US20100016911A1

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Publication number: US20100016911A1
Application number: US12/174,509
Authority: US
Inventors: N. Parker Willis; Richard E. Riley; Mark W. Cowan
Original assignee: EBR Systems Inc
Current assignee: EBR Systems Inc
Priority date: 2008-07-16
Filing date: 2008-07-16
Publication date: 2010-01-21
Also published as: US20160114176A1; US9731139B2

Abstract

A wireless cardiac stimulation device is disclosed comprising a controller-transmitter, a receiver, and a stimulating electrode, wherein the stimulating electrode and the receiver are separately implantable at cardiac tissue locations of the heart and are connected by a local lead. Having separately implantable receiver and stimulating electrodes improves the efficiency of ultrasound mediated wireless stimulation by allowing the receiver to be placed optimally for reception efficiency, thereby resulting in longer battery life, and by allowing the stimulating electrode to be placed optimally for stimulus delivery. Another advantage is a reduced risk of embolization, since the receiver and stimulating electrode ensemble is attached at two locations of the heart wall, with the connecting local leads serving as a safety tether should either the receiver or the stimulating electrode become dislodged.

Description

FIELD OF THE INVENTION

The field of the present invention relates generally to implanted devices for tissue stimulation, monitoring, and other therapeutic or diagnostic functions, and specifically to implantable devices for the stimulation of cardiac tissue, for example pacemakers or implantable cardioverter-defibrillators (ICDs). More specifically, it pertains to such devices utilizing wireless energy transfer, for example through ultrasonic means.

DESCRIPTION OF THE RELATED ART

Conventional wired cardiac pacemaker and defibrillator systems comprise Implantable Pulse Generators (IPGs) configured to be located subcutaneously and connect via leads to stimulator electrodes implanted in the heart. However, because the IPG is connected to leads, the location and surgical process must consider lead insertion into a vascular access.

An ultrasound based wireless cardiac stimulation system has been disclosed in currently pending applications by the applicant (e.g., U.S. patent application Ser. No. 11/315,023). This system employs ultrasonic energy transfer from a subcutaneously implantable controller-transmitter device (C-T), which is directed towards one or more receiver-stimulator (R-S) devices implanted at desired sites in the heart, for example in the left ventricle. Ultrasonic transducers and circuitry in the R-S convert the transmitted ultrasonic energy into electrical energy capable of stimulating the cardiac tissue. The system, C-T, and R-S are described in co-pending U.S. patent applications Nos. (Publication Number) 20060136004, 20060136005, 20070027508, 20070055184, 20070078490 and 20070060961 and Ser. No. 11/752,775, which are herein incorporated by reference in their entirety.

Energy and battery life computations show that the range between the C-T and the R-S has a dramatic impact on the efficiency of energy transfer between them. Therefore, it is desirable to reduce the distance between the C-T and the R-S and thereby improve the efficiency of wireless pacing. An optimal location for cardiac stimulation is believed to be the posterio-lateral LV wall, and an optimal subdermal location for an IPG is the fifth intercostal space. These locations are approximately 10 cm apart. It is desirable to have a cardiac stimulation system that simultaneously optimizes the stimulation location and minimizes the wireless energy delivery range between the C-T and the R-S, thereby providing optimal battery life and optimal stimulation location. The present embodiments provide such a system.

SUMMARY OF THE INVENTION

Embodiments of the present invention are directed to wireless cardiac stimulation devices comprising a controller-transmitter (C-T), a receiver, and a stimulating electrode, wherein the stimulating electrode and the receiver are separately implantable at different locations of the heart and are connected by a local lead. Separating the receiver from the stimulating electrode improves the efficiency of ultrasound mediated wireless stimulation by allowing the receiver to be placed optimally for reception efficiency, thereby resulting in longer battery life or reduced battery size. Separation of the receiver and stimulating electrode also allows the stimulating electrode to be placed optimally for stimulus delivery, and provides for improved connective reliability.

In one aspect, the C-T is implanted subcutaneously such that its transmission passes through an intercostal space, and the receiver is implanted at the apex of the left ventricle (LV) of the heart, thereby minimizing the distance between the receiver and the C-T. The stimulating electrode is implanted, separately from the receiver, at an optimal posterio-lateral LV location, and connected to the receiver via a local lead for transfer of electrical energy. One advantage of such a system is the longer battery life due to the reduction in distance between the wireless transmitter and the receiver. Another advantage is a reduced risk of embolization, since the receiver and stimulating electrode are attached at two locations of the heart wall, with the connecting local lead serving as a safety tether should either the receiver or the stimulating electrode become dislodged.

In one aspect, the system comprises a plurality of stimulating electrodes, thereby providing multi-site stimulation. In another aspect, the receiver itself comprises a stimulating electrode, thereby providing dual-site stimulation. In another aspect, the receiver and stimulating electrode are implanted in different ventricles, thereby providing biventricular stimulation, with the local lead crossing the ventricular septum to connect the receiver and stimulating electrode.

Another aspect of the invention is methods of using acoustic energy to stimulate cardiac tissue by (a) subcutaneously implanting a transmitter; (b) implanting a receiver at a first cardiac tissue location, wherein the receiver receives acoustic energy transmitted by the transmitter and produces a biologically stimulating electrical output in response to the received acoustic energy; and (c) implanting a stimulating electrode at a second cardiac tissue location, wherein the stimulating electrode is connected to the receiver by a local lead, and wherein the stimulating electrode receives the biologically stimulating electrical output from the receiver and delivers said output to cardiac tissue. Additionally, the first cardiac tissue location can be chosen to optimize acoustic energy transmission from the transmitter to the receiver. Another embodiment of the above method involves implanting additional stimulating electrodes, wherein the stimulating electrodes are connected to the receiver by the local lead. Alternatively, the additional stimulating electrodes are connected to the receiver by additional local leads.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention has other advantages and features which will be more readily apparent from the following detailed description of the invention and the appended claims, when taken in conjunction with the accompanying drawings, in which:

FIG. 1 shows an example embodiment of a system for electrically stimulating the heart, comprising separately implantable receiver and stimulating electrode implanted at endocardial locations of the heart wall.

FIGS. 2aand2bshow other example embodiments of a system for electrically stimulating the heart, comprising a separately implantable receiver and/or stimulating electrode implanted at an epicardial location of the heart wall.

FIG. 3 shows an example embodiment of a receiver.

FIGS. 4a-4cshow example embodiments of systems configured with a single receiver and a plurality of stimulating electrodes.

FIG. 5 shows an example embodiment of a system configured with a plurality of receivers and a plurality of stimulating electrodes.

FIG. 6 shows the reception range of an exemplary fixed-focus transducer.

DETAILED DESCRIPTION OF THE EMBODIMENTS

In the following description, for purposes of explanation, numerous specific details are set forth in order to provide a thorough understanding of the invention. It will be apparent, however, to one skilled in the art that the invention can be practiced without these specific details.

An ultrasound based wireless cardiac stimulation system is disclosed which improves the efficiency of ultrasound mediated wireless stimulation and results in longer battery life. The system comprises two separately implantable subsystems. The first subsystem is a receiver-stimulator (R-S) configured to be implanted within the heart to provide electrical stimulation. The second subsystem is a controller-transmitter (C-T) configured to be implanted subcutaneously to wirelessly power and control the R-S.

To increase the operational efficiency and battery life of the system, the R-S itself comprises two separately implantable elements that are connected by a local lead. The first is an implantable receiver element (hereinafter also referred to as “receiver”), and the second is an implantable stimulating electrode element (hereinafter also referred to as “stimulating electrode”). The receiver wirelessly receives energy from the C-T, converts the received energy to electrical energy, and electrically powers the stimulating electrode via the local lead. The stimulating electrode receives the electrical energy and provides electrical stimulation to the tissue.

It is an advantageous aspect that the separation of the receiver from the stimulating electrode allows two goals to be simultaneously met. First, it allows the receiver to be implanted closest to the C-T, thereby minimizing the travel range of the wireless energy transmission from the C-T to the receiver. Second, it allows the stimulating electrode to be implanted at an optimal location within the heart for the delivery of electrical stimulation to heart tissue, independent of the location of the implanted receiver.

Reducing the distance between the C-T and the receiver allows more of the transmitted acoustic energy to be harvested by the receiver, since (a) less of the acoustic energy is spread to where the receiver cannot harvest it, providing a quadratic increase in gain as a function of the inverse of the distance between the C-T and the receiver, and (b) there is less intervening tissue between the C-T and the receiver that could lead to undesired energy dissipation. This means that the C-T needs to transmit less energy to achieve the same stimulation output. This provides not only a longer battery life, but also simpler C-T and receiver design, for example by using fewer transducers in the construction of the C-T and/or the receiver (such as only one transducer, in some embodiments).

Optionally, as disclosed in co-pending U.S. Patent Application Ser. No. 61/016,869, the C-T itself may comprise an implantable transmitter as well as a separately implantable battery for powering the transmitter via a subcutaneously routable electrical cable, thereby improving patient comfort and providing a larger usable aperture.

While the present embodiments refer to stimulating the heart, it is understood herein that the disclosed embodiments can be used to stimulate any living tissue in humans or animals. For example, published PCT application WO2007149936 with common inventor and assignee of this application, which is incorporated herein by reference, describes using a wireless stimulation system for stimulating various tissues.

FIG. 1 shows one embodiment of a system100 for electrically stimulating theheart101, comprising separately implantable receiver and stimulating electrode elements. The system100 comprises aC-T102, as well as an R-S comprising areceiver103, astimulating electrode104, and alocal lead105 connecting thereceiver103 andstimulating electrode104.

C-T

102 is configured to be implanted subcutaneously so as to be close to a location in the heart where thereceiver103 is to be implanted. In one embodiment, theC-T102 is implanted subcutaneously such that its transmission passes through an intercostal space, such as the 5^thintercostal space.FIG. 1 showsC-T102 implanted thusly, with the transmission passing through an intercostal space betweenribs106.

Thereceiver103 is configured to be implanted at a location within the heart where it can be closest to theC-T102. In one embodiment, thereceiver103 is implanted at the septal apex of the LV, as shown inFIG. 1. This could be done using traditional interventional techniques, wherein a delivery catheter is advanced percutaneously into the left ventricle and the receiver is delivered and fixed at a preferred site. The fixation could be accomplished using various tissue fixing mechanisms such as barbs, tines, etc.

In such an embodiment where theC-T102 is implanted at an intercostal space and thereceiver103 is implanted at the septal apex of the LV, the distance between the C-T102 and thereceiver103 is minimized to approximately 2-4 cm, allowing efficient energy transfer from the C-T102 to thereceiver103, and therefore providing for longer battery life forC-T102.

WhileFIG. 1 shows thereceiver103 andstimulation electrode104 implanted at an endocardial location of the heart wall, in other embodiments one or both may be implanted at an epicardial location. Such an embodiment is shown inFIG. 2a,with thereceiver103 andstimulation electrode104 implanted at epicardial locations.

In one such embodiment, thereceiver103 can be placed on the anterior of the heart by using a minimally invasive surgical approach, as shown inFIG. 2a.Once thereceiver103 is fixed to the anterior surface of the heart and within the desired range of theC-T102, a stimulatingelectrode104 could be localized at an endocardial location by penetrating the stimulatingelectrode104 through theheart wall101 from the epicardial surface. A small diameter trocar or such implement could enable the implantation of thereceiver103 and the stimulatingelectrode104 from the external surface (as opposed to interventional means). Alternatively, the stimulatingelectrode104 may be placed at an epicardial location to provide stimulation (as shown inFIG. 2b).

As shown inFIG. 3, thereceiver103 comprisesinternal circuitry107 for converting acoustic energy to electrical energy that is transmitted to the stimulatingelectrode104. In one embodiment, thecircuitry107 comprises one or more transducers which produce electrical energy in response to the acoustic energy received from theC-T102. The transducers may comprise piezoelectric material, such as a polycrystalline ceramic piezoelectric material or a single crystal piezoelectric material.

Circuitry

107 further comprises one or more conversion circuits, wherein each conversion circuit is electrically connected to a corresponding transducer such that the electrical energy output from the transducers is converted to a biologically stimulating electrical output. For example, the conversion circuitry may comprise one or more rectifiers, as well as optional protection circuitry (such as comprising one or more Zener diodes) to protect the rectifiers from damage due to high voltages.

The stimulatingelectrode104 is configured to be implanted at a cardiac tissue location, separately from thereceiver103, at a location that is optimal for delivering the stimulating electrical output to the heart. The stimulatingelectrode104 comprises one or more electrodes (cathode) for delivering the electrical output to tissue, and is powered by thereceiver103 via alocal lead105. In one embodiment, as shown inFIG. 1, the stimulatingelectrode104 is implanted at a posterio-lateral location in the LV. As shown inFIG. 3, thereceiver103 comprises ananode108 electrically connected tocircuitry107 via anelectrical connection109. Theanode108 may comprise part or all of the exterior of thereceiver103 or alternatively may be placed anywhere along the length of the local lead (not shown). Typically, the anode is a large surface area electrode relative to the cathode having a low current density to preferentially stimulate the tissue at the cathode, in this embodiment at the stimulatingelectrode104. Alternatively, the anode can be designed to have a small surface area to intentionally stimulate the tissue at the receiver location, thereby providing dual site stimulation from both the anode and cathode.

As described above, separating the implant locations of thereceiver103 and stimulatingelectrode104 allows the system100 to simultaneously optimize wireless energy transfer efficiency as well as stimulation location. Furthermore, separating thereceiver103 from the stimulatingelectrode104 also reduces the risk of embolization, since the R-S ensemble is now attached at two locations in the heart wall, with thelocal lead105 serving as a safety tether should either thereceiver103 or the stimulatingelectrode104 become dislodged.

Optionally, the system100 may be extended to provide multi-site stimulation. For example, the system100 may comprise a plurality of stimulation electrodes to provide multi-site stimulation. In one such embodiment, thereceiver103 itself comprises a stimulation electrode, so that the heart is stimulated at thereceiver103 site in addition to stimulation provided at the stimulatingelectrode104 site.

In another embodiment for multi-site stimulation, the system100 comprises more than one stimulating electrode, each connected to thereceiver103 via a single or multiple local leads.FIG. 4ashows one such embodiment, wherein multiple

stimulating electrodes

104a,104b,and104c(at endocardial locations of the heart) are connected via multiple

local leads

105a,105b,and105cto a receiver103 (also at an endocardial location), thereby providing multi-site stimulation.FIG. 4bshows another such embodiment, wherein multiple

stimulating electrodes

104aand104b(at epidardial locations) are connected via multiple

local leads

105aand105bto a receiver103 (also at an epicardial location), thereby providing multi-site stimulation. Alternatively or in combination, two or more of the stimulating electrodes may be contained on a single local lead, such as shown inFIG. 4cwithreceiver103 connected in series to stimulating

electrodes

104aand104bvialocal lead105.

In another embodiment for multi-site stimulation, the system100 may be configured with a plurality of receivers.FIG. 5 shows one such embodiment, wherein afirst receiver103ais implanted at a cardiac tissue location of the LV and connected to a firststimulating electrode104avia a firstlocal lead105a,and asecond receiver103bis implanted at a cardiac tissue location of the RV and connected to a secondstimulating electrode104bvia a secondlocal lead105b.Analogously, system100 may comprise more than two receivers, each of which may electrically power one or more stimulating electrodes via one or more local leads.

Optionally, the system100 may be configured to provide biventricular stimulation. In one such embodiment, thereceiver103 comprises a stimulation electrode for providing electrical stimulation, and is implanted at a cardiac tissue location of the septal apex of the right ventricle (RV), allowing thereceiver103 to function as an RV lead for biventricular stimulation. In another embodiment, thereceiver103 may be implanted at a cardiac tissue location of the RV, with thelocal lead105 having a very small profile (i.e. a small surface area lead) and puncturing through the ventricular septum to the LV and connecting thereceiver103 with one or morestimulating electrodes104. Crossing the ventricular septum with such a small profile local lead would cause minimal to no trauma.

It is an advantageous aspect that the present systems100 can be manufactured to minimize energy loss and thereby maximize battery life. In one particular example implementation, theC-T102 comprises a fixed-focus transducer110 with no steering capabilities, as shown inFIG. 6.

Another example implementation comprises ahigh frequency receiver103 with a small receiver surface area and a small number of transducers. For example,receiver103 may be an 800 kHz high frequency receiver with three transducer elements and a receiver surface area of approximately 3 mm². In such an embodiment, theC-T102 produces a homing signal using an array of transducers to track the location ofreceiver103. It can be estimated that to produce a steering range of approximately 2 radians for a distance of approximately 3 cm, a 6×6 array of about 36 transducer elements could be used, with each transducer element having an element size of about 1 mm².

While the above is a complete description of the preferred embodiments of the invention, various alternatives, modifications, and equivalents may be used. Therefore, the above description should not be taken as limiting the scope of the invention which is defined by the appended claims.

Claims

1. An implantable cardiac stimulator device for converting acoustic energy to electrical energy, comprising:

an implantable receiver which produces a biologically stimulating electrical output in response to acoustic energy, the receiver configured to be implanted at a first cardiac tissue location to optimize acoustic energy reception;

a first implantable stimulating electrode which receives the biologically stimulating electrical output from the receiver and delivers said output to cardiac tissue, the stimulating electrode configured to be implanted at a second cardiac tissue location to optimize delivery of stimulation energy to cardiac tissue; and

a first local lead connecting the receiver and the first stimulating electrode.

2. The device ofclaim 1, wherein the receiver comprises:

one or more transducers which produce electrical energy in response to acoustic energy; and

one or more conversion circuits, wherein each conversion circuit is electrically connected to a corresponding transducer such that the electrical energy output from the transducers is converted to the biologically stimulating electrical output.

3. The device ofclaim 2, wherein the transducers comprise piezoelectric material.

4. The device ofclaim 3, wherein the piezoelectric transducer material is one of a polycrystalline ceramic piezoelectric material or a single crystal piezoelectric material.

5. The device ofclaim 2, wherein the conversion circuits comprise rectifiers.

6. The device ofclaim 5, further comprising protection circuitry to protect the rectifiers from damage due to high voltages.

7. The device ofclaim 6, wherein the protection circuitry comprises a Zener diode.

8. The device ofclaim 1, wherein the receiver is further configured to deliver the stimulating electrical output to cardiac tissue, thereby allowing multi-site stimulation.

9. The device ofclaim 8, wherein the receiver comprises a stimulation electrode for delivering the stimulating electrical output to cardiac tissue.

10. The device ofclaim 1, further comprising a second implantable stimulating electrode, thereby allowing multi-site stimulation.

11. The device ofclaim 11, further comprising a second local lead connecting the receiver and the second stimulating electrode.

12. The device ofclaim 1, wherein the receiver is configured to be implanted at an endocardial or epicardial location.

13. The device ofclaim 1, wherein the first stimulating electrode is configured to be implanted at an endocardial or epicardial location.

14. The device ofclaim 1, wherein the receiver is configured to be implanted at a cardiac tissue location at the septal apex of the right ventricle of the heart, wherein the first stimulating electrode is configured to be implanted at a cardiac tissue location of the left ventricle of the heart, and wherein the first local lead is configured to puncture through the ventricular septum of the heart to connect the receiver and the first stimulating electrode.

15. The implantable cardiac stimulator device ofclaim 1, wherein the first local lead tethers the receiver to the stimulating electrode and retains the receiver and the stimulator within the heart when the receiver or stimulator is dislodged from the implanted location.

16. The device ofclaim 15, wherein the local lead prevents embolization due to the dislocation of the receiver or stimulator from the implanted location.

17. An implantable cardiac stimulator system for converting acoustic energy to electrical energy, comprising:

a first implantable stimulating electrode which receives the biologically stimulating electrical output from the receiver and delivers said output to cardiac tissue, the stimulating electrode configured to be implanted at a second cardiac tissue location to optimize delivery of stimulation energy to cardiac tissue;

a first local lead connecting the receiver and the first stimulating electrode; and

a controller-transmitter for transmitting acoustic energy towards the receiver.

18. The system ofclaim 17, wherein the controller-transmitter is subcutaneously implanted.

19. The system ofclaim 18, wherein the controller-transmitter and the receiver are located such that acoustic energy is optimally transmitted to the receiver with minimal energy loss.

20. The system ofclaim 19, wherein the optimal transmission is achieved by locating the receiver in close proximity to the transmitter.

21. A method of using acoustic energy to stimulate cardiac tissue, comprising:

subcutaneously implanting a transmitter;

implanting a receiver at a first cardiac tissue location, wherein the receiver receives acoustic energy transmitted by the transmitter and produces a biologically stimulating electrical output in response to the received acoustic energy; and

implanting a stimulating electrode at a second cardiac tissue location, wherein the stimulating electrode is connected to the receiver by a local lead, and wherein the stimulating electrode receives the biologically stimulating electrical output from the receiver and delivers said output to cardiac tissue.

22. The method ofclaim 21, wherein the first cardiac tissue location is chosen to optimize acoustic energy transmission from the transmitter to the receiver.

23. The method ofclaim 22, further comprising implanting additional stimulating electrodes, wherein the stimulating electrodes are connected to the receiver by the local lead.

24. The method ofclaim 22, further comprising implanting additional stimulating electrodes, wherein the stimulating electrodes are connected to the receiver by additional local leads.

25. A method of stimulating cardiac tissue by converting acoustic energy to electrical energy, comprising:

transmitting acoustic energy from a subcutaneously implanted transmitter;

receiving acoustic energy at a first cardiac location;

producing a biologically stimulating electrical output in response to the received acoustic energy; and

delivering the biologically stimulating electrical output via a local lead to a stimulating electrode implanted at a second cardiac tissue location, thereby stimulating cardiac tissue.

26. The method ofclaim 25, wherein the first cardiac tissue location is chosen to optimize acoustic energy reception from the transmitter.

27. The method ofclaim 26, further comprising delivering the biologically stimulating electrical output to additional stimulating electrodes implanted at additional cardiac tissue locations via the local lead.

28. The method ofclaim 26, further comprising delivering the biologically stimulating electrical output to additional stimulating electrodes implanted at additional cardiac tissue locations via additional local leads.