64 results about "Cerebral blood volume" patented technology

Apparatus for modifying a property of a brain of a patient is provided, including one or more electrodes (7), adapted to be applied to a site selected from a group of sites consisting of: a sphenopalatine ganglion (SPG) (6) of the patient and a neural tract originating in or leading to the SPG. A control unit (8) is adapted to drive the one or more electrodes to apply a current to the site capable of inducing (a) an increase in permeability of a blood-brain barrier (BBB) of the patient, (b) a change in cerebral blood flow of the patient, and/or (c) an inhibition of parasympathetic activity of the SPG.

A method for increasing cerebral blood flow in a patient. A electrical stimulating device is provided. The electrical stimulating device is applied to the patient at a region adjacent the cervical sympathetic chain, the brain stem, the head, or the sympathetic nervous system. The electrical stimulating device is applied by any route selected from transcutaneous, subcutaneous, and subarachnoid. The electrical stimulating device is activated to stimulate or inhibit nerve impulses of the cervical sympathetic chain, thereby producing vasodilation in the cerebral vasculature, thereby increasing cerebral blood flow. Devices for increasing cerebral blood flow in a patient are also described.

A shunt for regulating blood pressure between a patient's left atrium and right atrium comprises an anchor comprising a neck region, first and second end regions, and a conduit affixed with the anchor that formed of a biocompatible material that is resistant to transmural and translation tissue ingrowth and that reduces a risk of paradoxical embolism.

The present invention relates to devices and systems that alter intracranial compliance, cerebral blood flow and/or intracranial pressure pulsatility/waveform by oscillating the contraction and expansion of a compressible composition within the cranial or spinal cavities such that they increase intracranial capacity. The contraction and expansion of the compressible composition in the oscillating compliance devices can be due to an individual's intracranial pressure, the result of the expansion and compression of a reservoir which is mediated by the contractility of the heart or driven by a pump gaited to a biorhythm. The invention also relates to methods for protecting an individual's brain from abnormal arterial pulsations and for altering an individual's cerebral blood flow using the devices and systems of the invention. The oscillating compliance devices can be used to treat several diseases and/or conditions characterized by altered/abnormal intracranial compliance, cerebral blood flow and/or intracranial pressure pulsatility/waveform, including hydrocephalus, stroke, dementia and migraine headaches, vasospasms, congestive heart failure, cardiopulmonary bypass or carotid endarterectomy.

A method for non-contrast enhanced 4D time resolved dynamic magnetic resonance angiography using arterial spin labeling of blood water as an endogenous tracer and a multiphase balanced steady state free precession readout is presented. Imaging can be accelerated with dynamic golden angle radial acquisitions and k-space weighted imaging contrast (KWIC) image reconstruction and it can be used with parallel imaging techniques. Quantitative tracer kinetic models can be formed allowing cerebral blood volume, cerebral blood flow and mean transit time to be estimated. Vascular compliance can also be assessed using 4D dMRA by synchronizing dMRA acquisitions with the systolic and diastolic phases of the cardiac cycle.

An apparatus and methodological framework are provided, named perfusion angiography, for the quantitative analysis and visualization of blood flow parameters from DSA images. The parameters, including cerebral blood flow (CBF) and cerebral blood volume (CBV), mean transit time (MTT), time-to-peak (TTP), and T_max, are computed using a bolus tracking method based on the deconvolution of time-density curves on a pixel-by-pixel basis. Individual contrast concentration curves of overlapping vessels can be delineated with multivariate Gamma fitting. The extracted parameters are each transformed into parametric maps of the target that can be color coded with different colors to represent parameter values within a particular set range. Side by side parametric maps with corresponding DSA images allow expert evaluation and condition diagnosis.

A detector for detecting the saturation level of cerebral blood oxygen is composed of probe, synchronous amplifier, A/D converter, single-chip computer system, and display. It features that two LEDs generating different wavelengthes and two light receivers with two photoelectric silicon cells are installed in its probe. The obtained data contains two parts: one is the information about superficial tissue and another is the information about superficial tissue and cerebral blood oxygen. Subtracting one part from another can obtain the information about cerebral blood oxygen. Its advantages include simple structure, high sensitivity and reliability, and low cost.

A method of estimating cerebral blood flow includes obtaining a measure of time-varying blood volume in the head, using an impedance plethysmography (102 and 104), obtaining a measure of time-varying blood volume in the scalp, and using the time-varying blood volume in the head and scalp to estimate cerebral blood flow.

This invention measures cerebral blood volume changes to evaluate, from properties of low-frequency components of such changes and heart rate changes calculated by analysis, a distribution of cerebral blood vessel hardness and its with-time change to thereby estimate and display diseased and dangerous portions based on the evaluation. Briefly, the above-noted object is attainable by a biological measurement system having a cerebral blood volume measurement unit which measures a regional cerebral blood volume of a body under test, an analyzer unit that analyzes a signal measured by the cerebral blood volume measurement unit, an extraction unit for extracting, based on an output of the analysis unit, information concerning a regional cerebral blood vessel state of the test body, and a display unit which displays a measurement result of the cerebral blood volume measurement unit, an analysis result of the analyzer unit or an extraction result of the extraction unit.

Disclosed embodiments relate to an apparatus for detecting brain conditions. The apparatus for detecting brain conditions may include: a layer which is located adjacent to the brain of a living body; a light source which is formed on the layer and irradiates light to the brain; and an optical sensor which is formed on the layer adjacent to the light source and detects the light scattered from the brain. Since detection is possible at a location relatively adjacent to the brain, the apparatus for detecting brain conditions may improve accuracy and reliability of detection. The apparatus for detecting brain conditions may be used to detect brain conditions such as cerebral oxygenation, cerebral blood volume, cerebral blood flow, etc. or to monitor brain activities, or to diagnose and/or localize the disease foci in case of neurovascular disease such as stroke including hemorrhage or bleeding, into or around the brain or brain tumors or epilepsy, etc. Since the apparatus for detecting brain conditions has a relatively flexible structure, damage to the brain tissue may be minimized.

This invention provides a method for treating a mammalian subject afflicted with a disorder associated with reduced neurogenesis in the subject's hippocampal dentate gyrus which comprises administering to the subject a therapeutically effective amount of a compound which increases cerebral blood volume in the subject's hippocampal dentate gyrus by a percentage greater than that by which it increases the cerebral blood volume in the subject's hippocampal CA1 region, thereby treating the subject.

The current invention provides a method of identifying a ischemic lesion. The method includes loading perfusion imaging data into an electronic memory element and deriving perfusion maps from the perfusion imaging data, where the perfusion maps include a cerebral blood volume (CBV) map and an arterial delay time (DT) map, which utilize arterial delay and dispersion effects. Ischemic pixels are determined from the perfusion imaging data, where the DT is greater than a predetermined first threshold value and the CBV is below a second threshold value and the infarct portion of the ischemic lesion is determined, where DT is greater than a predetermined third threshold value and/or the CBV is below a forth threshold value. A cluster analysis is applied to all of the determined ischemic lesion and infarct pixels and the penumbra is then determined, where mismatch regions between the ischemic lesion and the infarct core define the penumbra.

The invention relates to a method for calculating brain blood volume. The method is used for calculating the brain blood volume on the stable status CT (Computed Tomography) brain perfusion imaging principle. The method comprises the following steps of (1) carrying out common whole brain CT scanning to obtain a brain tissue structure image before contrast agent injection; injecting the contrast agent to the vessel exciting area to reach the stable status, and obtaining the brain tissue structure image of the same position; (3) deleting an overhigh brain blood volume value with a vessel pixel deleting method, and deleting the interference of the artery in the existing area to the brain blood content measuring value; (4) and calculating the brain blood flow value of the brain tissue by calculating the ratio of the brain tissue to the signal change in the vessel according to a formula. With the method, all brain scanning can be carried out and the radial dosage of the perfusion scanning can be reduced, thus the method for calculating brain blood volume can be widely applied into the clinical trial.

The invention provides an automatic image processing and displaying method based on a magnetic resonance cerebral perfusion image, which is used for assisting in evaluating cerebral ischemia disease risks and is characterized by comprising spatial deformation, multi-parameterization, brain map coverage and a method for evaluating ischemic cerebral disease risks. The image space deformation methodcomprises the following steps: head movement correction, which is used for adjusting a space difference generated by head movement in a cerebral perfusion imaging process; and standard brain registration: taking the standard brain as a reference to realize standardization of the imported cerebral perfusion image. The multi-parameterization is used for converting the original nuclear magnetic datainto cerebral image perfusion parameters such as cerebral blood flow, cerebral blood volume and artery arrival time, wherein the coverage brain map is used for enabling the parameterized cerebral perfusion image data to cover standard brain maps of different templates to form different regions of interest, and calculating average parameter values of the different regions of interest.The standard cerebral map comprises a cerebral artery blood supply area and an early CT scoring area of an Albetan stroke project. The ischemic brain disease risk assessment method is used for comparing the averageparameter value of the region of interest with a reference range, displaying the differentiation degree and automatically displaying the region of interest beyond the reference range. According to the invention, multi-parameter automatic partitioning and quantitative processing from nuclear magnetic cerebral perfusion original number to ischemic cerebral disease early-stage risk assessment are realized, and an effective assessment method is provided for early-stage screening, early-stage diagnosis and early-stage treatment of cerebral ischemic diseases.

The invention discloses a cerebral blood flow measuring device, a cerebral blood flow measuring system and a helmet, wherein the cerebral blood flow measuring device comprises at least one group of light source device and at least two groups of detection devices; the light source device comprises a single longitudinal mode crystal laser, an optical switch and radiation optical fibers; an output end of the single longitudinal mode crystal laser is connected to an input end of an optical switch; an output end of the optical switch is connected to the at least two radiation optical fibers so as to switch a beam of inputted laser light into at least two beams of laser light and output the at least two beams of laser light; by virtue of the radiation optical fibers, the laser light is transmitted to a to-be-measured part; each detection device comprises a single mode fiber, a collimation device and a silicon photomultiplier; by virtue of the collimation device, received laser light, which is outputted by the single mode fiber, is uniformly transmitted to a receiving window of the silicon photomultiplier; and the silicon photomultiplier is used for converting a received optical signal into an electric signal and for outputting the electric signal. The cerebral blood flow measuring device disclosed by the invention has the advantages of being high in time sampling rate, high in signal to noise ratio, small in volume, good in portability and the like.

A device has a source for emitting near infrared radiation into cerebral tissue, a sensor for detecting radiation exiting from the tissue, and an evaluation unit which detects the exiting radiation as an input signal having pulsatile and non-pulsatile components and is programmed to determine the concentration of an injected indicator in the tissue from the non-pulsatile signal component, iteratively determine an inflow function characterizing cerebral blood flow by varying a mean transit time until reaching a stop criterion, determine indicator concentration relative to cerebral blood volume from the inflow function and the pulsatile signal component, calculate cerebral blood volume by dividing indicator concentration in the tissue by indicator concentration relative to cerebral blood volume, calculate cerebral blood flow by dividing the cerebral blood volume by the mean transit time when the stop criterion has been reached, and scale the inflow function using values determined from the pulsatile signal component.

Methods and systems that detect and differentiate epileptogenic from eloquent and normal cortices are provided. A method for identifying epileptogenic cortices in a brain may include detecting areas in the brain that are undergoing cerebral blood volume low frequency oscillations, detecting areas in the brain that are undergoing blood oxygenation low frequency oscillations; mapping clusters of the brain in which the cerebral blood volume low frequency oscillations are negatively correlated with the blood oxygenation low frequency oscillations, and analyzing the time based relationship between the clusters of the brain that are undergoing negatively correlated low frequency oscillations to determine cause areas, which are areas of the brain that are causing negatively correlated low frequency oscillations to occur elsewhere.

The invention discloses a cerebral blood flow auto-regulation index output method, a storage medium and ultrasonic equipment. The method includes: acquiring cerebral blood flow data and continuous blood pressure data of multiple channels, wherein sampling points of each channel are synchronous; selecting cerebral blood flow data and continuous blood pressure data of each channel according to preset data quantity to obtain a sample data segment of each channel; synchronously analyzing the sample data segment of each channel, and displaying analysis results of each channel on a display interface by groups. Since the cerebral blood flow data and continuous blood pressure data are acquired synchronously, the synchronously selected data segments are analyzed and the analysis results are displayed on the display interface by groups, real-time synchronous displaying of multiple groups of cerebral blood flow auto-regulation indexes in a transcranial Doppler system is realized, and convenience in use is brought to users.

The invention provides a method for evaluating the automatic regulation function of cerebral blood flow of an individual. The method comprises the following steps that 1, external counterpulsation operation is applied to the individual; 2, continuous blood pressure monitoring and cerebral blood flow speed monitoring are conducted on the individual before the external counterpulsation operation, during the external counterpulsation operation and after the external counterpulsation operation; 3, blood pressure changes and cerebral blood flow speed changes, responding to the external counterpulsation operation, of the individual are recorded, and the automatic regulation function of the cerebral blood flow of the individual is evaluated on the basis of the changes. The invention further provides a system for implementing the method.

Embodiments of the present invention disclose a cerebral blood volume correction method and apparatus. The method comprises steps of: detecting bifurcation points of arteries on each frame of image in an image sequence of cerebral arterial geometries of a patient; for any group of arteries of a same status, selecting areas of interest for the arteries on each frame of image; for each area of interest, extracting a blood flow TIC of the area of interest from the image sequence; according to the TIC of each area of interest, calculating blood flow parameter values of the corresponding artery; for any group of arteries of a same status, calculating blood flow differences between different arteries, and according to the blood flow differences, generating a CBV compensation factor M for each artery; based on the anatomical structure of the 3D CBV image cross section of cerebral arteries of the patient, dividing the cross section into a plurality of artery blood-supply areas, and according to the M of the corresponding artery in each artery blood-supply area, correcting the CBV value of the artery blood-supply area. The cerebral blood volume correction method and apparatus, and angiography equipment provided by the present invention reduce the impact of uneven CM distribution on cerebral perfusion symmetry.