首页> 外文学位 >Cost-Effectiveness of Current Anticoagulation Care versus Genetic Testing of CYP2C9 and VKORC1 Prior to Long-Term Warfarin Anticoagulation Care: The Implementation of Discrete Event Simulation Model on the Natural History of Venous Thromboembolism.
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Cost-Effectiveness of Current Anticoagulation Care versus Genetic Testing of CYP2C9 and VKORC1 Prior to Long-Term Warfarin Anticoagulation Care: The Implementation of Discrete Event Simulation Model on the Natural History of Venous Thromboembolism.

机译:当前抗凝治疗的成本效果与长期华法林抗凝治疗之前的CYP2C9和VKORC1遗传检测的关系:基于静脉血栓栓塞自然史的离散事件模拟模型的实现。

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摘要

Genetic test for CYP2C9 and VKORC1 genes to guide warfarin dosing for patients with VTE holds a promise of being able to reduce clinical complications. However, lack of evidence and uncertainties surrounding this new technology lead to the question of whether gene testing is cost-effective in the societal perspective.;A discrete event simulation model was conducted to evaluate the cost-effectiveness of CYP2C9 and VKORC1 genotype-guided warfarin on the natural history of VTE. The model depicted patients' health states as the disease evolve with time, and captured its associated costs (2007 U.S. dollars) and quality of life. Data was extrapolated with the criteria of including VTE patients of age >=18 years on warfarin with INR target of 2-3. Probabilities, costs and humanistic properties were obtained from the literature, HCUP (NIS & SEDD), and the Medicare Reimbursement Schedule databases. Sensitivity analysis was performed for uncertainty parameters in the model. All costs and benefits were discounted at 3%.;This study had a significant difference in the prevalence of bleeding complication between Standard anticoagulation (6.1%) and the genotype --guided groups (5.8%). No differences were found in the prevalence of recurrent VTE episode. Approximately, ;In conclusion, the data analysis in this study showed that both CYP2C9 and VKORC1 genotype-guided warfarin anticoagulation therapy is not cost --effective in all population and that patient with higher risk of complications are more likely to benefit from this new innovation. For the genotype-guided test to be cost-effective in the population with VTE, the cost of the test would have to be
机译:CYP2C9和VKORC1基因的基因检测可指导VTE患者的华法林剂量,有望减少临床并发症。然而,由于这项新技术缺乏证据和不确定性,因此提出了从社会角度来讲基因测试是否具有成本效益的问题。;建立了一个离散事件模拟模型来评估CYP2C9和VKORC1基因型指导的华法林的成本效益。关于VTE的自然历史。该模型描述了随着疾病的发展患者的健康状况,并记录了相关的费用(2007年美元)和生活质量。数据以包括≥18岁的华法林VTE患者(INR目标值为2-3)纳入标准。概率,成本和人文属性来自文献,HCUP(NIS&SEDD)和Medicare报销时间表数据库。对模型中的不确定性参数进行了敏感性分析。所有成本和收益均折现为3%。该研究在标准抗凝(6.1%)和基因型指导组(<5.8%)之间的出血并发症发生率上有显着差异。复发性VTE发作的发生率未发现差异。大约,总而言之,本研究中的数据分析表明,CYP2C9和VKORC1基因型指导的华法林抗凝治疗并非在所有人群中都具有成本效益,而且并发症风险较高的患者更可能受益于这项新创新。为了使基因型指导的测试在具有VTE的人群中具有成本效益,测试的成本必须<

著录项

  • 作者

    Teschemaker, Anna R.;

  • 作者单位

    Howard University.;

  • 授予单位 Howard University.;
  • 学科 Biology Genetics.;Health Sciences General.;Health Sciences Pharmacy.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 196 p.
  • 总页数 196
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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