PTH是目前唯一能够增加骨合成代谢的药物,每天皮下注射一次PTH能够增加BMD, 减少骨折,所以有人想象是否可以用钙离子受体抑制剂促进内源性PTH合成以增加骨合成或者发现一种PTH的类似物可以增加骨合成却不增加骨吸收,而有关PTH与各种药物的联合治疗还有待进一步研究。
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1700632871 表3 各种防治OP药物的用法及常规推荐剂量
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1700632876 【思考题】
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1700632878 1.骨质疏松症有哪些防范措施?
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1700632880 2.试述骨质疏松症的药物治疗。
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1700632882 参考文献
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1700632884 [1] 徐永清,陆声.骨质疏松性骨折的预防和治疗.创伤外科杂志,2006,8(6).
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1700632886 [2] McLellan AR, Gallacher SJ. The fracture liaison service: success of a program for the evaluation and management of patients with osteoporotic fracture. Osteoporos Int, 2003, 14:1028-1034.
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1700632888 [3] 李洲,马宝通.骨质疏松性骨折的预防研究进展.中华临床医学杂志,2007,8(11):31-34.
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1700632890 [4] Trivedi DP, Doll R, Khaw KT. Effect of four monthly oral vitamin D3(cholecalciferol)supplementation on fractures and mortality in men and women living in the community: Randomised double blind controlled trial. BMJ, 2003, 326:469-472.
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1700632892 [5] Grant AM, Avenell A, Campbell MK, et al. Oral vitamin D3 and calcium for secondary prevention of low-trauma fractures in elderly people(Randomised Evaluation of Calcium Orvitamin D, RECORD): A randomised placebocontrolled trial. Lancet, 2005, 365:1621-1628.
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1700632894 [6] Porthouse J, Cockayne S, King C, et al. Randomised controlled trial of calcium and supplementation with cholecalciferol(vitamin D3)for prevention of fractures in primary care. BMJ, 2005, 330:1003-1006.
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1700632896 [7] Jackson RD, LaCroix AZ, Gass M, et al. Calcium plus vitamin D supplementation and the risk of fractures. N Engl J Med, 2006, 354:669-683.
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1700632898 [8] Boonen S, Rizzoli R, Meunier PJ, et al. The need for clinical guidance in the use of calcium and vitamin D in the mangement of osteoporosis: a consensus report. Osteoporos Int, 2004, 15:511-519.
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1700632900 [9] Greenblatt D. Treatment of postmenopausal osteoporosis. Pharmacotherapy, 2005, 25:574-584.
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1700632902 [10] Cranney A, Wells G, Willan A, et al. For the Osteoporosis Methodology Group and the Osteoporosis Research Advisory Group. Meta-analyses of therapies for postmenopausal osteoporosis. Ⅱ. Meta-analysis of alendronate for the treatment of postmenopausal women. Endocr Rev, 2002, 23:508-516.
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1700632904 [11] Schnitzer T, Bone HG, Crepaldi G, et al. For the Alendronate Once-Weekly Study Group. Therapeutic equivalence of alendronate 70mg once-weekly and alendronate 10mg daily in the treatment of osteoporosis. Aging,(MiIano), 2000, 12:1-12.
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1700632906 [12] Bone HG, Hosking D, Devogelaer JP, et al. For the Alendronate Phase Ⅲ Osteoporosis Treatment Study Group. Ten years’ experience with alendronate for osteoporosis in postmenopausal women. N Engl J Med, 2004, 350:1189-1199.
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1700632908 [13] Recker R, Ensrud K, Diem S, et al. Normal bone histomorphometry and 3D microarchitecture after 10 years alendronate treatment of postmenopausal women. J Bone Miner Res, 2004, 19:45.
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1700632910 [14] Harris ST, Watts NB, Genant HK, et al. For the Vertebral Efficacy with Risedronate Therapy(VERT)Study Group. Effects of risedronate treatment on vertebral and nonvertebral fractures in women with postmenopausal osteoporosis: A randomized controlled trial. JAMA, 1999, 282:1344-1352.
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