Objective: To report a patient case identifying risk for recurrent venous thromboembolism (VTE) associated with heterozygous Factor V Leiden mutation. Case Summary: A 54-year-old Caucasian male was diagnosed with heterozygous Factor V Leiden mutation in 2008 after experiencing a deep vein thrombosis (DVT) and bilateral pulmonary embolism. The patient was treated appropriately and started on anticoagulation therapy with warfarin through an anticoagulation management clinic. After approximately 17 months of warfarin therapy without incident, warfarin was discontinued. Within 2 months after discontinuation of anticoagulation therapy, the patient experienced his second DVT and left pulmonary artery embolus. Discussion: The risk of recurrent venous thromboembolism (VTE) in patients with heterozygous Factor V Leiden mutation is documented as an approximate 1.4-fold increase compared to patients without thrombophilia. However, the risk increases dramatically when nonreversible (age) or reversible risk factors (obesity, smoking, and long air fl ights) are present in this population. Conclusion: Based on recent literature, heterozygous Factor V Leiden mutation exponentially increases the risk of recurrent VTE, especially in the presence of other risk factors. Health care providers should complete a comprehensive review of the patients' other risk factors when deciding on duration of anticoagulation therapy for patients with positive heterozygous Factor V Leiden mutation. Even though thrombophilias may increase the risk of VTE, current literature states that thrombophilia should not be considered a major factor in determining the duration of anticoagulation therapy after VTE. The guidelines state that standard therapy (3 to 12 months) of anticoagulation is acceptable in the prevention of recurrent VTE in patients with thrombophilias including Factor V Leiden mutation.
Key Words-heterozygous5 Our case report documents a patient with heterozygous V enous thromboembolism (VTE) is a major medical issue that results from a combination of genetic, acquired, and modifi able risk factors.1 Patients with VTE have a higher incidence of death compared to patients without VTE.2 Thrombophilias have been associated with an increased risk of fi rst and recurrent VTE, with Factor V Leiden mutation being the most common genetic risk factor.3 Factor V Leiden mutation occurs in 40% to 50% of cases of hereditary thrombophilia; only 3% to 8%