The invention relates to a method and apparatus for identifying image shift. In known image capture or acquisition devices such as the IviewGT (trademark) system available from Elekta AB problems arise with offset of acquired images. Referring to
The invention will be described by way of example with reference to the figures of which:
In overview, a method of identifying an image shift is provided in which a reference element position is identified, for example a faulty pixel or a reference marker. The identified position in a captured image is compared with a predetermined expected position to identify image shift. For example, imaging panel defects can be employed; such defects can appear where the pixels do not behave as expected, for example remaining black or white or displaying another unexpected artefact, or responding differentially compared to other pixels. Where reference markers are employed, these can be identified in a calibration phase or identified by the manufacturer, and are typically filtered out of the image when the image is acquired, but can act as a “finger print” for the panel.
If the acquired image shifts, the position of the reference element will also shift; image processing software can identify the shift and correct the image or prevent the image from being used. As a result, the onus on the user to identify faulty images is significantly reduced, increasing the inherent safety of the imaging device by adjusting, correcting or shifting the image, or discarding it.
The imaging panels can be used, for example, in a radio therapy device.
The device comprises both MR imaging apparatus 112 and radiotherapy (RT) apparatus which may comprise a Linac device. The MR imaging apparatus is shown in cross-section in the diagram. In operation, the MR scanner produces MR images of the patient, and the Linac device produces and shapes a beam of radiation and directs it toward a target region within a patient's body in accordance with a radiotherapy treatment plan. The depicted device does not have the usual ‘housing’ which would cover the MR imaging apparatus 112 and RT apparatus in a commercial setting such as a hospital.
The MR-Linac device 100 depicted in
The RT apparatus comprises a source of radiation 106 and a radiation detector (not shown). Typically, the radiation detector is positioned diametrically opposed to the radiation source 106. The radiation detector is suitable for, and configured to, produce radiation intensity data. In particular, the radiation detector is positioned and configured to detect the intensity of radiation which has passed through the subject. The radiation detector may also be described as radiation detecting means, and may form part of a portal imaging system.
The radiation source 106 may comprise a beam generation system. For a Linac, the beam generation system may comprise a source of RF energy 102, an electron gun 106, and a waveguide 104. The radiation source is attached to the rotatable gantry 116 so as to rotate with the gantry 116. In this way, the radiation source 106 is rotatable around the patient so that the treatment beam 110 can be applied from different angles around the gantry 116. In a preferred implementation, the gantry is continuously rotatable. In other words, the gantry can be rotated by 360 degrees around the patient, and in fact can continue to be rotated past 360 degrees. The gantry may be ring-shaped. In other words, the gantry may be a ring-gantry.
The source 102 of radiofrequency waves, such as a magnetron, is configured to produce radiofrequency waves. The source 102 of radiofrequency waves is coupled to the waveguide 104 via circulator 118, and is configured to pulse radiofrequency waves into the waveguide 104. Radiofrequency waves may pass from the source 102 of radiofrequency waves through an RF input window and into an RF input connecting pipe or tube. A source of electrons 106, such as an electron gun, is also coupled to the waveguide 104 and is configured to inject electrons into the waveguide 104. In the electron gun 106, electrons are thermionically emitted from a cathode filament as the filament is heated. The temperature of the filament controls the number of electrons injected. The injection of electrons into the waveguide 104 is synchronised with the delivery of the radiofrequency waves into the waveguide 104. The design and operation of the radiofrequency wave source 102, electron source and the waveguide 104 is such that the radiofrequency waves accelerate the electrons to very high energies as the electrons propagate through the waveguide 104.
The design of the waveguide 104 depends on whether the Linac accelerates the electrons using a standing wave or travelling wave, though the waveguide typically comprises a series of cells or cavities, each cavity connected by a hole or ‘iris’ through which the electron beam may pass. The cavities are coupled in order that a suitable electric field pattern is produced which accelerates electrons propagating through the waveguide 104. As the electrons are accelerated in the waveguide 104, the electron beam path may be controlled by a suitable arrangement of steering magnets, or steering coils, which surround the waveguide 104. The arrangement of steering magnets may comprise, for example, two sets of quadrupole magnets.
Once the electrons have been accelerated, they may pass, in some Linac configurations, into a flight tube. The flight tube may be connected to the waveguide by a connecting tube. This connecting tube or connecting structure may be called a drift tube. The electrons travel toward a heavy metal target which may comprise, for example, tungsten. Whilst the electrons travel through the flight tube, an arrangement of focusing magnets act to direct and focus the beam on the target.
To ensure that propagation of the electrons is not impeded as the electron beam travels toward the target, the waveguide 104 is evacuated using a vacuum system comprising a vacuum pump or an arrangement of vacuum pumps. The pump system is capable of producing ultra-high vacuum (UHV) conditions in the waveguide 104 and in the flight tube. The vacuum system also ensures UHV conditions in the electron gun. Electrons can be accelerated to speeds approaching the speed of light in the evacuated waveguide 104.
The waveguide includes a source of radiation configured to direct a beam 110 of therapeutic radiation toward a patient positioned on the patient support surface 114. The source of radiation may comprise a heavy metal target toward which the high energy electrons exiting the waveguide are directed. When the electrons strike the target, X-rays are produced in a variety of directions. A primary collimator may block X-rays travelling in certain directions and pass only forward travelling X-rays to produce a treatment beam 110. The X-rays may be filtered and may pass through one or more ion chambers for dose measuring. The beam can be shaped in various ways by beam-shaping apparatus, for example by using a multi-leaf collimator 108, before it passes into the patient as part of radiotherapy treatment.
In some implementations, the source of radiation 106 is configured to emit either an X-ray beam or an electron particle beam. Such implementations allow the device to provide electron beam therapy, i.e. a type of external beam therapy where electrons, rather than X-rays, are directed toward the target region. It is possible to ‘swap’ between a first mode in which X-rays are emitted and a second mode in which electrons are emitted by adjusting the components of the Linac. In essence, it is possible to swap between the first and second mode by moving the heavy metal target in or out of the electron beam path and replacing it with a so-called ‘electron window’. The electron window is substantially transparent to electrons and allows electrons to exit the flight tube.
The subject or patient support surface 114 is configured to move between a first position substantially outside the bore, and a second position substantially inside the bore. In the first position, a patient or subject can mount the patient support surface. The support surface 114, and patient, can then be moved inside the bore, to the second position, in order for the patient to be imaged by the MR imaging apparatus 112 and/or imaged or treated using the RT apparatus. The movement of the patient support surface is effected and controlled by a subject support surface actuator, which may be described as an actuation mechanism. The actuation mechanism is configured to move the subject support surface in a direction parallel to, and defined by, the central axis of the bore. The terms subject and patient are used interchangeably herein such that the subject support surface can also be described as a patient support surface. The subject support surface may also be referred to as a moveable or adjustable couch or table.
The radiotherapy apparatus/device depicted in
The controller is a computer, processor, or other processing apparatus. The controller may be formed by several discrete processors; for example, the controller may comprise an MR imaging apparatus processor, which controls the MR imaging apparatus; an RT apparatus processor, which controls the operation of the RT apparatus; and a subject support surface processor which controls the operation and actuation of the subject support surface. The controller is communicatively coupled to a memory, i.e. a computer readable medium.
The Linac device also comprises several other components and systems as will be understood by the skilled person. For example, in order to ensure the Linac does not leak radiation, appropriate shielding is also provided.
As discussed above, image capture issues can arise in known imaging systems for example of the type discussed above in MR-Linacs as a result of image shift, offset or wraparound. According to
When the image is captured, in instances where there is image shift, an arrangement such as that shown in
It will be noted that the shifted image can be detected in alternative manners, for example by modifying imaging hardware to put reference markers in the image such that rather than having a faulty pixel 302, a reference marker is provided. Once again, once the image is captured, any shift in position of the reference marker can be presented by a shift vector or other transformation representation, and the shift can be rectified by reversing the transformation.
In one embodiment the reference marker can be a pixel or other marker deliberately placed at the time of, or after manufacture of the imaging detector. A reference value, for example an intensity value as a percentage of maximum output, associated with the pixel can be set to permit it to be identified consistently. As a result, the pixel can be identified from one image to the next allowing image shift to be accurately and consistently determined.
In an embodiment specific shapes or patterns of pixels or markers could be inserted to allow them to be differentiated from each other. Yet further, or alternatively, the marker can be provided by predefining the location value of one or more pixels to provide an encoded geometric location of the pixel or pixels. A coded pattern can, additionally, reduce the risk of areas being transposed by failures of the device, for example where the device is a ‘tiled’ device. Imaging devices based for example on amorphous silicon sensors can be singular or tiled, but in either case the readout and processing electronics are often modular and can encounter failures in addressing potential causes of incorrect imaging, for example distinguishing between a transposition or a wrap—again knowledge of the relative position/shape/coding of multiple reference markers can provide additional reconstruction information.
Operation of the approach is shown in
It will be noted that the approaches described herein can be implemented in any appropriate manner. For example, where images are captured using a CCD panel, then in a calibration step the bad pixel location can be identified. This can be a standard calibration process using data that is currently used to edit out faulty pixels in the acquired image or can be an additional calibration stage specifically to identify the location for subsequent steps as discussed above. The image capture panel can be of any appropriate kind for example the Iview or XVI panels such as those used in the Elekta Unity product. Alternatively, and as discussed above, the reference marker can be deliberately introduced by having an inactive or otherwise differentiated pixel in the capture array, the position of which is known from manufacture information or calibration and used in the image shift detection approach as discussed in more detail above.
As discussed above the imaging panel can be used in any appropriate apparatus for example a radiotherapy device. Any type of appropriate imaging hardware can be used, for example any type of readout device where a known reference marker or an encoded pattern is used to validate (and reject) or correct the image data. It will further be seen that by harnessing the information provided by faulty pixel location the lifetime of the device can be prolonged rather than simply discarding the device as faulty.
Number | Date | Country | Kind |
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2018757.1 | Nov 2020 | GB | national |
Filing Document | Filing Date | Country | Kind |
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PCT/EP2021/083223 | 11/26/2021 | WO |