Quantitative characterization of fibrillatory spatiotemporal organization

• US 5,868,680 A
• Filed: 09/23/1997
• Issued: 02/09/1999
• Est. Priority Date: 09/23/1997
• Status: Expired due to Fees

• Current Assignee: Regents of the University of California (University of California)
• Original Assignee: Regents of the University of California (University of California)
• Inventors: Steiner, Paul R., Lesh, Michael D.
• Primary Examiner(s): Kamm, William E.
• Assistant Examiner(s): LAYNO, CARL HERNANDZ
• Application Number:
  US08/936,083
• Time in Patent Office: 504 Days
• Field of Search: 600/518, 600/515, 607/5
• US Class Current: 600/518
• CPC Class Codes: A61B 5/363 Detecting tachycardia or bradycardia

Abstract

Described is a method for monitoring the spatiotemporal organization of atrial arrhythmias, especially atrial fibrillation, based on an analysis of sequences of activation patterns obtained from a particular set of atrial recording sites. This analysis measures the degree of order change in the sequence of activation patterns, or of the time between order changes. Electrogram signals produced by atrial fibrillation are acquired simultaneously from sites adjacent to atrial tissue using multipole electrode catheters. These signals subsequently are filtered and processed to obtain a group of time series which manifest peaks at the latencies of maximal energy in the original data; when these peaks occur are the latencies that are defined as activation events. The activation events from each sampled site are ordered with respect to activation events from each of the other sites, and are translated into corresponding activation patterns, which are determined by the specific spatiotemporal activation sequence associated with each activation event. Each activation pattern in the sequence then is compared with subsequent observed patterns to determine if any spatiotemporal order change has occurred, and if so, to what extent; also, the distribution of observed activation patterns is evaluated for an additional characterization of atrial fibrillation.

Claims

1. A method for characterizing the spatiotemporal organization of atrial fibrillation, comprising the steps of:

(a) acquiring electrogram signals during atrial fibrillation from a plurality of sites adjacent to a region of atrial tissue;

(b) determining activation patterns from said electrogram signals; and

(c) determining spatiotemporal organization of electrical propagation from said activation patterns.

2. A method as recited in claim 1, further comprising the step of detecting atrial fibrillation from said spatiotemporal organization.

3. A method as recited in claim 1, further comprising the step of activating a defibrillation device in response to detection of specific characteristics of said spatiotemporal organization.

4. A method for detecting and characterizing the spatiotemporal organization of atrial fibrillation based upon the spatiotemporal relationship of activation events detected at sites representing spatial samples within an atrial region of interest, comprising the steps of:

(a) simultaneously acquiring electrogram signals during atrial fibrillation from a plurality of sites adjacent to a region of atrial tissue;

(b) determining the latencies of the activation events at each site;

(c) determining sequences of activation patterns from said activation event latencies; and

(d) translating said sequences of activation patterns to sequences of spatiotemporal patterns having a common spatiotemporal reference.

5. A method as recited in claim 4, further comprising the step of detecting atrial fibrillation from said sequences of spatiotemporal patterns.

6. A method as recited in claim 4, further comprising the step of activating a defibrillation device in response to detection of specific characteristics of said sequences of spatiotemporal patterns.

7. A method for detecting and characterizing the spatiotemporal organization of atrial fibrillation based upon the spatiotemporal relationship of activation events detected at sites representing spatial samples within an atrial region of interest, comprising the steps of:

(a) simultaneously acquiring electrogram signals during atrial fibrillation from a plurality of sites adjacent to a region of atrial tissue;

(b) determining activation events at each site from said electrogram signals;

(c) determining sequences of activation patterns from said activation events; and

(d) determining spatiotemporal organization of electrical propagation within said atrial region of interest from said sequences of activation patterns wherein atrial fibrillation is detected and characterized from said spatiotemporal organization.

8. A method as recited in claim 7, wherein said step of determining said spatiotemporal organization includes the step of deriving said spatiotemporal organization from a manifest sequence of said activation patterns.

9. A method as recited in claim 7, wherein said step of determining said spatiotemporal organization includes the step of deriving said spatiotemporal organization from a manifest statistical distribution of said activation patterns.

10. A method as recited in claim 7, wherein said step of determining said spatiotemporal organization includes the step of deriving said spatiotemporal organization from a manifest trajectory of said activation patterns.

11. A method as recited in claim 7, wherein said step of determining said spatiotemporal organization includes the step of deriving said spatiotemporal organization from a manifest sequence and manifest statistical distribution of said activation patterns.

12. A method as recited in claim 7, wherein said step of determining said spatiotemporal organization includes the step of deriving said spatiotemporal organization from a manifest sequence and manifest trajectory of said activation patterns.

13. A method as recited in claim 7, wherein said step of determining said spatiotemporal organization includes the step of deriving said spatiotemporal organization from a manifest sequence of spatiotemporal patterns derived from said activation patterns.

14. A method as recited in claim 7, wherein said step of determining said spatiotemporal organization includes the step of deriving said spatiotemporal organization from a manifest statistical distribution of spatiotemporal patterns derived from said activation patterns.

15. A method as recited in claim 7, wherein said step of determining said spatiotemporal organization includes the step of deriving said spatiotemporal organization from a manifest trajectory of spatiotemporal patterns derived from said activation patterns.

16. A method as recited in claim 7, wherein said step of determining activation events comprises the steps of:

(a) screening the acquired signals and excluding signals having high noise levels or poor signal quality; and

(b) filtering the screened signals, and obtaining a resultant set of time series having peaks at the latencies of maximal energy within a prescribed upper frequency bandwidth, wherein said peaks occur at times that define activation events associated with the original signals.

17. A method as recited in claim 7, wherein said step of determining sequences of activation patterns from said activation events comprises the steps of:

(a) placing together in temporal order all activation events that have been detected from a set of electrodes positioned at the atrial region; and

(b) determining an activation pattern associated with each event, whereby an event is assigned to be in a consistent temporal position within its associated activation pattern, and then uniformly determining the temporal sequence of activation events for a consistent spatial ordering of the sites within the region of interest.

18. A method as recited in claim 7, wherein said step of determining sequences of activation patterns from said activation events comprises the steps of:

(a) placing together in temporal order all activation events that have been detected from a set of electrodes positioned at the atrial region; and

(b) determining an activation pattern associated with each event, whereby each event is assigned to be in a consistent spatial position within its associated activation pattern, and then uniformly determining the spatial sequence of activation events for a consistent temporal ordering of the sites within the region of interest.

19. A method as recited in claim 17, further comprising the step of translating the sequence of activation patterns to a sequence of spatiotemporal patterns having a common spatiotemporal reference.

20. A method as recited in claim 18, further comprising the step of translating the sequence of activation patterns to a sequence of spatiotemporal patterns having a common spatiotemporal reference.

21. A method as recited in claim 7, wherein said step of determining spatiotemporal organization of electrical propagation from manifest sequences of activation patterns comprises the steps of:

(a) deriving a sequence of spatiotemporal patterns from the activation patterns;

(b) comparing each spatiotemporal pattern with subsequent patterns in the sequence to determine the presence or absence of a pattern match across a range of spatiotemporal pattern sequence increments;

(c) computing a quantitative spatiotemporal organization characterization based upon the relative proportion of pattern stability across a range of distances that separate subgroupings; and

(d) plotting said characterization of sampled distances vs. activation event increment vs. proportion of spatiotemporal pattern stability, to provide information that can be compared to expected plots associated with random spatiotemporal activation.

22. A method as recited in claim 7, further comprising the step of detecting atrial fibrillation from said spatiotemporal organization.

23. A method as recited in claim 7, further comprising the step of activating a defibrillation device in response to detection of atrial fibrillation.

24. A method as recited in claim 7, further comprising the step of activating a defibrillation device in response to the detection of specific characteristics of the spatiotemporal organization of atrial fibrillation.

25. A method as recited in claim 8, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest sequence of activation patterns comprises the steps of:

(a) deriving a sequence of spatiotemporal patterns from the activation patterns;

(b) comparing each spatiotemporal pattern with its subsequent spatiotemporal pattern in the sequence to determine the presence or absence of a pattern match; and

(c) computing a metric result based upon the proportion of sequential matching of spatiotemporal patterns.

26. A method as recited in claim 8, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest sequence of activation patterns comprises the steps of:

(a) deriving a sequence of spatiotemporal patterns from the activation patterns;

(b) comparing each spatiotemporal pattern with its subsequent pattern in the sequence to quantify the amount of order change occurring amongst all sites; and

(c) computing a metric result based upon the amount of spatiotemporal order change that occurs with each subsequent increment of the spatiotemporal pattern sequence.

27. A method as recited in claim 8, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest sequence of activation patterns comprises the steps of:

(a) deriving a sequence of spatiotemporal patterns from the activation patterns;

(b) evaluating each spatiotemporal pattern with another pattern occurring at a specified increment in the sequence of spatiotemporal patterns to determine the presence or absence of a spatiotemporal pattern match; and

(c) computing a metric result based on the proportion of sequential matching of spatiotemporal patterns at the specified increment.

28. A method as recited in claim 8, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest sequence of activation patterns comprises the steps of:

(a) deriving a sequence of spatiotemporal patterns from the activation patterns;

(b) evaluating each spatiotemporal pattern with all other spatiotemporal patterns occurring within a specified increment of the sequence of spatiotemporal patterns, to determine the presence or absence of any change among the spatiotemporal patterns within that interval; and

(c) computing a metric result based upon the proportion of spatiotemporal patterns in the sequence for which all associated spatiotemporal patterns within the increment interval remain unchanged.

29. A method as recited in claim 8, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest sequence of activation patterns comprises the steps of:

(a) mathematically comparing the temporal intervals between activation events associated with every possible pairing of sites in an activation pattern with the temporal intervals between activation events associated with the corresponding site pairs of a subsequent activation pattern in the sequence; and

(b) deriving a metric result quantifying spatiotemporal organization from a function of the comparison values so derived.

30. A method as recited in claim 8, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest sequence of activation patterns comprises the steps of:

(a) mathematically comparing the temporal intervals between activation events associated with every possible pairing of sites in an activation pattern with the temporal intervals between the next occurring activation events associated with the same site pairs; and

(b) deriving a metric result quantifying spatiotemporal organization from a function of the comparison values so derived.

31. A method as recited in claim 30, wherein said step of deriving a metric result quantifying spatiotemporal organization from a function of the derived comparison values comprises the steps of:

(a) calculating the absolute value of the difference between the temporal interval associated with activations at a pair of sites in an activation pattern and the corresponding temporal interval for activations at those same sites in a subsequent pattern that is comprised of the next occurring activation events, for every possible pairing of sites in said activation pattern;

(b) summating said absolute values associated with the site pairings of an activation pattern, and doing so for successive activation patterns in the sequence; and

(c) deriving a metric result from said summations to quantify spatiotemporal organization.

32. A method as recited in claim 31, wherein said step of deriving a metric result from said summations to quantify spatiotemporal organization may include temporal normalization of the metric result, comprising the steps of:

(a) calculating the temporal interval between an activation event of an activation pattern and the next activation event at that same site, for each site of the activation pattern;

(b) deriving a temporal normalization factor from the mean of the intervals so derived for every site of an activation pattern;

(c) dividing the summation associated with each activation pattern by the temporal normalization factor associated with that same activation pattern to obtain temporally normalized summation values; and

(d) deriving a metric result from said temporally normalized summation values to quantify spatiotemporal organization.

33. A method as recited in claim 8, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest sequence of activation patterns comprises the steps of:

(a) mathematically comparing the temporal intervals between activation events associated with every possible pairing of sites in an activation pattern with the temporal intervals between the previous occurring activation events associated with the same site pairs; and

(b) deriving a metric result quantifying spatiotemporal organization from a function of the comparison values so derived.

34. A method as recited in claim 33, wherein said step of deriving a metric result quantifying spatiotemporal organization from a function of the derived comparison values comprises the steps of:

(a) calculating the absolute value of the difference between the temporal interval associated with activations at a pair of sites in an activation pattern and the corresponding temporal interval for activations at those same sites in a subsequent pattern that is comprised of the previous occurring activation events, for every possible pairing of sites in said activation pattern;

(b) summating said absolute values associated with the site pairings of an activation pattern, and doing so for successive activation patterns in the sequence; and

(c) deriving a metric result from said summations to quantify spatiotemporal organization.

35. A method as recited in claim 34, wherein said step of deriving a metric result from said summations to quantify spatiotemporal organization may include temporal normalization of the metric result, comprising the steps of:

(a) calculating the temporal interval between an activation event of an activation pattern and the previous activation event at that same site, for each site of the activation pattern;

(b) deriving a temporal normalization factor from the mean of the intervals so derived for every site of an activation pattern;

(c) dividing the summation associated with each activation pattern by the temporal normalization factor associated with that same activation pattern to obtain temporally normalized summation values; and

(d) deriving a metric result from said temporally normalized summation values to quantify spatiotemporal organization.

36. A method as recited in claim 9, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest statistical distribution of activation patterns comprises the steps of:

(a) analyzing the statistical distributions of the observed activation patterns in relation to the entire range of activation patterns that exists for the specified number of spatial sites being considered; and

(b) deriving a metric result based upon a statistical description of said distributions.

37. A method as recited in claim 9, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest statistical distribution of activation patterns comprises the steps of:

(a) deriving spatiotemporal patterns from the activation patterns;

(b) analyzing the statistical distributions of the observed spatiotemporal patterns in relation to the entire range of spatiotemporal patterns that exists for the specified number of spatial sites being considered; and

(c) deriving a metric result based upon a statistical description of said distribution.

38. A method as recited in claim 9, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest statistical distribution of activation patterns comprises the steps of:

(a) analyzing the distributions of the observed activation patterns in relation to the entire range of activation patterns that exists for the specific number of spatial sites being considered, to identify relative proportions within the distributions of one or more subgroupings of related activation patterns; and

(b) deriving a metric result based upon said proportions.

39. A method as recited in claim 9, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest statistical distribution of activation patterns comprises the steps of:

(a) deriving spatiotemporal patterns from the activation patterns;

(b) analyzing the distributions of the observed spatiotemporal patterns in relation to the entire range of spatiotemporal patterns that exists for the specific number of spatial sites being considered, to identify relative proportions within the distributions of one or more subgroupings of related spatiotemporal patterns; and

(c) deriving a metric result based upon said proportions.

40. A method as recited in claim 9, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest statistical distribution of activation patterns comprises the steps of:

(a) analyzing the relative distributions of the observed activation patterns to identify the manifestation of the preferential occurrence of activation patterns; and

(b) deriving a metric result based upon the predominance of a particular activation pattern.

41. A method as recited in claim 9, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest statistical distribution of activation patterns comprises the steps of:

(a) deriving spatiotemporal patterns from the activation patterns;

(b) analyzing the relative distributions of the observed spatiotemporal patterns to identify the manifestation of the preferential occurrence of spatiotemporal patterns; and

(c) deriving a metric result based upon the predominance of a particular spatiotemporal pattern.

42. A method as recited in claim 9, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest statistical distribution of activation patterns comprises the steps of:

(a) analyzing the relative distributions of the observed activation patterns to identify the manifestation of the preferential occurrence of related subgroupings of activation patterns; and

(b) deriving a metric result based upon the predominance of a particular related subgrouping of activation patterns.

43. A method as recited in claim 9, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest statistical distribution of activation patterns comprises the steps of:

(a) deriving spatiotemporal patterns from the activation patterns;

(b) analyzing the relative distributions of the observed spatiotemporal patterns to identify the manifestation of the preferential occurrence of related subgroupings of spatiotemporal patterns; and

(c) deriving a metric result based upon the predominance of a particular related subgrouping of spatiotemporal patterns.

44. A method as recited in claim 11, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest sequence and manifest statistical distribution of said activation patterns, comprises the steps of:

(a) deriving spatiotemporal patterns from the activation patterns;

(b) comparing each spatiotemporal pattern with its subsequent pattern in the sequence to determine the presence or absence of a pattern match;

(c) analyzing the relative distributions of the observed spatiotemporal patterns in relation to the entire range of spatiotemporal patterns that exists for the specific number of spatial sites being considered, to identify the manifestation of the preferential occurrence of spatiotemporal patterns; and

(d) deriving a metric result based upon the predominance of a particular spatiotemporal pattern which quantifies the relationship of pattern dominance to the occurrence of matching sequential spatiotemporal patterns.

45. A method as recited in claim 9, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest sequence and manifest statistical distribution of said activation patterns, comprises the steps of:

(a) deriving spatiotemporal patterns from the activation patterns;

(b) comparing each spatiotemporal pattern with its subsequent pattern in the sequence to determine the presence or absence of a pattern match;

(c) analyzing the relative distributions of the observed spatiotemporal patterns in relation to the entire range of spatiotemporal patterns that exists for the specific number of spatial sites being considered, to identify the manifestation of the preferential occurrence of related subgroupings of spatiotemporal patterns; and

(d) deriving a metric result based upon the predominance of a particular related subgrouping of spatiotemporal patterns which quantifies the relationship of pattern dominance to the occurrence of matching sequential spatiotemporal patterns.

46. A method as recited in claim 12, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest sequence and trajectory of said activation patterns, comprises the steps of:

(a) analyzing the statistical distributions of the observed increments in the sequence of activation patterns in relation to the entire range of possible increments that exists for the specified number of spatial sites being considered; and

(b) deriving a metric result based upon a numeric and/or graphical description of said distributions.

47. A method as recited in claim 12, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest sequence and trajectory of said activation patterns, comprises the steps of:

(a) analyzing the statistical distributions of the observed increments in the sequence of activation patterns in relation to the entire range of possible increments that exists for the specified number of spatial sites being considered; and

(b) deriving a metric result based upon a numeric and/or graphical description of the relative proportions of particular related trajectory subgroupings.

48. A method as recited in claim 12, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest sequence and trajectory of said activation patterns, comprises the steps of:

(a) analyzing the statistical distributions of the observed increments in the sequence of activation patterns to identify relative proportions of the emergence of specific activation patterns from other activation patterns, including the same activation pattern; and

(b) deriving a metric result based upon a numeric description of said distributions, a graphical description of said distributions, or both a numeric and graphical description of said distributions.

49. A method as recited in claim 12, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest sequence and trajectory of said activation patterns, comprises the steps of:

(a) analyzing the statistical distribution of the observed increments in the sequence of activation patterns to identify relative proportions of the dissipation of each specific activation pattern into other specific activation patterns, including the same activation pattern; and

(b) deriving a metric result based upon a numeric description of said distributions, a graphical description of said distributions, or both a numeric and graphical description of said distributions.

50. A method as recited in claim 12, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest sequence and trajectory of said activation patterns, comprises the steps of:

(a) analyzing the statistical distribution of the observed increments in the sequence of activation patterns to identify relative proportions of the emergence of each specific activation pattern from other specific activation patterns, including the same activation pattern; and

(b) deriving a metric result based upon a numeric description of said distributions, a graphical description of said distributions, or both a numeric and graphical description of the predominance of a particular related subgrouping of trajectories.

51. A method as recited in claim 12, wherein said step of determining spatiotemporal organization of electrical propagation from a manifest sequence and trajectory of said activation patterns, comprises the steps of:

(a) analyzing the statistical distribution of the observed increments in the sequence of activation patterns to identify relative proportions of the dissipation of each specific activation pattern into other specific activation patterns, including the same activation pattern; and

(b) deriving a metric result based upon a numeric description of said distributions, a graphical description of said distributions, or both a numeric and graphical description of the predominance of a particular related subgrouping of trajectories.

52. A method for mapping atrial fibrillation by assessing spatiotemporal organization at multiple targeted atrial regions, comprising the steps of:

(a) simultaneously acquiring electrogram signals during atrial fibrillation from a plurality of sites adjacent to each targeted region of atrial tissue;

(b) determining activation events at each site from said electrogram signals;

(c) determining sequences of activation patterns for each targeted region from the activation events associated with that region;

(d) determining spatiotemporal organization of electrical propagation within each targeted atrial region from sequences of activation patterns associated with that region; and

(e) comparing spatiotemporal organization in different atrial regions wherein atrial fibrillation can be detected and characterized from said comparison.

53. A method as recited in claim 52, further comprising the step of detecting atrial fibrillation from said spatiotemporal organization regional comparison.

54. A method as recited in claim 52, further comprising the step of activating a defibrillation device in response to detection of specific characteristics of said spatiotemporal organization regional comparison.