The present application relates to Magnetic Resonance (MR) arts. It finds particular application in conjunction with magnetic resonance imaging (MRI) but may also find application in magnetic resonance spectroscopy (MRS).
Magnetic Resonance Imaging (MRI) uses a pre-scan to calibrate and create initial references before each scan sequence. A typical pre-scan includes a coil survey, a sense reference, a B0 mapping, and a B1 mapping. A coil survey typically lasts more than 10 seconds. A sense reference typically lasts more than 10 seconds. A B0 mapping lasts more than 15 seconds, and a B1 mapping lasts between 15 and 30 seconds. The total pre-scan can last longer than one minute. If the coil or the patient position change, then the information is inaccurate. Ideally, all of these pre-scans need be repeated. Otherwise, the reconstructed image may contain serious artefacts. However, the repetition of these reference scans prolong the total acquisition time.
Moreover, the pre-scan is usually run at a low resolution to save time. If the coil elements are small, a low resolution image may not provide sufficiently accurate coil sensitivity maps. A lack of sufficiently accurate coil sensitivity maps result in residual aliasing artefacts in SENSE images.
A typical imaging subject is scanned with an average of 4 or more imaging sequences. The imaging sequences are typically performed on the same region of interest but focus on different aspects of the subject anatomy, achieve different contrasts, and the like. Since the same subject is scanned in the same system using the same RF coil, the information such as B0, B1−, optimized acquisition trajectory and reconstruction parameters, etc, can be shared among these scans for different contrasts to improve the image quality. The present application provides a new and improved MR imaging using shared information which overcomes the above-referenced problems and others using one set of pre-scans.
In accordance with one aspect, a magnetic resonance method is provided in which a pre-scan sequence is followed by a plurality of scanning sequences without pre-scan sequences in between and in which information of the pre-scan sequence is refined by each scan sequence.
In accordance with another aspect, a magnetic resonance system includes a magnet which generates a B0 field in an examination region, a gradient coil system which creates magnetic gradients in the examination region, and an RF system which induces resonance in and receives resonance signals from a subject in the examination region. The system further includes one or more processors which are programmed to control the RF and gradient coil systems to perform a pre-scan sequence to generate pre-scan data. The pre-scan data is processed to create pre-scan information. The RF system and the gradient coil system are controlled to use the pre-scan information to perform a first sequence to generate first sequence data, as well as refined pre-scan data. The one or more processors controls at least one of the RF and gradient coil systems using the refined pre-scan data to perform a second sequence to generate second sequence data and/or reconstruction of the second sequence data into an image representation using refined pre-scan information.
In accordance with another aspect, a magnetic resonance method includes performing a magnetic resonance pre-scan sequence to generate pre-scan information, performing a first sequence to generate first sequence data, and refining the pre-scan information with the first sequence data to create refined pre-scan information. A second scan sequence is performed to generate second scan data and at least one of the second scan sequence is reconstructed using the refined pre-scan information and/or the refined pre-scan sequence information is used when performing the second scan sequence.
In accordance with another aspect, a magnetic resonance method is provided in which an RF and gradient coil system are controlled to perform a pre-scan sequence to generate pre-scan information and perform a first imaging sequence to generate first image sequence data. The first image data is reconstructed using the pre-scan information to generate a first image representation. The first imaging sequence data is used to refine the pre-scan information. The RF and gradient coil systems are controlled to perform a second imaging sequence to generate second imaging data. The second imaging sequence data are reconstructed using the refined pre-scan information to generate a second image representation.
One advantage is that total time for a subject in a scanner is reduced.
Another advantage is that pre-scans between sequences due to patient or coil motion are reduced or eliminated.
Another advantage is that the order of scans can be optimized.
Another advantage resides in correcting motion across imaging sequences.
Another advantage resides in accelerating individual sequences using a priori information.
Another advantage is that the accuracy of pre-scan information and reconstructed images are improved.
Another advantage resides in avoiding mis-registration due to motion.
Another advantage resides in replacing corrupted data with uncorrupted data.
Another advantage is that the information from prior images guides the sampling trajectory.
Another advantage is that the parameters used in reconstruction can be optimized using prior images.
Still further advantages of the present invention will be appreciated to those of ordinary skill in the art upon reading and understand the following detailed description.
The invention may take form in various components and arrangements of components, and in various steps and arrangements of steps. The drawings are only for purposes of illustrating the preferred embodiments and are not to be construed as limiting the invention.
With reference to
One or more processors 30 include a sequence controller 32 such as a sequence control computer algorithm, a sequence control module, or the like. As explained in greater detail below, the sequence controller 32 controls the one or more RF transmitters 18, the gradient controller 22, and the one or more RF receivers 20 to conduct a pre-scan magnetic resonance sequence followed by a plurality of different magnetic resonance sequences, such as a T1 weighted imaging sequence, a T2 weighted imaging sequence, a diffusion weighted imaging sequence, or the like. The magnetic resonance signals from the pre-scan sequence are stored in a pre-scan data or information buffer 34. The one or more processors 30 includes the pre-scan information system 36 which derives pre-scan information from the pre-scan data, such as coil sensitivity maps, a B0 map, a B1 map, and the like as is explained in greater detail below.
The sequence controller 32 uses the pre-scan information to adjust the parameters of the first imaging sequence and controls the RF transmitter, RF receivers, and the gradient controller 22 to generate the first imaging sequence which is stored in a k-space data memory 40. The one or more processors 30 further include a reconstruction module, series of program instructions, ASICs or the like. The reconstruction processor 12 reconstructs the first scan data from the k-space memory 40 into a first image representation which is stored in a first image memory 441. The reconstruction is performed using the pre-scan information from the pre-scan information system 36. The pre-scan information system, in turn, uses the first scan data from the k-space memory 40 and data from the reconstructed image from the first image memory 441 to update, refine, and improve the accuracy of the pre-scan information. The sequence controller 32 uses the improved pre-scan information to conduct the second imaging scan which is reconstructed into a second image representation that is stored in a second image representation memory 442. The pre-scan information system 36 again updates, improves, and makes the pre-scan information more accurate. This process is repeated generating the third and subsequent images in the sequence with the pre-scan information being updated, improved, and rendered more accurate before each subsequent scan sequence. Also, k-space or image data from earlier sequences can be used by the reconstruction processor to accelerate or refine the images of later sequences.
With reference to
With reference to
In a sense, the first image scan sequence functions both to generate a first image representation, but also as a pre-scan for a second imaging sequence. When the next sequence ends 60, the resulting imaging data is saved as a reconstructed image and/or saved as intermediate data for later image reconstruction. When a next imaging sequence 70 is started, unlike the prior art, no pre-scan is conducted. Rather, the revised pre-scan information is used instead.
In
As the next imaging sequence 70 begins, pre-scan information is retrieved from the data stores 100′, 110′, 120′, 130′, 140, 150, 160. Specific data loaded prior to the next imaging sequence(s) depends upon what is available and what the next scan can use. The data stores 210 available depend upon the prior sequence(s). For example, periodic motion information is available if previous sequences include the appropriate anatomical regions and techniques to measure periodic motion. If the previous scan is a limb, then periodic motion may not be available. If for example, a previous cardiac imaging sequence is performed, then the cardiac landmarks 160 have already been identified, periodic motion identified 140 and measured for reference, and the maps of pre-scan information updated 100′, 110′, 120′, 130′. These data stores 210 are then used as input to the next imaging sequence 70 data collection, or its image reconstruction. Where creating data stores 210 is performed in either a pre-scan 50 or earlier imaging sequence, later sequences either use or revise the data stores. New data stores are added when new information becomes available. When motion corrupts data collection, prior data stores are used to correct, replace, or refresh the motion corrupted data. The accuracy of image registration is measured and tracked between the different imaging sequences which avoid mis-registration. The data stores 210 are again updated 100″, 110″, 120″, 130″, 140′, 150′, 160′, 170′, 180′ using data from the second imaging sequence 70.
In one embodiment illustrated in
In another example, the first imaging sequence 60 is a T1 weighted imaging sequence with an acceleration factor of 2. The second imaging sequence 70 is a T2 sequence with an acceleration factor of 5. The RF coil sensitivity map 100 is initially created in the pre-scan 50 and placed in a data store 210. The T1 imaging sequence 60 uses and revises the RF coil sensitivity map 100′ in the data store which is then preserved and used in the T2 imaging sequence 70. The T2 imaging sequence 70 can be run faster due to the more accurate and complete RF coil sensitivity map 100′, optimized acquisition trajectory 180, and optimized reconstruction parameter 170 created with the T1 imaging sequence 60. The T2 images are reconstructed using RF coil sensitivity map 100′.
In this example, the T1 image is used to identify the region of the k-space which is of primary interest. In the T2 and subsequent images, the sequence controller can tailor the k-space directory accordingly, e.g., to sample the region of primary interest more heavily.
With reference again to
With reference to
The changes in methodology may be implemented through changes in software. The changes in software are reflected in the user interface where an operator selects the imaging sequences and then the software orders the sequences. The imaging station serves as the user interface or an alternative processor may be used.
The invention has been described with reference to the preferred embodiments. Modifications and alterations may occur to others upon reading and understanding the preceding detailed description. It is intended that the invention be constructed as including all such modifications and alterations insofar as they come within the scope of the appended claims or the equivalents thereof.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/IB2012/055471 | 10/10/2012 | WO | 00 | 4/17/2014 |
| Number | Date | Country | |
|---|---|---|---|
| 61548241 | Oct 2011 | US |