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预防性地塞米松使用对唑来膦酸治疗早期不良反应的影响 被引量:3

Effect of Prophylactic Use of Dexamethasone on Incidence of Early Adverse Reactions of Zoledronic Acid Treatment
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摘要 目的探讨预防性使用地塞米松对唑来膦酸治疗后不良反应发生率的影响。方法入组80例计划使用唑来膦酸治疗的原发性骨质疏松症患者,随机分为对照组(40例)和实验组(40例)。对照组静脉滴注生理盐水500 m L水化后再缓慢静脉滴注唑来膦酸5 mg,实验组则在水化的生理盐水中加入5 mg地塞米松,其余处理均与对照组相同,观察两组患者治疗后早期药物不良反应的发生情况。结果实验组治疗后出现发热、关节痛、头痛的发生率分别是10.0%、12.5%、17.5%,均明显低于对照组的47.5%、75.0%、50.0%(P<0.05)。两组间血压及血糖无统计学差异(P>0.05)。结论预防性使用地塞米松可明显降低唑来膦酸治疗后一过性药物不良反应的发生率,为骨质疏松症患者提供了一个更安全且更易于接受的治疗方案。 Objective To discuss the influence of prophylactic use of dexamethasone on the incidence of early adverse reactions of zoledronic acid treatment. Methods 80 patients with primary osteoporosis who were planned to treat with zoledronic acid were randomly divided into control group and experiment group equally. Both groups were treated with zoledronic acid by intravenous infusion; In the hydration process, the control group was given physiological saline, while the experiment group was given dexamethasone injection. The early adverse reactions were observed. Results After the treatment, the incidences of fever, arthralgia and headache in the experiment group were significantly lower than those in the control group (all P〈0.05). There was no obvious changes in blood pressure and blood glucose after the treatment in both groups (P〉0.05). Conclusions Prophylactic use ofdexamethasone significantly reduces the incidence of transient adverse reactions of zoledronic acid, which provides a safer and more acceptable therapy for patients with osteoporosis.
出处 《临床医学工程》 2015年第9期1183-1184,共2页 Clinical Medicine & Engineering
关键词 地塞米松 原发性骨质疏松症 唑来膦酸 不良反应 Dexamethasone Osteoporosis Zoledronic acid Adverse reaction
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参考文献10

  • 1吕靖,马彩玲.绝经后骨质疏松症的治疗新进展[J].医学综述,2007,13(1):62-63. 被引量:37
  • 2周丕琪,沈霖,杨艳萍,谢晶.密固达治疗骨质疏松症患者的临床观察[J].中国中医骨伤科杂志,2011,19(6):36-37. 被引量:39
  • 3Black DM, Delmas PD, Eastell R, et al. Once-yearly zoledronic acid for treatment of postmenopausal osteoporosis [ J] . N Engl J Med, 2007, 356 (18) : 1809-1822.
  • 4李晓冬,陈建庭,王建钧,王素伟,陈燕梅.珠海地区575名女性骨密度测定及骨质疏松症危险因素初析[J].现代医院,2012,12(4):8-11. 被引量:16
  • 5Kanis JA, Adams J, Borgstrom F, et al. The cost-effectiveness of alen- dronate in the management of osteoporosis [J] . Bone, 2008, 42 (1) : 4-15.
  • 6张啟维,王英民,薛庆云,张华俦.唑来膦酸治疗绝经后骨质疏松早期药物不良反应分析[J].中国新药杂志,2011,20(8):757-760. 被引量:19
  • 7McClung M, Recker R, Miller P, et al. Intravenous zoledronic acid 5 mg in the treatment of postmenopausal women with low bone density previ- ously treated with alendronate [J] . Bone, 2007, 41 (1) : 122-128.
  • 8Makras P, Anastasilakis AD, Polyzos SA, et al. No effect of rosuvas- tatin in the zoledronate-induced acute-phase response [J] . Calcif Tissue lnt, 2011, 88 (5) : 402-408.
  • 9Bertoldo F, Pancheri S, Zenari S, et al. Serum 25-hydroxyvitamin D levels modulate the acute-phase response associated with the first ni- trogen-containing bisphosphonate infusion [J] . J Bone Miner Res, 2010, 25 (3) : 447-454.
  • 10Thompson K, Rogers MJ. Statins prevent bisphosphonate-induced gam- ma, delta-T-cell proliferation and activation in vitro [ J] . J Bone Miner Res, 2004, 19 (2) : 278-288.

二级参考文献39

  • 1杨玲,殷晓进.锶与骨矿代谢[J].中国骨质疏松杂志,2004,10(3):384-387. 被引量:17
  • 2孙瑞台.骨质疏松症的运动疗法应用及研究进展[J].国外医学(物理医学与康复学分册),1994,14(4):149-151. 被引量:11
  • 3颜兴伟,杨玉金,王国平,王小梅,刘菁萍,许秀柏.骨质疏松症危险因素的病例-对照研究[J].中国慢性病预防与控制,2005,13(2):69-72. 被引量:34
  • 4彭幼玲,陈党生,郭洁珍.年龄、体质量及体质量指数对中老年女性骨密度的影响[J].南方医科大学学报,2006,26(6):878-879. 被引量:20
  • 5李保林,谭建伟,利云峰,庾伟中,杨冰.绝经后骨质疏松性腰椎骨折骨代谢指标的变化[J].实用骨科杂志,2007,13(7):402-404. 被引量:5
  • 6COMPSTON JE,SEEMAN E. Compliance with osteoporosis therapy is the weakest link[ J]. Lancet,2006,368(9540) :973 -974.
  • 7SIRIS ES, HARRIS ST, ROSEN CJ, et al. Adherence to bisphosphonate therapy and fracture rates in osteoporotic women : relationship to vertebral and nonvertebral fractures from 2 US claims databases[J]. Mayo Clin Proc,2006, 81 (8) :1013 - 1022.
  • 8BLACK DM,DELMAS PD,EASTELL R, et al. Once-yearly zoledronic acid for treatment of postmenopausal osteoporosis[ J]. N Engl Med,2007,356(18) :1809 - 1822.
  • 9LYLES KW, COLON-EMERIC CS, MAGAZINER JS,et al. Zoledronic acid and clinical fractures and mortality after hip fracture [J].N Engl J Med, 2007,357(18) :1799 - 1809.
  • 10DUNFORD JE, THOMPSON K, COXON FP,et al. Structure-activity relationships for inhibition of farnesyl diphosphate synthase in vitro and inhibition of bone resorption in vivo by nitrogen-containing bisphosphonates [ J ]. J Pharmacol Exp Ther, 2001,296 ( 2 ) : 235 - 242.

共引文献103

同被引文献39

  • 1Russell RGG. Bisphosphonates: The first 40 years[J]. Bone, 2011, 49(1) :2-19.
  • 2Schilcher J, Koeppen V, Aspenberg P, et al. Risk of atypical femoral fracture during and after bisphosphonate use [ J ]. New England Journal of Medicine, 2014, 371 (10) : 974-976.
  • 3Roelofs A J, Coxon F P, Ebetino F H, et al. Fluorescent risedronate analogues reveal bisphosphonate uptake by bone marrow monoeytes and localization around osteocytes in vivo. [ J]. Journal of Bone & Mineral Research the Official Journal of the American Society for Bone & Mineral Research, 2010, 25 (3) :606-16.
  • 4Hughes D E, Wright K R, Uy H L, et al. Bisphosphonates promote apoptosls in murine osteoclasts in vitro and in vivo. J Bone Miner Res 10 : 1478 - 1487 [ J]. Journal of Bone & Mineral Research, 2009, 10(10) :1478-87.
  • 5Plotkin L I, Aguirre J I, Kousteni S, et al. Bisphosphonates and estrogens inhibit osteocyte apoptosis via distinct molecular mechanisms downstream of extraeellular signal-regulated kinase activation. [ J]. Journal of Biological Chemistry, 2005,280(8) : 7317-25.
  • 6Rondeau J, Bitsch F, Bourgier E, et al. Structural Basis for the Exceptional in vivo Efficacy of Bisphosphonate Drugs [ J ]. Chemmedehem, 2006, 1 (2) :267-273.
  • 7Ebetino F H, Hogan A M L, Shuting S, et al. The relationship between the chemistry and biological activity of the bisphosphonates. [ J ]. Bone, 2011, 49 ( 1 ) :20-33.
  • 8Ory S, Brazier H, Pawlak G, et al. Rho GTPases in osteoelasts: Orchestrators of podosome arrangement[J]. European Journal of Cell Biology, 2008, 87(8-9) :469-77.
  • 9M 8nkknen H, Auriola S, Lehenkari P, et at. A new endogenous ATP analog (ApppI) inhibits the mitochondrial adenine nucleotide translocase (ANT) and is responsible for the apoptosis induced by nitrogen-containing bisphosphonates [ J ]. British Journal of Pharmacology, 2006, 147 (4) :437-45.
  • 10Karin O, Catherine V P. Significance and impact of- bisphosphonate-induced acute phase responses. [ J ]. International Journal of Radiation Oncology Biology Physics, 2012, 82(3) :1098-1107.

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