Impact of Prolonged Anticoagulation with Rivaroxaban on Provoked Venous Thromboembolism Recurrence: IMPROVE-VTE

被引:3
作者
Coleman, Craig, I [1 ,6 ]
Turpie, Alexander G. G. [2 ,6 ]
Bunz, Thomas J. [3 ,6 ]
Beyer-Westendorf, Jan [4 ,6 ]
Baker, William L. [5 ,6 ]
机构
[1] Univ Connecticut, Sch Pharm, Dept Pharm Practice, Storrs, CT 06269 USA
[2] Hartford Hosp, Evidence Based Practice Ctr, Hartford, CT 06115 USA
[3] McMaster Univ, Dept Med, Hamilton, ON, Canada
[4] New England Hlth Analyt LLC, Dept Pharmacoepidemiol, Granby, CO USA
[5] Univ Hosp Carl Gustav Carus, Div Hematol, Dept Med 1, Thrombosis Res Unit, Dresden, Germany
[6] Kings Coll London, Dept Hematol, Kings Thrombosis Serv, London, England
关键词
Anticoagulants; Extended duration; Provoked; Rivaroxaban; Venous thromboembolism; GUIDELINE; RISK;
D O I
10.1016/j.amjmed.2018.11.040
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: We sought to evaluate the real-world effectiveness and safety of prolonged anticoagulation with rivaroxaban following a provoked venous thromboembolism. METHODS: Using US MarketScan claims from November 2012 to March 2017, we identified adults with >= 1 primary hospitalization or emergency department diagnosis code for venous thromboembolism, a provoking (major or minor, persistent or transient) risk factor, at least 3 months of continuous rivaroxaban treatment, and >= 12 months of continuous insurance benefits prior to their qualifying venous thromboembolism. Patients were categorized as either continuing rivaroxaban or discontinuing anticoagulation (no anticoagulation or nonaspirin antiplatelet agents but may have received aspirin) after the initial 3 months of rivaroxaban treatment (index date). Differences in baseline covariates between cohorts were adjusted for using inverse probability-of-treatment weights based on propensity scores (absolute standardized differences <0.1 achieved for all covariates after adjustment). Twelve month incidences of recurrent venous thromboembolism or major bleeding were compared between cohorts using Cox regression (according to an intention-to-treat methodology) and reported as hazard ratios (HRs) with 95% confidence intervals (CIs). RESULTS: Among patients experiencing a provoked venous thromboembolism and treated with rivaroxaban for the first 3 months (N=4,990), continued rivaroxaban use beyond 3 months (median [25%, 75% range duration of additional rivaroxaban use = 3 [2, 5] months) was associated with a 44% (95% CI of 9%-66%) lower hazard of recurrent venous thromboembolism without altering major bleeding risk [HR of 0.87, 95% CI of 0.51-1.49] versus anticoagulation discontinuation (with or without aspirin use). CONCLUSIONS: Our study suggests continuing rivaroxaban after the initial 3 month period was associated with a decreased risk of recurrent venous thromboembolism. The observed reduction in recurrent venous thromboembolism with prolonged rivaroxaban use was not associated with a significant change in major bleeding risk. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:498 / 504
页数:7
相关论文
共 20 条
  • [1] [Anonymous], 2021, XARELTO RIVAROXABAN
  • [2] A Tutorial and Case Study in Propensity Score Analysis: An Application to Estimating the Effect of In-Hospital Smoking Cessation Counseling on Mortality
    Austin, Peter C.
    [J]. MULTIVARIATE BEHAVIORAL RESEARCH, 2011, 46 (01) : 119 - 151
  • [3] Incidence of recurrent venous thromboembolism in relation to clinical and thrombophilic risk factors: prospective cohort study
    Baglin, T
    Luddington, R
    Brown, K
    Baglin, C
    [J]. LANCET, 2003, 362 (9383) : 523 - 526
  • [4] Oral Rivaroxaban for Symptomatic Venous Thromboembolism.
    Bauersachs, Rupert
    Berkowitz, Scott D.
    Brenner, Benjamin
    Buller, Harry R.
    Decousus, Herve
    Gallus, Alex S.
    Lensing, Anthonie W.
    Misselwitz, Frank
    Prins, Martin H.
    Raskob, Gary E.
    Segers, Annelise
    Verhamme, Peter
    Wells, Phil
    Agnelli, Giancarlo
    Bounameaux, Henri
    Cohen, Alexander
    Davidson, Bruce L.
    Piovella, Franco
    Schellong, Sebastian
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (26) : 2499 - 2510
  • [5] The REporting of studies Conducted using Observational Routinely-collected health Data (RECORD) Statement
    Benchimol, Eric I.
    Smeeth, Liam
    Guttmann, Astrid
    Harron, Katie
    Moher, David
    Petersen, Irene
    Sorensen, Henrik T.
    von Elm, Erik
    Langan, Sinead M.
    [J]. PLOS MEDICINE, 2015, 12 (10)
  • [6] Clinical outcomes of prolonged anticoagulation with rivaroxaban after unprovoked venous thromboembolism
    Berger, Jeffrey S.
    Seheult, Roger
    Laliberte, Francois
    Crivera, Concetta
    Lejeune, Dominique
    Xiao, Yongling
    Schein, Jeff
    Lefebvre, Patrick
    Kaatz, Scott
    [J]. RESEARCH AND PRACTICE IN THROMBOSIS AND HAEMOSTASIS, 2018, 2 (01) : 58 - 68
  • [7] Healthcare costs associated with rivaroxaban or warfarin use for the treatment of venous thromboembolism
    Coleman, Craig I.
    Baugh, Christopher
    Crivera, Concetta
    Milentijevic, Dejan
    Wang, Sheng-Wei
    Lu, Lang
    Nelson, Winnie W.
    [J]. JOURNAL OF MEDICAL ECONOMICS, 2017, 20 (02) : 200 - 203
  • [8] An automated database case definition for serious bleeding related to oral anticoagulant use
    Cunningham, Andrew
    Stein, C. Michael
    Chung, Cecilia P.
    Daugherty, James R.
    Smalley, Walter E.
    Ray, Wayne A.
    [J]. PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2011, 20 (06) : 560 - 566
  • [9] Gandhi S.K., 1999, J MANAGE CARE PHARM, V5, P215, DOI DOI 10.18553/JMCP.1999.5.3.215
  • [10] Hansen L., 2018, The Truven Health MarketScan databases for life sciences researchers