Abstract: An implantable drug-delivery sleeve for an elongate component of an implantable medical device. The sleeve includes a tubular substrate having a lumen configured to receive the elongate component so as to allow relative displacement of the substrate and the elongate component, wherein the substrate is shaped so as to be retained stationary at a desired position along the elongate component, and a drug releasably carried by the substrate.

Abstract: A method for delivering drugs from an implantable medical device to an implantee, comprising implanting the medical device having a receptacle configured to receive a drug release capsule, the drug release capsule having at least one drug disposed thereon, placing the drug release capsule in the receptacle subsequent to the implanting, and permitting the release of the at least one drug from the drug release capsule to the recipient.

Abstract: An implantable device for mounting to a patient's bone includes a housing and at least one osseointegrating protuberance. The housing includes a surface having an abutting portion configured to abut the bone when the housing is implanted in the patient, the abutting portion defining a housing axis orthogonal to the surface. The at least one osseointegrating protuberance: extends from the surface of the housing; is adapted to abut the patient's bone; and has a substantially smooth shaft.

Abstract: Various embodiments are generally directed recurringly cycling the driving of a platter media of a hard drive with a motor, allowing rotation of the platter media to slow only to a threshold rotational speed to balance power conservation with delays in accessing data. A method comprises driving platter media of a hard drive to rotate at a selected normal rotational speed, retrieving data stored on the platter media when the platter media rotates at the normal rotational speed, ceasing to drive the platter media to rotate to allow the platter media to rotate under rotational inertia imparted to the platter media, monitoring a current rotational speed of the platter media, and resuming driving the platter media to rotate based on the current rotational speed falling to a lower threshold rotational speed selected to be less than the normal rotational speed. Other embodiments are described and claimed.

Abstract: Methods and systems to facilitate the collaborative development, discovery and implementation of evidence-based, clinical pathways are disclosed. Clinicians, medical professionals or researchers, may use the Platform 105 in multiple implementation, such as integrated with a third-party system like an EHR 104 to build and find clinical pathways through a graphical interface, creating relational data records between steps in pathways. Further, users of the Platform 105 may be able to associate relevant content such as published evidence, supplemental content items (e.g., videos, images, documents, ICD, CPT, SNOMED codes, and external web pages), and other associated pathways which reside in the system's database. Users of the Platform 105 may be able organize themselves into groups and networks to develop single pathways collaboratively. Users may be able to find specific pathways in the Platform 105 through semantic search, querying for relationships which exist inside of individual pathways.

Abstract: Controlling the interaction between an external device and an implanted device, including a method of controlling interaction between an external device and an implanted device, the method including at least the steps of: establishing communications between the implanted device and the external device; the external device determining an identification of the implant and comparing the identification with identifications in a stored list; if the device matches one of said identifications, then using a corresponding set of operating parameters to interact with said implant; and otherwise, not interacting with said device.

Abstract: A device, system and method for inserting a pre-curved electrode array (100) held in a substantially straight configuration by a straightening member (101) into a cochlea of a subject. As the electrode array (100) is inserted into the cochlea by the device, the straightening member (101) is held by the device such that the electrode array (100) advances off the straightening member (101) such that it is free to take on its pre-curved configuration in the cochlea of the subject.

Abstract: An ABI pad having a configuration and composition to provide the ABI pad with sufficient flexibility to permit the pad to be curved, molded or otherwise conformed to the cochlear nucleus, brainstem or other therapeutically-beneficial site, while ensuring the ABI pad maintains structural integrity over the anticipated operational life of the implant. The ABI pads are manufactured from silicone or other biocompatible material having a durometer sufficient to ensure the durability of the ABI pad over the anticipated operational life of the implant. To attain substantial flexibility, the thickness or cross section of the ABI pad is as minimal as possible to increase flexibility while not adversely affecting the noted durability of the pad. In one embodiment, the ABI pads are formed with an aperture in its interior region resulting in an ABI pad having minimal material mass while having sufficient structural integrity to reliably support the electrodes and associated wires.

Abstract: An implantable electrode array includes an elongated carrier (20) and a plurality of electrodes mounted within the carrier. A actuator adjusts the curvature of the carrier and can be controlled by varying an electric potential applied to the actuator. The actuator is based on an electrochemical cells and may be a conducting polymer based actuator.

Abstract: A training system is disclosed. The training system includes a server. The server includes a processor, data storage, a data input/output interface, and a voice interface. The data input/output interface is configured to provide a web-based interface to a data terminal and to receive, from the data terminal and via the web-based interface, both an identifier identifying at least one voice terminal and at least one response. The voice interface is configured to transmit at least one audio test signal corresponding to at least one audio test to the at least one voice terminal. The response is a response to the at least one audio test. In one embodiment, the voice terminal and the data terminal are combined in a single device.

Abstract: An implantable electrode array for insertion into an implantee's body. The array comprises an elongate carrier having a proximal end and a distal end. A plurality of electrodes are supported by the carrier at respective longitudinally spaced locations thereon between the proximal end and the distal end. The carrier is comprised of at least a first portion that preferentially adopts a first at least partially curved configuration and at least a second portion that preferentially adopts a second different configuration to that of the first portion. The second portion is closer to the distal end than the first portion and both the first and second portions each have at least one electrode supported thereon.

Abstract: Controlling the interaction between an external device and an implanted device, including a method of controlling interaction between an external device and an implanted device, the method including at least the steps of: establishing communications between the implanted device and the external device; the external device determining an identification of the implant and comparing the identification with identifications in a stored list; if the device matches one of said identifications, then using a corresponding set of operating parameters to interact with said implant; and otherwise, not interacting with said device.

Abstract: A method for manufacturing an electrode assembly. The method comprises: forming a comb having a plurality of electrode contacts, wherein the surface of at least one of the electrode contacts comprises a plurality of indentations such that the effective surface area per area unit of a center region of the at least one electrode contact is larger than the effective surface area per area unit of the of the region of the surface outside the center region; assembling an array of electrode contacts from the comb; molding a carrier member about the assembled array of electrode contacts, wherein a surface of the at least one electrode contact is covered by a layer of the carrier member material; and removing the layer of carrier member material on the surface of the at least one electrode contact.

Abstract: A protective faceplate (37) for an implantable component of a tissue-stimulating prosthesis, such as a prosthetic hearing implant. The faceplate (37) comprising a first or outer surface and an opposed second or inner surface. The implantable component can be removably or non-removably mountable to the second surface and adapted to extend into a cavity formed in a bone of a recipient.

Abstract: Various embodiments are generally directed recurringly cycling the driving of a platter media of a hard drive with a motor, allowing rotation of the platter media to slow only to a threshold rotational speed to balance power conservation with delays in accessing data. A method comprises driving platter media of a hard drive to rotate at a selected normal rotational speed, retrieving data stored on the platter media when the platter media rotates at the normal rotational speed, ceasing to drive the platter media to rotate to allow the platter media to rotate under rotational inertia imparted to the platter media, monitoring a current rotational speed of the platter media, and resuming driving the platter media to rotate based on the current rotational speed falling to a lower threshold rotational speed selected to be less than the normal rotational speed. Other embodiments are described and claimed.

Abstract: An implantable drug-delivery sleeve for an elongate component of an implantable medical device. The sleeve includes a tubular substrate having a lumen configured to receive the elongate component so as to allow relative displacement of the substrate and the elongate component, wherein the substrate is shaped so as to be retained stationary at a desired position along the elongate component, and a drug releasably carried by the substrate.

Abstract: An implantable tissue-stimulating prosthesis such as a cochlear implant system comprising an elongate carrier member having a distal end, a proximal end, and at least one electrode positioned thereon; at least one electrical conductor extending from one or more of the at least one electrode; a lead extending from the carrier member and enclosing the at least one electrical conductor; and a holding member constructed and arranged to radially extend outwardly from the surface of the carrier member to facilitate grasping of the holding member during implantation of the carrier member in a patient.

Abstract: An implantable electrode array assembly configured to stimulate tissue of a recipient, including an elongate member configured to be inserted into a recipient, wherein at least a portion of the elongate member includes a bio-active substance.

Abstract: An implantable tissue-stimulating prosthesis such as a cochlear implant system comprising an elongate carrier member having a distal end, a proximal end, and at least one electrode positioned thereon; at least one electrical conductor extending from one or more of the at least one electrode; a lead extending from the carrier member and enclosing the at least one electrical conductor; and a holding member constructed and arranged to radially extend outwardly from the surface of the carrier member to facilitate grasping of the holding member during implantation of the carrier member in a patient.

Abstract: An apparatus and method for implanting and securing an implanted medical device in a recipient. The implantable medical device of the generally includes a stimulating lead assembly that comprises an elongate carrier member having at least one stimulating element positioned thereon. The stimulating lead assembly further has an expandable portion thereon configured to be inserted into said reference structure in a first dimension, expand to a second dimension, and interact with a portion of the reference structure to help longitudinally secure the carrier member in the recipient.