Stimulus timing for a stimulating medical device

• US 9,713,715 B2
• Filed: 03/29/2016
• Issued: 07/25/2017
• Est. Priority Date: 02/05/2009
• Status: Active Grant

• Current Assignee: Cochlear Limited
• Original Assignee: Cochlear Limited
• Inventors: Smith, Zachary Mark
• Primary Examiner(s): VOORHEES, CATHERINE M
• Application Number:
  US15/083,814
• Publication Number:
  US 20160206879A1
• Time in Patent Office: 483 Days
• CPC Class Codes: A61N 1/36038 Cochlear stimulation
• CPC Class Codes: H04R 25/505 using digital signal processing

Abstract

Methods and systems are disclosed for determining the timing of stimulation applied using a medical device. In embodiments, the medical device filters a received signal to obtain a plurality of band-pass filtered signals, each corresponding to one or more stimulation channels. The medical device then determines the envelopes of these band-pass filtered signals. Next, the medical device determines the stimulation timing (i.e., the pulse times) for the corresponding stimulation channel based on the timing of a particular phase (e.g., a peak, a minimum, etc.) of the envelope. A pulse amplitude for the stimulation channel may then be determined, and stimulation applied using the determined amplitude and pulse time.

Claims

1. A stimulating medical device, comprising:

one or more band-pass filters configured to filter a received signal to obtain a set of band-pass filtered signals;

one or more envelope detectors configured to determine an envelope for at least one band-pass filtered signal of the set of band-pass filtered signals; and

one or more pulse time selectors configured to determine a variable pulse rate for stimulation pulses at a stimulation channel of the stimulating medical device, wherein the stimulation channel is associated with the at least one band pass filtered signal and the variable pulse rate corresponds to a frequency of the envelope of the at least one band-pass filtered signal.

2. The stimulating medical device of claim 1, further comprising:

a plurality of electrodes,

wherein the stimulation channel terminates in one or more of the plurality of electrodes, and wherein the one or more of the plurality of electrodes are configured to deliver the stimulation pulses to a recipient using the variable pulse rate.

3. The stimulating medical device of claim 2, further comprising:

one or more amplitude selectors configured to determine, based on the envelope, one or more pulse amplitudes for the stimulation pulses,

wherein the one or more of the plurality of electrodes are configured to deliver the stimulation pulses to a recipient using the variable pulse rate and the one or more pulse amplitudes.

4. The stimulating medical device of claim 1, wherein the one or more one or more band-pass filters comprise a plurality of band-pass filters configured to determine a plurality of band-pass filtered signals that each correspond to one of a plurality of stimulation channels of the stimulating medical device, wherein the one or more envelope detectors comprise a plurality of envelope detectors configured to determine a plurality of envelopes, wherein each of the plurality of envelopes corresponds to one of the plurality of band-pass filtered signals, and wherein the one or more pulse time selectors comprise a plurality of pulse time selectors configured to determine independently variable pulse rates for each of the plurality of stimulation channels, wherein each of the variable pulse rates corresponds to a frequency of the envelope of the band-pass filtered signal associated with the corresponding stimulation channel.

5. The stimulating medical device of claim 4, further comprising:

a plurality of amplitude selectors configured to determine, based on the one or more envelopes for each of the plurality of band-pass filtered, one or more pulse amplitudes for stimulation pulses at each of the corresponding plurality of stimulation channels.

6. The stimulating medical device of claim 5, further comprising:

a plurality of electrodes, wherein each of the plurality of stimulation channels terminates in a set of one or more of the plurality of electrodes, and wherein the sets of one or more electrodes are configured to deliver the stimulation pulses to a recipient using the corresponding variable pulse rate and the one or more pulse amplitudes.

7. The stimulating medical device of claim 5, further comprising a maxima selector configured to:

select a plurality of maxima from the one or more pulse amplitudes associated with the plurality of stimulation channels; and

arbitrate between the selected maxima to determine a set of stimulation pulse rates and corresponding pulse amplitudes for use in delivery of stimulation pulses to the recipient.

8. A method, comprising:

filtering a received signal to obtain a set of band-pass filtered signals;

determining an envelope for at least one band-pass filtered signal of the band-pass filtered signals;

determining a variable pulse rate for a stimulation channel of a stimulating medical device, wherein the stimulation channel is associated with the at least one band pass filtered signal, and wherein the variable pulse rate corresponds to a frequency of the envelope of the at least one band-pass filtered signal; and

delivering stimulation pulses via the stimulation channel using the variable pulse rate.

9. The method of claim 8, wherein the set of band-pass filtered signals includes a plurality of band-pass filtered signals each corresponding to one of a plurality of stimulation channels of the stimulating medical device, and further comprising:

determining a plurality of envelopes, wherein each of the plurality of envelopes corresponds to one of the plurality of band-pass filtered signals;

determining independently variable pulse rates for each of the plurality of stimulation channels, wherein each of the variable pulse rates corresponds to a frequency of the envelope of the band-pass filtered signal associated with the corresponding stimulation channel; and

delivering stimulation pulses via the plurality of stimulation channels using the corresponding pulse rate.

10. The method of claim 9, further comprising:

determining, based on the one or more envelopes for each of the plurality of band-pass filtered, one or more pulse amplitudes for stimulation pulses at each of the corresponding plurality of stimulation channels; and

delivering stimulation pulses via the plurality of stimulation channels using the corresponding variable pulse rates and the one or more pulse amplitudes.

11. The method of claim 10, further comprising:

selecting a plurality of maxima from the one or more pulse amplitudes associated with the plurality of stimulation channels; and

arbitrating between the selected maxima to determine a set of stimulation pulse rates and corresponding pulse amplitudes for use in delivery of stimulation pulses to the recipient.

12. The method of claim 8, wherein each stimulation channel corresponds to one or more electrodes for use in delivering stimulation pulses.

13. A bilateral implant system, comprising:

a first cochlear implant fitted to a first ear of a recipient; and

a second cochlear implant fitted to a second ear of the recipient,

wherein the first and second cochlear implants each comprise;

one or more band-pass filters configured to filter a received signal to obtain a set of band-pass filtered signals;

one or more envelope detectors configured to determine an envelope for at least one band-pass filtered signal of the band-pass filtered signals; and

one or more pulse time selectors configured to determine a variable pulse rate for stimulation pulses at a stimulation channel of the respective cochlear implant, wherein the stimulation channel is associated with the at least one band pass filtered signal, and wherein the variable pulse rate corresponds to a frequency of the envelope of the at least one band-pass filtered signal.

14. The bilateral implant system of claim 13, wherein the first and second cochlear implants further comprise first and second sets of low-pass filters, respectively, wherein the first and second sets of low-pass filters are configured to filter the envelopes generated by the first and second sound cochlear implants, respectively, and wherein the first and second sets of low-pass filters have upper cutoff frequencies that limit a pulse rate.

15. The bilateral implant system of claim 14, wherein the upper cutoff frequencies are in a range of approximately 300 hertz (Hz) to approximately 600 Hz.

16. The bilateral implant system of claim 15, wherein the upper cutoff frequencies are approximately 450 Hz.

17. The bilateral implant system of claim 14, wherein the upper cutoff frequencies of the first and second sets of low-pass filters are selected to limit the pulse rate in each stimulation channel to within a perceptually relevant range for the recipient.

18. The bilateral implant system of claim 13, wherein the first and second cochlear implants each operate in accordance with a fixed latency.

19. The bilateral implant system of claim 13, wherein the first and second cochlear implants each comprise:

a plurality of electrodes, wherein the stimulation channels of the first and second sound processing units each terminates in one or more electrodes, and wherein the one or more electrodes are configured to deliver the stimulation pulses to a recipient using the variable pulse rate.

20. The bilateral implant system of claim 19, wherein the first and second cochlear implants each comprise:

one or more amplitude selectors configured to determine, based on the envelope, one or more pulse amplitudes for the stimulation pulses,

wherein the one or more electrodes in the first and second cochlear implants, respectively, are configured to deliver the stimulation pulses to a recipient using the variable pulse rate and the one or more pulse amplitudes.