31 results about "Diastolic phase" patented technology

Methods and apparatus for mitral valve repair are disclosed herein where the posterior mitral leaflet is supported or buttressed in a frozen or immobile position to facilitate the proper coaptation of the leaflets. An implantable apparatus may be advanced and positioned intravascularly beneath the posterior leaflet of the mitral valve. The apparatus may include one or more individual balloon members, each of which may be optionally configured with supporting integrated structures. A magnet chain catheter may be positioned within the coronary sinus and adjacent to the mitral valve to magnetically secure the apparatus in position beneath the posterior mitral leaflet. Alternatively, a split-ring device may be placed about the chordae tendineae supporting the mitral valve such that the ring slides along the chordae tendineae alternately against the mitral leaflet and towards the papillary muscles during systole and diastole.

An annuloplasty ring to resize a dilated aortic root during valve sparing surgery includes a scalloped space frame having three trough sections connected to define three crest sections. The annuloplasty ring is mounted outside the aortic root, and extends in height between a base plane and a spaced apart commissure plane of the aortic root. At least two adjacent trough sections are coupled by an annulus-restraining member or tether that limits the maximum deflection of the base of the annuloplasty ring. In use, the tether is preferably located in proximity to the base plane of the aortic root. The annuloplasty ring is movable between a first, substantially conical configuration occurring during a diastolic phase of the cardiac cycle, and a second, substantially cylindrical configuration occurring during a systolic phase of the cardiac cycle. The attachment of the annuloplasty ring in proximity to the cardiac valve annulus allows the ring to regulate the dimensions of a dynamic aortic root during the different phases of the cardiac cycle.

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.

The invention relates to a method for realizing the three-dimension ultrasonic cardiogram four-chamber section image automatic check, which comprises that 1, extracting one three-dimension data from the end-diastolic phase of heart from the heart full-volume data; 2, extracting 180 section images from the three-dimension data to build an image database; 3, calculating out the similarity between each image of database and the template image, to be selected and using wavelet system statistic character to check out the image with highest similarity in the left image, to record the position in the data as the four-chamber watch position. The invention realizes the automatic search function of four-chamber section; therefore, medical staff can use real-time three-dimension ultrasonic technique to diagnose the patient.

A contactless system for measuring and continuously monitoring arterial blood pressure includes a light source configured to illuminate light having at least one predetermined wavelength at a predetermined area of a human subject having an artery therein. A detector responsive to reflected light from the predetermined area is configured to continuously acquire images of the artery in the predetermined area. A processor is configured to process the images and determine: when an image at a proximal location of the predetermined area is darker indicating transition of a pulse wave into the artery at the proximal location and at a proximal time and when an image at a distal location of the predetermined area is darker indicating transition of the pulse wave into the artery at a distal location at a distal time, determine the difference in time between the distal time and the proximal time to calculate a pulse transit time (PTT), determine a length between the proximal location and the distal location, determine a diameter of the artery during a systolic phase of a cardiac pulse, determine a diameter of the artery during a diastolic phase of a cardiac pulse, calculate a pulse wave velocity of the pulse wave, calculate pulse pressure (ΔP), calculate an elastic modulus (E) of the artery, and contactlessly and continuously calculate the arterial blood pressure for each cardiac cycle of the human subject.

A system for crossing a heart valve with a guidewire includes an advancement motor and a controller. The controller controls when the advancement motor advances and retracts the guidewire. The controller is coupled to an electrocardiogram device and determines the systolic and diastolic phase of the heart from information/data from the electrocardiogram device. The guidewire advances or retracts based on the controller's determination of the systolic or diastolic phase corresponding with the heart valve being in an open configuration. The system may include a catheter including a lumen through which the guidewire is disposed. The system may further include a sensor. The sensor is in communication with the controller, and the controller will stop advancement of the guidewire if the controller determines the guidewire has not advanced between open leaflets of the heart valve based upon information/data from the sensor.

A valve repair device for repairing a native heart valve of a patient includes a pair of clasps, where each clasp is configured to attach to native valve leaflet. The ends of the pair of clasps can move away from one another to a partially open position when the native valve leaflets open during a diastolic phase of a cardiac cycle, and the ends of the pair of clasps can move toward one another when the native valve leaflets close during a systolic phase of a cardiac cycle.

A method, an apparatus, and a kit including the apparatus and a fluorescence agent are provided for measuring a time-varying change in an amount of blood in a tissue volume, and include exciting a fluorescence agent in the blood, acquiring a time-varying light intensity signal during a pulsatile flow of the blood through the tissue volume, the pulsatile flow having a systolic and a diastolic phase resembling a conventional photoplethysmogram, and processing the acquired signal by applying a modified Beer-Lambert law to obtain a measurement of the time-varying change in the amount of blood in the tissue volume. The instantaneous molar concentration of the fluorescence agent is determined by utilizing a concentration-mediated change in a fluorescence emission spectrum of the fluorescence agent. There is further provided a fluorescence agent for use in the method.

The invention relates to a method of MR imaging, wherein a portion of a body (10) placed in the examination volume of a MR device (1) is subjected to an imaging sequence (IMG) of RF pulses and switched magnetic field gradients. The imaging sequence (IMG) is a stimulated echo sequence including i) at least two preparation RF pulses (α) radiated toward the portion of the body (10) during a preparation period (21), and ii) one or more reading RF pulses (β) radiated toward the portion of the body (10) during an acquisition period (22) temporally subsequent to the preparation period (21). One or more FID signals (I₁) and one or more stimulated echo signals (I₂) are acquired during the acquisition period (22). A B₁ map indicating the spatial distribution of the RF field of the RF pulses within the portion of the body (10) is derived from the acquired FID (I₁) and stimulated echo (I₂) signals. It is an object of the invention to provide an improved B₁ mapping method which can be applied in magnetic resonance angiography (MRA) and, in particular, in cardiac imaging, where the acquisition of a complete B₁ map needs to be performed within the diastolic phase of the heartbeat. The invention proposes that the portion of the body (10) is subjected to a suppression sequence (BB) for suppression of MR signals emanating from blood prior to the imaging sequence (IMG). Moreover, the invention relates to a MR device (1) and to a computer program for a MR device (1).

A cardiac ventricular assist device or VAD includes a pumping unit with a variable-volume chamber capable of receiving a mass of blood, and a control unit to control the pumping unit to obtain contraction of the variable-volume chamber, with consequent expulsion of the blood collected in the chamber, and expansion of the variable-volume chamber consequent on the flow of blood into the chamber. A flow line is included, such as a transcutaneous line, for a gaseous flow caused by the contraction and expansion of the variable-volume chamber. A sensor sensitive to the gaseous flow in the flow line generates a flow-meter signal that is indicative of the expulsion and inflow of blood with regard to the variable-volume chamber. The control unit is sensitive to said flow-meter signal and utilises that signal to control the pumping unit, for example to cause the pumping unit to operate in a condition of synchronous counterpulsation with regard to the natural heart, that is with the variable-volume chamber capable of receiving blood from the assisted heart when it is in a systolic phase and the variable-volume chamber that expels the blood collected in the chamber, when the assisted heart is in a diastolic phase.

Embodiments of the present invention provide an improved transformation method whereby the peripheral pulse waveform is filtered to separate different phases which make up the waveform. The separate phases are transformed before being re-combined to provide an estimated intra-arterial transfer function. For example, in one embodiment the peripheral pulse waveform is filtered by a first high pass filter, and a copy of the peripheral pulse waveform filtered by a second high pass filter, having a different cut-off frequency. The two filtered waveforms may then be further processed, for example by being added back to original wave-form, and are then multiplexed together in a time division manner to provide a final waveform. For example, the part of the first filtered waveform corresponding to the systolic phase may be combined with the part of the second filtered waveform corresponding to the diastolic phase to produce the final waveform, and the respective filter cut-off frequencies may be chosen to extract characteristics of the respective phases of the heart.

The embodiment of the invention relates to an ejection fraction data processing method and device based on a cardiac ultrasound video. The method comprises the steps that the cardiac ultrasound video is acquired; performing image framing to obtain a first framed image sequence; performing left ventricle lengthwise axis key point identification on each first sub-frame image based on an image target key point identification model; performing left ventricle semantic segmentation processing on each first framing image based on an image semantic segmentation model to generate a second framing image with a left ventricle segmented sub-image; screening processing of framing images at the end of a systolic period and at the end of a diastolic period is carried out on the second framing image sequence; performing left ventricular volume calculation to generate corresponding left ventricular volume parameters; generating a systolic end volume mean value and a diastolic end volume mean value; and ejection fraction data is calculated and generated according to the volume mean value of the end of the systolic period and the end of the diastolic period. By means of the method, the manual intervention link in a traditional method can be eliminated, and the ejection fraction calculation precision and accuracy can be improved.

An extracorporeal circulation management device pumps blood in synchronization with heartbeats of a patient based on measurements of blood flow. Maximum and minimum blood flow measurement samples are compared with upper and lower threshold values to identify candidate timing for a systolic phase and diastolic phase of the heartbeat. During pulsatile pumping of the blood using the candidate timing, differences in the pulsatile flow measurements are determined. Based on the size of the difference, a final correction may be made to identification of the systolic and diastolic phases, and the corrected phase information is used to start and stop the motor unit.

The invention relates to a minimally invasive path of an extracorporeal blood pump aorta counterpulsation circulation auxiliary device and an implantation method. The implantation method of the extracorporeal blood pump aorta counterpulsation minimally invasive path is characterized in that: making a cutting mark in the center of sternum corresponding to a selected part on an aortic valve, drilling a circular hole, implanting and fixing a counterpulsation pump pipeline into an ascending aorta through minimally invasive surgery, and connecting the pipeline to an external counterpulsation pump balloon after exhausting. The method has the advantages that: the circular hole is drilled in the center of the sternum, a hose is implanted into the ascending aorta and fixed through minimally invasive surgery, and the hose is connected to the external counterpulsation pump balloon after exhausting. Through pressure or electrocardio waveforms, a controller achieves synchronous counterpulsation assistance through the diastolic period of the counterpulsation pump, and the purposes of assisting circulation and treating heart failure are achieved. The cure rate of acute heart failure can be greatly improved; after implantation, physical strength permitted, the patient is allowed to take food, urinate, defecate and move out of bed by himself/herself; the ICU residence time is shortened; and long-time assistance is achieved, and no obvious complications exist.

The invention relates to an apparatus configured to display an aortic valve image and an indicator when the aortic valve is in its open-state and/or when the valve is in its closed-state. The indicator is supposed to be in an overlay to the image of the aortic valve, such that a physician can see on the same display image the information needed to advance a guide wire or catheter through the aortic valve of a heart. This may prevent damaging ensures not to damage the aortic valve. The physician receives the relevant information, when the aortic valve is in its open-state and thus being in a state to be passed by the catheter. The information, whether the aortic valve is in its open-state or in its closed-state, corresponds to the systolic phase and the distal phase of the heart, respectively. The information, when the heart is in its systolic phase and when it is in the diastolic phase may be extracted from an ECG measurement. From the detection of these cardiac phases, the closed-state of the valve and/or the open-state of the valve can be estimated using general knowledge about flood flow during the cardiac cycle.