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心房颤动的遗传风险可能促使患者坚持华法林治疗:一项成本效益分析。

Genetic risk for atrial fibrillation could motivate patient adherence to warfarin therapy: a cost effectiveness analysis.

作者信息

Shiffman Dov, Perez Marco V, Bare Lance A, Louie Judy Z, Arellano Andre R, Devlin James J

机构信息

Quest Diagnostics, 1401 Harbor Bay Parkway, Alameda, CA, 94502, USA.

Stanford University School of Medicine, 291 Campus Drive, Stanford, CA, 94305, USA.

出版信息

BMC Cardiovasc Disord. 2015 Sep 29;15:104. doi: 10.1186/s12872-015-0100-7.

Abstract

BACKGROUND

Atrial fibrillation (AF) increases risk of stroke, and although this stroke risk can be ameliorated by warfarin therapy, some patients decline to adhere to warfarin therapy. A prospective clinical study could be conducted to determine whether knowledge of genetic risk for AF could increase adherence to warfarin therapy for patients who initially declined therapy. As a prelude to a potential prospective clinical study, we investigated whether the use of genetic information to increase adherence could be cost effective.

METHODS

Markov model assessed costs and utilities of two care strategies for AF patients who declined warfarin therapy. In the usual care strategy patients received aspirin. In the test strategy genetic risk for AF was assessed (genotype of the 4q25 locus) and some patients with a positive genetic test (≥1 risk allele) were assumed to adhere to warfarin therapy. The remaining patients received aspirin. The incremental cost-effectiveness ratio (ICER) was the ratio of the costs differential and the quality adjusted life-years (QALYs) differential for the two strategies.

RESULTS

We found that the 4q25 genetic testing strategy, compared with the usual care strategy (aspirin therapy), would be cost-effective (ICER $ 47,148) if 2.1 % or more of the test positive patients were to adhere to warfarin therapy. The test strategy would become a cost saving strategy if 5.3 % or more of the test positive patients were to adhere to warfarin therapy. If 20 % of test positive patients were to adhere to warfarin therapy in a hypothetical cohort of 1000 patients, 7 stroke events would be prevented and 3 extra-cranial major bleeding events would be caused over 5 years, resulting in a cost savings of ~ $250,000 and a net gain of 9 QALYs.

DISCUSSION

A clinical study to assess the impact of patient knowledge of genetic risk of AF on adherence to warfarin therapy would be merited because even a modest increase in patient adherence would make a genetic testing strategy cost-effective.

CONCLUSION

Providing patients who declined warfarin therapy with information about their genetic risk of AF would be cost effective if this genetic risk information resulted in modest increases in adherence.

摘要

背景

心房颤动(AF)会增加中风风险,尽管华法林治疗可降低这种中风风险,但一些患者拒绝接受华法林治疗。可以开展一项前瞻性临床研究,以确定房颤遗传风险信息是否能提高最初拒绝治疗的患者对华法林治疗的依从性。作为潜在前瞻性临床研究的前奏,我们调查了利用遗传信息提高依从性是否具有成本效益。

方法

马尔可夫模型评估了拒绝华法林治疗的房颤患者两种护理策略的成本和效用。在常规护理策略中,患者接受阿司匹林治疗。在测试策略中,评估房颤的遗传风险(4q25位点的基因型),一些基因检测呈阳性(≥1个风险等位基因)的患者被假定会坚持华法林治疗。其余患者接受阿司匹林治疗。增量成本效益比(ICER)是两种策略成本差异与质量调整生命年(QALY)差异的比值。

结果

我们发现,如果2.1%或更多检测呈阳性的患者坚持华法林治疗,与常规护理策略(阿司匹林治疗)相比,4q25基因检测策略将具有成本效益(ICER为47,148美元)。如果5.3%或更多检测呈阳性的患者坚持华法林治疗,测试策略将成为一种节省成本的策略。在一个假设的1000名患者队列中,如果20%检测呈阳性的患者坚持华法林治疗,5年内可预防7次中风事件,但会导致3次颅外大出血事件,节省成本约250,000美元,净增加9个QALY。

讨论

开展一项临床研究来评估患者对房颤遗传风险的了解对其华法林治疗依从性的影响是值得的,因为即使患者依从性有适度提高,也会使基因检测策略具有成本效益。

结论

如果房颤遗传风险信息能适度提高依从性,那么向拒绝华法林治疗的患者提供其房颤遗传风险信息将具有成本效益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a592/4587718/902d5d8f0a48/12872_2015_100_Fig1_HTML.jpg

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