IMPLANTABLE ULTRASONIC DEVICE

Abstract

An implantable electrical stimulation device including an implant sized and configured to be implanted subcutaneously, the implant being configured to rectify a received pulse train of ultrasound into a single electrical pulse configured to stimulate a tibial nerve of a patient.

Claims

1. An implantable electrical stimulation device, comprising: an implant sized and configured to be implanted subcutaneously, the implant including an inductive coil and a plurality of piezoelectric elements in communication with each other to rectify a received pulse train of ultrasound into a single electrical pulse to stimulate a tibial nerve of a patient.

2. The device of claim 1, wherein the implant further includes a fixation element configured to retain the implant in a position proximate the tibial nerve.

3. The device of claim 2, wherein the fixation element is transitionable from a first position during deployment to a second position during subcutaneous fixation.

4. The device of claim 2, wherein the fixation element includes a plurality of tines.

5. (canceled)

6. The device of claim 1, wherein the implant further includes an electrode configured to conduct the single electrical pulse to the tibial nerve.

7. The device of claim 1 , wherein the implant is passively powered.

8. The device of claim 1, wherein the implant is configured to output a voltage having an amplitude up to 20V for the single electrical pulse.

9. A method for treating urinary incontinence, comprising: subcutaneously implanting an implant proximate a tibial nerve of a patient, the implant being configured to rectify a received pulse train of ultrasound into a single electrical pulse configured to stimulate the tibial nerve of the patient; and delivering a pulse train of ultrasound to the implant and electrically stimulating the tibial nerve.

10. The method of claim 9, wherein subcutaneously implanting the implant includes piercing skin proximate an ankle of the patient and stimulating a target area for implantation of the implant with a stimulation device to determine a suitable location for implantation of the implant.

11. The method of claim 10, wherein subcutaneously implanting the implant includes fixating the implant with subcutaneous fascia.

12. The method of claim 9, wherein delivering a pulse train of ultrasound to the implant includes delivering ultrasound from an ultrasound patch adhered to the surface of skin of the patient.

13. A system for stimulating a tibial nerve of a patient, comprising: an implant delivery device, the implant delivery device being configured to deliver an implant subcutaneously proximate the tibial nerve, the implant including an inductive coil and a plurality of piezoelectric elements configured to rectify a received pulse train of ultrasound into a single electrical pulse to stimulate the tibial nerve of the patient; and an ultrasound device coupled to the skin of the patient and configured to deliver the pulse train of ultrasound to the implant.

14. The system of claim 13, wherein the implant delivery device is configured to stimulate a target area for implantation of the implant with a stimulation device to determine a suitable location for implantation of the implant.

15. The system of claim 13, wherein the implant delivery device includes a needle defining a lumen therein, and wherein the implant is slideably disposed within the lumen.

16. The system of claim 13, wherein the implant further includes a fixation element configured to retain the implant in a position proximate the tibial nerve.

17. The system of claim 16, wherein the fixation element is transitionable from a first position during deployment to a second position during subcutaneous fixation.

18. The system of claim 16, wherein the fixation element includes a plurality of tines.

19. (canceled)

20. The system of claim 13, wherein the implant further includes an electrode configured to conduct the single electrical pulse to the tibial nerve.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0026] A more complete understanding of the present invention, and the attendant advantages and features thereof, will be more readily understood by reference to the following detailed description when considered in conjunction with the accompanying drawings wherein:

[0027] FIG. 1 is a cross-sectional schematic view of an exemplary implanted subcutaneous electrical stimulation device;

[0028] FIG. 2 is a cross-sectional schematic view of the electrical stimulation device shown in FIG. 1;

[0029] FIG. 3 is a chart showing the rectification of exemplary ultrasound inputs into electrical outputs by the implant shown in FIG. 2;

[0030] FIG. 4 is a chart shown exemplary electrical output parameters of the implant shown in FIG. 2; and

[0031] FIG. 5 is a cross-sectional schematic view of an exemplary system for implanting the implant shown in FIG. 2.

DETAILED DESCRIPTION

[0032] It should be understood that various aspects disclosed herein may be combined in different combinations than the combinations specifically presented in the description and accompanying drawings. It should also be understood that, depending on the example, certain acts or events of any of the processes or methods described herein may be performed in a different sequence, may be added, merged, or left out altogether (e.g., all described acts or events may not be necessary to carry out the techniques). In addition, while certain aspects of this disclosure are described as being performed by a single module or unit for purposes of clarity, it should be understood that the techniques of this disclosure may be performed by a combination of units or modules associated with, for example, a medical device.

[0033] In one or more examples, the described techniques may be implemented in hardware, software, firmware, or any combination thereof. If implemented in software, the functions may be stored as one or more instructions or code on a computer-readable medium and executed by a hardware-based processing unit. Computer-readable media may include non-transitory computer-readable media, which corresponds to a tangible medium such as data storage media (e.g., RAM, ROM, EEPROM, flash memory, or any other medium that can be used to store desired program code in the form of instructions or data structures and that can be accessed by a computer).

[0034] Instructions may be executed by one or more processors, such as one or more digital signal processors (DSPs), general purpose microprocessors, application specific integrated circuits (ASICs), field programmable logic arrays (FPGAs), or other equivalent integrated or discrete logic circuitry. Accordingly, the term “processor” as used herein may refer to any of the foregoing structure or any other physical structure suitable for implementation of the described techniques. Also, the techniques could be fully implemented in one or more circuits or logic elements.

[0035] Referring now to the drawings in which like reference designators refer to like elements, there is shown in FIG. 1 an exemplary implant constructed in accordance with the principles of the present application and designated generally a “10.” The implant 10 may be sized and configured to be implanted subcutaneously, for example, underneath a human or animal patient's skin by ankle, thigh, pelvis, and the like. In one configuration, the implant 10 is sized to be implanted within subcutaneous fascia proximate the tibial nerve. For example, as shown in FIG. 1, the implant may include a fixation element 12 configured to affix and retain the implant 10 within a target subcutaneous area. The fixation element 12 may include, but is not limited to, a plurality of tines, which may be composed of flexible and/or shape memory material such as Nitinol, or barbs, hooks, hook and loop fasteners, or other anchors. In one configuration, the fixation element is transitionable from a first position during deployment from a position outside the body to a second position during subcutaneous fixation. For example, the fixation element 12 may transition from a position during insertion in which the plurality of tines is substantially parallel with a major axis of the implant 10, to a position in which the plurality of tines extends in a direction substantially orthogonal to the major axis of the implant. In the configuration shown in FIG. 1, the plurality of tines extends into the deep fascia to prevent migration of the implant 10.

[0036] The implant 10 may be configured to rectify a received pulse train of ultrasound into a single electrical pulse configured to stimulate a tibial nerve of a patient, as discussed in more detail below. For example, as shown in FIG. 1, an ultrasound patch 14 may be adhered or otherwise positioned on the skin proximate the implant 10 to deliver ultrasound underneath the skin and to the implant 10 including pulse trains of ultrasound. In other configurations, other ultrasound devices may be used to deliver ultrasound to the implant 10.

[0037] Referring now to FIG. 2, the implant 10 may include a housing 16 sized and configured to retain the various components of the implant. The housing 16 may further define an interior 18 sized to receive an inductive coil 20 for communication with the device 14 and a plurality of piezoelectric elements 22, such as PZT rods. The piezoelectric elements 22 are configured to rectify ultrasound pulses into electrical pulses for stimulation of nerves, and in particular, the tibial nerve of the patient. The implant 10 may further include a circuit board 24 having processing circuitry configured to control operation of the implant 10 to rectify received pulse trains of ultrasound. In one configuration, the implant includes its own rechargeable power source (not shown) or passively powered by the ultrasound device 14. The configuration of the implant 10 shown in FIG. 2 is merely an exemplary arrangement of the components disposed therein and other configurations are contemplated by this disclosure. In one configuration, one or more electrodes 26 are in communication with the circuit board 24, the plurality of piezoelectric elements 22 and the inductive coil to deliver the rectified electrical waveform to target nerve, for example, the tibial nerve. In the configuration shown in FIG. 2, the electrode 26 is cylindrical and is coupled to the distal end of the implant between the fixation elements 12.

[0038] Referring now to FIGS. 3 and 4, in one configuration, the implant 10 is configured to output an electrical waveform having a minimum of 0V to a maximum of 10V assuming sufficient coupling of the ultrasound device 14 to the implant 10 and a depth of approximately 0.5 to 3 cm insertion of the implant subcutaneously with about 1 kOhm tissue impedance. In other configurations, the implant 10 may output waveforms of various other amplitudes depending on the depth of insertion of the implant and the tissue impedance. For example, the maximum output of the implant 10 may be up to 20V. In one configuration, a pulse width of an outputted electrical waveform may range, for example, between 20 microseconds to 400 microseconds and between a frequency of 10 Hz to 10 kHz. FIG. 3 shows examples of some ultrasound waveform inputs received by the implant and the corresponding rectified electrical waveform outputs.

[0039] Referring now to FIG. 5, an exemplary implant delivery device 28 is configured to pierce, cut, or otherwise penetrate the skin of the patient for delivery and implantation of the implant 10. In one configuration, the device 28 may include a needle, tube, or other piercing element 30 at its distal end and configured to pierce the skin and create an opening for delivery of the implant 10. In one configuration, the piercing element 30 is hollow and sized to slidably receive the implant 10, and in other configurations may be solid. The device 28 may further include an electrical stimulation element 32 configured to electrically test a target area of treatment to determine a suitable location for the implant 10. In particular, the stimulation element 32 may include a stimulation engine 34 in communication with an electrode 36 configured to apply a test electrical pulse to stimulate the target implant area to determine if, for example, the tibial nerve is stimulated. If the tibial nerve is stimulated, the implant 10 is implanted at the location where stimulation is observed. The test level pulse may be less than or equal to a therapeutic electrical pulse delivered by the implant 10 to the tibial nerve. In one configuration, the device 28 includes a plunger 38 slidably received within a housing 40 to advance the test electrode 36 toward the target tissue region. In one configuration, the stimulation engine 34 and one or more batteries 42 may be disposed within the plunger 38 and in other configurations may be disposed elsewhere within or to device 28. In the configuration shown in FIG. 5, the device 28 includes a retractor actuator 44 configured advance and retract the plunger 38 within the housing 40, a stimulation actuator 46 to start and stop the stimulation engine 32, and an amplitude control actuator 48 to control the amplitude of the test level stimulation.

[0040] In an exemplary use of the device 28, the user may pierce the skin of the patient in a location in which the tibial nerve may be accessed, for example, by the ankle or other portion of the leg. A target area for implantation of the implant 10 is electrically stimulated with the stimulation device 32 to determine a suitable location for implantation of the implant 10. The implant 10 is then implanted at the suitable location. In one configuration the device 28 implants the implant 10 only and in other configurations a separate device (not shown) may be used to pierce the skin, or vice versa. In the configuration shown in FIG. 5, the implant is disposed proximal to tube 30 within the housing 40. The implant 10 may be side-loaded into the housing 40 and positioned distal to the distal end of plunger 38. The plunger 38 is advanced distally within the housing 40 and pushes on the implant 10 to advance the implant out from the housing 40. It is further contemplated that piercing the patient's skin and implanting the implant 10 may be achieved through separate medical devices.

[0041] It will be appreciated by persons skilled in the art that the present invention is not limited to what has been particularly shown and described herein above. In addition, unless mention was made above to the contrary, it should be noted that all of the accompanying drawings are not to scale. A variety of modifications and variations are possible in light of the above teachings without departing from the scope and spirit of the invention, which is limited only by the following claims.