The present invention generally relates to the field of medical imaging, and systems for obtaining diagnostic images such as nuclear medicine images and magnetic resonance (MR) images. In particular, the present invention relates to phantoms used to calibrate medical imaging systems and methods for doing so.
Nuclear medicine is a unique medical specialty wherein radiation is used to acquire images which show the function and anatomy of organs, bones, or tissues of the body. Radiopharmaceuticals are introduced into the body, either by injection or ingestion, and are attracted to specific organs, bones, or tissues of interest. Such radiopharmaceuticals produce gamma photon emissions which emanate from the body and are captured by a scintillation crystal, with which the photons interact to produce flashes of light or “events.” Events are detected by an array of photodetectors, such as photomultiplier tubes, and their spatial locations or positions are calculated and stored. In this way, an image of the organ or tissue under study is created from detection of the distribution of the radioisotopes in the body.
One particular nuclear medicine imaging technique is known as Positron Emission Tomography, or PET. PET is used to produce images for diagnosing the biochemistry or physiology of a specific organ, tumor, or other metabolically active site. Measurement of the tissue concentration of a positron emitting radionuclide is based on coincidence detection of the two gamma photons arising from positron annihilation. When a positron is annihilated by an electron, two 511 keV gamma photons are simultaneously produced and travel in approximately opposite directions. Gamma photons produced by an annihilation event can be detected by a pair of oppositely disposed radiation detectors capable of producing a signal in response to the interaction of the gamma photons with a scintillation crystal. Annihilation events are typically identified by a time coincidence between the detection of the two 511 keV gamma photons in the two oppositely disposed detectors, i.e., the gamma photon emissions are detected virtually simultaneously by each detector. When two oppositely disposed gamma photons each strike an oppositely disposed detector to produce a time coincidence event, they also identify a line of response, or LOR, along which the annihilation event has occurred.
An example of a PET method and apparatus is described in U.S. Pat. No. 6,858,847, which patent is incorporated herein by reference in its entirety. After being sorted into parallel projections, the LORs defined by the coincidence events are used to reconstruct a three-dimensional distribution of the positron-emitting radionuclide within the patient. PET is particularly useful in obtaining images that reveal bioprocesses, e.g., the functioning of bodily organs such as the heart, brain, lungs, etc., and bodily tissues and structures such as the circulatory system.
On the other hand, Magnetic Resonance Imaging (MRI) is primarily used for obtaining high quality, high resolution anatomical and structural images of the body. MRI is based on the absorption and emission of energy in the radio frequency range primarily by the hydrogen nuclei of the atoms of the body and the spatial variations in the phase and frequency of the radio frequency energy being absorbed and emitted by the imaged object. The major components of an MRI imager include a cylindrical magnet; gradient coils within the magnet; an RF coil within the gradient coil; and an RF shield that prevents the high-power RE pulses from radiating outside of the MR imager and keeps extraneous RF signals from being detected by the imager. A patient is placed on a patient bed or table within the magnet and is surrounded by the gradient and RF coils.
The magnet produces a Bo magnetic field for the imaging procedure. The gradient coils produce a gradient in the Bo field in the X, Y, and Z directions. The RF coil produces a B1 magnetic field necessary to rotate the spins of the nuclei by 90° or 180°. The RF coil also detects the nuclear magnetic resonance signal from the spins within the body. A radio frequency source produces a sine wave of the desired frequency.
The concept of merging PET and MR imaging modalities into a single device is generally known in the art. See, e.g., U.S. Pat. No. 4,939,464 or co-pending U.S. patent application Ser. No. 11/532,665 filed Sep. 18, 2006 (Publication Number 2007/0102641), the contents of which are incorporated herein by reference in their entirety.
Both of these imaging modalities, as well as others, require the use of phantoms for calibration and quality control or quality assurance, which should be performed regularly to ensure continued proper functioning of the scanners. (In essence, a phantom is an object with known properties, e.g., emission activity distribution, attenuation distribution, water distribution, etc., which properties are registered by a given imaging scanner.) In addition to calibration/quality control of the individual imaging modalities in a hybrid (i.e., multiple-mode) system, phantoms are used to ensure proper alignment of the various imaging modalities. Thus, for the specific example of an MR/PET hybrid imaging system, a field-of-view (FOV) alignment phantom, an MR water phantom, a PET normalization phantom, and a PET uniform phantom (at least) will be used to set up and calibrate the system.
Depending on the particular phantoms and the particular imaging modalities in connection with which they are used, the various phantoms an operator uses may be easily distinguished in some cases or, in other cases, they may be easily confused by the system operator. Therefore, because the imaging time for MR and PET (and possibly other modalities, too) is on the order of several: minutes, if the system operator selects the wrong phantom and/or calibration/quality control protocol during the calibration/QC process, the procedure will not complete successfully and substantial, valuable time for imaging with the system may be lost.
The present invention provides for automatic recognition or identification of the various phantoms that are used to calibrate and ensure accuracy of a given imaging system, and is particularly useful—but by no means limited to—in connection with hybrid (multiple-modality) imaging systems. Most advantageously, the present invention further entails automatically initiating the appropriate calibration/quality control protocol in connection with which a give phantom is used.
Thus, in one aspect, the invention features a self-identifying phantom. In some embodiments, the self-identifying phantom includes a phantom, per se, and a distinguishable, machine-readable identification feature associated with the phantom, per se—without which identification feature the phantom, per se, could still be used to calibrate/assure image quality of the medical imaging device. Possible machine-readable features include plugs that engage the local coil ports provided on some MR imaging systems; RFID tags; and barcodes. In other embodiments, the machine-readable identification feature works in conjunction with features located on a cradle in which the phantom, per se, is supported for calibration. Examples of such features include optical-based features (e.g., light passages through the phantom or a portion of it) and contact-based or proximity-based features (e.g., switches, electrical contacts, magnets/Hall effect sensors, etc.)
In another aspect, the invention features a medical imaging system. The medical imaging system includes imaging apparatus and a stand-alone phantom-recognizing device associated with the medical imaging device—without which stand-alone phantom-recognizing device the imaging apparatus could still be used to image a patient. Possible stand-alone phantom-recognizing devices include RFID-scanners; barcode-readers; and cameras (with associated optical-image-recognition software).
In another aspect, the invention features a medical imaging system. The medical imaging system includes a medical imaging device with an operational control system and control software residing on the medical imaging system. The control software includes image-analyzing software that analyzes an image produced by the medical imaging device and that, based thereon, recognizes and identifies an object being imaged by the medical imaging system. For example, discrete locations of emissions activity can be identified even without the system being calibrated or perfectly tuned, and the position, distribution, overall shape of the distribution, etc., can be used to recognize and identify a given phantom being imaged by the system.
These and other features of the invention will be described more fully below.
The invention will now be described in greater detail in connection with the figures, in which:
Three different embodiments 10a, lob, and 10c of a hybrid imaging system constructed according to certain aspects of the invention are illustrated in
Thus, each of the hybrid imaging systems 10a, 10b, and 10c exemplarily constitutes an MR/PET imaging systems. Accordingly, each includes an MR housing 12 that houses the magnetic field-generating coils (not shown) and that supports gradient coils 14, 16, 18, and 20. Additionally, RF sensing probes 22, 24—part of the MR “half” of the hybrid system—are provided. As for the PET “half” of the hybrid system, a number of PET detectors (scintillator crystals) are provided, e.g., in the form of a ring of crystals 26a that extends circumferentially around the central, patient-receiving cavity of the systems as shown in
A patient bed 28 is centrally located centrally within the patient-receiving cavity of each of the systems 10a, 10b, and 10c. Additionally, a port 30 into which are plugged any of a variety of local coils (which are used to image specific structures from “up close”) is schematically illustrated as provided, for example, on the patient bed 28. The port 30 is used to transfer information between a local coil and the imaging system, which information—e.g., the type of local coil that has been connected to the port 30—can be used to control the imaging protocol used by the imaging system. Alternatively, the port 30 is used to transmit signals/electrical power to the connected local coil.
Furthermore, each of the hybrid systems 10a, 10b, and 10c is depicted as including a stand-alone phantom-recognizing device. In the embodiment 10a illustrated in
As explained above, various phantoms are used to calibrate and ensure imaging quality of an MR/PET hybrid system (as well as other single-mode or hybrid imaging systems), and according to one aspect of the present invention, the phantoms are configured to facilitate automatic identification of the phantom being used at any given time. Thus, five different exemplary embodiments of self-identifying phantoms are illustrated in
In one embodiment illustrated in
Thus, when a given phantom 100 is used to calibrate/run quality control on an imaging system, its identification plug 104 is connected to the imaging system's port 30 and the imaging system's operational control system (illustrated schematically by the flowchart 1 within the imaging system 10a's, 10b's, or 10c's control console 34 in
Other embodiments of self-identifying phantoms 200, 300, 400, and 500 are illustrated in
Similarly, the self-identifying phantom 300 (
Two further embodiments of self-identifying phantoms 400, 500 with distinguishable, machine-readable identification features associated with them are illustrated in
In the embodiment illustrated in
Information as to the presence or absence of an open passageway at each light source location suitably is provided to the imaging system through connector 410 (
The embodiment of a self-identifying phantom 500 illustrated in
According to another aspect of the invention, in many cases, phantoms that do not have any associated distinguishable, machine-readable identification features can still be used for automatic identification. In particular, phantoms often can be distinguished visually fairly easily based on their shapes and/or dimensions. For example, as illustrated in
Alternatively, in many instances, the attribute of a given phantom that is detected by an imaging system and that is used to perform the calibration/quality assurance can be detected with sufficient clarity or resolution for its spatial distribution to be identified even before the imaging system has been calibrated or recalibrated. For example, emissions activity can be localized to a discrete number of spheres 640, 940, or it may be distributed throughout a predefined number and arrangement of cylindrical rods 740 that are located throughout the phantom, and the positions of those spheres/rods often can be identified sufficiently by an image analysis module within the operational control system's software 1—which module analyzes images of the phantom produced by the particular imaging mode, not an optical image of the phantom—to be able to identify the specific phantom being imaged even without the system having been calibrated or recalibrated. Alternatively, if the emissions activity is uniformly distributed throughout the phantom, as represented by the stars in
Thus, even if specialized phantoms with distinguishable, machine-readable identification features are not used, it may be possible to identify the phantoms being used automatically (i.e., without operator intervention) so long as the imaging system, per se, is configured with appropriate image-analyzing software.
The foregoing disclosure is only intended to be exemplary of the methods and apparatus of the present invention. Departures from and modifications to the disclosed embodiments may occur to those having skill in the art. The scope of the invention is set forth in the following claims.