US20110071609A1 - Biasing and fixation features on leads - Google Patents
Biasing and fixation features on leads Download PDFInfo
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- US20110071609A1 US20110071609A1 US12/952,885 US95288510A US2011071609A1 US 20110071609 A1 US20110071609 A1 US 20110071609A1 US 95288510 A US95288510 A US 95288510A US 2011071609 A1 US2011071609 A1 US 2011071609A1
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- Prior art keywords
- loop
- lead body
- biasing feature
- lead
- distal end
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- 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
-
- 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 to medical devices and devices for securing a lead. More specifically, the invention relates to devices and methods for positioning and fixing a lead within a vessel of the heart.
- Implantable medical devices for treating irregular contractions of the heart with electrical stimuli are well known in the art. Some of the most common forms of such implantable devices are defibrillators and pacemakers. Various types of electrical leads for defibrillators and pacemakers have been suggested in the prior art.
- a broad group of leads may be characterized by the fact that they are placed transvenously. These leads are introduced into the patient's vasculature at a venous access site and travel through veins to the locations where the leads' electrodes will implant in or otherwise contact coronary tissue.
- One large subfamily of the group of transvenously-placed leads are those that are implanted in the endocardium (the tissue lining the inside of the heart) of the right atrium or ventricle.
- Another subfamily of the group of transvenously-placed leads are those that are placed in the branch vessels of the coronary venous system to stimulate the left ventricle.
- left ventricular stimulation either alone or in conjunction with right ventricular stimulation.
- cardiac resynchronization therapy also commonly referred to as biventricular pacing
- Left ventricular stimulation requires placement of a lead in or on the left ventricle in the lateral or posterior-lateral aspect/region of the heart.
- One technique for left ventricular lead placement is to advance a lead endovenously into the coronary sinus and then advance the lead through a branch vein onto the surface of the left ventricle so as to stimulate the myocardium of the heart.
- the left ventricle beats forcefully as it pumps oxygenated blood throughout the body. Repetitive beating of the heart, in combination with patient movement, can sometimes dislodge the lead from the branch vessel. Over time, the electrodes may lose contact with the heart muscle, or move from their original location and orientation.
- the present invention is a lead assembly for placement in a coronary vessel of the heart.
- the coronary vessel has a pericardial wall portion and a myocardial wall portion.
- the lead assembly comprises a lead body extending from a proximal end adapted for coupling to a pulse generator to a distal end adapted for implantation in the heart, an electrode positioned at the distal end of the lead body, and a loop biasing feature located at the distal end of the lead body.
- the loop biasing feature includes a resilient loop positioned to bias a portion of the electrode towards the myocardial wall portion of the coronary vessel by exerting a force against the pericardial wall portion.
- the loop biasing feature further includes a collar for coupling the loop biasing feature to the lead body.
- the present invention is a lead assembly for placement in a coronary vessel of the heart.
- the coronary vessel has a pericardial wall portion and a myocardial wall portion.
- the lead assembly comprises a lead body extending from a proximal end adapted for coupling to a pulse generator to a distal end adapted for implantation in the heart.
- the lead body includes a lumen extending from the proximal end to the distal end.
- An electrode is positioned at the distal end of the lead body.
- a loop biasing feature is located at the distal end of the lead body.
- the loop biasing feature includes a resilient loop positioned to bias a portion of the electrode towards the myocardial wall.
- a cord is coupled to the loop and extends to the proximal end of the lead body. A tensile force applied to the cord causes the loop to flatten towards the lead body and a portion of the loop to slide into the lumen.
- the present invention is a method of implanting a lead in a coronary vessel of the heart.
- the coronary vessel has a pericardial wall portion and a myocardial wall portion.
- the method comprises providing a lead body extending from a proximal end adapted for coupling to a pulse generator to a distal end adapted for implantation in the heart, an electrode positioned at the distal end of the lead body, and a loop biasing feature located at the distal end of the lead body.
- the loop biasing feature includes a resilient loop. The resilient loop is compressed towards the lead body by inserting the lead into a guide catheter. The distal end of the lead body is advanced into the coronary vessel to a fixation location. The electrode is biased towards the myocardial wall portion of the coronary vessel by engaging the loop biasing feature.
- FIG. 1 shows an exemplary implantable medical device in relation to a heart.
- FIG. 2 shows a side view of the distal end of a lead assembly according to one embodiment of the present invention in relation to a branch vessel of the coronary sinus.
- FIG. 3 shows a side view of the distal end of the lead assembly of FIG. 2 detailing tissue in-growth.
- FIG. 4 shows a side view of the distal end of the lead assembly of FIG. 3 partially removed from the branch vessel.
- FIGS. 5A-5D show a loop biasing feature according to alternative embodiments of the present invention.
- FIG. 6 shows a side view of the distal end of a lead assembly according to another embodiment of the invention.
- FIG. 7 shows a side view of the distal end of a lead assembly according to yet another embodiment of the invention.
- FIGS. 8A-8B show a loop biasing feature according to yet another alternative embodiment of the present invention.
- FIGS. 9A-9C show a loop biasing feature according to an alternative embodiment of the present invention.
- FIG. 10 shows a side view of a distal end of a lead assembly according to one embodiment of the present invention positioned within a guide catheter.
- FIG. 11 shows a side view of a distal end of a lead assembly according to another embodiment of the present invention positioned within a guide catheter.
- FIG. 12A shows a side view of a lead assembly according to yet another embodiment of the invention.
- FIG. 12B shows a cross-sectional view of the lead assembly of FIG. 12A taken along line 12 A- 12 A.
- FIG. 13 shows a side view of a distal end of a lead assembly according to another embodiment of the invention.
- FIG. 14 shows a side view of a distal end of a lead assembly according to another embodiment of the present invention.
- FIG. 15 shows a side view of a distal end of a lead assembly according to another embodiment of the present invention.
- FIG. 1 is a schematic drawing of a cardiac rhythm management system 5 including a pulse generator 8 coupled to an exemplary lead assembly 10 deployed in a patient's heart 12 from a superior vena cava 13 .
- the heart 12 includes a right atrium 15 and a right ventricle 16 , a left atrium 17 and a left ventricle 18 , a coronary sinus ostium 19 in the right atrium 15 , a coronary sinus 21 , and various cardiac vessels including a great cardiac vein 23 and other branch vessels of the coronary sinus 21 including an exemplary branch vessel 25 .
- FIG. 2 shows a portion of the lead assembly 10 according to one embodiment of the present invention.
- the lead assembly 10 is shown implanted in the branch vessel 25 .
- the branch vessel 25 has a myocardial wall portion 26 a nearer to a myocardium 26 of the heart 12 and a pericardial wall portion 27 a nearer to a pericardium 27 of the heart 12 .
- the lead assembly 10 includes a lead body 28 extending from a proximal end 29 (see FIG. 1 ) adapted for coupling to the pulse generator 8 to a distal end 30 adapted for insertion into the heart 12 .
- An electrode 31 is positioned at the distal end 30 of the lead body 28 for pacing and sensing electrical stimuli.
- lead assembly 10 is shown as a monopolar-type lead having a single electrode 31 , it is also contemplated that one or more electrodes may be positioned on the lead body 28 to allow for unipolar, bipolar or multi-polar pacing and sensing. It is also contemplated that one or more electrodes may be positioned on the lead body 28 to allow pacing and sensing at a selected electrode in a preferred position.
- the lead assembly 10 further includes a loop biasing feature 32 at the distal end 30 of the lead body 28 .
- the loop biasing feature 32 includes a resilient loop 34 of material protruding from the lead body 28 .
- the loop 34 forms a closed curve with the lead body 28 .
- the size of the lead biasing feature 32 and the loop 34 may vary with respect to the size of the lead assembly 10 .
- the loop 34 extends a distance between approximately 0.003 and 0.250 inches from the lead body 28 .
- the loop 34 has a radius between approximately 0.025 and 10.0 inches.
- the loop 34 may have an included angle between approximately 10 and 179 degrees.
- the loop 34 is resilient. It rebounds or springs back into shape after bending or being compressed.
- the resilient loop 34 allows the loop biasing feature 32 to exert a force against the pericardial wall portion 27 a .
- the loop biasing feature exerts a force between 1 and 800 grams when fully compressed.
- the force exerted by the loop biasing feature 32 when the loop 34 is extended is a function of the vessel size and the loop shape and size.
- the loop biasing feature 32 may be formed from a material having a predetermined shape.
- the loop biasing feature 32 may be made of a variety of materials, including, for example, molded or extruded silicone rubber, polyurethane or other polymeric materials.
- the loop biasing feature 32 may also be made of a flexible coil, cable or wire, coated or uncoated with a material as described above. In other embodiments, the loop biasing feature 32 can be made of any material and have any shape that is capable of exerting a force against the pericardial wall portion 27 a.
- the loop biasing feature 32 further includes a collar 38 coupling the loop 34 to the lead body 28 .
- the collar 38 is initially slidable along the lead body 28 so as to selectively position the loop 34 at various locations along the lead body 28 , as well as to permit addition and/or removal of the loop biasing feature 32 from the lead body 28 .
- a groove 47 is formed in the lead body 28 for receiving the collar 38 and retaining the collar 38 in position.
- the groove 47 may be sized as shown such that the collar 38 is isodiametric with the remainder of the lead body 28 .
- an adhesive or other fixator (not shown) may be employed to fix the collar 38 to the lead body 28 , or the loop biasing feature 32 may be otherwise mechanically coupled to the lead body 28 , or integrally formed with the lead body 28 .
- the loop biasing feature 32 protrudes from the lead body 28 in such a manner as to frictionally engage the pericardial wall portion 27 a of the branch vessel 25 as shown in FIG. 2 .
- the loop biasing feature 32 thus biases the electrode 31 away from the pericardial wall 27 a and towards the myocardial wall 26 a of the branch vessel 25 .
- the loop biasing feature 32 increases the frictional force between the lead body 28 and the branch vessel 25 , thus helping to fix the lead body 28 within the branch vessel 25 .
- the loop biasing feature 32 is positioned adjacent to the electrode 31 so as to bias a portion of the electrode 31 opposite the loop 34 towards the myocardial wall 26 a .
- one or more loop biasing features 32 may be positioned at various locations on the lead body 28 , not necessarily adjacent to the electrode 31 , so as to bias the one or more electrodes 31 towards the myocardial wall 26 a .
- the loop biasing features 32 may be positioned at the same distal location on the lead body 28 (as shown in FIGS. 8 and 9 A- 9 C) or may be staggered along the length of the lead body 28 (not shown).
- a loop biasing feature 32 may therefore be selected to take advantage of the complex shape of the branch vessel 25 so as to bias and fix the electrode 31 towards the myocardial wall 26 a .
- a loop biasing feature 32 may include one or more loops 34 , one or more collars 38 , or any variation in the number of loops 34 and collars 38 .
- the loop biasing feature 32 defines a tissue in-growth area 48 between the lead body 28 and the loop 34 .
- the tissue in-growth area 48 is an open region into which scar tissue or clotting material may grow upon implantation, further fixing the lead assembly 10 in place.
- FIG. 3 shows tissue 49 , which has grown into the tissue in-growth area 46 .
- a pharmaceutical agent such as a clotting agent, or other therapeutic treatment 52 is embedded or coated onto the loop biasing feature 32 , as shown in FIGS. 2 and 3 , or nearby on the lead body 28 , to facilitate tissue in growth on and about the tissue in-growth area 48 .
- a pharmaceutical agent such as a clotting agent, or other therapeutic treatment 52 is embedded or coated onto the loop biasing feature 32 , as shown in FIGS. 2 and 3 , or nearby on the lead body 28 , to facilitate tissue in growth on and about the tissue in-growth area 48 .
- a pharmaceutical agent such as a clotting agent, or other therapeutic treatment 52 is embedded or coated onto the loop bias
- the loop 34 can be coated with or encapsulated by a drug so as to be a delivery mechanism for delivering drugs or other therapeutic treatments such as steroids to the heart 12 (not shown).
- the tissue 49 is shown completely extending from the pericardial wall 27 a to the lead body 28 in the area of the loop 34 , but in other embodiments, the tissue 49 need not extend completely from the pericardial wall 27 a to the lead body 28 .
- the tissue 49 may partially encompass the loop 34 .
- the lead assembly 10 may further include a drug collar 56 on the lead body 28 for delivering drugs or other therapeutic treatments such as steroids to the heart 12 .
- the loop biasing feature 32 includes an optional necked down region 46 of the loop 34 connecting the loop 34 to the collar 38 .
- the necked down region 46 of the loop 34 is thinner than the remainder of the loop 34 , so as to break at a pre-determined axial load.
- the predetermined axial load can be between 1 and 800 grams. In another embodiment, the predetermined axial load can be 100 grams.
- the necked down region 46 is at an end of the loop 34 .
- the necked down region 46 may be located anywhere on the loop biasing feature 32 , including, for example, in the center of the loop 34 .
- the loop 34 can pull off of the lead body 28 or out of the lead body 28 .
- the loop 34 can remain connected to the lead body 28 after the necked down region 46 has been broken.
- FIGS. 5A-5D show alternative embodiments of the loop biasing feature 32 .
- the necked down region 46 has the same dimensions as the loop 34 , but has been weakened by heat, radiation, or any other suitable means for weakening the necked down region 46 .
- the loop biasing feature 32 can also include a hole 47 in the necked down region 46 , as shown in the top view of FIG. 5B . This hole 47 weakens the loop 34 , thus reducing the axial force necessary to break the loop 34 .
- the side view of FIG. 5C illustrates an alternative embodiment of the loop biasing feature 32 where the necked down region 46 includes a notch 49 .
- 5D illustrates an embodiment where the necked down region 46 is thinner in a plane parallel to the top of the loop biasing feature 32 .
- Any combination of holes 47 , notches 49 , and necked down regions 46 can be used to alter the axial force required to break the loop 34 .
- the loop 34 does not include a necked down or weakened region 46 , and the cross-sectional area of the loop 34 controls the axial force needed to break the loop 34 .
- FIGS. 6 and 7 show additional embodiments of the loop biasing feature 32 where the loop biasing feature 32 includes a fixation structure.
- the loop 34 may be formed with a tine 60 , as shown in FIG. 5 , or scales 64 , as shown in FIG. 6 , to increase fixation or friction between the loop biasing feature 32 and the branch vessel 25 . These features may reduce unintended dislodgement of the lead assembly 10 from a selected fixation location.
- FIGS. 8A and 8B show yet another alternative embodiment of the loop biasing feature 32 where the loop biasing feature 32 includes two loops 34 .
- the groove along the heart 12 where the vessel 25 lies may be somewhat oval.
- certain positions of loops 34 around the circumference of the lead body 28 may preferentially orient the lead assembly 10 and loop biasing feature 32 into a position where the electrode 31 faces towards the heart 12 and the loops 34 face away from the heart 12 . This can result in better electrical contact with the heart 12 .
- the location of the loop or loops 34 around the circumference of the lead body 28 may therefore be critical.
- FIGS. 8A-8B depict an embodiment for such orientation. Although two loops 34 are shown in FIGS. 8A and 8B , the loop biasing feature 32 could include any number of loops 34 .
- FIGS. 9A-9C show another alternative embodiment of the loop biasing feature 32 where the loop biasing feature 32 includes more than one loop 34 .
- the loop biasing feature 32 includes two loops 34 a and a loop 34 b interposed between the loops 34 a .
- the loops 34 a , 34 b are similar to the tines 60 .
- the loops 34 a resist motion of the lead tip 30 in the proximal direction and the loop 34 b resists motion of the lead tip 30 in the distal direction.
- the loops 34 folds down into down onto the lead body 28 so that it can more easily slide thru a catheter (not shown) and vessels 25 , or deploy in a more predictable manner.
- the loop biasing feature 32 may optionally include holes 47 located in the necked down region 46 to facilitate removal of the lead assembly 10 .
- FIGS. 8A-8B and 9 A- 9 C show two loops 34 , the loop biasing feature 32 could have additional loops 34 having any desired shape and optionally including a necked down region 46 , a hole 47 , or a notch 49 .
- the lead assembly 10 may be delivered into the branch vessel 25 with a variety of techniques as are known in the art, including through the use of a guide catheter and/or stylet.
- FIG. 10 shows an embodiment of the lead assembly 10 positioned for delivery into the branch vessel (not shown) through a lumen 70 of a guide catheter 72 .
- a stylet, guidewire, or another catheter may be used to advance the lead assembly 10 through the lumen 70 .
- the loop 34 flattens down against the lead body 28 .
- the diameter of the guide catheter 72 may be sized smaller than the combined diameter of the lead body 28 and the loop 34 . In one embodiment, as illustrated in FIG.
- a groove 74 is formed into an outer surface 76 of the lead body 28 to receive the flattened loop 34 . This further reduces the diameter of the lead assembly 10 and of the guide catheter 72 .
- the groove 74 extends over the electrode 31 .
- the loop biasing feature 32 may be positioned on the lead body 28 such that the loop 34 and/or the groove 74 do not pass over the electrode 31 (not shown).
- FIGS. 12A and 12B show a lead assembly 110 according to another embodiment of the invention.
- the lead assembly 110 includes a lead body 128 extending from a proximal end 129 adapted for coupling to a pulse generator (not shown) to a distal end 130 adapted for insertion into the heart 12 .
- An electrode 131 is positioned at the distal end 130 of the lead body 128 .
- the lead assembly 110 further includes a loop biasing feature 132 at the distal end 130 of the lead body 128 .
- the loop biasing feature 132 includes a loop 134 of cord, filament or cable material protruding from the lead body 128 .
- the loop 134 has a distal end 135 fixed to the lead body 128 by, for example, adhesive, a crimp tube, compressive fit, or any other suitable manner (not shown).
- a proximal end 136 of the loop 134 is coupled to a cord 180 extending through a cord lumen 184 formed in the lead body 128 .
- proximal and distal ends 136 , 135 of the loop 134 exit and enter the cord lumen 184 through a pair of ports 188 in the lead body 128 .
- a proximal end 192 of the cord 180 is coupled to an optional grasp feature 196 .
- a pocket 198 is provided in an outer surface 176 of the lead body 128 for receiving the grasp feature 196 .
- a slidable tube 193 is positioned over the lead body 128 for covering the proximal end 192 of the cord 180 and the pocket 198 .
- a groove 174 is formed in the outer surface 176 of the lead body 128 for receiving the flattened loop 134 .
- a tensile force applied to the cord 180 causes the loop distal end to detach, thus facilitating removal of the lead assembly 110 .
- the loop 134 and the cord 180 are not separate components, but rather the loop 134 is formed of a portion of the cord 180 which is sufficiently rigid to bias the lead body 128 towards the epicardium 27 and the myocardium 26 .
- pharmaceutical agents 152 can be added to the lead assembly 110 to facilitate tissue in-growth into a tissue in-growth area 148 defined between the loop 134 and the lead body 128 .
- the lead body 128 could include a surface treatment such as a plasma treatment.
- the loop 134 protrudes from the lead body 128 in such a manner as to engage the pericardial wall 27 a as previously described.
- the loop biasing feature 132 thus biases the electrode 131 towards the myocardial wall 26 a and also helps to fix the lead body 128 within the branch vessel 25 (not shown).
- a proximally directed force exerted on the grasp feature 196 as illustrated by arrow 197 , tensions the cord 180 , thereby flattening the loop 134 towards the lead body 128 for implanting, revising or removing the lead assembly 110 .
- the cord 180 permits the loop biasing feature 132 to be neutralized by reducing a distance d between the loop 134 and the exterior surface 176 of the lead body 128 .
- the loop 134 twists or bends on itself so as to flatten towards the lead body 128 during implantation.
- the cord 180 is typically formed of a lubricious material such as ethylene tetrafluoroethylene (ETFE), polytetrafluoroethylene (PTFE) or expanded polytetrafluoroethylene (ePTFE) or other strong polymer such as polyester, aramid, Kevlar®, or is coated with such a material so as to reduce friction between the cord 180 and the cord lumen 184 .
- a lubricious material such as ethylene tetrafluoroethylene (ETFE), polytetrafluoroethylene (PTFE) or expanded polytetrafluoroethylene (ePTFE) or other strong polymer such as polyester, aramid, Kevlar®, or is coated with such a material so as to reduce friction between the cord 180 and the cord lumen 184 .
- suitable materials include coextruded PTFE/Kevlar®, and can be polymer coated cable or nitinol wire. This reduces the axial force necessary to tension the cord 180 so as to neutralize
- FIG. 12B shows a cross-sectional view of the lead body 128 , showing the cord 180 and cord lumen 184 .
- the lead body 128 may include additional lumens 199 for uses such as delivery of payloads or receiving a conductive member.
- the cord 180 and/or the electrode 131 can be radio-opaque to allow the implanter to visualize deployment and electrode orientation with respect to the myocardial wall 26 a to provide optimal or desirable orientation.
- the loop 134 is preformed with the curvature shown.
- the loop 134 is thus biased outwardly into the loop shape protruding from the lead body 128 by virtue of the preformed curvature.
- the loop 134 may be preformed with different shapes than that shown in FIG. 12A .
- the loop 134 may be preformed with multiple curvatures (as shown in FIG. 13 ), or may have a variable cross-section along the length of the loop 134 (not shown).
- the loop 34 can have a thickness such that the loop 34 shields or otherwise insulates a portion of the electrode 31 to prevent stimulation of the nerves located near the pericardium 27 and coronary vessels or the diaphragm (not shown).
- the loop 134 is biased outward by a spring mechanism 195 , as illustrated in FIG. 14 .
- the spring mechanism 195 is shown in a window view in FIG. 14 for illustrative purposes only.
- the loop 134 is connected to the spring mechanism 195 such that the loop 134 is biased distally, or outwardly, from the lead body 128 .
- the spring 195 can optionally be coupled to a cord 180 extending through the lumen 184 . In the embodiment of FIG. 14 , a proximally directed tensioning force on the cord 180 flattens the loop 134 , thus aiding in removal of the lead assembly 110 from the vessel 25 .
- the spring 195 is located at the distal tip 130 of the lead assembly 110 and surrounding a portion 196 of the loop 134 .
- the spring 195 pushes the loop 134 distally or outwardly.
- the loop 134 can optionally be coupled to a cord 180 extending through the lumen 184 .
- application of a proximally directed tensioning force to the cord 180 flattens the loop 134 , thereby aiding in removal of the lead assembly 110 from the vessel 25 .
- the lead assembly does not include the spring 195 .
- the loop biasing feature 132 itself can be stiff enough to provide a biasing force.
- the loop 134 can be optionally coupled to a cord 180 extending through a lumen 184 for lead removal as described with respect to FIG. 14 .
- the lead assembly 110 may include multiple loops 134 and the loops 134 may be preformed with multiple curvatures.
- the loop biasing features 132 may include any combination of necked down regions 146 , holes 147 , or notches 149 .
Abstract
A lead assembly for placement in a coronary vessel of the heart, the coronary vessel having a pericardial wall portion and a myocardial wall portion. The lead assembly comprises a lead body extending from a proximal end adapted for coupling to a pulse generator to a distal end adapted for implantation in the heart, an electrode positioned at the distal end of the lead body, and a loop biasing feature located at the distal end of the lead body. The loop biasing feature includes a resilient loop positioned to bias a portion of the electrode towards the myocardial wall portion of the coronary vessel by exerting a force against the pericardial wall portion. The loop biasing feature further includes a collar for coupling the loop biasing feature to the lead body. A method of implanting the lead assembly.
Description
- This application is a continuation of U.S. application Ser. No. 11/548,838, filed Oct. 12, 2006, which is a continuation in part of U.S. application Ser. No. 11/424,440, filed Jun. 15, 2006, all of which are incorporated herein by reference in their entirety.
- The present invention relates to medical devices and devices for securing a lead. More specifically, the invention relates to devices and methods for positioning and fixing a lead within a vessel of the heart.
- Implantable medical devices for treating irregular contractions of the heart with electrical stimuli are well known in the art. Some of the most common forms of such implantable devices are defibrillators and pacemakers. Various types of electrical leads for defibrillators and pacemakers have been suggested in the prior art.
- A broad group of leads may be characterized by the fact that they are placed transvenously. These leads are introduced into the patient's vasculature at a venous access site and travel through veins to the locations where the leads' electrodes will implant in or otherwise contact coronary tissue. One large subfamily of the group of transvenously-placed leads are those that are implanted in the endocardium (the tissue lining the inside of the heart) of the right atrium or ventricle. Another subfamily of the group of transvenously-placed leads are those that are placed in the branch vessels of the coronary venous system to stimulate the left ventricle.
- The treatment of heart failure often requires left ventricular stimulation either alone or in conjunction with right ventricular stimulation. For example, cardiac resynchronization therapy (also commonly referred to as biventricular pacing) is an emerging treatment for heart failure, which requires stimulation of both the right and the left ventricle to increase cardiac output. Left ventricular stimulation requires placement of a lead in or on the left ventricle in the lateral or posterior-lateral aspect/region of the heart. One technique for left ventricular lead placement is to advance a lead endovenously into the coronary sinus and then advance the lead through a branch vein onto the surface of the left ventricle so as to stimulate the myocardium of the heart. Although methods and tools have been developed to navigate the lead through the vasculature, and in particular to direct the lead into a selected branch vessel of the coronary sinus, it can be difficult to orient the electrodes to face and stimulate the myocardium. If the electrodes come into contact with the pericardial wall portion of the branch vessel, rather than the myocardial wall portion, a degraded site for sensing and pacing may result.
- The left ventricle beats forcefully as it pumps oxygenated blood throughout the body. Repetitive beating of the heart, in combination with patient movement, can sometimes dislodge the lead from the branch vessel. Over time, the electrodes may lose contact with the heart muscle, or move from their original location and orientation.
- There is a need for an improved lead and method of implantation for orienting the lead into the coronary sinus branch vessels such that the lead electrodes contact the myocardium, and also to provide controlled fixation and removal of the lead.
- In one embodiment, the present invention is a lead assembly for placement in a coronary vessel of the heart. The coronary vessel has a pericardial wall portion and a myocardial wall portion. The lead assembly comprises a lead body extending from a proximal end adapted for coupling to a pulse generator to a distal end adapted for implantation in the heart, an electrode positioned at the distal end of the lead body, and a loop biasing feature located at the distal end of the lead body. The loop biasing feature includes a resilient loop positioned to bias a portion of the electrode towards the myocardial wall portion of the coronary vessel by exerting a force against the pericardial wall portion. The loop biasing feature further includes a collar for coupling the loop biasing feature to the lead body.
- In another embodiment, the present invention is a lead assembly for placement in a coronary vessel of the heart. The coronary vessel has a pericardial wall portion and a myocardial wall portion. The lead assembly comprises a lead body extending from a proximal end adapted for coupling to a pulse generator to a distal end adapted for implantation in the heart. The lead body includes a lumen extending from the proximal end to the distal end. An electrode is positioned at the distal end of the lead body. A loop biasing feature is located at the distal end of the lead body. The loop biasing feature includes a resilient loop positioned to bias a portion of the electrode towards the myocardial wall. A cord is coupled to the loop and extends to the proximal end of the lead body. A tensile force applied to the cord causes the loop to flatten towards the lead body and a portion of the loop to slide into the lumen.
- In yet another embodiment, the present invention is a method of implanting a lead in a coronary vessel of the heart. The coronary vessel has a pericardial wall portion and a myocardial wall portion. The method comprises providing a lead body extending from a proximal end adapted for coupling to a pulse generator to a distal end adapted for implantation in the heart, an electrode positioned at the distal end of the lead body, and a loop biasing feature located at the distal end of the lead body. The loop biasing feature includes a resilient loop. The resilient loop is compressed towards the lead body by inserting the lead into a guide catheter. The distal end of the lead body is advanced into the coronary vessel to a fixation location. The electrode is biased towards the myocardial wall portion of the coronary vessel by engaging the loop biasing feature.
- While multiple embodiments are disclosed, still other embodiments of the present invention will become apparent to those skilled in the art from the following detailed description, which shows and describes illustrative embodiments of the invention. Accordingly, the drawings and detailed description are to be regarded as illustrative in nature and not restrictive.
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FIG. 1 shows an exemplary implantable medical device in relation to a heart. -
FIG. 2 shows a side view of the distal end of a lead assembly according to one embodiment of the present invention in relation to a branch vessel of the coronary sinus. -
FIG. 3 shows a side view of the distal end of the lead assembly ofFIG. 2 detailing tissue in-growth. -
FIG. 4 shows a side view of the distal end of the lead assembly ofFIG. 3 partially removed from the branch vessel. -
FIGS. 5A-5D show a loop biasing feature according to alternative embodiments of the present invention. -
FIG. 6 shows a side view of the distal end of a lead assembly according to another embodiment of the invention. -
FIG. 7 shows a side view of the distal end of a lead assembly according to yet another embodiment of the invention. -
FIGS. 8A-8B show a loop biasing feature according to yet another alternative embodiment of the present invention. -
FIGS. 9A-9C show a loop biasing feature according to an alternative embodiment of the present invention. -
FIG. 10 shows a side view of a distal end of a lead assembly according to one embodiment of the present invention positioned within a guide catheter. -
FIG. 11 shows a side view of a distal end of a lead assembly according to another embodiment of the present invention positioned within a guide catheter. -
FIG. 12A shows a side view of a lead assembly according to yet another embodiment of the invention. -
FIG. 12B shows a cross-sectional view of the lead assembly ofFIG. 12A taken along line 12A-12A. -
FIG. 13 shows a side view of a distal end of a lead assembly according to another embodiment of the invention. -
FIG. 14 shows a side view of a distal end of a lead assembly according to another embodiment of the present invention. -
FIG. 15 shows a side view of a distal end of a lead assembly according to another embodiment of the present invention. - While the invention is amenable to various modifications and alternative forms, specific embodiments have been shown by way of example in the drawings and are described in detail below. The intention, however, is not to limit the invention to the particular embodiments described. On the contrary, the invention is intended to cover all modifications, equivalents, and alternatives falling within the scope of the invention as defined by the appended claims.
-
FIG. 1 is a schematic drawing of a cardiacrhythm management system 5 including apulse generator 8 coupled to anexemplary lead assembly 10 deployed in a patient'sheart 12 from asuperior vena cava 13. As shown, theheart 12 includes aright atrium 15 and aright ventricle 16, aleft atrium 17 and aleft ventricle 18, acoronary sinus ostium 19 in theright atrium 15, acoronary sinus 21, and various cardiac vessels including a greatcardiac vein 23 and other branch vessels of thecoronary sinus 21 including anexemplary branch vessel 25. -
FIG. 2 shows a portion of thelead assembly 10 according to one embodiment of the present invention. Thelead assembly 10 is shown implanted in thebranch vessel 25. Thebranch vessel 25 has amyocardial wall portion 26 a nearer to amyocardium 26 of theheart 12 and apericardial wall portion 27 a nearer to apericardium 27 of theheart 12. Thelead assembly 10 includes alead body 28 extending from a proximal end 29 (seeFIG. 1 ) adapted for coupling to thepulse generator 8 to adistal end 30 adapted for insertion into theheart 12. Anelectrode 31 is positioned at thedistal end 30 of thelead body 28 for pacing and sensing electrical stimuli. While thelead assembly 10 is shown as a monopolar-type lead having asingle electrode 31, it is also contemplated that one or more electrodes may be positioned on thelead body 28 to allow for unipolar, bipolar or multi-polar pacing and sensing. It is also contemplated that one or more electrodes may be positioned on thelead body 28 to allow pacing and sensing at a selected electrode in a preferred position. - The
lead assembly 10 further includes aloop biasing feature 32 at thedistal end 30 of thelead body 28. In the embodiment generally shown inFIG. 2 , theloop biasing feature 32 includes aresilient loop 34 of material protruding from thelead body 28. As shown inFIG. 2 , theloop 34 forms a closed curve with thelead body 28. The size of thelead biasing feature 32 and theloop 34 may vary with respect to the size of thelead assembly 10. In one embodiment, theloop 34 extends a distance between approximately 0.003 and 0.250 inches from thelead body 28. In one embodiment, theloop 34 has a radius between approximately 0.025 and 10.0 inches. Theloop 34 may have an included angle between approximately 10 and 179 degrees. - The
loop 34 is resilient. It rebounds or springs back into shape after bending or being compressed. Theresilient loop 34 allows theloop biasing feature 32 to exert a force against thepericardial wall portion 27 a. In one embodiment, the loop biasing feature exerts a force between 1 and 800 grams when fully compressed. The force exerted by theloop biasing feature 32 when theloop 34 is extended is a function of the vessel size and the loop shape and size. Theloop biasing feature 32 may be formed from a material having a predetermined shape. Theloop biasing feature 32 may be made of a variety of materials, including, for example, molded or extruded silicone rubber, polyurethane or other polymeric materials. Theloop biasing feature 32 may also be made of a flexible coil, cable or wire, coated or uncoated with a material as described above. In other embodiments, theloop biasing feature 32 can be made of any material and have any shape that is capable of exerting a force against thepericardial wall portion 27 a. - In the embodiment illustrated in
FIG. 2 , theloop biasing feature 32 further includes acollar 38 coupling theloop 34 to thelead body 28. Thecollar 38 is initially slidable along thelead body 28 so as to selectively position theloop 34 at various locations along thelead body 28, as well as to permit addition and/or removal of theloop biasing feature 32 from thelead body 28. In the illustrated embodiment, agroove 47 is formed in thelead body 28 for receiving thecollar 38 and retaining thecollar 38 in position. Thegroove 47 may be sized as shown such that thecollar 38 is isodiametric with the remainder of thelead body 28. In other embodiments, an adhesive or other fixator (not shown) may be employed to fix thecollar 38 to thelead body 28, or theloop biasing feature 32 may be otherwise mechanically coupled to thelead body 28, or integrally formed with thelead body 28. - The
loop biasing feature 32 protrudes from thelead body 28 in such a manner as to frictionally engage thepericardial wall portion 27 a of thebranch vessel 25 as shown inFIG. 2 . Theloop biasing feature 32 thus biases theelectrode 31 away from thepericardial wall 27 a and towards themyocardial wall 26 a of thebranch vessel 25. In addition, theloop biasing feature 32 increases the frictional force between thelead body 28 and thebranch vessel 25, thus helping to fix thelead body 28 within thebranch vessel 25. - In the illustrated embodiment, the
loop biasing feature 32 is positioned adjacent to theelectrode 31 so as to bias a portion of theelectrode 31 opposite theloop 34 towards themyocardial wall 26 a. In other embodiments, however, one or more loop biasing features 32 may be positioned at various locations on thelead body 28, not necessarily adjacent to theelectrode 31, so as to bias the one ormore electrodes 31 towards themyocardial wall 26 a. In other embodiments, the loop biasing features 32 may be positioned at the same distal location on the lead body 28 (as shown in FIGS. 8 and 9A-9C) or may be staggered along the length of the lead body 28 (not shown). The position of theloop biasing feature 32 may therefore be selected to take advantage of the complex shape of thebranch vessel 25 so as to bias and fix theelectrode 31 towards themyocardial wall 26 a. In other embodiments, aloop biasing feature 32 may include one ormore loops 34, one ormore collars 38, or any variation in the number ofloops 34 andcollars 38. - The
loop biasing feature 32 defines a tissue in-growth area 48 between thelead body 28 and theloop 34. The tissue in-growth area 48 is an open region into which scar tissue or clotting material may grow upon implantation, further fixing thelead assembly 10 in place.FIG. 3 showstissue 49, which has grown into the tissue in-growth area 46. In some embodiments, a pharmaceutical agent, such as a clotting agent, or othertherapeutic treatment 52 is embedded or coated onto theloop biasing feature 32, as shown inFIGS. 2 and 3 , or nearby on thelead body 28, to facilitate tissue in growth on and about the tissue in-growth area 48. One such exemplary clotting agent is the QuikClot® brand hemostatic agent (available from Z-Medica Corporation of Wallingford, Conn.). Theloop 34 can be coated with or encapsulated by a drug so as to be a delivery mechanism for delivering drugs or other therapeutic treatments such as steroids to the heart 12 (not shown). InFIG. 3 , thetissue 49 is shown completely extending from thepericardial wall 27 a to thelead body 28 in the area of theloop 34, but in other embodiments, thetissue 49 need not extend completely from thepericardial wall 27 a to thelead body 28. Thetissue 49, for example, may partially encompass theloop 34. In other embodiments, thelead assembly 10 may further include adrug collar 56 on thelead body 28 for delivering drugs or other therapeutic treatments such as steroids to theheart 12. - In the illustrated embodiment, the
loop biasing feature 32 includes an optional neckeddown region 46 of theloop 34 connecting theloop 34 to thecollar 38. As shown inFIGS. 2 and 3 , the necked downregion 46 of theloop 34 is thinner than the remainder of theloop 34, so as to break at a pre-determined axial load. In one embodiment, the predetermined axial load can be between 1 and 800 grams. In another embodiment, the predetermined axial load can be 100 grams. By breaking theloop 34, as illustrated inFIG. 4 , the biasing and frictional force between thelead assembly 10 and thebranch vessel 25 is reduced and theloop 34 can be pulled out of thetissue 49 surrounding theloop 34. This can be used to disengage theloop biasing feature 32 from thebranch vessel 25 to facilitate removal of thelead assembly 10. In the embodiment generally illustrated inFIGS. 2-4 , the necked downregion 46 is at an end of theloop 34. In other embodiments, the necked downregion 46 may be located anywhere on theloop biasing feature 32, including, for example, in the center of theloop 34. Theloop 34 can pull off of thelead body 28 or out of thelead body 28. Theloop 34 can remain connected to thelead body 28 after the necked downregion 46 has been broken. -
FIGS. 5A-5D show alternative embodiments of theloop biasing feature 32. In the embodiment shown in the side view ofFIG. 5A , the necked downregion 46 has the same dimensions as theloop 34, but has been weakened by heat, radiation, or any other suitable means for weakening the necked downregion 46. Alternatively, theloop biasing feature 32 can also include ahole 47 in the necked downregion 46, as shown in the top view ofFIG. 5B . Thishole 47 weakens theloop 34, thus reducing the axial force necessary to break theloop 34. The side view ofFIG. 5C illustrates an alternative embodiment of theloop biasing feature 32 where the necked downregion 46 includes anotch 49. The top view shown inFIG. 5D illustrates an embodiment where the necked downregion 46 is thinner in a plane parallel to the top of theloop biasing feature 32. Any combination ofholes 47,notches 49, and necked downregions 46 can be used to alter the axial force required to break theloop 34. In an alternative embodiment, theloop 34 does not include a necked down or weakenedregion 46, and the cross-sectional area of theloop 34 controls the axial force needed to break theloop 34. -
FIGS. 6 and 7 show additional embodiments of theloop biasing feature 32 where theloop biasing feature 32 includes a fixation structure. For example, theloop 34 may be formed with atine 60, as shown inFIG. 5 , or scales 64, as shown inFIG. 6 , to increase fixation or friction between theloop biasing feature 32 and thebranch vessel 25. These features may reduce unintended dislodgement of thelead assembly 10 from a selected fixation location. -
FIGS. 8A and 8B show yet another alternative embodiment of theloop biasing feature 32 where theloop biasing feature 32 includes twoloops 34. In some circumstances, the groove along theheart 12 where thevessel 25 lies may be somewhat oval. As a result, certain positions ofloops 34 around the circumference of thelead body 28 may preferentially orient thelead assembly 10 andloop biasing feature 32 into a position where theelectrode 31 faces towards theheart 12 and theloops 34 face away from theheart 12. This can result in better electrical contact with theheart 12. The location of the loop orloops 34 around the circumference of thelead body 28 may therefore be critical.FIGS. 8A-8B depict an embodiment for such orientation. Although twoloops 34 are shown inFIGS. 8A and 8B , theloop biasing feature 32 could include any number ofloops 34. -
FIGS. 9A-9C show another alternative embodiment of theloop biasing feature 32 where theloop biasing feature 32 includes more than oneloop 34. In this embodiment, theloop biasing feature 32 includes twoloops 34 a and aloop 34 b interposed between theloops 34 a. Theloops tines 60. Theloops 34 a resist motion of thelead tip 30 in the proximal direction and theloop 34 b resists motion of thelead tip 30 in the distal direction. As shown inFIG. 9C , theloops 34 folds down into down onto thelead body 28 so that it can more easily slide thru a catheter (not shown) andvessels 25, or deploy in a more predictable manner. Theloop biasing feature 32 may optionally includeholes 47 located in the necked downregion 46 to facilitate removal of thelead assembly 10. Although the embodiments illustrated inFIGS. 8A-8B and 9A-9C show twoloops 34, theloop biasing feature 32 could haveadditional loops 34 having any desired shape and optionally including a neckeddown region 46, ahole 47, or anotch 49. - The
lead assembly 10 may be delivered into thebranch vessel 25 with a variety of techniques as are known in the art, including through the use of a guide catheter and/or stylet.FIG. 10 shows an embodiment of thelead assembly 10 positioned for delivery into the branch vessel (not shown) through alumen 70 of aguide catheter 72. A stylet, guidewire, or another catheter (not shown) may be used to advance thelead assembly 10 through thelumen 70. As thelead assembly 10 passes through thelumen 70, theloop 34 flattens down against thelead body 28. Thus, the diameter of theguide catheter 72 may be sized smaller than the combined diameter of thelead body 28 and theloop 34. In one embodiment, as illustrated inFIG. 11 , agroove 74 is formed into anouter surface 76 of thelead body 28 to receive the flattenedloop 34. This further reduces the diameter of thelead assembly 10 and of theguide catheter 72. In the illustrated embodiment, thegroove 74 extends over theelectrode 31. In other embodiments, theloop biasing feature 32 may be positioned on thelead body 28 such that theloop 34 and/or thegroove 74 do not pass over the electrode 31 (not shown). -
FIGS. 12A and 12B show alead assembly 110 according to another embodiment of the invention. Thelead assembly 110 includes alead body 128 extending from aproximal end 129 adapted for coupling to a pulse generator (not shown) to adistal end 130 adapted for insertion into theheart 12. Anelectrode 131 is positioned at thedistal end 130 of thelead body 128. - The
lead assembly 110 further includes aloop biasing feature 132 at thedistal end 130 of thelead body 128. Theloop biasing feature 132 includes aloop 134 of cord, filament or cable material protruding from thelead body 128. In the illustrated embodiment, theloop 134 has adistal end 135 fixed to thelead body 128 by, for example, adhesive, a crimp tube, compressive fit, or any other suitable manner (not shown). Aproximal end 136 of theloop 134 is coupled to acord 180 extending through acord lumen 184 formed in thelead body 128. The proximal anddistal ends loop 134 exit and enter thecord lumen 184 through a pair ofports 188 in thelead body 128. Aproximal end 192 of thecord 180 is coupled to anoptional grasp feature 196. Apocket 198 is provided in anouter surface 176 of thelead body 128 for receiving thegrasp feature 196. Aslidable tube 193 is positioned over thelead body 128 for covering theproximal end 192 of thecord 180 and thepocket 198. In one embodiment, as illustrated inFIG. 11 , a groove 174 is formed in theouter surface 176 of thelead body 128 for receiving the flattenedloop 134. In an alternative embodiment where the loopdistal end 135 is fixed to thelead body 128 through an adhesive, crimp tube, compressive fit, or any other suitable manner, a tensile force applied to thecord 180 causes the loop distal end to detach, thus facilitating removal of thelead assembly 110. - In some embodiments, the
loop 134 and thecord 180 are not separate components, but rather theloop 134 is formed of a portion of thecord 180 which is sufficiently rigid to bias thelead body 128 towards theepicardium 27 and themyocardium 26. As previously discussed, in some embodiments,pharmaceutical agents 152 can be added to thelead assembly 110 to facilitate tissue in-growth into a tissue in-growth area 148 defined between theloop 134 and thelead body 128. Alternatively, thelead body 128 could include a surface treatment such as a plasma treatment. - The
loop 134 protrudes from thelead body 128 in such a manner as to engage thepericardial wall 27 a as previously described. Theloop biasing feature 132 thus biases theelectrode 131 towards themyocardial wall 26 a and also helps to fix thelead body 128 within the branch vessel 25 (not shown). A proximally directed force exerted on thegrasp feature 196, as illustrated byarrow 197, tensions thecord 180, thereby flattening theloop 134 towards thelead body 128 for implanting, revising or removing thelead assembly 110. Stated another way, thecord 180 permits theloop biasing feature 132 to be neutralized by reducing a distance d between theloop 134 and theexterior surface 176 of thelead body 128. In other embodiments, theloop 134 twists or bends on itself so as to flatten towards thelead body 128 during implantation. - The
cord 180 is typically formed of a lubricious material such as ethylene tetrafluoroethylene (ETFE), polytetrafluoroethylene (PTFE) or expanded polytetrafluoroethylene (ePTFE) or other strong polymer such as polyester, aramid, Kevlar®, or is coated with such a material so as to reduce friction between thecord 180 and thecord lumen 184. Examples of other suitable materials include coextruded PTFE/Kevlar®, and can be polymer coated cable or nitinol wire. This reduces the axial force necessary to tension thecord 180 so as to neutralize theloop biasing feature 132 and reposition or extract thelead assembly 110. -
FIG. 12B shows a cross-sectional view of thelead body 128, showing thecord 180 andcord lumen 184. As illustrated inFIG. 12B , thelead body 128 may includeadditional lumens 199 for uses such as delivery of payloads or receiving a conductive member. Thecord 180 and/or theelectrode 131 can be radio-opaque to allow the implanter to visualize deployment and electrode orientation with respect to themyocardial wall 26 a to provide optimal or desirable orientation. - In the embodiment illustrated in
FIG. 12A , theloop 134 is preformed with the curvature shown. Theloop 134 is thus biased outwardly into the loop shape protruding from thelead body 128 by virtue of the preformed curvature. In other embodiments, theloop 134 may be preformed with different shapes than that shown inFIG. 12A . For example, theloop 134 may be preformed with multiple curvatures (as shown inFIG. 13 ), or may have a variable cross-section along the length of the loop 134 (not shown). In alternative embodiments, theloop 34 can have a thickness such that theloop 34 shields or otherwise insulates a portion of theelectrode 31 to prevent stimulation of the nerves located near thepericardium 27 and coronary vessels or the diaphragm (not shown). - In yet another embodiment, the
loop 134 is biased outward by aspring mechanism 195, as illustrated inFIG. 14 . Thespring mechanism 195 is shown in a window view inFIG. 14 for illustrative purposes only. Theloop 134 is connected to thespring mechanism 195 such that theloop 134 is biased distally, or outwardly, from thelead body 128. Thespring 195 can optionally be coupled to acord 180 extending through thelumen 184. In the embodiment ofFIG. 14 , a proximally directed tensioning force on thecord 180 flattens theloop 134, thus aiding in removal of thelead assembly 110 from thevessel 25. - In the embodiment shown in
FIG. 15 , thespring 195 is located at thedistal tip 130 of thelead assembly 110 and surrounding aportion 196 of theloop 134. Thespring 195 pushes theloop 134 distally or outwardly. In the illustrated embodiment, theloop 134 can optionally be coupled to acord 180 extending through thelumen 184. As discussed with respect toFIG. 14 , application of a proximally directed tensioning force to thecord 180 flattens theloop 134, thereby aiding in removal of thelead assembly 110 from thevessel 25. In an alternative embodiment, the lead assembly does not include thespring 195. Theloop biasing feature 132 itself can be stiff enough to provide a biasing force. In this embodiment, theloop 134 can be optionally coupled to acord 180 extending through alumen 184 for lead removal as described with respect toFIG. 14 . Thelead assembly 110 may includemultiple loops 134 and theloops 134 may be preformed with multiple curvatures. The loop biasing features 132 may include any combination of necked downregions 146, holes 147, or notches 149. - Various modifications and additions can be made to the exemplary embodiments discussed without departing from the scope of the present invention. For example, while the embodiments described above refer to particular features, the scope of this invention also includes embodiments having different combinations of features and embodiments that do not include all of the described features. Accordingly, the scope of the present invention is intended to embrace all such alternatives, modifications, and variations as fall within the scope of the claims, together with all equivalents thereof.
Claims (20)
1. A method of implanting a lead in a coronary vessel of the heart, the coronary vessel having a pericardial wall portion and a myocardial wall portion, the method comprising:
providing a lead body extending from a proximal end adapted for coupling to a pulse generator to a distal end adapted for implantation in the heart, a pace/sense electrode positioned at the distal end of the lead body, and a loop biasing feature located at the distal end of the lead body, the loop biasing feature including a resilient loop;
compressing the resilient loop towards the lead body by inserting the lead into a guide catheter;
advancing the distal end of the lead body into the coronary vessel to a fixation location; and
biasing the pace/sense electrode towards the myocardial wall portion of the coronary vessel by engaging the loop biasing feature.
2. The method of claim 1 , further comprising engaging the loop biasing feature by removing the catheter.
3. The method of claim 1 , further comprising revising the implantation location by tensioning a cord coupled to the loop biasing feature.
4. The method of claim 1 , wherein the loop biasing feature further comprises a predefined break region, and the method further comprises breaking the predefined break region in order to remove the lead body.
5. The method of claim 4 , wherein the predefined break location comprises a necked down region, and breaking the predefined break region comprises breaking the necked down region.
6. The method of claim 1 , wherein the loop biasing feature further comprises a collar for coupling the loop biasing feature to the lead body.
7. The method of claim 6 , wherein the lead body further comprises a groove configured to accommodate the collar.
8. The method of claim 1 , wherein the loop biasing feature further includes a fixation structure.
9. The method of claim 1 , wherein the loop biasing feature further includes a plurality of resilient loops.
10. A method of implanting a lead in a coronary vessel of the heart, the coronary vessel having a pericardial wall portion and a myocardial wall portion, the method comprising:
providing a lead body extending from a proximal end adapted for coupling to a pulse generator to a distal end adapted for implantation in the heart, an electrode positioned at the distal end of the lead body, and a loop biasing feature located at the distal end of the lead body, the loop biasing feature including a resilient loop, the loop biasing feature including a collar for coupling the loop biasing feature to the lead body, the lead body including a groove to accommodate the collar;
compressing the resilient loop towards the lead body by inserting the lead into a guide catheter;
advancing the distal end of the lead body into the coronary vessel to a fixation location; and
biasing the electrode towards the myocardial wall portion of the coronary vessel by engaging the loop biasing feature.
11. The method of claim 10 , further comprising engaging the loop biasing feature by removing the catheter.
12. The method of claim 10 , further comprising revising the implantation location by tensioning a cord coupled to the loop biasing feature.
13. The method of claim 10 , wherein the loop biasing feature further comprises a predefined break region, and the method further comprises breaking the predefined break region in order to remove the lead body.
14. The method of claim 13 , wherein the predefined break location comprises a necked down region, and breaking the predefined break region comprises breaking the necked down region.
15. The method of claim 10 , wherein the loop biasing feature further includes a fixation structure.
16. The method of claim 10 , wherein the loop biasing feature further includes a plurality of resilient loops.
17. A method of implanting a lead in a branch vessel of the coronary sinus, the branch vessel having a pericardial wall portion and a myocardial wall portion, the method comprising:
providing a lead body extending from a proximal end adapted for coupling to a pulse generator to a distal end adapted for implantation in the heart, a pace/sense electrode positioned at the distal end of the lead body, and a loop biasing feature located at the distal end of the lead body, the loop biasing feature including a resilient loop;
compressing the resilient loop towards the lead body by inserting the lead into a guide catheter;
advancing the distal end of the lead body into the branch vessel to a fixation location; and
biasing the pace/sense electrode towards the myocardial wall portion of the branch vessel by engaging the loop biasing feature.
18. The method of claim 17 , further comprising engaging the loop biasing feature by removing the catheter.
19. The method of claim 17 , wherein the electrode comprises a pace/sense electrode.
20. The method of claim 17 , wherein the loop biasing feature further comprises a necked down region defining a predefined break region, and the method further comprises breaking the necked down region in order to remove the lead body.
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US11/548,838 US7865248B2 (en) | 2006-06-15 | 2006-10-12 | Biasing and fixation features on leads |
US12/952,885 US20110071609A1 (en) | 2006-06-15 | 2010-11-23 | Biasing and fixation features on leads |
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US10456581B2 (en) | 2015-11-20 | 2019-10-29 | Cardiac Pacemakers, Inc | Single pass coronary venous lead for multiple chamber sense and pace |
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US8532790B2 (en) * | 2010-04-13 | 2013-09-10 | Medtronic, Inc. | Slidable fixation device for securing a medical implant |
US8478431B2 (en) * | 2010-04-13 | 2013-07-02 | Medtronic, Inc. | Slidable fixation device for securing a medical implant |
WO2012149511A2 (en) | 2011-04-28 | 2012-11-01 | Synecor Llc | Neuromodulation systems and methods for treating acute heart failure syndromes |
AU2012299373A1 (en) | 2011-07-11 | 2014-02-27 | Interventional Autonomics Corporation | System and method for neuromodulation |
US20130072995A1 (en) | 2011-07-11 | 2013-03-21 | Terrance Ransbury | Catheter system for acute neuromodulation |
US9446240B2 (en) | 2011-07-11 | 2016-09-20 | Interventional Autonomics Corporation | System and method for neuromodulation |
US11219775B2 (en) * | 2018-05-01 | 2022-01-11 | Cardiac Pacemakers, Inc. | Retention mechanism for an implantable lead |
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US10456581B2 (en) | 2015-11-20 | 2019-10-29 | Cardiac Pacemakers, Inc | Single pass coronary venous lead for multiple chamber sense and pace |
Also Published As
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US7865248B2 (en) | 2011-01-04 |
US20070293925A1 (en) | 2007-12-20 |
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