Abstract: Systems and methods for wireless energy transfer are described. A transmitter unit has a transmitter resonator with a coil that is coupled to a power supply to wirelessly transmit power to a receiver unit. A receiver unit has a receiver resonator with a coil coupled to a device load. The receiver unit can include a ferrite enclosure to prevent transmission of magnetic flux into electronics of the receiver unit, and can include ferrite fins to increase a coupling between the transmitter resonator and the receiver resonator.

Abstract: Disclosed are systems for wireless energy transfer including transcutaneous energy transfer. Embodiments are disclosed for user interface (UI) hubs to connect multiple batteries and to output system information to a patient. Embodiments are further disclosed for garment and devices to be worn by a patient requiring treatment. The garments are configured for desired placement of a transmitter coil relative to the body and for facilitating patient comfort and quality of life. Methods for manufacturing and using the devices and system are also disclosed.

Abstract: A needle guard is used when suturing the cuff of an attachment ring to the heart. The needle guard is disposed in the attachment ring to prevent other parts of the attachment ring from being punctured by a suturing needle. The needle guard can include one or more grooves to inhibit relative movement between the needle guard and the attachment ring during suturing. The needle guard is removed upon completion of suturing and to allow insertion into attachment ring of an inflow conduit of a heart assist device. An articulated clamp is used to compress the attachment ring into engagement with the inflow conduit. The attachment include an annular rib that grabs the inflow conduit.

Abstract: Methods and apparatus for wireless power transfer and communications are provided. In one embodiment, a resonator of a wireless power transfer system comprises a plurality of links connected to another with hinges to form a coil housing, the coil housing being adjustable at the hinges to conform to a body of a patient, and a flexible conductor wire attached to the coil housing, the flexible conductor wire being configured to transmit or receive wireless power. The resonator can be infinitely adjusted at the hinges to conform the shape of the resonator to a patient's body. In some embodiments, a locking mechanism can be configured to lock the resonator into a preferred position.

Abstract: A bearing assembly for use in a blood pump includes a first component that has a convex bearing surface and a first outer surface proximate the convex bearing surface. The bearing assembly includes a second component that a concave bearing surface and a second outer surface proximate the concave bearing surface, the concave bearing surface being configured to receive the convex bearing surface. A plurality of grooves are defined through the convex bearing surface and first outer surface or through the concave bearing surface and the second outer surface.

Abstract: A coupling system includes an applicator tool and an attachment ring mounted on the applicator tool. Clips are contained within the applicator tool and are deployed through the attachment ring in order to anchor the attachment ring to biological tissue. When deployed, tips of the clips follow a curved trajectory through an annular cuff of the attachment ring and through the underlying tissue. The tips loop back out of the tissue and to a location where they are later trapped or clamped by the attachment ring. While the tips are trapped or clamped, the applicator tool cinches the clips by pulling rear segments of the clips. Thereafter, the applicator tool disconnects from the attachment ring which remains anchored to the tissue and serves as a coupling for a cannula. The cannula can have movable lock members that secure it to the attachment ring.

Abstract: A coupling system includes an applicator tool, an anastomotic prosthesis mounted on the applicator tool, and an engagement device. The applicator tool deploys a securement through the prosthesis and tissue which leaves the prosthesis attached to the tissue. The engagement device selectively engages the applicator tool onto the tissue, with the use of suction, in order to facilitate accurate placement of the prosthesis on the tissue and facilitate deployment of the securement into the tissue. The applicator tool and the tissue are able to move together while the engagement device prevents or inhibits relative movement between the applicator tool and the tissue. A method for securing an anastomotic prosthesis to tissue includes applying of suction to engage an applicator tool to the tissue while a securement is deployed out of the applicator tool and into the prosthesis and the tissue.

Abstract: A bearing assembly for use in a blood pump includes a first component that has a convex bearing surface and a first outer surface proximate the convex bearing surface. The bearing assembly includes a second component that a concave bearing surface and a second outer surface proximate the concave bearing surface, the concave bearing surface being configured to receive the convex bearing surface. A plurality of grooves are defined through the convex bearing surface and first outer surface or through the concave bearing surface and the second outer surface.

Abstract: A coupling system includes an applicator tool and an attachment ring mounted on the applicator tool. Clips are contained within the applicator tool and are deployed through the attachment ring in order to anchor the attachment ring to biological tissue. When deployed, tips of the clips follow a curved trajectory through an annular cuff of the attachment ring and through the underlying tissue. The tips loop back out of the tissue and to a location where they are later trapped or clamped by the attachment ring. While the tips are trapped or clamped, the applicator tool cinches the clips by pulling rear segments of the clips. Thereafter, the applicator tool disconnects from the attachment ring which remains anchored to the tissue and serves as a coupling for a cannula. The cannula can have movable lock members that secure it to the attachment ring.

Abstract: A coupling system includes an applicator tool, an anastomotic prosthesis mounted on the applicator tool, and an engagement device. The applicator tool deploys a securement through the prosthesis and tissue which leaves the prosthesis attached to the tissue. The engagement device selectively engages the applicator tool onto the tissue, with the use of suction, in order to facilitate accurate placement of the prosthesis on the tissue and facilitate deployment of the securement into the tissue. The applicator tool and the tissue are able to move together while the engagement device prevents or inhibits relative movement between the applicator tool and the tissue. A method for securing an anastomotic prosthesis to tissue includes applying of suction to engage an applicator tool to the tissue while a securement is deployed out of the applicator tool and into the prosthesis and the tissue.

Abstract: A coring knife can be used to make a circular incision. The coring knife includes an abutment that is inserted into an initial slit through the heart wall. The abutment can be inserted into the slit while oriented in a direction that minimizes its insertion profile. After insertion, the abutment is reoriented by turning a key so that its abutment surface faces toward a circular cutting edge of the coring knife on the other side of the heart wall. The circular incision through the heart wall is made by pressing the circular cutting edge of the coring knife against the abutment.

Abstract: A sensor may be adapted to reduce motion artifacts by damping the effects of outside forces and sensor motion. A sensor is provided with a motion damping structure adapted to reduce the effect of motion of a sensor emitter and/or detector. Further, a method of damping outside forces and sensor motion is also provided.

Abstract: A system that monitors water displacement in tissue during patient therapy includes a generator supplying electrosurgical energy to tissue, a spectrometer operably coupled to the generator, and a processor communicating with the generator and with the spectrometer having a light source for exposing tissue to light and a light sensor. The light sensor is configured to sense changes in light through tissue in response to tissue treatment and communicate the changes to the processor to determine tissue hydration levels and motility. A plurality of optical fibers may be configured in an array to communicate light between the generator and tissue. An optical temperature monitor may communicate with the processor and be coupled to an optical fiber. The optical fibers may have an optic fiber distance between adjacent optical fibers. The system may be incorporated within an electrosurgical pencil or a forceps. A corresponding method of detecting hydration is also disclosed.

Abstract: A sensor for pulse oximetry or other applications utilizing spectrophotometry may be adapted to reduce motion artifacts by fixing the optical distance between an emitter and detector. A flexible sensor is provided with a stiffening member to hold the emitter and detector of the sensor in a relatively fixed position when applied to a patient. Further, an annular or partially annular sensor is adapted to hold an emitter and detector of the sensor in a relatively fixed position when applied to a patient. A clip-style sensor is provided with a spacer that controls the distance between the emitter and detector.

Abstract: A needle guard is used when suturing the cuff of an attachment ring to the heart. The needle guard is disposed in the attachment ring to prevent other parts of the attachment ring from being punctured by a suturing needle. The needle guard can include one or more grooves to inhibit relative movement between the needle guard and the attachment ring during suturing. The needle guard is removed upon completion of suturing and to allow insertion into attachment ring of an inflow conduit of a heart assist device. An articulated clamp is used to compress the attachment ring into engagement with the inflow conduit. The attachment include an annular rib that grabs the inflow conduit.

Abstract: An anastomotic system including a plurality of needles loaded with sutures and a delivery tool. The sutures include a suture core and crimp or fastener member at a proximal end of the core. An anchoring sleeve is optionally provided at a distal end. The anchoring sleeve is configured to collapse and prevent retraction of the suture after insertion through the tissue wall. A method of deploying the needles using the delivery tool is also disclosed.

Abstract: Systems and methods for wireless energy transfer are described. A transmitter unit has a transmitter resonator with a coil that is coupled to a power supply to wirelessly transmit power to a receiver unit. A receiver unit has a receiver resonator with a coil coupled to a device load. The receiver unit can include a ferrite enclosure to prevent transmission of magnetic flux into electronics of the receiver unit, and can include ferrite fins to increase a coupling between the transmitter resonator and the receiver resonator.

Abstract: Systems and methods for wireless energy transfer are described. A transmitter unit has a transmitter resonator with a coil that is coupled to a power supply to wirelessly transmit power to a receiver unit. A receiver unit has a receiver resonator with a coil coupled to a device load. At least one of the resonators is a malleable, non-planar resonator that can be bent and shaped to conform to a patient's anatomy.

Abstract: A bearing assembly for use in a blood pump includes a first component that has a convex bearing surface and a first outer surface proximate the convex bearing surface. The bearing assembly includes a second component that a concave bearing surface and a second outer surface proximate the concave bearing surface, the concave bearing surface being configured to receive the convex bearing surface. A plurality of grooves are defined through the convex bearing surface and first outer surface or through the concave bearing surface and the second outer surface.

Abstract: A needle guard is used when suturing the cuff of an attachment ring to the heart. The needle guard is disposed in the attachment ring to prevent other parts of the attachment ring from being punctured by a suturing needle. The needle guard can include one or more grooves to inhibit relative movement between the needle guard and the attachment ring during suturing. The needle guard is removed upon completion of suturing and to allow insertion into attachment ring of an inflow conduit of a heart assist device. An articulated clamp is used to compress the attachment ring into engagement with the inflow conduit. The attachment include an annular rib that grabs the inflow conduit.