Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
  • A61N1/00—Electrotherapy; Circuits therefor
  • A61N1/02—Details
  • A61N1/04—Electrodes
  • A61N1/05—Electrodes for implantation or insertion into the body, e.g. heart electrode
  • A61N1/056—Transvascular endocardial electrode systems
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
  • A61N1/00—Electrotherapy; Circuits therefor
  • A61N1/02—Details
  • A61N1/04—Electrodes
  • A61N1/05—Electrodes for implantation or insertion into the body, e.g. heart electrode
  • A61N1/056—Transvascular endocardial electrode systems
  • A61N1/057—Anchoring means; Means for fixing the head inside the heart
  • A61N2001/0578—Anchoring means; Means for fixing the head inside the heart having means for removal or extraction
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
  • A61N1/00—Electrotherapy; Circuits therefor
  • A61N1/02—Details
  • A61N1/04—Electrodes
  • A61N1/05—Electrodes for implantation or insertion into the body, e.g. heart electrode
  • A61N1/056—Transvascular endocardial electrode systems
  • A61N2001/0585—Coronary sinus electrodes

Definitions

• the present invention relates generally to implantable leads and, more particularly, to a medical electrical lead employing a load bearing sleeve arrangement.
• Implantation of pacing and defibrillation leads in coronary vessels is becoming increasingly common as atrial and heart failure therapies become more widely accepted. Implanting and stabilizing such leads in the coronary sinus, great vein, and the branch veins is critical to the efficacy of these and other therapies. It is often desirable or necessary to remove leads implanted in cardiac structures, such as the coronary sinus vasculature, for various reasons. Removal of these leads is problematic, especially if coil electrodes are employed on the lead.
• a medical electrical lead employing a load bearing sleeve arrangement.
• a medical electrical lead includes an outer sleeve, having proximal and distal ends, and is formed of a first material.
• At least one electrical conductor is situated within the outer sleeve and extends between the proximal and distal ends of the outer sleeve.
• At least one electrode is electrically coupled to the electrical conductor.
• a load bearing sleeve extends between the proximal and distal ends of the outer sleeve.
• the load bearing sleeve is formed of a second material different from the first material.
• the load bearing sleeve offers resistance to axial loading forces applied to the lead.
• the first material of the outer sleeve is preferably formed from a flexible polymer material
• the second material of the load bearing sleeve is formed from an ultra-high molecular weight polymeric material.
• the first material of the outer sleeve can be silicone or polyurethane
• the second material of the load bearing sleeve can be PTFE or ePTFE.
• the load bearing sleeve extends along at least a majority of the length of the outer sleeve.
• the load bearing sleeve can, for example, be substantially coextensive with the outer sleeve.
• the load bearing sleeve can be entirely encompassed by the outer insulating sleeve.
• portions of the load bearing sleeve proximate an electrode or other transition can emerge from the interior of the lead body so as to cover the electrode or transition.
• the load bearing sleeve submerges into the lead body distal of the electrode/transition in configurations in which the lead body extends beyond the subject electrode/transition.
• the electrical conductor can be configured as a coil conductor, and the load bearing sleeve can be situated within a longitudinally extending cavity of the coil conductor.
• the longitudinally extending cavity of the load bearing sleeve in such a configuration defines an open lumen of the lead.
• the open lumen can be dimensioned to receive a guide wire, a sensor, a stylet or other implement or instrument.
• a medical electrical lead of the present invention includes an outer sleeve formed of a first material and an electrical conductor situated within the outer sleeve which extends between the proximal and distal ends of the outer sleeve. At least one electrode is electrically coupled to the electrical conductor.
• a load bearing sleeve extends between the proximal and distal ends of the outer sleeve. A majority of the length of the load bearing sleeve is positioned within the outer sleeve.
• the load bearing sleeve is formed of a second material having a tensile strength greater than that of the first material of the outer sleeve and a tensile elongation less than that of the first material.
• An inner surface of a portion of the load bearing sleeve extends over an outer surface of the at least one electrode, and an outer surface of the load bearing sleeve portion is exposed through a gap in the outer sleeve.
• a method of implanting a medical electrical lead into a cardiac structure of a patient's heart involves providing a guiding catheter for longitudinally guiding the lead.
• the lead preferably has a construction which incorporates a load bearing sleeve arrangement.
• the implantation method involves inserting the guiding catheter into a chamber of the patient's heart via an access vessel.
• the lead is nserted through the guiding catheter via the open lumen to implant the lead wi thin or on the cardiac structure,
• the implantation method nvolves providing a guide wire for longitudinally guiding the lead.
• the guide wire is inserted through the guiding catheter into the cardiac structure.
• the lead is inserted through the guiding catheter and over the guide wire via the open lumen to implant the lead within or on the cardiac structure.
• a sensor catheter can be inserted through the open lumen to assist in locating the cardiac structure.
• Figure 1 is a partial sectional view of a human heart and a lead system employing left and right side leads comprising pacing and cardioversion/defibrillation electrodes;
• Figure 2 is a sectional view of a medical electrical lead employing a load bearing sleeve arrangement in accordance with an embodiment of the present invention
• Figure 3 is a sectional view of a medical electrical lead employing a load bearing sleeve arrangement in accordance with another embodiment of the present invention
• Figure 4 is a sectional view of a medical electrical lead employing a load bearing sleeve arrangement in accordance with a further embodiment of the present invention
• FIGS. 5A and 5B are partial sectional views of a medical electrical lead employing a load bearing sleeve arrangement in accordance with yet another embodiment of the present invention.
• Figure 6 is a sectional view of a medical electrical lead employing a load bearing sleeve arrangement in accordance with a further embodiment of the present invention.
• the present invention is directed to a medical electrical lead which employs a load bearing sleeve arrangement. More particularly, embodiments of the present invention are directed to a medical electrical lead having an outer insulating sleeve and an inner load bearing sleeve.
• the load bearing sleeve extends along a majority of the outer sleeve length.
• the load bearing sleeve can be substantially coextensive with the outer sleeve of the medical electrical lead.
• the load bearing sleeve can be discontinuous or perforated in certain locations, such as at an electrode location.
• the medical electrical lead can be configured such that one or more electrodes of the lead are positioned proximate an outer surface of the load bearing sleeve.
• the lead can also be configured such that one or more electrodes of the lead are positioned proximate an inner surface of the load bearing sleeve.
• the load bearing sleeve is positioned between the outer sleeve and a coil conductor of the medical electrical
• the load bearing sleeve can be disposed within a medical electrical lead so as to define an open inner lumen of the lead.
• the open lumen can be used to receive a guide wire for over-the-wire implant procedures.
• the open lumen can also be dimensioned to receive a sensor catheter.
• two load bearing sleeves can be used: one that defines an inner lumen of the lead, and a second that is situated between a lead conductor(s) and the outer insulating sleeve of the lead.
• Other configurations are possible, including use of one or more load bearing sleeves to define one or more lumens of a medical electrical lead.
• the load bearing sleeve is preferably formed from a material having a tensile strength greater than that of the outer insulating sleeve.
• the load bearing sleeve can have a tensile strength greater than about 5,500 psi, and the outer insulating sleeve can have a tensile strength of less than about 5,000 psi.
• the tensile elongation of the load bearing sleeve is preferably significantly less than that of the outer insulating sleeve.
• the load bearing sleeve can have a tensile elongation of less than 100%, and the outer insulating sleeve can have a tensile elongation of 300%-1000% or more.
• the load bearing sleeve is preferably formed from a ultra-high molecular weight polymeric material, such as PTFE (polytetrafluoroethylene) or ePTFE (expanded polytetrafluoroethylene), for example.
• the outer insulating sleeve can be formed from materials commonly used for medical electrical lead, such as silicone or polyurethane.
• a medical electrical lead of the present invention is particularly well suited for use with left side pacing and cardioversion/defibrillation devices, it being understood that advantages of the present invention can be realized in right side lead systems.
• pacing and defibrillation leads implanted in the coronary vessels are becoming more common as left atrial and left ventricular therapies become more accepted.
• relatively high axial loads must typically be applied to such leads during lead extraction.
• the integrity of such a lead fabricated using conventional techniques can be compromised if the lead is subjected to excessively high axial forces.
• a medical electrical lead fabricated in accordance with the present invention advantageously provides for improved axial loading characteristics over conventional leads.
• Left side leads for example, can be fabricated to incorporate a load bearing sleeve in a manner described herein to significantly enhance the extractability performance of such leads.
• An important advantage realized by employing a load bearing sleeve in a medical electrical lead of the present invention concerns a significant improvement in axial loading characteristics as compared to many conventional designs. It is appreciated in the art that right sided leads generally require high axial loads for extraction. Left sided leads require substantially lower axial loads for extraction, but are smaller and more flexible than right sided leads, typically resulting in generally less robust designs. In accordance with the principles of the present invention, improved axial loading characteristics are achieved for right sided leads, while inclusion of a load bearing sleeve in left sided lead provides additional robustness to such implementations.
• an implantable medical device which includes a cardiac function management (CFM) device 100 electrically and physically coupled to an intracardiac lead system 102.
• the intracardiac lead system 102 is implanted in a human body with portions of the intracardiac lead system 102 inserted into a heart 101.
• the intracardiac lead system 102 is used to detect and analyze electric cardiac signals produced by the heart 101 and to provide electrical energy to the heart 101 under certain predetermined conditions to treat cardiac arrhythmias.
• the intracardiac lead system 102 includes one or more electrodes used for pacing, sensing, or defibrillation.
• the intracardiac lead system 102 includes a right ventricular lead system 104, a right atrial lead system 105, and a left atrial/ventricular lead system 106.
• the right ventricular lead system 104 is configured as an integrated bipolar pace/shock lead.
• One, some, or all of the lead systems shown in Figure 1 can be configured to include a load bearing sleeve arrangement of the present invention.
• the implantable medical device shown in Figure 1 can employ a single lead for use in a single heart chamber or multiple heart chambers. It is also understood that a medical electrical lead of the present invention can incorporate one or more electrodes, including one or more of a pacing electrode, cardioversion/defibrillation electrode, and monitoring electrode, for example.
• the right ventricular lead system 104 includes an SVC-coil 116, an RV-coil 114, and an RV-tip electrode 112.
• the RV-coil 114 which may alternatively be configured as an RV-ring electrode, is spaced apart from the RV-tip electrode 1 2, which is a pacing electrode for the right ventricle.
• the right atrial lead system 105 includes a RA-tip electrode 156 and an RV-tip electrode 156 and an RV-tip electrode 156 and an RV-tip electrode 156.
• the RA-tip 156 and RA-ring 154 electrodes may provide respectively pacing pulses to the right atrium of the heart and detect cardiac signals from the right atrium.
• the right atrial lead system 105 is configured as a J-lead.
• the intracardiac lead system 102 is shown positioned within the heart 101 , with the right ventricular lead system 104 extending through the right atrium 120 and into the right ventricle 118.
• the RV-tip electrode 112 and RV-coil electrode 114 are positioned at appropriate locations within the right ventricle 118.
• the SVC-coil 116 is positioned at an appropriate location within the right atrium chamber 120 of the heart 101 or a major vein leading to the right atrium chamber 120 of the heart 101.
• the RV-coil 114 and SVC-coil 116 depicted in Figure 1 are defibrillation electrodes.
• An LV-tip electrode 113 and an LV-ring electrode 117 are inserted through the coronary venous system and positioned adjacent to the left ventricle 124 of the heart 101.
• the LV-ring electrode 117 is spaced apart from the LV-tip electrode, 113 which is a pacing electrode for the left ventricle. Both the LV-tip 113 and LV-ring 117 electrodes may also be used for sensing the left ventricle providing two sensing sites within the left ventricle.
• the left atrial/left ventricular lead system 106 further includes an LA-tip 136 and LA-ring 134 electrode positioned adjacent the left atrium 122 for pacing and sensing the left atrium 122 of the heart 101.
• the left atrial/left ventricular lead system 106 includes endocardia! pacing leads that are advanced through the superior vena cava (SVC), the right atrium 120, the valve of the coronary sinus, and the coronary sinus 150 to locate the LA- tip 136, LA-ring 134, LV-tip 113 and LV-ring 117 electrodes at appropriate locations adjacent to the left atrium and ventricle 122, 124, respectively.
• SVC superior vena cava
• left atrial/ventricular lead placement involves creating an opening in a percutaneous access vessel, such as the left subclavian or left cephalic vein.
• the left atrial/left ventricular lead 106 is guided into the right atrium 120 of the heart via the superior vena cava.
• the left atrial/left ventricular lead system 106 is deployed into the coronary sinus ostium, the opening of the coronary sinus 150.
• the lead system 106 is guided through the coronary sinus 150 to a coronary vein of the left ventricle 124.
• This vein is used as an access pathway for leads to reach the surfaces of the left atrium 122 and the left ventricle 124 which are not directly accessible from the right side of the heart.
• Lead placement for the left atrial/left ventricular lead system 106 may be achieved via the subclavian vein access and a preformed guiding catheter for insertion of the LV and LA electrodes 113, 117, 136, 134 adjacent the left ventricle 124 and left atrium 122, respectively.
• the left atrial/left ventricular lead system 106 is implemented as a single-pass lead.
• the lead system further includes a terminal end for establishing physical and electrical connection with a connector block of the CFM device 100.
• the CFM device can be configured as, or incorporate functions of, a pacemaker, cardioverter, defibrillator, cardiac monitor, re-synchronizer or a device that incorporates the functions of two or more of these devices.
• Figure 2 there is illustrated a sectional view of a medical electrical lead which incorporates a load bearing sleeve arrangement in accordance with an embodiment of the present invention.
• the sectional view of Figure 2 is taken at a region of the lead which encompasses an electrode.
• the electrode is generally representative of a defibrillation electrode or a pacing electrode, such as a platinum/iridium electrode, and the electrical conductor that electrically connects with the electrode is generally representative of a coil conductor, such as a single or multiple filar coil conductor, or a cable.
• a medical electrical lead includes an outer insulating sleeve 202, which can be formed from a conventional material suitable for implantable leads.
• the insulating sleeve 202 can be fabricated from silicone, polyurethane, or other biocompatible, flexible material.
• An electrode 204 is shown positioned in a gap formed between adjacent sections 202A, 202B of the outer sleeve 202. The interfaces between the electrode 204 and respective outer sleeve sections 202A, 202B can be sealed using conventional techniques.
• the electrode 204 is representative of a cardioversion/defibrillation electrode.
• Appropriate electrical connections are made between the electrode 204 and the electrical conductor 208 of the lead.
• electrical connections that breach the load bearing sleeve such as some crimping and swaging operations, in isolated areas may be used.
• a load bearing sleeve 206 is shown disposed within the lead, such that all of the load bearing sleeve 206 is surrounded by the outer insulating sleeve 202.
• most of the load bearing sleeve 206 is surrounded by the outer insulating sleeve 202, but one or more sections of the load bearing sleeve 206 can emerge from the interior of the lead body at particular locations, such as at electrode or transition locations.
• the lead includes a central lumen within which a coil conductor 208 is situated.
• a medical electrical lead of the present invention can include two, three, or more lumens.
• a lead of the preset invention can include one or more open lumens, closed lumens, or a combination of open and closed lumens.
• Such lumens can be dimensioned to receive steering tendons, a guide wire, finishing wire, sensor, instrument, or other type of catheter, for example.
• a lumen can also be dimensioned to receive a stylet, although the load bearing sleeve arrangement of the present invention can obviate the need for a conventional stylet in many applications.
• a lumen of such a lead can be provided with a lubricious sleeve or coating, such as a PTFE or ePTFE sleeve, for example.
• a lubricious sleeve or coating such as a PTFE or ePTFE sleeve, for example.
• the load bearing sleeve 206 is disposed entirely within the lead (i.e., encompassed by the outer sleeve 202) and extends along the length of the lead or some majority portion of the lead. As shown, the load bearing sleeve 206 is positioned within the lead lumen, it being understood that the specific location of the load bearing sleeve 206 within the lead structure can be varied.
• the coil conductor 206 is positioned within the load bearing sleeve 206.
• the hollow coil conductor may thus define an inner lumen of the lead, which can be an open or closed lumen.
• a solid (i.e., non-hollow) conductor is employed, such as a cable
• no such inner lumen would be defined within the load bearing sleeve 206 depicted in Figure 2.
• the load bearing sleeve 206 can be dimensioned to receive a solid electrical conductor along with one or more other elements, such as a sensor catheter for example.
• a sensor catheter can incorporate a pressure sensor, an oxygen sensor or a temperature sensor, for example.
• the load bearing sleeve 206 is dimensioned to receive a hollow coil conductor 208.
• the coil conductor 208 is dimensioned to receive a guide wire suitable for left heart chamber over-the-wire lead implant procedures, for example.
• the coil conductor 208 is preferably provided with a lubricious sleeve, liner, or coating.
• the coil conductor 208 can be provided with a lubricous load bearing sleeve, in addition to, or exclusive of, the load bearing sleeve 206. An example of one such variation in configuration will be described below with reference to Figure 6.
• the lubricious material provided within the coil conductor 208 preferably has a low-energy surface that inhibits platelet adhesion.
• a suitable lubricious material that provides a low-energy surface for this usage is ePTFE. Such a surface advantageously provides for enhanced tactile feedback to the physician during use of the over-the-wire lead arrangement.
• the load bearing sleeve 206 is preferably formed from a material having a tensile strength greater than that of the outer insulating sleeve 202.
• the load bearing sleeve 206 has a tensile strength greater than about 5,500 psi, and the outer insulating sleeve 202 has a tensile strength of less than about 5,000 psi.
• the tensile elongation of the load bearing sleeve 206 is preferably less than 100%, and that of the outer insulating sleeve is preferably 300%-1000% or more.
• the load bearing sleeve 206 can have a wall thickness ranging between about 0.001 inches and about 0.01 inches. According to one particular configuration, the load bearing sleeve 206 has a wall thickness ranging between about 0.002 inches and about 0.006 inches.
• the load bearing sleeve 206 is preferably formed from a ultra-high molecular weight polymeric material, such as PTFE or ePTFE, for example. It has been determined that leads with substantial amounts of exposed ePTFE have demonstrated high rates of dislodgment. Extensive use of ePTFE within the interior of a medical electrical lead, rather than on the exterior, provides for a more robust lead implementation, which can withstand higher levels of axial loading without adversely affecting performance as compared to conventional leads.
• the electrical characteristics of a medical electrical lead of the present invention can be selectively altered by judicious selection of the electrode/load bearing sleeve configuration.
• variations in electrode surface exposure and coverage can be achieved by implementing designs in which the electrode is fully exposed (i.e., not covered by the load bearing sleeve), entirely covered by the load bearing sleeve, or partially covered by the load bearing sleeve.
• Varying the level of electrode exposure/coverage can result in varying several electrical characteristics of the lead electrodes, such as the polarization characteristics of the lead electrodes.
• different current distributions can be achieved by selectively altering the level of electrode exposure/coverage.
• FIG. 3 illustrates another embodiment of a medical electrical lead which employs a load bearing sleeve arrangement 306 in accordance with the principles of the present invention.
• the lead includes an outer insulating sleeve 302 and an electrode 304 situated within a gap formed between adjacent sections 302A, 302B of the outer sleeve 302.
• a load bearing sleeve 306 is discontinuous at the region proximate the electrode 304.
• the load bearing sleeve 306 can be formed to have a discontinuity at each of the electrodes 304 that are situated along the length of the lead.
• electrode 304 is situated within a gap formed between adjacent sections 306A, 306B of the load bearing sleeve 306.
• the electrode 304 is connected to the electrical conductor 308, which can be a coil conductor for example, and protrudes through the load bearing sleeve 306 and the outer insulating sleeve 302.
• the electrode 304 is generally flush with respect to the outer surface of the outer insulating sleeve 302.
• a suitable sealing material or arrangement is employed between the electrode 304 and the adjacent outer sleeve sections 302A, 302B and load bearing sleeve sections 306A, 306B, respectively.
• the embodiment of a medical electrical lead shown in Figure 4 is similar to that shown in Figure 3, in that the load bearing sleeve arrangement 406 includes a discontinuity at a location proximate the electrode 404.
• an electrically conductive element, material, or filler 410 is employed at an interface between the electrode 404 and the electrical conductor 408.
• the filler or element 410 provides for conduction of electrical current between the electrode 404 and conductor 408, and can be sized to provide a desired outer surface profile of the lead.
• the element 410 can, if desired, be implemented to intimately connect with adjacent edges of adjacent load bearing sleeve sections 406A, 406B, such as through use of known mechanical or chemical/adhesion means.
• FIGS 5A and 5B illustrate variations of another embodiment of the present invention.
• a load bearing sleeve 506 is positioned within the lead such that most of the load bearing sleeve 506 is encompassed by an outer insulating sleeve 502.
• the load bearing sleeve 506 emerges from the interior of the lead body so as to extend over the electrode 510.
• the load bearing sleeve 506 returns to the sub-surface of the lead body after passing the distal end of the electrode 510.
• the load bearing sleeve need not return to the lead body sub-surface.
• the load bearing sleeve 506 is not severed at the region proximate the electrode 510, but remains continuos along its length.
• the exposed portion of the load bearing sleeve 506A covering the electrode 510 can include perforations.
• the bent or bulged section of the load bearing sleeve 502 proximate the electrode 510 can be pre-formed or formed at the time of lead fabrication.
• the wall thickness of the bent or bulged section of the load bearing sleeve 502 proximate the electrode 510 can be different from that of other sections of the load bearing sleeve 502.
• the thickness of the load bearing sleeve wall in the bent or bulged region can be less than that of the non-bent portions of the load bearing sleeve 506, such as by up to about 50% less in thickness.
• the embodiment shown in Figures 5A and 5B provides the desired improvement in axial loading characteristics while not adversely contributing to implant instability and lead dislodgment.
• ePTFE for example, is a material that prevents or inhibits tissue in-growth (e.g., fibrotic encapsulation or any other form of cellular adhesion).
• tissue in-growth e.g., fibrotic encapsulation or any other form of cellular adhesion.
• extensive use of ePTFE as an outer sleeve of an implantable medical electrical lead has been associated with high lead dislodgment rates.
• limiting the external use of ePTFE primarily at the electrode regions of a medical electrical lead in accordance with the principles the present invention avoids such lead dislodgment problems and provides
• FIG. 6 A further embodiment of a medical electrical lead implemented in accordance with the present invention is depicted in Figure 6.
• the load bearing sleeve 606 is disposed within a lumen defined within the interior of a coil electrode 608.
• the coil electrode 608, in this configuration, is situated between the inner surface of the outer insulating sleeve 602 and the outer surface of the load bearing sleeve 606.
• the electrode 604 is shown positioned in a gap formed between adjacent sections 602A, 602B of the outer sleeve 602, and electrically connects with the coil electrode 608.
• the load bearing sleeve 608 defines an inner lumen of the medical electrical lead.
• This configuration is particularly well-suited for use in over-the-wire implantation procedures, as the interior surface of the load bearing sleeve 608 preferably defines a lubricious surface.
• a second load bearing sleeve can be situated between the coil conductor 608 and the outer insulating sleeve 602 in a manner previously discussed.
• a medical electrical lead incorporating a load bearing sleeve in accordance with the principles of the present invention can be used in a variety of medical procedures.
• a method of implanting a medical electrical lead into a cardiac structure of a patient's heart involves use of a guiding catheter for longitudinally guiding the lead.
• the lead has an open lumen and includes an outer sleeve formed of a first material.
• a coil conductor is situated within the outer sleeve and extends between proximal and distal ends of the outer sleeve. At least one electrode is electrically coupled to the coil conductor.
• the lead further includes a load bearing sleeve that extends between the proximal and distal ends of the outer sleeve.
• the load bearing sleeve is formed of a second material different from the first material. The load bearing sleeve offers resistance to axial loading forces applied to the lead.
• the procedure involves inserting the guiding catheter into a chamber of the patient's heart via an access vessel.
• the procedure further involves inserting the lead through the guiding catheter via the open lumen to implant the lead within or on the cardiac structure.
• a guide wire is provided for longitudinally guiding the lead.
• the procedure involves inserting the guide wire through the guiding catheter into the cardiac structure.
• the lead is inserted through the guiding catheter and over the guide wire via the open lumen to implant the lead within or on the cardiac structure.
• a sensor catheter In another procedure, a sensor catheter is provided. The procedure involves inserting the sensor catheter through the open lumen to assist in locating the cardiac structure.
• the cardiac structure can be a cardiac vessel, such as a left side coronary vessel, for example.
• a medical electrical lead of the present invention may also be configured to include a lead stabilization mechanism in combination with a load bearing sleeve arrangement.
• a lead stabilization mechanism employs an adhesion site or sites at strategic locations on the lead, including electrically active and/or electrically inactive locations of the lead.
• a polymer outer sleeve or coating of the lead provides for improved lead extractability, while the adhesion sites provide for increased stability at selected locations of the lead.
• the lead has a sleeve arrangement which includes one or more adhesion sites provided at one or more of the first lead locations.
• the adhesion sites promote tissue in-growth or attachment between the adhesion sites and cardiac tissue contacting the adhesion sites to enhance stabilization of the implantable lead.
• the cardiac tissue may represent tissue of a cardiac structure of the heart or coronary vasculature of the heart.
• the adhesion sites define apertures in the sleeve at one or more first locations of the sleeve.
• the adhesion sites may comprise exposed portions of one or more of the electrodes or other exposed portions of the lead's insulation or covering.
• the adhesion sites include a structure having a porous surface that promotes cardiac tissue in-growth or attachment at the adhesion sites.
• a metallic annular structure may be disposed at the adhesion site.
• a metallic ring for example, having porous surface characteristics may be employed to promote cellular adhesion at the adhesion site.
• the annular structure may incorporate an electrode, sensor or drug delivery arrangement.
• An annular electrode structure for example, may incorporate a sensing, pacing or shocking electrode.
• the adhesion sites comprise a material that promotes cardiac tissue in-growth or attachment at the adhesion sites.
• the first material may comprise a first polymer material that substantially prevents tissue in-growth between the first locations and cardiac tissue contacting the first locations.
• the adhesion sites in contrast, comprise a second polymer material that promotes tissue in-growth or attachment between the adhesion sites and cardiac tissue contacting the adhesion sites.
• the second polymer material may, for example, have a porosity, pore sizes or distribution of pore sizes that differ from that of the first polymer material.
• the second polymer material may differ in terms of hydrophobicity relative to the first polymer material.
• the first material comprises a first type of PTFE
• a second material of the adhesion sites comprises a second type of PTFE.
• the first type of PTFE comprises a first type of ePTFE
• the second type of PTFE comprises a second type of ePTFE.
• the second type of ePTFE preferably differs from the first type of ePTFE in terms of one or more of porosity, pore sizes or distribution of pore sizes.

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• 2003
  • 2003-01-29 US US10/353,793 patent/US7155293B2/en not_active Expired - Fee Related
• 2004
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