STRUCTURAL INTERVENTIONS

AMPLATZER™ SEPTAL OCCLUDER CLINICAL DATA

The primary treatment option for atrial septal defects (ASD) is percutaneous, transcatheter closure, and Abbott’s 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%

NEW VERSION AVAILABLE
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 v1.0 | Item approved for Global OUS use only.

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MAT-2000631 v8.0 | Item approved for Global OUS use only.

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