Single-pass A-V lead for pacing with stimulation of right ventricular outflow tract

Claim 2

A single-pass A-V lead for producing an improved sequence of activation for use in a dual-chamber cardiac pacemaker comprising: an insulated lead body having a proximal end for connection to a pacemaker and a distal end for placement within the heart, the lead body having at least one lumen adapted for the insertion of a stylet, the lumen extending axially from an exit port at the proximal end; a right ventricular outflow tract (RVOT) pacing electrode at the distal tip of the lead body and electrically connected to a first conductor that extends within the lead body to the proximal end; an atrial electrode on the lead body and positioned in spaced relationship to the distal tip, the atrial electrode connected to a second conductor that extends within the lead body to the proximal end; and the lead body comprising a preformed ventricular portion that assumes a curved configuration when the stylet is withdrawn from the lumen, the curvature of the preformed ventricular portion being sufficient to bias the RVOT electrode against a wall of the RVOT so that ventricular stimulation occurs using the RVOT pacing electrode which results in a fastener sequence of activation than apical stimulation.

Claim 3

The single-pass A-V lead, as defined in claim 1, wherein the lead body further comprises a preformed atrial portion that forms a laterally projecting bow when the stylet is withdrawn from the lumen, the atrial electrode being located substantially at an outward facing surface of the bow, and wherein the preformed ventricular portion is oriented relative to the preformed atrial portion so as to urge the RVOT electrode generally toward the atrial electrode when the stylet is withdrawn.

Claim 4

The single-pass A-V lead, as defined in claim 2, wherein the preformed atrial and ventricular portions are configured such that heart tissue separating the RVOT and right atrium is squeezed between the RVOT and atrial electrodes when the stylet is withdrawn.

Claim 5

The single-pass A-V lead, as defined in claim 2, wherein the preformed atrial and ventricular portions are configured such that, when the stylet is withdrawn, the atrial electrode is urged against the interatrial septum and the RVOT electrode is urged against a wall of the RVOT that is adjacent to the aorta.

Claim 6

The single-pass A-V lead, as defined in claim 2, wherein the lead body is configured such that, when the stylet is withdrawn, the laterally projecting bow and a major curve of the preformed ventricular portion fall generally within a single plane.

Claim 7

The single-pass A-V lead, as defined in claim 2, wherein the lead body is configured such that, when the stylet is withdrawn, the laterally projecting bow falls generally within a first plane, and wherein a major curve of the preformed ventricular portion falls generally within a second plane.

Claim 8

The single-pass A-V lead, as defined in claim 6, wherein the first and second planes are rotated between 30 and 90 degrees relative to one another.

Claim 9

The single-pass A-V lead, as defined in claim 6, wherein the lead body further comprises an inward bend within a last 1.5 centimeter ventricular portion thereof, the inward bend projecting the RVOT electrode out of the second plane.

Claim 10

The single-pass A-V lead, as defined in claim 2, wherein the preformed atrial and ventricular portions are configured to fall generally within respective first and second planes such that heart tissue separating the RVOT and right atrium is squeezed between the RVOT and atrial electrodes when the stylet is withdrawn.

Claim 11

The single-pass A-V lead, as defined in claim 2, wherein the distal end of the lead body is unbranched, the atrial electrode is formed in-line with the lead body, and wherein an inward-facing surface of the atrial electrode is coated with an insulating material to prevent discharge of current into the bloodstream.

Claim 12

The single-pass A-V lead, as defined in claim 1, wherein the lead body further comprises a preformed atrial portion, and wherein the preformed atrial and ventricular portions are configured so as to urge the RVOT electrode and the atrial electrode in opposing directions when the stylet is withdrawn to thereby generate a biasing force to hold the atrial and RVOT electrodes in position.

Claim 13

The single-pass A-V lead, as defined in claim 11, wherein the preformed atrial portion forms a laterally projecting bow when the stylet is withdrawn from the lumen, and wherein the atrial electrode is located substantially at an outwardly facing surface of the bow.

Claim 14

The single-pass A-V lead, as defined in claim 11, wherein the preformed atrial and ventricular portions are configured such that the atrial electrode presses against the right atrial free wall of the heart.

Claim 15

The single-pass A-V lead, as defined in claim 11, wherein the distal end of the lead body is unbranched, the atrial electrode is formed in-line with the lead body, and wherein an inward-facing surface of the atrial electrode is coated with an insulating material to reduce unnecessary discharge of current into the bloodstream.

Claim 16

The single-pass A-V lead, as defined in claim 1 wherein the lead body has an atrial branch and a ventricular branch and has a first lumen adapted for the insertion of a first stylet and a second lumen adapted for the insertion of a second stylet, the first lumen extending axially from a first exit port at the proximal end into the atrial branch and the second lumen extending axially from a second exit port at the proximal end into the ventricular branch, and wherein the atrial electrode is located at the distal tip of the atrial branch and the RVOT electrode is located at the distal tip of the ventricular branch, and wherein the preformed ventricular portion of the lead body is formed in the ventricular branch and assumes the curved configuration when the second stylet is withdrawn from the second lumen.

Claim 17

The single-pass A-V lead, as defined in claim 15, wherein the atrial branch comprises a preformed portion that assumes a curved configuration when the first stylet is withdrawn from the atrial branch, the curvature of the preformed portion of the atrial branch being sufficient to bias the atrial electrode against a wall of the right atrium.

Claim 18

A single-pass A-V lead for implantation within a human heart, comprising: an insulated lead body having a proximal end for connection to a pacemaker and an unbranched distal end for placement within the heart, the lead body having a lumen adapted for the insertion of a stylet, the lumen extending axially from an exit port at the proximal end substantially to the distal end; a ventricular electrode at the distal tip of the lead body and electrically connected to a first conductor that extends within the lead body to the proximal end; and a curved, atrial electrode formed in-line with the lead body, the atrial electrode located at a prebent, atrial portion of the lead body that forms a laterally projecting bow when the stylet is withdrawn such that the atrial electrode is pressed against a wall of the atrium, and wherein an inward-facing surface of the atrial electrode is coated with an insulating material to reduce discharge of current into the bloodstream and to thereby consume battery life of a pacemaker to which the single-pass A-V lead connects.

Claim 19

A single-pass A-V lead for implantation within a human heart, comprising: an insulated lead body having a proximal end for connection to a pacemaker and an unbranched distal end for placement within the heart, the lead body having a lumen adapted for the insertion of a stylet, the lumen extending axially from an exit port at the proximal end substantially to the distal end; a ventricular electrode at the distal tip of the lead body and electrically connected to a first conductor that extends within the lead body to the proximal end; and a curved, atrial electrode formed in-line with the lead body, the atrial electrode located at a prebent, atrial portion of the lead body that forms a laterally projecting bow when the stylet is withdrawn such that the atrial electrode is pressed against a wall of the atrium, and wherein an inward-facing surface of the atrial electrode is coated with an insulating material to reduce discharge of current into the bloodstream and to thereby consume battery life of a pacemaker to which the single-pass A-V lead connects.

Claim 20

The single-pass A-V lead, as defined in claim 17, wherein the lead body comprises a prebent ventricular portion adapted to project the ventricular electrode against a wall of the right ventricular outflow tract.

Claim 21

The single-pass A-V lead, as defined in claim 18, wherein the prebent ventricular portion forms a loop when the stylet is withdrawn in free space.

Claim 22

The single-pass A-V lead, as defined in claim 19, wherein the laterally projecting bow falls generally within a first plane and the loop falls generally within a second plane.

Claim 23

The single-pass A-V lead, as defined in claim 20, wherein the first and second planes are rotated between 30 and 90 degrees relative to one another.

Claim 24

A single-pass A-V lead for implantation within a human heart, comprising: an insulated lead body having a proximal end for connection to a pacemaker and a branched distal end having an atrial branch and a ventricular branch, the lead body having a first lumen adapted for the insertion of a first stylet, the first lumen extending axially from a first exit port at the proximal end into the atrial branch, the lead body also having a second lumen adapted for the insertion of a second stylet, the second lumen extending axially from a second exit port at the proximal end into the atrial branch; an atrial electrode on the atrial branch and electrically connected to a first conductor that extends within the lead body to the proximal end; means for biasing the atrial electrode against a wall of the right atrium, the means for biasing comprising a preformed portion of the atrial branch that assumes a curved configuration when the first stylet is withdrawn from the atrial branch; a right ventricular outflow tract (RVOT) electrode on the ventricular branch and electrically connected to a second conductor that extends within the lead body to the proximal end; and means for positioning the RVOT electrode against a wall of the RVOT, the means comprising a preformed portion of the ventricular branch that assumes a curved configuration when the second stylet is withdrawn from the ventricular branch.

Claim 25

A single-pass A-V lead for implantation within a human heart, comprising: an insulated lead body having a proximal end for connection to a pacemaker and a branched distal end having an atrial branch and a ventricular branch, the lead body having a first lumen adapted for the insertion of a first stylet, the first lumen extending axially from a first exit port at the proximal end into the atrial branch, the lead body also having a second lumen adapted for the insertion of a second stylet, the second lumen extending axially from a second exit port at the proximal end into the atrial branch; an atrial electrode on the atrial branch and electrically connected to a first conductor that extends within the lead body to the proximal end; means for biasing the atrial electrode against a wall of the right atrium, the means for biasing comprising a preformed portion of the atrial branch that assumes a curved configuration when the first stylet is withdrawn from the atrial branch; a right ventricular outflow tract (RVOT) electrode on the ventricular branch and electrically connected to a second conductor that extends within the lead body to the proximal end; and means for positioning the RVOT electrode against a wall of the RVOT, the means comprising a preformed portion of the ventricular branch that assumes a curved configuration when the second stylet is withdrawn from the ventricular branch.

Claim 26

The single-pass A-V lead, as defined in claim 22, wherein the preformed portion of the atrial branch is configured so as to bias the atrial electrode against the right atrial appendage of the heart.

Claim 27

The single-pass A-V lead, as defined in claim 22, wherein the preformed portion of the ventricular branch is configured so as to bias the RVOT electrode against the wall in a direction generally toward the right atrium of the heart.

Claim 28

The single-pass A-V lead, as defined in claim 22, wherein the preformed portion of the ventricular branch is configured to substantially form a loop when the second stylet is withdrawn.

Claim 31

The method, as defined in claim 26, wherein the first force and the second force are substantially equal in magnitude and opposite in direction.

Claim 32

The method, as defined in claim 26, wherein the step of maintaining comprises applying the first force and the second force to opposing sides of a septal wall that separates the right atrium from the RVOT.

Claim 33

The method, as defined in claim 26, wherein the step of maintaining comprises applying the first force to the right atrial free wall and the second force to the interventricular septum.

Claim 34

A pacing lead for providing an improved sequence of activation, comprising: an insulated lead body having a proximal end for connection to a pacemaker and a distal end for placement within a human heart, the lead body having at least one lumen adapted for the insertion of a stylet, the lumen extending axially from an exit port at the proximal end; and a right ventricular outflow tract (RVOT) pacing electrode at the distal tip of the lead body and electrically connected to a conductor that extends within the lead body to the proximal end; wherein a ventricular portion of the lead body is preformed to assume a curved configuration when the stylet is withdrawn from the lumen, and wherein the preformed ventricular portion is configured to position the RVOT electrode within the RVOT when the lead is properly implanted within the human heart so that ventricular stimulation occurs using the RVOT pacing electrode which results in a fastener sequence of activation than apical stimulation.

Claim 35

A pacing lead for providing an improved sequence of activation, comprising: an insulated lead body having a proximal end for connection to a pacemaker and a distal end for placement within a human heart, the lead body having at least one lumen adapted for the insertion of a stylet, the lumen extending axially from an exit port at the proximal end; and a right ventricular outflow tract (RVOT) pacing electrode at the distal tip of the lead body and electrically connected to a conductor that extends within the lead body to the proximal end; wherein a ventricular portion of the lead body is preformed to assume a curved configuration when the stylet is withdrawn from the lumen, and wherein the preformed ventricular portion is configured to position the RVOT electrode within the RVOT when the lead is properly implanted within the human heart so that ventricular stimulation occurs using the RVOT pacing electrode which results in a fastener sequence of activation than apical stimulation.

Claim 36

A pacing lead, as in claim 30, wherein the preformed ventricular portion is configured to bias the RVOT electrode against a wall of the RVOT when the lead is properly implanted within the human heart.

Claim 37

A pacing lead, as in claim 31, further comprising an atrial electrode on an atrial portion of the lead, the atrial portion being preformed to assume a curved configuration when the stylet is withdrawn from the lumen, the atrial portion being configured to bias the atrial electrode against a wall of the right atrium of the heart to thereby generate a counteracting force for biasing the RVOT electrode against the wall of the RVOT.

Claim 40

The method, as defined in claim 33, wherein the step of withdrawing comprises biasing the electrode against a wall of the RVOT to thereby maintain the electrode in position within the RVOT.

Claim 41

The method, as defined in claim 34, wherein the pacing lead further comprises an atrial electrode on an atrial portion thereof, the atrial portion being preformed to assume a curved configuration when the stylet is withdrawn from the lumen, and wherein the method further comprises the step of biasing the atrial electrode against a wall of the right atrium of the heart to thereby provide a counteracting force the biasing of the electrode against the wall of the RVOT.