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Mortality Risk Associated With Outpatient Diagnosis Of Acute Lower Extremity Deep Vein Thrombosis
Jennifer Avise, Laura Peterson, MD, Justin Hurie, MD, Matthew Edwards, MD, Jeanette Stafford, Gabriela Velazquez, MD, Randolph Geary, MD, Nitin Garg, MD, Matthew A. Corriere, MD.
Wake Forest School of Medicine, Winston Salem, NC, USA.

OBJECTIVES: Risk of acute lower extremity deep vein thrombosis (LE-DVT) and associated morbidity and mortality during hospitalization is well-characterized. We evaluated mortality risk associated acute LE-DVT diagnosed in outpatients.
METHODS: Outpatients with unilateral duplex ultrasounds positive for acute LE-DVT over a 2 year period were identified from a clinical vascular laboratory. Electronic medical records were queried to determine DVT pharmacotherapy, medical history, DVT location, and mortality. Mortality risk was evaluated using logistic regression.
RESULTS: 111 acute LE-DVT were identified in outpatients over 2 years. Initial treatment consisted of enoxaparin ± warfarin in 71 patients (64%) and anticoagulation with oral Xa inhibitors in 19 (17%), while 21 patients (19%) were managed with alternative treatments (including unfractionated heparin, thrombolysis, and/or inferior vena cava filter insertion). Mortality over a median follow up of 8.9 months was 12.6%, including 8/75 patients (10.7%) with proximal and 6/36 patients (16.7%) with calf DVT. Treatment type (classified as Xa inhibitors, enoxaparin ± warfarin, or alternative treatments) was associated with mortality, with increased risk specifically associated with alternative treatments (OR 6.6, 95% CI [1.8-23.8], P=0.004 vs. enoxaparin ± warfarin). No association between DVT location and mortality was observed.
CONCLUSIONS: Short-term mortality associated with outpatient acute LE-DVT is significant and similar between patients with calf vein versus proximal thrombosis. Alternative treatments were associated with significant higher mortality risk; further investigation is required to determine whether this risk reflects more severe presentation, contraindications to standard pharmacotherapy, or other factors.


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