Terms in this set (20)

Inherited thrombophilia

Factor V Leiden or prothrombin mutation

Protein S or C deficiency

Antithrombin (AT) deficiency
Factor V Leiden or prothrombin mutation
Protein S or C deficiency
Antithrombin (AT) deficiency
Acquired conditions

Malignancy

Presence of a central venous catheter

Surgery (especially orthopedic)

Trauma

Pregnancy

Oral contraceptive use

Hormone replacement therapy

History of Tamoxifen, Thalidomide, or Lenalidomide use

Immobilization

Heart failure

Antiphospholipid antibody syndrome

Myeloproliferative disorders (disorders that cause platelets, white blood cells, and red blood cells to grow abnormally in the bone marrow), such as polycythemia vera, essential thrombocytosis, primary or idiopathic myelofibrosis, or chronic myelogenous leukemia

Polycythemia vera

Essential thrombocythemia

Paroxysmal nocturnal hemoglobinuria

Inflammatory bowel disease

Nephrotic syndrome
Malignancy
Presence of a central venous catheter
Surgery (especially orthopedic)
Trauma
Pregnancy
Oral contraceptive use
Hormone replacement therapy
History of Tamoxifen, Thalidomide, or Lenalidomide use
Immobilization
Heart failure
Antiphospholipid antibody syndrome
Myeloproliferative disorders (disorders that cause platelets, white blood cells, and red blood cells to grow abnormally in the bone marrow), such as polycythemia vera, essential thrombocytosis, primary or idiopathic myelofibrosis, or chronic myelogenous leukemia
Polycythemia vera
Essential thrombocythemia
Paroxysmal nocturnal hemoglobinuria
Inflammatory bowel disease
Nephrotic syndrome
;