Abstract: An implantable device monitors a pressure of fluid within an inflatable portion of a gastric band. The implantable device comprises a tube defining a lumen, and a pressure sensor positioned within at least one of the lumen or the tube. The pressure sensor is configured to sense the pressure of the fluid within the inflatable portion of the gastric band. The pressure sensor is also configured to transmit a pressure signal based on the pressure to a microcontroller, which transmits the pressure signal to a remote control device. The pressure sensor confers strain relief upon at least a portion of the tube, and the pressure sensor shields at least a portion of the tube from puncture by a needle.

Abstract: A method of determining an optimal coil shape for use in magnetic stimulation includes identifying a stimulation location and a constraint at the stimulation location. A first electromagnetic effect at the stimulation location is determined. The first electromagnetic effect is induced by a first electrical quantity assigned to a first current element at a first current element location with a first orientation. A second electromagnetic effect at the stimulation location is also determined. The second electromagnetic effect is induced by a second electrical quantity assigned to a second current element at the first current element location with a second orientation. Based on the first electromagnetic effect and the second electromagnetic effect, an optimal orientation of a current element at the first current element location is determined. The optimal orientation is such that the constraint is satisfied. Repeating the process at a plurality of locations yields the optimal coil shape.

Abstract: Described are pelvic implants (e.g., urinary incontinence sling, hammock, etc.) that provide treatment for pelvic floor disorders such as incontinence, stress urinary incontinence, prolapse (e.g., cystocele, enterocele, rectocele, vault prolapse), fecal incontinence, and the like, wherein the implant involves the ability to adjust dimensions of an implant before, during, or after implantation. In a preferred embodiment the implant (680) comprises a support portion piece (682) and an extension portion piece (688, 690) adjustably connected to the support portion piece through a frictional adjusting element (696) comprising an aperture through which a segment of extension portion extends.

Abstract: A method, apparatus and a system for thermally-assisted pulsed electromagnetic field stimulation for treatment of osteoarthritis are disclosed. In one embodiment, the system comprises a multi-coil applicator adapted for positioning near or around of the treated joint, a pulse generator functionally coupled to the applicator, a power supply, and a feedback loop for stabilizing the temperature of the joint. The feedback loop includes a heating element, a temperature sensor and an electronic controller for maintaining the temperature of the joint in the range of 38 to 42 degree C. At elevated temperatures the healing effect of PEMF stimulation on the cartilage is maximized and overall efficiency of the treatment is improved. To produce a high electric field, the coils of the applicator are made with a low number of turns, for example less than 5 turns, and are spatially arranged to cover the whole joint without “dead” zones.

Abstract: Described herein are methods of treating a patient to prevent or correct cardiac remodeling following myocardial infarction. In general these methods may include inserting or implanting a device in a heart chamber to support the affected region within 72 hours after myocardial infarction. The device may be a support device (e.g., a resilient frame) and/or a partitioning device.

Abstract: An apparatus and method for performing warming therapy is described. In one exemplary embodiment, the apparatus includes a base for supporting a medical patient and a humidifier module removably coupled to the base. The humidifier module may include a main reservoir and an evaporator reservoir separated by a channel. Both the main and evaporator reservoirs may be protected by a cover, which may be made removable. The design of the humidifier module is such that the component parts thereof may be easily removed, so that the reservoir body including the main reservoir and the evaporator reservoir may be easily cleaned, such as through use of an autoclave.

Abstract: An apparatus and method for providing patient access in a warming therapy device (e.g., incubator, warmer, etc.) is described. In one exemplary embodiment, the apparatus includes a mattress tray assembly having at least two axes of rotation, and in another exemplary embodiment, the apparatus includes a mattress tray assembly having at least four axes of rotation.

Abstract: A method for radiation treatment includes adjusting a plurality of adjustable elements on a radiation treatment bra to establish a reference breast geometry and aligning the patient to a radiation treatment machine by projecting a light field through windows provided in the radiation treatment bra during a radiation treatment planning session. To begin actual radiation treatment, the reference breast geometry is reestablished by repeating the original adjustments of the adjustable elements, as necessary. Alignment is re-established by viewing tattoos through the windows in conjunction with the light field.

Abstract: Brachytherapy treatment apparatus are provided that include an elongate body including a core member and an outer member surrounding and movable relative to the core member. One or more helical catheters are provided on a distal portion of the elongate body, e.g., including distal ends coupled to the core member and proximal ends coupled to the outer member. The outer member is movable relative to the core member, e.g., axially and/or rotationally, to direct the helical catheters between a collapsed configuration for introduction through a tissue tract to a target location, e.g., a lumpectomy cavity, and an expanded configuration. Each helical catheter includes a lumen, and, after expansion to the expanded configuration, a source of radiation may be introduced along the helical catheters and/or a lumen of the core member for delivering radiation to the target location. Optionally, the apparatus may include a balloon surrounding or within the helical members.

Abstract: An orthotic obstructive sleep apnea treatment device is provided that includes a hyoid bone attachment element disposed to attach a ferric element to a hyoid bone, where the ferric element is disposed to face along a treatment vector from the hyoid bone, and the treatment vector is oriented relative to a sagittal plane of a human. The orthotic obstructive sleep apnea treatment device further includes an external orthotic neck device having a contoured housing with a shape disposed to conform about a neck of the human subject, where the housing includes a force delivery element disposed at an exterior-front neck region of the human subject and is disposed to provide an attractive force to the ferric element along the treatment vector. A force sensor is disposed to measure a force exerted on the hyoid bone, a skin contact pressure, tissue compression between the ferric element and the force delivery element.

Abstract: The invention relates to an apparatus for stimulating local and higher homeostatic autoregulatory mechanisms during the sleep phase and the rest of relaxation phase of the organism by means of a pulsed electromagnetic field. Said apparatus comprises a pulse generator, a control device, and a filed generating device. The pulse generator is designed in such a way as to generate a pulsed electromagnetic field along with the control device and the filed generating device by applying 5 special series of pulses in which the frequency is the same for all signals, ranging from 8 to 15 Hz, the series of pulses are repeated multiple times, and the control time amounts to at least 3.5 h within a period of 7 to 9 hours.

Abstract: A sound enrichment system for provision of tinnitus relief, the sound enrichment system includes a noise generator, an environment classifier that is configured to determine a classification of an ambient sound environment of the sound enrichment system, a processing system for adjusting a noise signal based at least in part on the classification, wherein the noise signal is obtained using the noise generator, and an output transducer for conversion of the adjusted noise signal to an acoustic signal for presentation to a user. A method of providing a noise enriched sound signal for provision of relief of tinnitus includes obtaining a noise signal, adjusting the noise signal based at least in part on a sound environment classification, generating an acoustic noise signal from the adjusted noise signal, and presenting the acoustic noise signal to a tinnitus suffering person.

Abstract: A sexual stimulation apparatus which may comprise a plurality of light sources for photostimulation and microbe reduction of the vagina, clitoris, or both; a plurality of vibrators for mechanical stimulation of the vagina, clitoris, or both; a plurality of modes of operation for achieving improved sexual stimulation in a user; a handle for ease of operation; a controller and programmable memory for containing modes of operation and driving the light sources and vibrators of the invention; a vaginal finger; a clitoral finger; a handle for ease of use; a keypad for user entry of commands; a charging and programming port; and a power source which may be a rechargeable battery which may be rechargeable by direct, inductive or other means; and a handle for ease of operation. The invention also comprises a flexible covering that provides smooth sliding engagement with the vagina and clitoris of a user.

Abstract: The present invention includes a device and method for relaxing and promoting healing to an individual by synchronization of kinesthetic and aural whole tone sounds.

Abstract: An infant care system and apparatus includes a horizontal surface to support an infant. A microenvironment region is defined around the horizontal surface by at least one wall. A graphical display is disposed within the microenvironment region. A diagnostic imaging device is at least partially disposed within the microenvironment region to obtain diagnostic images of an infant disposed within the microenvironment region.

Abstract: In a general aspect, a method of treating urinary incontinence can include slidably interfitting a first push tube into a first dilator tube disposed at an end of a sling assembly and slidably interfitting the first push tube onto an end of a shaft of a delivery device. The method can also include inserting the shaft transvaginally through a vaginal wall and removing the shaft to implant a portion of the sling assembly in periurethral tissue. The method can also include slidably interfitting a second push tube into a second dilator tube disposed at a second end of the sling assembly and slidably interfitting the second push tube onto the end of the shaft. The method can still further include inserting the shaft transvaginally through the vaginal wall and removing the shaft from the patient to implant a second portion of the sling assembly in periurethral tissue.

Abstract: An in-vivo dose detector (41) for an HDR brachytherapy system (1; 31), wherein the detector is insertable into and movable through a catheter (15), and comprises a sensor (53) operable to detect radiation from a source (52) used to irradiate a tissue to be treated (9) in the course of an HDR brachytherapy treatment. A brachytherapy system and a method of dose monitoring are also disclosed.

Abstract: Systems and methods for optimizing sleep and post-sleep performance. In an embodiment, a system comprising a device and sleep mask are provided. The mask may comprise electroencephalographic (EEG) sensors and one or more stimulation elements configured to stimulate the senses of a wearer of the mask. The mask may be releasably and electrically coupled to a device which receives EEG signals from the mask, determines current and target sleep states based, at least in part, on the EEG signals, and uses this determination to tailor a sleep architecture of the wearer by controlling the stimulation elements. The mask may be a soft mask which utilizes conductive thread embroidered into one or more textile layers. In an embodiment, the stimulation elements may comprise one or more heating elements, electroluminescent panels, and speakers. In addition, the EEG sensors may comprise hybrid sensors comprising hydrogel in a conductive spacer fabric.

Abstract: Radiosurgical treatments of tissues of the heart mitigate arrhythmias and treat other tumerous and non-tumerous disease using an implanted fiducial positioned in or near the heart using cardiac catheterization techniques. The fiducials may be implanted after diagnostic and planning images of the target tissues have been acquired. Fiducial implantation may take place the day of a scheduled radiosurgical treatment. Techniques to accommodate post-planning fiducial implantation may include registration of the implanted fiducial location with the treatment plan, and active fiducials may limit collateral imaging radiation exposure while enhancing tracking accuracy.

Abstract: The invention provides, in various embodiments, systems, devices and methods relating to adjustable length implantable sling assemblies for providing support to anatomical locations. In certain embodiments, the sling includes at least one elastic member to aid in the placement and tensioning of the sling.