The present invention relates to medical implants, and more specifically to a novel ossicular prosthesis arrangement.
A normal ear transmits sounds as shown in
Hearing is impaired when there are problems in the ability to transduce external sounds into meaningful action potentials along the neural substrate of the cochlea 104. To improve impaired hearing, auditory prostheses have been developed. For example, when the impairment is related to operation of the middle ear 103, a conventional hearing aid may be used to provide acoustic-mechanical stimulation to the auditory system in the form of amplified sound.
Middle ear implants also have been developed that employ electromagnetic transducers to mechanically stimulate the structures of the middle ear 103. A coil winding is held stationary by attachment to a non-vibrating structure within the middle ear 103 and a microphone signal current is delivered to the coil winding to generate an electromagnetic field. A magnet is attached to an ossicle within the middle ear 103 so that the magnetic field of the magnet interacts with the magnetic field of the coil. The magnet vibrates in response to the interaction of the magnetic fields, causing vibration of the bones of the middle ear 103. See U.S. Pat. No. 6,190,305, which is incorporated herein by reference.
Middle ear implants using electromagnetic transducers can present some problems. Many are installed using complex surgical procedures which present the usual risks associated with major surgery and which also require disarticulating (disconnecting) one or more of the bones of the middle ear 103. Disarticulation deprives the patient of any residual hearing he or she may have had prior to surgery, placing the patient in a worsened position if the implanted device is later found to be ineffective in improving the patient's hearing.
Novel surgical approaches try to deal with these issues by fixing an electromechanical transducer to the ossicle bones and placing an engagement member of the transducer against the oval or round window of the cochlear outer surface. The transducer is pressed toward the window membrane by filling fascia into the space between the transducer and a fixing anatomical structure. Fascia has the advantage of being biocompatible and having suitable damping properties to stabilize the fixing of the transducer and the engagement member to prevent their wandering out of place. But this approach very much depends on the exact execution of the filling of fascia and yields non-reproducible results. And either too much or too little exerted pressure on the membrane yields a distorted acoustic signal as perceived by the patient.
Embodiments of the present invention are directed to a middle ear implant arrangement responding to the above problems with the transducer loading structure from claim 1. Further advantageous embodiments of the present invention are in the dependent claims.
An implantable electromechanical transducer with an inner end and an outer end, converts an input electrical stimulation signal into a corresponding output mechanical stimulation signal. A cochlear engagement member at the inner end of the transducer has a cochlear engagement surface for coupling the mechanical stimulation signal to an outer cochlear surface of a recipient patient. A transducer loading structure has: i. an inner end adapted to releasably engage the transducer, ii. an outer end elongated along a central end axis for engaging a fixed anatomical structure within the middle ear of the recipient patient, and iii. a center spring structure connecting the inner end and the outer end and adapted to expand along a central spring axis to develop a spring force between the fixed anatomical structure and the outer end of the transducer.
More specifically, the center spring structure may include a first spring section toward the outer end of the transducer loading structure extending radially outward away from the central spring axis, and a second spring section toward the inner end of the transducer loading structure extending radially outward away from the central spring axis opposite to the first spring section. At least one of the spring sections may have a rectangular, hexagonal or elliptic cross-section. In addition or alternatively, the first spring section may have a larger cross-section and/or a larger spring-constant than the second spring section. At least one of the spring sections may include a relatively narrow sub-section. Some or all of the transducer loading structure may have chamfered edges.
The spring force may develop within a predetermined range when compressing the loading structure not more than a predetermined length along the end axis. The outer end of the engagement member may include a cone-shaped end, a spherical-shaped end, or a bolt-shaped end. The outer end of the engagement member may be adapted to releasably engage within an outer end sleeve. The transducer loading structure may be substantially flat. The transducer loading structure may be integrally formed, for example, of Nitinol.
Various embodiments of the present invention are directed to a middle ear implant arrangement based on a loading structure for a hearing implant transducer that is adapted to develop a spring force that presses one end of the electromechanical transducer to firmly engage it against an outer surface of the implant patient's cochlea.
A transducer loading structure 206 has an inner end 211 that fits over and engages the outer end 208 of the electromechanical transducer 201, and a limiter flange 209 that engages snuggly against the FMT signal lead 202. The transducer loading structure 206 also has an outer end 212 that engages a fixed anatomical structure within the middle ear of the recipient patient, for example, bone mass within the middle ear of the recipient patient such as the temporal bone. The transducer loading structure 206 is adapted to expand along a central spring axis 207 to develop a spring force between the fixed anatomical structure and the outer end 208 of the electromechanical transducer 201 to firmly engage the engagement surface 205 against the outer cochlea surface.
For example, the transducer loading structure 206 may be formed of a compressible material such as implant grade silicone that may be compressed and shortened by surgical forceps during implantation surgery so that the inner end 211 of the loading structure 206 can be fit over the outer end 208 of the transducer 201 while rotating the outer end 212 of the loading structure 206 into position against the fixed bone mass. When the surgeon removes the forceps the loading structure expands along the center axis 213 of the transducer 201 to engage the engagement surface 205 against the cochlear membrane. The resulting firm engagement between the transducer 201 and the cochlea optimizes the coupling of the mechanical stimulation signal between the transducer 201 and the cochlea. It also secures the transducer 201 into a fixed position from which it does not drift over time, thereby maintaining that proper coupling over a prolonged lifetime of the device.
The outer end 212 of the loading structure 206 may be fixed in place against the bone mass by an end receiving recess in a fixed anchor plate of any biocompatible rigid material such as titanium. Such an end receiving recess may be based on a snap-in structure such as a spring flange that allows for rotational movement of the loading structure 206 while securing the outer end 212 in place up to some given tractive force that is sufficient for reliable fixation but small enough for easy surgical insertion and removal. Such recessed anchor plate provides reliable fixation to the bone mass with free rotational movement but avoids osseous-disintegration. The recess may be movable in at least one direction relative to the plate such that the outer end 212 of the loading structure 206 can be brought in place while the plate is e.g. fixed with screws to the anchoring bone mass and the force applied to the outer surface of the cochlea may therewith be adjusted. The movable recess may then be fixed to the plate.
The inner end of the transducer loading structure may be adapted as shown in
The outer end 301 of the transducer loading structure 300 may have a cone-shaped end, a spherical-shaped end, or a bolt-shaped end 308 which releasably engages within an outer end sleeve 501 as shown in
In the embodiment shown in
At least one of the spring sections 303 and/or 304 may have a rectangular, hexagonal or elliptic cross-section, which may vary in size and shape over distance. And some or all of the transducer loading structure 300 may have chamfered edges, which may help minimize trauma to nearby tissue when inserting the arrangement into position in the middle ear. In some embodiments, the cross-section and/or the spring-constant of the first spring section 303 may be larger than that of the second spring section 304. This may help control or absorb vibrations and/or be helpful to avoid contacting bone mass.
The transducer loading structure 300 may be integrally formed which may allow for easy manufacturing such as preferably by a chemical etching process. The transducer loading structure 300 should be made of a material that is biocompatible and sufficiently elastic to exert the desired spring force, for example, Nitinol that is 55.9% nickel and 44.09% titanium by weight.
The transducer loading structure 300 shown in
In some systems, the transducer may be held securely within a transducer holding structure 600 as shown in
Although various exemplary embodiments of the invention have been disclosed, it should be apparent to those skilled in the art that various changes and modifications can be made which will achieve some of the advantages of the invention without departing from the true scope of the invention.
This application claims priority from U.S. Provisional Patent Application 61/663,788, filed Jun. 25, 2012, which is incorporated herein by reference.
Number | Date | Country | |
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61663788 | Jun 2012 | US |