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Arnd Doerfler

Publications and source records attributed to Arnd Doerfler.

4 recordsLinked to original sources

A novel use of time separation technique to improve flat detector CT perfusion imaging in stroke patients

CT perfusion imaging (CTP) is used in the diagnostic workup of acute ischemic stroke (AIS). CTP may be performed within the angio suite using flat detector CT (FDCT) to help reduce patient management time. In order to significantly improve FDCT perfusion (FDCTP) imaging, data-processing algorithms need to be able to compensate for the higher levels of noise, slow rotation speed, and a lower frame rate of current FDCT devices. We performed a realistic simulation of FDCTP acquisition based on CTP data from seven subjects. We used the time separation technique (TST) as a model-based approach for FDCTP data processing. We propose a novel dimension reduction in which we approximate the time attenuation curves by a linear combination of trigonometric functions. Our goal was to show that the TST can be used even without prior assumptions on the shape of the attenuation profiles. We first demonstrated that a trigonometric basis is suitable for dimension reduction of perfusion data. Using simulated FDCTP data, we have shown that a trigonometric basis in the TST provided better results than the classical straightforward processing even with additional noise. Average correlation coefficients of perfusion maps were improved for cerebral blood flow (CBF), cerebral blood volume, mean transit time (MTT) maps. In a moderate noise scenario, the average Pearson's coefficient for the CBF map was improved using the TST from 0.76 to 0.81. For the MTT map, it was improved from 0.37 to 0.45. Furthermore, we achieved a total processing time from the reconstruction of FDCTP data to the generation of perfusion maps of under 5 min. In our study cohort, perfusion maps created from FDCTP data using the TST with a trigonometric basis showed equivalent perfusion deficits to classic CT perfusion maps. It follows, that this novel FDCTP technique has potential to provide fast and accurate FDCTP imaging for AIS patients.

physics.med-ph

Noise and dose reduction in CT brain perfusion acquisition by projecting time attenuation curves onto lower dimensional spaces

CT perfusion imaging (CTP) plays an important role in decision making for the treatment of acute ischemic stroke with large vessel occlusion. Since the CT perfusion scan time is approximately one minute, the patient is exposed to a non-negligible dose of ionizing radiation. However, further dose reduction increases the level of noise in the data and the resulting perfusion maps. We present a method for reducing noise in perfusion data based on dimension reduction of time attenuation curves. For dimension reduction, we use either the fit of the first five terms of the trigonometric polynomial or the first five terms of the SVD decomposition of the time attenuation profiles. CTP data from four patients with large vessel occlusion and three control subjects were studied. To compare the noise level in the perfusion maps, we use the wavelet estimation of the noise standard deviation implemented in the scikit-image package. We show that both methods significantly reduce noise in the data while preserving important information about the perfusion deficits. These methods can be used to further reduce the dose in CT perfusion protocols or in perfusion studies using C-arm CT, which are burdened by high noise levels.

physics.med-ph

MRzero -- Fully automated discovery of MRI sequences using supervised learning

Purpose: A supervised learning framework is proposed to automatically generate MR sequences and corresponding reconstruction based on the target contrast of interest. Combined with a flexible, task-driven cost function this allows for an efficient exploration of novel MR sequence strategies. Methods: The scanning and reconstruction process is simulated end-to-end in terms of RF events, gradient moment events in x and y, and delay times, acting on the input model spin system given in terms of proton density, T1 and T2, and $Δ$B0. As a proof of concept, we use both conventional MR images and T1 maps as targets and optimize from scratch using the loss defined by data fidelity, SAR penalty, and scan time. Results: In a first attempt, \textit{MRzero} learns gradient and RF events from zero, and is able to generate a target image produced by a conventional gradient echo sequence. Using a neural network within the reconstruction module allows arbitrary targets to be learned successfully. Experiments could be translated to image acquisition at the real system (3T Siemens, PRISMA) and could be verified in the measurements of phantoms and a human brain \textit{in vivo}. Conclusions: Automated MR sequence generation is possible based on differentiable Bloch equation simulations and a supervised learning approach.

physics.med-ph

Contrast-to-noise ratio analysis of microscopic diffusion anisotropy indices in q-space trajectory imaging

Diffusion anisotropy in diffusion tensor imaging (DTI) is commonly quantified with normalized diffusion anisotropy indices (DAIs). Most often, the fractional anisotropy (FA) is used, but several alternative DAIs have been introduced in attempts to maximize the contrast-to-noise ratio (CNR) in diffusion anisotropy maps. Examples include the scaled relative anisotropy (sRA), the gamma variate anisotropy index (GV), the surface anisotropy (UAsurf), and the lattice index (LI). With the advent of multidimensional diffusion encoding it became possible to determine the presence of microscopic diffusion anisotropy in a voxel, which is theoretically independent of orientation coherence. In accordance with DTI, the microscopic anisotropy is typically quantified by the microscopic fractional anisotropy (uFA). In this work, in addition to the uFA, the four microscopic diffusion anisotropy indices (uDAIs) usRA, uGV, uUAsurf, and uLI are defined in analogy to the respective DAIs by means of the average diffusion tensor and the covariance tensor. Simulations with three representative distributions of microscopic diffusion tensors revealed distinct CNR differences when differentiating between isotropic and microscopically anisotropic diffusion. q-Space trajectory imaging (QTI) was employed to acquire brain in-vivo maps of all indices. For this purpose, a 15 min protocol featuring linear, planar, and spherical tensor encoding was used. The resulting maps were of good quality and exhibited different contrasts, e.g. between gray and white matter. This indicates that it may be beneficial to use more than one uDAI in future investigational studies.

physics.med-ph