Estimating acute response to cardiac resynchronization therapy

1. A medical system, comprising:

an electrode for delivering at least one pacing pulse to a pacing site of a patient's heart during a cardiac cycle;

an energy delivery and sensing unit coupled to the electrode;

a hemodynamic sensor;

another sensor;

a memory configured to store at least a threshold that distinguishes between acute responsiveness and non-responsiveness to cardiac resynchronization therapy (CRT) for a patient population, patient population data, and a fusion algorithm; and

a controller coupled to the memory, the hemodynamic sensor, the another sensor, and the energy delivery and sensing unit, the controller configured to:

measure systolic timing intervals of a plurality of different events of the cardiac cycle derived from a plurality of signals sensed during the cardiac cycle, at least one of the plurality of signals produced by the hemodynamic sensor and indicating a systolic timing interval of a mechanical cardiac event of the plurality of different events of the cardiac cycle, and at least another of the plurality of signals produced by the another sensor,

implement the fusion algorithm to combine the measured systolic timing intervals of the plurality of different events of the cardiac cycle and the patient population data to compute an estimate of probability of acute responsiveness to cardiac resynchronization therapy CRT for the pacing site,

compare the estimate to the threshold, and

generate an output indication of acute responsiveness or non-responsiveness of the pacing site to CRT based on the comparison of the estimate to the threshold.

2. The medical system of claim 1 , wherein all of the plurality of systolic timing intervals are intervals of different mechanical events of the cardiac cycle.

3. The medical system of claim 1 , wherein the controller is configured to measure signal amplitude from at least one of the signals of the plurality and implement the fusion algorithm using the measured systolic timing intervals and the at least one measured signal amplitude.

4. The medical system of claim 1 , wherein controller implementation of the fusion algorithm comprises use of a linear regression parameter generated from the measured systolic timing intervals in computing the estimate.

5. The medical system of claim 1 , wherein at least one of the signals of the plurality from which at least one of the systolic timing intervals is measured comprises an electrical cardiac signal indicating electrical activity of the heart during the cardiac cycle.

6. The medical system of claim 1 , wherein the hemodynamic sensor comprises a cardiac stroke impedance sensor.

7. The medical system of claim 1 , wherein the hemodynamic sensor comprises a heart sounds sensor.

8. The medical system of claim 1 , wherein the hemodynamic sensor comprises a cardiac stroke impedance sensor and a heart sounds sensor, the controller measuring the systolic timing intervals derived from features of signals produced by the cardiac stroke impedance sensor and the heart sounds sensor.

9. The medical system of claim 1 , wherein the system is configured for implantation in a patient.

10. The medical system of claim 1 , wherein at least a portion of the system is configured for implantation in a patient and another portion of the system is configured for operation external to the patient.

11. The medical system of claim 1 , wherein the plurality of systolic timing intervals are intervals of different electromechanical events of the cardiac cycle.

12. The medical system of claim 1 , wherein the computed estimate of acute responsiveness is a binary indication between acute responsiveness and non-responsiveness to CRT for the pacing cite.

13. The medical system of claim 1 , wherein the controller is further configured to calculate a confidence indication indicative of relative acute responsiveness to CRT for the pacing site.

14. The medical system of claim 13 , wherein the controller is further configured to set an atrio-ventricular delay for the CRT based on the estimate of acute responsiveness to CRT and the confidence indication.

15. The medical system of claim 1 , further comprising circuitry configured to output a human perceivable indication indicative of the computed estimate of acute responsiveness to CRT.

16. The medical system of claim 1 , wherein the systolic timing intervals are measured in response to delivery of the at least one pacing pulse using one or more atrio-ventricular delay values.

17. The medical system of claim 1 , wherein the hemodynamic sensor comprises an arteriole blood pressure sensor configured for implantation and to measure pressure of the arteriole system.

18. A medical system for delivering at least one pacing pulse to a pacing site of a patient's heart during a cardiac cycle, the system comprising:

means for measuring systolic timing intervals of a plurality of different events of the cardiac cycle, at least one of the systolic timing intervals based on a mechanical cardiac event, the measuring means comprising at least a hemodynamic sensor and another sensor;

means for storing patient population data;

means for implementing a fusion algorithm to combine the measured systolic timing intervals of the plurality of different events of the cardiac cycle and the patient population data to compute an estimate of acute responsiveness to cardiac resynchronization therapy (CRT);

means for comparing the estimate to a threshold, the threshold distinguishing between acute responsiveness and non-responsiveness to CRT for a patient population; and

means for producing an indication of acute responsiveness to CRT for the pacing site in response to the comparison.