Intravenous channel cardiac electrode and lead assembly and method

Claim 2

A lead assembly for intravenously conducting electrical signals to or from a patient's heart, the lead assembly comprising in combination: a. a core lead having first and second ends, said core lead including i. first flexible sleeve means; ii. a first conductor surrounded by material of said first flexible sleeve means, said first conductor extending approximately between the first and second ends of said core lead; iii. first electrode means attached to said first flexible sleeve means approximately at the first end of said core lead, said first electrode means being electrically connected to said first conductor; b. a first removable stylet extending through said first flexible sleeve means to facilitate control of said core lead, said core lead being preformed to tend to assume a straight configuration when said first stylet is removed from said core lead; c. a channel lead having first and second ends, said channel lead including i. second flexible sleeve means, said second flexible sleeve means having an elongated channel for receiving said core lead, said channel extending through a major portion of the length of said channel lead, said channel extending from a first opening in said channel lead to a second opening in said channel lead, said first opening being located at said first end of said channel lead, said second opening being a side port opening located a first predetermined distance from said second end of said channel lead; ii. a second conductor surrounded by material of said second flexible sleeve means, said second conductor being disposed outside of said channel and extending approximately between the first and second ends of said second flexible sleeve means; iii. second electrode means attached to said second flexible sleeve means approximately at the first end of said channel lead, said second electrode means being electrically connected to said second conductor; and d. a second removable stylet extending through said second flexible sleeve means to facilitate control of said channel lead, said core lead being disposed in said channel of said channel lead, the first end of said core lead extending from said first opening and the second end of said core lead extending from said second opening, said first opening being located within the patient's heart when said channel lead is positioned to conduct the electrical signals to a predetermined portion of the patient's heart, said channel lead being performed to tend to assume a bent, J-shaped configuration located approximately at the location of said side port opening to cause said second end of said channel lead to move into the atrial appendage of the patient's heart when said second stylet is removed, said side port opening being located near the lowest portion of said bent, J-shaped configuration when the second end of said channel lead is in the highest or superior portion of the atrial appendage, said core lead extending through said side port opening deep into the right ventricle of the patient's heart.

Claim 3

The lead assembly of claim 1 wherein said first and second flexible sleeve means are composed of silicone rubber.

Claim 4

The lead assembly of claim 2 wherein said first conductor means is a helically wound coil conductor.

Claim 5

The lead assembly of claim 2 wherein said core lead and said channel lead each include a circumferential sealing ring of silicone rubber extending from said first and second flexible sleeve means adjacent the second ends of said core lead and said channel lead, respectively, for sealing said core lead and said channel lead to receptacles of an electronic signal producing and/or receiving apparatus.

Claim 6

The lead assembly of claim 2 wherein the second end of said channel lead is divided into first and second branches, said channel extending through the first branch, said lead assembly including ties for tightening silicone rubber material of said first branch against said core lead to form a seal between the silicone rubber material of said first branch and the silicone rubber material of said core lead to prevent blood from seeping from the patient's heart through said channel.

Claim 7

The lead assembly of claim 2 wherein said core lead and said channel lead are both bipolar leads.

Claim 8

The lead assembly of claim 1 wherein said core lead further includes third electrode means electrically connected to said first conductor at the second end of said core lead for electrically connecting said core lead to an electronic signal sending and/or receiving apparatus, and wherein said channel lead further includes fourth electrode means electrically connected to said second conductor at the second end of said channel lead.

Claim 9

A lead assembly for intravenously conducting electrical signals to or from a patient's heart, the lead assembly comprising in combination: a. a core lead having first and second ends, said core lead including i. first flexible sleeve means; ii. a first conductor surrounded by material of said first flexible sleeve means, said first conductor extending approximately between the first and second ends of said core lead; iii. first electrode means attached to said first flexible sleeve means approximately at the first end of said core lead, said first electrode means being electrically connected to said first conductor; b. a first removable stylet extending through said first flexible sleeve means to facilitate control of said core lead, said core lead being preformed to tend to assume a straight configuration when said first stylet is removed from said core lead; c. a channel lead having first and second ends, said channel lead including i. second flexible sleeve means, said second flexible sleeve means having an elongated channel for receiving said core lead, said channel extending through a major portion of the length of said channel lead, said channel extending from a first opening in said channel lead, said first opening being located at said first end of said channel lead, said second opening being a side port opening located a first predetermined distance from said second end of said channel lead; iii. a second conductor surrounded by material of said second flexible sleeve means, said second conductor being disposed outside of said channel and extending approximately between the first and second ends of said second flexible sleeve means; iii. second electrode means attached to said second flexible sleeve means approximately at the first end of said channel lead, said second electrode means being electrically connected to said second conductor; and d. a second removable stylet extending through said second flexible sleeve means to facilitate control of said channel lead, said core lead being disposed in said channel of said channel lead, the first end of said core lead extending from said first opening and the second end of said core lead extending from said second opening, said first opening being located within the patient's heart when said channel lead is positioned to conduct the electrical signals to a predetermined portion of the patient's heart, said channel lead being preformed to tend to assume a bent, L-shaped configuration located approximately at the location of said side port opening to cause said second end of said channel lead to move into the coronary sinus of the patient's heart when said second stylet is removed, said side port opening being located near the entrance to the coronary sinus when the second end of said channel lead is in the deepest portion of the coronary sinus, said core lead extending through said side port opening deep into the right ventricle of the patient's heart.

Claim 10

A lead assembly for intravenously conducting electrical signals to or from a patient's heart, the lead assembly comprising in combination: a. a core lead having first and second ends, said core lead including i. first flexible sleeve means; ii. a first conductor surrounded by material of said first flexible sleeve means, said first conductor extending approximately between the first and second ends of said core lead; iii. first electrode means attached to said first flexible sleeve means approximately at the first end of said core lead, said first electrode means being electrically connected to said first conductor; b. a first removable stylet extending through said first flexible sleeve means to facilitate control of said core lead, said core lead being preformed to tend to assume a straight configuration when said first stylet is removed from said core lead; c. a channel lead having first and second ends, said channel lead including i. second flexible sleeve means, said second flexible sleeve means having an elongated channel for receiving said core lead, said channel extending through a major portion of the length of said channel lead, said channel extending from a first opening in said channel lead, said first opening being located at said first end of said channel lead, said second opening being a side port opening located a first predetermined distance from said second end of said channel lead; iii. a second conductor surrounded by material of said second flexible sleeve means, said second conductor being disposed outside of said channel and extending approximately between the first and second ends of said second flexible sleeve means; iii. second electrode means attached to said second flexible sleeve means approximately at the first end of said channel lead, said second electrode means being electrically connected to said second conductor; and d. a second removable stylet extending through said second flexible sleeve means to facilitate control of said channel lead, said core lead being disposed in said channel of said channel lead, the first end of said core lead extending from said first opening and the second end of said core lead extending from said second opening, said first opening being located within the patient's heart when said channel lead is positioned to conduct the electrical signals to a predetermined portion of the patient's heart, said channel lead being preformed to tend to assume a bent, L-shaped configuration located approximately at the location of said side port opening to cause said second end of said channel lead to move into the coronary sinus of the patient's heart when said second stylet is removed, said side port opening being located near the entrance to the coronary sinus when the second end of said channel lead is in the deepest portion of the coronary sinus, said core lead extending through said side port opening deep into the right ventricle of the patient's heart.

Claim 13

The method of claim 9 further including the step of sealing the channel of the channel lead to the core lead to prevent sliding of the core lead in the channel and to prevent leakage of blood from the heart through the channel.

Claim 14

The method of claim 9 including the step of sealing the channel lead to the vein prior to step (e) to prevent sliding of the channel lead in the vein and to prevent loss of blood from the heart through the incision.

Claim 19

The method of claim 13 wherein said sterile intravenous solution is normal saline solution.

Claim 22

c. guiding the first end of the channel lead through a venous path to the entrance of a first predetermined cavity of the patient's heart; d. withdrawing a stylet from the channel lead, the channel lead being preformed to assume a bent configuration with a bend located approximately at the location of said side port opening when the stylet is withdrawn in order to direct the first end of the core lead into said predetermined cavity in the patient's heart adjacent to said venous path, said channel lead being preformed to tend to assume said bent configuration to cause the second end of said channel lead to move into said predetermined cavity of the patient's heart when the stylet is removed, said side port opening being located near the lowest portion of said bend when the second end of said channel lead is in the deepest portion of said predetermined cavity; e. guiding the first end of said channel lead deep into said predetermined cavity; and f. guiding the first end of said core lead through the channel, out of said side port opening, into the right ventrical of the patient's heart.

Claim 23

c. guiding the first end of the channel lead through a venous path to the entrance of a first predetermined cavity of the patient's heart; d. withdrawing a stylet from the channel lead, the channel lead being preformed to assume a bent configuration with a bend located approximately at the location of said side port opening when the stylet is withdrawn in order to direct the first end of the core lead into said predetermined cavity in the patient's heart adjacent to said venous path, said channel lead being preformed to tend to assume said bent configuration to cause the second end of said channel lead to move into said predetermined cavity of the patient's heart when the stylet is removed, said side port opening being located near the lowest portion of said bend when the second end of said channel lead is in the deepest portion of said predetermined cavity; e. guiding the first end of said channel lead deep into said predetermined cavity; and f. guiding the first end of said core lead through the channel, out of said side port opening, into the right ventrical of the patient's heart.

Claim 24

A lead assembly for intravenously conducting electrical signals through a venous path to or from a patient's heart, the lead assembly comprising in combination: a. a core lead having first and second ends, said core lead including i. first flexible sleeve means; ii. a first conductor surrounded by material of said first flexible sleeve means, said first conductor extending approximately between the first and second ends of said core lead; iii. first electrode means attached to said first flexible sleeve means approximately at the first end of said core lead, said first electrode means being electrically connected to said first conductor; b. a first removable stylet extending through said first flexible sleeve means to facilitate control of said core lead, said core lead being preformed to tend to assume a straight configuration when said first stylet is removed from said core leads; c. a channel lead having first and second ends, said channel lead including i. second flexible sleeve means, said second flexible sleeve means having an elongated channel for receiving said core lead, said channel extending through a major portion of the length of said channel lead, said channel extending from a first opening in said channel lead to a second opening in said channel lead, said first opening being located at said first end of said channel lead, said second opening being a side port opening located a first predetermined distance from said second end of said channel lead; ii. a second conductor surrounded by material of said second flexible sleeve means, said second conductor being disposed outside of said channel and extending approximately between the first and second ends of said second flexible sleeve means; iii. second electrode means attached to said second flexible sleeve means approximately at the first end of said channel lead, said second electrode means being electrically connected to said second conductor; and d. a second removable stylet extending through said second flexible sleeve means to facilitate control of said channel lead, said core lead being disposed in said channel lead, the first end of said core lead extending from said first opening and the second end of said core lead extending from said second opening, said first opening being located within the patient's heart when said channel lead is positioned to conduct the electrical signals to a predetermined portion of the patient's heart, said channel lead being preformed to tend to assume a bent configuration located approximately at the location of said side port opening to cause said second end of said channel lead to move into a predetermined cavity in the patient's heart adjacent to said venous path when said second stylet is removed, said side port opening being located near the entrance to said predetermined cavity when the second end of said channel lead is in the deepest portion of said predetermined cavity, said core lead extending slidably through said side port opening deep into the right ventricle of the patient's heart.

Claim 25

A lead assembly for intravenously conducting electrical signals through a venous path to or from a patient's heart, the lead assembly comprising in combination: a. a core lead having first and second ends, said core lead including i. first flexible sleeve means; ii. a first conductor surrounded by material of said first flexible sleeve means, said first conductor extending approximately between the first and second ends of said core lead; iii. first electrode means attached to said first flexible sleeve means approximately at the first end of said core lead, said first electrode means being electrically connected to said first conductor; b. a first removable stylet extending through said first flexible sleeve means to facilitate control of said core lead, said core lead being preformed to tend to assume a straight configuration when said first stylet is removed from said core leads; c. a channel lead having first and second ends, said channel lead including i. second flexible sleeve means, said second flexible sleeve means having an elongated channel for receiving said core lead, said channel extending through a major portion of the length of said channel lead, said channel extending from a first opening in said channel lead to a second opening in said channel lead, said first opening being located at said first end of said channel lead, said second opening being a side port opening located a first predetermined distance from said second end of said channel lead; ii. a second conductor surrounded by material of said second flexible sleeve means, said second conductor being disposed outside of said channel and extending approximately between the first and second ends of said second flexible sleeve means; iii. second electrode means attached to said second flexible sleeve means approximately at the first end of said channel lead, said second electrode means being electrically connected to said second conductor; and d. a second removable stylet extending through said second flexible sleeve means to facilitate control of said channel lead, said core lead being disposed in said channel lead, the first end of said core lead extending from said first opening and the second end of said core lead extending from said second opening, said first opening being located within the patient's heart when said channel lead is positioned to conduct the electrical signals to a predetermined portion of the patient's heart, said channel lead being preformed to tend to assume a bent configuration located approximately at the location of said side port opening to cause said second end of said channel lead to move into a predetermined cavity in the patient's heart adjacent to said venous path when said second stylet is removed, said side port opening being located near the entrance to said predetermined cavity when the second end of said channel lead is in the deepest portion of said predetermined cavity, said core lead extending slidably through said side port opening deep into the right ventricle of the patient's heart.