Patient-Specific Decision-Making for Warfarin Therapy in Nonvalvular Atrial Fibrillation How Will Screening With Genetics and Imaging Help?

被引:35
作者
Eckman, Mark H. [1 ,2 ]
Wong, Lawrence K. S. [3 ]
Soo, Yannie O. Y. [3 ]
Lam, Wynnie [3 ]
Yang, Song Ran [4 ]
Greenberg, Steven M. [5 ]
Rosand, Jonathan [5 ,6 ]
机构
[1] Univ Cincinnati, Med Ctr, Div Gen Internal Med, Cincinnati, OH 45267 USA
[2] Univ Cincinnati, Med Ctr, Ctr Clin Effectiveness, Cincinnati, OH 45267 USA
[3] Chinese Univ Hong Kong, Dept Neurol, Hong Kong, Hong Kong, Peoples R China
[4] Sun Yat Sen Univ, Dept Neurol, Guangzhou 510275, Guangdong, Peoples R China
[5] Massachusetts Gen Hosp, Dept Neurol, Hemorrhag Stroke Res Grp, Boston, MA 02114 USA
[6] Massachusetts Gen Hosp, Ctr Human Genet Res, Boston, MA 02114 USA
关键词
atrial fibrillation; cerebral hemorrhage; decision support techniques; genetics; magnetic resonance imaging;
D O I
10.1161/STROKEAHA.108.523159
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-Intracerebral hemorrhage (ICH) accounts for a majority of long-term morbidity and mortality associated with bleeding while on warfarin. Both ICH and warfarin-related ICH appear to have a genetic component. Furthermore, advanced neuroimaging using MRI can now identify individuals at increased risk of ICH. We explore whether screening strategies that include genetic profiling and neuroimaging might improve the safety of chronic anticoagulation for atrial fibrillation by identifying individuals from whom warfarin should be withheld. Methods-We used a Markov state transition decision model. Effectiveness was measured in quality-adjusted life-years. Data sources included the English language literature using MEDLINE searches and bibliographies from selected articles along with empirical data from our institutions. The base case was a 69-year-old man with newly diagnosed nonvalvular atrial fibrillation. Results-For patients at average risk for thromboembolic events and known to possess a hypothetical genetic profile increasing risk for warfarin ICH, anticoagulation remains the preferred strategy until the relative hazard of ICH exceeds 23.8. Genetic profiling would be favored for patients at low risk of thromboembolism (1.5% per year) if the hypothetical gene variant(s) conferred a relative risk of ICH > 4.1. Screening strategies in which patients underwent genotyping and MRI before anticoagulation did not improve aggregate patient outcomes unless the predictive power of MRI exceeded current best guess estimates and patients were at low to moderate risk of thromboembolism. Conclusion-Currently identified genetic markers of bleeding risk do not confer a risk of ICH sufficiently high to warrant routine genetic testing for patients at average risk of thromboembolism. Even if patients undergo screening with MRI as well as genotyping, currently available data on the role of MRI on risk of ICH and warfarin ICH do not support use of these tests for withholding anticoagulation in patients with atrial fibrillation. (Stroke. 2008; 39: 3308-3315.)
引用
收藏
页码:3308 / 3315
页数:8
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