Synopsis
For
interventional procedures, MRI-guidance has the advantage of soft-tissue
visualization and no ionizing radiation exposure, compared with X-ray guidance.
The features of an interventional MRI suite include specialized systems for
image acquisition and display, communication, anesthesia, and hemodynamic
recording. For each type of interventional procedure, MR compatible devices (e.g.
needles, catheters, guidewires) need to be carefully chosen. With careful planning and diligent staff
training, a standard MRI suite may be adequately equipped to safely perform
clinical interventional procedures.Highlights
·
Essential
features of an interventional suite include interactive, real-time imaging,
in-room displays, and a communication system.
·
Most
components of an interventional suite are commercially available.
·
The
availability of MR-safe interventional devices is limited, but it is an active
area of development.
Target
Audience
Clinicians
and scientists who are planning to begin an interventional MRI program. Information will be presented on how to plan
for a new facility or retrofit an existing one to enable MRI-guided procedures.
Introduction
Interventional
MRI provides excellent soft tissue visualization without ionizing radiation (1),
and is being used to guide a wide array of clinical procedures in areas
including neurosurgery, oncology and cardiology (see ref. (2) for a recent review). An interventional MRI suite requires
incremental hardware modifications plus real-time, interactive imaging sequences
(3). The
major scanner vendors all offer suitable real-time sequences, and some offer
additional features such as thermometry or active device tracking. The
purpose of this presentation is to describe the additional systems needed in an
interventional MRI suite and discuss developing technologies in the field.
Equipment
Display: In an interventional MRI procedure the real-time
images need to be displayed to the operators inside the MRI suite using MR-safe
LCD monitors or shielded projectors (Figure 1). Where operators
and staff will be during procedures should be considered to determine the
optimal placement of the displays. Displays
may need to be mirrored to either side of the magnet bore. Multiple displays are often required in order
to display additional information, such as previously acquired images and
hemodynamics. In the control room, a
video matrix switch may be used to dynamically change the display configuration
for different procedures. Video signals
in the control room should be converted to optical signals and passed into the
MRI suite via fiber through a waveguide.
Communication: It is critical that staff in the MR suite
and control room can communicate during a procedure. Additionally, staff in the room may need to
communicate directly with the patient.
Commercial systems are available which consist of multiple headsets and
provide adequate sound suppression to enable communication during
scanning. These systems are wireless,
but may require fiber connections through a waveguide to processing units
outside the MR suite.
Hemodynamics:
Hemodynamic
monitoring and recording requirements vary by procedure. MR-safe monitoring systems that measure ECG,
non-invasive and invasive blood pressure, and SpO2 are commercially
available. Cardiovascular procedures
usually require high-fidelity hemodynamic recording
capabilities, typically available in cardiac angiography suites. These systems have more ECG and invasive
blood pressure channels, higher data sampling rates, and are usually connected
to patient database systems. Systems for
electrophysiology procedures may also require measurement of intracardiac electrograms. Measurement of high-fidelity ECG in MRI is
challenging because of RF and gradient interference, but several groups have
developed solutions (4,5). While an MR compatible hemodynamic recording
system is not yet commercially available, efforts are ongoing.
Devices
Most
interventional devices are made from metal and pose a heating risk and/or
produce large artifacts in MRI. Some
devices have been specifically designed for use in MRI, including needles made
from non-ferrous materials and non-metallic guidewires. Commercial MRI compatible electrophysiology
systems are also under development (6,7). Certain catheters contain no metallic
braiding and have been shown to be safe in MRI.
When using a device specifically designed for MRI, the instructions for
use should be carefully reviewed for restrictions on magnetic field strength
and other use conditions. Other off the
shelf devices may be screened for metal with fluoroscopy.
Workflow & Safety
Special
consideration should be given to workflow and safety in an interventional MR
suite. Some suites may have adjoining
X-ray angiography suites and specialized transfer systems to move patients
between the two modalities (Figure
2). Staff
which may typically work with X-ray angiography or CT should undergo MRI safety
training, and all personnel should be carefully screened before entering the
suite. It is recommended to run drills for
patient transfer and emergency evacuation regularly. The interventional MR technologist assumes additional roles and responsibilities,
including sterile draping of the scanner system, preparation of an MR-safe
procedure table, and running real-time imaging to guide the procedure (8).
Conclusion
The
interventional MRI suite includes additional features to enable operators to
conduct procedures in the suite during real-time imaging. Most of the equipment necessary for an
interventional MRI suite is now available from commercial vendors. Procedures have been limited by a lack of MR
compatible devices, but there are several off the shelf devices which are MR-safe,
and there is active development in areas such as MRI guided electrophysiology
which holds promise for clinical translation in the near future. MRI guided
interventions have become routine clinical practice at several institutions,
and demand for interventional MRI suites is expected to grow as more MR
compatible devices become commercially available.
Acknowledgements
Thanks to Robert J. Lederman, William H. Schenke, and Jonathan R. Mazal for their contributions.References
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