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Samples in periodicals archive:
This final volume in the series is designed to provide clinicians a better understanding of the acute deep vein thrombosis disease process and its etiology, and a current review of optimal patient care.
New pooled safety data from the RE-COVERTM and RE-COVERTM II phase III trials in acute deep vein thrombosis (DVT) and pulmonary embolism (PE) consistently favour treatment with PradaxaA 150mg bid over treatment with warfarin.
registry study of the company's OmniWave(TM) Endovascular System (OES) in patients undergoing percutaneous mechanical thrombectomy of acute deep vein thrombosis (DVT).
Boehringer Ingelheim today announced the submission of an application to the European Medicines Agency (EMA) for use of Pradaxa (dabigatran etexilate) for the treatment of acute deep vein thrombosis (DVT) and pulmonary embolism (PE) and the prevention of recurrent DVT and PE.
S and Europe for the prevention of venous thromboembolism in patients undergoing major orthopedic or abdominal surgery and for treatment of acute deep vein thrombosis and acute pulmonary embolism.
Inpatient treatment of acute deep vein thrombosis with or without pulmonary embolism, when administered in conjunction with warfarin sodium.
As the Company moves forward to explore the potential treatment of acute deep vein thrombosis (DVT) in fiscal 2006, it is likely that the DVX catheter would be the preferred investigational device for any clinical studies.
In the trial, 1,240 patients with acute deep vein thrombosis received ximelagatran (36 mg twice daily) and 1,249 patients received standard therapy with enoxaparin for 5 days followed by warfarin for 6 months.