Patent Application
20220395214
The present invention relates to medical systems, and in particular, but not exclusively to, catheter-based systems.
A wide range of medical procedures involve placing probes, such as catheters, within a patient's body. Location sensing systems have been developed for tracking such probes. Magnetic location sensing is one of the methods known in the art. In magnetic location sensing, magnetic field generators are typically placed at known locations external to the patient. A magnetic field sensor within the distal end of the probe generates electrical signals in response to these magnetic fields, which are processed to determine the coordinate locations of the distal end of the probe. These methods and systems are described in U.S. Pat. Nos. 5,391,199, 6,690,963, 6,484,118, 6,239,724, 6,618,612 and 6,332,089, in PCT International Publication No. WO 1996/005768, and in U.S. Patent Application Publications Nos. 2002/0065455 and 2003/0120150 and 2004/0068178, whose disclosures are all incorporated herein by reference. Locations may also be tracked using impedance or current based systems.
One medical procedure in which these types of probes or catheters have proved extremely useful is in the treatment of cardiac arrhythmias. Cardiac arrhythmias and atrial fibrillation in particular, persist as common and dangerous medical ailments, especially in the aging population.
Diagnosis and treatment of cardiac arrhythmias include mapping the electrical properties of heart tissue, especially the endocardium and the heart volume, and selectively ablating cardiac tissue by application of energy. Such ablation can cease or modify the propagation of unwanted electrical signals from one portion of the heart to another. The ablation process destroys the unwanted electrical pathways by formation of non-conducting lesions. Various energy delivery modalities have been disclosed for forming lesions, and include use of microwave, laser and more commonly, radiofrequency energies to create conduction blocks along the cardiac tissue wall. In a two-step procedure, mapping followed by ablation, electrical activity at points within the heart is typically sensed and measured by advancing a catheter containing one or more electrical sensors into the heart, and acquiring data at a multiplicity of points. These data are then utilized to select the endocardial target areas at which the ablation is to be performed.
Electrode catheters have been in common use in medical practice for many years. They are used to stimulate and map electrical activity in the heart and to ablate sites of aberrant electrical activity. In use, the electrode catheter is inserted into a major vein or artery, e.g., femoral artery, and then guided into the chamber of the heart of concern. A typical ablation procedure involves the insertion of a catheter having a one or more electrodes at its distal end into a heart chamber. A reference electrode may be provided, generally taped to the skin of the patient or by means of a second catheter that is positioned in or near the heart. RF (radio frequency) current is applied to the tip electrode(s) of the ablating catheter, and current flows through the media that surrounds it, i.e., blood and tissue, toward the reference electrode. The distribution of current depends on the amount of electrode surface in contact with the tissue as compared to blood, which has a higher conductivity than the tissue. Heating of the tissue occurs due to its electrical resistance. The tissue is heated sufficiently to cause cellular destruction in the cardiac tissue resulting in formation of a lesion within the cardiac tissue which is electrically non-conductive.
Therefore, when placing an ablation or other catheter within the body, particularly near the endocardial tissue, it is desirable to have the distal tip of the catheter in direct contact with the tissue. The contact can be verified, for example, by measuring the contact between the distal tip and the body tissue. U.S. Patent Application Publication Nos. 2007/0100332, 2009/0093806 and 2009/0138007, describe methods of sensing contact pressure between the distal tip of a catheter and tissue in a body cavity using a force sensor embedded in the catheter.
There is provided in accordance with an embodiment of the present disclosure, a medical system, including a catheter configured to be inserted into a chamber of a heart, and including electrodes configured to capture electrical activity of tissue of the chamber over time, a display, and processing circuitry configured to compute a propagation of a cardiac activation wave over an anatomical map of the chamber from a start time in a cardiac cycle to an end time in the cardiac cycle responsively to the captured electrical activity, render to the display a sub-region of the anatomical map, select a time-bounded portion of the propagation of the cardiac activation wave commencing at a time after the start time responsively to when the propagation would commence to be rendered in the sub-region of the anatomical map, and render to the display the time-bound portion of the propagation of the cardiac activation wave on the sub-region of the anatomical map.
Further in accordance with an embodiment of the present disclosure the processing circuitry is configured to select the time-bounded portion of the propagation of the cardiac activation wave ending at a time before the end time responsively to when the propagation of the cardiac activation wave would complete to be rendered in the sub-region of the anatomical map.
Still further in accordance with an embodiment of the present disclosure the processing circuitry is configured to automatically repeat rendering of the time-bound portion of the propagation of the cardiac activation wave on the sub-region of the anatomical map.
Additionally, in accordance with an embodiment of the present disclosure the processing circuitry is configured to render the sub-region of the anatomical map from a viewpoint within the anatomical map.
Moreover, in accordance with an embodiment of the present disclosure the processing circuitry is configured to render the sub-region of the anatomical map from a viewpoint within the anatomical map, while the viewpoint is static during rendering of the time-bound portion of the propagation of the cardiac activation wave on the sub-region of the anatomical map.
Further in accordance with an embodiment of the present disclosure, the system includes a user interface to receive user input of a manipulation of a virtual camera to change a rendered view of the anatomical map from within the anatomical map, wherein the processing circuitry is configured to render the sub-region of the anatomical map responsively to the user input.
Still further in accordance with an embodiment of the present disclosure the processing circuitry is configured to render the sub-region of the anatomical map from a viewpoint outside of the anatomical map.
Additionally, in accordance with an embodiment of the present disclosure, the system includes a user interface to receive user input of a selection of the sub-region of the anatomical map, wherein the processing circuitry is configured to render the sub-region of the anatomical map responsively to the user input.
Moreover, in accordance with an embodiment of the present disclosure, the system includes a user interface to receive user input of a speed of the rendering of the time-bounded portion of the propagation of the cardiac activation wave, wherein the processing circuitry is configured to render to the display the time-bound portion of the propagation of the cardiac activation wave on the sub-region of the anatomical map responsively to the user input of the speed.
Further in accordance with an embodiment of the present disclosure, the system includes a user interface to receive user input of a width of the cardiac activation wave, wherein the processing circuitry is configured to render to the display the time-bound portion of the propagation of the cardiac activation wave on the sub-region of the anatomical map responsively to the user input of the width of the cardiac activation wave.
There is also provided in accordance with another embodiment of the present disclosure, a medical method, including computing a propagation of a cardiac activation wave over an anatomical map of a chamber of a heart from a start time in a cardiac cycle to an end time in the cardiac cycle responsively to electrical activity of tissue of the chamber captured by electrodes of a catheter inserted into the chamber, rendering a sub-region of the anatomical map to a display, selecting a time-bounded portion of the propagation of the cardiac activation wave commencing at a time after the start time responsively to when the propagation would commence to be rendered in the sub-region of the anatomical map, and rendering the time-bound portion of the propagation of the cardiac activation wave on the sub-region of the anatomical map to the display.
Still further in accordance with an embodiment of the present disclosure the selecting includes selecting the time-bounded portion of the propagation of the cardiac activation wave ending at a time before the end time responsively to when the propagation of the cardiac activation wave would complete to be rendered in the sub-region of the anatomical map.
Additionally, in accordance with an embodiment of the present disclosure, the method includes automatically repeating rendering of the time-bound portion of the propagation of the cardiac activation wave on the sub-region of the anatomical map.
Moreover, in accordance with an embodiment of the present disclosure the rendering the sub-region includes rendering the sub-region of the anatomical map from a viewpoint within the anatomical map.
Further in accordance with an embodiment of the present disclosure the rendering the sub-region includes rendering the sub-region of the anatomical map from a viewpoint within the anatomical map, while the viewpoint is static during rendering of the time-bound portion of the propagation of the cardiac activation wave on the sub-region of the anatomical map.
Still further in accordance with an embodiment of the present disclosure, the method includes receiving user input of a manipulation of a virtual camera to change a rendered view of the anatomical map from within the anatomical map, wherein the rendering the sub-region includes rendering the sub-region of the anatomical map responsively to the user input.
Additionally, in accordance with an embodiment of the present disclosure the rendering the sub-region includes rendering the sub-region of the anatomical map from a viewpoint outside of the anatomical map.
Moreover, in accordance with an embodiment of the present disclosure, the method includes receiving user input of a selection of the sub-region of the anatomical map, wherein the rendering the sub-region includes rendering the sub-region of the anatomical map responsively to the user input.
Further in accordance with an embodiment of the present disclosure, the method includes receiving user input of a speed of the rendering of the time-bounded portion of the propagation of the cardiac activation wave, wherein the rendering the sub-region includes rendering the time-bound portion of the propagation of the cardiac activation wave on the sub-region of the anatomical map responsively to the user input of the speed.
Still further in accordance with an embodiment of the present disclosure, the method includes a user interface to receive user input of a width of the cardiac activation wave, wherein the processing circuitry is configured to render to the display the time-bound portion of the propagation of the cardiac activation wave on the sub-region of the anatomical map responsively to the user input of the width of the cardiac activation wave.
There is also provided in accordance with still another embodiment of the present disclosure, a software product, including a non-transient computer-readable medium in which program instructions are stored, which instructions, when read by a central processing unit (CPU), cause the CPU to compute a propagation of a cardiac activation wave over an anatomical map of a chamber of a heart from a start time in a cardiac cycle to an end time in the cardiac cycle responsively to electrical activity of tissue of the chamber captured by electrodes of a catheter inserted into the chamber, render a sub-region of the anatomical map to a display, select a time-bounded portion of the propagation of the cardiac activation wave commencing at a time after the start time responsively to when the propagation would commence to be rendered in the sub-region of the anatomical map, and render the time-bound portion of the propagation of the cardiac activation wave on the sub-region of the anatomical map to the display.
The present invention will be understood from the following detailed description, taken in conjunction with the drawings in which:
As mentioned previously, in a two-step procedure, mapping followed by ablation, electrical activity at points within the heart is typically sensed and measured by advancing a catheter containing one or more electrodes into the heart, and acquiring data at a multiplicity of points. These data are then utilized to select the target areas at which the ablation is to be performed.
The mapping may be used to compute a propagation of a cardiac activation wave over a chamber of the heart from a start time in a cardiac cycle to an end time in the cardiac cycle responsively to captured electrical activity, such as local activation times (LATs). The propagation of the cardiac activation wave may be rendered to a display, typically in slow motion (or at any suitable selected speed), over an anatomical map of the chamber using colors and/or symbols. The propagation is then analyzed via a physician to determine if and where to ablate the tissue of the chamber of the heart.
The physician may be viewing a sub-region of the anatomical map, for example, the physician may want to zoom into a sub-region of the anatomical map or view a sub-region of the anatomical map from inside the anatomical map (e.g., from the viewpoint of a virtual camera in which only the sub-region of the map can be viewed at any one time). Assuming that the selected sub-region of the anatomical map is not at the start of the wave propagation, and the physician then runs the propagation of the cardiac activation wave over the anatomical map of the chamber of the heart, the physician will not see the propagation on the selected rendered sub-region of the anatomical map until after some delay, i.e., until the wave finally reaches the selected rendered sub-region of the anatomical map after “running” over the non-rendered portions of the map. In general, the above problem may be observed whenever the desired wave propagation range is smaller than the whole wave propagation range. If the wave propagation is run in a loop mode whereby the wave propagation runs from beginning to end and then repeats from the beginning etc., the delay may be even greater as the physician needs to wait while the wave propagation is running over the non-rendered portions of the anatomical map prior to, and after, the selected rendered sub-regions of the map currently being viewed. Once the wave propagation enters the selected rendered sub-region, the wave propagation disappears quickly until the next repeat of the wave propagation after another delay. The delay in the wave being visible in the selected sub-region of the anatomical map may be confusing to the physician and wastes valuable time during a cardiac procedure especially when the physician needs to repeatedly run the wave propagation in order to determine if and where to ablate the tissue of the chamber of the heart based on the wave propagation.
Embodiments of the present invention solve the above problems by automatically computing the earliest time (according to a cardiac cycle time of the wave propagation) that the wave would arrive in the selected sub-region of the anatomical map currently in view on a display. Rendering of the wave propagation to the display then starts from the computed earliest time in the cardiac cycle of the wave propagation. Therefore, upon the physician running the wave propagation, the wave propagation is automatically rendered without any substantial delay over the selected sub-region currently in view.
Similarly, the latest time (according to the cardiac cycle time of the wave propagation) when the wave would leave the sub-region currently in view may be computed and rendering of the wave propagation may be stopped at around that point. Therefore, when the wave propagation is run by the physician, the wave propagation may immediately start to render in the sub-region currently in view until the wave propagation leaves the sub-region, and be repeatedly rendered in the sub-region without any significant delay.
Embodiments of the present invention are useful whether the sub-region of the anatomical map is viewed from a viewpoint (e.g., a virtual camera) within the anatomical map or from a viewpoint outside the anatomic map.
In some embodiments, the physician may select a sub-region from the outside of the anatomical map by marking, or pointing to, a portion of the anatomical map. The selected sub-region is then optionally enlarged, or otherwise highlighted or marked, providing the physician with better visibility of the sub-region and the rendering of the wave propagation on the sub-region.
In some embodiments, the virtual camera may be manipulated by the physician using a suitable user interface (e.g., mouse, joystick or other pointing device) thereby selecting the sub-region of the anatomical map to be viewed on the display.
In some embodiments, parameters of the wave propagation rendering, such as rendering speed and/or wave width, may be selected by the physician to allow the physician to better understand the wave propagation in a given region. For example, if the physician selects a sub-region associated with fast wave propagation, the physician may slow down the wave propagation to carefully view the wave propagation in the sub-region. In some embodiments, the parameters may be automatically set according to any suitable parameters, for example, the size of the selected region, and/or the fraction of the size of the selected region compared to size of the region over which the whole wave propagation is originally computed.
Reference is now made to
The medical procedure system 20 is used to determine the position of the catheter 40, seen in an inset 25 of
The catheter 40 includes a position sensor 53 disposed on the shaft 22 in a predefined spatial relation to the proximal ends of the flexible arms 54. The position sensor 53 may include a magnetic sensor 50 and/or at least one shaft electrode 52. The magnetic sensor 50 may include at least one coil, for example, but not limited to, a dual-axis or a triple axis coil arrangement to provide position data for location and orientation including roll. The catheter 40 includes multiple electrodes 55 (only some are labeled in
The medical procedure system 20 may determine a position and orientation of the shaft 22 of the catheter 40 based on signals provided by the magnetic sensor 50 and/or the shaft electrodes 52 (proximal-electrode 52a and distal-electrode 52b) fitted on the shaft 22, on either side of the magnetic sensor 50. The proximal-electrode 52a, the distal-electrode 52b, the magnetic sensor 50 and at least some of the electrodes 55 are connected by wires running through the shaft 22 via a catheter connector 35 to various driver circuitries in a console 24. In some embodiments, at least two of the electrodes 55 of each of the flexible arms 54, the shaft electrodes 52, and the magnetic sensor 50 are connected to the driver circuitries in the console 24 via the catheter connector 35. In some embodiments, the distal electrode 52b and/or the proximal electrode 52a may be omitted.
The illustration shown in
A physician 30 navigates the catheter 40 to a target location in a body part (e.g., heart 26) of a patient 28 by manipulating the shaft 22 using a manipulator 32 near the proximal end of the catheter 40 and/or deflection from a sheath 23. The catheter 40 is inserted through the sheath 23, with the flexible arms 54 gathered together, and only after the catheter 40 is retracted from the sheath 23, the flexible arms 54 are able to spread and regain their intended functional shape. By containing flexible arms 54 together, the sheath 23 also serves to minimize vascular trauma on its way to the target location.
Console 24 comprises processing circuitry 41, typically a general-purpose computer and a suitable front end and interface circuits 44 for generating signals in, and/or receiving signals from, body surface electrodes 49 which are attached by wires running through a cable 39 to the chest and to the back, or any other suitable skin surface, of the patient 28.
Console 24 further comprises a magnetic-sensing sub-system. The patient 28 is placed in a magnetic field generated by a pad containing at least one magnetic field radiator 42, which is driven by a unit 43 disposed in the console 24. The magnetic field radiator(s) 42 is/are configured to transmit alternating magnetic fields into a region where the body-part (e.g., the heart 26) is located. The magnetic fields generated by the magnetic field radiator(s) 42 generate direction signals in the magnetic sensor 50. The magnetic sensor 50 is configured to detect at least part of the transmitted alternating magnetic fields and provide the direction signals as corresponding electrical inputs to the processing circuitry 41.
In some embodiments, the processing circuitry 41 uses the position-signals received from the shaft electrodes 52, the magnetic sensor 50 and the electrodes 55 to estimate a position of the catheter 40 inside an organ, such as inside a cardiac chamber. In some embodiments, the processing circuitry 41 correlates the position signals received from the electrodes 52, 55 with previously acquired magnetic location-calibrated position signals, to estimate the position of the catheter 40 inside a cardiac chamber. The position coordinates of the shaft electrodes 52 and the electrodes 55 may be determined by the processing circuitry 41 based on, among other inputs, measured impedances, or on proportions of currents distribution, between the electrodes 52, 55 and the body surface electrodes 49. The console 24 drives a display 27, which shows the distal end of the catheter 40 inside an anatomical map of the heart 26.
The method of position sensing using current distribution measurements and/or external magnetic fields is implemented in various medical applications, for example, in the Carto® system, produced by Biosense Webster Inc. (Irvine, Calif.), and is described in detail in U.S. Pat. Nos. 5,391,199, 6,690,963, 6,484,118, 6,239,724, 6,618,612, 6,332,089, 7,756,576, 7,869,865, and 7,848,787, in PCT Patent Publication WO 96/05768, and in U.S. Patent Application Publication Nos. 2002/0065455 A1, 2003/0120150 A1 and 2004/0068178 A1.
The Carto®3 system applies an Active Current Location (ACL) impedance-based position-tracking method. In some embodiments, using the ACL method, the processing circuitry 41 is configured to create a mapping (e.g., current-position matrix (CPM)) between indications of electrical impedance and positions in a magnetic coordinate frame of the magnetic field radiator(s) 42. The processing circuitry 41 estimates the positions of the shaft electrodes 52 and the electrodes 55 by performing a lookup in the CPM.
Processing circuitry 41 is typically programmed in software to carry out the functions described herein. The software may be downloaded to the computer in electronic form, over a network, for example, or it may, alternatively or additionally, be provided and/or stored on non-transitory tangible media, such as magnetic, optical, or electronic memory.
The system 20 also includes a user interface 57 to receive user input such as a selection of a sub-region of the anatomical map for display, manipulation of a virtual camera used in viewing the sub-region of the anatomical map, a rendering speed of a wave propagation of a cardiac activation wave, and/or a width of a cardiac activation wave being rendered. The user interface 57 may include a keyboard and/or touch screen, a foot pedal, and optionally a pointing device such as a mouse, stylus and/or joystick.
The catheter 40 described above includes eight flexible arms 54 with six electrodes 55 per arm 54. Any suitable catheter may be used instead of the catheter 40, for example, a catheter with a different number of flexible arms and/or electrodes per arm, or a different probe shape such as a balloon catheter or a lasso catheter, by way of example only.
The medical procedure system 20 may also perform ablation of heart tissue using any suitable catheter, for example using the catheter 40 or a different catheter and any suitable ablation method. The console 24 may include an RF signal generator 34 configured to generate RF power to be applied by an electrode or electrodes of a catheter connected to the console 24, and one or more of the body surface electrodes 49, to ablate a myocardium of the heart 26. The console 24 may include a pump (not shown), which pumps irrigation fluid into an irrigation channel to a distal end of a catheter performing ablation. The catheter performing the ablation may also include temperature sensors (not shown) which are used to measure a temperature of the myocardium during ablation and regulate an ablation power and/or an irrigation rate of the pumping of the irrigation fluid according to the measured temperature.
Reference is now made to
The anatomical map 62 may be generated using any suitable anatomical map generation method, for example, but not limited to, Fast Anatomical Mapping (FAM). FAM is described in U.S. Pat. No. 10,918,310 to Cohen, et al. In FAM, a smooth shell is generated around a three-dimensional (3D) cloud of data points, such as a cloud of computed electrode positions of the electrodes 55. The propagation of the cardiac activation wave 60 may be computed using any suitable method, for example, but not limited to, one or more of the methods disclosed in U.S. Pat. Nos. 10,136,828, 6,226,542, 6,301,496, and in 6,892,091.
Reference is now made to
The processing circuitry 41 is configured to render to the display 27 the sub-region 64 of the anatomical map 62 of a chamber of the heart 26. The processing circuitry 41 is configured to select a time-bounded portion of the propagation of the cardiac activation wave 60 commencing at a time (referred herein as “adjusted start time”) after the cycle start time T0 (and optionally ending at a time (referred herein as “adjusted end time”) before the cycle end time T7) responsively to when the propagation would commence to be rendered in the sub-region 64 of the anatomical map 62 (and optionally when the propagation of the cardiac activation wave 60 would complete to be rendered in the sub-region 64 of the anatomical map 62). Therefore, the processing circuitry 41 is configured to compute the adjusted start time and optionally the adjusted end time for rendering the propagation of the cardiac activation wave 60 according to when the propagation would be rendered in the sub-region 64. Therefore, the time-bounded portion is defined by the adjusted start time and optionally the adjusted end time. In the example of
The processing circuitry 41 is configured to render to the display 27 the time-bound portion of the propagation of the cardiac activation wave 60 on the sub-region 64 of the anatomical map 62 by rendering the generated propagation of the cardiac activation wave 60 from the adjusted start time (e.g., T2) to the adjusted end time (e.g., T6). The time-bound portion of the propagation of the cardiac activation wave 60 may be repeatedly rendered from the adjusted start time (e.g., T2) to the adjusted end time (e.g., T6) in loop-mode thereby enabling the physician 30 to carefully inspect the propagation of the wave over the sub-region 64.
The anatomical map 62 and the sub-region 64 shown in
Reference is now made to
The anatomical map 62 may be viewed from the viewpoint of a virtual camera 66 within the anatomical map 62 so that a field of view 68 of the virtual camera 66 is rendered to the display 27. The field of view 68 is delineated by two dotted lines 76.
An arrow 70 shows how the cardiac activation wave 60 propagates over the internal wall 74 of the anatomical map 62 from time T0 to time T7. It can be seen that the cardiac activation wave 60 enters the sub-region 64 at time T2 and leaves the sub-region 64 at time T6. Therefore, when the physician 30 selects running the propagation of the cardiac activation wave 60 while the sub-region 64 is being viewed from the virtual camera 66, the propagation is rendered from time T2 until time T6 and not during the time periods T0 to T2 and T6 to T7.
Reference is now made to
The processing circuitry 41 is configured to generate the anatomical map 62 of the chamber of the heart 26 and render the anatomical map 62 or a part thereof to the display 27. The processing circuitry 41 is configured to compute (block 82) a propagation of the cardiac activation wave 60 over the anatomical map 62 of a chamber of the heart 26 (
In some embodiments, the user interface 57 is configured to receive user input (block 84) of a selection of the sub-region 64 of the anatomical map 62 of the chamber of the heart 26. The sub-region 64 may be selected by the physician 30 from the surface of the anatomical map 62, for example, by selecting a region or point on the map 62, e.g., using a pointing device or a touch sensitive screen. The processing circuitry 41 is configured to render (block 86) the sub-region 64 of the anatomical map 62 responsively to the user input. In some embodiments, the processing circuitry 41 is configured to render the sub-region 64 of the anatomical map 62 from a viewpoint outside of the anatomical map 62.
In some embodiments, the user interface 57 is configured to receive (block 84) user input of a manipulation of the virtual camera 66 to change a rendered view of the anatomical map 62 from within the anatomical map 62 to a view of the sub-region 64 from within the anatomical map 62. The processing circuitry 41 is configured to render (block 86) to the display 27 the sub-region 64 of the anatomical map 62 from a viewpoint (e.g., the virtual camera 66) within the anatomical map 62 responsively to the user input of the manipulation of the virtual camera 66.
The processing circuitry 41 is configured to select (block 88) a time-bounded portion of the propagation of the cardiac activation wave 60 commencing at a time (e.g., an adjusted start time T2) after the cycle start time (e.g., T0) responsively to when the propagation would commence to be rendered in the sub-region 64 of the anatomical map 62. In some embodiments, the processing circuitry 41 is configured to select the time-bounded portion of the propagation of the cardiac activation wave 60 ending at a time (e.g., adjusted end time T6) before the cycle end time (e.g., T7) responsively to when the propagation of the cardiac activation wave 60 would complete to be rendered in the sub-region 64 of the anatomical map 62.
The user interface 57 may be configured to receive (block 90) user input of a rendering speed of the time-bounded portion of the propagation of the cardiac activation wave 60 and/or a width of the cardiac activation wave 60 over the sub-region 64 of the anatomical map 62. The time-bound portion may be rendered at real-time speed (i.e., at the speed the cardiac activation wave 60 propagates over the chamber of the heart 26) or slow or faster than real-time speed. The width of the cardiac activation wave 60 provides a measure of the LAT values included in the sliding window of the propagation of the cardiac activation wave 60 over the sub-region 64 of the anatomical map 62 at any one time. For example, if the selected width is 40 milliseconds, the range of LAT values shown on the anatomical map 62 at any one time is within a range width of 40 milliseconds (ms) (e.g., from −100 ms to −60 ms at time T2, or from 10 ms to 50 ms at time T6, etc.) and as the cardiac activation wave 60 propagates over the anatomical map 62, the sliding window of LAT values is constantly shifted but has a static width of 40 ms.
The processing circuitry 41 is configured to render (block 92) to the display 27 the time-bound portion of the propagation of the cardiac activation wave 60 on the sub-region 64 of the anatomical map 62. In other words, the processing circuitry 41 is configured to render to the display 27 the propagation of the cardiac activation wave 60 from the adjusted start time (until the adjusted end time). In some embodiments, the processing circuitry 41 is configured to render the sub-region 64 of the anatomical map 62 from a viewpoint (e.g., from the virtual camera 66) within the anatomical map 62. In some embodiments, the processing circuitry 41 is configured to render the sub-region 64 of the anatomical map 62 from a viewpoint (e.g., from the virtual camera 66) within the anatomical map 62, while the viewpoint (e.g., the virtual camera 66) is static during rendering of the time-bound portion of the propagation of the cardiac activation wave 60 on the sub-region 64 of the anatomical map 62. In some embodiments, the processing circuitry 41 is configured to render the sub-region 64 of the anatomical map 62 from a viewpoint outside of the anatomical map 62.
In some embodiments, the processing circuitry 41 is configured to render to the display 27 the time-bound portion of the propagation of the cardiac activation wave 60 on the sub-region 64 of the anatomical map 62 responsively to the user input of the rendering speed at the step of block 90. In some embodiments, the processing circuitry 41 is configured to render to the display 27 the time-bound portion of the propagation of the cardiac activation wave 60 on the sub-region 64 of the anatomical map 62 responsively to the user input of the width of the cardiac activation wave 60 at the step of block 90.
The processing circuitry 41 may be configured to automatically repeat (block 94) rendering of the time-bound portion of the propagation of the cardiac activation wave 60 on the sub-region 64 of the anatomical map 62.
As used herein, the terms “about” or “approximately” for any numerical values or ranges indicate a suitable dimensional tolerance that allows the part or collection of components to function for its intended purpose as described herein. More specifically, “about” or “approximately” may refer to the range of values ±20% of the recited value, e.g., “about 90%” may refer to the range of values from 72% to 108%.
Various features of the invention which are, for clarity, described in the contexts of separate embodiments may also be provided in combination in a single embodiment. Conversely, various features of the invention which are, for brevity, described in the context of a single embodiment may also be provided separately or in any suitable sub-combination.
The embodiments described above are cited by way of example, and the present invention is not limited by what has been particularly shown and described hereinabove. Rather the scope of the invention includes both combinations and sub-combinations 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.
