Posture detection using pressure and other physiologic sensors

• US 8,731,665 B1
• Filed: 10/24/2007
• Issued: 05/20/2014
• Est. Priority Date: 10/24/2007
• Status: Active Grant

• Current Assignee: Pacesetter Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: Pacesetter Incorporated (Abbott Laboratories Incorporated)
• Inventors: Min, Xiaoyi, Jalali, Laleh, Koh, Steve, Bornzin, Gene A., Park, Euljoon
• Primary Examiner(s): Koharski, Christopher D
• Assistant Examiner(s): So, Elizabeth K
• Application Number:
  US11/923,286
• Time in Patent Office: 2,400 Days
• Field of Search: None
• US Class Current: 607/18
• CPC Class Codes: A61N 1/365 controlled by a physiological parameter, e.g. heart potential evoked response A61N1/371
• CPC Class Codes: A61N 1/36535 controlled by body position or posture

Abstract

Systems and methods are provided for detecting the orientation and/or movement of a patient having an implantable cardiac stimulation device and evaluating whether a change in the patient'"'"'s cardiac activity can be at least in part due to a change in the patient'"'"'s orientation. In one particular embodiment, signals from an orientation sensor and/or a pressure sensor are evaluated to determine static positional orientation of the patient and determine based on the static orientation whether the patient'"'"'s cardiac activity is abnormal.

Claims

1. An implantable cardiac stimulation system for a patient comprising:

at least one lead adapted to be implanted within the patient so as to be able to provide electrical stimulation to the heart of the patient;

at least one electrical sensor that senses internal electrogram signals which include signals indicative of intrinsic heart activity and evoked heart activity in response to the delivery of therapeutic electrical stimulations via the at least one lead;

a pressure sensor that senses a pressure within at least one chamber of the heart;

an orientation sensor that detects parameters of the patient that are indicative of an orientation of the patient, wherein the orientation sensor comprises at least one accelerometer and wherein the orientation of the patient is determined using both the pressure sensor and the accelerometer;

a controller that induces the cardiac system to deliver electrical stimulation to the heart of the patient via the at least one lead wherein the controller receives internal electrogram signals from the at least one electrical sensor and signals from the orientation sensor, wherein the controller evaluates the internal electrogram signals from the at least one electrical sensor to determine whether the internal electrogram signals are potentially indicative of possible abnormality in the patient'"'"'s heart function and when the controller determines that the internal electrogram signals are potentially indicative of possible abnormalities in the patient'"'"'s heart function, the controller then evaluates the orientation sensor to determine whether the possible abnormalities are due, at least in part, to a change in the orientation of the patient.

2. The device of claim 1, wherein the controller is adapted to evaluate whether the possible abnormalities are due to a change in the orientation of the patient and the controller is configured to store the internal electrogram signals relating to the possible abnormality in a memory and set a flag in the memory for future follow up, when the controller determines that the possible abnormalities are not due to a change in the patient'"'"'s orientation.

3. The device of claim 1, wherein the controller is adapted to evaluate whether the possible abnormalities are due to a change in the orientation of the patient and the controller is configured to change the parameters of the electrical stimulation applied to the heart, when the controller determines that the possible abnormalities are not due to a change in the patient'"'"'s orientation.

4. The device of claim 1, wherein the at least one lead is adapted to both provide electrical stimulation and also detect electrical activity of the heart so that the at least one lead comprises the at least one electrical sensor.

5. The device of claim 1, wherein an amplitude of internal electrogram signal changes as a result of a change in the patient'"'"'s orientation.

6. The device of claim 5, wherein the controller monitors the evoked heart activity to determine whether the evoked heart activity has amplitude that is less than a pre-determined threshold and when the amplitude is less than a pre-determined threshold, the controller determines the signals to be potentially indicative of possible abnormalities.

7. The device of claim 6, wherein the controller then determines using the orientation sensor whether the possible abnormality is an artifact of the patient'"'"'s orientation.

8. The device of claim 1, wherein the accelerometer is positioned inside the implantable cardiac stimulation device.

9. The device of claim 1, wherein the accelerometer is configured to detect the patient'"'"'s static positional orientation.

10. The device of claim 1, wherein the accelerometer is configured to detect the patient'"'"'s movement.

11. An implantable cardiac stimulation device for a patient comprising:

at least one lead adapted to be implanted within the patient so as to be able to provide electrical stimulation to the heart of the patient;

at least one electrical sensor that senses internal electrogram signals which include signals indicative of intrinsic heart activity and evoked heart activity in response to the delivery of therapeutic electrical stimulations via the at least one lead;

a pressure sensor that senses a pressure within at least one chamber of the heart;

an orientation sensor that detects parameters of the patient that are indicative of the orientation of the patient; and

a controller that induces the at least one lead to provide electrical stimulation to the heart of the patient wherein the controller receives internal electrogram signals from the at least one electrical sensor and signals from the orientation sensor, and the pressure sensor and wherein the controller evaluates the internal electrogram signals from the at least one electrical sensor to determine whether the internal electrogram signals are potentially indicative of possible abnormality in the patient'"'"'s heart function and when the controller determines that the internal electrogram signals are potentially indicative of possible abnormalities in the patient'"'"'s heart function, the controller then evaluates signals received from the pressure sensor and the orientation sensor to determine whether the possible abnormalities are due, at least in part, to a change in the orientation of the patient and uses the signals to adjust the electrical stimulation therapy being provided to the heart via the at least one lead.

12. The device of claim 11, wherein the orientation sensor comprises an accelerometer.

13. The device of claim 12, wherein the orientation sensor comprises a plurality of accelerometer arranged in an orthogonal shape.

14. The device of claim 11, wherein the at least one lead is adapted to both provide electrical stimulation and also detect electrical activity of the heart so that the at least one lead comprises the at least one electrical sensor.

15. The device of claim 11, wherein the controller evaluates the signals received from the pressure sensor and the orientation sensor to detect if the patient has stood up and evaluates the signals received from the pressure sensor to detect whether the patient suffers from orthostatic hypotension.