Coordinating musculoskeletal and cardiovascular hemodynamics

• US 9,457,190 B2
• Filed: 03/17/2014
• Issued: 10/04/2016
• Est. Priority Date: 03/15/2013
• Status: Active Grant

• Current Assignee: Pulson, Inc.
• Original Assignee: Pulson, Inc.
• Inventors: Bleich, Jeffery L., Mannheimer, Paul, Buxbaum, Darin Howard
• Primary Examiner(s): EVANISKO, GEORGE ROBERT
• Application Number:
  US14/216,960
• Publication Number:
  US 20140277241A1
• Time in Patent Office: 932 Days
• US Class Current: 1/1
• CPC Class Codes: A61N 1/36507 controlled by gradient or slope of the heart potential
• CPC Class Codes: A61N 1/36542 controlled by body motion, e.g. acceleration
• CPC Class Codes: A61N 1/36585 controlled by two or more physical parameters

Abstract

The present invention is generally directed to methods, systems, and computer program products for coordinating musculoskeletal and cardiovascular hemodynamics. In some embodiments, a heart pacing signal causes heart contractions to occur with an essentially constant time relationship with respect to rhythmic musculoskeletal activity. In other embodiments, prompts (e.g., audio, graphical, etc.) are provided to a user to assist them in timing of their rhythmic musculoskeletal activity relative to timing of their cardiovascular cycle. In further embodiments, accurately indicating a heart condition during a cardiac stress test is increased.

Claims

1. A method for coordinating cardiovascular pump timing with detected musculoskeletal pump timing to facilitate favorable cardiovascular hemodynamics in an individual, the method comprising:

accessing ongoing signals from at least one musculoskeletal activity sensor positioned in or on an individual;

processing the accessed signals from the musculoskeletal activity sensor;

detecting from the processed signals that the individual is engaged in a rhythmic physical activity, the rhythmic physical activity having an associated musculoskeletal pump timing;

determining a target cardiovascular pump timing for the individual, which would achieve favorable cardiovascular hemodynamics during the rhythmic physical activity;

determining a target heartrate corresponding to the rhythmic physical activity;

determining whether an intrinsic heartrate of the individual is less than or equal to the target heartrate; and

when the intrinsic heartrate is less than the target heartrate, providing a pacing signal to the heart of the individual to pace the heart at the target heartrate and the target cardiovascular pump timing such that a maximal musculoskeletal pumping of blood occurs substantially during cardiac diastole.

2. The method of claim 1, wherein the pacing signal is provided in accordance with conventional pacing algorithms.

3. The method of claim 1, wherein at least one musculoskeletal activity sensor is positioned within an artificial pacemaker implanted in the individual.

4. The method of claim 1, wherein at least one musculoskeletal activity sensor is an external wireless sensor.

5. The method of claim 1, wherein the musculoskeletal activity sensor comprises at least one of:

a uniaxial accelerometer, a multi-axial accelerometer, a gyroscope, a magnetometer, a piezoelectric material, or a pressure sensor.

6. The method of claim 1, wherein the musculoskeletal activity sensor comprises at least one physiologic sensor responsive to body motions, the at least one physiologic sensor selected from a group consisting of a:

respiratory sensor, cardiac function sensor, motion sensor, force sensor, temperature sensor, electromyographic (EMG) sensor, electrocardiographic (ECG) sensor, electroencephalographic (EEG) sensor, andphotoplethysmographic (PPG) sensor.

7. The method of claim 1, wherein processing the accessed signals from the musculoskeletal activity sensor comprises determining at least one of rhythmic physical activity frequency, maximal muscle contraction timing, timing of rhythmic changes in inertia, timing of physical impact, magnitude of rhythmic changes in inertia, step timing, changes in elevation, duration of foot-ground contact time, a measure of foot strike ergonomics, a measure of physical posture, or a measure of balance.

8. The method of claim 1, wherein the rhythmic physical activity comprises at least one of walking, running, swimming, climbing, rowing, and biking.

9. The method of claim 1, wherein determining a target cardiovascular pump timing for the individual comprises identifying a timing that results in left ventricular ejection occurring in between skeletal muscle contractions during the musculoskeletal pump cycle.

10. The method of claim 1, wherein the target cardiovascular pump timing is determined by:

delivering varying pacing signals to the heart such that ventricular contraction is systematically triggered at different timing locations during the musculoskeletal pump cycle, measuring a physiological response of the patient while the pacing signals are varied, and identifying a cardiovascular pump timing that produces an optimal physiological response.

11. The method of claim 10, wherein the measured physiological response of the patient comprises at least one of:

contractility, blood pressure, cardiac output, tissue oxygenation, tissue pH, or minute volume.

12. The method of claim 1, wherein the target heartrate equals an integer multiple of a cadence of the rhythmic physical activity.

13. A method, for artificially pacing a patient'"'"'s heart, comprising:

detecting a recurrent aspect of a rhythmic musculoskeletal activity of the patient;

determining a target heartrate for the detected rhythmic musculoskeletal activity;

determining whether an intrinsic heartrate of the patient is less than or equal to the target heartrate for the rhythmic musculoskeletal activity; and

when the intrinsic heartrate is less than the target heartrate, providing a pacing signal to the heart, wherein;

the pacing signal causes heart contractions in a cardiac cycle to occur with a predominantly constant timing relationship with respect to the detected recurrent aspect of the rhythmic musculoskeletal activity,

the detected recurrent aspect of the rhythmic musculoskeletal activity has a consistent timing relationship with a maximal musculoskeletal pumping during the rhythmic musculoskeletal activity of the patient, and

the pacing, signal results in the maximal musculoskeletal pumping occurring, predominantly within a diastolic period of the cardiac cycle.

14. The method of claim 13, wherein the pacing signal is provided in the predominantly constant timing relationship with respect to the detected recurrent aspect of the rhythmic musculoskeletal activity only when the frequency of the recurrent aspect of the rhythmic musculoskeletal activity is within a pre-defined range.

15. The method of claim 13, wherein the pacing signal comprises electrical stimulations repeated at a timing determined on the basis of at least one of:

a percent of a step to step interval, a fixed time delay relative to the detected rhythmic musculoskeletal activity, a calculated time after the detected rhythmic musculoskeletal activity, or a calculated time before a predicted next rhythmic musculoskeletal activity.

16. The method of claim 13, wherein the pacing signal to the heart is provided by an artificial pacemaker.

17. The method of claim 13, wherein the recurrent aspect of the rhythmic musculoskeletal activity of the patient is detected from an electrical signal received from a musculoskeletal activity sensor positioned in or on the patient.

18. The method of claim 17, wherein the musculoskeletal activity sensor comprises at least one of a uniaxial accelerometer, a multi-axial accelerometer, a gyroscope, a magnetometer, a piezoelectric material, or a pressure sensor.

19. The method of claim 17, wherein the musculoskeletal activity sensor comprises at least one physiologic sensor responsive to body motions, the at least one physiologic sensor selected from a group consisting of a:

respiratory sensor, cardiac function sensor, motion sensor, force sensor, temperature sensor, electromyogram (EMG) sensor, electrocardiogram ECG) sensor, electroencephalogram (EEG) sensor, and photoplethysmogram (PPG) sensor.

20. The method of claim 13, wherein performance of the method is triggered by at least one of a detected increase in metabolic demands as identified by minute ventilation, a sensed rhythmic musculoskeletal activity detected by an activity sensor, a pre-programmed activation, or an activation signal from a user-controlled external device.