Abstract: An electrode for use with a cochlear implant system includes an electrode array with electrode contacts distributed along the electrode array, and an electrode lead adjacent to the electrode array. The electrode lead has (1) a flexible region configured to allow the electrode lead to bend, (2) an attachment mechanism with an internal portion positioned within and along a longitudinal direction of the electrode lead, and an external portion configured to be bent and secured to bone, the external portion having an attachment element configured to secure the attachment mechanism to the bone, and (3) a securing element extending from the electrode lead and located further back from the flexible region toward a rear end of the electrode lead, the securing element configured to secure the electrode lead to the bone. A method of securing the electrode to bone is also disclosed.

Abstract: A method includes receiving, by a receiver device, a request sent from a transmitter device. The request is identified by a case name and at least one of a type of the request and a due date of the request. The request has a transmitter priority designated by the transmitter device. The method also includes assigning, by the receiver device, a receiver priority for the request received by the receiver device. The method also includes determining a final priority by the receiver device. The final priority is based upon a combination of the transmitter priority and the receiver priority. The method further includes handling the request within the receiver device based on the final priority.

Abstract: The invention relates to the application of photon energy to energize dental materials to enhance their physical handling characteristics, efficacy, ability to be delivered, reactivity, polymerization, and/or post-cure mechanical properties, among other attributes.

Abstract: An abdominal closure method and device is disclosed where the device generally includes a first tissue securement member configured for securement to a first tissue region and a second tissue securement member configured for securement to a second tissue region. The first and second tissue securement members are coupled to the connecting member and the connecting member is positionable at a distance from the first and second tissue regions. Additionally, one or more biasing elements may be connected to the first and second tissue securement members to approximate the first and second tissue regions towards one another via respective securement members.

Abstract: A system to acquire and decode patient clinical information is provided. The system includes an off-the-shelf device. The off-the-shelf device includes at least a processor and memory communicatively coupled to the processor and a low power, long range wireless transmission means communicating with a medical device through one of its ports. The memory includes a plurality of modules for execution by the processor, wherein the modules are configured at least for detecting information about a medical device it is communicatively coupled to; acquiring patient clinical information from the medical device; transforming the patient clinical information into an open standard format; transmitting the transformed patient clinical information securely over a network using a low power, long range wireless protocol. The system also includes a central server configured for receiving the transmitted data for storing and analysis.

Abstract: A method of fitting a cochlear implant in an ipsilateral ear of a subject, the cochlear implant having an electrode array with one or more electrode contacts, includes applying broad-band white noise stimulus to a contralateral ear in order to mask efferent nerve fibers, applying a single pulse stimulus to the ipsilateral ear and then measuring base-line evoked compound action potential (CAP) signals in the ipsilateral ear for an electrode contact during a refractory period, applying a sequence of separated single pulse stimuli to the contralateral ear and then measuring attenuated CAP signals in the ipsilateral ear for the electrode contact during the refractory period, comparing the measured attenuated CAP signals to the measured base-line CAP signals in order to determine a CAP threshold for the electrode contact and adjusting processing parameters of the cochlear implant based on the CAP threshold.

Abstract: A therapeutic thermal energy measuring system, method and application for a meridian thermal therapy device. The therapeutic thermal energy measuring system for a meridian thermal therapy device comprises: a time setting module for setting a time; a temperature setting module or an intensity level setting module for setting a temperature or an intensity level; a therapeutic thermal energy measuring module for measuring therapeutic thermal energy on the basis of a preset time and a preset temperature or intensity level, and outputting a result, and/or performing real-time measurement of therapeutic thermal energy on the basis of a preset temperature or intensity level and cumulative working hours of a treatment head of the meridian thermal therapy device, and outputting a result. The therapeutic heat energy measuring system can solve a bottleneck problem of having no way of quantizing therapeutic thermal energy in meridian thermal therapy.

Abstract: Provided is a system and method for a removable syringe micro pump. The removable syringe micro pump includes a pump housing having a first end and opposite thereto an attaching end, and at least one sidewall there between, the housing having a base proximate to the first end and, the attaching end having an attacher structured and arranged to temporarily engage a syringe. At least one wave spring is nested within the housing and attached proximate to the base. The wave spring having has a compressed first position wherein the wave spring is disposed within the pump housing, and a second extended position wherein, the release of tension extends the spring normally away from the pump housing. The wave spring has a diameter pre-selected to pass within a barrel of the engaged syringe. And engage a plunger seal of the syringe. An associated method of use is also provided.

Abstract: A multimodal medical device for the diagnosis and/or thermal treatment of a disease includes an instrument for performing thermal therapy; and an imaging system having multiple tomographic imaging modes, including optical coherence tomography (OCT), ultrasound imaging, photoacoustic (PA) imaging, fluorescence imaging and/or thermal imaging to provide guidance for accurate diagnosis and treatment of the disease.

Abstract: Disclosed is a method for measuring cholesterol by using a cholesterol dependent cytolysin (CDC), which is a cholesterol binding protein, and an antibody specifically recognizing HDL-C or LDL-C. The method according to the subject matter is capable of rapidly measuring low density lipoproteins and high density lipoproteins at low cost, and thus can be effectively applied in various fields requiring the measurement of low density lipoproteins and high density lipoproteins.

Abstract: There is described a method, a system, and a device for the anchoring of and into a corpus disposed distally in a conduit by engaging a stranded tube with the corpus and unwinding the wound threads of the stranded tube into unwound threads. Engagement includes the use of handling and manipulation shaft to dispose the stranded tube proximally, distally, or in the interior to the corpus. Unwinding, of the stranded tube is achieved by rotating a tube tool against the stranded tube. Unwinding liberates the helically coiled unwound strands in “corkscrew” rotation into the corpus. Proximal retrieval of a corpus is achieved by proximal retrieval of the stranded tube anchoring the corpus. An unwound stranded tube is operable as a fastener, as an electrical lead, and as a support for a device.

Abstract: The present invention relates, according to some embodiments, method of treating eye diseases, such as AMD by administering Semaphorin 3C (Sema3C) or a variant thereof having amino acid modifications at furin-like pro-protein convertase cleavage sites, rendering these sites resistant to cleavage.

Abstract: Provided is a warming device which can efficiently warm a blood product and inhibit a liquid in a warming flow path from exceeding an upper limit temperature thereof when liquid delivery of the blood product is stopped. The warming device includes the warming flow path in which the blood product flows and a heat plate which is in contact with the warming flow path to supply heat to the warming flow path. On the heat plate, a heater in a predetermined pattern corresponding to the warming flow path is disposed. The heater is disposed such that an amount of heat generation toward the warming flow path decreases in stages from an upstream side toward a downstream side in the warming flow path and that a decrease rate of the amount of heat generation at each of the stages decreases from the upstream side toward the downstream side.

Abstract: The present disclosure relates to a connector for connecting flow channels, flow regulators and/or reservoirs for directing flow. In some embodiments, the connector is a medical connector for connecting fluid flow controlling elements used in medical applications, particularly in infusion systems, such as tubes, syringes, needles, catheters and fluid reservoirs. The connector reduces the risk of contamination during handling and enhances safety when administering therapeutic solutions into a patient.

Abstract: The present invention relates to pharmaceutical compositions comprising a combination of a therapeutically-effective amount of the antiviral compound aciclovir and a therapeutically-effective amount of the COX-2 inhibitor celecoxib. The invention is further related to methods of treating functional somatic syndromes by administering a therapeutically-effective combination of aciclovir and celecoxib.

Abstract: A non-pneumatic tourniquet including a tourniquet ring configured to resiliently constrict around a body part of a subject. The tourniquet ring defines a plurality of openings. A handle moves the tourniquet ring onto the body part and includes a first strap having a first end secured to the tourniquet ring at one of the openings and a second end secured to the tourniquet ring at one of the openings. A second strap has a first end secured to the tourniquet ring at one of the openings and a second end secured to the tourniquet ring at one of the openings.

Abstract: The present disclosure in some embodiments relates to a computer-based method for improving the pharmaceutical understanding of a user. The method includes receiving medication data from a source, wherein the medication data is related to a user's prescribed, dispensed, or claimed medicines; associating a unique ID for each user with the medication data for the user; providing a user interface, whereby the data for a user is accessible to the user only after the user has provided an authentication, wherein the medication data accessible to the user via the user interface comprises the one or more medications the user is taking.

Abstract: A device is initially rolled up can unfold into its original spherical dome shape after insertion through a surgical incision.

Abstract: A vestibular electrode is described that is for implantation into a vestibular semi-circular canal. An intra-labyrinthine electrode carrier with a C-shaped cross-section has an inner concave surface and an outer convex surface, and is configured to fit through an electrode opening in an outer surface of the bony labyrinth into the perilymph fluid without breaking the membranous labyrinth so as to fit the inner concave surface of the electrode carrier adjacent to the membranous labyrinth and the outer convex surface adjacent to the bony labyrinth. There are one or more electrode contacts on a surface of the electrode carrier that are configured for electrical interaction with adjacent neural tissue.