AMPLATZER™ SEPTAL OCCLUDER CLINICAL DATA
The primary treatment option for atrial septal defects (ASD) is percutaneous, transcatheter closure, and the Amplatzer™ Septal Occluder is the proven standard of care1,2—with more than 20 years of global clinical experience in ASD closure.3
GREATER SAFETY COMPARED WITH SURGICAL CLOSURE
The Amplatzer™ Septal Occluder is the most studied transcatheter atrial septal defect (ASD) closure device available today, with over 20 years of demonstrated clinical experience.1,2
The following 3 studies, together, cover over 1,500 patient-years of device experience.2-4
U.S. PIVOTAL TRIAL: LOWER RATES OF ADVERSE EVENTS VS SURGERY2
This study was conducted to determine the safety and efficacy of transcatheter ASD closure involving 442 device-closure patients and 911.5 total patient-years of device experience.2 The U.S. Pivotal Trial revealed:
- An adverse event rate 3 times lower for Amplatzer Septal Occluder as compared to surgical closure
- No erosion events
AMPLATZERTM SEPTAL OCCLUDER PATIENTS | |
---|---|
Procedure Attempt Success | 95.7% |
Immediate Procedure Success | 97.6% |
24-hour closure rate | 96.7% |
6-month closure rate | 97.2% |
12-month closure rate | 98.5% |
Major complications | 1.6% |
Minor complications | 6.1% |
AMPLATZER SEPTAL OCCLUDER POST-APPROVAL STUDY3
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This study is evaluating the long-term safety and efficacy of the Amplatzer Septal Occluder. The results below are from 1,000 patients reported in July 2011.3
Procedural success rate 97.9% One-month closure rate 98.5% Two-year closure rate 97.9%
MAGIC ATRIAL SEPTAL DEFECT STUDY4
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This study evaluated the initial safety and results of unrestricted multi-institution routine use of the Amplatzer Septal Occluder in 478 patients.4
Procedural success rate 96% 24-hour closure rate 99%
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MAT-2201795 v2.0 | Item approved for OUS use only.