Unipolar reference electrode for electrophysiology mapping catheter
An apparatus includes a shaft and an end effector at a distal end of the shaft. The end effector has a distal end and a proximal end with a longitudinal intermediate point between the distal and proximal ends. The end effector is sized to fit in an anatomical passageway within a cardiovascular system. The end effector includes at least one sensor electrode and a reference electrode. The at least one sensor electrode is configured to contact cardiovascular tissue and thereby pick up potentials. The reference electrode is configured to pick up a potential from fluid in contact with the reference electrode. The reference electrode is located proximal to the longitudinal intermediate point of the end effector. The end effector is configured to prevent the reference electrode from contacting tissue.
1 . An apparatus, comprising:
(a) a shaft; and
(b) an end effector at a distal end of the shaft, the end effector having a distal end and a proximal end with a longitudinal midpoint between the distal and proximal ends of the end effector, the end effector being sized to fit in an anatomical passageway within a cardiovascular system, the end effector comprising:
(i) a plurality of elongated spines having proximal ends at the distal end of the shaft, the plurality of elongated spines extending distally from the distal end of the shaft, each spine carrying at least one sensor electrode, the at least one sensor electrode being configured to contact cardiovascular tissue and thereby pick up potentials, and
(ii) a central end effector shaft that is shorter than the plurality of spines and fixedly connected to the distal end of the shaft, the central end effector shaft having a proximal portion extending distally from the distal end of the shaft and a distal portion terminating in a distal end that is proximal to the longitudinal midpoint of the end effector and near the proximal ends of the plurality of elongated spines, the proximal portion of the central end effector shaft carrying a circumferential reference electrode spaced from the distal end of the distal portion and configured to pick up a potential from fluid in contact with the reference electrode,
the plurality of spines and the central end effector shaft being configured to prevent the reference electrode from contacting tissue such that any tissue contact with the central end effector shaft occurs at the distal end of the distal portion of the central end effector shaft thereby shielding the circumferential reference electrode from contact with the tissue.
2 . The apparatus of claim 1 , the end effector defining a profile having a first portion proximal to the longitudinal midpoint and a second portion proximal to the longitudinal midpoint, the first portion of the profile being proximal to the second portion of the profile, the profile of the end effector having:
(A) a first cross-sectional area at a proximal plane located at the proximal end of the end effector, the proximal plane defining a proximal boundary of the first portion of the profile,
(B) a second cross-sectional area at an intermediate plane defining a boundary between the first and second portions of the profile, the second cross-sectional area being substantially equal to the first cross-sectional area, and
(C) a third cross-sectional area at a distal plane defining a distal boundary of the second portion of the profile.
3 . The apparatus of claim 2 , the reference electrode being positioned in the first portion of the profile.
4 . The apparatus of claim 2 , the first portion of the profile being generally cylindrical.
5 . The apparatus of claim 2 , the first portion of the profile being generally polygonal.
6 . The apparatus of claim 2 , the second portion of the profile being generally frusto-conical.
7 . The apparatus of claim 6 , the second portion of the profile being generally bellmouth-shaped.
8 . The apparatus of claim 6 , the second portion of the profile being generally pyramid-shaped.
9 . The apparatus of claim 2 , the second portion of the profile diverging outwardly from the intermediate plane to the distal plane.
10 . The apparatus of claim 1 , the at least one sensor electrode comprising a plurality of sensor electrodes carried on each of the plurality of spines.
11 . The apparatus of claim 1 , the spines of the plurality of spines being disposed in parallel to each other and connected at a proximal region of the spines to define a generally planar configuration.
12 . The apparatus of claim 1 , a first pair of spines of the plurality of spines being connected at a first proximal region to define a first plane and a second pair of spines of the plurality of spines being connected at a second proximal region to define a second plane different from the first plane.
13 . The apparatus of claim 1 , the shaft defining a longitudinal axis, a portion of each of the plurality of spines extending outwardly away from the longitudinal axis.
14 . The apparatus of claim 1 , the shaft defining a longitudinal axis, each of the plurality of spines comprising respective free ends oriented away from the longitudinal axis.
15 . The apparatus of claim 1 , the shaft defining a longitudinal axis, the central end effector shaft extending from the distal end of the shaft along the longitudinal axis of the shaft such that the reference electrode is positioned on the central end effector shaft and partially enshrouded by the spines.
16 . The apparatus of claim 1 , the central end effector shaft being further configured to dispense irrigation fluid.
17 . The apparatus of claim 1 , the shaft defining a longitudinal axis, the plurality of spines being configured to bow outwardly and converge distally with respect to the longitudinal axis to form a basket configuration.
18 . The apparatus of claim 17 , the central end effector shaft carrying the reference electrode such that it is positioned in an interior region of the basket configuration.
19 . The apparatus of claim 1 , the reference electrode being positioned proximally in relation to the at least one sensor electrode.
20 . The apparatus of claim 1 , the plurality of spines and the central end effector shaft being configured to prevent the central end effector shaft from contacting tissue when the plurality of spines are generally flattened on the tissue.
21 . The apparatus of claim 1 , the plurality of spines and the central end effector shaft being configured to prevent the reference electrode from contacting tissue when the plurality of spines are generally flattened on the tissue such that any tissue contact with the central end effector shaft occurs at the distal end of the distal portion of the central end effector shaft thereby shielding the reference electrode from contact with the tissue.
22 . The apparatus of claim 14 , the plurality of spines and the central end effector shaft being configured to prevent the central end effector shaft from contacting tissue when the plurality of spines are generally flattened on the tissue.
23 . The apparatus of claim 14 , the plurality of spines and the central end effector shaft being configured to prevent the reference electrode from contacting tissue when the plurality of spines are generally flattened on the tissue such that any tissue contact with the central end effector shaft occurs at the distal end of the distal portion of the central end effector shaft thereby shielding the reference electrode from contact with the tissue.
24 . An apparatus, comprising:
(a) a shaft extending along a longitudinal axis; and
(b) an end effector at a distal end of the shaft, the end effector being sized to fit in an anatomical passageway within a cardiovascular system, the end effector defining a profile oriented with respect to the longitudinal axis that generates about the longitudinal axis a frusto-conical portion and a cylindrical portion proximal to the frusto-conical portion, the end effector comprising:
(i) at least one tissue-contacting electrode, the at least one tissue-contacting electrode being configured to contact cardiovascular tissue and thereby pick up potentials,
(ii) a non-tissue contact electrode configured to pick up a reference potential from fluid in contact with the non-tissue contact electrode, the non-tissue contact electrode being positioned in the cylindrical portion of the profile,
(iii) a plurality of elongated spines having proximal ends at the distal end of the shaft, the plurality of elongated spines extending distally from the distal end of the shaft, the at least one tissue-contacting electrode being carried on at least one of the plurality of elongated spines, and
(iv) a central end effector shaft that is shorter than the plurality of elongated spines and fixedly connected to the distal end of the shaft, the central end effector shaft having a proximal portion extending distally from the distal end of the shaft and a distal portion terminating in a distal end that is proximal to a longitudinal midpoint of the end effector and near the proximal ends of the plurality of elongated spines, the proximal portion of the central end effector shaft carrying the non-tissue contact electrode spaced from the distal end of the distal portion,
the end effector being configured to prevent the non-tissue contact electrode from contacting tissue such that any tissue contact with the central end effector shaft occurs at the distal end of the distal portion of the central end effector shaft thereby shielding the non-tissue contact electrode from contact with the tissue.
25 . The apparatus of claim 24 , in which the apparatus is capable of being reprocessed into a reusable apparatus for subsequent reuse.
26 . The apparatus of claim 25 , in which the reprocessed apparatus is cleaned and sterilized with a solution for reuse in a subject.
27 . The apparatus of claim 26 , in which the solution comprises a chemical selected from the group consisting of: 3300-3800 ppm peracetic acid; 2.65% glutaraldehyde; 3.4% glutaraldehyde with 26% isopropanol; 3.5% glutaraldehyde; 5.75% ortho-phthaldehyde; 0.55% ortho-phthaldehyde; hypochlorite with hypochlorous acid 650-675 ppm active free chlorine; 1.12% glutaraldehyde with 1.93% phenol/phenate; 2.5% glutaraldehyde; 3.2% glutaraldehyde; 3% glutaraldehyde; 7.35% hydrogen peroxide with 0.23% peracetic acid; 1.0% hydrogen peroxide with 0.08% peracetic acid; 2.4% glutaraldehyde; 3.4% glutaraldehyde; 2.0% hydrogen peroxide; 0.60% ortho-phthalaldehyde; hypochlorous acid/hypochlorite 400-450 ppm with active free chlorine; and combinations thereof.
28 . The apparatus of claim 24 , the end effector being configured to prevent the central end effector shaft from contacting tissue when the plurality of spines are generally flattened on the tissue.
29 . The apparatus of claim 24 , the end effector being configured to prevent the non-tissue contact electrode from contacting tissue when the plurality of spines are generally flattened on the tissue such that any tissue contact with the central end effector shaft occurs at the distal end of the distal portion of the central end effector shaft thereby shielding the non-tissue contact electrode from contact with the tissue.
30 . An apparatus, comprising:
(a) a shaft; and
(b) a tip shaft fixedly connected to a distal end of the shaft and having a proximal portion extending distally from a distal end of the shaft and a distal portion terminating in a distal end, the tip shaft defining a hollow interior and a distal opening in fluid communication with the hollow interior;
(c) a plurality of spines having proximal ends at the distal end of the shaft, the plurality of spines extending distally from the distal end of the shaft along a longitudinal axis to define a virtual volume about the tip shaft, the plurality of spines being longer than the tip shaft such that the distal end of the distal portion of the tip shaft is proximal of a longitudinal midpoint between the distal end of the shaft and distal ends of the plurality of spines and near the proximal ends of the plurality of spines; and
(d) a circumferential non-tissue contact electrode carried by the proximal portion of the tip shaft at a position spaced proximally from the distal opening at the distal end of the distal portion of the tip shaft, the non-tissue contact electrode being configured to pick up a reference potential, and the plurality of spines and the tip shaft being configured to prevent the non-tissue contact electrode from contacting tissue such that any tissue contact with the tip shaft occurs at the distal end of the distal portion of the tip shaft thereby shielding the circumferential non-tissue contact electrode from contact with the tissue.
31 . The apparatus of claim 30 , in which the circumferential non-tissue contact electrode is disposed on an inner circumferential surface of the hollow interior of the tip shaft.
32 . The apparatus of claim 30 , in which the circumferential non-tissue contact electrode is disposed on an outer circumferential surface of the tip shaft.
33 . The apparatus of claim 30 , the plurality of spines and the tip shaft being configured to prevent the tip shaft from contacting tissue when the plurality of spines are generally flattened on the tissue.
34 . The apparatus of claim 30 , the plurality of spines and the tip shaft being configured to prevent the non-tissue contact electrode from contacting tissue when the plurality of spines are generally flattened on the tissue such that any tissue contact with the tip shaft occurs at the distal end of the distal portion of the tip shaft thereby shielding the non-tissue contact electrode from contact with the tissue.
35 . A method of using the apparatus of claim 1 , the method comprising:
(a) placing a first sensor electrode of the at least one sensor electrode in contact with tissue in a patient's cardiovascular system;
(b) positioning the reference electrode in contact with fluid in the patient's cardiovascular system without contact with tissue in the patient's cardiovascular system;
(c) processing electrical signals from the first sensor electrode and the reference electrode;
(d) plotting an electrocardiogram signal based on the processed electrical signals;
(e) communicating fluid through a lumen of the central end effector shaft, the reference electrode being coaxially positioned about the lumen.
36 . The method of claim 35 , the at least one sensor electrode comprising the first sensor electrode and a second sensor electrode, the method further comprising:
(a) placing the second sensor electrode in the patient's cardiovascular system without placing the second sensor electrode in contact with tissue in the patient's cardiovascular system;
(b) measuring impedance between the reference electrode and the first sensor electrode;
(c) measuring impedance between the reference electrode and the second sensor electrode; and
(d) determining that the first sensor electrode is in contact with tissue and that the second sensor electrode is not in contact with tissue based on the measured impedances.
37 . The method of claim 36 , the measured impedance between the reference electrode and the first sensor electrode being greater than the measured impedance between the reference electrode and the second sensor electrode, the step of determining that the first sensor electrode is in contact with tissue and that the second sensor electrode is not in contact with tissue comprising determining that the measured impedance between the reference electrode and the first sensor electrode is greater than the measured impedance between the reference electrode and the second sensor electrode.
38 . The method of claim 35 , the step of plotting comprising displaying a unipolar signal waveform with reduction of far field signals in a range from 50% to 100% compared to Wilson Central Terminal (WCT) reference signals.