Abstract: A system is provided comprising an optically-guided catheter having a proximal end, a distal end, and at least one lumen. A light-emitting means is coupled to the catheter, the catheter is inserted into place in the patient, and light is emitted as a point or points from a selected location, usually the distal tip, of the catheter to which it is coupled. The system further comprises an external detection device that detects the transdermally projected light, emitted by the light-emitting point from within the patient, thereby indicating precise placement of the catheter within the patient.

Abstract: In the present invention, because no examples are known of binding of magnetic particle to mesenchymal cell or chondrocyte which might be used in regenerative medicine, whether or not a cell having the magnetic particle bound thereto is retained in local by external magnetism after administration and whether or not the cell can exhibit intrinsic activity is studied. According to the present invention, a magnetic cell comprising mesenchymal cell or cultured chondrocyte having magnetic particle bound to the surface thereof is provided, and when the cell is administered in vivo and an external magnetic field is applied, the cell can be retained for a long time at a disease site. Moreover, a drug delivery system can be constructed by causing the magnetic cells to contain a drug.

Abstract: A suburethral implant for treating stress urinary incontinence (SUI) includes an elongated plate-like member which is slightly curved in transverse cross-section, and a pair of spaced apart arms having hooked ends or barbs which extend from the plate-like member. A device for deploying the suburethral implant for treating SUI includes a vaginal probe for insertion in the vaginal canal of a patient, and a urethra locator probe for the simultaneous insertion in the urethra of a patient. The urethra probe is spaced apart from and overlies the vaginal probe. The vaginal probe includes a wall in which is formed an exit port. A suburethral implant introducer assembly is extendable and retractable through the exit port on the vaginal probe. The introducer assembly has a distal end on which is removably mounted a suburethral implant.

Abstract: A magnetic field applicator system wherein a plurality of magnets are generally fixed within an applicator base, each of the plurality of magnets having a magnetic axis at an angle different to other magnets in the plurality of magnets. The magnetic axis may be random with respect to others within the plurality of magnets. Also disclosed is a system for making the magnetic field applicator system.

Abstract: A fixation section and a rim form a myocardial patch for implant in the pericardial space. The fixation section is adapted to promote fibrosis to secure the patch in place. The rim is secured to and surrounds at least a portion of the fixation section and has a lumen. The patch is adapted to transition between a collapsed state and an expanded state. A stylet is passed through the lumen to force the patch into a collapsed state and is removed when the patch is positioned to allow the patch to expand and engage the epicardial surface.

Abstract: Systems for suppressing motion sickness are provided. In this regard, an exemplary system comprises a display device and a display controller. The display device is operative to display a first image and a second image. The display controller communicates with the display device and is operative to control display of the second image such that the second image moves relative to the display device in response to at least one of: motion of the first image relative to the display device, and motion of the display device. Methods and other systems also are provided.

Abstract: Described are methods of treating urinary incontinence using a urinary sling and a tissue path that passes through the obturator foramen, along with related surgical implants, devices, systems, and kits.

Abstract: Disclosed is a surgical system for positioning an implant in a patient. The surgical system includes an insertion needle and a connector. The insertion needle has a distal end with a channel formed therein. The channel has a first end and a second end. The first end extends to the distal end. The second is laterally offset from the first end and does not extend to the distal end. The connector has a first end and a second end. The first end is attached to the implant that is to be positioned in the patient. The second end has a recess formed therein. The recess generally conforms to the distal end of the insertion needle. The connector has an inwardly directed extension that extends into the recess. The inwardly directed extension engages the insertion needle through the channel.

Abstract: In general, the invention is directed to techniques for locating an implanted object using an external antenna. The implanted object may be, for example, an internal antenna that facilitates recharging of and/or communication with an implantable medical device. An external device coupled to the external antenna drives the antenna with a plurality of waveforms. Asymmetry in the loading profile of the external antenna when it is driven by the plurality of waveforms allows the external device or another device to determine the location of the implanted object relative to the external antenna. The external device or other device may provide information to a user based on the determined location of the implanted object relative to the external antenna, such as information to help a user position the external antenna with respect to an internal antenna in embodiments in which the implanted object is an internal antenna.

Abstract: A cap having ear pieces and an eyepiece. The ear pieces are preferably connected to an audio device that can play stored audio and/or rebroadcast ambient sounds at a reduced audio level. The ear pieces preferable provide sound attenuation of at least 20 dB. The stored audio may include sounds that simulate sounds heard by a fetus while in the womb. The eye piece is preferably removable.

Abstract: A gastrointestinal implant system includes an adjustable restriction device having a contact surface configured for at least partially engaging a surface of a gastrointestinal tract of a mammal. The implant system further includes an implantable interface including a first driving element, the first driving element being moveable and operatively coupled to the adjustable restriction device by an actuator configured to change the dimension or configuration of the contact surface in response to movement of the first driving element. The system also includes an external adjustment device having a second driving element configured to non-invasively engage the first driving element of the implantable interface from a location external to the mammal. In the system, actuation of the second driving element of the external adjustment device produces movement in the first driving element of the implantable interface and results in a change in the dimension or configuration of the contact surface.

Abstract: The invention relates to a device for treatment with magnetic fields, which provides an easily transportable and storable device for the treatment with magnetic fields, which is also convenient for patients and in particular is economical to produce. The device comprises: a first device for generation of a first magnetic field, a second device for generation of a second magnetic field and a support with an upper side and a lower side, whereby the support is embodied for applying the treated body regions of the patient thereto.

Abstract: A transcranial magnetic stimulation (“TMS”) induction coil device includes an attachment portion for attachment to a tracking device and providing that the tracking device, when attached to the TMS coil device, is at a predetermined location and orientation in relation to a casing of the TMS coil device. The casing of the TMS coil device also includes a reference point for confirming the accuracy of the attachment of the tracking device to the TMS coil device at the predetermined location and orientation in relation to the casing.

Abstract: A device for fixing and tensioning at least one pulling thread for applying a neovagina comprises a base body on which at least one fixing element is arranged for fixing the at least one pulling thread with tensioning. The fixing element is able to turn about an axis of rotation in order to tension the at least one pulling thread, and a blocking device is provided for the fixing element, by means of which blocking device the fixing element can be blocked at least in a direction of rotation opposite to the direction of rotation for tensioning the at least one pulling thread.

Abstract: A system comprises a first signal handling unit sized and shaped for insertion to a reference distance within a first body cavity and a probe sized and shaped for insertion into a second body cavity the probe including an energy emitting head and a second signal handling unit, wherein one of the first and second signal handling units comprises a transmitter and the other of the first and second signal handling units comprises one of a receiver adapted to receive signals from the transmitter and a signal reflecting element, wherein, when the other of the first and second signal handling units comprises a signal reflecting element, the one of the first and second signal handling units comprises a receiver in combination with a controller operatively connected to the receiver, the controller generating an output varying as a distance between the first and second signal handling units varies.

Abstract: Described are implants, tools, and related methods, for use in pelvic surgery to treat conditions such as prolapse and incontinence, including one embodiment of a method that uses a transcoccyx tissue path; other embodiments that use particular implants with various features relating to, e.g., end portions; and other embodiments relating to particular tools.

Abstract: In one embodiment a therapeutic member includes a radioactive source and a material (e.g., a bio-absorbable polymeric material) that encapsulates the radioactive source. An outer surface of the encapsulating material includes a plurality of protrusions to reduce a tendency of the member to migrate and rotate within a patient's body after implantation. In an embodiment, the encapsulating material includes an anchor mechanism that extends from at least one of the longitudinal ends of the radioactive source to reduce a tendency of the member to migrate and rotate within a patient's body after implantation. Embodiments of the present invention are also directed to strands that include similar protrusions and/or anchor mechanisms. Additionally, embodiments of the present invention are directed to spacers that resist migration and rotation. Embodiments are also directed to radiopaque markers that resist migration and rotation. This abstract is not intended to be a complete description of the invention.

Abstract: Methods and applicator apparatus are disclosed for brachytherapy treatment of tissue surrounding a cavity in a patient, particularly a resection cavity. In treatment regimes requiring recovery time between successive radiation treatments, applicators of the invention are retained under the skin, with the skin allowed to at least partially heal, and are re-accessed later for one or more subsequent treatments. To reduce patient discomfort an anesthetic agent can be infused through the applicator to patient tissue, for insertion, balloon inflation or removal of the applicator.

Abstract: A device for delivery of a cardiac support device for treating cardiac disease of a heart includes a multistage deployment mechanism and an actuating mechanism for controlling the positions of the deployment mechanism. The deployment mechanism is operable to change between a retracted state and an extended state, and includes a plurality of independent stages, including, in one embodiment, a first stage including a guide structure for location adjacent a portion of the patient's heart when in the extended state. A second stage is movably coupled to the first stage, and is guided by the guide structure between the retracted and extended states. The second stage further releasably engages and supports the cardiac support device and positions the cardiac support device at the desired implantation location, guided by the guide structure of the stage. In some embodiments, the deployment mechanism may include additional stages.

Abstract: A device for detecting and influencing the physiological and/or pathological state of the human or animal body, including a housing which has a first housing wall that, in turn, has an outer surface provided for placing against a body to be treated. A rotor is situated inside the housing and is rotationally driven about an axis that is essentially perpendicular to the first housing wall. First magnets are mounted on the rotor, and their magnetic fields are oriented in the same direction that is parallel to the rotation axis. At least one additional magnet is situated essentially coaxial to the rotation axis with a polarity of each being oriented in an opposite direction to the first magnets.