44 results about "Heart walls" patented technology

A system for mapping electrical activity of a patient's heart includes a set of electrodes spaced from the heart wall and a set of electrodes in contact with the heart wall. Voltage measurements from the electrodes are used to generate three-dimensional and two-dimensional maps of the electrical activity of the heart.

Method and apparatus for detecting and analyzing heart mechanical activity at a region of interest of a patient's heart are provided. The method comprises acquiring a time sequence of 2-dimensional X-ray images of a region of interest over at least part of a cardiac cycle; detecting coronary vessels in the X-ray images; tracking the coronary vessels through the sequence of images to identify movements of the coronary vessels; and analyzing the movements of the coronary vessels to quantify at least one parameter characterizing heart wall motion in the region of interest.

Disclosed are devices, a systems, and methods for determining the dipole densities on heart walls. In particular, a triangularization of the heart wall is performed in which the dipole density of each of multiple regions correlate to the potential measured at various locations within the associated chamber of the heart. To create a database of dipole densities, mapping information recorded by multiple electrodes located on one or more catheters and anatomical information is used. In addition skin electrodes may be implemented.

The invention relates to an apparatus for monitoring hemodynamic performance of a cardiac chamber. In one embodiment, the apparatus takes real time measurements of the volume and pressure of the cardiac chamber and prepares a PV loop. The apparatus may include an intracardiac echocardiogram catheter with a pressure sensor positioned to measure intracardiac pressure when the distal end of the catheter is deployed in a cardiac chamber. The apparatus may further include control circuitry that receives heart wall surface image data signals from the ultrasound transducer and intracardiac pressure data signals from the pressure senor and generates pressure-volume loop data signals from the surface image data signals and intracardiac pressure data signals in real time.

An external heart wall stress reduction apparatus is provided to create a heart wall shape change. The device is generally disposed to the exterior of a heart chamber to reshape the chamber into a lower stress configuration.

The present invention is a conduit device designed to be placed within a wall of a heart, such as through a prepared opening or hole in the heart wall. The conduit is hollow and extends to form a sleeve over a portion of the heart pump, such as a VAD, which traverses the heart wall and enters a chamber of the heart. The conduit provides for a simplified and noninvasive approach to removal and/or replacement of the heart pump.

A medical device 1 for use in treatment of a valve comprises a treatment element 2 which is configured for location at a region of coaption of leaflets 3 of a valve to resist fluid flow in a retrograde direction through an opening 7 of the valve. The device also comprises a support 4 for the treatment element 2, and an anchor 8 for anchoring the support 4 to a heart wall. The treatment element 2 and/or at least a part of the support 4 comprises a hydrogel.

A system for stabilizing the heart via a helical needle, providing access to the interior of the heart via an introducer sheath, and forming a purse string suture using suture delivered by the helical needle. A helical needle projects distally from the device and terminates in a sharp distal tip. The helical needle is advanced into the heart wall, and is used to stabilize the heart and to pass a purse string suture through the heart tissue. An access port provides access to the interior of the heart via an opening passing through the heart wall in an area circumscribed by the helical needle. The helical needle may have a deflection segment adjacent the distal tip that is more flexible than the rest of the helical distal portion of the helical needle.

A surgical stabilizer for use with a surgical site retractor has a base, a bendable arm, and a distal cuff adapted to resiliently hold a tube of an elongated port-access device. The cuff may have a body defining a partial enclosure within which is held a highly flexible gasket having a slit for resiliently receiving the tube. The surgical site retractor may have a collapsible ring and a flexible outer portion attached thereto, the ring being sized to pass through an intercostal incision and expand therein under adjacent ribs to prevent removal, and the flexible outer portion extending out of the incision and drawing over the stabilizer base to mutually secure the retractor and base. The port-access tube may be for a heart valve delivery system using an elongated port-access device for transapically delivering a prosthetic heart valve to the aortic valve annulus. A method involves partly installing the surgical site retractor, anchoring the base of the stabilizer with the flexible outer portion, deploying the port-access tube from outside the body through the incision and through a puncture in the heart wall, and resiliently capturing a tube of the port-access within the partial enclosure of the stabilizer cuff. A second bendable arm on the base having a clip may be used to hold still a proximal end of the port-access device.

An ablation device, including a catheter and an ablation element incorporating one or more balloons at the distal end of the catheter, has a continuous passageway extending through it from the proximal end of the catheter to the distal side of the expandable ablation element. The ablation device ablates tissue by subjecting it to ultrasound energy, cryogenic energy, chemical, laser beam, microwave, or radiation energy. A probe carrying electrodes is introduced through this passageway and deploys, under the influence of its own resilience, to a structure incorporating a loop which is automatically aligned with the axis of the expandable ablation device, so that minimal manipulation is required to place the probe. Pulmonary vein potential is monitored in real time via the electrodes. The probe may have an atraumatic tip with a ball formed at the leading edge. The atraumatic tip prevents any tissue damage such as perforation of heart wall.

The present disclosure provides an apical connector for use in a heart wall. The apical connector may include a port defining an aperture therethrough, an anchoring device extending distally from the port and configured for advancing at least partially through the heart wall, and a cannula configured for advancing through the aperture of the port and at least partially through the heart wall. The cannula may include a locking tab configured to engage the port and lock the cannula with respect to the port.

A handpiece for a medical laser system comprising a barrel for having a passage for transmitting a laser beam and a contacting wall on one end of said barrel including an aperture in communication with the passage, a solid face extending radially outward from the aperture to the periphery of said contacting wall, and a knurled surface on the face for preventing movement of the contacting wall with respect to the heart wall during surgery.

A handpiece for use in transmyocardial revascularization heart-synchronized pulsed laser system includes a barrel having a passage for transmitting a laser beam; a surface at the distal end of the barrel for contacting the wall of the heart; an aperture located at the distal end of the barrel and the enlarged surface for transmitting the laser beam; and means for focusing the laser beam proximate to the aperture to vaporize the tissue of the heart wall and create a hole to the interior heart chamber.

An actuation system for assisting the operation of a natural heart is disclosed. The actuation system includes a framework for interfacing with the natural heart and a power system that can be coupled to the framework. The framework includes an internal framework element and an external framework element. The power system is configured to engage an exterior surface of the heart wall, and includes an actuator mechanism for exerting force on the heart wall, a driving mechanism for actuating the actuator mechanism, a transmission mechanism coupled between the actuator mechanism and the driving mechanism for transmitting power to the actuator mechanism, and a carrier device coupled between the actuator mechanism and the driving mechanism and configured for housing the transmission mechanism. The modular power system is configured for being freely exchanged and replaced in the actuation system while leaving the framework elements in place and generally undisturbed. A guide structure such as a wire or tube can also be included for guiding or advancing the power system to its position adjacent to the heart surface.

Ultrasound systems and methods provide a workflow to automatically identify a fetal heartbeat. A region of interest (ROI) is identified in an ultrasound image and an ROI is identified that contains the fetal heart. The ultrasound system produces spatially different M-mode lines associated with the ROI. The ultrasound system can identify a fetal heartbeat by tracking the changing position of the heart wall and estimate the fetal heart rate, e.g. by measuring from peak-to-peak of two subsequent waves. The echo signals for the M-mode lines can also be ranked according to the likely presence of a fetal heartbeat in the echo data.