Several exemplary embodiments of the present invention will now be described in detail with reference to the accompanying drawings:
In the drawings, the same or similar elements are denoted by the same reference numerals even though they are depicted in different drawings.
In the following description, a detailed description of known functions and configurations incorporated herein has been omitted for conciseness.
The medical imaging system further comprises a processor 110 and a memory 111. The processor can run an algorithm for performing a dual scan, and the memory 111 can store the algorithm.
In many instances, a data acquisition console 200 (e.g., with a user interface and/or display) is located proximate a patient during use for a technologist 107 to manipulate during data acquisition. In addition to the data acquisition console 200, images are often developed via a processing computer system which is operated at another image processing computer console including, e.g., an operator interface and a display, which may often be located in another room, to develop images. By way of example, the image acquisition data may, in some instances, be transmitted to the processing computer system after acquisition using the acquisition console.
In accordance with an embodiment of the present invention, a dual energy computed tomography (CT) approach is provided in order to solve the problem of distinguishing bones from different concentrations of contrast agents. If the CT is performed using two energies at the same time, e.g., 80 kVp and 140 kVp, then the ratio of HU(kVp)/HU(kVp) helps to distinguish the contrast agent from bone in accordance with an embodiment of the present invention.
In addition, in accordance with an embodiment of the present invention, the dual energy CT provides some additional anatomical and physiological information, for example, regarding fat tissue. The dual-energy approach enables transformation of the linear attenuation mu at the CT effective energy to one decomposed into the Compton and photoelectric components, and allows detailed information on the composition of the material to be obtained. The dual-energy CT scan can identify more subtle differences in composition, such as for determination of the extent of fatty liver disease.
A criticism of dual energy approaches is that dual energy increases the patient's exposure to radiation. In accordance with an embodiment of the present invention, this can be mitigated by acquiring a CT diagnostic scan with technique factors, 140 kVp or 130 kVp and 60 mA, giving a body-core exposure of approximately 7 mGy, and by acquiring the second of the dual energy CT scans with moderated technique factors, 80 kVp and 30 mA, giving a body-core exposure of approximately 1 mGy. The image resulting from the second CT scan will have much higher noise, but, since the contrast agent is spread out over a large area, the increased noise does not significantly reduce the effectiveness of the dual-energy algorithm. The overall CT body-core exposure of 8 mGy is comparable to that of a single diagnostic CT scan.
It should be appreciated by those skilled in the art that the specific numbers provided are exemplary. For example a range of 60 kVp to 160 kVp can be used without departing from the scope of the present invention. Some of the determining factors concerning what specific parameters to use may comprise radiation exposure, noise, type of contrast agent used, size of area to be scanned, and size of patient and so on.
The following comprises the material and exemplary methods used. In terms of the calibration a GAMMEX® 467 electron density CP phantom (GAMMEX RMI®, Middleton, Wis., USA) was used to define a kVp-dependent transformation from HU into 511 keV linear attenuation values.
This transformation was measured on several CT scanners. In Table 1, all measured scanners are shown. The kVp settings were those that the user interfaces of the scanners offered. It should be appreciated by those skilled in the art that other brands and types of scanners can be used without departing from the scope of the present invention.
In accordance with an embodiment of the present invention, in order to verify the algorithm, dual-energy CT measurements were performed on a Biograph 6 PET/CT scanner (Siemens MI) at three kVp settings: 110, 130 and 80 kVp. On this CT scanner, standard parameters for a conventional diagnostic CT study were 110 kVp, 100-150 mA, depending on the part of the body that was imaged (lung/abdomen) and the size of the patient. For a small region of interest (ROI) located deep inside the body, the patient exposure with this scanner was about 8 mGy. For the dual-energy measurements, technique factors of about 60 mA at 130 kVp and about 30 mA at 80 kVp were chosen, in order not to exceed the patient exposure of the conventional study at 110 kVp and 100 mA. In order to approach the same image quality for diagnosis, the dual energy CT studies were reconstructed independently and added together.
As described above, CT scans of this phantom were performed, CT images were reconstructed by the CT scanner software and hardware, and the mean H.U. values of ROIs within each syringe and within the water phantom were measured. Care was taken to maintain the ROI boundaries well within the syringe walls. For each ROI, 1000HU were added to the means, and the resulting numbers for 80 kVp were divided by those for 130 kVp. These ratios were plotted against the HU values at 80 kVp. Finally, the results from the GAMMEX® phantom were added to the plot as shown in
The patient 106 was scanned with a Siemens Biograph 16 scanner at 80 kVp and 140 kVp. Although not necessary for demonstrating the efficacy of this dual-energy approach, the dose of the 80 kVp scan was that of a diagnostic CT. Care was taken to limit the patient's movement between the dual-energy scans. ROIs were drawn over various tissues in the 80 kVp scan, and the mean HU for each ROI was measured with the scanner software. The ROIs were reproduced on the 140 kVp scan and the measurement was repeated as shown in
Although oral-contrast-enhanced pixels in the CT image can have the same Hounsfield units as bone pixels, it is known that their associated 511 keV linear attenuation values are different. In fact, it has been shown that oral contrast in vivo, though it can result in enhancements of the CT image by hundreds of H.U., it has 511 keV linear attenuation values close to that of water. This is in contrast to bone, which has a higher linear attenuation than water at 511 keV due to its greater density. Since prior art methods and conventional kVp-dependent methods do not distinguish between oral-contrast-enhanced pixels and bone pixels in the transformation, these methods treat these pixels as bone and will overestimate the 511 keV linear attenuation for regions of oral contrast enhancement.
For routine clinical scans at 120 kVp, the resulting overestimation in reconstructed PET activity has been reported as having a maximum value in the 20-30% range, and a similar overestimation would be expected using this method, as bone and oral contrast agents are not distinguished.
The clinical validation of the kVp-dependent transformation is clearly demonstrated in
Since this prior art method is optimized for 120 kVp, the results determined using this method from the CT images acquired at 80 kVp will be most in error.
While the present invention has been shown and described with reference to certain embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the spirit and scope of the invention as defined by the appended claims.
This application claims priority from U.S. Provisional Patent Application Ser. No. 60/789,341 filed on Apr. 5, 2006, the disclosure of which is incorporated by reference in its entirety herein.
Number | Date | Country | |
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60789341 | Apr 2006 | US |