Computer Aided Detection and Measurement of Peripheral Arterial Diseases from CTA Images
Professor Jamshid Dehmeshki Kingston University, London The University Hospital of Lausanne
Computer Aided Detection and Measurement of Peripheral Arterial - - PDF document
Computer Aided Detection and Measurement of Peripheral Arterial Diseases from CTA Images Professor Jamshid Dehmeshki Kingston University, London The University Hospital of Lausanne Outline Anatomical overview of Peripheral Arteries
Professor Jamshid Dehmeshki Kingston University, London The University Hospital of Lausanne
➢ Anatomical overview of Peripheral Arteries Diseases (PAD) ➢ Investigation of PAD in Computed Tomography Angiography (CTA) ➢ Methodology – Automatic Computer Aided Detection (CAD) and Automatic Computer Aided Measurement (CAM) of PAD ➢ Evaluation – computational implementation and evaluation ➢ Conclusıon
extremities
people in the U.K and 10 million of Americans per year
➢ PAD has a mortality rate higher than breast cancer . ➢ PAD is a marker of coronary artery disease (CVD) , ischemic heart disease (IHD) and cerebrovascular disease ➢ The disease is undertreated and under detected
atherosclerosis
atherosclerosis
Imaging techniques
➢ CTA a common imaging technique for investigation of the disease Current problems
➢ Large amount of data
(2D) views ➢ Variety of arteries size and shape, abnormalities ➢ Image quality: parameters of CT scanning, contrast agent, PVA always present Radiologist ➢ High inter-observer and intra-observer variability ➢ Error, fatigue vs. performance ➢ Cost
➢A system that can fully detect and measure peripheral arterial diseases in CTA datasets automatically ➢A tool for radiologist to reduce investigation time, human error improving clinical assessment
CAD - CAM
Proposed Methodology
➢ I - the input Dicom image ➢ l f0 - initial foreground value ➢ lb0 - background value ➢ Optimum threshold is calculated iteratively
➢ Automatic seed selection ➢ Region growing criteria:
➢ Over segmentation from previous step (region growing): artery and bone are connected
➢ Erosion is not sufficient to delineate areas of continuity between bone and artery ➢ Use a prior information and spatial information ➢ Anatomical prior: properties of artery and bones
intensity values
homogeneous intensity(exception: calcifications)
➢ Erosion is not sufficient to delineate areas
➢ Use a prior information and spatial information ➢ Anatomical prior: properties of artery and bones
intensity values
homogeneous intensity(exception: calcifications)
➢ We have extracted the peripheral arteries and we want to investigate the presence of stenosis ➢ Requires a centreline that preserves geometry and topology
➢ Centreline contains spurious branches and redundant voxels
➢Removal of these unwanted voxels is done using:
search to remove branches
➢Create continuous smooth line
splines ➢
➢ The obtained centreline is a discrete representation of voxels
➢ Create continuous smooth line
Rom splines ➢ Artery measurements are performed in cross section images ➢ Cross section images are orthogonal planes to the arteries ➢Cross section images are obtained using a sliced- based rendering technique
➢ We have created the cross section images where the measurement can be performed ➢ Area ➢ Equivalent Diameter
➢ Maxima (pmax)and Minima (pmin) are chosen ➢ A stenotic area is automatically identified if
➢ The vessel profile is a 1D representation of
the measurements ➢ Looking for significant extrema points
➢ A MAP-MRF expectation maximization method is used ➢Partial volume effect is a mixture of tissues in one pixel ➢ In the current context is mixture between the peripheral artery and surrounding tissue
➢ Finding the contribution of each tissue in one pixel would provide an accurate measurement of area/diameter
➢ By using an a priori penalty as a spatial constraint within a
Markov Random field framework we can model the tissue mixture ➢ The EM algorithm is used to estimate the tissue mixture
➢ A new measurement is performed
taking into account the partial volume effect, reflected by the determined percentage contribution of each tissue , λ, in one pixel
➢ Stenosis is measured based on a reference measurement in a healthy artery distal or proximal to a stenotic site and the measurement in the most severe site of stenosis
➢ Degree of stenosis is determined according to the area percentage, by a scale 5 point :
➢ Length of stenosis shows severity of the disease and is expressed through two categories:
➢ Twenty CTA datasets provided by CHUV, Lausanne but 18 were used ➢ GE Multi-slice helical CT ➢ Different sizes from 512 x 512 x 900 to 512 x 512 x 1050 ➢ Resolution: 0.703125 x 0.703125 x 1.25
➢ Mimics the shape and attenuation properties of the artery ➢ Diameter ranges from 1 to 8 mm ➢ Stenosis is simulated ➢ Different acquisition protocols (10)
➢ Applied on 18 datasets ➢ Optimal threshold: 140-200 HU Results ➢ Visual evaluation showed that all arterial segments were present
➢ Applied on 18 datasets ➢ 6 neighbourhood connectivity system Results ➢ The arteries were extracted correctly in 2 datasets ➢ In 16 datasets the extracted arteries were connected to the bone
➢ Applied on 15 segmented data, each partitioned in 35 segments (total
➢ Ground truth: 149 segments with stenosis: 132 soft plaque, 17 calcifications Parameters ➢ The width of the 1D Gaussian filter was set to 9 ➢ The parameter k in the discrete curve analysis was fixed to 20 ➢ The parameter θs was set to 0.55
Results ➢ The method identified 116 stenosis caused by soft plaque ➢ 33 stenotic areas were missed (17 calcified) ➢ Identified 15 false positives stenoses
➢ The peripheral arteries were extracted with a sensitivity of 83.3% ➢ The undetected stenosis in the calcified arterial segments influences the sensitivity
➢ Evaluated on phantom data and compared to threshold method Parameters ➢ A MAP-MRF method
➢ Threshold method
➢ Evaluated on phantom data and compared to threshold method Results ➢ The measurement of the simulated artery in the phantom, using MAP- MRF method showed a percentage error of 8%.
➢ A fully automatic CAD-CAM system for detection and measurement of
peripheral arterial diseases in CTA images has been developed and implemented ➢ Results for stenosis detection showed a sensitivity of 78% and specificity of 96% (15 false positive in all datasets), with an increase in sensitivity (to 88%) if calcified areas were excluded
➢ The partial volume effect was corrected and CAM component showed an average errot of 8% when evaluated on phantom data ➢ The computation time for processing 1000 slices is 8 min, while radiologist examination is 1- 4 hours
➢ Computational improvement
➢ Identification and quantification of stenoses in calcified areas ➢ Functionality for CAD system to deal with other pathologies (occlusions and aneurysm ) ➢ Additional anatomical a priori information