C Mri User Manual Version 3.0
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We offer an MR Conditional/MRI Ready pacing system so you can better meet the needs of your patients.
Oct 15, 2015 The EADC-ADNI HarP for Manual Hippocampal Segmentation project provided manually segmented 100 ADNI MR images for analysis of this study. The scans were obtained on a variety of commercial 1.5 Tand 3.0 T MR imaging scanners on subjects across the continuum of cognitive health including healthy controls, MCI, and AD as described in recent work. Imaging Procedures Manual for CT/MRI and Angiography in SITS Open, version 1 – 2015-11-06 1.0 Introduction The purpose of this manual is to standardize DSA, MRI and CT image acquisition procedures among the centres participating in the SITS Open Protocol version 4.0 date 20151105 study. UCRL-MA-130653 Rev. 2 User’s Manual for the USNT Module of the NUFT Code, Version 3.0 (NP-phase, NC-Component, Thermal) John J. Nitao Earth and Environmental Sciences.
Assurity MRI™ Pacemaker
The Assurity MRI pacemaker is conditionally safe for use in the MRI environment when used with MRI Ready leads from Abbott and in accordance to the instructions in the user manual.
- Enables full-body, 1.5T MRI scans when used with Abbott MRI Ready leads; see MRI Scan Parameters—Lead Models.
- The SJM MRI Activator™ Device allows you to enable previously stored MRI settings before an MRI scan without the need for a traditional programmer.
For additional information, including additional MRI scanning information, contraindications and potential adverse events, please refer to the MRI Ready Systems Manual.
Assurity MRI In-Service
Programming MRI Mode
SJM MRI Activator
IMPLANTABLE CARDIAC MONITOR
SJM Confirm™ Implantable Cardiac Monitor
The SJM Confirm™ implantable cardiac monitor (ICM) DM2102 is conditionally safe for use in the MRI environment when used in accordance to the instructions in the user manual. Patients with newly implanted or previously implanted devices can undergo MR scanning when following specific scanning conditions.
These conditions include:
- Closed bore-cylindrical magnet.
- Static magnetic field strength of 1.5 Tesla (T) only.
- Maximum gradient slew rate 200 T/m/s per axis.
- Whole-body specific absorption rate (SAR) less than or equal to 2.0 W/kg.
- The uninterrupted duration of active scanning (when radio frequency and gradients are on) over the chest during MRI must not exceed 60 minutes.
- Confirmation of absence of other contraindicated implantable devices and/or leads, including abandoned leads, lead extenders and lead adaptors.
In non-clinical testing, the SJM Confirm ICM produced a temperature rise of less than 3°C at a maximum MR system-reported whole-body-averaged SAR of 3.9 W/kg as displayed on the MR scanner console for 60 minutes of MR scanning in a 1.5 T closed-bore MR scanner (manufacturer Philips, model Intera 1.5, software version: 9.5.2).
For additional information, including contraindications and potential adverse events please refer to the SJM Confirm ICM User’s Manual. It is important to read the information in the MRI Procedure section of the user manual before conducting an MRI scan on a patient with an implanted SJM Confirm implantable cardiac monitor.
IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (ICD)
Fortify Assura™ ICD
The Fortify Assura™ ICD allows full-body, 1.5T MRI scans that meet certain scan conditions, when combined with specific lead and lead lengths that are MR Conditional.*
- Meets industry-standard MRI testing requirements
- Capable of full body 1.5T MRI imaging scans
ELLIPSE™ ICD
The Ellipse™ ICD System allows full-body, 1.5T MRI scans* that meet certain scan conditions.
- Meets industry-standard MRI testing requirements
- Capable of full body 1.5T MRI imaging scans
C Mri User Manual Version 3.0 Download
HEART FAILURE MANAGEMENT RESOURCES
CardioMEMS™ HF System
Non-clinical testing demonstrated that the CardioMEMS™ PA sensor is MR Conditional. A patient with this device can be scanned safely, immediately after implantation under the following conditions:
- Static magnetic field of 1.5 Tesla (T) or 3.0 T.
- Maximum spatial gradient magnetic field of 720 Gauss/cm (7200 mT/m) or less.
In non-clinical testing, the CardioMEMS™ PA sensor produced the temperatures in the table below during MRI performed for 15 minutes of scanning (per pulse sequence) in the 1.5 T/64 MHz* and 3 T/128 MHz* MR systems. These temperature changes will not pose a hazard to the patient under the conditions indicated.
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Table 2. MRI Related Heating
1.5 Tesla | 3 Tesla | |
MR system reported whole body averaged SAR | 2.9 W/kg | 2.9 W/kg |
Calorimetry measured values, whole body averaged SAR | 2.1 W/kg | 2.7 W/kg |
Highest temperature change | 1.9°C | 2.3°C |
MR image quality may be compromised if the area of interest is in the same area or relatively close to the position of the sensor. Selecting optimal MR imaging parameters to compensate for the presence of the sensor may be necessary. The maximum artifact size (as seen on the gradient echo pulse sequence) extends approximately 5 mm relative to the size and shape of the sensor.
Table 3. Artifact Information
Pulse sequence | T1-SE | GRE | GRE | |
Signal void size | 305 mm2 | 34 mm2 | 645 mm2 | 101 mm2 |
Plane orientation | Parallel | Perpendicular | Parallel | Perpendicular |
MULTIPOINT™ PACING PRODUCTS
Quadra Assura MP™ CRT-D and Quartet™ Quadripolar LV Lead
The Quadra Assura MP™ CRT-D and the Quartet™ Quadripolar LV lead allow full-body, 1.5T MRI scans* that meet certain scan conditions.
- Meet industry-standard MRI testing requirements
- Capable of full body 1.5T MRI imaging scans