Method of supplying energy to subcutaneous cardioverter-defibrillator and pacer
A power supply for an implantable cardioverter-defibrillator for subcutaneous positioning between the third rib and the twelfth rib and for providing cardioversion/defibrillation energy to the heart, the power supply comprising a capacitor subsystem for storing the cardioversion/defibrillation energy for delivery to the patient's heart; and a battery subsystem electrically coupled to the capacitor subsystem for providing electrical energy to the capacitor subsystem.
1. A method of supplying energy for alleviating a cardiac dysfunction, the method comprising:
implanting a device having a power source and an energy storage system into a patient;
providing a lead system having one or more electrodes for the device, the lead system provided such that it is disposed internally to a patient without contacting the patient's heart;
coupling the power source to the energy storage system;
storing energy in the energy storage system; and
discharging the energy from the energy storage system to the patient the step of discharging the energy including using at least one electrode disposed in the lead system;
wherein the step of discharging the energy uses a first electrode tat is part of the lead system and a second electrode disposed on the device itself, wherein the amount of energy discharged is selected to achieve a pacing function.
2. A method of supplying energy for alleviating a cardiac dysfunction, the method comprising:
implanting a device having a power source and an energy storage system into a patient;
providing a lead system having one or more electrodes for the device, the lead system provided such tat it is disposed internally to a patient without contacting the patient's heart;
coupling the power source to the energy storage system;
storing energy in the energy storage system; and
discharging the energy from the energy storage system to the patient, the step of discharging the energy including using at least one electrode disposed in the lead system;
wherein the step of discharging the energy uses only a first electrode that is part of the lead system and a means for dispensing current to tissue disposed on the device itself wherein the amount of energy discharged is selected to achieve a defibrillation function.
3. The method of claim 2 , further comprising determining whether the patient has an abnormally slow heart rate.
4. A method of supplying an electrical stimulus to a patient's heart comprising:
providing a lead assembly including a first electrode implanted in a patient, the lead assembly provided such that it does not contact the patient's heart;
providing a device including a battery and a means for storing energy, the device being coupled to the lead assembly;
providing a second electrode implanted such that it does not contact the patient's heart;
sensing far-field signals using a sensing electrode pair including the first electrode to monitor a portion of the patient's cardiac rhythm;
determining whether the patient's cardiac rhythm requires electrical therapy; and, if so:
supplying energy from the battery to the energy storage means; and
discharging energy stored in the energy storage means to the patient using a stimulus electrode pair including the second electrode; wherein:
the lead assembly includes a third electrode disposed such that it does not touch the heart;
the sensing electrode pair includes the first electrode and the second electrode; and
the stimulus electrode pair includes the second electrode and the third electrode.
5. A method of supplying energy for alleviating a cardiac dysfunction, the method comprising:
implanting a device having a power source and an energy storage system into a patient;
providing a lead system having one or more electrodes for the device, the lead system provided such that it is disposed internally to a patient without contacting the patient's heart;
coupling the power source to the energy storage system;
storing energy in the energy storage system; and
discharging the energy from the energy storage system to the patient, the step of discharging the energy including using at least one electrode disposed in the lead system;
wherein the step of implanting a device includes implanting the device at about the left axillary line.
6. The method of claim 5 , wherein the step of providing the lead system includes providing a lead extending medially from the device.
7. A method of supplying energy for alleviating a cardiac dysfunction, the method comprising:
implanting a device having a power source and an energy storage system into a patient;
providing a lead system having one or more electrodes for the device, the lead system provided such that it is disposed internally to a patient without contacting the patient's heart
coupling the power source to the energy storage system;
storing energy in the energy storage system; and
discharging the energy from the energy storage system to the patient, the step of discharging the energy including using at least one electrode disposed in the lead system;
wherein the step of implanting a device includes implanting the device approximately level with the cardiac apex.
8. A method of supplying energy for alleviating a cardiac dysfunction, the method comprising:
implanting a device having a power source and an energy storage system into a patient;
providing a lead system having one or more electrodes for the device, the lead system provided such that it is disposed internally to a patient without contacting the patient's heart;
coupling the power source to the energy storage system;
storing energy in the energy storage system; and
discharging the energy from the energy storage system to the patient, the step of discharging the energy including using at least one electrode disposed in the lead system;
wherein the step of implanting a device includes implanting the device along the inframammary crease.
9. A method of supplying an electrical stimulus to a patient's heart comprising:
providing a lead assembly including a first electrode implanted in a patient, the lead assembly provided such that it does not contact the patient's heart;
providing a device including a battery and a means for storing energy, the device being coupled to the lead assembly;
providing a second electrode implanted such that it does not contact the patient's heart;
sensing far-field signals using a sensing electrode pair including the first electrode to monitor a portion of the patient's cardiac rhythm;
determining whether the patient's cardiac rhythm requires electrical therapy; and, if so:
supplying energy from the battery to the energy storage means; and
discharging energy stored in the energy storage means to the patient using a stimulus electrode pair including the second electrode;
wherein the step of providing the lead system includes providing a lead extending medially from the device;
wherein the step of implanting a device includes implanting the device at about the left axiflary line.
10. The method of claim 9 , wherein the step of implanting a device includes implanting the device between approximately The third rib and the twelfth rib of the patient.
11. The method of claim 9 , wherein the step of implanting a device includes implanting the device approximately level with the cardiac apex.
12. The method of claim 9 , wherein the step of implanting a device includes implanting the device along the inframammary crease.
13. The method of claim 9 , wherein the step of providing a lead assembly includes providing the lead assembly outside of the patient's vasculature.
14. A method of supplying an electrical stimulus to a patient's heart comprising:
providing a lead assembly including a first electrode implanted in a patient outside of the patient's vasculature;
providing a device including a battery, means for storing energy and a housing having a second electrode thereon, the device being coupled to the lead assembly and placed between approximately the third rib and the twelfth rib of the patient at approximately the left axillary line along approximately the inframammary crease;
sensing far-field signals using a sensing electrode pair including the first electrode to monitor a portion of the patient's cardiac rhythm;
determining whether the patient's cardiac rhythm requires electrical therapy; and, if so:
supplying energy from the battery to the energy storage means; and
discharging energy stored in the energy storage means to the patient using a stimulus electrode pair including the second electrode.
15. The method of claim 14 , wherein:
the lead assembly includes a third electrode disposed outside of the patient's vasculature;
the sensing electrode pair includes the first electrode and the second electrode; and
the stimulus electrode pair includes the second electrode and the third electrode.