The following relates generally to the imaging arts, remote imaging assistance arts, remote imaging examination monitoring arts, quality assurance procedure arts, and related arts.
Regular quality assurance (QA) of a medical imaging system ensures consistent diagnostic image quality. Depending on the modality and the image quality assurance standards (QAS) adopted by a given healthcare provider, QA procedures can be performed on daily, weekly, or monthly bases with varying degrees of complexity. Depending on the level of complexity, medical imaging system QA is often time consuming and can require a set of specialized materials and tools (software/hardware). Furthermore, to perform these procedures, trained staff, such as a medical physicist or a corresponding service engineer, can also be required.
A typical QA procedure used for assessing a medical imaging system may employ a selected one of a set of standardized quality phantoms, and tools to support the measurements. The quality tests are then run by a service engineer (on site or remotely) together with a radiology technologist (RT). The data acquired during such scans is processed on the machine and a report is be generated to detect any irregularities. More complex QA tasks, and QA tasks for certain modalities, may involve the physical presence of either a service engineer (SE) or medical physicist on site. It typically is not feasible for the manufacturer to send service engineers to oversee routine daily or weekly QA routines. Furthermore, in the case of an SE supporting the RT remotely, the lack of visual information and more comprehensive verification of phantom or tool positioning can lead to reduced measurement quality for QA tasks overseen remotely by the SE.
The following discloses certain improvements to overcome these problems and others.
In one aspect, a non-transitory computer readable medium stores instructions executable by at least one electronic processor to perform a method of monitoring a quality assurance (QA) procedure performed using a medical device. The method includes receiving a signal indicating a start of the QA procedure; analyzing video of the medical device acquired after receiving the signal to detect one or more errors during the QA procedure; and providing a remedial action addressing the detected one or more errors.
In another aspect, an apparatus includes a medical imaging device; and instructions stored in a non-transitory computer readable medium executable by at least one electronic processor to perform a method of monitoring a QA procedure performed using the medical imaging device. The method includes receiving an image acquired by the medical imaging device during the QA procedure; analyzing the received image to identify a deficiency of the medical imaging device; determining an adjustment to the medical imaging device for resolving the identified deficiency of the medical imaging device; and proposing the adjustment via a display device.
In another aspect, a method of monitoring a QA procedure performed using a medical device includes receiving a signal indicating a start of the QA procedure; analyzing video of the medical device acquired after receiving the signal to detect one or more errors during the QA procedure; providing a remedial action addressing the detected one or more errors; displaying the video of the medical device on a remote expert workstation located remotely from the medical device; and providing two-way communication between the remote expert workstation and an electronic device disposed with the medical device to perform the remedial action.
One advantage resides in providing for a QA procedure with support from a remote expert to a local operator performing the QA procedure.
Another advantage resides in providing for a QA procedure for a medical imaging device with assistance in aspects such as selection and placement of an imaging phantom.
Another advantage resides in providing for a QA procedure with immediate analysis of QA images and actionable guidance for improving imaging quality based on the analysis.
Another advantage resides in reduced errors, repeats, and reduced wasted time for medical procedures.
A given embodiment may provide none, one, two, more, or all of the foregoing advantages, and/or may provide other advantages as will become apparent to one of ordinary skill in the art upon reading and understanding the present disclosure.
The example embodiments are best understood from the following detailed description when read with the accompanying drawing figures. It is emphasized that the various features are not necessarily drawn to scale. In fact, the dimensions may be arbitrarily increased or decreased for clarity of discussion. Wherever applicable and practical, like reference numerals refer to like elements.
The following is motivated in part by the recognition made herein, based on feedback obtained from medical imaging device service engineers, which has identified problems with quality assurance (QA) procedures as a prominent source of unnecessary product servicing and component returns. In a typical QA procedure, an object, such as an imaging phantom, is used as a test subject, and imaging system performance is assessed based on acquired images of the phantom. In practice, it appears that customers (e.g., hospital radiology departments and other medical imaging device operators) are commonly performing QA procedures with the phantom and/or auxiliary components such as MR imaging coils misplaced, or even using the wrong phantom. These mistakes in performing QA procedures can lead to unnecessary service calls and reduced customer satisfaction.
Disclosed herein are approaches for remotely supervising QA procedures. A camera is placed in the imaging bay, and possibly a second camera may be arranged to image the examination region (e.g., inside the bore of an MRI or CT). The camera provides real time visual monitoring of a QA procedure in progress.
The disclosed approaches advantageously leverage infrastructure that may already be present in the context of a Radiology operations command center (ROCC) or similar imaging assistance system, which provides infrastructure for imaging centers or integrated delivery networks (IDNs) to interact with pools of technologist (“tech”; also referred to herein as “radiation technologist” or “RT”) talent to share tech expertise across an entire imaging network. By providing a communication channel (e.g., telephonic, videoconferencing, or so forth) and remote imaging device controller console sharing, an ROCC empowers more experienced techs to provide guidance and oversight for junior techs when working with an imaging modality or workflow they may not be familiar or comfortable with. The ROCC infrastructure may include a bay camera and possibly also a “bore” camera arranged to image the examination region, and these can be repurposed as disclosed herein to provide automated or semi-automated QA support.
The QA procedure supervision may be provided by a remote service engineer (RSE), or may be provided in an automated fashion using a supervisory script or artificial intelligence (AI) component. Feedback from the RSE or AI supervisor to the on-site radiology technologist (RT) performing the QA procedure can be provided via an application program running on a computer or mobile device, or in the case of RSE supervision by telephonic or videoconference link.
Various approaches can be used to detect errors in the QA procedure in progress based on the video feedback. The phantom can be identified using a suitable object recognition component, such as a convolutional neural network (CNN) trained to recognize the correct phantom versus other likely incorrect phantoms (e.g., a different one from another manufacturer or that is used in a different type of QA procedure). To detect mispositioning of the phantom or other component, if a light visor is used for aligning the phantom or other component then the camera can directly observe any displacement between the phantom or other component and the alignment mark(s) provided by the light visor. If the camera is a three-dimensional (3D) camera then this is straightforward. If the camera is a two-dimensional (2D) camera, then a suitable algorithm can be used to estimate 3D position from the 2D camera image, Such algorithms can include, for example, deep learning methods to estimate the depth information including a distance from camera to each object point and therefore reconstruct the 3D position of the object (see, e.g., e.g. PlaneNet: Piece-wise Planar Reconstruction from a Single RGB Image et al 2018), using geometrical relationships between 3D world coordinates and 2D camera image coordinates using known object dimensions, known camera properties (e.g., intrinsic parameter, extrinsic parameters, location, etc.) and the detected object in the 2D image (see, e.g., Bradski, G., and A. Kaehler. Learning OpenCV: Computer Vision with the OpenCV Library. Sebastopol, CA: O'Reilly, 2008).
A common problem in QA procedures is misorientation or (in the case of deformable phantoms) incorrect shaping of the phantom. This can be detected using a CNN or other machine learning component in a fashion similar to the object recognition component.
Various remedial actions can be taken. In one approach, the RSE or automated script or AI supervisor provides verbal or visual feedback indicating a wrong phantom or misalignment, or other detected errors in the QA procedure in progress. In the case of a wrong phantom or misshapen deformable phantom, a display can show the correct phantom/shape.
In some embodiments disclosed herein, a projector is integrated with the imaging device to provide the feedback. For example, a projector could project an image of the correct phantom and its correct position on the table. A holographic projector could even show this in 3D.
In other embodiments disclosed herein, proactive remediation of mistakes being made during the QA procedure is also contemplated. For example, if the table has automated positioning that is remotely controllable by the script or AI supervisor then this can be used to automatically correct translational mispositioning on the table so that the phantom is positioned at scanner isocenter (i.e., center of the field-of-view) during the QA procedure. In the case of MRI, the magnetic field gradients defining imaging isocenter could be adjusted to provide analogous translational correction by moving the isocenter to coincide with the position of the imaging phantom.
In another embodiment, an augmented reality (AR) headset or AR eyeglasses could be used to provide the feedback as superimposed AR content. A forward-looking camera of the AR headset or glasses could also augment or be substituted for the bay and/or bore camera(s) to provide video of the QA procedure.
The disclosed system is also contemplated to provide various validation aspects based on the images acquired by the imaging device during the QA procedure. For example, an image feature that can be linked to an a priori known underlying cause can be recognized by analysis of the QA procedure images and the RT advised to check for that possible underlying cause. As a specific example, the system may guide the RT through an imaging device adjustment process, acquiring further QA procedure images, and so forth until the issue is resolved.
With reference to
The image acquisition device 2 can be a Magnetic Resonance (MR) image acquisition device, a Computed Tomography (CT) image acquisition device; a positron emission tomography (PET) image acquisition device; a single photon emission computed tomography (SPECT) image acquisition device; an X-ray image acquisition device; an ultrasound (US) image acquisition device; or a medical imaging device of another modality. The imaging device 2 may also be a hybrid imaging device such as a PET/CT or SPECT/CT imaging system. While a single image acquisition device 2 is shown by way of illustration in
As used herein, the term “medical imaging device bay” (and variants thereof) refer to a room containing the medical imaging device 2 and also any adjacent control room containing the medical imaging device controller 10 for controlling the medical imaging device. For example, in reference to an MRI device, the medical imaging device bay 3 can include the radiofrequency (RF) shielded room containing the MRI device 2, as well as an adjacent control room housing the medical imaging device controller 10, as understood in the art of MRI devices and procedures. On the other hand, for other imaging modalities such as ultrasound (US) imaging, the imaging device controller 10 may be located in the same room as the imaging device 2, so that there is no adjacent control room and the medical bay 3 is only the room containing the medical imaging device 2. The imaging device controller 10 includes an electronic processor 20′, at least one user input device such as a mouse 22′, a keyboard, and/or so forth, and a display device 24′. The imaging device controller 10 presents a device controller graphical user interface (GUI) 28′ on the display 24′ of the imaging device controller 10, via which the local operator LO accesses device controller GUI screens for entering the imaging examination information such as the name of the local operator LO, the name of the patient and other relevant patient information (e.g. gender, age, etc.) and for controlling the (typically robotic) patient support to load the patient into the bore or imaging examination region of the imaging device 2, selecting and configuring the imaging sequence(s) to be performed, acquiring preview scans to verify positioning of the patient, executing the selected and configured imaging sequences to acquire clinical images, display the acquired clinical images for review, and ultimately store the final clinical images to a Picture Archiving and Communication System (PACS) or other imaging examinations database. In addition, while
As diagrammatically shown in
In other embodiments, the live video feed 17 of the display 24′ of the imaging device controller 10 is, in the illustrative embodiment, provided by a video cable splitter 15 (e.g., a DVI splitter, a HDMI splitter, and so forth). In other embodiments, the live video feed 17 may be provided by a video cable connecting an auxiliary video output (e.g. aux vid out) port of the imaging device controller 10 to the remote workstation 12 operated by the remote expert RE. Alternatively, a screen mirroring data stream 18 is generated by screen sharing software 13 running on the imaging device controller 10 which captures a real-time copy of the display 24′ of the imaging device controller 10, and this copy is sent from the imaging device controller 10 to the remote workstation 12. Other approaches besides the illustrative video cable splitter 15 or screen sharing software 13 are contemplated for capturing a real-time copy of the display 24′ of the imaging device controller 10 which is then sent to the workstation 12 of the remote expert RE. While in an ROCC this real-time copy of the display 24′ of the imaging device controller 10 is used to provide status information to the remote expert RE for use in assisting the local operator LO, in embodiments disclosed herein the real-time copy of the display 24′ of the imaging device controller 10 is also leveraged (optionally along with other available information) to determine one or more performance metrics of the local operator LO.
The communication link 14 also provides a natural language communication pathway 19 for verbal and/or textual communication between the local operator LO and the remote expert RE, in order to enable the latter to assist the former in performing the imaging examination. For example, the natural language communication link 19 may be a Voice-Over-Internet-Protocol (VOIP) telephonic connection, a videoconferencing service, an online video chat link, a computerized instant messaging service, or so forth. Alternatively, the natural language communication pathway 19 may be provided by a dedicated communication link that is separate from the communication link 14 providing the data communications 17, 18, e.g., the natural language communication pathway 19 may be provided via a landline telephone. In another example, the natural language communication pathway 19 may be provided via an ROCC device 8, such as a mobile device (e.g., a tablet computer or a smartphone), or can be a wearable device worn by the local operator LO, such as an augmented reality (AR) display device (e.g., AR goggles), a projector device, a heads-up display (HUD) device, etc., each of which having a display device 36. For example, an “app” can run on the ROCC device 8 (operable by the local operator LO) and the remote workstation 12 (operable by the remote expert RE) to allow communication (e.g., audio chats, video chats, and so forth) between the local operator and the remote expert.
The medical imaging device controller 10 in the medical imaging device bay 3 also includes similar components as the remote workstation 12 disposed in the remote service center 4. Except as otherwise indicated herein, features of the medical imaging device controller 10 disposed in the medical imaging device bay 3 similar to those of the remote workstation 12 disposed in the remote service center 4 have a common reference number followed by a “prime” symbol (e.g., processor 20′, display 24′, GUI 28′) as already described. In particular, the medical imaging device controller 10 is configured to display the imaging device controller GUI 28′ on a display device or controller display 24′ that presents information pertaining to the control of the medical imaging device 2 as already described, such as imaging acquisition monitoring information, presentation of acquired medical images, and so forth. It will be appreciated that the real-time copy of the display 24′ of the controller 10 provided by the video cable splitter 15 or the screen mirroring data stream 18 carries the content presented on the display device 24′ of the medical imaging device controller 10. The communication link 14 allows for screen sharing from the display device 24′ in the medical imaging device bay 3 to the display device 24 in the remote service center 4. The GUI 28′ includes one or more dialog screens, including, for example, an examination/scan selection dialog screen, a scan settings dialog screen, an acquisition monitoring dialog screen, among others. The GUI 28′ can be included in the video feed 17 or provided by the video cable splitter 15 or by the mirroring data stream 17′ and displayed on the remote workstation display 24 at the remote location 4.
Furthermore, as disclosed herein the server 14s performs a method or process 100 of monitoring a quality assurance (QA) procedure performed using the medical device 2. The QA procedure monitoring method 100 advantageously leverages information sources provided by the ROCC, such as the content of the display 24′ of the imaging device controller 10.
With reference to
With continuing reference to
At an operation 106, a remedial action addressing the detected one or more errors is provided. The remedial action operation 106 can also be performed in a variety of manners. In one example, a visualization 40 of the remedial action is displayed on the display device 36 of the ROCC device 8 (e.g., regardless of whether the ROCC device 8 comprises a tablet or smartphone, an AR device (so that the AR content of the remedial action is superimposed on the medical device 2), a projector, an HUD device, and so forth) so that it is observable by the local operator LO. In another example, the remedial action operation 106 can include controlling a position of the medical device 2 (e.g., moving a patient bench of the medical device 2). In a further example, the remedial action operation 106 can include performing a validation process to determine if the detected one or more errors corresponds to a predetermined matter with the medical device 2.
In a particular embodiment, the medical device 2 comprises a medical imaging device 2. In such embodiments, the signal receiving operation 102 includes receiving an image acquired by the medical imaging device during the QA procedure in which the image comprises the signal that indicates a start of a QA procedure. The analysis operation 104 comprises analyzing the received image to identify a deficiency (e.g., an image quality issue) of the medical imaging device 2, and determining an adjustment to the medical imaging device 2 for resolving the identified deficiency of the medical imaging device 2.
In one example, the remedial action operation 106 comprises proposing the adjustment via the display device 36 of the ROCC device 8. In another example, the remedial action operation 106 includes, when the ROCC device 8 is a HUD device 8, determining a mispositioning of an object based on position of the object compared with alignment marks produced by the projector and observed in the video 17. In another example, the remedial action operation 106 includes, when the ROCC device 8 is a projector device 8, projecting a marker indicating a correct placement of an object on an imaging support of the imaging device 2. In another example, the remedial action operation 106 can include controlling a robotic subject support of the medical imaging device 2 or magnetic field gradient coils of an MRI imaging device 2 to correct a mispositioning of a phantom relative to an isocenter of the imaging device 2.
Referring back to
The remote workstation 12 of the selected remote expert RE, and/or the medical imaging device controller 10 being run by the local operator LO, is configured to perform a method or process 200 for providing assistance from the remote expert RE to the local operator LO. For brevity, the method 200 will be described as being performed by the remote workstation 12. The non-transitory storage medium 26 stores instructions which are readable and executable by the at least one electronic processor 20 (of the workstation 12, as shown, and/or the electronic processor or processors of a server or servers on a local area network or the Internet) to perform disclosed operations including performing the method or process 200.
With reference to
The following describes another example of the method 100. In order to enable a more simplified workflow during the QA of medical imaging devices 2, a semi-automated approach comprising several key steps is proposed and is summarized in a method 300 depicted as a flowchart shown in
At an operation 302, a notification from either the RSE, the system itself or based on the QAS employed in the healthcare institution is provided. Any frequency can be considered, however in the case of involvement of the RSE it may be limited by the service contract. From the manufacturer all the necessary phantom(s) and tool(s) are supplied. If these do not suffice the required QAS of the healthcare provider, additional ones can also be incorporated in the overall approach. In another scenario, the RT starts the QA procedure on his or her own, in which case the triggering operation 302 may be omitted.
At an operation 304, once the RT is notified with the signal, the RT can configure the medical device 2 (e.g., X-ray tube/detector placement, coil placement, etc.) and correctly place the required items. At some point during either operation 302 or operation 304 the QA procedure supervision is initiated. This can occur by various mechanisms. In one approach, the operation 302 notifies both the RT and the RSE of the start of the QA procedure. In another approach, the operation 302 notifies the RT of the start of the QA procedure and also invokes the AI-based supervision. In another approach, the RT manually calls the RSE or manually starts the AI-based supervision as part of the setup operation 304. In another approach, if the QA procedure entails bringing up a special QA procedure menu on the controller of the imaging device 2 then the RSE notification or AI-based supervision invocation can be triggered when the special QA procedure menu is brought up. These are merely some illustrative approaches.
At an operation 306, in one embodiment, the medical bay 3 features the digital camera 16, either integrated in the medical device 2 or placed externally while allowing sufficient visibility. Throughout this process the RT is guided by the RSE or by the medical device 2 based on visual data coming from the camera 17. In case of the RSE, audio-visual information 17, 18 is conveyed to the ROCC device 8 to support the RT. In the case of automatic guidance by the medical device 2, recognition algorithms are employed on the camera's visual feed to verify the actions of the RT.
In some embodiments, for the QA procedure, quality phantoms need to be positioned in a specific way on the patient table, often requiring special phantom holders. After positioning of the phantom, a light visor is used for alignment and then the phantom is moved into the iso-center of the magnet using the patient table tumble switch. During this QA procedure, the display device 36 of the ROCC device 8 next to a bore of the medical imaging device 2 shows the position overlaid in red onto a table to where the phantom shall then be put. The image stream 17 of the camera 16 is used to detect the phantom on the patient table. To do so, machine-learning (ML) based algorithms (i.e., the CNN 48) using pre-trained image nets (e.g., U-net) are suitable. The algorithm identifies the phantom (if it is the correct phantom). A notification that the phantom is incorrect is displayed on the ROCC device 8, or communicated via the natural language pathway 19. Optionally, the automatically identified imaging phantom may also be highlighted on the ROCC device 8 by a bounding box or the like superimposed on the video display. As another variant, if the incorrect imaging phantom is being used, the ROCC device 8 may display an image of the correct image phantom to assist the RT in selecting the correct phantom.
If the CNN 48 determines that the phantom is the correct one, then the position and orientation of the phantom is determined. Once the phantom is placed on the correct location on the table, the phantom position location color on the ROCC device 8 is switched to green, and optionally a voice command is given to the RT to step back from the patient table and leave the room indicating that the table is now moving to the correct scanning position and once the door is closed the scan starts. Alternatively, if the imaging phantom is incorrectly placed then a valid region for the phantom is shown on the ROCC device 8. The phantom position is determined by the CNN 48 by evaluating the images and the offset to the correct position in the medical imaging device 2 is calculated and the table is moved automatically into the medical imaging device 2. If a projector is present, then the appropriate phantom position region is suitably projected on top of the table. Specific phantom holders are sometimes required, but in case it is sufficient to accurately know the position of the phantom it is determined by the CNN 48 and then communicated to the medical imaging device 2 for correct table positioning but also adaptation of the QA scan protocol adjustment with respect to the correct setting of the imaging volume.
In some embodiments, the RT is supplied with the ROCC device 8 as an AR headset or glasses 8 by the manufacturer. The AR glasses allow the RSE or the CNN 48 to access to a visual feed coming from the RT's viewpoint. In return the RT interactively receives annotations and audio/text to the AR glasses 8 themselves in order to guide them through the set-up procedure.
At an operation 308, once the QA set-up is deemed acceptable, a set of measurements are executed. These measurements run through a set of algorithms employed on the medical imaging device 2. In some QA procedures, the measurements involve acquiring one or more images of the imaging phantom using the medical imaging device 2. The measurements may be the acquired images per se, or the measurements may be information extracted from the acquired images by post-acquisition image processing. For example, the measurements might include a measurement of a spatial resolution obtained by the acquired images, or a measurement of pixel intensities, of image contrast metrics, and/or so forth. Where the measurements involve post-acquisition image processing, they may be done automatically by the controller of the medical imaging device 2 or manually (or semi-manually) by the RT.
At an operation 310, a verification of phantom placement is performed to assess the quality metrics obtained in operation 308. In some examples, the CNN 48 can analyze the quality metrics to learn from new performed procedures. The QA metrics and placement information are presented in the form of textual information, dashboards, and images to the RT (via the ROCC device 8) and RSE (via the remote workstation 12).
If adjustments to item placement or measurements are required, then the respective operations 304-310 are repeated as indicated by the flowback arrow in
In one example, a required adjustment can include adjusting a coil placed on the patient (e.g., a head coil or a neck coil) during an imaging procedure. In another example, a different type of coil can be substituted for a previously-used coil. In another example, a required adjustment can include changing a phantom used during the imaging procedure. In another example, a required adjustment can further include using one or more pencil dosimeters placed in an acrylic phantom to be used in CT dose index (CTDI) dose measurements. The placement of the dosimeter(s) can be verified by a camera or imaging data acquired by the medical imaging device 120. These are merely examples, and should not be construed as limiting.
The preceding description of the disclosed embodiments is provided to enable any person skilled in the art to practice the concepts described in the present disclosure. As such, the above disclosed subject matter is to be considered illustrative, and not restrictive, and the appended claims are intended to cover all such modifications, enhancements, and other embodiments which fall within the true spirit and scope of the present disclosure. Thus, to the maximum extent allowed by law, the scope of the present disclosure is to be determined by the broadest permissible interpretation of the following claims and their equivalents and shall not be restricted or limited by the foregoing detailed description.
In the foregoing detailed description, for the purposes of explanation and not limitation, representative embodiments disclosing specific details are set forth in order to provide a thorough understanding of an embodiment according to the present teachings. Descriptions of known systems, devices, materials, methods of operation and methods of manufacture may be omitted so as to avoid obscuring the description of the representative embodiments. Nonetheless, systems, devices, materials, and methods that are within the purview of one of ordinary skill in the art are within the scope of the present teachings and may be used in accordance with the representative embodiments. It is to be understood that the terminology used herein is for purposes of describing particular embodiments only and is not intended to be limiting. The defined terms are in addition to the technical and scientific meanings of the defined terms as commonly understood and accepted in the technical field of the present teachings.
It will be understood that, although the terms first, second, third, etc. may be used herein to describe various elements or components, these elements or components should not be limited by these terms. These terms are only used to distinguish one element or component from another element or component. Thus, a first element or component discussed below could be termed a second element or component without departing from the teachings of the inventive concept.
The terminology used herein is for purposes of describing particular embodiments only and is not intended to be limiting. As used in the specification and appended claims, the singular forms of terms “a,” “an” and “the” are intended to include both singular and plural forms, unless the context clearly dictates otherwise. Additionally, the terms “comprises,” “comprising,” and/or similar terms specify the presence of stated features, elements, and/or components, but do not preclude the presence or addition of one or more other features, elements, components, and/or groups thereof. As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items.
Unless otherwise noted, when an element or component is said to be “connected to,” “coupled to,” or “adjacent to” another element or component, it will be understood that the element or component can be directly connected or coupled to the other element or component, or intervening elements or components may be present. That is, these and similar terms encompass cases where one or more intermediate elements or components may be employed to connect two elements or components. However, when an element or component is said to be “directly connected” to another element or component, this encompasses only cases where the two elements or components are connected to each other without any intermediate or intervening elements or components.
The present disclosure, through one or more of its various aspects, embodiments and/or specific features or sub-components, is thus intended to bring out one or more of the advantages as specifically noted below. For purposes of explanation and not limitation, example embodiments disclosing specific details are set forth in order to provide a thorough understanding of an embodiment according to the present teachings. However, other embodiments consistent with the present disclosure that depart from specific details disclosed herein remain within the scope of the appended claims. Moreover, descriptions of well-known apparatuses and methods may be omitted so as to not obscure the description of the example embodiments. Such methods and apparatuses are within the scope of the present disclosure.
Number | Date | Country | Kind |
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22164389.3 | Mar 2022 | EP | regional |
Filing Document | Filing Date | Country | Kind |
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PCT/EP2022/081894 | 11/15/2022 | WO |
Number | Date | Country | |
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63285248 | Dec 2021 | US |