Disclosed herein are in vivo non-invasive methods and devices for the measurement of the hemodynamic parameters, such as such as blood pressure, stroke volume, cardiac output, performance of the aortic and mistral heart valves, arterial blood velocity profile, blood viscosity and the blood flow induced arterial wall shear stress, hypertensive/hypotensive and vasodilation/vasocontraction state and aging status of a subject, and the mechanical anelastic in vivo properties of the arterial blood vessels. An exemplary method requires obtaining the peripheral pulse volume waveform (PVW), the peripheral pulse pressure waveform (PPW), and the peripheral pulse velocity waveform (PUW) from the same artery; calculating the time phase shift between the PPW and PVW, and the plot of pulse pressure versus pulse volume; and determining the blood pressures and power law components of the anelastic model from the waveforms PPW and PVW, the cardiac output and heart valves performances from the waveforms PPW and PUW, and the anelastic in vivo properties of the descending, thoracic and abdominal aorta. The disclosed methods and devices can be used to diagnose and treat cardiovascular disease in a subject in need thereof.

A system and method is disclosed for measurement of pulse wave velocity of a vessel. An intravascular device comprises a first and a second marker provided at different locations along the length of the intravascular device of which positions are localizable by a tracking apparatus. The intravascular device provides plurality of measurements along the length of the vessel, while the intravascular device is moved from a first position to a second position, corresponding to a first and a second time. At the second time the position of the first marker in the vessel corresponds to the position of the second marker at the first time. The pulse wave velocity value of the vessel is ascertained based on measurements associated for the first time and the second time from the plurality of measurements and based on the distance between the locations of the two markers along the length of the intravascular device.

The invention provides a method for generating a transvalvular pressure quantification within a cavity. The method includes acquiring a plurality of color Doppler ultrasound image frames, wherein the image frames comprise a view of a valve, one of which is then presented to a user. The user may then provide an input to indicate the location of the valve within the image frame. The location of the valve is then tracked within the remaining image frames based on the user input. A vector flow is estimated based on the color Doppler image frames and the tracked location of the valve, which may be used to estimate the flow across the valve(s) and in the cavity.

The invention provides a method for generating a transvalvular pressure quantification within a cavity. The method includes acquiring a plurality of color Doppler ultrasound image frames, wherein the image frames comprise a view of a valve, one of which is then presented to a user. The user may then provide an input to indicate the location of the valve within the image frame. The location of the valve is then tracked within the remaining image frames based on the user input. A vector flow is estimated based on the color Doppler image frames and the tracked location of the valve, which may be used to estimate the flow across the valve(s) and in the cavity.

There is provided a method for determining a pulse transmission time, an arteriosclerosis detection apparatus and a system, the method comprising: receiving a single-lead electro-cardio signal; receiving a pulse wave signal of at least one of body parts, the pulse wave signal being detected by a micro ultrasonic detector arranged at the respective body parts; and determining the pulse transmission time by taking an R wave of the single-lead electro-cardio signal as a starting point and taking a feature point of the pulse wave signal of the at least one of the body parts as an end point.

The present invention, in some embodiments thereof, relates to methods and/or apparatus for measuring the effectiveness of a renal denervation treatment. In some embodiments, a method for determining effectiveness of the denervation treatment comprises tracking at least one of arterial wall movement, arterial blood flow rate, arterial blood flow velocity, blood pressure and arterial diameter at one or more selected locations in the renal artery over time, and assessing the effectiveness of said renal denervation treatment according to results obtained by tracking.

The present invention, in some embodiments thereof, relates to methods and/or apparatus for measuring the effectiveness of a renal denervation treatment. In some embodiments, a method for determining effectiveness of the denervation treatment comprises tracking at least one of arterial wall movement, arterial blood flow rate, arterial blood flow velocity, blood pressure and arterial diameter at one or more selected locations in the renal artery over time, and assessing the effectiveness of said renal denervation treatment according to results obtained by tracking.

A system for controlling blood pressure includes a wearable interface having an internal contact surface, the wearable interface configured to at least partially encircle a first portion of a first limb of a subject, a sensing module carried by the wearable interface and configured to determine at least a change in blood pressure of the first limb of the subject, and an energy application module carried by the wearable interface and configured to apply energy of two or more types to the first limb of the subject.

A system for controlling blood pressure includes a wearable interface having an internal contact surface, the wearable interface configured to at least partially encircle a first portion of a first limb of a subject, a sensing module carried by the wearable interface and configured to determine at least a change in blood pressure of the first limb of the subject, and an energy application module carried by the wearable interface and configured to apply energy of two or more types to the first limb of the subject.

In part, the disclosure relates to computer-based methods, and systems suitable for evaluating a cardiac system using a diagnostic metric such as a pressure value-based ratio. Selection of a subset or portion of a cardiac cycle is avoided in one embodiment to increase reliability and usability of a diagnostic ratio and parameters described herein. In one embodiment, a minimum or a relative extrema of a series of diagnostic metrics plotted on a per cycle basis are used to inform diagnosis of a stenosis or other intravascular event or phenomena.