LIVE WEBINAR BROADCAST | WEDNESDAY, MARCH 7 @ 8:30PM EST
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• Identify which patients will benefit the most from this lower dose, shorter duration EKOS™ therapy
• Learn how PE patients’ Right Ventricular Dysfunction can be effectively treated in as little as 2 hours
• Hear about the remarkable 1-year post-treatment results in efficacy, safety, and quality of life measures
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Victor F. Tapson,
MD, FCCP, FRCP
Professor of Medicine
Division of Pulmonary and
Critical Care Medicine
Cedars-Sinai
Medical Center
Los Angeles, CA
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FDA CLEARED INDICATIONS:
The EkoSonic® Endovascular System is indicated for the ultrasound-facilitated, controlled, and selective infusion of physician-specified fluids, including thrombolytics, into the vasculature for the treatment of pulmonary embolism; the controlled and selective infusion of physician-specified fluids, including thrombolytics, into the peripheral vasculature; and the infusion of solutions into the pulmonary arteries. Instructions for use, including warnings, precautions, potential complications, and contraindications can be found at www.ekoscorp.com. Caution: Federal (USA) law restricts these devices to sale by or on the order of a physician. CE Mark: The Ekosonic™ Endovascular System is intended for the controlled and selective infusion of physician-specified fluids, including thrombolytics, into the peripheral vasculature. Intended for the treatment of pulmonary embolism patients with ≥ 50% clot burden in one or both main pulmonary arteries or lobar pulmonary arteries, and evidence of right heart dysfunction based on right heart pressures (mean pulmonary artery pressure ≥ 25 mmHg) or echocardiographic evaluation.
EKOS and EkoSonic are registered trademarks of EKOS Corporation, a BTG International group company. "Acoustic pulse thrombolysis" is a trademark of EKOS Corporation. BTG and the BTG roundel logo are registered trademarks of BTG International Ltd in US, EU, and certain other territories and trademarks of BTG International Ltd elsewhere. © 2017 EKOS Corporation.
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