Abstract

BackgroundAtrial 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.MethodsMarkov 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.ResultsWe 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.DiscussionA 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.ConclusionProviding 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.

Highlights

  • Atrial fibrillation (AF) increases risk of stroke, and this stroke risk can be ameliorated by warfarin therapy, some patients decline to adhere to warfarin therapy

  • We first investigated the fraction of the test positive patients that would need to adhere to warfarin therapy in order to make the test strategy cost effective

  • We found that under the base-case assumptions (Table 1), the test strategy would be cost-effective compared with the usual care if 2.1 % or more of the test positive patients choose to adhere to warfarin therapy

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Summary

Introduction

Atrial fibrillation (AF) increases risk of stroke, and 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. Any strategy that would increase adherence to warfarin therapy among eligible AF patients has the potential to prevent fatal and non-fatal stroke events. Providing patients with information about their genetic-based risks has the potential to improve adherence and clinical outcomes. Patients’ knowledge of genetic test results increased adherence (63 vs 45 %) to statin therapy in the AKROBATS study [19]

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