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Article

Update on the management of venous thromboembolism

John R. Bartholomew, MD
Cleveland Clinic Journal of Medicine December 2017, 84 (12 suppl 3) 39-46; DOI: https://doi.org/10.3949/ccjm.84.s3.04
John R. Bartholomew
Section Head, Department of Vascular Medicine, Heart and Vascular Institute, Cleveland Clinic
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Article Figures & Data

Tables

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    TABLE 1

    Risk factors for bleeding with anticoagulation therapy

    Age older than 65
    Anemia
    Antiplatelet therapy
    History of bleeding
    Poor anticoagulant control
    Alcohol abuse
    Cancer
    Diabetes
    Liver failure
    Frequent falls
    Nonsteroidal anti-inflammatory drug use
    Renal failure
    Recent surgery
    Previous stroke
    Thrombocytopenia
    • Data from reference 3.

    • View popup
    TABLE 2

    Anticoagulation agents for patients with venous thromboembolism by treatment phase

    PatientAcute
    (0 to ~7 days)
    Long-term
    (~7 days to ~3 months)
    Extended
    (~3 months to indefinite)
    Most patientsUFH, LMWH, fondaparinux or DOACs (rivaroxaban or apixaban)DOACs (rivaroxaban, apixaban, dabigatran, or edoxaban) or VKA (warfarin)
    • Use same anticoagulant used in long-term phase

    • If first or second VTE is unprovoked proximal DVT of the leg or PE with low or moderate bleeding risk

    Renal failure (CrCL < 30 mL/min) or liver failure with coagulopathyUFHVKA (warfarin)Warfarin
    Hemodynamically unstable PE patientUFH or LMWHN/AN/A
    Pregnancy or cancer patientUFH or LMWHLMWHLMWH
    Once-daily dosingFondaparinux or LMWH at 1.5 mg/kg/dayVKA (warfarin), rivaroxaban (after 21 days) or edoxabanVKA (warfarin), edoxaban, rivaroxaban
    Recurrent VTEN/AIf on a non-LMWH anticoagulant, convert to LMWH
    If on LMWH, increase the dose
    If on a non-LMWH anticoagulant, convert to LMWH
    If on LMWH, increase the dose
    Need for reversal agentUFH
    LMWH (partially reversible)
    VKA (warfarin)
    Dabigatran
    Warfarin
    Dabigatran
    • CrCL = creatinine clearance; DOAC = direct oral anticoagulant; DVT = deep vein thrombosis; LMWH = low-molecular-weight heparin; N/A = not applicable; PE = pulmonary embolism; UFH = unfractionated heparin; VKA = vitamin K antagonist; VTE = venous thromboembolism

    • Data from references 3 and 4.

    • View popup
    TABLE 3

    Clinical features associated with a high risk of recurrent venous thrombosis

    EvidenceClinical relevance
    Absence of a temporary risk conditionStrongHigh
    Pulmonary embolism or proximal deep vein thrombosisStrongHigh
    More than 2 thrombotic eventsStrongRestricted, consider bleeding risk during prolonged anticoagulation
    Male sexStrongHigh
    Residual vein thrombosisStrongLow
    Vena cava filterStrongHigh
    Continued estrogen useStrongHigh
    CancerStrongHigh
    Postthrombotic syndromeModerateModerate
    OverweightWeakLow
    • Reprinted from The Lancet (Kyrle PA, Rosendaal FR, Eichinger S. Risk assessment for recurrent venous thrombosis. Lancet 2010; 376:2032–2039). © 2010 with permission from Elsevier. https://www.sciencedirect.com/journal/the-lancet.

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Cleveland Clinic Journal of Medicine: 84 (12 suppl 3)
Cleveland Clinic Journal of Medicine
Vol. 84, Issue 12 suppl 3
1 Dec 2017
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Update on the management of venous thromboembolism
John R. Bartholomew
Cleveland Clinic Journal of Medicine Dec 2017, 84 (12 suppl 3) 39-46; DOI: 10.3949/ccjm.84.s3.04

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Update on the management of venous thromboembolism
John R. Bartholomew
Cleveland Clinic Journal of Medicine Dec 2017, 84 (12 suppl 3) 39-46; DOI: 10.3949/ccjm.84.s3.04
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