A Real-World Experience With the Supera Interwoven Nitinol Stent in Femoropopliteal Arteries
Autor: | Olaf Schouten, Victor C. Bourke, Shannon D. Thomas, Ramon L. Varcoe, Andrew F. Lennox, Michael Myint |
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Rok vydání: | 2016 |
Předmět: |
Male
Time Factors medicine.medical_treatment Constriction Pathologic Kaplan-Meier Estimate Femoral artery 030204 cardiovascular system & hematology 0302 clinical medicine Risk Factors Popliteal Artery Treatment Failure 030212 general & internal medicine Aged 80 and over education.field_of_study Endovascular Procedures Middle Aged Limb Salvage Femoral Artery Female Stents Radiology New South Wales medicine.symptom Cardiology and Cardiovascular Medicine Adult medicine.medical_specialty Population Prosthesis Design Amputation Surgical Disease-Free Survival Peripheral Arterial Disease 03 medical and health sciences medicine.artery Angioplasty Alloys medicine Humans Vascular Patency Radiology Nuclear Medicine and imaging education Aged Retrospective Studies business.industry Angiography Digital Subtraction Intermittent Claudication Intermittent claudication Popliteal artery Surgery Amputation business Claudication |
Zdroj: | Journal of Endovascular Therapy. 23:433-441 |
ISSN: | 1545-1550 1526-6028 |
DOI: | 10.1177/1526602816639543 |
Popis: | Purpose: To evaluate the safety and midterm patency of the Supera interwoven nitinol stent in a real-world population and determine deployment and patient-related factors that may predispose to loss of patency. Methods: A retrospective analysis was conducted of 111 consecutive limbs from 97 patients (mean age 75.3 years; 68 men) with severe atherosclerotic disease of the superficial femoral and popliteal arteries that were treated with Supera stents between June 2012 and October 2014. Half the patients had claudication (56%); the remainder had rest pain (19%) and tissue loss (26%). Forty-eight (43%) lesions were chronic total occlusions, and more than half were classified as TransAtlantic Inter-Society Consensus C (22%) or D (30%). Results: All 146 Supera stents (1.32 stents per limb) were deployed successfully, extending over a mean length of 175.5±130.5 mm to treat lesions averaging 151.5±127.1 mm long. At 30 days, Kaplan-Meier estimated freedom from death, target lesion revascularization, and amputation was 97.3%. Primary patency and freedom from clinically driven target lesion revascularization rates were 87.1% and 95.0% at 6 months, respectively, and 78.9% and 87.6% at 12 months, respectively. Four distinct mechanisms for failure were identified in the 13 limbs in which patency was lost; stent intussusception (n=4), compromised inflow or outflow (n=2), gross oversizing (n=1), and neoplastic thrombophilia (n=1); the cause of 5 occlusions could not be identified. Conclusion: In this heterogeneous group that included long and complex atheromatous femoropopliteal lesions, the Supera stent achieved excellent clinical and patency results at 1 year. Further improvement may be achieved through careful patient selection and the avoidance of deployment pitfalls. |
Databáze: | OpenAIRE |
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