Abstract: A method for rapid computation of three-dimensional displacement and Lagrange strain in a high resolution filed of phase data obtained with Displacement Encoding with Stimulated Echoes (DENSE) in magnetic resonance images of the myocardium. The method includes semi-automated segmentation of a region of a heart, phase unwrapping the images in three dimensions, and a custom radial point interpolation method (RPIM). The RPIM is a meshfree numerical analysis method that uses radial basis functions and polynomial functions to calculate the Lagrange strain of DENSE displacement data acquired from the myocardium.

Abstract: A method for rapid computation of three-dimensional displacement and Lagrange strain in a high resolution filed of phase data obtained with Displacement Encoding with Stimulated Echoes (DENSE) in magnetic resonance images of the myocardium. The method includes semi-automated segmentation of a region of a heart, phase unwrapping the images in three dimensions, and a custom radial point interpolation method (RPIM). The RPIM is a meshfree numerical analysis method that uses radial basis functions and polynomial functions to calculate the Lagrange strain of DENSE displacement data acquired from the myocardium.

Abstract: The strain at different locations in a subject's heart is determined by acquiring a series of MR images using a tagging pulse sequence (SPAMM) that produces a grid of lines in the reconstructed images. Circumferential strain, longitudinal strain, and the minimum principal strain angle, are all calculated at locations in the heart. These raw strain values are normalized by comparing them with corresponding values in a stored reference heart model. The normalized values at each location are combined to form a composite multiparametric strain index that is indicative of myocardial contractile function and these values are employed to modulate the color at corresponding locations in an anatomical image of the subject's heart.

Abstract: The strain at different locations in a subject's heart is determined by acquiring a series of MR images using a tagging pulse sequence (SPAMM) that produces a grid of lines in the reconstructed images. Circumferential strain, longitudinal strain, and the minimum principal strain angle, are all calculated at locations in the heart. These raw strain values are normalized by comparing them with corresponding values in a stored reference heart model. The normalized values at each location are combined to form a composite multiparametric strain index that is indicative of myocardial contractile function and these values are employed to modulate the color at corresponding locations in an anatomical image of the subject's heart.

Abstract: In one embodiment described in the specification, a surgically implantable reciprocating pump employs a check valve as the piston, which is driven by a permanent magnet linear electric motor to assist either side of the natural heart. The pump is implanted in the aorta or pulmonary artery using vascular attachment cuffs such as flexible cuffs for suturing at each end with the pump output directly in line with the artery. The pump is powered by surgically implanted rechargeable batteries. In another embodiment, pairs of pumps are provided to replace or assist the natural heart or to provide temporary blood flow throughout the body, for example, during operations to correct problems with the natural heart.

Abstract: In one embodiment described in the specification, a surgically implantable reciprocating pump employs a check valve as the piston, which is driven by a permanent magnet linear electric motor to assist either side of the natural heart. The pump is implanted in the aorta or pulmonary artery using vascular attachment cuffs such as flexible cuffs for suturing at each end with the pump output directly in line with the artery. The pump is powered by surgically implanted rechargeable batteries. In another embodiment, pairs of pumps are provided to replace or assist the natural heart or to provide temporary blood flow throughout the body, for example, during operations to correct problems with the natural heart.

Abstract: In one embodiment described in the specification, a surgically implantable reciprocating pump employs a check valve as the piston, which is driven by a permanent magnet linear electric motor to assist either side of the natural heart. The pump is implanted in the aorta or pulmonary artery using vascular attachment cuffs such as flexible cuffs for suturing at each end with the pump output directly in line with the artery. The pump is powered by surgically implanted rechargeable batteries. In another embodiment, pairs of pumps are provided to replace or assist the natural heart or to provide temporary blood flow throughout the body, for example, during operations to correct problems with the natural heart.

Abstract: In one embodiment described in the specification, a surgically implantable reciprocating pump employs a check valve as the piston, which is driven by a permanent magnet linear electric motor to assist either side of the natural heart. The pump is implanted in the aorta or pulmonary artery using vascular attachment cuffs such as flexible cuffs for suturing at each end with the pump output directly in line with the artery. The pump is powered by surgically implanted rechargeable batteries. In another embodiment, pairs of pumps are provided to replace or assist the natural heart or to provide temporary blood flow throughout the body, for example, during operations to correct problems with the natural heart.

Abstract: In one embodiment described in the specification, a surgically implantable reciprocating pump employs a check valve as the piston, which is driven by a permanent magnet linear electric motor to assist either side of the natural heart. The pump is implanted in the aorta or pulmonary artery using vascular attachment cuffs such as flexible cuffs for suturing at each end with the pump output directly in line with the artery. The pump is powered by surgically implanted rechargeable batteries. In another embodiment, pairs of pumps are provided to replace or assist the natural heart or to provide temporary blood flow throughout the body, for example, during operations to correct problems with the natural heart.

Abstract: In one embodiment described in the specification, a surgically implantable reciprocating pump employs a check valve as the piston, which is driven by a permanent magnet linear electric motor to assist either side of the natural heart. The pump is implanted in the aorta or pulmonary artery using vascular attachment cuffs such as flexible cuffs for suturing at each end with the pump output directly in line with the artery. The pump is powered by surgically implanted rechargeable batteries. In another embodiment, pairs of pumps are provided to replace or assist the natural heart or to provide temporary blood flow throughout the body, for example, during operations to correct problems with the natural heart.

Abstract: In one embodiment described in the specification, a surgically implantable reciprocating pump employs a check valve as the piston, which is driven by a permanent magnet linear electric motor to assist either side of the natural heart. The pump is implanted in the aorta or pulmonary artery using vascular attachment cuffs such as flexible cuffs for suturing at each end with the pump output directly in line with the artery. The pump is powered by surgically implanted rechargeable batteries. In another embodiment, pairs of pumps are provided to replace or assist the natural heart or to provide temporary blood flow throughout the body, for example, during operations to correct problems with the natural heart.

Abstract: In one embodiment described in the specification, a surgically implantable reciprocating pump employs a check valve as the piston, which is driven by a permanent magnet linear electric motor to assist either side of the natural heart. The pump is implanted in the aorta or pulmonary artery using vascular attachment cuffs such as flexible cuffs for suturing at each end with the pump output directly in line with the artery. The pump is powered by surgically implanted rechargeable batteries. In another embodiment, pairs of pumps are provided to replace or assist the natural heart or to provide temporary blood flow throughout the body, for example, during operations to correct problems with the natural heart.

Abstract: In one embodiment described in the specification, a surgically implantable reciprocating pump employs a check valve as the piston, which is driven by a permanent magnet linear electric motor to assist either side of the natural heart. The pump is implanted in the aorta or pulmonary artery using vascular attachment cuffs such as flexible cuffs for suturing at each end with the pump output directly in line with the artery. The pump is powered by surgically implanted rechargeable batteries. In another embodiment, pairs of pumps are provided to replace or assist the natural heart or to provide temporary blood flow throughout the body, for example, during operations to correct problems with the natural heart.

Abstract: A surgical device and method are disclosed for closing the sternum following a median sternotomy. Instead of using stainless steel wire or a flat steel band, a strand of thin flexible suture material is used which is compressible in its radial dimension (either because of a hollow tubular shape, or due to solid material properties), while remaining strong and inelastic in its longitudinal dimension. The longitudinal strength may be maintained by using selected plastics, or by using nylon fibers or other materials for reinforcement. When not compressed, the strand has a diameter slightly larger than the diameter of the needle used to place the strand in position around the sternal halves, between the ribs. After insertion, the expandable suture material will provide gentle pressure against the surrounding tissue to minimize bleeding in the needle track.

Abstract: This invention relates to a method of surgically implanting a blood pump into the ascending aorta or pulmonary artery of a patient with a diseased or damaged heart ventricle. One preferred type of pump which is well-suited for such implantation has an impeller design that generates central axial flow (CAF). After implantation of the CAF pump, blood flows through the hollowed-out rotor shaft of an electric motor. The CAF rotor shaft contains angled vanes mounted on the inner surface of the hollow shaft, extending only part of the distance toward an imaginary axis at the center of the rotor shaft. Rotation of the hollow shaft with its angled vanes pumps blood through the pumping unit. The vanes contact and impart forward motion to a portion of the blood at the periphery of the flow path, generating an outer fluid annulus which is being directly propelled by the vanes.