Relationship Between Time in Therapeutic Range and Comparative Treatment Effect of Rivaroxaban and Warfarin: Results From the ROCKET AF Trial

被引:82
作者
Piccini, Jonathan P. [1 ]
Hellkamp, Anne S. [1 ]
Lokhnygina, Yuliya [1 ]
Patel, Manesh R. [1 ]
Harrell, Frank E., Jr. [3 ]
Singer, Daniel E. [4 ,5 ]
Becker, Richard C. [1 ]
Breithardt, Guenter [6 ]
Halperin, Jonathan L. [7 ]
Hankey, Graeme J. [8 ,9 ]
Berkowitz, Scott D. [10 ]
Nessel, Christopher C. [11 ]
Mahaffey, Kenneth W. [1 ]
Fox, Keith A. A. [12 ,13 ]
Califf, Robert M. [2 ]
机构
[1] Duke Univ, Med Ctr, Duke Clin Res Inst, Durham, NC 27705 USA
[2] Duke Univ, Med Ctr, Duke Translat Med Inst, Durham, NC 27705 USA
[3] Vanderbilt Univ, Sch Med, Nashville, TN 37212 USA
[4] Massachusetts Gen Hosp, Dept Med, Boston, MA 02114 USA
[5] Harvard Univ, Sch Med, Boston, MA USA
[6] Hosp Univ Munster, Munster, Germany
[7] Mt Sinai Med Ctr, Icahn Sch Med Mt Sinai, Cardiovasc Inst, New York, NY 10029 USA
[8] Univ Western Australia, Sch Med & Pharmacol, Nedlands, WA 6009, Australia
[9] Royal Perth Hosp, Dept Neurol, Stroke Unit, Perth, WA 6001, Australia
[10] Bayer HealthCare Pharmaceut, Montville, NJ USA
[11] Janssen Res & Dev, Raritan, NJ USA
[12] Univ Edinburgh, Edinburgh, Midlothian, Scotland
[13] Royal Infirm Edinburgh NHS Trust, Edinburgh, Midlothian, Scotland
来源
JOURNAL OF THE AMERICAN HEART ASSOCIATION | 2014年 / 3卷 / 02期
关键词
rivaroxaban; time in therapeutic range; warfarin; NONVALVULAR ATRIAL-FIBRILLATION; NORMALIZED RATIO CONTROL; ANTICOAGULATION CONTROL; STROKE PREVENTION; ORAL ANTICOAGULATION; OPTIMAL INTENSITY; PHYSICIAN; EFFICACY; OUTCOMES; QUALITY;
D O I
10.1161/JAHA.113.000521
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Time in therapeutic range (TTR) is a standard quality measure of the use of warfarin. We assessed the relative effects of rivaroxaban versus warfarin at the level of trial center TTR (cTTR) since such analysis preserves randomized comparisons. Methods and Results-TTR was calculated using the Rosendaal method, without exclusion of international normalized ratio (INR) values performed during warfarin initiation. Measurements during warfarin interruptions >7 days were excluded. INRs were performed via standardized finger-stick point-of-care devices at least every 4 weeks. The primary efficacy endpoint (stroke or non-central nervous system embolism) was examined by quartiles of cTTR and by cTTR as a continuous function. Centers with the highest cTTRs by quartile had lower-risk patients as reflected by lower CHADS(2) scores (P<0.0001) and a lower prevalence of prior stroke or transient ischemic attack (P<0.0001). Sites with higher cTTR were predominantly from North America and Western Europe. The treatment effect of rivaroxaban versus warfarin on the primary endpoint was consistent across a wide range of cTTRs (P value for interaction=0.71). The hazard of major and non-major clinically relevant bleeding increased with cTTR (P for interaction=0.001), however, the estimated reduction by rivaroxaban compared with warfarin in the hazard of intracranial hemorrhage was preserved across a wide range of threshold cTTR values. Conclusions-The treatment effect of rivaroxaban compared with warfarin for the prevention of stroke and systemic embolism is consistent regardless of cTTR.
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页数:10
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