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Amplia MRI Quad CRT-D

Cardiac Resynchronization Therapy Defibrillators (CRT-D)

MRI Access

CRT Patients are not Receiving MRIs

Amplia-41-CRT-Patients-2

Data from 2012 were used to project MRI utilization in the CRT patient cohort over 4 years: whereas the actual MRI utilization rate over 4 years was measured in the non-CRT cohort.


*

CRT patients likely to receive an MRI is between 1.45% and 2.40%.

CRT Patients are not Receiving MRIs and are Likely to Need them

Amplia-Patients-Scan

With Amplia MRI™, patients have access to 1.5T and 3T full-body MRI scanning

Amplia Product Shot

BUILT TO BE SCANNED

Our SureScan™ devices and leads work in any combination to provide simplified scanning conditions

We engineered our devices with enhancements to ensure patient safety against:

  • force, torque and heating
  • unintended cardiac stimulation
  • device interactions in the MRI

Amplia-MRI-Board


References

1

Medtronic data on file 2016: Data from MarketScan® 2012 Commercial and Medicare Database, Truven Health Analytics.

2

Gold MR, Kanal E, Schwitter J, et al. Preclinical evaluation of implantable cardioverter-defibrillator developed for magnetic resonance imaging use. Heart Rhythm. March 2015;12(3):631-638.

3

Wilkoff BL, Bello D, Taborsky M, et al. Magnetic resonance imaging in patients with a pacemaker system designed for the magnetic resonance environment. Heart Rhythm. January 2011;8(1):65-73.

4

Ramza B, et al. Are There Cumulative Effects of Multiple MRI on MR-conditional Pacemakers? Presented at HRS, May 2014.

5

Gimbel JR, Bello D, Schmitt M, et al. Randomized trial of pacemaker and lead system for safe scanning at 1.5 Tesla. Heart Rhythm. May 2013;10(5):685-691.

6

Evaluation of Approved Pacing Lead (Model 5076) for Use in MRI Environment, clinicaltrials.gov, NCT01755143.

7

Confirmatory Clinical Trial of the Evera MRI System for Conditionally-Safe MRI Access, clinicaltrials.gov, NCT02117414.

8

Poor, Corinne. MRI™ SureScan™ Units Sold from FY09 – FY15. June 2015. Medtronic Data on File.