Cost-Effectiveness of Genotype-Guided and Dual Antiplatelet Therapies in Acute Coronary Syndrome

被引:75
|
作者
Kazi, Dhruv S.
Garber, Alan M.
Shah, Rashmee U.
Dudley, R. Adams
Mell, Matthew W.
Rhee, Ceron
Moshkevich, Solomon
Boothroyd, Derek B.
Owens, Douglas K.
Hlatky, Mark A.
机构
[1] Univ Calif San Francisco, San Francisco Gen Hosp, San Francisco, CA USA
[2] Univ Calif San Francisco, Philip R Lee Inst Hlth Policy Studies, San Francisco, CA 94143 USA
[3] Harvard Univ, Cambridge, MA 02138 USA
[4] Harvard Univ, Sch Med, Boston, MA USA
[5] Univ Pittsburgh, Med Ctr, Pittsburgh, PA USA
[6] Ctr Primary Care Outcomes Res, Grad Sch Business, Stanford, CA USA
[7] Ctr Hlth Policy, Stanford, CA USA
[8] Stanford Univ, Sch Med, Stanford, CA 94305 USA
[9] Vet Affairs Palo Alto Hlth Care Syst, Palo Alto, CA USA
关键词
SIROLIMUS-ELUTING STENTS; PLATO PLATELET INHIBITION; ARTERY-BYPASS SURGERY; TIMI; 38; TRIAL; CYP2C19; GENOTYPE; MYOCARDIAL-INFARCTION; CARDIOVASCULAR EVENTS; CLINICAL-OUTCOMES; FOCUSED UPDATE; CLOPIDOGREL;
D O I
10.7326/M13-1999
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The choice of antiplatelet therapy after acute coronary syndrome (ACS) is complicated: Ticagrelor and prasugrel are novel alternatives to clopidogrel, patients with some genotypes may not respond to clopidogrel, and low-cost generic formulations of clopidogrel are available. Objective: To determine the most cost-effective strategy for dual antiplatelet therapy after percutaneous coronary intervention for ACS. Design: Decision-analytic model. Data Sources: Published literature, Medicare claims, and life tables. Target Population: Patients having percutaneous coronary intervention for ACS. Time Horizon: Lifetime. Perspective: Societal. Intervention: Five strategies were examined: generic clopidogrel, prasugrel, ticagrelor, and genotyping for polymorphisms of CYP2C19 with carriers of loss-of-function alleles receiving either ticagrelor (genotyping with ticagrelor) or prasugrel (genotyping with prasugrel) and noncarriers receiving clopidogrel. Outcome Measures: Direct medical costs, quality-adjusted life-years (QALYs), and incremental cost-effectiveness ratios (ICERs). Results of Base-Case Analysis: The clopidogrel strategy produced $179301 in costs and 9.428 QALYs. Genotyping with prasugrel was superior to prasugrel alone, with an ICER of $35 800 per QALY relative to clopidogrel. Genotyping with ticagrelor was more effective than genotyping with prasugrel ($30 200 per QALY relative to clopidogrel). Ticagrelor was the most effective strategy ($52 600 per QALY relative to genotyping with ticagrelor).. Results of Sensitivity Analysis: Stronger associations between genotype and thrombotic outcomes rendered ticagrelor substantially less cost-effective ($104 800 per QALY). Genotyping with prasugrel was the preferred therapy among patients who could not tolerate ticagrelor. Limitation: No randomized trials have directly compared genotyping strategies or prasugrel with ticagrelor. Conclusion: Genotype-guided personalization may improve the cost-effectiveness of prasugrel and ticagrelor after percutaneous coronary intervention for ACS, but ticagrelor for all patients may be an economically reasonable alternative in some settings.
引用
收藏
页码:221 / 232
页数:12
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