A system and method for generating a parametric map of a subject's brain includes receiving non-contrast computed tomography (NCCT) imaging data and receiving computed tomography perfusion (CTP) data. The method further includes creating a baseline image by utilizing the NCCT data and generating a parametric map using the CTP data and the baseline image.

Uptake of hypoxia-sensitive PET tracers is dependent on tissue transport properties, specifically, distribution volume. Variability in tissue transport properties reduces the sensitivity of static PET imaging to hypoxia. When tissue transport (v.sub.d) effects are substantial, correlations between the two methods of determining hypoxic fractions are greatly reduced—that is, trapping rates k.sub.3 are only modestly correlated with tumour-to-blood ratio (TBR). In other words, the usefulness of dynamic- and static-PET based hypoxia surrogates, trapping rate k.sub.3 and TBR, in determining hypoxic fractions is reduced in regions where diffusive equilibrium is achieved slowly. A process is provided for quantifying hypoxic fractions using a novel biomarker for hypoxia, hypoxia-sensitive tracer binding rate k.sub.b, based on PET imaging data. The same formalism can be applied to model the kinetics of non-binding CT and MT contrast agents, giving histopathological information about the imaged tissue.

The disclosure discloses a method, a device, a system and a computer storage medium for obtaining the CT perfusion imaging parameter maps of brain. The method includes: obtaining CT perfusion images, pre-processing the CT perfusion images, and obtaining discrete contrast agent concentration curves C(n) of each pixel point in the brain tissue; reading the acquisition time information of the CT perfusion images to obtain the acquisition time arrays T(n); intercepting the acquisition time arrays T(n) to obtain the relative acquisition time arrays t(n); combining the discrete contrast agent concentration curves C(n) with the corresponding relative acquisition time arrays t(n) to obtain the discrete time-concentration curves C(t.sub.n) of each pixel point in the brain tissue; after fitting or interpolating the discrete time-concentration curves C(t.sub.n), re-discretizing at the same time interval, and obtaining the discrete time-concentration curves C(n)′ of each pixel point in brain tissue.

Embodiments include a system for determining cardiovascular information for a patient. The system may include at least one computer system configured to receive patient-specific data regarding a geometry of the patient's heart, and create a three-dimensional model representing at least a portion of the patient's heart based on the patient-specific data. The at least one computer system may be further configured to create a physics-based model relating to a blood flow characteristic of the patient's heart and determine a fractional flow reserve within the patient's heart based on the three-dimensional model and the physics-based model.

Methods and systems are provided for extracting cardiac frequency angiographic phenomena for an unconstrained vascular object from an angiographic study. In one example, a computer may obtain a series of angiographic image frames obtained at a rate faster than cardiac frequency. Each image frame may comprise a plurality of pixels, and each pixel may have a corresponding intensity. The computer may apply an optical flow technique to the angiographic image frames to generate a plurality of paths corresponding to a displacement of respective pixels from image frame to image frame. The computer may further generate a spatiotemporal reconstruction of cardiac frequency angiographic phenomena based on the plurality of paths and the corresponding intensities associated with respective pixels of the paths, and output for display the spatiotemporal reconstruction of cardiac frequency angiographic phenomena in one or more images.

The present invention relates to a device (1) for fractional flow reserve determination. The device (1) comprises a model generator (10) configured to generate a three-dimensional model (3DM) of a portion of an imaged vascular vessel tree (VVT) surrounding a stenosed vessel segment (SVS), based on a partial segmentation of the imaged vascular vessel tree (VVT). Further, the device comprises an image processor (20) configured to calculate a blood flow (Q) through the stenosed vessel segment (SVS) based on an analysis of a time-series of X-ray images of the vascular vessel tree (VVT). Still further, the device comprises a fractional-flow-reserve determiner (30) configured to determine a fractional flow reserve (FFR) based on the three-dimensional model (3DM) and the calculated blood flow.

The present disclosure is directed to a method and system for automatically predicting a physiological parameter based on images of vessel. The method includes receiving the images of a vessel acquired by an imaging device. The method further includes determining a sequence of temporal features at a sequence of positions on a centerline of the vessel based on the images of the vessel, and determining a sequence of structure-related features at the sequence of positions on the centerline of the vessel. The method also includes fusing the sequence of structure-related features and the sequence of temporal features at the sequence of positions respectively. The method additionally includes determining the physiological parameter for the vessel at the sequence of positions, by using a sequence-to-sequence neural network configured to capture sequential dependencies among the sequence of fused features.

Embodiments of the disclosure provide methods and systems for multi-modality joint analysis of a plurality of vascular images. The exemplary system may include a communication interface configured to receive the plurality of vascular images acquired using a plurality of imaging modalities. The system may further include at least one processor, configured to extract a plurality of vessel models for a vessel of interest from the plurality of vascular images. The plurality of vessel models are associated with the plurality of imaging modalities, respectively. The at least one processor is also configured to fuse the plurality of vessel models associated with the plurality of imaging modalities to generate a fused model for the vessel of interest. The at least one processor is further configured to provide a diagnostic analysis result based on the fused model of the vessel of interest.

A medical image processing apparatus according to an embodiment includes processing circuitry. The processing circuitry acquires medical images of multiple time phases. The processing circuitry generates a vascular territory image showing plural vascular territories included in the subject tissue. The processing circuitry sets a region of interest in the subject tissue. The processing circuitry sets at least two regions out of the vascular territories and an ischemia area in the region of interest based on the vascular territory image. The processing circuitry calculates a ratio of each of the at least two regions to the region of interest. The processing circuitry outputs information about the ratio.

This disclosure discloses a method for analyzing clinical data. The Method includes extracting a first feature information by applying a neural network to the clinical data; predicting a disease status related parameter by applying a regression model to the extracted first feature information; generating a second feature information based on the extracted first feature information and the disease status related parameter; and predicting a disease status classification result by applying a classification model to the second feature information. The method can improve the prediction accuracy and the diagnosis efficiency of doctors.