Patent Application
20110160832
a. Field of the Invention
This invention relates to a system and method for assessing coupling of a lead to tissue. In particular, the invention relates to a system and method in which the amount of energy between an electrode and a fixation element on the lead is used to assess the degree of coupling of the lead to tissue.
b. Background Art
A number of conventional medial diagnostic and treatment methods exist in which electric signals are applied to tissues in a body. For example, electric signals are commonly used to control heart rates and rhythms in order to maintain or restore a regular heart rate or rhythm in patients suffering from bradyarrhythmias, tachyarrhythmias or fibrillation. The electrical signals are provided to the heart tissue using electrodes disposed on leads that are fed intravenously from an external device or internally from an implanted pacemaker or implantable cardioverter defibrillator (ICD).
Leads are generally attached to the heart tissue using a fixating element such a hook, tines, or a helix or screw extending from the lead. Proper affixation of the lead to the tissue is important to ensure proper placement of the electrodes. Improperly placed electrodes can reduce the useful life of the device by draining power from the device and can also result in less than optimal diagnosis and/or treatment of a condition.
A clinician typically monitors placement and affixation of leads through fluoroscopic imaging. The use of fluoroscopy, however, has several drawbacks. Fluoroscopy requires a subjective judgment on the part of the clinician as to whether the lead has been placed properly and affixed to the tissue. This assessment can be difficult where the leads are being affixed to cardiac tissue because fluoroscopic images are two-dimensional projections and blood and myocardium attenuate x-rays similarly. Fluoroscopic imaging also exposes the patient and clinician to radiation
The inventors herein have recognized a need for a system and method for assessing coupling of a lead to tissue that will minimize and/or eliminate one or more of the above-identified deficiencies.
It is desirable to provide a system and method for assessing the coupling of a lead to tissue.
A system for assessing the coupling of a lead to tissue in accordance with one embodiment of the present teachings includes a lead body including an electrode disposed proximate a distal end of the lead body. The lead body further includes a fixation element disposed near the distal end of the lead body. The fixation element is configured to anchor the distal end of the lead body in the tissue. The system further includes a meter configured to generate a signal indicative of an amount of energy between the electrode and the fixation element. The system further includes an electronic control unit configured to determine a degree of coupling between the lead and the tissue responsive to the signal.
A method for assessing the coupling of a lead to tissue in accordance with one embodiment of the present teachings includes the step of generating a signal indicative of an amount of energy between an electrode disposed proximate a distal end of a lead body and a fixation element disposed near the distal end of the lead body, the fixation element configured to anchor the distal end of the lead body in the tissue. The method further includes the step of determining a degree of coupling between the lead and the tissue responsive to the signal.
The above-described system and method are advantageous because they provide a less subjective assessment for assessing the coupling of a lead to tissue. In particular, the use of the amount of energy between the electrode and fixation element provides a measurable quantity indicative of the relative locations of the electrode and fixation element and the degree of coupling of the fixation element to tissue. The inventive system and method also minimize or eliminate the need for fluoroscopic imaging. As a result, exposure of the patient and clinician to radiation is reduced.
The foregoing and other aspects, features, details, utilities and advantages of the present invention will be apparent from reading the following description and claims, and from reviewing the accompanying drawings.
Referring now to the drawings wherein like reference numerals are used to identify identical components in the various views,
Lead 12 is provided for examination, diagnosis and/or treatment of internal body tissues such as tissue 14. In accordance with one embodiment of the present teachings, lead 12 comprises a pacing lead used for controlling heart rhythms. It should be understood, however, that the present invention can be implemented and practiced with a variety of leads. Lead 12 may include a connector or interface 22 and a lead body 24 having a proximal end 26 and a distal 28 end (as used herein, “proximal” refers to a direction toward the end of the catheter near the clinician, and “distal” refers to a direction away from the clinician and (generally) inside the body of a patient). Lead 12 may also include one or more electrodes 30 and a fixation element 32. Lead 12 may also include other conventional components not illustrated herein such as sensors, additional electrodes, and corresponding conductors or leads.
Connector 22 provides mechanical and electrical connections for cables, wires, or other electrical conductors 34, 36 extending from pulse generator 16 and meter 18. Connector may also provide fluid connections and additional mechanical and/or electrical connections depending on the application for lead 12. Connector 22 is conventional in the art and is disposed at a proximal end of lead 12.
Lead body 24 is an elongated, deformable, tubular structure configured for movement with the body (e.g., within the vascular structure). Lead body 24 supports electrodes 30 and fixation element 32 and associated conductors. Lead body 24 may also include additional electronics for signal processing or conditioning. For example, meter 18 may be integrated therein. Lead body 24 may also permit transport, delivery and/or removal of fluids (including irrigation fluids and bodily fluids), medicines and/or surgical tools or instruments. Lead body 24 may be made from biocompatible materials that provide sufficient flexibility and insulation including, for example, silicon and polyurethane. Lead body 24 defines one of more passageways or lumens configured to house and/or transport electrical conductors, fluids or surgical tools. Body 24 extends between proximal end 26 where it is connected to connector 22 and distal end 28 which is disposed proximate the target site in tissue 14. Body 24 may be introduced into a blood vessel or other structure within the body through a conventional introducer. Body 24 may then be steered or guided through the body to a desired location such as tissue 14 with guide wires or other means known in the art.
Electrodes 30 may be provided for a variety of diagnostic and therapeutic purposes including, for example, electrophysiological studies, lead identification and location, pacing, cardiac mapping and ablation. In the illustrated embodiment, electrode 30 comprises a ring electrode disposed at the tip or distal end 28 of lead 12. It should be understood, however, that the number, orientation and purpose of electrodes 30 may vary.
Fixation element 32 is provided to anchor, or secure the position of, the distal end 28 of lead body 24 in tissue 14. Fixation element 32 may be a passive or active fixation element. For example, fixation element may comprise one or more tines extending from lead body 24, a hook, or—as shown in FIGS. 2-3—a helix 38 or screw. Fixation element 32 may be made from a conducting metal or metal alloy such as Nitinol or stainless steel. Fixation element 32 may provide only an anchoring function or, alternatively, may perform additional functions including use as an electrode. In the helix embodiment illustrated in
Pulse generator 16 generates, delivers and controls RF energy used by lead 12. Generator 16 is conventional in the art and may comprise one of the pacemakers sold under the trademark “AFFINITY” by St. Jude Medical, Inc. or a conventional cardiac resynchronization therapy (CRT) device sold under the trademark “FRONTIER” by St. Jude Medical, Inc. Generator 16 is configured to generate a signal at a predetermined frequency in accordance with one or more user specified parameters (e.g., power, time, etc.) and under the control of various feedback sensing and control circuitry as is know in the art.
Meter 18 is provided to measure the amount of energy between electrode 30 and fixation element 32 and to generate a signal indicative of the amount of energy in response thereto. In one embodiment of the invention, the amount of energy between the electrode 30 and fixation element 32 represents a capacitance and meter 18 comprises a capacitance meter. In another embodiment of the invention, the amount of energy between the electrode 30 and fixation element 32 represents an inductance and meter 18 comprises an inductance meter. In yet other embodiments of the invention, the amount of energy between the electrode 30 and fixation element 32 represents a voltage or a current and meter 18 comprises a volt-meter or ammeter (or amp-meter), respectively. Meter 18 is conventional in the art and may be integrated into lead 12 or an external element, pulse generator 16 or a microprocessor or circuit forming electronic control unit 20. Meter 18 is electrically connected to electrode 30 and fixation element 32 through conductors 44, 46.
ECU 20 is provided to determine a degree of coupling between lead 12 and tissue 14 responsive to the signal received from meter 18. ECU 20 preferably comprises a programmable microprocessor or microcontroller, but may alternatively comprise an application specific integrated circuit (ASIC). ECU 20 may include a central processing unit (CPU) and an input/output (I/O) interface through which ECU 20 may receive a plurality of input signals including signals from meter 18 and generate a plurality of output signals including those used to control generation of electrical signals by electrode 30. In accordance with one aspect of the present invention, ECU 20 may be programmed with a computer program (i.e., software) encoded on a computer storage medium for performing one or more of the above functions.
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A system and method in accordance with the present teachings offers one or more of a number of advantages. The system and method provide a less subjective assessment for assessing the coupling of a lead 12 to tissue 14. In particular, the use of the amount of energy between the electrode 30 and fixation element 32 provides a measurable quantity indicative of the relative locations of the electrode 30 and fixation element 32 and the degree of coupling of the fixation element 32 to tissue. The inventive system and method also minimize or eliminate the need for fluoroscopic imaging. As a result, exposure of the patient and clinician to radiation is reduced.
Although several embodiments of this invention have been described above with a certain degree of particularity, those skilled in the art could make numerous alterations to the disclosed embodiments without departing from the scope of this invention. All directional references (e.g., upper, lower, upward, downward, left, right, leftward, rightward, top, bottom, above, below, vertical, horizontal, clockwise and counterclockwise) are only used for identification purposes to aid the reader's understanding of the present invention, and do not create limitations, particularly as to the position, orientation, or use of the invention. Joinder references (e.g., attached, coupled, connected, and the like) are to be construed broadly and may include intermediate members between a connection of elements and relative movement between elements. As such, joinder references do not necessarily infer that two elements are directly connected and in fixed relation to each other. It is intended that all matter contained in the above description or shown in the accompanying drawings shall be interpreted as illustrative only and not as limiting. Changes in detail or structure may be made without departing from the invention as defined in the appended claims.
