The disclosure relates generally to diagnostic imaging and in particular to radiographic imaging systems used for obtaining volume images of patient extremities.
3-D volume imaging has proved to be a valuable diagnostic tool that offers significant advantages over earlier 2-D radiographic imaging techniques for evaluating the condition of internal structures and organs. 3-D imaging of a patient or other subject has been made possible by a number of advancements, including the development of high-speed imaging detectors, such as digital radiography (DR) detectors that enable multiple images to be taken in rapid succession.
Cone beam computed tomography (CBCT) or cone beam CT technology offers considerable promise as one type of diagnostic tool for providing 3-D volume images. Cone beam CT systems capture volumetric data sets by using a high frame rate digital radiography (DR) detector and an X-ray source, typically affixed to a gantry that rotates about the object to be imaged, directing, from various points along its orbit around the subject, a divergent cone beam of X-rays toward the subject. The CBCT system captures projections throughout the rotation, for example, one 2-D projection image at every degree of rotation. The projections are then reconstructed into a 3D volume image using various techniques. Among well known methods for reconstructing the 3-D volume image from the 2-D image data are filtered back projection and iterative algebraic reconstruction approaches.
Recent advances in CBCT offer improved capability for volume imaging of patient extremities, such as portions of the leg, arm, and shoulder, for example. A CBCT system for providing this function is described, for example, in commonly assigned U.S. Pat. No. 8,348,506 entitled “Extremity imaging apparatus for cone beam computed tomography” to Yorkston et al., incorporated herein by reference. Using this type of system, highly detailed volume images of the complex bone structures and joint arrangements characteristic of extremities can be obtained and analyzed as a useful diagnostic tool.
While CBCT has proved to be of valuable assistance for extremity diagnosis and treatment, however, there are some problems that constrain the overall accuracy of the information that is obtained. For example, one aspect of interest for extremity diagnosis and treatment and for bone condition overall relates to bone material density (BMD). Quantitative Computed Tomography (QCT) is a technique used to measure BMD. QCT obtains the attenuation data acquired for each bone voxel, expressed in Hounsfield Units (HU), and interprets this data as being linearly related to bone mineral density at that spatial location. Straightforward conversion of the HU data to BMD information can thus provide highly useful information to the diagnostician.
Obtaining accurate Hounsfield Unit data from the acquired image content, however, requires calibration. Most standard CT systems have a platform, e.g., a bed, used to move the patient into and through the scanning system. For stationary QCT systems there is often a set of calibration targets implanted into the bed or other platform in order to assure that the acquired data response of the radiography detector can be calibrated relative to objects of known HU values. Various alternative methods have been proposed for calibration during CT image acquisition, such as using a solid phantom placed beneath or against the patient, addressing the need for regular, ongoing calibration procedure without taking the imaging system out of service.
Methods suitable for CT system calibration, however, are not applicable to CBCT systems, particularly for portable systems and extremity imaging apparatus that are designed to adapt to variable patient location, limb orientation, and positioning. No bed or stationary platform is used; instead, the patient may be standing or sitting, according to the exam type, and may be instructed to extend the extremity of interest to an appropriate depth within the bore of an imaging system.
Executing or verifying calibration as a separate procedure before each patient imaging examination proves to be impractical, requiring considerable time, an experienced operator, and high expense. Moreover, as with computed tomography systems in general, maintaining ongoing accuracy of the CBCT imaging apparatus can be a problem due to spatial drift. With respect to Hounsfield units (HU), for some CBCT apparatus for example, there can be characteristic drift of HU values perceptible along the axial direction during scanning of patient anatomy. Change in system response can also be a consideration, with frequent re-calibration recommended to minimize drift between exams.
Thus, it can be seen that there would be significant benefit in a CBCT calibration solution that is suitable for extremity imaging.
It is an object of the present disclosure to advance the art of diagnostic imaging and calibration for acquiring volume images of extremity body parts, particularly jointed or load-bearing, paired extremities such as knees, legs, ankles, fingers, hands, wrists, elbows, arms, and shoulders.
It is a feature of the present disclosure that it provides a mechanism for straightforward, automated calibration of the CBCT apparatus without requiring extensive operator training or procedures and without discomfort to the patient.
According to an aspect of the present disclosure there is provided a wearable calibration target comprising: a band that is configured to wrap about a patient's limb; and one or more calibration patches coupled to the band, wherein each of the one or more calibration patches is formed from a material having a known attenuation to X-ray radiation.
These objects are given only by way of illustrative example, and such objects may be exemplary of one or more embodiments of the disclosure. Other desirable objectives and advantages inherently achieved by the disclosure may occur or become apparent to those skilled in the art. The invention is defined by the appended claims.
The foregoing and other objects, features, and advantages of the invention will be apparent from the following more particular description of the embodiments of the invention, as illustrated in the accompanying drawings. The elements of the drawings are not necessarily to scale relative to each other.
The following is a detailed description of the preferred embodiments of the invention, reference being made to the drawings in which the same reference numerals identify the same elements of structure in each of the several figures.
In the context of the present disclosure, the term “extremity” has its meaning as conventionally understood in diagnostic imaging parlance, referring to knees, legs, ankles, fingers, hands, wrists, elbows, arms, and shoulders and any other anatomical extremity. The term “subject” is used to describe the extremity of the patient that is imaged, such as the “subject leg”, for example. The term “paired extremity” is used in general to refer to any anatomical extremity wherein normally two or more are present on the same patient. In the context of the present invention, the paired extremity is not imaged unless necessary; only the subject extremity is imaged.
To describe the present invention in detail, a number of the examples given herein for embodiments of the present invention focus on imaging of the load-bearing lower extremities of the human anatomy, such as the leg, the knee, the ankle, and the foot, for example. However, these examples are considered to be illustrative and non-limiting.
In the context of the present disclosure, the term “arc” or, alternately, “circular arc”, has its conventional meaning as being a portion of a circle of less than 360 degrees or, considered alternately, of less than 2π radians for a given radius.
The term “actuable” has its conventional meaning, relating to a device or component that is capable of effecting an action in response to a stimulus, such as in response to an electrical signal, for example.
As used herein, the term “energizable” relates to a device or set of components that perform an indicated function upon receiving power and, optionally, upon receiving an enabling signal.
An extremity imaging apparatus for Cone Beam Computed Tomography is described in WO 2014/058775 (Litzenberger) filed as PCT/US2013/063673, and in WO 2014/058771 (Litzenberger) filed as PCT/US2013/063666, both of which are incorporated herein in their entirety by reference. The imaging apparatus for cone beam computed tomography imaging of an extremity of a patient includes: a support structure that includes a support column; a vertical translation element for positioning in a height direction to a height position along the support column, and a scanner.
The perspective view of
By way of illustrative example,
An embodiment of the present disclosure addresses the need for providing a calibration target to facilitate automated calibration of a CBCT apparatus by providing one or more calibration targets in the form of a calibration target device. In a preferred arrangement, the calibration target device is a wearable device, such as in the form of a band or bracelet, that can be configured to be worn/wrapped about an arm, wrist, leg, or other limb or otherwise fitted around/adjacent/near the imaged extremity or configured to be attached to a piece of cloth/clothing fitted about the arm, wrist, leg, or limb.
The calibration target device can include one or more discrete/individual calibration target elements or patches of the same or different materials, arranged so that these target elements can be identified for processing in either the individual projection images or the reconstructed volume image.
The perspective view of
Each calibration target patch 50 is formed from a suitable radio-opaque material having a known/predetermined size and exhibiting a known/predetermined attenuation to X-ray radiation, allowing straightforward computation of HU values. Patches 50 can be formed from materials of the same or different radiometric densities and any number of patches 50 can be used.
According to an embodiment of the present disclosure, patches 50 are formed from reference standards that are conventionally used in the CT calibration arts, formed of materials such as calcium hydroxyapatite, potassium phosphate, and distilled water. Other suitable radio-opaque materials for calibration, wherein the materials have known/predetermined attenuation to X-ray energy, could similarly be used.
The arrangement of calibration target elements/patches 50 can be configured according to the exam type. For example, particular practitioners may consider different patches 50 of particular materials to be more useful for imaging one type of limb than for imaging another type of limb.
Calibration target elements or patches 50 can be of any suitable shape and size, including plate-shaped, spherical, or other geometric shape. Shapes can relate to the material that is used in the patch; different materials could be provided as patches 50 having different shapes and colors. The patches 50 can have the corresponding reference material encased, such as in a radio-opaque plastic or other material. Patches 50 can be re-positioned around the band, shifted in position (i.e., slideably movable), and can be added to or removed from wearable target device 60 as needed. Patches 50 can be connected/coupled to a support 62 (illustrated as a band/bracelet) using any of a number of type of clips, clasps, snaps, fittings, adhesives, string or connective material, hook-and-loop fasteners, or other mountings/connectors/fasteners. As such, the calibration patches 50 can be removably attachable to band 62. That is, patch 50 can be attached and detached from band 62 without the destruction of patch 50. In such a manner, patches 50 of calibration target device 60 are disposed/positioned relative to a limb of a patient.
In one embodiment, patches 50 can dangle from portions of band 62, so that the calibration target elements are spaced apart from the patient's skin.
In an alternate embodiment, calibration target elements or patches 50 are built into the band 62, such as woven or sewed into the band, protected from contact. To promote sanitary conditions, band 62 can be comprised of an anti-bacterial material.
According to another alternate embodiment of the present disclosure, radiotransparent band 62 can extend over or around the joint or other extremity part to be imaged, covering the anatomy of interest with radiotransparent portions of the band and providing calibration target elements or patches 50 along outer edges of the band 62.
Band 62 can be a fixed circumferential size or can be adjustable to a number of discrete size settings. Band 62 can be stiff, such as a hinged ring or shell, or can be conformal and flexible, such as formed from a cloth or flexible synthetic material that conforms readily to the outer surface shape of the limb, fitting comfortably against the skin or clothing of the patient. Band 62 can be washable or disposable following removal of patches 50. Different sizes/colors of band 62 can be used for patients of different dimensions. Band 62 can be formed from a radio-transparent material.
Wearable target device 60 can be elastic and can have a fastener or clasp 52, such as a Velcro® brand hook-and-loop fastener, buckle, or other latching or fastening mechanism, such as a lacing mechanism, for example. Clasp 52 can allow adaptable sizing of band 62 (including its diameter) in order to tighten or loosen the band along/about the limb.
Wearable target device 60 can be worn on the limb or other extremity in any suitable position such that patches 50 are spaced apart from the imaged object.
More than one wearable target device 60 can be used for a patient, allowing multiple patch or target elements 50 to be imaged, such as at different locations along the axial direction. The schematic diagram of
To promote sanitary conditions, (all or a portion of) target device 60 can be disposed within a disposable sheath, such as a plastic disposable film/bag.
Using an embodiment of the present disclosure, calibration of the CBCT system can be achieved using image data from the reconstructed 3D volume. By identifying voxels reconstructed from the target elements or patches 50 of known radio-opaque density, the needed data for calibration can be obtained, allowing an accurate range of HU values to be measured. This allows functions using quantitative image data, such as BMD, to have improved accuracy.
Since the target patches 50 (appearing in the sequence of acquired 2D projection images) are of a known radio-opaque density, the needed data for calibration can be obtained, allowing an accurate range of HU values to be measured.
The invention has been described in detail, and may have been described with particular reference to a suitable or presently preferred embodiment, but it will be understood that variations and modifications can be effected within the spirit and scope of the invention. The presently disclosed embodiments are therefore considered in all respects to be illustrative and not restrictive. The scope of the invention is indicated by the appended claims, and all changes that come within the meaning and range of equivalents thereof are intended to be embraced therein.
This application claims the benefit of U.S. Provisional application U.S. Ser. No. 62/629,221, provisionally filed on Feb. 12, 2018, entitled “CALIBRATION TARGET FOR QUANTITATIVE COMPUTED TOMOGRAPHY”, in the name of Lawrence A. Ray, which is incorporated herein by reference in its entirety.
Number | Date | Country | |
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62629221 | Feb 2018 | US |