19,687 research outputs found
Automatic Characterization of Myocardial Perfusion in Contrast Enhanced MRI
The use of contrast medium in cardiac MRI allows joining the high-resolution anatomical information provided by standard magnetic resonance with functional information obtained by means of the perfusion of contrast agent in myocardial tissues. The current approach to perfusion MRI characterization is the qualitative one, based on visual inspection of images. Moving to quantitative analysis requires extraction of numerical indices of myocardium perfusion by analysis of time/intensity curves related to the area of interest. The main problem in quantitative image sequence analysis is the heart movement, mainly due to patient respiration. We propose an automatic procedure based on image registration, segmentation of the myocardium, and extraction and analysis of time/intensity curves. The procedure requires a minimal user interaction, is robust with respect to the user input, and allows effective characterization of myocardial perfusion. The algorithm was tested on cardiac MR images acquired from voluntaries and in clinical routine
Does quantification of myocardial perfusion SPECT study differ while image reconstruction is carried out using iteration algorithm instead of filtered back-projection? - preliminary report
BACKGROUND: The purpose of this study was to compare the performance
of two reconstruction algorithms: conventional filtered back-projection (FBP)
and an iterative algorithm -ITW- in quantitative analysis of myocardial perfusion
SPECT studies. The defect size and defect severity were assessed on 99m Tc -
MIBI images reconstructed using both methods and estimation of sensitivity in
the detection of perfusion deficits and myocardial viability were performed
as well.
METHODS AND RESULTS: The study group comprised 43 patients (38 men and
5 women) in the age of 40-73 years (mean 59 years). Heart perfusion scintigraphy
was performed following an injection of 22 to 25 mCi 99m Tc-MIBI for exercise
and rest myocardial perfusion study. Images were reconstructed using
FBP and ITW algorithms. Defect size (DS) was quantified by a threshold program
and CEqual programme. Defect severity (nadir) was calculated as the ratio of
minimal/maximum counts from bull?s eye polar map. Coronary arteriography
was performed in all patients.
RESULTS: Defect size calculated by threshold method on resting images
did not differ between reconstruction methods (p=0.61 for cut-off 50% and p
= 0.24 for cut-off 60%); defect severity was higher on images reconstructed
with ITW (CI 0.95 = 2.4%¸5.2% of maximal counts).
CONCLUSIONS: Sensitivity for detection of heart perfusion defects and
estimation of myocardial viability were similar on images reconstructed by both
algorithms
Quantitative Myocardial Perfusion Imaging Versus Visual Analysis in Diagnosing Myocardial Ischemia
Objectives: This study sought to compare the diagnostic accuracy of visual and quantitative analyses of myocardial perfusion cardiovascular magnetic resonance against a reference standard of quantitative coronary angiography.
Background: Visual analysis of perfusion cardiovascular magnetic resonance studies for assessing myocardial perfusion has been shown to have high diagnostic accuracy for coronary artery disease. However, only a few small studies have assessed the diagnostic accuracy of quantitative myocardial perfusion.
Methods: This retrospective study included 128 patients randomly selected from the CE-MARC (Clinical Evaluation of Magnetic Resonance Imaging in Coronary Heart Disease) study population such that the distribution of risk factors and disease status was proportionate to the full population. Visual analysis results of cardiovascular magnetic resonance perfusion images, by consensus of 2 expert readers, were taken from the original study reports. Quantitative myocardial blood flow estimates were obtained using Fermi-constrained deconvolution. The reference standard for myocardial ischemia was a quantitative coronary x-ray angiogram stenosis severity of ≥70% diameter in any coronary artery of >2 mm diameter, or ≥50% in the left main stem. Diagnostic performance was calculated using receiver-operating characteristic curve analysis.
Results: The area under the curve for visual analysis was 0.88 (95% confidence interval: 0.81 to 0.95) with a sensitivity of 81.0% (95% confidence interval: 69.1% to 92.8%) and specificity of 86.0% (95% confidence interval: 78.7% to 93.4%). For quantitative stress myocardial blood flow the area under the curve was 0.89 (95% confidence interval: 0.83 to 0.96) with a sensitivity of 87.5% (95% confidence interval: 77.3% to 97.7%) and specificity of 84.5% (95% confidence interval: 76.8% to 92.3%). There was no statistically significant difference between the diagnostic performance of quantitative and visual analyses (p = 0.72). Incorporating rest myocardial blood flow values to generate a myocardial perfusion reserve did not significantly increase the quantitative analysis area under the curve (p = 0.79).
Conclusions: Quantitative perfusion has a high diagnostic accuracy for detecting coronary artery disease but is not superior to visual analysis. The incorporation of rest perfusion imaging does not improve diagnostic accuracy in quantitative perfusion analysis
Coronary microvascular ischemia in hypertrophic cardiomyopathy - a pixel-wise quantitative cardiovascular magnetic resonance perfusion study.
BACKGROUND: Microvascular dysfunction in HCM has been associated with adverse clinical outcomes. Advances in quantitative cardiovascular magnetic resonance (CMR) perfusion imaging now allow myocardial blood flow to be quantified at the pixel level. We applied these techniques to investigate the spectrum of microvascular dysfunction in hypertrophic cardiomyopathy (HCM) and to explore its relationship with fibrosis and wall thickness. METHODS: CMR perfusion imaging was undertaken during adenosine-induced hyperemia and again at rest in 35 patients together with late gadolinium enhancement (LGE) imaging. Myocardial blood flow (MBF) was quantified on a pixel-by-pixel basis from CMR perfusion images using a Fermi-constrained deconvolution algorithm. Regions-of-interest (ROI) in hypoperfused and hyperemic myocardium were identified from the MBF pixel maps. The myocardium was also divided into 16 AHA segments. RESULTS: Resting MBF was significantly higher in the endocardium than in the epicardium (mean ± SD: 1.25 ± 0.35 ml/g/min versus 1.20 ± 0.35 ml/g/min, P < 0.001), a pattern that reversed with stress (2.00 ± 0.76 ml/g/min versus 2.36 ± 0.83 ml/g/min, P < 0.001). ROI analysis revealed 11 (31%) patients with stress MBF lower than resting values (1.05 ± 0.39 ml/g/min versus 1.22 ± 0.36 ml/g/min, P = 0.021). There was a significant negative association between hyperemic MBF and wall thickness (β = −0.047 ml/g/min per mm, 95% CI: −0.057 to −0.038, P < 0.001) and a significantly lower probability of fibrosis in a segment with increasing hyperemic MBF (odds ratio per ml/g/min: 0.086, 95% CI: 0.078 to 0.095, P = 0.003). CONCLUSIONS: Pixel-wise quantitative CMR perfusion imaging identifies a subgroup of patients with HCM that have localised severe microvascular dysfunction which may give rise to myocardial ischemia
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Magnetic resonance multitasking for motion-resolved quantitative cardiovascular imaging.
Quantitative cardiovascular magnetic resonance (CMR) imaging can be used to characterize fibrosis, oedema, ischaemia, inflammation and other disease conditions. However, the need to reduce artefacts arising from body motion through a combination of electrocardiography (ECG) control, respiration control, and contrast-weighting selection makes CMR exams lengthy. Here, we show that physiological motions and other dynamic processes can be conceptualized as multiple time dimensions that can be resolved via low-rank tensor imaging, allowing for motion-resolved quantitative imaging with up to four time dimensions. This continuous-acquisition approach, which we name cardiovascular MR multitasking, captures - rather than avoids - motion, relaxation and other dynamics to efficiently perform quantitative CMR without the use of ECG triggering or breath holds. We demonstrate that CMR multitasking allows for T1 mapping, T1-T2 mapping and time-resolved T1 mapping of myocardial perfusion without ECG information and/or in free-breathing conditions. CMR multitasking may provide a foundation for the development of setup-free CMR imaging for the quantitative evaluation of cardiovascular health
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Impact of incomplete ventricular coverage on diagnostic performance of myocardial perfusion imaging.
In the context of myocardial perfusion imaging (MPI) with cardiac magnetic resonance (CMR), there is ongoing debate on the merits of using technically complex acquisition methods to achieve whole-heart spatial coverage, rather than conventional 3-slice acquisition. An adequately powered comparative study is difficult to achieve given the requirement for two separate stress CMR studies in each patient. The aim of this work is to draw relevant conclusions from SPECT MPI by comparing whole-heart versus simulated 3-slice coverage in a large existing dataset. SPECT data from 651 patients with suspected coronary artery disease who underwent invasive angiography were analyzed. A computational approach was designed to model 3-slice MPI by retrospective subsampling of whole- heart data. For both whole-heart and 3-slice approaches, the diagnostic performance and the stress total perfusion deficit (TPD) score-a measure of ischemia extent/severity-were quantified and compared. Diagnostic accuracy for the 3-slice and whole-heart approaches were similar (area under the curve: 0.843 vs. 0.855, respectively; P = 0.07). The majority (54%) of cases missed by 3-slice imaging had primarily apical ischemia. Whole-heart and 3-slice TPD scores were strongly correlated (R2 = 0.93, P < 0.001) but 3-slice TPD showed a small yet significant bias compared to whole-heart TPD (- 1.19%; P < 0.0001) and the 95% limits of agreement were relatively wide (- 6.65% to 4.27%). Incomplete ventricular coverage typically acquired in 3-slice CMR MPI does not significantly affect the diagnostic accuracy. However, 3-slice MPI may fail to detect severe apical ischemia and underestimate the extent/severity of perfusion defects. Our results suggest that caution is required when comparing the ischemic burden between 3-slice and whole-heart datasets, and corroborate the need to establish prognostic thresholds specific to each approach
Spatio-Temporal Modelling of Perfusion Cardiovascular MRI
Myocardial perfusion MRI provides valuable insight into how coronary artery and microvascular diseases affect myocardial tissue. Stenosis in a coronary vessel leads to reduced maximum blood flow (MBF), but collaterals may secure the blood supply of the myocardium but with altered tracer kinetics. To date, quantitative analysis of myocardial perfusion MRI has only been performed on a local level, largely ignoring the contextual information inherent in different myocardial segments. This paper proposes to quantify the spatial dependencies between the local kinetics via a Hierarchical Bayesian Model (HBM). In the proposed framework, all local systems are modelled simultaneously along with their dependencies, thus allowing more robust context-driven estimation of local kinetics. Detailed validation on both simulated and patient data is provided
Deep learning analysis of the myocardium in coronary CT angiography for identification of patients with functionally significant coronary artery stenosis
In patients with coronary artery stenoses of intermediate severity, the
functional significance needs to be determined. Fractional flow reserve (FFR)
measurement, performed during invasive coronary angiography (ICA), is most
often used in clinical practice. To reduce the number of ICA procedures, we
present a method for automatic identification of patients with functionally
significant coronary artery stenoses, employing deep learning analysis of the
left ventricle (LV) myocardium in rest coronary CT angiography (CCTA). The
study includes consecutively acquired CCTA scans of 166 patients with FFR
measurements. To identify patients with a functionally significant coronary
artery stenosis, analysis is performed in several stages. First, the LV
myocardium is segmented using a multiscale convolutional neural network (CNN).
To characterize the segmented LV myocardium, it is subsequently encoded using
unsupervised convolutional autoencoder (CAE). Thereafter, patients are
classified according to the presence of functionally significant stenosis using
an SVM classifier based on the extracted and clustered encodings. Quantitative
evaluation of LV myocardium segmentation in 20 images resulted in an average
Dice coefficient of 0.91 and an average mean absolute distance between the
segmented and reference LV boundaries of 0.7 mm. Classification of patients was
evaluated in the remaining 126 CCTA scans in 50 10-fold cross-validation
experiments and resulted in an area under the receiver operating characteristic
curve of 0.74 +- 0.02. At sensitivity levels 0.60, 0.70 and 0.80, the
corresponding specificity was 0.77, 0.71 and 0.59, respectively. The results
demonstrate that automatic analysis of the LV myocardium in a single CCTA scan
acquired at rest, without assessment of the anatomy of the coronary arteries,
can be used to identify patients with functionally significant coronary artery
stenosis.Comment: This paper was submitted in April 2017 and accepted in November 2017
for publication in Medical Image Analysis. Please cite as: Zreik et al.,
Medical Image Analysis, 2018, vol. 44, pp. 72-8
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