STRUCTURAL INTERVENTIONS

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 Success95.7%
Immediate Procedure Success97.6%
24-hour closure rate96.7%
6-month closure rate97.2%
12-month closure rate98.5%
Major complications1.6%
Minor complications6.1%

AMPLATZER SEPTAL OCCLUDER POST-APPROVAL STUDY3

  • Read more

    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 rate97.9%
    One-month closure rate98.5%
    Two-year closure rate97.9%

MAGIC ATRIAL SEPTAL DEFECT STUDY4

  • Read more

    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 rate96%
    24-hour closure rate99%


GET THE AMPLATZER PORTFOLIO APP

The Amplatzer Portfolio App helps physicians determine which Amplatzer Structural Interventions device to use by suggesting applicable devices based on respective Instructions for Use.
 

MAT-2201795 v2.0 | Item approved for OUS use only.

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MAT-2000631 v18.0 | Item approved for OUS use only.

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