This invention concerns an efficient algorithm for automatic detection and accurate segmentation of Abdominal Aortic Aneurysm (AAA). The algorithm first identifies the location of the lumen (the inner portion of aorta) and then segments it. The abdominal portion of the lumen is then found using anatomical and geometrical features. This portion of the lumen is straightened using geometrical transformation based on the smoothed centreline. The transformed lumen is then passed through a number of filters, based on geometrical, intensity, gradient and texture features, to search for the existence of the aneurysm. If aneurysm is detected, a deformable model is first initialized to the approximate borders of the aneurysm which are then refined using global and location information
An Abdominal Aortic Aneurysm (AAA) is a localised dilation (swelling or enlargement) of an aorta. An AAA usually consists of two sections—the lumen (the inner part) and the thrombus (the outer fatty part). Blood flows in the lumen and its visibility can be enhanced when CT Angiography (CTA) is used. The progressive growth of an aneurysm may eventually cause a rupture if not diagnosed or treated. This can be life threatening as the rupture would cause massive internal bleeding. The probability of a rupture occurring depends on its size. For example, patients exhibiting an AAA of 5 cm or more in diameter should be treated to replace the weakened section by open surgery or using a stentgraft (endovascular procedure). For a 4 cm AAA, if the aneurysm increases by 5 mm or more in six months, treatment should be considered. As a follow-up after the operation, a frequent life-long monitor will be used to ensure that no further expansion has occurred to prevent the chance of further ruptures.
In England and Wales, there are as many as 6,000 to 10,000 people who suffer from an AAA rupture each year; most of whom are men aged 65 and above [1]. In general, about 1 in 20 people in the UK over the age of 65 develop an aortic aneurysm [2]. In USA, as many as 200,000 people are diagnosed each year with the mortality rate of about 15,000 annually [3]. Thus, without doubt, the quantification of aneurysms in CT scans plays a significant role in monitoring the disease both before and after surgery.
Typically, CTA is conducted by injecting patients with a contrast agent to enhance the blood stream in the CT images. The radiologist then manually identifies the enlarged portions of the aorta on a number of cross-sectional images in order to obtain a full volume measure.
This extremely tedious and time-consuming process may take up to 30 minutes and is inconvenient for physicians. Furthermore, this approach becomes impractical as the datasets produced by the latest CT scan machines increase. In addition, such manual methods are subjective, prone to error and non-reproducible. In fact, the validity of the method is questionable as different measurements can arise for the same aneurysm region when performed by different radiologists or by the same radiologist at different times.
The detection and accurate segmentation of an AAA region is a challenging task since it is very difficult, though not impossible, to identify and differentiate between the boundaries of an AAA and the surrounding muscles or other vascular structures. There are a few research publications on computerized AAA segmentation from which computerized measurements can be achieved.
Reference [6] introduces a five-part energy function defined on polar coordinates using a snake method and validates the segmentation result based on 34 ultrasound images.
References [7-8] provide studies of various approaches to segmenting both the aneurysm and the aortic flow channel employing a level set framework using either edge strength or region intensity information. These methods are not fully automatic and require one or several external seed points for initialisation. Further, they have not been robustly validated.
There exist on the market a number of Computer Aided Detection (CAD) systems using image processing analysis that assist radiologists in detecting abnormalities in medical imaging more efficiently. The medical image processing methods are highly application oriented which means that different algorithms are developed to cater for different parts of human body such as the lung (CAD from Siemens [4b]), breast (GE-Mammography [5b]) and others.
The members of Mediar Ltd. have in the past designed and produced several scientific image processing algorithms, each developed for a specific medical imaging application. Some of the publications are provided in references [6b] to [10b]. In [6b] a description of an image processing algorithm is provided for the quantification of calcium plaque in heart using the Modified Expectation Maximization (MEM) method. Reference [7b] tackles the segmentation problem in brain from MRI images using Multiple Discriminant Analysis (MDA). References [8b] and [9b] present CAD systems in colon using several image processing methods such as fuzzy connectivity, shape index and clustering analysis. Reference [10b] gives a description of lung nodule segmentation using a shaped based region growing algorithm.
Despite the growing importance of having a dynamic approach that would help radiologists obtain accurate measurements of the Abdominal Aortic Aneurysm (AAA), there is no real computerized image processing analysis system commercially available. This is because the task of extracting the AAA region from the CT scans and measuring it accurately by a computerized image analysis system is problematic. This is due to the fact that the AAA boundaries often touch muscles and other tissues of similar intensities making it very difficult, though not impossible, to identify and differentiate between the boundaries of the adjacent tissues.
There is accordingly an immediate demand for a new and sophisticated image processing approach that uses scientific algorithms to effectively extract any AAA regions and produce precise measurements.
Although there are a few academic papers that have attempted to tackle this problem (see references [1 lb] to [20b]), they are not robust enough to be considered for future commercial use.
Reference [lib] introduces a five-part energy function defined on polar coordinates using a snake method and validates the segmentation result based on 34 ultrasound images.
References [12b-13b] provide studies of various approaches to segmenting both the aneurysm and the aortic flow channel employing a level set framework using either edge strength or region intensity information. Further, they have not been robustly validated. These methods are not fully automatic and require one or several external seed points for initialisation.
In reference [9], an active shape model (ASM) is used to segment the AAA. In this approach, the user has to draw a two-dimensional (2-D) contour on one slice which is propagated to the adjacent slice based on gray values similarity. The optimal fit is defined by maximum correlation of gray value profiles around the contour in successive slices.
In reference [10], an interactive AAA segmentation system is developed based on the active shape model. If an obtained contour is not sufficiently accurate, the user can intervene and provide an additional manual reference contour. Although accurate, the amount of user interaction is large, because slice-by-slice user-interaction is required. Further, the result may vary considerably with different attempts.
Reference [11] investigates a 3D active shape model method with a gray level appearance model based nonparametric classification technique for AAA segmentation. The method requires manually drawn top and bottom slices and a user input point in the approximate aneurysm centre of the central slice.
Another method is described in reference [12], where a level-set algorithm is used to segment the aneurysm from an initial region which is drawn as a sphere by the user. The sphere is deformed to identify the borders of the AAA. Although user interaction is minimal, the reported results are not accurate.
In reference [13], a method is described for the aortic aneurysm segmentation using a constrained contour evolution method. At each iteration, the snake points are driven by a rejecting force that depends on the difference between local Hounsfield Unit (HU) value and thrombus HU and an edge force directed along the derivative of the image gradient that is active only if the edge shape is compatible with the border of a thrombotic region. User interaction is vital to achieve good results.
Another method is presented in reference [14]. This method is based on a deformable model called a 3D active object. First, the algorithm segments the lumen (the inner portion of aorta), which is then used to initialize the segmentation of the AAA (the rest of the expanded fatty portion). A nonparametric gray level appearance model that is based on the intensity profile is used to drive the deformable model. Accurate results with less required user intervention were reported. However, a parameter estimation using a classifier is required for different datasets which calls for manual segmentation of AAA boundaries for a subset of the data. Once the system is trained, the user provides two seeds on the same slice and the algorithm extracts the AAA. This algorithm was only tested on pre-operative cases of a total of 17 patients.
Another method in AAA segmentation is presented in reference [15]. This method estimates a rough initial surface, and then refines it by using a level set segmentation scheme augmented with a global region and a local feature analyzer. One drawback is that the deformable model segmentation assumes that the aneurysm is roughly circular in a transaxial cross section, thus resulting in failure of the segmentation for non-circular shaped aneurysm. The system was only tested on 20 CTA AAA datasets.
Other prior art publications include WO 03/075209, WO 2004/081874 and US 2006/025674.
As the reliability of the measurement depends on how accurately the regions of interest can be segmented, an aim of the present invention is to improve the measurement methods and systems of the prior art.
More specifically, an aim of the invention is to concentrate on the development of an automatic and accurate segmentation of AAA as a first and essential stage for accurate measurement.
In comparison to the manual identification, segmentation and measurement of AAA, the proposed system and method offers more accurate, reproducible and cost-effective, plus faster results.
a) to 2(d) illustrates the detection and extraction of the lumen: (a) Original sagittal view, (b) 3D view of the segmented image, (c) 3D view of morphological operation on (b),(d) the extracted lumen wherein the white arrows point to the lumen;
a) to 4(c) represent lung regions: (a) Coronal view showing abdominal aorta at the lung regions, (b) axial view of a lung, (c) extracted holes of the segmented lung;
a) to 5(c) represent a Celiac Trunk: (a) sagittal view showing the Celiac Trunk (arrowed), (b) Projected sagittal view of a segmented aorta, (c) morphological operation on (b) where the top isolated object is the celiac trunk;
a) to 6(c) illustrate a geometrical transformation (3D views of the segmented lumen); a) original lumen, b) geometrically transformed lumen, c) overlap between a and b, the original position is highlighted with an arrow;
a) and (b) illustrate examples of the presence of aneurysm; the bottom images are the projection of coronal view of segmented aorta and the top images show the slices indicated by the white arrows; only the segmented lumen are shown in the bottom images: (a) lumen is bent and has large diameter, (b) lumen is straight with small diameter but irregular lumen cross section
a) and (b) illustrate fat regions, (a) original image, (b) segmented fat regions, 3D view of the segmented fat regions;
a) to (c) illustrate a method of filling the gap between bone edges of a spine where the top images are axial and the bottom images are sagittal views; (a) original image, (b) segmented fat and spine, (c) similar to (b) with gaps filled (arrowed) between the bone edges
a) and (b) are examples of blood vessel next to an aorta: (a) the 3D image clearly shows the difference in geometrical features between the blood vessel and the calcified region, no thrombus is shown in the 3D image, (b) the result shows that the blood vessel are retained as part of non-AAA regions;
The principle of the main steps of the method are outlined as follows:
Each of the abovementioned steps is described in more detail below.
Lumen identification is achieved through gathering prior knowledge of their shape, appearance and geometrical representations in relation to other tissues. Anatomically, the aorta (lumen) runs alongside the spine before branching off into the two main arteries that run down the legs. Further, the enhanced intensity level of lumen in the CT Angiography images assists in locating the lumen more accurately. The identification and extraction of the lumen is done as follow:
The abdominal portion of the lumen is located between the Celiac Trunk and Iliac Arteries junction. The Celiac Trunk is the first artery that stems out of the lumen below the diaphragm which is approximately where the lung ends. The Iliac Arteries junction is where the lumen is split into two major arteries. The algorithm for identifying the abdominal portion of the lumen is outlined below:
Using the centreline in Step 2c and the location of the Celiac Trunk and Iliac Arteries (Step 2b and 2c) as end points, the centreline is straightened by finding the shortest path between the two end points. The geometrical mapping that is obtained from the centreline transformation can be applied on the segmented or the original image. This way, all features collected from the lumen and the surrounding voxels will be virtually taken from the planes orthogonal to the original position of the lumen.
The geometrically transformed lumen is first examined for the indication of the aneurysm and then the objects attached to the lumen are evaluated. The search for aneurysm is presented below:
The extracted lumen (Step 2) is used as an initial surface and the non-AAA regions (Step 4d_i and 4d_ii) are used as barriers for a deformable model based segmentation, a. The AAA region is first approximated by robustly fitting a 3-D ellipsoid anisotropic Gaussian-based intensity model to the border of the non-AAA regions. A union of this region and the extracted lumen is used as an initial region to be refined at its border; this is given in the next step.
The deformable model, initialised in the previous step, is driven by the global and local information. The global information uses the graphical representations of anatomical structures and relationships that constitute the human body, whilst the local information utilises the 3D geometric features calculated at each voxel as a measure of local shape information.
The method is described in a more detailed manner in the following with reference to the drawings.
The CTA image is first smoothed using the anti-geometric diffusion method in the pre-processing stage. Lumen is then extracted from the pre-processed image using segmentation and morphological operation. The abdominal portion of the lumen is identified using geometrical information, mathematical morphology and connectivity cluster analysis. This is followed by the geometrical transformation to straighten the lumen using its centreline. Several evaluations are then carried out on the abdominal aortic section to search for the presence of aneurysm. If aneurysm is identified, the full segmentation of the AAA will follow.
Accurate segmentation of lumen is not necessary since lumen will be used as an initial region to detect and segment the aneurysm. The segmentation of the lumen is performed using a threshold-based segmentation with low and high threshold values of Ti and Th, these threshold limits were found experimentally to be 140 and 700 respectively. Due to the partial volume effect, the extracted lumen often has loose connection with objects of similar HU attenuation such as spine and kidneys through renal arteries. To separate lumen from other objects, the morphological erosion operation is applied which will result in several isolated 3D objects. For further elimination of the loose links, a special 3D labelling algorithm is applied whereby the core regions of the cross sections in the consecutive slices are used to identify the existence of the connectivity. The core of a region is obtained by first taking the distance transform and finding the centre point (maximum distance value). The region core is then identified as a blob that contains the centre point as well as all the points that have distance value of some percentage of the maximum distance. A 70% region core was used in this experiment.
The morphological operation and the special 3D labelling results in several isolated 3D objects. Among these isolated objects, the lumen can be identified as the object that is relatively long in Z direction and narrow (in coronal view), plus it resides approximately in the middle of the body.
The abdominal section of the lumen is identified automatically by finding the positions of the Celiac Trunk and the Iliac Arteries junction as shown in
The first step in identifying the abdominal portion of the lumen is to find the end location of the lung regions. Lung regions appear as hollowed objects in the CT images due to the presence of large volume of air, as shown in
The lung regions, extracted as hollowed objects, contain a number of smaller holes which are the result of cross sectional views of many blood vessels in the lung regions. The cross section of a segmented lung in
Where N is the total number of isolated objects (holes) inside the Kth object Ok, Ok(p) is the pth isolated object, Tcnt is an object count threshold, and
Where Tsize is the object size. Experimentally Tsize=5 and Tcnt=10 were chosen.
This process of identifying the lung regions is continued slice-by-slice until no lung region is found. This will be the approximate location of the diaphragm or the end of the lung regions.
The end location of the lung regions only provides an approximate position where the search for the Celiac Trunk can be carried out. The search volume will be within a volume of an enlarged lumen (20% enlargement) and limited to 20 mm above and below the end of lung location. By using an adaptive segmentation, a new lumen is obtained with the search volume to ensure that a fully detailed lumen is obtained; note that the previously extracted lumen lack detail due to the morphological operation. A projected sagittal view of the segmented aorta is then obtained which is shown in
Iliac Arteries junction is the last location to be found for the abdominal aortic identification. This is where the aorta splits into two major arteries running down the legs. To identify this location, the centre-line of the aorta is first obtained then is passed through a smoothing filter followed by a conversion to the cluster connectivity. Using this cluster connectivity, a cluster analysis based on length and angle is used for every branches stemming-out from the main centre-line (the lumen). As regard to this, the length of all branches, except for the Iliac arteries, is relatively short and their angle with respect to the main centre-line is relatively sharp.
The abdominal portion of the lumen is geometrical transformed to straighten the lumen by using its 3D centreline. The reason for the transformation is to ensure that the subsequent feature extraction would represent the information taken from the plain orthogonal to the lumen's original centreline.
Several features are used to detect the presence of aneurysm. First, the features from the extracted lumen are obtained and evaluated. If no aneurysm is detected, then features from the raw image are used for further evaluation. These features are outlined as follows:
If the aneurysm is not detected following the evaluation of the features 1-3, all the objects that are attached to the lumen are first extracted and then examined based on the features that can be obtained from the raw image such as HU attenuations, gradient and texture. These attached objects to the extracted lumen are treated as Potential Regions (PR) and are obtained as given in Equation 3.
PR=(Lexp−L)∩˜(non_AAA) (3)
Where L is the extracted lumen and Lexp is the expanded (enlarged) lumen, ∩ and ‘˜’ are intersection and logical NOT operations respectively. The non AAA symbol stands for regions that cannot be part of aneurysm. These regions include fat, spine and blood vessels. Due to their prominent features compared to those of the aneurysm regions, they can easily be separated and hence used as a solid obstacle during subsequent detection and segmentation of aneurysm. Before describing how the potential regions are obtained and evaluated, the description regarding the extraction of the non AAA regions is presented.
Fat regions are darker than the aneurysm and can easily be extracted by using a thresholded segmentation followed by morphological opening operation. In some large size aneurysm, small dark regions might exist, within the aneurysm, that could be natural or due to image acquisition artefact. As regard to this, fat regions with a relatively small size are ignored. The size limit for the fat region identification was found empirically to be 50 m3.
Spine is another object that is located very close to the aorta and hence it is useful to use it as a non AAA region. Extracting the spinal bones can easily be done due to their high HU values. However the spine is made of pieces of bones that are held together with a muscle like object called Disk. The Disks have HU values that are similar to that of the thrombus. This leads to the formation of openings in the slices where the Disk regions touch the borders of the aneurysm. These openings (or gaps) can easily be filled by interpolating between the bone edges of the spine, which are located a few slices above and below.
There are several tiny blood vessels that stem out of the lumen. They appear as small circles in consecutive axial images. They can easily be mistaken with the calcified regions when viewed on the axial images. Unlike the calcified regions, the blood vessels are not part of the aneurysm and thus should be included in the non-AAA regions. One prominent feature that can be used to distinguish between the blood vessels and the calcified regions is that the blood vessels have compact and circular cross section that span over a relatively large number of slices. Although calcified regions might have similar contrast and their cross sections might be compact and circular, they are generally small 3D objects with elongated surface that occupy a few slices. Therefore a combination of circularity-compactness and 3D connectivity analysis is used to identify the blood vessels.
As indicated in Equation 3, the Potential Regions (PRs) are obtained by subtracting the lumen from its expansion and finding the intersection of this result with the inverse of non-AAA regions. The PR regions are then used as a mask to extract the corresponding features from the raw image. The features are fed into a rule-based filter to identify whether the PR contains aneurysm or not. In order to make the process more robust, several expansions of the lumen is used (refer to Equation 1). The PR regions from different expansions are fed to the rule-based filters separately and a global filter is used to make the final decision based on the results obtained from those rule-based filters. This process is shown graphically in
The non AAA regions that were described earlier can be used as a strong barrier (mask) for finding the borders of the aneurysm. This mask is not totally closed up as there are some gaps and openings due to the existence of different tissues touching the aorta with some having similar intensity values as the aneurysm regions. These gaps create leakage path for any region segmentation. To avoid the leakage, an elliptical approximation of the aneurysm region is found first and then fine-tuned using a deformable model.
The distance map of the mask, the non-AAA regions, provides useful information of where the entire or parts of the aneurysm might be. The centre point, where the distance value is at its maximum, indicates the deepest part of the aneurysm basin. From this centre point, the core of the region is extracted with 70% of the maximum value; the core region extraction was described above. Note that the higher percentage of the core will create a core region that is more resemblance to the shape of the original region. The sharp edges of this core region are then reduced by applying the opening morphological operation of window size 3×3. This region is then ballooned out until it hits the edges of the mask region. The ballooning process is done by first finding the minimum distance between the edges of the core region and the mask and enlarging the core by the amount equal to the minimum distance value.
The ellipsoid approximation provides a very good estimate for defining the borders of the aneurysm. In most cases, the ellipsoid regions cover the exact borders of the aneurysm; in other cases, they would be located very close to the true borders of the aneurysm regions. As regards to this, the deformable model only needs to fine-tune the extend of the ellipsoid region.
40 CT Angiography scans were used to test the automatic detection and segmentation that is proposed in this paper. The patients were age between 55 and 85 with 4 female and 36 male. The GE LightSpeed VCT machine was used to obtain the images. Scan parameters were 120 kV, 300 to 400 mA and slice thickness 1.0 to 2.0 mm.
The AAA regions in CT data were annotated by three expert Radiologists. It should be noted that obtaining a ground truth (i.e. a “gold standard”) for defining the border of aneurysm in clinical data is challenging. There can be interobserver and intraobserver differences in manually outlined AAA provided by experts. Consequently, validating the acceptability of any AAA segmentation algorithm is subjective.
In this experiment the effect of different threshold limits on the detection and extraction of the lumen is shown. Since there was no annotation information for the lumen regions (i.e. it is expensive and time consuming to ask the radiologists to annotate both lumen and borders of aneurysm), one set of parameters were used as a test-bench and other results were compared to it. The test-bench was obtained by selecting a set of parameters that resulted in the correct extraction of the lumens for all 40 images based on the visual judgment of an expert radiologist. The parameters for this test-bench were selected as Tl=140 HU and Th=700 HU (see the earlier description above). Table 1 shows the result of trying out different parameters for detection and extraction of the lumen in 40 datasets. The Mean Overlap (MOv) is obtained as follows:
Where Ov is the overlap between two objects, V(C) and V(T) are the volume of the current and test object respectively; N is the number of CTA images.
For the results in Table 1, the erosion window size was set kept to 3×3×3 and the threshold values Tl and Th were changed. The algorithm performed well for Tl>300 HU when Th was kept to 700. It failed on one dataset for Tl=130 HU which was due to strong presence of spine; i.e. the lumen was detected but attached to the spine. The lower threshold values caused filling more gaps in-between spinal bones (including partial volume effect on the disk portions) thus leading to the formation of fairly strong links between lumen and spine. The second part of Table 1 provides the result of altering the upper threshold value Th. With the lower values for Th (<500 HU), many points were excluded from the segmentation results for the lumen causing it to break into pieces after passing through the morphological operation (see the description above). Therefore, the algorithm could not find a compact 3D object that had the geometrical feature of the lumen.
Table 2 shows the effect of the erosion operation on separating lumen from other objects in the segmented image. The results are compared to the test bench with parameters Tl=150 HU, Th=600 HU and the erosion window size of 7×7×1 (2D erosion slice by slice). Based on these results, the 2D erosion operation is faster than the 3D operation but the later is more robust for cases in this experiment. As trade off between robustness and speed, the 2D erosion operation of 7×7×1 can be chosen.
As was described above, a special 3D region labeling is applied on the segmented regions following the morphological erosion operation. This region labeling uses the core of the region cross sections in the consecutive slices to identify the existence of connectivity. The size of the region core depends on the percentage of the maximum value of the distance map. Since the region core is only used to identify the connectivity and not to determine the final size of the lumen, its size does not have significant effect on the result. This was proved in an experiment that was conducted using a range of sizes for the core region between 60% and 99% of the centre point's distance value; i.e. core region extraction was described above. These tests were applied on all the datasets using the parameters Tl=140, Th=700 and erosion size of 3×3×3. It was observed that the core sizes of above 70% did not have any significant effect on the result and below 70% some lumens were reduced in size since some cross sections were not added due to lack of connectivity. The algorithm was also tested on with the traditional 3D labeling. With this, the algorithm did not produced satisfactory results for two cases. In one case, the lumen was attached to the spine and in the other case the lumen was connected to one kidney through the renal artery.
This experiment investigates the sensitivity of the algorithm to the parameters Tsize and Tent in Equations 1 and 2 to find end of the lung location. Table 1 shows the results of finding the end of lung positions using different parameters. The minimum, maximum and average distance, in millimeter, between the end of lung location and the actual position of the Celiac Trunk are given. The latter location was provided by one of the radiologists. The algorithm failed on one data when the size limit for identifying the isolated objects was small (Tsize=3). This is because some of the artifacts from the segmented lung were identified as valid isolated objects. Apart from the choice of small size limit, the algorithm was robust for a range of experimental values; i.e. due to the paper limitation, many of the combinations of the parameters are not shown in Table 3. Out of these results, the parameters of Tsize=6, Tcnt=6 were chosen as a trade-off between robustness and accuracy.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/IB09/51588 | 4/16/2009 | WO | 00 | 5/9/2011 |
Number | Date | Country | |
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61045283 | Apr 2008 | US |