3.8 Review

Prevention of venous thromboembolism in obesity

Journal

EXPERT REVIEW OF CARDIOVASCULAR THERAPY
Volume 8, Issue 12, Pages 1711-1721

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1586/ERC.10.160

Keywords

deep vein thrombosis; fondaparinux; low-molecular-weight heparin; morbid obesity; pulmonary embolism; special populations; venous thromboembolism prophylaxis

Funding

  1. NIH [1K23HL092161, R43 HD066993]
  2. ARUP Laboratories
  3. Sanofi-Aventis
  4. Boehringer Ingelheim
  5. Pfizer
  6. Canyon's Pharmaceuticals
  7. Bristol-Meyers Squibb
  8. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH &HUMAN DEVELOPMENT [R43HD066993] Funding Source: NIH RePORTER
  9. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [K23HL092161] Funding Source: NIH RePORTER

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Venous thromboembolism (VTE) is a significant cause of morbidity and mortality in hospitalized patients. Where appropriate, evidence-based methods of prophylaxis are implemented and the burden of VTE can be reduced substantially. Obesity, including morbid obesity, is associated with a high risk of VTE and, unfortunately, fixed doses of US FDA-approved anticoagulant regimens, including unfractionated heparins, low-molecular-weight heparins and factor Xa inhibitors, may not provide optimal VTE prophylaxis in these patients. Although the data are still limited, a rapidly growing body of literature and cumulative evidence suggests that anticoagulant dose adjustments in morbidly obese patients may optimize pharmacodynamic activity and reduce VTE risk. With the prevalence of morbid obesity continuing to rise, more high-quality clinical data are needed to better understand the pathobiology of VTE in obesity and provide effective, yet safe, prevention strategies.

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