期刊文献+

老年心房颤动患者应用华法林个体化剂量的研究 被引量:5

A warfarin-dosing algorithm on atrial fibrillation in elderly patients
原文传递
导出
摘要 目的探讨老年心房颤动(房颤)患者应用华法林的个体化剂量。方法41例老年房颤患者,给予华法林抗凝治疗,治疗初始阶段每日监测国际标准化比值(INR),目标抗凝强度INR1.6~2.5。观察患者年龄、性别、身高、体质量等人口统计学指标以及合并用药、并存疾病等临床指标,测定血清白蛋白水平、INR等实验室指标,记录华法林剂量。结果单因素分析显示,个体华发林剂量分别与以下指标相关:年龄(r=-0.535,P〈0.01)、性别(rs=-0.494,P〈0.01)、身高(r=-0.484,P〈0.01)、体质量(r=-0.453,P〈0.01)、体表面积(r=-0.388,P〈0.05)、磺脲类降糖药物(rs=-0.446,P〈0.01)、白蛋白(r=-0.520,P〈0.01);多元逐步回归分析中,年龄、白蛋白、性别、磺脲类依次进入回归方程,个体化剂量回归方程式可以解释65.4%的华法林个体剂量的变异(R=0.808,R^2=65.4%)。结论老年房颤患者应用华法林抗凝治疗的个体化剂量可在治疗的初始阶段,根据患者的年龄、性别、是否合用磺脲类降糖药物及血清白蛋白水平等因素预测得到。 Objective To study the individualized dose of warfarin in treating atrial fibrillation in elderly patients. Methods Forty-one elderly in-patients with atrial fibrillation were recruited. Warfarin was used to start anti-coagulation therapy with the target INR value 1.6-2.5. The data of demographic variables, concomitant diseases, medications and laboratory values were collected, then correlated these factors with the maintenance dose of warfarin. Results Warfarin dose requirements were significantly associated with age(r=-0. 535, P〈0.01), sex(r=-0. 494, P〈0.01), height (r=0. 484, P〈0.01), weight (r= 0. 453, P〈0.01), body surface area(r= 0. 388, P〈0.05), concomitant use of a sulfonylurea medication (r = - 0. 446, P〈 0.01 ) and serum albumin level (r= 0. 520, P〈0.01). The multivariate regression model included the variables of age, sex, serum albumin level and concomitant use of a sulfonylurea medication. This algorithm explained 65.4 %of the variance in the maintenance dose of warfarin (R = 0. 808,R^2 = 65.4%). Conclusions The warfarin dose in treating atrial fibrillation in elderly patients can be estimated from demographic, clinical and laboratory factors that can be obtained at the time of warfarin initiation.
出处 《中华老年医学杂志》 CAS CSCD 北大核心 2008年第4期262-265,共4页 Chinese Journal of Geriatrics
基金 湖南省科技厅资助(06FJ3201)
关键词 心房颤动 华法林 老年 个体化剂量 Atrial fibrillation, Warfarin
  • 相关文献

参考文献10

  • 1Higashi MK, Veenstra DL, Kondo LM, et al. Association between CYP2C9 genetic variants and anticoagulation-related outcomesduring warfarin therapy. JAMA, 2002,287:1690-1698.
  • 2Douketis JD, Foster GA, Crowther MA, et al. Clinical risk factors and timing of recurrent venous thromboembolism during the initial 3 months of anticoagulant therapy. Arch Intern Med, 2000, 160: 3431-3436.
  • 3Valentin F, Lars ER, David SC, et al. ACC/AHA/ ESC 2006 Guidelines for the management of patients with atrial fibrillation-executive summary. Circulation, 2006,15:701-751.
  • 4Elizabeth AS, Tayyaba IK, Hilary AW, et al. The impact of CYP2C9 and VKORC1 genetic polymorphism and patient characteristics upon warfarin dose requirements: proposal for a new dosing regimen. Blood 2005, 106:2329-2333.
  • 5Kamali F, Khan TI, King BP, et al. Contribution of age, bodysize and CYP2C9 genotype to anticoagulant response to warfarin. Clin Pharmacol Ther, 2004,75: 204-212.
  • 6Elaine MH, David G, Susan R, et al. Warfarin maintenance dosing patterns in clinical practice: implications for safer anticoagulation in the elderly population. Chest, 2005,127 : 2049-2056.
  • 7Tham LS, Goh BC, Nafziger A, et al. A warfarindosing model in Asians that uses single-nucleotide polymorohisms in vitamin K epoxide reductase complex and cytochrome P450 2C9. Clin Pharmacol Ther, 2006,80:346-355.
  • 8Russell AW, Richard LB, Humberto JV. Impact of age, CYP2C9 genotype and concomitant medication on the rate of rise for prothrombin time during the first 30 days of warfarin therapy. Clin Med Res, 2005, 3: 207-213.
  • 9Sanoski CA, Bauman JL. Clinical observations with the Amiodarone/Warfarin Interaction : dosing relationships with long-termtherapy. Chest, 2002, 121: 19-23.
  • 10Brian FG, Charles E, Paul EM. Use of pharmacogenetics and clinical factors to predict the maintenance dose of warfarin. Thromb Haemost, 2004, 91 : 87-94.

同被引文献28

引证文献5

二级引证文献16

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部