Patent Application
20210161426
The present invention relates generally to cardiac mapping, and specifically to mapping local activation times of sinus rhythm and non-sinus rhythm cardiac cycles.
Cardiac arrhythmia, such as atrial fibrillation, is a heart rhythm that produces irregular heartbeats. Arrhythmias typically occur when regions of cardiac tissue abnormally conduct electric signals to adjacent tissue, thereby disrupting the normal cardiac cycle and causing asynchronous rhythm.
Mapping of electrical potentials in the heart is a commonly used tool for diagnosing and treating cardiac arrhythmias. Typically, time-varying electrical potentials in the endocardium are sensed and recorded as a function of position inside the heart, and then used to map a local electrogram or local activation time. Activation time differs from point to point in the endocardium due to the time required for conduction of electrical impulses through the heart muscle. The direction of this electrical conduction at any point in the heart is conventionally represented by an activation vector, which is normal to an isoelectric activation front, both of which may be derived from a map of activation time. The rate of propagation of the activation front through any point in the endocardium may be represented as a velocity vector.
Mapping the activation front and conduction fields aids the physician in identifying and diagnosing abnormalities, such as ventricular and atrial tachycardia and ventricular and atrial fibrillation, which result from areas of impaired electrical propagation in the heart tissue.
U.S. Patent Application 2015/0073246 to Chmiel et al., describes a method for manually mapping premature ventricular contractions (PVCs). The method includes recording a series of electrocardiogram (ECG) signals from a patient suffering from PVCs, and then selecting, by a physician, beats which show a sinus rhythm, and beats which show a PVC. The sinus beats are used for producing a physical map of the heart. Electrophysiological readings of local activation times (LATs), acquired during the PVC beats, are then overlaid on the sinus map, producing a so-called LAT hybrid map.
U.S. Pat. No. 5,271,411 to Ripley et al., describes a method for ECG signal analysis and cardiac arrhythmia detection. The method includes identifying a normal QRS complex and labeling QRS complexes acquired after identification the normal QRS complex based on multiple rules and their respective locations.
U.S. Pat. No. 4,336,810 to Anderson et al., describes a method for arrhythmia analysis of ECG recordings. The method includes receiving and comparing ECG signals to known templates that are based on classifications of previously-identified complexes. Based on the comparisons, each of the received signals can be designated as normal, ventricular ectopic, supraventricular ectopic, or unknown (ectopy of unknown origin).
U.S. Patent Application 2012/0165895 to Dong et al., describes a method for non-captured intrinsic discrimination in cardiac pacing response classification. The method includes discriminating non-captured intrinsic beats during evoked response detection and classification by comparing the features of a post-pace cardiac signal with expected features associated with a non-captured response with intrinsic activation. In some embodiments, the detection of a non-captured response with intrinsic activation may be based on the peak amplitude and timing of the cardiac signal.
U.S. Patent Application 2009/0099468 to Thiagalingam et al., describes a method for the automated processing of electrophysiological data. The method includes determining temporal locations by defining one or more reference channels containing a reference beat and comparing beats of the recorded electrogram data against the defined one or more reference channels. An index of the temporal locations and other information of the beats within the recorded electrogram data is created, and the index of temporal locations can be used to analyze recorded electrogram data in order to locate electrophysiological features suggestive of an abnormality.
There is provided, in accordance with an embodiment of the present invention, a method including receiving, by a processor, sets of signals during multiple cardiac cycles, each set of the signals indicating, for a medical probe inserted into a cardiac chamber, a three-dimensional (3D) location of a distal end of the probe, electrical potentials measured at the 3D location, and respective times during a given cardiac cycle when the electrical potentials were measured. comparing the received electrical potential measurements and the respective times to a first template for a sinus rhythm cardiac cycle and a second template for a non-sinus rhythm cardiac cycle so as to identify a sequence of cardiac cycles including consecutive first, second, and third cardiac cycles wherein the first and second cardiac cycles are in accordance with the first template and the third cardiac cycle is in accordance with the second template, generating a physical map of the cardiac chamber, based on the 3D locations, and rendering to a display, based on the received 3D locations and corresponding measured electrical potentials, an electroanatomic map including the local activation times for the non-sinus rhythm cardiac cycle overlaid on the physical map.
In some embodiments, the probe includes an intracardiac catheter having multiple electrodes that simultaneously generate respective sets of the signals.
In additional embodiments, the non-sinus rhythm cardiac cycle includes a premature ventricular contraction.
In further embodiments, generating the physical map includes generating the physical map based on the 3D locations indicated by the sets of signals received during the first and second cardiac cycles. In one embodiment, generating the physical map includes generating a first physical map based on the 3D locations indicated by the sets of signals received during the first cardiac cycle and a second physical map based on the 3D locations indicated by the sets of signals received during the second cardiac cycle, and selecting either the first or the second physical map. In another embodiment, the second physical map is in accordance with the first physical map.
In supplemental embodiments, rendering the electroanatomic map including the local activation times for the non-sinus rhythm cardiac cycle overlaid on the physical map includes overlaying the local activation time of the non-sinus rhythm cardiac cycle indicated by each given signal at a map location corresponding to the 3D location indicated by the given signal.
In some embodiments, comparing the received electrical potential measurements and the respective times to a given template includes comparing a given signal indicating the received electrical potential measurements and the respective times to the given template.
In additional embodiments, the method may include identifying a region of the map having earliest local activation times, and flagging, on the display, the identified region for ablation. In one embodiment, identifying the region of the map having earliest local activation times includes segmenting the map into multiple regions based on their respective local activation times, and identifying the region having the earliest local activation times.
There is also provided, in accordance with an embodiment of the present invention, an apparatus including a display, and a processor configured to receive sets of signals during multiple cardiac cycles, each set of the signals indicating, for a medical probe inserted into a cardiac chamber, a three-dimensional (3D) location of a distal end of the probe, electrical potentials measured at the 3D location, and respective times during a given cardiac cycle when the electrical potentials were measured, to compare the received electrical potential measurements and the respective times to a first template for a sinus rhythm cardiac cycle and a second template for a non-sinus rhythm cardiac cycle so as to identify a sequence of cardiac cycles including consecutive first, second, and third cardiac cycles wherein the first and second cardiac cycles are in accordance with the first template and the third cardiac cycle is in accordance with the second template, to generate a physical map of the cardiac chamber, based on the 3D locations, and to render to a display, based on the received 3D locations and corresponding measured electrical potentials, an electroanatomic map including the local activation times for the non-sinus rhythm cardiac cycle overlaid on the physical map.
There is further provided, in accordance with an embodiment of the present invention, a computer software product, operated in conjunction with a medical probe for insertion into a body cavity, the product including a non-transitory computer-readable medium, in which program instructions are stored, which instructions, when read by a computer, cause the computer to receive sets of signals during multiple cardiac cycles, each set of the signals indicating, for a medical probe inserted into a cardiac chamber, a three-dimensional (3D) location of a distal end of the probe, electrical potentials measured at the 3D location, and respective times during a given cardiac cycle when the electrical potentials were measured, to compare the received electrical potential measurements and the respective times to a first template for a sinus rhythm cardiac cycle and a second template for a non-sinus rhythm cardiac cycle so as to identify a sequence of cardiac cycles including consecutive first, second, and third cardiac cycles wherein the first and second cardiac cycles are in accordance with the first template and the third cardiac cycle is in accordance with the second template, to generate a physical map of the cardiac chamber, based on the 3D locations, and to render to a display, based on the received 3D locations and corresponding measured electrical potentials, an electroanatomic map including the activation times for the non-sinus rhythm cardiac cycle overlaid on the physical map.
The disclosure is herein described, by way of example only, with reference to the accompanying drawings, wherein:
Generating a local activation time (LAT) map of a heart with an arrhythmia is typically a difficult and time-consuming process. The LAT map is generated from information collected during sinus and non-sinus cardiac cycles, and the selection of the different types of cardiac cycles (also known as beats) by a medical professional (e.g., a physician) can be time consuming.
Embodiments of the present invention provide methods and systems for automatically generating an electroanatomic LAT hybrid map that maps premature ventricular contractions (PVCs) for an arrhythmic heart. As described hereinbelow, an intra-cardiac probe is inserted into a cardiac chamber, and sets of signals are received during multiple cardiac cycles, each set of the signals indicating a three-dimensional (3D) location of a distal end of the probe, electrical potentials measured at the 3D location, and respective times during a given cardiac cycle when the electrical potentials were measured.
The received electrical potential measurements and the respective times are compared to a first template for a normal sinus rhythm (also referred to herein simply as sinus rhythm) cardiac cycle and a second template for a non-sinus rhythm cardiac cycle so as to identify a sequence of cardiac cycles comprising consecutive first, second, and third cardiac cycles, wherein the first and second cardiac cycles are in accordance with the first template and the third cardiac cycle is in accordance with the second template. A physical map of the cardiac chamber is generated based on the received 3D locations, and based on the received 3D locations and corresponding measured electrical potentials, an electroanatomic map comprising the local activation times for the non-sinus rhythm cardiac cycle overlaid on the physical map is rendered to a display. The resultant map may then typically be used to select a region for ablation, since it indicates an origin of the PVC. Using templates to identify sinus and non-sinus cardiac cycles enables systems implementing embodiments of the present invention to rapidly generate electroanatomic LAT maps for an arrhythmic heart without requiring any user input to identify the sinus and non-sinus cardiac cycles. In some embodiments, the physical map may be generated solely based on the 3D coordinates received during the first and second cardiac cycles (i.e., the sinus rhythm cardiac cycles). By only using 3D location coordinates collected from the sinus rhythm cardiac cycles, embodiments of the present invention can produce a more stable physical map having fewer errors due to the unstable or “jumpy” nature of adjacent non-sinus cardiac cycles such as PVCs.
During a medical procedure, a medical professional 34 inserts medical probe 22 into a biocompatible sheath 80 (
Control console 24 is connected, by a cable 32, to body surface electrodes, which typically comprise adhesive skin patches 36 that are affixed to patient 30. Control console 24 comprises a processor 38 that, in conjunction with a current tracking module 40, determines position coordinates of the distal end 26 inside the heart based on impedances measured between adhesive skin patches 36 and electrodes 84 that are affixed to splines 82 as shown in
While embodiments herein show probe 20 comprising a multi-spline intracardiac catheter such as the Pentaray® NAV catheter, using other multi-electrode intracardiac catheters such as the Navistar® Thermocool® catheters are considered to be within the spirit and scope of the present invention. The Pentaray® NAV and Navistar® Thermocool® catheters are both produced by Biosense Webster Inc.
Processor 38 may comprise real-time noise reduction circuitry 42 typically configured as a field programmable gate array (FPGA), followed by an analog-to-digital (A/D) ECG (electrocardiograph) signal conversion integrated circuit 44. The processor can pass the signal from A/D ECG circuit 42 to another processor and/or can be programmed to perform one or more algorithms disclosed herein, each of the one or more algorithms comprising steps described hereinbelow. The processor uses circuitry 42 and circuit 44, as well as features of modules which are described in more detail below, in order to perform the one or more algorithms.
The medical system shown in
Control console 24 also comprises an input/output (I/O) communications interface 46 that enables the control console to transfer signals from, and/or transfer signals to electrodes 84 and adhesive skin patches 36. Based on signals received from electrodes 84 and/or adhesive skin patches 36, processor 38 can generate an electroanatomic local activation time (LAT) map 48 that presents measurements of cardiac conduction velocity, as described in the description referencing
During a procedure, processor 38 can present electroanatomic LAT map 48 to medical professional 34 on a display 50, and store data representing the electroanatomic LAT map in a memory 52. Memory 52 may comprise any suitable volatile and/or non-volatile memory, such as random access memory or a hard disk drive. In some embodiments, medical professional 34 can manipulate map 48 using one or more input devices 54. In alternative embodiments, display 50 may comprise a touchscreen that can be configured to accept inputs from medical professional 34, in addition to presenting map 48.
As shown in
In the configuration shown in
In some embodiments, electrode location records 64 have a one-to-one correspondence with electrodes 84, and processor 38 can initialize the set of electrode location records 64 by storing, to each electrode ID 67, a unique numeric value or text string indicating the corresponding electrode 84.
Each intracardiac ECG record 65 comprises an electrode ID 68 indicating a given electrode 84, and a set of intracardiac ECG signals 60C received from the indicated electrode. In some embodiments, intracardiac ECG records 65 have a one-to-one correspondence with electrodes 84, and processor 38 can initialize the set of intracardiac ECG records 65 by storing, to each electrode ID 68, a unique numeric value or text string indicating the corresponding electrode 84.
Each ECG template 66 comprises a cardiac cycle type 69 and a corresponding set of template ECG signals 70, each of the template ECG signals comprising a time 71 and an electrical potential 72. Examples of cardiac cycle types 69 include, but are not limited to, a normal sinus rhythm, and a non-sinus rhythm such as a premature ventricular contraction (PVC).
In operation, processor 38 can receive signals 60, and store the received signals to memory 52 using the following embodiments:
Control console 24 may also comprise an electrocardiogram (ECG) module 56 that can be configured to generate an ECG chart 58 from body surface ECG signals 60A. In some embodiments, processor 38 presents ECG chart 58 on display 50 (i.e., along with LAT map 48). In addition to presenting ECG chart 58 on display 50, processor 38 can store the ECG chart to memory 52. Further details of ECG chart 58 are described in the description referencing
In an insertion step 92, medical professional 34 inserts distal end 26 into the chamber so that splines 82 engage intracardiac tissue 110, and in a maneuvering step 94, medical professional 34 moves the splines at the distal end along intracardiac tissue 110 during multiple cardiac cycles. As medical professional 34 moves the splines along the intracardiac tissue during the multiple cardiac cycles, processor 38 receives, in a receiving step 96, body-surface ECG signals 60A, location signals 60B and intracardiac ECG signals 60C.
In identification step 98, processor 38 identifies, by comparing the received body-surface ECG signals 60A to ECG templates 66, three consecutive cardiac cycles comprising two sinus cardiac rhythm cycles followed by a non-sinus rhythm cardiac cycle. In some embodiments, comparing body-surface ECG signals 60A to templates 66 comprises comparing sampling times 61A and the electrical potentials 62A in the body-surface ECG signals to times 71 and electrical potentials 72 in the templates.
As described supra, a first given template 66 can be defined for a sinus rhythm cardiac cycle, and a second given template 66 can be defined for a non-sinus rhythm cardiac cycle such as a premature ventricular contraction. In embodiments of the present invention, processor 38 can identify the three cardiac cycles by comparing body-surface ECG signals 60A to templates 66 and detecting that the body-surface ECG signals during the first two cardiac cycles match a first given template 66 for a sinus rhythm cardiac cycle, and detecting that the body-surface ECG signals during the subsequent third cardiac cycle match a second given template 66 for a non-sinus rhythm cardiac cycle. Therefore, processor 38 can identify a first set sampling times 61 for the first two cardiac cycles and a second set of sampling times 61 for the third cardiac cycle.
To match, during a given cardiac cycle, body-surface ECG signals 60A to a given template 66, processor 38 can perform a correlation between the body-surface ECG signals and the given template, and detect a match by comparing the correlation to predefined thresholds, and determining there is a high correlation (i.e., within a defined threshold) between the body-surface ECG signals and the given template. For example, processor 38 can use a correlation threshold of 0.95 when comparing body-surface ECG signals 60A to a given template 66 for a non-sinus rhythm cardiac cycle, and can use a correlation threshold of 0.9 when comparing the body-surface ECG signals to a given template 62 for a sinus rhythm cardiac cycle.
Returning to the flow chart, in a first generation step 100, processor 38 generates, based on 3D coordinates indicated by locations 63, a physical map of the cardiac chamber. The physical map is described in the description referencing
Using a physical map comprising 3D coordinates indicated by locations 63 from location signals 60B whose respective sampling times 61B were during normal sinus-rhythm cardiac cycles can help create a more useful physical map since heart 28 is typically in sinus rhythm most of the time. For example, during an ablation procedure using an ablation catheter (not shown), if the non-sinus cardiac cycles comprise PVCs, heart 28 will typically be in sinus rhythm, with intermittent short PVC bursts. Therefore if processor 38 creates the physical map with 3D coordinates indicated by locations 63 from location signals 60B whose respective sampling times 61B were during a PVC cardiac cycle, a discrepancy likely exists between the locations of the map's points (PVC geometry) and distal end 26, as the ablation catheter location is displayed mostly in sinus rhythm. As a result, any ablated area may not be optimum to correct the patient's arrhythmia. It is believed that the geometry of the heart differs during sinus rhythm, compared to its geometry during non-sinus cardiac cycles such as PVCs.
In additional embodiments, processor 38 can generate the physical map by creating a first physical map for the 3D coordinates indicated by locations 63 from location signals 60B whose respective sampling times 61B were during the first (i.e., sinus rhythm) cardiac cycle, creating a second physical map for the 3D coordinates indicated by locations 63 from location signals 60B whose respective sampling times 61B were during the second (i.e., sinus rhythm) cardiac cycle, and selecting either the first of the second physical map as physical map. The physical map is described in the description referencing
In some embodiments, processor 38 can generate the physical map only if body-surface ECG signals 60A whose respective sampling times 61A were during the first and second sinus rhythm cardiac cycles match (i.e., within a specified threshold) a given template 66 for a sinus rhythm cardiac cycle. In other words, processor 38 can generate the physical map only if the first and the second maps are substantially the same (i.e., in accordance with one another).
In a second generation step 102, processor 38 generates, based on locations 63 (i.e., as indicated in the location signals) and the corresponding electrical potentials 62C measured by electrodes 84 (i.e., as indicated in the intracardiac ECG signals), map 48 comprising local activation times for the non-sinus rhythm cardiac cycle overlaid on the physical map. (U.S. Patent Application 2015/0073246, whose disclosure is incorporated herein by reference, describes overlaying PVC electrical data on a sinus rhythm physical map.) In other words, map 48 reflects the geometry of heart 28 during sinus rhythm, but has the local activation times of the heart while experiencing PVCs.
Finally, in a rendering step 104, processor 38 renders map 48 to display 50, and the method ends. To render map 48, processor 38 can render physical map 140 on display 50, and overlay, on the physical map rendered on the display, the local activation time of the non-sinus rhythm cardiac cycle indicated by each given intracardiac ECG signal 60C at a map location corresponding to the location indicated by the corresponding location signal (i.e., where sampling times 61B and 61C match). An example of overlaying the local activation times on the physical map is described in the description referencing
Therefore, in map 48, a first region 144 has a relatively early LAT, and is circumscribed by an area 146 that has a relatively later local activation time. In embodiments described herein, regions 144 and 146 comprise map locations that correspond to the 3D locations indicated by the received signals. In operation, since region 144 processor 38 can identify and flag region 144 (i.e., the region with the earliest LAT in map 48) as the region for ablation. Alternatively, medical professional can use input devices 54 to select and flag regions 144 and/or 146.
It will be appreciated that the embodiments described above are cited by way of example, and that the present invention is not limited to what has been particularly shown and described hereinabove. Rather, the scope of the present invention includes both combinations and subcombinations of the various features described hereinabove, as well as variations and modifications thereof which would occur to persons skilled in the art upon reading the foregoing description and which are not disclosed in the prior art.
