Real-time feedback for electrode contact during mapping

Information

  • Patent Grant
  • 10172536
  • Patent Number
    10,172,536
  • Date Filed
    Tuesday, July 26, 2016
    7 years ago
  • Date Issued
    Tuesday, January 8, 2019
    5 years ago
Abstract
A catheter system includes a mapping catheter including a plurality of mapping electrodes, each mapping electrode configured to sense signals associated with an anatomical structure. The catheter system further includes a processor operatively coupled to the plurality of mapping electrodes and configured to receive the signals sensed by the plurality of mapping electrodes, characterize the signals sensed by the plurality of mapping electrodes based on a signal parameter of the sensed signals, and generate an output of a quality of contact of the plurality of mapping electrodes with the anatomical structure based on the signal characterization.
Description
TECHNICAL FIELD

The present disclosure relates to mapping systems. More particularly, the present disclosure relates to a mapping system configured to provide real-time feedback for mapping electrode contact with an anatomical structure during mapping.


BACKGROUND

Physicians make use of catheters in medical procedures to gain access into interior regions of the body for diagnostic and therapeutic purposes. It is important for the physician to be able to precisely position the catheter within the body to gain contact with a desired tissue location. During these procedures, a physician steers the catheter through a main vein or artery into the interior region of the heart that is to be treated. The physician then further manipulates a steering mechanism to place the electrode carried on the distal tip of the catheter into direct contact with the endocardial tissue. The physician directs energy from the electrode through myocardial tissue either to an indifferent electrode (in a unipolar electrode arrangement) or to an adjacent electrode (in a bi-polar electrode arrangement) to ablate the tissue.


Before ablating heart tissue, physicians often examine the propagation of electrical impulses in heart tissue to locate aberrant conductive pathways and to identify the arrhythmia foci, which are ablated. The techniques used to analyze these pathways and locate foci are commonly called mapping.


SUMMARY

Disclosed herein are various embodiments of methods for providing real-time feedback for mapping electrode contact with an anatomical structure during mapping, as well as cardiac mapping systems employing such methods.


In an Example 1, a catheter system comprising: a catheter including a plurality of mapping electrodes, each mapping electrode configured to sense signals associated with an anatomical structure; and a processor operatively coupled to the plurality of mapping electrodes and configured to: receive the signals sensed by the plurality of mapping electrodes; determine a signal parameter associated with each of the plurality of mapping electrodes; and determine a quality of contact of each of the plurality of mapping electrodes with the anatomical structure based on the signal parameter.


In an Example 2, the catheter system of Example 1, further comprising a display device configured to provide a graphical display representative of the quality of contact of the plurality of mapping electrodes.


In an Example 3, the catheter system of Example 1, the catheter further comprising a contact determination mechanism, wherein the processor is configured to determine the quality of contact based on the signal parameter and an output of the contact determination mechanism.


In an Example 4, the catheter system of Example 3, the contact determination mechanism comprising at least one of a force sensor and an impedance sensor.


In an Example 5, the catheter system of Example 1, wherein the processor is further configured to generate a map of the anatomical structure based on electrodes having sensed signals with amplitudes greater than a threshold amplitude.


In an Example 6, the catheter system of Example 1, wherein the processor is configured to sense and characterize at least one of unipolar signals and bipolar signals.


In an Example 7, the catheter system of Example 1, wherein the catheter comprises an ablation catheter.


In an Example 8, the catheter system of Example 1, wherein the processor is further configured to identify contours of the anatomical structure based on the quality of contact of the plurality of mapping electrodes.


In an Example 9, the catheter system of Example 1, wherein the processor is further configured to determine an orientation of the plurality of mapping electrodes based on the quality of contact of the plurality of mapping electrodes.


In an Example 10, a method for mapping an anatomical structure, the method comprising: sensing signals associated with an anatomical structure with a plurality of mapping electrodes; characterizing the signals sensed by the plurality of mapping electrodes based on a signal parameter associated with the plurality of mapping electrodes; determining a quality of contact of the plurality of mapping electrodes with the anatomical structure based on the signal characterization; and generating a map of the anatomical structure based only on electrodes having sensed signals with a quality of contact exceeding a threshold value.


In an Example 11, the method of Example 10, wherein the determining step comprises combining the signal characterization with an output of a contact determination mechanism.


In an Example 12, the method of Example 11, wherein the contact determination mechanism comprises at least one of a force sensor and an impedance sensor.


In an Example 13, the method of Example 10, further comprising generating a map of the anatomical structure based only on electrodes having sensed signals with amplitudes greater than a threshold amplitude.


In an Example 14, the method of Example 10, further comprising identifying contours of the anatomical structure based on the quality of contact of the plurality of mapping electrodes.


In an Example 15, the method of Example 10, further comprising determining an orientation of the plurality of mapping electrodes based on the quality of contact of the plurality of mapping electrodes.


In an Example 16, a method for mapping an anatomical structure, the method comprising: positioning a plurality of mapping electrodes proximate to an anatomical structure; sensing signals with the plurality of mapping electrodes; characterizing the signals sensed by the plurality of mapping electrodes based on a signal parameter associated with the mapping electrodes; determining a quality of contact of the plurality of mapping electrodes with the anatomical structure based on the signal characterization; displaying a graphical display representative of the quality of contact of the plurality of electrodes; repositioning the plurality of mapping electrodes with respect to the anatomical structure; and updating the graphical display in real-time as the quality of contact of the plurality of electrodes changes when the plurality of electrodes are repositioned.


In an Example 17, the method of Example 16, wherein the sensing step comprises sensing bipolar signals with the pairs of the plurality of mapping electrodes.


In an Example 18, the method of Example 16, wherein the sensing step comprises sensing unipolar signals with each of the plurality of mapping electrodes.


In an Example 19, the method of Example 16, and further comprising generating a map of the anatomical structure based only on electrodes having sensed signals with amplitudes greater than a threshold amplitude.


In an Example 20, the method of Example 16, wherein the determining step comprises combining the signal characterization with an output of a contact determination mechanism, the contact determination mechanism comprising at least one of a force sensor and an impedance sensor.


While multiple embodiments are disclosed, still other embodiments of the present invention will become apparent to those skilled in the art from the following detailed description, which shows and describes illustrative embodiments of the invention. Accordingly, the drawings and detailed description are to be regarded as illustrative in nature and not restrictive.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a schematic view of an embodiment of a system for accessing a targeted tissue region in the body for diagnostic and therapeutic purposes.



FIG. 2 is a schematic view of an embodiment of a mapping catheter having a basket functional element carrying structure for use in association with the system of FIG. 1.



FIG. 3 is a schematic side view of an embodiment of the basket functional element including a plurality of mapping electrodes.



FIG. 4 is an illustration of a graphical display showing signal amplitudes for bipolar signals sensed by the plurality of mapping electrodes.



FIG. 5 is an illustration of a graphical display showing signal amplitudes for unipolar signals sensed by the plurality of mapping electrodes.





While the invention is amenable to various modifications and alternative forms, specific embodiments have been shown by way of example in the drawings and are described in detail below. The intention, however, is not to limit the invention to the particular embodiments described. On the contrary, the invention is intended to cover all modifications, equivalents, and alternatives falling within the scope of the invention as defined by the appended claims.


DETAILED DESCRIPTION


FIG. 1 is a schematic view of a system 10 for accessing a targeted tissue region in the body for diagnostic or therapeutic purposes. FIG. 1 generally shows the system 10 deployed in the left ventricle of the heart. Alternatively, system 10 can be deployed in other regions of the heart, such as the left atrium, right atrium, or right ventricle. While the illustrated embodiment shows the system 10 being used for ablating heart tissue, the system 10 (and the methods described herein) may alternatively be configured for use in other tissue ablation applications, such as procedures for ablating tissue in the prostrate, brain, gall bladder, uterus, and other regions of the body, including in systems that are not necessarily catheter-based.


The system 10 includes a mapping probe 14 and an ablation probe 16. In FIG. 1, each is separately introduced into the selected heart region 12 through a vein or artery (e.g., the femoral vein or artery) through suitable percutaneous access. Alternatively, the mapping probe 14 and ablation probe 16 can be assembled in an integrated structure for simultaneous introduction and deployment in the heart region 12.


The mapping probe 14 has a flexible catheter body 18. The distal end of the catheter body 18 carries a three-dimensional multiple electrode structure 20. In the illustrated embodiment, the structure 20 takes the form of a basket defining an open interior space 22 (see FIG. 2), although other multiple electrode structures could be used. The multiple electrode structure 20 carries a plurality of electrodes 24 configured to sense intrinsic physiological activity in the anatomical region on which the ablation procedure is to be performed.


The electrodes 24 are electrically coupled to a processing system 32. A signal wire (not shown) is electrically coupled to each electrode 24 on the basket structure 20. The wires extend through the body 18 of the probe 14 and electrically couple the electrodes 24 to the processing system 32 and the guidance system 34. The electrodes 24 sense intrinsic electrical activity in heart tissue. The sensed activity is processed by the processing system 32 to assist the physician in identifying the site or sites within the heart appropriate for ablation.


In some embodiments, the processing system 32 may be configured to measure the intrinsic electrical activity in the heart tissue adjacent to the electrodes 24. For example, in some embodiments, the processing system 32 is configured to detect intrinsic electrical activity associated with a dominant rotor in the anatomical feature being mapped. Studies have shown that dominant rotors have a role in the initiation and maintenance of atrial fibrillation, and ablation of the rotor path and/or rotor core may be effective in terminating the atrial fibrillation. The processing system 32 processes the sensed information to derive the location of a site appropriate for ablation using the ablation probe 16.


The ablation probe 16 includes a flexible catheter body 34 that carries one or more ablation electrodes 36. The one or more ablation electrodes 36 are electrically connected to a radio frequency generator 37 that is configured to deliver ablation energy to the one or more ablation electrodes 36. The ablation probe 16 is movable with respect to the anatomical feature to be treated, as well as the structure 20. The ablation probe 16 is positionable between or adjacent to electrodes 24 of the structure 20 as the one or more ablation electrodes 36 are positioned with respect to the tissue to be treated.


A guidance system 38 is electrically coupled to the mapping catheter 14 and the ablation catheter 16. The guidance system 38 collects and processes information regarding the location of the ablation probe 16 within the space 22 defined by the basket structure 20, in term of its position relative to the position of the electrodes 24. The guidance system 38 provides a position-identifying output that aids the physician in guiding the ablation electrodes 36 into contact with tissue at the site identified for ablation. The guidance system 38 can process and provide position-specific information in various ways.


In the illustrated embodiment, the guidance system 38 includes an output display device 40 (e.g., a CRT, LED display, or a printer). In some embodiments, the display device 40 is configured to display a representation of the mapping catheter 14 and ablation catheter 16 relative to the anatomical structure.



FIG. 2 illustrates an embodiment of the mapping catheter 14 including electrodes 24 at the distal end suitable for use in the system 10 shown in FIG. 1. The mapping catheter 14 has a flexible catheter body 18, the distal end of which carries the three dimensional structure 20 configured to carry the mapping electrodes or sensors 24. The mapping electrodes 24 sense intrinsic electrical activity in the heart tissue, which sensed activity is then processed by the processing system 32 and guidance system 38 to assist the physician in identifying the site or sites having a heart rhythm disorder. This process is commonly referred to as mapping. This information can then be used to determine an appropriate location for applying appropriate therapy (e.g., ablation) to the identified sites, and to navigate the one or more ablation electrodes 36 to the identified sites.


The illustrated three dimensional structure 20 comprises a base member 41 and an end cap 42 between which flexible splines 44 generally extend in a circumferentially spaced relationship. As discussed above, the three dimensional structure 20 takes the form of a basket defining an open interior space 22. In some embodiments, the splines 44 are made of a resilient inert material, such as, e.g., Nitinol metal or silicone rubber, and are connected between the base member 41 and the end cap 42 in a resilient, pretensed condition, to bend and conform to the tissue surface they contact. In the illustrated embodiment, eight splines 44 form the three dimensional structure 20. Additional or fewer splines 44 could be used in other embodiments. As illustrated, each spline 44 carries eight mapping electrodes 24. Additional or fewer mapping electrodes 24 could be disposed on each spline 44 in other embodiments of the three dimensional structure 20. In the illustrated embodiment, the three dimensional structure 20 is relatively small (e.g., 40 mm or less in diameter). In alternative embodiments, the three dimensional structure 20 is larger (e.g., 40 mm in diameter or greater).


A slidable sheath 50 is movable along the major axis of the catheter body 30. Moving the sheath 50 forward (i.e., toward the distal end) causes the sheath 50 to move over the three dimensional structure 20, thereby collapsing the structure 20 into a compact, low profile condition suitable for introduction into an interior space, such as, for example, into the heart. In contrast, moving the sheath 50 rearward (i.e., toward the proximal end) frees the three dimensional structure 20, allowing the structure 20 to spring open and assume the pretensed position illustrated in FIG. 2. Further details of embodiments of the three dimensional structure 20 are disclosed in U.S. Pat. No. 5,647,870, entitled “Multiple Electrode Support Structures,” which is hereby incorporated by reference in its entirety.


A signal wire (not shown) is electrically coupled to each mapping electrode 26. The wires extend through the body 30 of the mapping catheter 20 into a handle 54, in which they are coupled to an external connector 56, which may be a multiple pin connector. The connector 56 electrically couples the mapping electrodes 24 to the processing system 32 and guidance system 38. Further details on mapping systems and methods for processing signal generated by the mapping catheter are discussed in U.S. Pat. No. 6,070,094, entitled “Systems and Methods for Guiding Movable Electrode Elements within Multiple-Electrode Structure,” U.S. Pat. No. 6,233,491, entitled “Cardiac Mapping and Ablation Systems,” and U.S. Pat. No. 6,735,465, entitled “Systems and Processes for Refining a Registered Map of a Body Cavity,” the disclosures of which are incorporated herein by reference.


It is noted that other multi-electrode structures could be deployed on the distal end. It is further noted that the multiple mapping electrodes 24 may be disposed on more than one structure rather than, for example, the single mapping catheter 14 illustrated in FIG. 2. For example, if mapping within the left atrium with multiple mapping structures, an arrangement comprising a coronary sinus catheter carrying multiple mapping electrodes and a basket catheter carrying multiple mapping electrodes positioned in the left atrium may be used. As another example, if mapping within the right atrium with multiple mapping structures, an arrangement comprising a decapolar catheter carrying multiple mapping electrodes for positioning in the coronary sinus, and a loop catheter carrying multiple mapping electrodes for positioning around the tricuspid annulus may be used.


Additionally, although the mapping electrodes 24 have been described as being carried by dedicated probes, such as mapping catheter 14, the mapping electrodes can be carried on non-mapping dedicated probes. For example, an ablation catheter (e.g., the ablation catheter 16) can be configured to include one or mapping electrodes 24 disposed on the distal end of the catheter body and coupled to the signal processing system 32 and guidance system 38. As another example, the ablation electrode at the distal end of the ablation catheter may be coupled to the signal processing system 32 and guidance system 38 to also operate as a mapping electrode.


To illustrate the operation of the system 10, FIG. 3 is a schematic view of an embodiment of the basket structure 20 including a plurality of mapping electrodes 24 disposed on a plurality of splines 44. In the illustrated embodiment, the basket structure includes sixty-four mapping electrodes 24. The mapping electrodes 24 are disposed in groups of eight electrodes 24 (labeled E1, E2, E3, E4, E5, E6, E7, and E8) on each of eight splines 44 (labeled S1, S2, S3, S4, S5, S6, S7, and S8). While the sixty-four mapping electrodes 24 are shown disposed on a basket structure 20, the mapping electrodes 24 may alternatively be arranged in different numbers and on different structures.


When the basket structure 20 is introduced into the anatomical structure to be mapped (e.g., heart), some of the electrodes 24 are brought into contact with the anatomical structure to allow measurements of physiological activity in the anatomical structure. The physiological activity is then used to generate a map of the physiological activity in the anatomical structure to aid the clinician with diagnosis and treatment of the anatomical structure. However, because the contours of the anatomical structure may not correspond to the contours of the basket structure 20, some of the electrodes 24 in the basket structure 20 may make better contact with the anatomical structure than others of the electrodes 24. In order to assure quality data collection during mapping, the mapping system 10 according to the present disclosure is configured to provide the clinician with real-time feedback of electrode contact quality during the mapping process.


In some embodiments, the processing system 32 is configured to receive signals from each of the electrodes 24 and determine a quality of the contact of each of the electrodes 24 based on the received signals. In some embodiments, the processing system 32 measures bipolar signals based on sequential or simultaneous measurements across two of the electrodes 24 in the basket structure 20. For example, the processing system 32 may measure signals across adjacent electrodes 24 (e.g., E1-E2, E3-E4, E5-E6, E7-E8) on the same spline (S1-S8). In some embodiments, the processing system measures unipolar signals based on sequential or simultaneous signal measurements by each of the electrodes 24 individually.


The processing system 32 can be configured to establish the quality of contact of the electrodes 24 by characterizing the measured signals from the electrodes 24. For example, in some embodiments, the quality of contact of each of the mapping electrodes 24 is a function of the amplitude of the signal measured by the electrode 24 (i.e., higher signal amplitude correlates to better contact). As another example, the quality of contact of each of the mapping electrodes 24 is a function of the frequency distribution of the signals measured by the electrodes 24. More specifically, signals with a higher frequency component in bipolar measurements can be identified as channels making good contact with the anatomical structure. In some embodiments, the electrodes having a measured signal parameter that exceeds a threshold or falls within a predetermined range are identified as making good contact with the anatomical structure (i.e., contact sufficient to provide reliable mapping data). The signal measurements to determine quality of contact can be combined with other contact determination mechanisms, such as force and/or impedance sensors, that may be integrated onto the basket structure 20.


The processing system 32 can be configured to provide an output to the clinician that indicates the quality of contact of the electrodes 24. For example, as will be discussed below, the processing system 32 may provide information to the display device 40 that graphically represents the quality of contact of each of the electrodes 24.


As the basket structure 20 is moved through the anatomical structure, the processing system 32 continuously measures signals with the electrodes 24 to monitor any changes in the quality of contact with respect to each of the electrodes 24. In some embodiments, the processing system 32 updates the quality of contact of the electrodes 24 in real-time as the basket structure 20 is moved through the anatomical structure. In some embodiments, the display device 40 is configured to receive the updated quality of contact information from the processing system 32 and update the graphical display representative of the quality of contact of each of the electrodes 24 in real-time. The clinician may use this real-time updating to assure consistent quality contact with the anatomical structure is being made during the mapping procedure.


In addition, the clinician can identify anatomical landmarks or catheter orientation based on the graphical representation. For example, when mapping a cardiac structure, low amplitude signals would be expected as the electrodes 24 move past certain cardiac structures, such as valves. A clinician can rotate the basket structure 20 to see whether the low amplitude shift from electrodes 24 on one spline to electrodes 24 on another spline 44. The clinician can use this information to distinguish between an anatomical discontinuity and poor electrode contact.


When the electrodes 24 that are and are not making good contact with the anatomical structure have been identified, the processing system 32 may use this information to improve the visualization of physiological activity of the anatomical structure during mapping. For example, the processing system 32 may blank or ignore signals from electrodes 24 that are identified as making poor contact with the anatomical structure, since the signals sensed by these electrodes may be unreliable.


As discussed above, the display device 40 may be configured to display a graphical representation of the quality of contact of the electrodes 24. For example, FIG. 4 is an illustration of an embodiment of a graphical display showing signal amplitudes for bipolar signals sensed by the plurality of mapping electrodes 24. The display includes a panel 70 that depicts the bipolar signal amplitude measured by pairs of electrodes 24 on each of the splines 44. Particularly, the panel 70 shows bipolar signal amplitudes (in millivolts (mV)) across electrodes pairs E1-E2, E3-E4, E5-E6, and E7-E8 on each of the splines S1-S8. The scale 72 assigns a different color to each of the different bipolar signal amplitudes. In the embodiment illustrated in FIG. 4, the bipolar signal amplitude range displayed is from 0 mV to 4 mV. The electrode pairs with higher bipolar signal amplitudes indicate that the associated electrodes are in good contact with the anatomical structure, while the electrode pairs with lower bipolar signal amplitudes indicate that the associated electrodes are in poor electrical contact. Thus, in the illustrated example, if the amplitude threshold for good electrode contact is selected to be about 2 mV, the clinician may determine that electrode pairs E5-E6 on splines 51, S2, and S8 and electrode pair E7-E8 on splines S1-S4 and S8 are making poor contact. In an alternative embodiment, the clinician may set the display device 40 to display electrodes 24 making good contact, as determined by a threshold signal value, in a first color and electrodes 24 making poor contact in a second color.



FIG. 5 is an illustration of an embodiment of a graphical display showing signal amplitudes for unipolar signals sensed by the plurality of mapping electrodes 24. The display includes a panel 80 that depicts the unipolar signal amplitude measured by each electrode 24 on each of the splines 44. Particularly, the panel 80 shows unipolar signal amplitudes (in millivolts (mV)) at each electrode E1-E8 on each of the splines S1 -S8. The scale 82 assigns a different color to each of the different unipolar signal amplitudes ranging from 0 mV to 10 mV. The electrodes 24 with higher unipolar signal amplitudes indicate that the electrodes 24 are in good contact with the anatomical structure, while the electrodes 24 with lower unipolar signal amplitudes indicate that the electrodes 24 are in poor electrical contact. Thus, in the illustrated example, if the amplitude threshold for good electrode contact is set at about 2 mV, the clinician can determine that electrodes E7 and E8 on splines S2, S7, and S8 are making poor contact with the anatomical structure. In an alternative embodiment, the clinician may set the display device 40 to display electrodes 24 making good contact, as determined by a threshold signal value, in a first color and electrodes 24 making poor contact in a second color.


Various modifications and additions can be made to the exemplary embodiments discussed without departing from the scope of the present invention. For example, while the embodiments described above refer to particular features, the scope of this invention also includes embodiments having different combinations of features and embodiments that do not include all of the described features. Accordingly, the scope of the present invention is intended to embrace all such alternatives, modifications, and variations as fall within the scope of the claims, together with all equivalents thereof.

Claims
  • 1. A catheter system comprising: a catheter including (1) a contact determination mechanism, the contact determination mechanism comprising a force sensor; and (2) a plurality of mapping electrodes, each mapping electrode configured to sense signals associated with an anatomical structure; anda processor operatively coupled to the plurality of mapping electrodes and configured to: receive the signals sensed by the plurality of mapping electrodes;determine a signal parameter associated with each of the plurality of mapping electrodes;determine a quality of contact of each of the plurality of mapping electrodes with the anatomical structure based on the signal parameter and an output of the contact determination mechanism; andgenerate a map of the anatomical structure based only on electrodes having sensed signals with a quality of contact exceeding a threshold value, wherein the sensed signals include sensed signals with a quality of contact exceeding a threshold value and sensed signals with a quality of contact not exceeding the threshold value.
  • 2. The catheter system of claim 1, further comprising a display device configured to provide a graphical display representative of the quality of contact of the plurality of mapping electrodes.
  • 3. The catheter system of claim 1, wherein the processor is further configured to generate a map of the anatomical structure based on electrodes having sensed signals with amplitudes greater than a threshold amplitude.
  • 4. The catheter system of claim 1, wherein the processor is configured to sense and characterize at least one of unipolar signals and bipolar signals.
  • 5. The catheter system of claim 1, wherein the catheter comprises an ablation catheter.
  • 6. The catheter system of claim 1, wherein the processor is further configured to identify contours of the anatomical structure based on the quality of contact of the plurality of mapping electrodes.
  • 7. The catheter system of claim 1, wherein the processor is further configured to determine an orientation of the plurality of mapping electrodes based on the quality of contact of the plurality of mapping electrodes.
  • 8. A method for mapping an anatomical structure, the method comprising: sensing signals associated with an anatomical structure with a plurality of mapping electrodes;characterizing the signals sensed by the plurality of mapping electrodes based on a signal parameter associated with the plurality of mapping electrodes;determining a quality of contact of the plurality of mapping electrodes with the anatomical structure based on the signal characterization, wherein the determining step comprises combining the signal characterization with an output of a contact determination mechanism, the contact determination mechanism comprising a force sensor; andgenerating a map of the anatomical structure based only on electrodes having sensed signals with a quality of contact exceeding a threshold value, wherein the sensed signals include sensed signals with a quality of contact exceeding a threshold value and sensed signals with a quality of contact not exceeding the threshold value.
  • 9. The method of claim 8, further comprising generating a map of the anatomical structure based only on electrodes having sensed signals with amplitudes greater than a threshold amplitude.
  • 10. The method of claim 8, further comprising identifying contours of the anatomical structure based on the quality of contact of the plurality of mapping electrodes.
  • 11. The method of claim 8, further comprising determining an orientation of the plurality of mapping electrodes based on the quality of contact of the plurality of mapping electrodes.
  • 12. A method for mapping an anatomical structure, the method comprising: positioning a plurality of mapping electrodes proximate to an anatomical structure;sensing signals with the plurality of mapping electrodes;characterizing the signals sensed by the plurality of mapping electrodes based on a signal parameter associated with the mapping electrodes;determining a quality of contact of the plurality of mapping electrodes with the anatomical structure based on the signal characterization, wherein the determining step comprises combining the signal characterization with an output of a contact determination mechanism, the contact determination mechanism comprising a force sensor;displaying a graphical display representative of the quality of contact of the plurality of electrodes;repositioning the plurality of mapping electrodes with respect to the anatomical structure;updating the graphical display in real-time as the quality of contact of the plurality of electrodes changes when the plurality of electrodes are repositioned; andgenerating a map of the anatomical structure based only on electrodes having sensed signals with a quality of contact exceeding a threshold value, wherein the sensed signals include sensed signals with a quality of contact exceeding a threshold value and sensed signals with a quality of contact not exceeding the threshold value.
  • 13. The method of claim 12, wherein the sensing step comprises sensing bipolar signals with the pairs of the plurality of mapping electrodes.
  • 14. The method of claim 12, wherein the sensing step comprises sensing unipolar signals with each of the plurality of mapping electrodes.
  • 15. The method of claim 12, and further comprising generating a map of the anatomical structure based only on electrodes having sensed signals with amplitudes greater than a threshold amplitude.
CROSS-REFERENCE TO RELATED APPLICATION

This application is a continuation of U.S. application Ser. No. 14/136,607, filed Dec. 20, 2013, which claims the benefit of Provisional Application No. 61/739,980, filed Dec. 20, 2012, all of which are incorporated herein by reference in their entirety.

US Referenced Citations (135)
Number Name Date Kind
5383874 Jackson et al. Jan 1995 A
5398683 Edwards et al. Mar 1995 A
5437664 Cohen et al. Aug 1995 A
5447529 Marchlinski et al. Sep 1995 A
5562721 Marchlinski et al. Oct 1996 A
5598848 Swanson et al. Feb 1997 A
5647870 Kordis et al. Jul 1997 A
5722401 Pietroski et al. Mar 1998 A
5820568 Willis Oct 1998 A
5836990 Li Nov 1998 A
5840031 Crowley Nov 1998 A
5935079 Swanson Aug 1999 A
6050267 Nardella et al. Apr 2000 A
6056745 Panescu et al. May 2000 A
6063078 Wittkampf May 2000 A
6070094 Swanson et al. May 2000 A
6183468 Swanson et al. Feb 2001 B1
6233491 Kordis et al. May 2001 B1
6391024 Sun et al. May 2002 B1
6546270 Goldin et al. Apr 2003 B1
6569160 Goldin et al. May 2003 B1
6584345 Govari Jun 2003 B2
6663573 Goldin Dec 2003 B2
6735465 Panescu May 2004 B2
6804545 Fuimaono et al. Oct 2004 B2
6845257 Fuimaono et al. Jan 2005 B2
6950689 Willis et al. Sep 2005 B1
7099711 Fuimaono et al. Aug 2006 B2
7123951 Fuimaono et al. Oct 2006 B2
7181262 Fuimaono et al. Feb 2007 B2
7610073 Fuimaono et al. Oct 2009 B2
7662151 Crompton et al. Feb 2010 B2
7720420 Kajita May 2010 B2
7879029 Jimenez Feb 2011 B2
7894871 Wittkampf et al. Feb 2011 B2
7938828 Koblish May 2011 B2
7976541 McGee et al. Jul 2011 B2
7996085 Levin Aug 2011 B2
8048063 Aeby Nov 2011 B2
8103327 Harlev et al. Jan 2012 B2
8160690 Wilfley et al. Apr 2012 B2
8162935 Paul et al. Apr 2012 B2
8208991 Markowitz et al. Jun 2012 B2
8265745 Hauck et al. Sep 2012 B2
8267926 Paul et al. Sep 2012 B2
8290578 Schneider Oct 2012 B2
8317783 Cao et al. Nov 2012 B2
8340751 Markowitz et al. Dec 2012 B2
8369922 Paul et al. Feb 2013 B2
8380276 Schultz Feb 2013 B2
8400164 Osadchy et al. Mar 2013 B2
8403925 Miller et al. Mar 2013 B2
8406866 Deno et al. Mar 2013 B2
8449535 Deno et al. May 2013 B2
8454538 Wittkampf et al. Jun 2013 B2
8454589 Deno et al. Jun 2013 B2
8489184 Wilfley et al. Jul 2013 B2
8583215 Lichtenstein Nov 2013 B2
8603084 Fish et al. Dec 2013 B2
8603085 Jimenez Dec 2013 B2
8622935 Leo Jan 2014 B1
8644950 Hauck Feb 2014 B2
8672936 Thao et al. Mar 2014 B2
8679109 Paul et al. Mar 2014 B2
8728077 Paul et al. May 2014 B2
8755860 Paul et al. Jun 2014 B2
8906011 Gelbart et al. Dec 2014 B2
8998890 Paul et al. Apr 2015 B2
9125565 Hauck Sep 2015 B2
9149327 Lambert Oct 2015 B2
9168004 Gliner et al. Oct 2015 B2
9173586 Deno et al. Nov 2015 B2
9254163 Paul et al. Feb 2016 B2
9271782 Paul et al. Mar 2016 B2
9283026 Paul et al. Mar 2016 B2
9427167 Maskara et al. Aug 2016 B2
9510786 Gliner Dec 2016 B2
9681923 Barley Jun 2017 B2
20020068934 Edwards et al. Jun 2002 A1
20020128643 Simpson et al. Sep 2002 A1
20020165448 Ben-Haim et al. Nov 2002 A1
20050203375 Willis et al. Sep 2005 A1
20070181139 Hauck Aug 2007 A1
20070197929 Porath et al. Aug 2007 A1
20070265609 Thapliyal et al. Nov 2007 A1
20080161796 Cao et al. Jul 2008 A1
20080172049 Bredno et al. Jul 2008 A1
20080243214 Koblish Oct 2008 A1
20080281319 Paul et al. Nov 2008 A1
20080288038 Paul et al. Nov 2008 A1
20080312521 Solomon Dec 2008 A1
20080312713 Wilfley et al. Dec 2008 A1
20090093810 Subramaniam et al. Apr 2009 A1
20090163904 Miller et al. Jun 2009 A1
20090171345 Miller et al. Jul 2009 A1
20090177069 Razavi Jul 2009 A1
20090177111 Miller et al. Jul 2009 A1
20090209950 Starksen Aug 2009 A1
20090275827 Aiken et al. Nov 2009 A1
20090281541 Ibrahim et al. Nov 2009 A1
20090306643 Pappone et al. Dec 2009 A1
20100168557 Deno et al. Jul 2010 A1
20100241117 Paul et al. Sep 2010 A1
20100268059 Ryu et al. Oct 2010 A1
20100286550 Harlev et al. Nov 2010 A1
20110034915 Ibrahim et al. Feb 2011 A1
20110125150 Deno et al. May 2011 A1
20110137153 Govari et al. Jun 2011 A1
20110144509 Kahlert et al. Jun 2011 A1
20110237933 Cohen Sep 2011 A1
20120078129 Bailin Mar 2012 A1
20120136346 Condie et al. May 2012 A1
20120136348 Condie et al. May 2012 A1
20120150021 Schwartz Jun 2012 A1
20120184863 Harlev et al. Jul 2012 A1
20120184864 Harlev et al. Jul 2012 A1
20120184865 Harlev et al. Jul 2012 A1
20120209174 Moll et al. Aug 2012 A1
20120238897 Wilfley et al. Sep 2012 A1
20120253161 Harlev et al. Oct 2012 A1
20130023784 Schneider et al. Jan 2013 A1
20130060245 Grunewald et al. Mar 2013 A1
20130172875 Govari et al. Jul 2013 A1
20130190717 Dollar et al. Jul 2013 A1
20130190747 Koblish et al. Jul 2013 A1
20130226169 Miller et al. Aug 2013 A1
20140058375 Koblish Feb 2014 A1
20140100563 Govari et al. Apr 2014 A1
20140194867 Fish et al. Jul 2014 A1
20140228713 Thao et al. Aug 2014 A1
20140364843 Paul et al. Dec 2014 A1
20140364848 Heimbecher et al. Dec 2014 A1
20150005624 Hauck et al. Jan 2015 A1
20160008065 Gliner et al. Jan 2016 A1
20160242667 Fay et al. Aug 2016 A1
Foreign Referenced Citations (4)
Number Date Country
101066225 Nov 2007 CN
102131458 Jul 2011 CN
103379873 Oct 2013 CN
2014036439 Mar 2014 WO
Non-Patent Literature Citations (9)
Entry
“Frequency-Division Multiplexing”, Wikipedia, the Feree Encyclopedia, Printed May 20, 2013. <http://en.wikipedia.org/wiki/Frequency-division_multiplexing>.
“Time-Division_Multiplexing”, Wikipedia, the Free Encyclopedia, Printed May 20, 2013. <http://en.wikipedia.org/wiki/Time-division-multiplexing>.
International Preliminary Report on Patentability issued in PCT/US2013/077019, dated Jun. 23, 2015, 8 pages.
International Preliminary Report on Patentability issued in PCT/US2014/066427, dated Jun. 2, 2016, 7 pages.
International Search Report and Written Opinion issued in PCT/US2013/077019, dated Apr. 9, 2014, 13 pgs.
International Search Report and Written Opinion issued in PCT/US2014/066427, dated Apr. 7, 2015, 9 pages.
Gabriel, C., et al. The Dielectric Properties of Biological Tissues: I. Literature Survey. Phys. Med. Biol., 41:2231-2249, 1996.
International Search Report and Written Opinion issued in PCT/US2016/018689, dated Apr. 28, 2016, 11 pages.
International Preliminary Report on Patentability issued in PCT/US2016/018689, dated Aug. 31, 2017, 7 pages.
Related Publications (1)
Number Date Country
20160331267 A1 Nov 2016 US
Provisional Applications (1)
Number Date Country
61739980 Dec 2012 US
Continuations (1)
Number Date Country
Parent 14136607 Dec 2013 US
Child 15220066 US