Effect of extended-duration thromboprophylaxis on venous thromboembolism and major bleeding among acutely ill hospitalized medical patients: a bivariate analysis

被引:23
作者
Chi, G. [1 ]
Goldhaber, S. Z. [2 ]
Kittelson, J. M. [3 ]
Turpie, A. G. G. [4 ]
Hernandez, A. F. [5 ,6 ]
Hull, R. D. [7 ]
Gold, A. [8 ]
Curnutte, J. T. [8 ]
Cohen, A. T. [9 ,10 ]
Harrington, R. A. [11 ]
Gibson, C. M. [1 ]
机构
[1] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Dept Med, Cardiovasc Div, Boston, MA 02215 USA
[2] Harvard Med Sch, Brigham & Womens Hosp, Cardiovasc Div, Boston, MA 02215 USA
[3] Univ Colorado, Colorado Sch Publ Hlth, Dept Biostat & Informat, Anschutz Med Campus, Aurora, CO USA
[4] Hamilton Hlth Sci, Gen Div, Dept Med, Hamilton, ON, Canada
[5] Duke Univ, Durham, NC USA
[6] Duke Clin Res Inst, Durham, NC USA
[7] Univ Calgary, RAH Fac Med, Div Cardiol, Calgary, AB, Canada
[8] Portola Pharmaceut Inc, San Francisco, CA USA
[9] Kings Coll London, Guys Hosp, Dept Haematol Med, London, England
[10] Kings Coll London, St Thomas Hosp, Dept Haematol Med, London, England
[11] Stanford Univ, Dept Med, Div Cardiovasc Med, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
adverse drug reaction; anticoagulant; clinical efficacy; hemorrhage; venous thromboembolism; DEEP-VEIN THROMBOSIS; PREVENTION; PROPHYLAXIS; BETRIXABAN; TRIAL; RIVAROXABAN; ENOXAPARIN; WARFARIN; THERAPY; BENEFIT;
D O I
10.1111/jth.13783
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Among acutely ill hospitalized medical patients, extended-duration thromboprophylaxis reduces the risk of venous thromboembolism (VTE), but some pharmacologic strategies have been associated with greater risks of major bleeding, thereby offsetting the net clinical benefit (NCB). Methods: To assess the risk-benefit profile of anticoagulation regimens, a previously described bivariate method that does not assume a linear risk-benefit tradeoff and can accommodate different margins for efficacy and safety was performed to simultaneously assess efficacy (symptomatic VTE) and safety (major bleeding) on the basis of data from four randomized controlled trials of extended-duration (30-46 days) versus standard-duration (6-14 days) thromboprophylaxis among 28 227 patients (EXCLAIM, ADOPT, MAGELLAN and APEX trials). Results: Extended thromboprophylaxis with full-dose betrixaban (80 mg once daily) was superior in efficacy and non-inferior in safety to standard-duration enoxaparin, and showed a significantly favorable NCB, with a risk difference of -0.51% (-0.89% to -0.10%) in the bivariate outcome. Extended enoxaparin was superior in efficacy and inferior in safety (bivariate outcome: 0.03% [-0.37% to 0.43%]), whereas apixaban and rivaroxaban were non-inferior in efficacy and inferior in safety (-0.20% [-0.49% to 0.17%] and 0.23% [-0.16% to 0.69%], respectively). Reduced-dose betrixaban did not show a significant difference in either efficacy or safety (0.41% [-0.85% to 1.94%]). Conclusions: In a bivariate analysis that assumes non-linear risk-benefit tradeoffs, extended prophylaxis with full-dose betrixaban was superior to standard-duration enoxaparin, whereas other regimens failed to simultaneously achieve both superiority and non-inferiority with respect to symptomatic VTE and major bleeding in the management of acutely ill hospitalized medical patients.
引用
收藏
页码:1913 / 1922
页数:10
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