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Statistical SPECT reconstruction can be very time-consuming especially when compensations for collimator and detector response, attenuation, and scatter are included in the reconstruction. This work proposes an accelerated SPECT reconstruction algorithm based on graphics processing unit (GPU) processing. Ordered subset expectation maximization (OSEM) algorithm with CT-based attenuation modelling, depth-dependent Gaussian convolution-based collimator-detector response modelling, and Monte Carlo-based scatter compensation was implemented using OpenCL. The OpenCL implementation was compared against the existing multi-threaded OSEM implementation running on a central processing unit (CPU) in terms of scatter-to-primary ratios, standardized uptake values (SUVs), and processing speed using mathematical phantoms and clinical multi-bed bone SPECT/CT studies. The difference in scatter-to-primary ratios, visual appearance, and SUVs between GPU and CPU implementations was minor. On the other hand, at its best, the GPU implementation was noticed to be 24 times faster than the multi-threaded CPU version on a normal 128 x 128 matrix size 3 bed bone SPECT/CT data set when compensations for collimator and detector response, attenuation, and scatter were included. GPU SPECT reconstructions show great promise as an every day clinical reconstruction tool.

We introduce an a posteriori modeling error estimator for the effective computation of electric potential propagation in the heart. Starting from the Bidomain problem and an extended formulation of the simplified Monodomain system, we build a hybrid model, called Hybridomain, which is dynamically adapted to be either Bi- or Monodomain ones in different regions of the computational domain according to the error estimator. We show that accurate results can be obtained with the adaptive Hybridomain model with a reduced computational cost compared to the full Bidornain model. We discuss the effectivity of the estimator and the reliability of the results on simulations performed on real human left ventricle geometries retrieved from healthy subjects. (C) 2010 Elsevier B.V. All rights reserved.