A support system aimed at securing an assist device inside a patient's heart, the assist device comprising a pump inside a pump body and being in fluidic communication with an exit cylinder. The support system includes an upstream support element, aimed at securing the upstream extremity of the pump body to the patient's heart, a downstream support element, aimed at securing the exit cylinder to the patient's heart. The upstream support element and the downstream support element are two independent and autonomous functional elements, and the upstream support element and the downstream support element are aimed to removably secure the assist device inside the patient's heart.

A support system aimed at securing an assist device inside a patient's heart, the assist device comprising a pump inside a pump body and being in fluidic communication with an exit cylinder. The support system includes an upstream support element, aimed at securing the upstream extremity of the pump body to the patient's heart, a downstream support element, aimed at securing the exit cylinder to the patient's heart. The upstream support element and the downstream support element are two independent and autonomous functional elements, and the upstream support element and the downstream support element are aimed to removably secure the assist device inside the patient's heart.

Membranes are provided to be specially developed for use in chambers for artificial circulatory assistance which may be employed primarily in cardiovascular procedures, notably to produce arterial capacitance, to regulate blood pressure, to produce aortic counterpulsation and to pump blood. The membrane may have circular sections that may vary in size or not depending on the function to be performed and are interconnected so that the transition between one section and the other is smooth, regardless of the size of each section. Further, chambers and pumps may be used for cardiopulmonary bypass and a pumping system.

Membranes are provided to be specially developed for use in chambers for artificial circulatory assistance which may be employed primarily in cardiovascular procedures, notably to produce arterial capacitance, to regulate blood pressure, to produce aortic counterpulsation and to pump blood. The membrane may have circular sections that may vary in size or not depending on the function to be performed and are interconnected so that the transition between one section and the other is smooth, regardless of the size of each section. Further, chambers and pumps may be used for cardiopulmonary bypass and a pumping system.

The invention relates to a system for treating blood, which includes a single cassette capable of carrying out the various CRRT treatments.

A positive displacement pump that triggers with the beating of a mammalian heart, through the monitoring of an ECG signal is disclosed. A programmable delay from the detection of the forthcoming contraction of the heart enables the pump to syncopate the ejection of the fluid with the events occurring in the cardiovascular system. This delayed ejection could be used to overlay the ejected fluid from the pump with a pressure wave in the artery of systemic circulation through a catheter connection between the pump and a physiological model (e.g., cow, dog, human). The outcome of this use could be to raise the pulse pressure in the system to take advantage of physiological pathways that respond to this transient change in blood pressure. The novelty of this system stems from the adaptable control architecture designed to augment the pulsatile characteristics of the cardiovascular system. This inventive concept could be expanded to encompass the augmentation (dampen or enhance) of pulsatile characteristics in any oscillating flow system.

The invention relates to a monitoring and regulation device configured for implantation in the heart, including at least one pressure sensor located in a distally arranged section of a shaft and a regulation device configured for regulating blood flow and blood pressure. The regulation device includes the shaft, a first pressure valve, a second pressure valve, and a sliding element. The pressure sensor is configured to output data that is used to monitor vital parameters of a cardiovascular system. The shaft is tubular with a lumen that extends axially there through. The shaft has distal and proximal sections and a central section, wherein the distal and proximal sections are disc-shaped extended, thus forming a first double disc at the distal section and a second double disc at the proximal section. The central section links the first and second double discs. The central section of the shaft has an opening. The first pressure valve is disposed in the opening in the central section of the shaft. The second pressure valve is located in the lumen in the proximal section of the shaft. The sliding element is housed inside the lumen. The sliding element has an axially movable and rotatable cylindrical piston and a piston rod, wherein pushing the piston towards the distal section of the shaft or rotating the piston results in a partial or complete closing of the opening for controlling the blood flow.

Membranes are provided to be specially developed for use in chambers for artificial circulatory assistance which may be employed primarily in cardiovascular procedures, notably to produce arterial capacitance, to regulate blood pressure, to produce aortic counterpulsation and to pump blood. The membrane may have circular sections that may vary in size or not depending on the function to be performed and are interconnected so that the transition between one section and the other is smooth, regardless of the size of each section. Further, chambers and pumps may be used for cardiopulmonary bypass and a pumping system.

Membranes are provided to be specially developed for use in chambers for artificial circulatory assistance which may be employed primarily in cardiovascular procedures, notably to produce arterial capacitance, to regulate blood pressure, to produce aortic counterpulsation and to pump blood. The membrane may have circular sections that may vary in size or not depending on the function to be performed and are interconnected so that the transition between one section and the other is smooth, regardless of the size of each section. Further, chambers and pumps may be used for cardiopulmonary bypass and a pumping system.

A lid that retains a pump tube which is elastic; a finger driving unit that is disposed facing the lid with the pump tube interposed therebetween, and that causes a plurality of fingers to sequentially move in the direction of contacting and separating from the lid; and a pump tube opening/closing mechanism that causes the finger driving unit to advance towards and retract from the lid, and that closes and opens the pump tube which is disposed between the fingers and the lid.