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Description  |
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TECHNICAL AREA
The invention relates to the area of diagnostic imaging and more
specifically to a method and device for interfacing MRI with various other
diagnostic imaging modalities and treatment devices.
BACKGROUND OF THE INVENTION
Magnetic resonance imaging (MRI) is a recent but extremely powerful
noninvasive diagnostic tool. MRI utilizes a combination of a powerful
static magnetic field and radio frequency pulses which gather information
concerning the location and interrelation of atomic nuclei which possess
unpaired electron spin within the body. As hydrogen is the most prevalent
element to possess unpaired spin, MRI mainly images hydrogen ion
concentration. Based upon this information, a computer is able to generate
an anatomic image of the subject. For particular studies, MRI has a
distinct advantage over computed tomography (CT) scans. For example, it is
presently established that MRI is the diagnostic tool of choice in
evaluating the posterior fossa, an anatomical location that is poorly
visualized by CT. MRI is also superior to CT in delineating extremity
soft-tissue tumors and primary bone malignancies. Whereas CT scans a
region of interest in one plane, MRI permits imaging in any desired plane,
thus more easily permitting multidimensional mapping of tumors.
These advantages of MRI make it attractive for use in radiation treatment
planning. Over the past several years, CT has been used for this purpose
and has revolutionized radiation treatment by making available more
detailed information concerning tumor localization than was ever before
possible: (E. Hart, "The Role of the CT Scanner in RT Planning" 54(613)
Radiotherapy 20, 1988.) Still, as suggested above, certain anatomical
studies are better suited to MRI, and thus, MRI should potentially
complement CT in radiation treatment planning. It has also been suggested
that MRI may be synergistic with CT in the definition of tumor volume for
a number of disease states. (A. Lichter and B. Fraass, "Recent Advances in
Radiotherapy Treatment Planning" Oncoloy, May 1988, p. 43)
In order for these expectations to be met, there is a need to develop a
means to accurately interface MRI with other diagnostic imaging modalities
such as CT or positron emission tomography (PET) and to transfer tumor
localization data obtained from MRI and the other imaging modalities to
radiation treatment devices. It is important to realize that due to
spatial and temporal magnetic field fluctuations within the MRI field, the
displayed image is distorted to varying degrees in a non-uniform manner.
These fluctuations are dependent on multiple factors such as ambient
temperature, and extraneous magnetic fields in the immediate scanner
vicinity. Images appearing on the viewing screen (CRT), and ultimately on
the film hardcopy, are the result of system software manipulations
intended for viewer aesthetics. Further, the bony skeleton which is often
used as a reference in determining tumor location and size with other
imaging modalities is not well visualized on MRI. Thus, MRI does not
permit direct tumor measurement with the degree of consistency and
precision demanded in a treatment planning setting.
SUMMARY OF THE INVENTION
The present invention provides an inexpensive but effective means to
interface MRI with other diagnostic imaging modalities and radiation
treatment devices in a reproducible manner. The invention herein described
and claimed avoids the interfacing problems with MRI otherwise caused by
distortion and poor visualization of bone by employing a grid system. For
MRI, the system uses a grid structure of members of contrast material
visualized on MRI and a means for reproducibly positioning said grid
structure relative to a body part being imaged. With the grid properly
positioned, the image taken with the MRI will include both data relative
to the body part and artifact caused by the contrast agent of the grid. As
the true spatial relationship of the grid members is known, and the causes
of distortion affect the grid and the body part similarly, such grid
artifact functions as a reference in the same manner that the bony
skeleton serves as a reference with other imaging modalities. Thus, if a
tumor is the structure of interest being imaged, determinations of
location and size of the tumor are made by reference to the known spatial
relationship of the grid.
When the subject is studied using other imaging modalities, the system is
again employed changing only the contrast material as required. Using the
positioning means, the subject and the grid structure are aligned in the
same manner as when the MRI images were made. With the grid as a reference
one can readily and accurately compare MRI images with images made with
the other imaging modalities. Thus, by selection of contrast material, and
a means to precisely and consistently position the grid and the patient in
relation one to the other, the invention functions to reproducibly
interface MRI with other modalities such as CT, PET and radiation
treatment devices. Localization grids have been described for use with CT,
PET and MRI applications: (S. Goerss, et al: A Computerized Tomographic
Stereotactic Adaptation System, 10 Neurosurgery 375-379, 1982; P.C. Hajek,
et. al., Localization Grid for MR-guided Biopsy. 163(3) Radiology 825-826,
1987; S. Miura, et. al. Anatomical Adjustments in Brain Positron Emission
Tomography Using CT Images. 12(2) Journal of Computer Assisted Tomography
363-67, 1988; U.S. Pat. No. 4,583,538.) To varying degrees, these grids
are either difficult to use, expensive to manufacture, not conducive to
exact repositioning from scan to scan or not readily interchangeable
between MRI and the various other diagnostic modalities.
Accordingly, it is an object of this invention to provide a method and
apparatus which may be used to interface MRI with other imaging devices as
well as with radiotherapy treatment units.
Another object of this invention is to provide a method and apparatus to
interface MRI with other imaging devices as well as with surgical
intervention techniques.
Yet another object of the invention is to satisfy the above stated
objectives in an uncomplicated and inexpensive manner.
The novel features which are believed to be characteristic of the invention
both as to its organization and method of operation, together with further
objectives and advantages thereof, will be better understood from the
following drawings in which a presently preferred embodiment of the
invention is illustrated by way of example. It is to be expressly
understood, however, that the drawings are for the purpose of illustration
and description only and are not intended as a definition of the limits of
the invention.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1A: Perspective view of a grid structure having a portion of its side
wall cut away to expose tubing embedded in the wall.
FIGS. 1B through 1D: Perspective views of a variety of grid structures.
FIG. 2: Partial perspective view of a grid structure having removable
walls.
FIG. 3: Perspective view of the corner portions of a grid structure
illustrating the interconnected tubing network embedded within said wall,
and specifically showing the beginning and terminus portions which open at
the same edge and are able to be capped.
FIG. 4: Partial perspective view of the corner section of the grid
structure of FIG. 1D, illustrating the use of a screw plug at such corner
section.
FIG. 5: Perspective view showing the relation of the patient platform to
the patient bed of an imaging unit.
FIGS. 6A and 6B: Two embodiments of a patient platform with grid structure
slidably attached.
FIGS. 7A and 7B: Perspective view illustrating the use of saggital and
transverse lasers to align the patient platform and subject.
FIG. 8A: Perspective view of the subject on the patient platform with grid
structure slidably attached in preparation for moving into the gantry of
an imaging unit.
FIG. 8B: Perspective view of the subject on the patient platform with grid
attached positioned within the gantry of an imaging unit and diagrammatic
representation of the use of a computer algorithm to correct image
distortion.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
While this invention is susceptible of embodiment in many different forms,
it is shown in the drawings and will herein be described in detail,
preferred embodiments of the invention. It should be understood, however,
that the present disclosure is to be considered an exemplification of the
principles of the invention and is not intended to limit the invention to
the specific embodiments illustrated.
The grid system of the preferred embodiment has two basic components. FIG.
1A illustrates the first component of the system, the grid structure 11.
As illustrated, the grid structure of the preferred embodiment is a
rectangular structure having two open ends 12. The walls 13 of the grid
structure 11 are made of semi-rigid non-magnetic material such as
plexiglass. Embedded within the walls are tubes 16, also of a non-magnetic
material, containing contrast material. For use with MRI, the preferred
contrast material is Gadolinium diethylenetriaminepentaacetic acid
(Gd-DPTA). Optimal visualization on both T1- and T2-weighted spin-echo
pulse sequences has been obtained by Hajek, et. al., supra, using 5
mm-diameter tubes filled with 500 mM Gd-DPTA. It is to be understood that
other paramagnetic material may be substituted for Gd DPTA and still come
within the scope of the claims. For use with CT radiopaque contrast
material such as Barium is desirable.
The tubes containing contrast material are regularly spaced and arranged in
a mutually orthogonal fashion. Also, one of the tubes embedded in each
face of the grid structure is arranged so as to form a diagonal 18.
In the presently preferred embodiment, interfacing between diagnostic
modalities is accomplished by using identically constructed grid
structures having tubes containing contrast material specific for the
particular imaging modality being used. Thus, for example, one grid
structure having tubes containing Gd-DPTA is used with MRI and an
identical structure having tubes containing Barium is used with CT and
radiation treatment devices.
Alternatively, interfacing may be accomplished using a grid structure, as
illustrated in FIG. 2, wherein the walls 22 of said structure may be
removed and replaced with identically constructed walls with tubes
containing a different contrast material. Thus, one would have a set of
grid structure walls containing contrast material specific for MRI, a set
of walls containing contrast material specific for PET, and yet another
set of walls specific for CT and radiation treatment devices. Said grid
structure walls would be held in place by conventional framing means
manufactured of non-magnetic material 23. An example of suitable material
would be semi-rigid nylon or plastic. Alternatively, the walls themselves
could have interlocking means at their edges such as a mitered joint type
of assembly so as not to require an external frame to hold the walls in
place.
Interfacing between MRI, CT and radiotherapy treatment devices is also made
possible using a grid structure with tubes containing both paramagnetic
and radiopaque contrast material. An example would be a grid structure
with tubes containing a solution with sufficient amounts of both Gd-DPTA
and Barium sulfate.
An alternative to using separate grid structures or removable grid
structure walls is a means to empty and refill the tubing of the wall of
contrast material. FIG. 3 illustrates such an embodiment. In this
embodiment, the tubes of a wall form an interconnected network, the
beginning and terminal portions (26, 25) of which fit flush with the edge
of the wall. These end portions open to the outside are fitted with a
capping means such as a simple plug or screw cap 24. Thus, to empty the
tubing network of contrast material one removes the cap from the beginning
and terminus end of the tubing and tips the wall to let the material
drain. To refill, one tips the wall up and fills at the beginning until
the solution runs out the terminal end. Once refilled, the ends are
recapped.
The ability to empty and refill the tubes of the grid structure is
particularly useful when using the grid structure to interface with PET.
Imaging with PET is dependent on the emission of positrons. The materials
which are generally used as positron emitters have only a short half life
and are thus prepared shortly before use.
FIG. 1D illustrates yet another embodiment of the grid structure of the
invention. In this embodiment the grid structure 11 is an assembly of
hollow tubes 31 joined in a generally rectangular shape with additional
hollow tubes as diagonals 32 across four of the faces of said rectangle.
The hollow tubes of this embodiment are formed of a non-magnetic material
such as a rigid plastic and filled with a solution of contrast material.
As indicated above, the contrast material would be selected with regard to
the particular imaging modality being used. Further, as illustrated in
FIG. 4, the corners of the grid structure of the embodiment of FIG. 1D
contain a screwable plug 33 which allows emptying and refilling the hollow
tubes (31, 32) such that solutions containing other preferred types of
contrast material are readily substituted as the need arises.
FIGS. 1B and 1C illustrate other suitable configurations of the grid
structure. As will be appreciated, the exact configuration of a grid
structure is not important to the essence of the invention. In the same
manner, the invention may also be carried out by using contrast material
in solid rather than liquid form. For example, contrast material in a
defined pattern could be embedded in a matrix of nonmagnetic material or
embedded within solid rods or bars that are arranged so as to form a grid.
Although the exact configuration of the grid structure is unimportant, as
illustrated in FIG. 5 the grid structure 11 must be of a size sufficient
to fit about the body of the subject 29 being imaged but within the gantry
27 of the diagnostic imaging machine 28 being used.
The second component of the grid system is a means for reproducibly
positioning the grid system relative to the body part being imaged. In the
preferred embodiment, this is accomplished by using a grid locating means
and a crossed laser system. As illustrated in FIGS. 6A and 6B, the grid
locating means of the preferred embodiment is a patient platform 41 to
which the grid 11 is slidably attached such that it may be moved
horizontally along the length of said platform and positioned at the
appropriate place about the subject being imaged. Located on the top
surface of the platform and at either side of the grid is a scale in the
form of regularly spaced and numbered demarcations.
Slidable attachment means attaching the grid structure to the platform may
be accomplished by a tongue and groove mechanism, a roller and track
mechanism or other conventional means.
In the presently preferred embodiment FIG. 6A, the platform consists of an
upper member 43 and a lower member 44. The upper member is sufficiently
narrow to pass between the side walls of the grid structure, but
sufficiently wide so as not to allow lateral movement of the grid
structure. As can be seen in FIG. 6A, at each end the members are joined
to a spacer 46 such that the upper member is separated from the lower
member by a space sufficient to accommodate the bottom wall 48 of the grid
structure. The fit of the bottom wall in this space should be such that
sliding of the grid back and forth is accomplished without difficulty but
it should not be so great as to allow vertical movement of the grid
structure. It is desirable to have sufficient horizontal movement of the
grid structure such that it can be moved the entire length of an average
sized subject centered on the platform. Using the above described
construction, the horizontal movement of the grid structure is dictated by
the strength and rigidity of the upper member. It is desirable that the
upper member support the subject without deformation so that the grid
structure is not pinched and prevented from horizontal movement. Thus, the
stronger and more rigid the upper member, the greater the span between the
supporting spacers 46, and the greater the horizontal movement of the grid
structure. As with the grid structure 11, the platform must be
manufactured of nonmagnetic material.
FIG. 5 illustrates the relationship of the platform 41 to the patient bed
30 of an imaging unit 28. As illustrated in FIG. 5, the patient platform
41 approximates the dimensions of the patient bed 30 in terms of length
and width and rests on top of said patient bed. The patient bed for the
conventional MRI unit as well as for the conventional CT unit has a
generally convex surface 36. The provision of a patient platform as
illustrated in FIG. 5 transforms the generally convex surface of the
patient bed to a flat surface. Means may be provided to conform the bottom
surface of the patient platform 41 to the concavity 36 of the patient bed
so as to prevent said patient platform from moving about while it rests on
the surface of the patient bed. Commercial patient platforms are available
from such manufacturers as Pickering and General Electric Medical Systems.
Said commercial patient platforms can be adapted to receive the grid
structure as illustrated in FIG. 5 and would fall within the scope of the
claims of this invention.
FIGS. 7A and 7B illustrate the crossed laser system which, together with
the grid locating means, is used to reproducibly position the subject in
relation to the grid. As illustrated in FIGS. 7A and 7B, the saggital
laser 51 aligns the platform and subject in the X and Z coordinates
whereas the transverse laser 52 aligns the subject and platform in the Y
and Z coordinates. Crossed laser systems are available commercially and
can be readily adapted to the use described herein. An example of a
commercially available system is the Patient Positioning Systems from
Gammex Inc., P.O. Box 26708 Milwaukee, Wis. 53226.
METHOD OF USE
In FIG. 7A, the patient platform 41 with grid structure 11 is mounted on
the patient bed of the imaging unit 28. The patient platform is then
aligned via the crossed laser system utilizing sagittal 51 and transverse
52 lasers. The use of a crossed laser technique to align structures in
three dimensional space is known in the art. In relation to the present
invention, the sagittal and transverse lasers are fixed and define a point
in X, Y and Z coordinates to which the patient platform is related. The
sagittal laser defines the X and Z coordinates of the patient platform 41
in relation to the imaging unit table 30, while the transverse laser
allows for adjustments in the Y and Z coordinates. By recording the X, Y
and Z coordinates of the imaging unit table with respect to some initial
point of laser intersection on the table, the location of the patient
platform 41 is reproducible from room to room, or from imaging device to
imaging device.
With the subject 29 for imaging stationed on the patient platform 41,
standard body immobilization techniques such as body casting or pleximolds
can be employed. As illustrated in FIG. 7B, the sagittal and transverse
lasers are then used to position the subject with relation to the table
and the desired X, Y and Z coordinates. Positioning of the subject 29 is
accomplished by employing marks or ink tattoos 44 on either the subject or
immobilization devices.
The grid structure 11 is then positioned so as to flank the region of
interest of the subject 29 which is to be imaged. In the preferred
embodiment, the location of the grid structure, once positioned, is
indicated by the numbered demarcations 42 provided on each side of the
platform. These numbered demarcations are recorded, and the table with the
grid structure platform and subject is then passed into the gantry 27 of
the imaging device 28 and the region of interest is scanned as illustrated
in FIGS. 8A and 8B.
When the subject is studied with imaging modalities other than MRI the
appropriate contrast material is selected and the above described
procedure is repeated. For example, if the subject is also to be studied
using CT, a grid structure and patient platform identical but for the
contrast material contained within the tubes is mounted on the CT patient
bed. In the case of CT, barium or other radiopaque contrast material is
used. The platform is aligned using the cross laser system as described
above; the subject is stationed on the platform; the subject is laser
aligned and the grid structure is then positioned over the region of
interest using the numbered demarcations.
Using the above method, the region of interest as studied with MRI is
defined in terms of the grid. As the grid pattern and the position of the
subject relative to the grid is identical in the CT studies as with the
MRI studies direct comparison between the studies of the two different
modalities can be made in spite of the distortion obtained with MRI.
As should be appreciated, the above-described grid system and procedure can
be used to interface MRI with any other imaging modality including PET and
Digital Subtraction Angiography.
The grid system and procedure also provides a means to more accurately
follow the course of a disease state and to judge the effectiveness of a
treatment plan on that disease state. For example, if one is treating a
tumor with radiotherapy, it is desirable to periodically repeat MRI and CT
scans of the tumor in order to monitor the treatment. Because of the
distortion obtained with MRI, it is difficult to assess minute changes in
tumor location and size. Using the grid system and procedure described
above, one avoids the inherent distortion obtained with MRI. Because the
system and procedure permit exact repositioning of the subject relative to
the grid structure during repeated scans and because the tumor is defined
in terms of the grid, small changes in tumor size or location can be
monitored.
For radiotherapy purposes, using the methods and apparatus of the present
invention, a tumor defined by MRI (including coronal and sagittal
sections) may thus be more accurately translated to CT images (which are
by necessity transverse), with a resultant improvement in target volume
determination. In the case of computer enhanced dosimetry, CT imaging
cannot be bypassed as it provides important electron density information.
In the case of coplaner radiation, a tumor may be defined in X, Y and Z
coordinates, and a simpler connect-the-dot method of target volume
determination is employed. The accuracy of this can be easily checked at a
therapy simulator or treatment machine using an array of lead wires
instead of the gadolinium chloride or barium sulfate which are well
visualized via MRI and CT respectively. The invention is also adaptable to
MRI-guided needle biopsy, or PET-guided biopsy.
METHOD OF USING THE GRID SYSTEM TO CORRECT MRI DISTORTION
Although the invention herein described can be used inspite of the
distortion caused by magnetic field fluctuations in MRI, it may also be
used as a means to correct such distortion. As before mentioned, the
magnetic field fluctuations distort the image of the grid artifact in the
same manner as such magnetic field fluctuations distort the image of the
subject. The grid artifacts which can be directly related to the known
spatial relationship of the grid thus act as indices of the degree of
distortion present in a particular image. By manipulating the image so as
to bring the grid artifacts into proper relation to one another, the image
distortion of the subject would be simultaneously corrected. Such
manipulation can be done using conventional mathematical computations
which are known in the art.
As illustrated in FIG. 8B, the above described method can be accomplished
by using a computer algorithm which applies the required mathematical
procedures to remove image distortion. In this manner, the computer
algorithm means can be incorporated with the software of the MRI to
recognize the misalignment of grid artifact 54, manipulate the uncorrected
image to bring the grid artifact into proper alignment and thus produce a
corrected image.
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Description  |
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