Catheter with coronary sinus ostium anchor
First Claim
1. A method of operating a medical device in a patient, comprising:
- positioning an inflatable first chamber of a medical device adjacent a first tissue region, the first tissue region including cardiac tissue, the inflatable first chamber including an expandable portion that is electrically conductive, the expandable portion being configured to be expanded to a maximum cross-sectional diameter of the inflatable chamber when the medical device is in use;
directing a cryogenic coolant through a first fluid flow path into the inflatable first chamber to expand the expandable portion of the inflatable first chamber;
positioning an inflatable second chamber of the medical device adjacent a second tissue region, the second tissue region including a portion of the coronary sinus, the inflatable second chamber including an expandable portion that is configured to be expanded to a maximum cross-sectional diameter of the inflatable second chamber when the medical device is in use;
directing a cryogenic coolant through a second fluid flow path into the inflatable second chamber to expand the expandable portion of the inflatable second chamber;
anchoring the expanded inflatable first chamber to the first tissue region through cryoadhesion and anchoring the expanded inflatable second chamber to the second tissue region through cryoadhesion;
positioning at least one of a diagnostic element and a therapeutic element of the medical device adjacent a third tissue region;
operating the at least one of a diagnostic element and therapeutic element proximate to the third tissue region; and
obtaining positional information from the expandable electrically conductive portion of the inflatable first chamber and transmitting the positional information from the electrically conductive portion of the inflatable first chamber to a position sensing system.
1 Assignment
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Accused Products
Abstract
A method of treating cardiac tissue is provided, including positioning a first chamber of a medical device adjacent an atrial wall; directing a cryogenic coolant into the first chamber; anchoring the first chamber to the atrial wall through cryoadhesion; directing a distal portion of the medical device into the coronary sinus; and positioning a cardiac lead through at least a portion of the coronary sinus with the distal portion. The method may include measuring a temperature of the first chamber; removing the first chamber from the atrial wall once a predetermined threshold temperature of the first chamber is reached; anchoring a second chamber of the medical device to a portion of the coronary sinus; and/or perfusing blood flow through at least a portion of the second chamber.
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Citations
13 Claims
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1. A method of operating a medical device in a patient, comprising:
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positioning an inflatable first chamber of a medical device adjacent a first tissue region, the first tissue region including cardiac tissue, the inflatable first chamber including an expandable portion that is electrically conductive, the expandable portion being configured to be expanded to a maximum cross-sectional diameter of the inflatable chamber when the medical device is in use; directing a cryogenic coolant through a first fluid flow path into the inflatable first chamber to expand the expandable portion of the inflatable first chamber; positioning an inflatable second chamber of the medical device adjacent a second tissue region, the second tissue region including a portion of the coronary sinus, the inflatable second chamber including an expandable portion that is configured to be expanded to a maximum cross-sectional diameter of the inflatable second chamber when the medical device is in use; directing a cryogenic coolant through a second fluid flow path into the inflatable second chamber to expand the expandable portion of the inflatable second chamber; anchoring the expanded inflatable first chamber to the first tissue region through cryoadhesion and anchoring the expanded inflatable second chamber to the second tissue region through cryoadhesion; positioning at least one of a diagnostic element and a therapeutic element of the medical device adjacent a third tissue region; operating the at least one of a diagnostic element and therapeutic element proximate to the third tissue region; and obtaining positional information from the expandable electrically conductive portion of the inflatable first chamber and transmitting the positional information from the electrically conductive portion of the inflatable first chamber to a position sensing system. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11)
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12. A method of treating a patient, comprising:
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performing a first procedure, the first procedure including; positioning a first chamber of a first medical device adjacent a first tissue region, the first chamber including an expandable portion that is electrically conductive; expanding the expandable portion of the first chamber to a maximum diameter of the first chamber such that the expandable portion of the first chamber is in contact with the first tissue region; positioning a second chamber of the first medical device adjacent a second tissue region, the second chamber including an expandable portion and one or more perfusion apertures; expanding the expandable portion of the second chamber to a maximum cross-sectional diameter of the second chamber such that the expandable portion of the second chamber is in contact with the second tissue region; anchoring the first chamber to the first tissue region through cryoadhesion and anchoring the second chamber to the second tissue region through cryoadhesion; positioning at least one of a diagnostic element and a therapeutic element of the first medical device adjacent a third tissue region different from the first and second tissue regions; operating the at least one of a diagnostic element and therapeutic element proximate to the third tissue region; obtaining positional information from the expandable electrically conductive portion of the first chamber and the at least one of a diagnostic element and a therapeutic element; generating a first map based on the positional information; and performing a second procedure, the second procedure including; positioning the first chamber of the first medical device adjacent a fourth tissue region, the second tissue region and the fourth tissue region being substantially co-located; expanding the expandable portion of the first chamber to the maximum cross-sectional diameter of the first chamber such that the expandable portion of the first chamber is in contact with the fourth tissue region; positioning the second chamber of the first medical device adjacent a fifth tissue region; expanding the expandable portion of the second chamber to the maximum cross-sectional diameter of the second chamber such that the expandable portion of the second chamber is in contact with the fifth tissue region; anchoring the first chamber to the fourth tissue region through cryoadhesion and anchoring the second chamber to the fifth tissue region through cryoadhesion; positioning the at least one of a diagnostic element and a therapeutic element adjacent a sixth tissue region different from the fourth and fifth regions; operating the at least one of a diagnostic element and therapeutic element proximate to the sixth tissue region; obtaining positional information from the electrically conductive portion of the first chamber at the at least one of a diagnostic element and a therapeutic element; generating a second map based on the positional information; and registering the second map to the first map.
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13. A method of treating cardiac tissue, comprising:
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directing a distal portion of a medical device into a coronary sinus, the medical device including a first chamber and a second chamber; positioning the first chamber of the medical device adjacent an atrial wall, the first chamber including an expandable portion that is electrically conductive and configured to be expanded to a maximum cross-sectional diameter of the first chamber when the device is in use; directing a cryogenic coolant into the first chamber; anchoring the first chamber to the atrial wall through cryoadhesion; positioning the second chamber of the medical device adjacent a tissue region in the coronary sinus, the second chamber including an expandable portion that is configured to be expanded to a maximum cross-sectional diameter of the second chamber when the medical device is in use; directing a cryogenic coolant into the second chamber; anchoring the second chamber to the tissue region in the coronary sinus through cryoadhesion; positioning an implantable cardiac lead through at least a portion of the coronary sinus with the distal portion of the medical device; and transmitting positional data from the electrically conductive portion of the first chamber to a position sensing system.
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Specification