The present application relates generally to systems and methods for facilitating wired power and data transmission, and more specifically, for facilitating wired power and data transmission using two connector portions configured to be repeatedly mechanically coupled to and decoupled from one another.
Medical devices have provided a wide range of therapeutic benefits to recipients over recent decades. Medical devices can include internal or implantable components/devices, external or wearable components/devices, or combinations thereof (e.g., a device having an external component communicating with an implantable component). Medical devices, such as traditional hearing aids, partially or fully-implantable hearing prostheses (e.g., bone conduction devices, mechanical stimulators, cochlear implants, etc.), pacemakers, defibrillators, functional electrical stimulation devices, and other medical devices, have been successful in performing lifesaving and/or lifestyle enhancement functions and/or recipient monitoring for a number of years.
The types of medical devices and the ranges of functions performed thereby have increased over the years. For example, many medical devices, sometimes referred to as “implantable medical devices,” now often include one or more instruments, apparatus, sensors, processors, controllers or other functional mechanical or electrical components that are permanently or temporarily implanted in a recipient. These functional devices are typically used to diagnose, prevent, monitor, treat, or manage a disease/injury or symptom thereof, or to investigate, replace or modify the anatomy or a physiological process. Many of these functional devices utilize power and/or data received from external devices that are part of, or operate in conjunction with, implantable components.
In one aspect disclosed herein, an apparatus comprises a first element and a second element configured to be repeatedly mechanically coupled to and decoupled from one another. The apparatus further comprises a first seal between the first element and the second element. The first seal is configured to inhibit moisture ingress from an environment surrounding the first and second elements to a first region enclosed at least partially by the first seal. The apparatus further comprises a second seal between the first element and the second element. The second seal is configured to inhibit moisture ingress from the first region to a second region enclosed at least partially by the second seal. One of the first and second seals comprises two first surfaces of the first and second elements in contact with one another, and another one of the first and second seals comprises a second surface and a resiliently bendable protrusion of the first and second elements in contact with one another.
In another aspect disclosed herein, an apparatus comprises an elastic protrusion, a surface facing the elastic protrusion, and a first region between the elastic protrusion and the surface. The first region is configured to receive a pair of oppositely facing sealing surfaces such that the surface engages one of the sealing surfaces to form a first moisture seal and the elastic protrusion engages and is bent by another of the sealing surfaces to form a second moisture seal.
In another aspect disclosed herein, a method comprises providing a first mating portion comprising a first plurality of electrical conduits and a second mating portion comprising a second plurality of electrical conduits configured to engage and be in electrical communication with the first plurality of electrical conduits. The method further comprises pressing a first surface of the first mating portion against a second surface of the second mating portion such that he first and second surfaces form a first moisture barrier between the first and second mating portions. The method further comprises pressing and bending an elastic protrusion of the second mating portion using a third surface of the first mating portion such that the elastic protrusion and the third surface form a second moisture barrier between the first and second mating portions.
Implementations are described herein in conjunction with the accompanying drawings, in which:
Certain implementations described herein provide small electrical multi-pin plug-and-socket connectors (e.g., for use in wearable devices or medical devices) that provide enhanced inhibition to moisture ingress from a surrounding environment into an enclosed region without compromising component size, electrical conductivity, and/or sealing. The plug and the socket have a first seal that inhibits moisture ingress into a first region from the environment and a second seal that inhibits moisture ingress into a second region from the first region. For example, one of the two seals can include a snap seal formed by surfaces of the plug and the socket in contact with one another and the other of the two seals can include a lip seal formed by a rigid surface and a resiliently bendable protrusion in contact with one another.
The teachings detailed herein are applicable, in at least some implementations, to any type of system or device (e.g., medical device configured to be worn by a recipient) having two electrical connector portions expected to be repeatedly mechanically coupled to and decoupled from one another and to withstand moisture ingress into a region bounded at least partially by the two portions. For example, the system can be an implantable medical device (e.g., implantable sensory prostheses; auditory prosthesis system) comprising an external first sub-system (e.g., sound processor external to a recipient) and an internal second sub-system (e.g., actuator and/or stimulator implanted on or within the recipient and configured to generate stimulation signals that are perceived by the recipient as sounds). The first sub-system can comprise two electrical connector portions (e.g., a first electrical connector portion that is a component of the external sound processor and a second electrical connector portion that is a component of an electrical cable in operative communication with an external communication unit (e.g., communication coil) configured to wirelessly (e.g., transcutaneously) transmit power and/or data (e.g., control signals) to the second sub-system and to wirelessly (e.g., transcutaneously) communicate with the second sub-system. Examples of auditory prosthesis systems compatible with certain implementations described herein include but are not limited to: electro-acoustic electrical/acoustic systems, cochlear implant devices, implantable hearing aid devices, middle ear implant devices, Direct Acoustic Cochlear Implant (DACI), middle ear transducer (MET), electro-acoustic implant devices, other types of auditory prosthesis devices, and/or combinations or variations thereof, or any other suitable hearing prosthesis system with or without one or more external components Implementations can include any type of medical device that can utilize the teachings detailed herein and/or variations thereof.
Merely for ease of description, apparatus and methods disclosed herein are primarily described with reference to an illustrative medical device, namely a cochlear implant. However, the teachings detailed herein and/or variations thereof may also be used with a variety of other wearable components/devices (e.g., medical devices) that provide a wide range of therapeutic benefits to recipients, patients, or other users. In some implementations, the teachings detailed herein and/or variations thereof can be utilized in other types of implantable medical devices beyond auditory prostheses. For example, apparatus and methods disclosed herein and/or variations thereof may also be used with one or more of the following: vestibular devices (e.g., vestibular implants); visual devices (e.g., bionic eyes); visual prostheses (e.g., retinal implants); sensors; cardiac pacemakers; drug delivery systems; defibrillators; functional electrical stimulation devices; catheters; brain implants; seizure devices (e.g., devices for monitoring and/or treating epileptic events); sleep apnea devices; electroporation; etc. The concepts described herein and/or variations thereof can be applied to any of a variety of implantable medical devices comprising an implanted component configured to use magnetic induction to communicate transcutaneously with an external component (e.g., receive control signals from the external component and/or transmit sensor signals to the external component) while using magnetic induction to receive power from the external component. In still other implementations, the teachings detailed herein and/or variations thereof can be utilized in other types of systems beyond components/devices (e.g., medical devices) utilizing magnetic induction for both wireless power transfer and data communication. For example, such other components, devices, and/or systems can include one or more of the following: wearable devices (e.g., smartwatches), consumer products (e.g., smartphones; IoT devices), and electric vehicles (e.g., automobiles).
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The sound processing unit 126 of certain implementations includes a power source (not shown in
The power source of the external component 142 is configured to provide power to the auditory prosthesis 100, where the auditory prosthesis 100 includes a battery (e.g., located in the internal component 144, or disposed in a separate implanted location) that is recharged by the power provided from the external component 142 (e.g., via a transcutaneous energy transfer link). The transcutaneous energy transfer link is used to transfer power and/or data to the internal component 144 of the auditory prosthesis 100. Various types of energy transfer, such as infrared (IR), electromagnetic, capacitive, and inductive transfer, may be used to transfer the power and/or data from the external component 142 to the internal component 144. During operation of the auditory prosthesis 100, the power stored by the rechargeable battery is distributed to the various other implanted components as needed.
The internal component 144 comprises an internal receiver unit 132, a stimulator unit 120, and an elongate stimulation assembly 118. In some implementations, the internal receiver unit 132 and the stimulator unit 120 are hermetically sealed within a biocompatible housing, sometimes collectively referred to as a stimulator/receiver unit. The internal receiver unit 132 comprises at least one internal inductive communication coil 136 (e.g., a wire antenna coil comprising multiple turns of electrically insulated single-strand or multi-strand platinum or gold wire), and generally, a magnet (not shown in
The elongate stimulation assembly 118 has a proximal end connected to the stimulator unit 120, and a distal end implanted in the cochlea 140. The stimulation assembly 118 extends from the stimulator unit 120 to the cochlea 140 through the mastoid bone 119. In some embodiments, the stimulation assembly 118 can be implanted at least in the basal region 116, and sometimes further. For example, the stimulation assembly 118 can extend towards an apical end of the cochlea 140, referred to as the cochlea apex 134. In certain circumstances, the stimulation assembly 118 can be inserted into the cochlea 140 via a cochleostomy 122. In other circumstances, a cochleostomy can be formed through the round window 121, the oval window 112, the promontory 123, or through an apical turn 147 of the cochlea 140.
The elongate stimulation assembly 118 comprises a longitudinally aligned and distally extending array 146 (e.g., electrode array; contact array) of stimulation elements 148 (e.g., electrical electrodes; electrical contacts; optical emitters; optical contacts). The stimulation elements 148 are longitudinally spaced from one another along a length of the elongate body of the stimulation assembly 118. For example, the stimulation assembly 118 can comprise an array 146 comprising twenty-two (22) stimulation elements 148 that are configured to deliver stimulation to the cochlea 140. Although the array 146 of stimulation elements 148 can be disposed on the stimulation assembly 118, in most practical applications, the array 146 is integrated into the stimulation assembly 118 (e.g., the stimulation elements 148 of the array 146 are disposed in the stimulation assembly 118). As noted, the stimulator unit 120 generates stimulation signals (e.g., electrical signals; optical signals) which are applied by the stimulation elements 148 to the cochlea 140, thereby stimulating the auditory nerve 114.
While
In certain implementations, the socket 310 comprises a first set of electrical connectors 330 (e.g., electrically conductive protrusions, pins, receptacles, recesses, and/or forks) and the plug 320 comprises a second set of electrical connectors 340 (e.g., electrically conductive protrusions, pins, receptacles, recesses, and/or forks) configured to be in mechanical and electrical communication with (e.g., to mate with) the first set of electrical connectors 330. Both the first set of electrical connectors 330 and the second set of electrical connectors 340 are at least partially within (e.g., extend into) the second region 270 and are in electrical communication with respective electrical conduits (e.g., bonded, soldered, or welded to wires) in electrical communication with respective circuitry. Upon the socket 310 and the plug 320 being coupled to one another, the electrical connectors 330 of the socket 310 are in mechanical and electrical communication with the electrical connectors 340 of the plug 320 such that the respective circuitry are in electrical communication with one another.
In certain implementations, the plug 320 is a portion of an electrical cable assembly 350 and the socket 310 is configured to be mounted on or within a component (e.g., sound processing unit 126) comprising circuitry that is in electrical communication with the electrical connectors 330. In certain such implementations, the socket 310 is mounted with a moisture-resistant seal between the socket 310 and the surrounding component (e.g., a seal formed by compression of an O-ring 360 between surfaces of the socket 310 and the component).
In certain implementations, the first seal 230 comprises a snap seal comprising the two first surfaces 212, 222 of the first and second elements 210, 220 in contact with one another. For example, the first element (e.g., socket 310) can comprise one first surface 212, the second element 220 (e.g., plug 320) can comprise the other first surface 222, and the first element 210 and the second element 220 can be configured to snap together and the two first surfaces 212, 222 can be configured to contact and press against one another upon the first and second elements 210, 220 being snapped together (see, e.g.,
In certain implementations, the second seal 260 comprises a lip seal comprising the second surface 214 and the resiliently bendable protrusion 224 of the first and second elements 210, 220 in contact with one another. For example, the first element 210 (e.g., socket 310) can comprise the second surface 214 and the second element 220 (e.g., plug 320) can comprise the resiliently bendable protrusion 224, while in another example, the first element 210 can comprise the resiliently bendable protrusion 224 and the second element 220 can comprise the second surface 214. The first element 210 of certain such implementations can comprise a portion (e.g., elongate portion 370) comprising a thermoplastic material (e.g., polyetherimide or PEI) with the second surface 214 comprising an inner surface (e.g., a surface facing towards the second region 270) of the portion (see, e.g.,
In certain implementations, the protrusion 224 and the first surface 222 are substantially circular and concentric with one another (e.g., in a plane perpendicular to the cross-sectional plane of
In certain implementations, a force applied by the first surface 222 (e.g., the inner surface of the outer molding 372) against the first surface 212 presses the elongate portion 370 against the resiliently bendable protrusion 224. Certain such implementations in which the first and second seals 230, 260 share a common component (e.g., elongate portion 370) and the forces applied to the common component by the first surface 222 and the protrusion 224 pressing against the common component are in substantially opposite and substantially colinear directions can advantageously improve the sealing by one or both of the first seal 230 and the second seal 260 compared to configurations in which the first and second seals 230, 260 do not share a common component of the first and second elements 210, 220 and/or the forces applied to the common component are not in substantially opposite and substantially colinear directions. In certain implementations, the first and second seals 230, 260 are configured to prevent moisture from reaching the second region 270 even when exposed to high moisture environments (e.g., submerged in water at a depth of one meter for a period of one hour).
In certain implementations, the apparatus 200 is an external portion of a medical system (e.g., a portion that is not implanted on or within the recipient). For example,
In an operational block 620, the method 600 further comprises pressing a first surface (e.g., having a first hardness) of the first mating portion against a second surface (e.g., having a second hardness greater than the first hardness) of the second mating portion, the first and second surfaces forming a first moisture barrier between the first and second mating portions. In an operational block 630, the method 600 further comprises pressing and bending an elastic protrusion of the second mating portion using a third surface (e.g., a substantially rigid surface) of the first mating portion, the elastic protrusion and the third surface forming a second moisture barrier between the first and second mating portions. For example, the first moisture barrier and the second moisture barrier can inhibit moisture ingress from an environment outside the first and second mating portions into an inner region bounded by the first and second mating portions.
Although commonly used terms are used to describe the systems and methods of certain implementations for ease of understanding, these terms are used herein to have their broadest reasonable interpretations. Although various aspects of the disclosure are described with regard to illustrative examples and implementations, the disclosed examples and implementations should not be construed as limiting. Conditional language, such as, among others, “can,” “could,” “might,” or “may,” unless specifically stated otherwise, or otherwise understood within the context as used, is generally intended to convey that certain implementations include, while other implementations do not include, certain features, elements and/or steps. Thus, such conditional language is not generally intended to imply that features, elements and/or steps are in any way required for one or more implementations or that one or more implementations necessarily include logic for deciding, with or without user input or prompting, whether these features, elements and/or steps are included or are to be performed in any particular implementation. In particular, the terms “comprises” and “comprising” should be interpreted as referring to elements, components, or steps in a non-exclusive manner, indicating that the referenced elements, components, or steps may be present, or utilized, or combined with other elements, components, or steps that are not expressly referenced.
It is to be appreciated that the implementations disclosed herein are not mutually exclusive and may be combined with one another in various arrangements. In addition, although the disclosed methods and apparatuses have largely been described in the context of conventional cochlear implants, various implementations described herein can be incorporated in a variety of other suitable devices, methods, and contexts. More generally, as can be appreciated, certain implementations described herein can be used in a variety of wearable device contexts that can utilize small electrical connectors comprising multiple portions that are configured to be repeatedly coupled to and decoupled from one another.
Language of degree, as used herein, such as the terms “approximately,” “about,” “generally,” and “substantially,” represent a value, amount, or characteristic close to the stated value, amount, or characteristic that still performs a desired function or achieves a desired result. For example, the terms “approximately,” “about,” “generally,” and “substantially” may refer to an amount that is within ±10% of, within ±5% of, within ±2% of, within ±1% of, or within ±0.1% of the stated amount. As another example, the terms “generally parallel” and “substantially parallel” refer to a value, amount, or characteristic that departs from exactly parallel by ±10 degrees, by ±5 degrees, by ±2 degrees, by ±1 degree, or by ±0.1 degree, and the terms “generally perpendicular” and “substantially perpendicular” refer to a value, amount, or characteristic that departs from exactly perpendicular by ±10 degrees, by ±5 degrees, by ±2 degrees, by ±1 degree, or by ±0.1 degree. The ranges disclosed herein also encompass any and all overlap, sub-ranges, and combinations thereof. Language such as “up to,” “at least,” “greater than,” less than,” “between,” and the like includes the number recited. As used herein, the meaning of “a,” “an,” and “said” includes plural reference unless the context clearly dictates otherwise. Also, as used in the description herein, the meaning of “in” includes “into” and “on,” unless the context clearly dictates otherwise.
While the methods and systems are discussed herein in terms of elements labeled by ordinal adjectives (e.g., first, second, etc.), the ordinal adjective are used merely as labels to distinguish one element from another (e.g., one signal from another or one circuit from one another), and the ordinal adjective is not used to denote an order of these elements or of their use.
The invention described and claimed herein is not to be limited in scope by the specific example implementations herein disclosed, since these implementations are intended as illustrations, and not limitations, of several aspects of the invention. Any equivalent implementations are intended to be within the scope of this invention. Indeed, various modifications of the invention in form and detail, in addition to those shown and described herein, will become apparent to those skilled in the art from the foregoing description. Such modifications are also intended to fall within the scope of the claims. The breadth and scope of the invention should not be limited by any of the example implementations disclosed herein, but should be defined only in accordance with the claims and their equivalents.
Filing Document | Filing Date | Country | Kind |
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PCT/IB2022/050028 | 1/3/2022 | WO |
Number | Date | Country | |
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63136371 | Jan 2021 | US |