|Numéro de publication||US20050054913 A1|
|Type de publication||Demande|
|Numéro de demande||US 10/839,861|
|Date de publication||10 mars 2005|
|Date de dépôt||5 mai 2004|
|Date de priorité||5 mai 2003|
|Numéro de publication||10839861, 839861, US 2005/0054913 A1, US 2005/054913 A1, US 20050054913 A1, US 20050054913A1, US 2005054913 A1, US 2005054913A1, US-A1-20050054913, US-A1-2005054913, US2005/0054913A1, US2005/054913A1, US20050054913 A1, US20050054913A1, US2005054913 A1, US2005054913A1|
|Inventeurs||Jeffrey Duerk, Daniel Elgort, Chris Flask, Claudia Hillenbrand, Jonathan Lewin, Frank Wacker, Eddy Wong|
|Cessionnaire d'origine||Duerk Jeffrey L., Daniel Elgort, Chris Flask, Hillenbrand Claudia M., Lewin Jonathan S., Wacker Frank K., Wong Eddy Y.|
|Exporter la citation||BiBTeX, EndNote, RefMan|
|Citations de brevets (2), Référencé par (30), Classifications (7)|
|Liens externes: USPTO, Cession USPTO, Espacenet|
This application incorporates by reference in entirety, and claims priority to and benefit of, U.S. Provisional Patent Application No. 60/468,173, filed on 05 May 2003. This application also incorporates by reference in entirety, the contents of simultaneously-filed U.S. utility application titled “MRI Probe Designs for Minimally Invasive Intravascular Tracking and Imaging Applications,” by E. Y. Wong et al., which claims priority to U.S. Provisional application 60/468,172 filed on 05 May 2003. This application also incorporates by reference in entirety, and claims priority to and benefit of, U.S. Provisional Patent Application No. 60/468,172 filed on 05 May 2003.
This invention was made with government support under Contract Number R01CA81431-02; and R33CA88144-01, both awarded by the NCI. The Government has certain rights in the invention.
In a typical magnetic resonance imaging (MRI) system, a subject such as a human body is placed in a static magnetic field that orients the proton magnetic dipoles. A field gradient is imposed along the z-axis in the direction of the main magnetic field such that a narrow plane of protons resonate within a band of frequencies. A phase encoding gradient along the x-axis is activated for a short time during which the dipoles acquire a different phase. A frequency encoding gradient along the y-axis is then activated to frequency encode the positions of the dipoles while a receiver coil is activated to record the signal. Typically, 128, 256, or 512 data points are recorded along the frequency encoded axis. As each recorded data point corresponds to a respective pixel in the image to be generated, the number of recorded data points determines the resolution of that image.
A Fourier Transform (FT) algorithm is used to decode frequency information contained in a proton signal at each location in the imaged plane to corresponding intensity levels. The resulting image is then displayed as shades of gray in a matrix arrangement of pixels. MRI may be used to reconstruct images for any standard orientation, such as transverse, coronal, or sagittal slices for example, or for any oblique orientation. MRI can also be used for interventional procedures, such as guiding medical devices through vessels and placing such devices inside vessels.
Interventionalists can perform procedures efficiently and safely if provided access to relevant image information. For example, an interventionalist may require information about a current position/orientation of a device, such as a catheter, in the body, which could be overlaid with a three-dimensional (3D) reference map showing the catheter's current position in real time. Real-time imaging can also overcome problems associated with patient movement.
In imaging most tissues with MRI, the hydrogen protons from water are preferably detected as most soft tissues are composed of greater than approximately eighty percent water. A device with a different resonance frequency can be attached to or incorporated in the catheter, with software in the scanner alternating between localizing the catheter and collecting image data.
Adjusting the MR image parameters (e.g., slice position, orientation, resolution, TE, TR, etc.) during an interventional catheter-based procedure can be a cumbersome process that may require the interventionalist or technologist to leave the magnet room and use a keyboard and a mouse in combination with a graphical user interface. Other conventional adaptive image parameter systems verify the feasibility of using feedback based on a catheter's insertion speed to adjust, in real-time, the value of specific adaptive image parameters. These systems, however, provide little clinical utility because they are neither sufficiently flexible nor robust for use in intravascular MR guided procedures.
It would therefore be desirable to provide a system and process that automatically and continuously adjusts specific image parameters in real time, based on a catheter's speed of insertion.
In one embodiment, the invention is directed to a system and method that, inter alia, incorporates real-time imaging sequences, flexible catheter tracking methods, adaptive parameter modes, and a user-friendly interface for the interventional physician.
This adaptive tracking system uses, in various embodiments, real-time tracking techniques to continually monitor a catheter tip's 3D position (including, for example, position relative to a target anatomy or position relative to the MR imager's receive coils), orientation, insertion speed, and a combination of physiological parameters, such as, without limitation, breathing rate, heart rate, etc. The device position and orientation information is used to automatically adjust the scan plane for real-time imaging. Insertion speed may be used to automatically adjust pre-specified adaptive image parameters in real-time. Image resolution, FOV, Bandwidth, TE, TR, and temporal resolution are employed as adaptive parameters; many other image parameters can also be used.
The systems and methods described herein represent a “hands free” interventional MRI systems and methods that automatically and adaptively adjust imaging parameters and react to changing clinical requirements in real-time. The systems and methods disclosed herein provide the interventional radiologist with a means to effect a change in specific image parameters, in real-time, using the catheter itself.
According to one embodiment, the invention is directed at a method of adaptively adjusting at least one MR imaging parameter for an interventional procedure. The method includes (a) adaptively tracking an MR-guided probe inserted into an object by (i) locating the probe by acquiring first probe coordinates with respect to a reference coordinate system, and (ii) calculating a velocity of the probe relative to the object by acquiring second probe coordinates with respect to the reference coordinate system (typically the MR scanner/imager's coordinate system, which may or may not be an orthogonal coordinate system), and (b) based at least partially on the calculated velocity, adjusting a subset of the at least one MR imaging parameter to adaptively track the probe, image a target region of the object, or both.
According to one practice, acquiring the first probe coordinates includes acquiring a plurality of one-dimensional frequency-encoded projections to determine at least one of a three-dimensional position of the probe and an orientation of the probe. Various imaging parameters that may be adjusted by the systems and methods disclosed herein include a subset of: field of view, image spatial resolution, image scan plane position, scan plane orientation, temporal resolution, bandwidth, slice thickness, imaging pulse sequence, image contrast, TR, TE, active receiver channels, k-space trajectory, excitation flip angle, MR scanner table position (e.g., to keep the probe proximal to an isocenter of the table).
According to one aspect, adjusting the one or more imaging parameters is at least partially based on an auxiliary parameter. The parameter includes an element belonging to a subset of: position of the probe relative to a target region of the object, position of the probe relative to the MR imager's receive coils, probe orientation, a physiological parameter associated with the object, and a combination these.
According to another embodiment, the invention is directed at A method of adaptively adjusting at least one MR imaging parameter for an interventional procedure. The method includes (a) locating an MR-guided probe inserted into an object by acquiring first probe coordinates with respect to a reference coordinate system, and (b) based at least partially on a parameter associated with the located probe, adjusting a subset of the at least one MR imaging parameter to adaptively to track the probe, to image a target region of the object, or both.
Further features and advantages of the present invention will be apparent from the following description of preferred embodiments and from the claims.
The following figures depict certain illustrative embodiments of the invention in which like reference numerals refer to like elements. These depicted embodiments are to be understood as illustrative of the invention and not as limiting in any way.
The invention is directed to a system and method for real-time catheter tracking and adaptive imaging using MRI. In particular, the system and method described herein can be used to track and position catheters and stents in a human body.
Referring now to the figures, and in particular to
As seen in
Various device localization techniques can be used, with one exemplary technique incorporating a single coil tip tracking method depicted in
The second tracking method, depicted in
Both localization methods require the collection of a limited number of 1D projections (the first tracking method requires 3 projections for catheter position, whereas the second tracking method requires 8 projections for catheter position and orientation). These localization projections are collected prior to the acquisition of each set of image data. The raw k-space projection data is sent to the image reconstruction computer where the data processing software (written in C++ and developed in ICE) determines the location of the tracking markers. The software then computes six values: three positional values that define the 3D position of the catheter and three angles that define the 3D orientation of the catheter. When using the first localization method, the three angles are set to fixed values that define a standard transverse, sagittal or coronal plane. Values are defined within the scanner's X, Y, and Z coordinate space and the positions have units of pixels.
Using standard methods provided in ICE, a dedicated real-time link is established between the image reconstruction computer and the hardware control computer, which executes the pulse sequence software on the scanner. The six position and orientation values are sent via this real-time link, where the pulse sequence software (written in C++ and developed in IDEA) accepts and stores them for use. The position and orientation values are then converted from magnet XYZ coordinate space, to a coordinate system defined by the patient using Read, Phase, and Slice-Shift axis. The 3D positions are also converted from units of pixels, to millimeters. A real-time software kernel ensures that these computations are performed within a 20 ms pause located after the collection of the localization projections and before acquisition of the next set of rapid image data. The new catheter position and orientation information is then used to automatically define the new scan plane just prior to image data acquisition.
The pulse sequence software uses localization data from multiple time points to calculate the speed of the device. A variable-point finite difference digital filter is used for this calculation. The number of time points used in the digital filter is adjustable via the user interface, allowing the clinician to control the system's sensitivity to sudden changes in catheter speed. The catheter speed is then used to adjust the value of selected image acquisition parameters (e.g., image resolution, temporal resolution, bandwidth, field of view, slice thickness). A variable image parameter, P(V), is expressed as a function of the device speed, V, with limits for the device speed set, for example, before each procedure. The value of this function determines how each adaptive parameter is set, relative to its full range of acceptable values. P(V) need not be calculated more than once before all of the selected image parameters can be updated.
Referring now to
If the current speed of the catheter is found to be less than the designated user-defined threshold VThresh, then the selected image parameters will be set to one predetermined value Pmin (which may be ideal for imaging with a stationary or slowly-moving catheter). Similarly, if the calculated catheter speed is larger than the designated threshold Vthresh, then the selected image parameters will be set to a different predetermined value Pmax (which may be better suited for a faster moving catheter).
A binary function may be inadequate to adjust to a changing insertion speed. Accordingly, a continuous mode can be employed that uses a smoothly-varying function of catheter speed, such as a sigmoidal function, to adjust the adaptive image parameters (Eq. 2):
This function is depicted in
A user-defined range for each specific image parameter is set prior to the experiment. Subsequently, during the intervention, the binary and/or continuous set functions are used to set the values of the parameters relative to their specified respective ranges. The clinician is able to designate which image parameters to treat as adaptive parameters via the user interface. The parameter set function calculations and the image parameter update are performed by the real-time kernel immediately prior to the acquisition image data.
In the exemplary system and method, a variety of pulse sequences have been integrated into the adaptive tracking software. One pulse sequence is a True-FISP pulse sequence (TR=5 ms, TE=2.5 ms, FA=70°, matrix=[128×128 to 1024×1024], FOV=[150 mm to 300 mm]). Another pulse sequence is a FISP sequence (TR=5 ms, TE=2.5 ms, FA=70°, matrix=[128×128 to 1024×1024], FOV=[150 mm to 300 mm]). Another pulse sequence is a FLASH sequence (TR=8 ms, TE=4 ms, FA=150, matrix=[128×128 to 1024×1024], FOV=[150 mm to 300 mm]). Yet another pulse sequence is a Radial True-FISP sequence (TR=3.6 ms, TE=1.8 ms, FA=70 degrees, Matrix=128×128, FOV=[50 mm to 400 mm], Radial Lines=[64 to 512]).
To evaluate the system's feasibility and performance in vitro and in vivo, trials were conducted in two vessel phantoms and eight porcine imaging experiments, using methods approved by our Institutional Animal Care and Use Committee. To quantify the system's reliability and precision, 100 image frames were collected (in vivo) in which the system updated the slice position and orientation so that it was centered on the tip of a stationary catheter. This procedure was then repeated on a catheter that was moving at clinically relevant speeds within a vessel phantom. The experiments measured image data with two active receive channels: the imaging coil and the tracking coil. The data from these two channels was combined before displaying the image so that the tracking markers appeared in the image as areas of high signal amplitude. The distance between the position of the tracking markers within the image and the center of the image was used as a measure of the system's accuracy.
The system was able to accurately localize a motionless catheter 100% of the time and a moving catheter 98% of the time. The small error rate is substantially due to the system misidentifying flowing spins outside the imaging plane as the signal from the tracking markers. When using the single coil tracking method, the system collected all of the necessary tracking data within 15 ms, whereas the figure for the two-marker method was about 25 ms. An additional 20 ms was then required to perform the localization, velocity calculations, and updating of the image parameter values. The system ran continuously and responded in real-time to calculated changes in all eight in-vivo and both phantom trials. Following parameter determination, the system successfully responded to changes in device speed by dynamically adjusting specified image parameters. In all cases, the slice plane location and orientation was automatically placed at the catheter tip using information extracted during the localization phase.
The adaptive interface was further tested by performing MR imaging-guided renal artery stent placement, which was performed in two pigs using a catheter-based system that interactively adjusts the scan plane and automatically adjusts a number of imaging parameters in a manner described above.
Although renal MR angiograms have become state-of-the-art for the diagnosis of renovascular disease, conventional fluoroscopy remains the guidance method of choice for renovascular intervention. However, MRI-guided stent placement has recently become recognized as a feasible alternative.
Miniature radiofrequency coils were implemented into a catheter to determine the exact 3D position of the device in real time. As mentioned above, multiple coils can be implemented to derive information about the device orientation.
In the experiment, multiple MR image-guided procedures were performed in two fully anesthetized pigs using a 1.5 T scanner (Magnetom Sonata, Siemens Medical Solutions, Erlangen, Germany). Gadomer-17 (Schering AG, Berlin, Germany), an intravascular contrast agent for prolonged vascular enhancement, was used to acquire a gradient echo baseline 3D-MRA and to improve artery opacification during the intervention. A 5F C1-catheter equipped with two short single loop coils at the tip was then used to catheterize the renal arteries using a transfemoral approach.
The three-dimensional position and orientation of the catheter micro-coils were determined every 300 ms by means of an analytic radial tracking method using the two active catheter-based coils. The position data was used to define the MR scan plane position and orientation of a steady-state free-precession (SSFP) sequence acquired with a frame rate of three images per second. The field of view (FOV) of the images was adjusted according to the speed of the catheter movement: an FOV was enabled for a slowly-moving catheter and a larger FOV was used at higher catheter speeds. Using a balloon catheter equipped with one short single loop coil proximal to the balloon (e.g., immediately proximal thereto), MR guidance was then used to place a stent over a wire into the ostium of the renal arteries of both pigs.
The procedure time was measured, and the stent position was verified using conventional angiography. The high-amplitude signal from the coil of the instrumented balloon catheter was used to exactly position the stent at the level of the renal artery ostium in both pigs. The stent deviation as measured with conventional angiography was less than 3 mm. The procedure times were 14 and 19 minutes, including the MRI acquisition.
The systems and methods described herein demonstrate a method for intravascular imaging that significantly improves the performance of image-guided intravascular procedures. With this, the physician has means with which to control the scanner and dynamically alter specific image parameters during an MR procedure. Allowing the MR scanner to respond to a moving catheter by adjusting the value of imaging parameters creates a more natural interface with the MR scanner for the clinician during intravascular procedures by eliminating the need for manual adjustment of the scan plane position or specific image parameters during the intervention. These scan plane adjustments are applied to imaging slices that are also following the location and orientation of the catheter. Hence, advancing the catheter more slowly will automatically improve the resolution or SNR properties of the images, or can even effect a total change in tissue contrast to allow more accurate characterization of vessel wall pathology if the clinician wishes to see more detail in a certain region of interest.
The interventional systems and methods described herein can be incorporated into virtually any imaging protocol. The tuned coils operating as capacitively-coupled localization markers can be manufactured to be small enough to fit a variety of clinical catheters. Other fiducial marker designs may also be incorporated with ease into the systems and methods disclosed herein. For example, and without limitation, multiple inductor types can be used (e.g. single-loop, solenoid, and opposed solenoid inductors); capacitively-coupled tuned resonant circuit markers may be connected to a single receiver channel or multiple channels as phased-arrays; these phased-array markers may also be used for catheter-based vessel wall imaging). According to one practice, inductively-coupled tuned resonant circuit markers may be used. According to another practice, markers filled with a distinct signal source, such as a fluid with a large chemical shift relative to water, can also be used. An underlying theme is that a localized signal is available that may be readily segmented from a non-marker background signal.
The systems and methods according to the invention have been able to reliably (with accuracy of at least 98%) localize a catheter to within 2 mm and 1 degree of rotational error; these values are comparable to existing commercially-available MR-tracking technology which is unable to provide real-time tracking with adaptive imaging. The observed small localization error rate of at most about 2% occurs at least in part because the imaging plane contains the tracking markers and tends to saturate the spins surrounding the markers, making it possible for signals outside the imaging plane (and farther away from the tracking markers) to be mistakenly identified as the tracking markers.
The problem can be addressed by allowing more time for signal recovery, introducing a non-selective saturation between imaging and localization, or constraining the extent of rotational or positional shifts between sequential images. During normal use, the system minimizes localization errors by monitoring the distance that the catheter has moved between each image frame. The slice position and adaptive parameters are not updated if the detected change in catheter position distance is greater than a pre-determined value corresponding to the preset maximum clinically permissible insertion speed. In practice, this ensures that a catheter localization failure during a given frame will generally not cause the slice to be placed at an incorrect position and the adaptive image parameters to be set to incorrect values.
The systems and methods described herein use standard clinical hardware, with the exception of the small markers that were affixed to the catheter. The systems and methods also use standard clinical gradient and RF hardware, control computer hardware, and reconstruction computer.
The software interface was also merged into the standard clinical interface provided by the vendor. These features make the systems and methods according to the invention easy and inexpensive to implement and intuitive for most who are experienced with the operation of the MR imager.
The adaptive tracking system requires, at most, an additional 60 ms per image. This allows real-time imaging sequences to continue to operate in real time, while providing a great deal of increased functionality and flexibility. The ability to respond, in real time, to changes in device velocity allows the scanner to automatically adjust a number of image parameters. Without requiring the clinician to intervene, the scanner can automatically increase resolution and decrease frame rate as the catheter slows, or increase the field of view (FOV) as the catheter's speed increases.
Moreover, according to one practice an adaptive tracking system uses markers with a resonant frequency that is distinct from a resonant frequency of surrounding tissue; in this practice, the MR scanner employed has RF hardware configured to transmit and/or receive signals at this distinct frequency and a marker has an internal signal source characterized by a resonant frequency substantially equal to the distinct frequency at the scanner's field strength.
While the invention has been disclosed in connection with the preferred embodiments shown and described in detail, various modifications and improvements thereon will become readily apparent to those skilled in the art. Accordingly, the spirit and scope of the present invention is to be limited only by the following claims.
|Brevet cité||Date de dépôt||Date de publication||Déposant||Titre|
|US5715822 *||28 sept. 1995||10 févr. 1998||General Electric Company||Magnetic resonance devices suitable for both tracking and imaging|
|US6171240 *||5 déc. 1997||9 janv. 2001||Picker International, Inc.||MRI RF catheter coil|
|Brevet citant||Date de dépôt||Date de publication||Déposant||Titre|
|US7539860 *||18 mars 2004||26 mai 2009||American Express Travel Related Services Company, Inc.||Single use user IDS|
|US7606611 *||26 juil. 2005||20 oct. 2009||Siemens Aktiengesellschaft||Method and apparatus for determining the azimuthal orientation of a medical instrument from MR signals|
|US7606612||19 mai 2005||20 oct. 2009||Case Western Reserve University||System and method to perform parallel imaging|
|US7660622 *||7 oct. 2004||9 févr. 2010||General Electric Company||Method and system for positioning a tracking sensor for optimal accuracy|
|US7863897 *||8 sept. 2008||4 janv. 2011||The General Hospital Corporation||Method and apparatus for characterizing the temporal resolution of an imaging device|
|US7996062 *||13 oct. 2009||9 août 2011||Case Western Reserve University||Double-contrast technique for MRI-guided vascular interventions|
|US8320647||26 mars 2008||27 nov. 2012||Olea Medical||Method and system for processing multiple series of biological images obtained from a patient|
|US8369930||16 juin 2010||5 févr. 2013||MRI Interventions, Inc.||MRI-guided devices and MRI-guided interventional systems that can track and generate dynamic visualizations of the devices in near real time|
|US8396532||16 juin 2010||12 mars 2013||MRI Interventions, Inc.||MRI-guided devices and MRI-guided interventional systems that can track and generate dynamic visualizations of the devices in near real time|
|US8693755 *||31 mars 2011||8 avr. 2014||Siemens Medical Solutions Usa, Inc.||System for adjustment of image data acquired using a contrast agent to enhance vessel visualization for angiography|
|US8768433||21 déc. 2012||1 juil. 2014||MRI Interventions, Inc.||MRI-guided devices and MRI-guided interventional systems that can track and generate dynamic visualizations of the devices in near real time|
|US8779771 *||19 août 2011||15 juil. 2014||Siemens Aktiengesellschaft||Magnetic resonance imaging system and method embodying a magnetic resonance marking system and method|
|US8824754 *||11 nov. 2011||2 sept. 2014||General Electric Company||Method and apparatus for generating variable resolution medical images|
|US8825133||24 janv. 2013||2 sept. 2014||MRI Interventions, Inc.||MRI-guided catheters|
|US8886288||10 janv. 2013||11 nov. 2014||MRI Interventions, Inc.|
|US8948841||22 juin 2006||3 févr. 2015||Polyvalor, Limited Partnership||MR-tracking based on magnetic signature selective excitation|
|US9123100||1 nov. 2012||1 sept. 2015||Olea Medical||Method and system for processing multiple series of biological images obtained from a patient|
|US20060025678 *||26 juil. 2005||2 févr. 2006||Peter Speier||Method and apparatus for determining the azimuthal orientation of a medical instrument from MR signals|
|US20060079756 *||7 oct. 2004||13 avr. 2006||Lloyd Charles F||Method and system for positioning a tracking sensor for optimal accuracy|
|US20060142658 *||21 nov. 2003||29 juin 2006||Michael Perkuhn||Fabric-integrated conductivity sensor|
|US20060293586 *||19 mai 2005||28 déc. 2006||Case Western Reserve University||System and method to perform parallel imaging|
|US20110311113 *||22 déc. 2011||Siemens Medical Solutions Usa, Inc.||System for Adjustment of Image Data Acquired Using a Contrast Agent to Enhance Vessel Visualization for Angiography|
|US20120043965 *||19 août 2011||23 févr. 2012||Bjoern Heismann||Magnetic resonance imaging system and method embodying a magnetic resonance marking system and method|
|US20120057767 *||11 nov. 2011||8 mars 2012||General Electric Company||Method and apparatus for generating variable resolution medical images|
|EP2910187A1 *||24 févr. 2014||26 août 2015||Université de Strasbourg (Etablissement Public National à Caractère Scientifique, Culturel et Professionnel)||Automatic multimodal real-time tracking of moving instruments for image plane alignment inside a MRI scanner|
|WO2006136029A1 *||22 juin 2006||28 déc. 2006||Ecole Polytech||Mr-tracking based on magnetic signature selective excitation|
|WO2010125486A1 *||14 avr. 2010||4 nov. 2010||Koninklijke Philips Electronics N.V.||Interventional mr imaging with motion compensation|
|WO2010144402A2 *||8 juin 2010||16 déc. 2010||Surgivision, Inc.||Mri-guided surgical systems with preset scan planes|
|WO2010144402A3 *||8 juin 2010||3 mars 2011||Surgivision, Inc.||Mri-guided surgical systems with preset scan planes|
|WO2015124795A1 *||24 févr. 2015||27 août 2015||UNIVERSITE DE STRASBOURG (Etablissement Public National à Caractère Scientifique, Culturel et Professionnel)||Automatic multimodal real-time tracking of a moving marker for image plane alignment inside a mri scanner|
|Classification aux États-Unis||600/423|
|Classification internationale||G01R33/563, G01R33/28, G06T11/00|
|Classification coopérative||G01R33/287, G01R33/563|