IMPLANTABLE CARDIAC MONITOR
First Claim
1. An implantable cardiac monitor (ICM) configured to be deployed subcutaneous, submuscular, or substernal at a position that enables the ICM to detect cardiac activity, the ICM comprising:
- a first electrode secured relative to the ICM;
a second electrode secured relative to the ICM and spaced from the first electrode;
a third electrode secured relative to the ICM and spaced from the first electrode and the second electrode;
a housing that is configured for subcutaneous, submuscular or substernal deployment and to support the first electrode, the second electrode and the third electrode, the housing comprising;
a body portion having a first end and a second end;
a tail portion extending from the body portion to a tail end;
the first electrode disposed adjacent the first end of the body portion;
the second electrode disposed adjacent the second end of the body portion;
the third electrode disposed adjacent the tail end of the tail portion;
a controller disposed within the housing and operably coupled to the first electrode, the second electrode and the third electrode;
the controller configured to select a pair of the first electrode, the second electrode and the third electrode to use for sensing P-waves resulting from atrial contraction; and
the controller configured to communicate information about the sensed P-waves to a second medical device.
1 Assignment
0 Petitions
Accused Products
Abstract
An implantable cardiac monitor (ICM) may be configured to be deployed subcutaneous, submuscular, or substernal at a position that enables the ICM to detect cardiac activity. In some cases, the ICM includes a housing that includes a body portion and a tail portion. A first electrode may be disposed adjacent a first end of the body portion, a second electrode may be disposed adjacent a second end of the body portion and a third electrode may be disposed adjacent a tail end of the tail portion. A controller may be disposed within the housing and may be operably coupled to the first electrode, the second electrode and the third electrode. The controller may be configured to select a pair of the first electrode, the second electrode and the third electrode to use for sensing cardiac electrical activity and to communicate information about the sensed activity to a second medical device.
40 Citations
20 Claims
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1. An implantable cardiac monitor (ICM) configured to be deployed subcutaneous, submuscular, or substernal at a position that enables the ICM to detect cardiac activity, the ICM comprising:
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a first electrode secured relative to the ICM; a second electrode secured relative to the ICM and spaced from the first electrode; a third electrode secured relative to the ICM and spaced from the first electrode and the second electrode; a housing that is configured for subcutaneous, submuscular or substernal deployment and to support the first electrode, the second electrode and the third electrode, the housing comprising; a body portion having a first end and a second end; a tail portion extending from the body portion to a tail end; the first electrode disposed adjacent the first end of the body portion; the second electrode disposed adjacent the second end of the body portion; the third electrode disposed adjacent the tail end of the tail portion; a controller disposed within the housing and operably coupled to the first electrode, the second electrode and the third electrode; the controller configured to select a pair of the first electrode, the second electrode and the third electrode to use for sensing P-waves resulting from atrial contraction; and the controller configured to communicate information about the sensed P-waves to a second medical device. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 13, 14, 15)
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11. The ICM of claim 11, wherein the controller is configured to communicate information about the sensed P-waves to the second medical device via conducted communication using a pair of the first electrode, the second electrode and the third electrode.
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12. The ICM of claim 12, wherein the controller is configured to select which two of the first electrode, the second electrode and the third electrode to use for conducted communication with the second medical device.
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16. An implantable cardiac monitor (ICM) configured to be deployed subcutaneous, submuscular or substernal at a position that enables the ICM to detect signs of cardiac activity, the ICM comprising:
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a housing; a first electrode secured relative to the housing; a second electrode secured relative to the housing and spaced from the first electrode; a third electrode secured relative to the housing and spaced from the first electrode and the second electrode; a controller disposed within the housing and operably coupled to the first electrode, the second electrode and the third electrode; the controller configured to select a pair of the first electrode, the second electrode and the third electrode for sensing cardiac electrical activity; and the controller configured to select a pair of the first electrode, the second electrode and the third electrode for communication with a second medical device. - View Dependent Claims (17, 18, 19)
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20. An implantable cardiac monitor (ICM) configured to be deployed subcutaneous, submuscular, or substernal at a position that enables the ICM to detect cardiac activity, the ICM comprising:
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a first electrode secured relative to the ICM; a second electrode secured relative to the ICM and spaced from the first electrode; a third electrode secured relative to the ICM and spaced from the first electrode and the second electrode; a controller operably coupled to the first electrode, the second electrode and the third electrode; a housing that is configured for subcutaneous, submuscular or substernal deployment and to support the first electrode, the second electrode and the third electrode, the housing comprising; a body portion having a first end and a second end, wherein the body portion comprises a hermitically sealed metallic enclosure that houses the controller; a flexible tail portion extending from the body portion to a tail end, the flexible tail portion comprises a polymeric body carrying the third electrode; the controller configured to use a selected pair of the first electrode, the second electrode and the third electrode for sensing cardiac activity; and the controller configured to communicate information about the cardiac activity to a second medical device.
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Specification