Inherited thrombophilia |
Factor V Leiden mutation |
Prothrombin G20210A mutation |
Protein S deficiency |
Protein C deficiency |
Antithrombin deficiency |
Other disorders and risk factors |
Presence of a central venous catheter |
Malignancy |
Surgery, especially orthopedic |
Trauma |
Immobilization |
Pregnancy |
Oral contraceptives |
Hormone replacement therapy |
Certain cancer therapies (eg, tamoxifen, thalidomide, lenalidomide, asparaginase) |
Heart failure |
Congenital heart disease |
Antiphospholipid syndrome |
Older age (≥65 years) |
Obesity |
Severe liver disease |
Myeloproliferative neoplasms |
Polycythemia vera |
Essential thrombocythemia |
Paroxysmal nocturnal hemoglobinuria |
Inflammatory bowel disease |
Nephrotic syndrome |