Electricity: measuring and testing – Particle precession resonance – Using a nuclear resonance spectrometer system
Reexamination Certificate
1998-10-05
2002-05-28
Arana, Louis (Department: 2862)
Electricity: measuring and testing
Particle precession resonance
Using a nuclear resonance spectrometer system
C324S307000
Reexamination Certificate
active
06396270
ABSTRACT:
The present invention relates to magnetic resonance imaging (MRI), and in particular to quantitation and standardization of both medical and industrial applications of MRI.
BACKGROUND OF THE INVENTION
Magnetic resonance measurements have been used in both non-medical and medical applications. In a typical non-medical application, a sample or a body of non-living matter is subjected to a static magnetic field and an oscillating radiofrequency field. The radiofrequency field electrically excites hydrogen atoms in the sample or body. After the oscillating field is turned off, the intensity of proton oscillation is measured, e.g., using an antenna, typically configured to detect the intensity of oscillations in a plurality of locations in a two-dimensional plane.
In a typical medical application of MRI, a patient is placed within the bore of a large, donut-shaped magnet. The magnet creates a static magnetic field that extends along the long (head-to-toe) axis of the patient's body. An antenna (e.g., a coil of wire) is also positioned within the bore of the large magnet, and is used to create an oscillating radiofrequency field that selectively excites hydrogen atoms (protons) in the patient's body into oscillation. The oscillating field is then turned off, and the antenna is used as a receiving element, to detect the proton oscillations as a function of position within the body. Typically, the intensity of the oscillations is measured throughout a two-dimensional plane. When the intensities are displayed as a function of position in this plane, the result is an image that often bears a striking resemblance to the actual anatomic features in that plane. Although MRI typically involves visual display of data, “imaging” can involve purely digital analysis and output so that, in this context, “imaging” does not necessarily require visually-perceptible output.
The intensity of proton oscillations detected at a given point in the patient's body is proportional to the proton density at that point. Because different types of tissues have different proton densities, different tissue types usually have different image intensities, and therefore appear as distinct structures in the MR image. However, the signal intensity also depends on physical and chemical properties of the tissues being imaged. In a simplified model of MRI, the detected signal intensity, as a function of position coordinates x and y in the plane being imaged is proportional to:
(1−
e
−TR/T
1
)
e
−TE/T
2
(1)
The parameters TR (recovery time) and TE (echo delay time) are under the control of the operator of the MR imaging system, and are constants for any given image. However, T
1
and T
2
are functions of the tissue under examination, and therefore vary with position in the x-y plane. By suitable selection of parameters TR and TE, either the T
1
or the T
2
term in Equation 1 can be made to dominate, thereby producing so-called “T
1
-weighted” and “T
2
-weighted” images, respectively.
One of the more important medical uses to which MRI has been put to date is to noninvasively scan a portion of a patient's body, in an attempt to identify benign or malignant tumors. When MRI is used in this fashion, it is necessary to have some methodology for concluding that a given portion of an MR image represents tumor, as opposed to other tissue types such as fat, cyst, etc. One known approach to identifying tissue type has been to acquire multiple MR images of the same region of the patient's body, using different imaging parameters, e.g., using different value of the TR and TE parameters. To take a simplified example, if it were known that a given tumor produced a high image intensity at a first parameter setting, a low image intensity at a second parameter setting, and a high image intensity at a third parameter setting, then a portion of a patient's body that produced that pattern of intensities (high, low, high) could be tentatively identified as tumor.
Pattern recognition approaches of this type are described in U.S. Pat. No. 5,003,979. This patent describes a system for the detection and display of lesions in breast tissue, using MRI techniques.
Many previous applications of magnetic resonance measurements have been directed to determining whether a substance or tissue is or is not of a particular type (e.g., whether a portion of a body being imaged is or is not fat). Other applications have been directed to determining whether a portion of a body being imaged falls into one of a small number of discrete categories (e.g., fat, cyst, or tumor). Non-parametric magnetic resonance imaging techniques have typically not been used for effectively and efficiently quantitizing a continuous property (such as viscosity or concentration of a substance within a body or sample).
In previous MRI techniques, analysis of results have often included a subjective or non-automatic component, such as a step of classifying or identifying portions of an image using judgment of a skilled observer. Accordingly, it would be useful to include techniques to more objectively or automatically categorize or analyze MR data.
In many cases, comparison of the pattern of intensities of a patient's tissue to “standard” patterns for different tissue types does not produce results of sufficient accuracy. One problem appears to be that attempts to define a single “standard” pattern for a given tissue type does not take sufficient account of possible variability in tissue of a given type. Another problem appears to be that there is substantial variability from one patient or sample to the next as well as from one MRI machine to the next or within different regions or fields of view of the same MRI machine.
Cancer treatment often includes detecting when a primary tumor has spread to other sites in the patient's body, to produce so-called secondary tumors, known as metastases. This process, using MRI or other imaging techniques, is often complicated by the fact that a remote lesion discovered during staging could represent either a metastasis or a benign incidental finding. A number of benign lesions (such as hepatic hemangiomas and nonfunctioning adrenal adenomas) occur as frequently in patients with a known primary tumor as they do in the general population.
Resolving this dilemma requires additional imaging studies or biopsy, but often significant uncertainty persists. Biopsy may expose the patient to substantial risk when the lesion in the brain or mediastinum, or when the patient has impaired hemostasis. Even when biopsy does not present a significant risk to the patient, it may be technically challenging, such as sampling focal lesions in vertebral marrow.
SUMMARY OF THE INVENTION
For the reasons set forth above, it would be useful to have a method that could use MR data to estimate the value of a continuous property such as concentration, viscosity or the like for both industrial applications and medical applications. It would further be useful to have a method which reduces or eliminates the need for subjective analysis of MRI data.
It would also be useful to provide a method that takes account of variability among “standard” substances or tissue types, takes account of variability from patient to patient, among different MRI machines and within different regions or fields of view of the same MRI machine. Particularly with regard to medical applications, it would be useful to provide a method that could noninvasively measure the similarity between a known primary tumor and a remote lesion of unknown tissue type. The clinician would use the measured similarity to determine the likelihood that the two lesions represent the same tissue. Such a method could be used to distinguish a pathological fracture from a benign osteoporotic compression fracture in a patient with a known primary tumor. Similarly, the method could be used to distinguish a metastasis from an infarction in a patient with lung cancer who presents with a supratentorial solitary enhancing lesion. Using the computed similarity to
Arana Louis
Townsend and Townsend and Crew
University of Washington
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