ALTO Case performed by Dr. Henao and team скачать в хорошем качестве

ALTO Case performed by Dr. Henao and team

Watch Dr. Steve Henao and the team perform the first commercial ALTO case in the western United States. The ALTO® Abdominal Stent Graft System is used for Endovascular Aneurysm Repair (EVAR) to treat Abdominal Aortic Aneurysm (AAA). INDICATIONS FOR USE: The ALTO® Abdominal Stent Graft System is indicated for treatment of patients with infrarenal abdominal aortic aneurysms having the vascular morphology suitable for endovascular repair with the device, which includes the following: ∙ Adequate iliac/femoral access compatible with vascular access techniques (femoral cutdown or percutaneous), devices, and/or accessories, ∙ A proximal aortic landing zone for the sealing ring 7 mm below the inferior renal artery. ∙ An aortic sealing zone comprised of healthy aorta defined as: – Lack of significant thrombus greater than 8 mm in thickness; at any point along the aortic circumference at the level of 7mm below the inferior renal artery, – Lack of significant calcification at the level of 7 mm below the inferior renal artery, – Conicity less than 10% as measured from the inferior renal artery to the aorta 7 mm below the inferior renal artery, – An inner wall diameter of no less than 16 mm and no greater than 30 mm at 7 mm below the inferior renal artery, and – An aortic angle of less than or equal to 60 degrees ∙ A distal iliac landing zone: – With a length of at least 10 mm, and – With an inner wall diameter of no less than 8 mm and no greater than 25 mm. CONTRAINDICATIONS: The system is contraindicated for use in patients who have a condition that threatens to infect the graft and in patients with known sensitivities or allergies to the device materials including polytetrafluoroethylene [PTFE], polyethylene glycol [PEG]-based polymers, contrast agents, fluorinated ethylene propylene [FEP], titanium, nickel, platinum, or iridium. Refer to Instructions for Use for more information concerning Indications, Contraindications, Specific Anatomic Considerations, Warnings, Precautions, and Adverse Events. CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician. NOTE: Not all product components are available in every country. Please consult with your Endologix representative to confirm product availability. ©2021 Endologix LLC. All rights reserved. MM2330 Rev 01