System and method for generating activation timing maps
View Patent ↗Cardiac activation timing is mapped using a catheter-mounted roving electrode instead of a fixed (e.g., coronary sinus) electrode. The roving electrode is used to measure an initial electrophysiological signal at an initial cardiac location as a reference signal, which is defined as a reference signal. Local activation time(s) for other cardiac location(s), also measured using the catheter-mounted roving electrode, are determined relative to the reference signal. The stability of the reference signal can be monitored, such as by comparing activation rates or cycle lengths between an instantaneously-measured electrophysiological signal and the initial electrophysiological signal. Smaller differences between the two (e.g., less than about 5%) can be compensated for, while larger differences can result in redefining the reference signal.
1. A method of mapping cardiac activation timing, comprising:
defining an initial electrophysiological signal measured by a catheter-mounted roving electrode at an initial cardiac location as a reference signal, the initial electrophysiological signal having an initial activation rate; and
measuring local activation time for a cardiac location other than the initial cardiac location relative to the reference signal using the catheter-mounted roving electrode.
2. The method according to claim 1 , wherein measuring local activation for a cardiac location other than the initial cardiac location relative to the reference signal using the catheter-mounted roving electrode comprises measuring local activation times for a plurality of cardiac locations other than the initial cardiac location relative to the reference signal using the catheter-mounted roving electrode, thereby generating a local activation time map.
3. The method according to claim 2 , further comprising outputting a graphical representation of the local activation time map on a three dimensional cardiac model.
4. The method according to claim 2 , further comprising monitoring stability of the reference signal.
5. The method according to claim 4 , wherein monitoring stability of the reference signal comprises:
measuring an instantaneous electrophysiological signal using the catheter-mounted roving electrode, the instantaneous electrophysiological signal having an instantaneous activation rate; and
computing a difference between the instantaneous activation rate and the initial activation rate.
6. The method according to claim 5 , wherein the instantaneous electrophysiological signal is measured at the initial cardiac location.
7. The method according to claim 5 , wherein the instantaneous electrophysiological signal is measured at a cardiac location other than the initial cardiac location.
8. The method according to claim 5 , wherein measuring local activation times for a plurality of cardiac locations other than the initial cardiac location relative to the reference signal using the catheter-mounted roving electrode further comprises compensating for the difference between the instantaneous activation rate and the initial activation rate.
9. The method according to claim 5 , further comprising redefining the reference signal using the instantaneous electrophysiological signal when the difference between the instantaneous activation rate and the initial activation rate exceeds a preset threshold amount.
10. The method according to claim 9 , wherein the preset threshold amount is 5% of the initial activation rate.
11. The method according to claim 9 , wherein the preset threshold amount is user-adjustable.
12. A method of mapping cardiac activation timing, comprising:
introducing an electrophysiology catheter including at least one electrode into a patient's heart;
placing the electrophysiology catheter at an initial cardiac location;
measuring an initial electrophysiological signal at the initial cardiac location using the at least one electrode;
defining the initial electrophysiological signal as a reference signal;
moving the electrophysiology catheter to a plurality of locations other than the initial cardiac location; and
measuring, at each of the plurality of locations other than the initial cardiac location, a local activation time relative to the reference signal, using the at least one electrode, thereby generating a local activation time map.
13. The method according to claim 12 , further comprising outputting a graphical representation of the local activation time map on a three dimensional cardiac model.
14. The method according to claim 12 , further comprising monitoring stability of the reference signal.
15. The method according to claim 14 , wherein monitoring stability of the reference signal comprises computing a difference between (1) an activation rate of an electrophysiological signal measured at at least one of the plurality of locations other than the initial cardiac location and (2) an activation rate of the initial electrophysiological signal.
16. The method according to claim 15 , wherein monitoring stability of the reference signal further comprises comparing the computed difference to a preset threshold.