High-energy capacitors for implantable defibrillators

• US 6,556,863 B1
• Filed: 10/02/1998
• Issued: 04/29/2003
• Est. Priority Date: 10/02/1998
• Status: Expired due to Fees

• Current Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Original Assignee: Cardiac Pacemakers Incorporated (Boston Scientific Corporation)
• Inventors: Poplett, James M., Tong, Robert R., Christenson, Luke J., OʼPhelan, Michael J.
• Primary Examiner(s): LAYNO, CARL HERNANDZ
• Application Number:
  US09/165,779
• Time in Patent Office: 1,670 Days
• Field of Search: 607/4, 607/5, 29/250.3
• US Class Current: 607/5
• CPC Class Codes: A61N 1/3782 producing a voltage above the power source level
• CPC Class Codes: A61N 1/3956 Implantable devices for applying electric shocks to the heart, e.g. for cardioversion
• CPC Class Codes: H01G 9/045 based on aluminium
• CPC Class Codes: H01G 9/055 Etched foil electrodes
• CPC Class Codes: Y10T 428/12431 Foil or filament smaller than 6 mils

Abstract

Implantable defibrillators are implanted into the chests of patients prone to suffering ventricular fibrillation, a potentially fatal heart condition. A critical component in these devices is an aluminum electrolytic capacitors, which stores and delivers one or more life-saving bursts of electric charge to a fibrillating heart. To reduce the size of these devices, capacitor manufacturers have developed special aluminum foils, for example core-etched and tunnel-etched aluminum foils. Unfortunately, core-etched foils don'"'"'t work well in multiple-anode capacitors, and tunnel-etched foils are quite brittle and tend to break when making some common types of capacitors. Accordingly, the inventors devised a new foil structure having one or more perforations and one or more cavities with a depth less than the foil thickness. In an exemplary embodiment, each perforation and cavity has a cross-sectional area, with the perforations having a larger, for example, 2 to 100 times larger, average cross-sectional area than the cavities. Other embodiments of the invention include foil assemblies, capacitors, and implantable defibrillators that benefit from properties of the new foil structure.

Claims

1. A defibrillation or cardioversion device comprising:

one or more leads for sensing electrical signals of a patient or for applying electrical energy to the patient;

a monitoring circuit for monitoring heart activity of the patient through one or more of the leads; and

a therapy circuit for delivering electrical energy through one or more of the leads to a heart of the patient, wherein the therapy circuit includes one or more capacitors which include a foil that comprises;

first and second opposing surfaces which define a foil thickness, with the first opposing surface having one or more cavities each having a maximum depth less than the foil thickness and the second opposing surface having one or more cavities each having a maximum depth less than the foil thickness;

wherein the cavities of the first surface have a first average maximum depth and the cavities of the second surface have a second average maximum depth, with the first and second average maximum depths being less than one-half the foil thickness; and

one or more perforations through the foil

2. An implantable defibrillation or cardioversion device comprising:

one or more leads for sensing electrical signals of a patient or for applying electrical energy to the patient;

a monitoring circuit for monitoring heart activity of the patient through one or more of the leads; and

a therapy circuit for delivering electrical energy through one or more of the leads to a heart of the patient, wherein the therapy circuit includes one or more capacitors, with each capacitor including at least one foil that comprises;

first and second opposing sides each having one or more of cavities having an average depth less than one-half the foil thickness; and

three or more perforations through the foil, wherein the average cross-sectional area of the perforations is about 2 to 100 times larger than the average cross-sectional area of the cavities.

3. The device of claim 2, wherein the average depth of the cavities is about one-third or one-fourth of the foil thickness.

4. The device of claim 2 wherein each perforation has a generally circular cross-section.

5. The device of claim 2 wherein the one foil comprises at least one of aluminum, tantalum, hafnium, niobium, titanium, and zirconium.

6. The device of claim 4 wherein one or more of the cavities define a perimeter which circumscribes one or more of the perforations and wherein the foil is at least partly rolled.

7. The device of claim 2 wherein at least a portion of the one foil is rolled.

8. The device of claim 2 wherein the one foil is part of an anode structure.

9. An implantable defibrillation or cardioversion device comprising:

an electrical circuit including one or more capacitors, with each capacitor including at least one foil that comprises;

first and second opposing sides each having one or more of cavities having an average depth less than one-half the foil thickness; and

two or more perforations through the foil, wherein the average cross-sectional area of the perforations is about 2 to 100 times larger than the average cross-sectional area of the cavities.

11. The device of claim 9 wherein each perforation has a generally circular cross-section.

12. The device of claim 9 wherein the one foil comprises at least one of aluminum, tantalum, hafnium, niobium, titanium, and zirconium.

13. A method comprising:

providing at least a portion of defibrillation or cardioversion device; and

installing at least one capacitor in at least the portion of the defibrillator or cardioversion device, with the capacitor including one or more metal foils that comprise;

first and second opposing sides each having two or more of cavities having an average depth less than one-half the foil thickness; and

two or more perforations through the foil, wherein the average cross-sectional area of the perforations is about 2 to 100 times larger than the average cross-sectional area of the cavities.

10. The device of claim 14 wherein the average depth of the cavities is about one-third or one-fourth of the foil thickness.

14. The method of claim 13 wherein the average depth of the cavities is about one-third or one-fourth of the foil thickness.

15. A defibrillation or cardioversion device comprising:

one or more leads for sensing electrical signals of a patient or for applying electrical energy to the patient;

a monitoring circuit for monitoring heart activity of the patient through one or more of the leads; and

a therapy circuit for delivering electrical energy through one or more of the leads to a heart of the patient, wherein the therapy circuit includes one or more capacitors which include a foil that comprises;

first and second opposing surfaces which define a foil thickness, with the first opposing surface having one or more cavities each having a maximum depth less than the foil thickness and the second opposing surface having one or more cavities each having a maximum depth less than the foil thickness; and

one or more perforations through the foil, wherein the one or more perforations include at least three perforations and each of the perforations has an associated average maximum cross-sectional area between 500 square-microns and 32 square-millimeters, inclusive.

16. An implantable defibrillation or cardioversion device comprising:

one or more leads for sensing electrical signals of a patient or for applying electrical energy to the patient;

a monitoring circuit for monitoring heart activity of the patient through one or more of the leads; and

a therapy circuit for delivering electrical energy through one or more of the leads to a heart of the patient, wherein the therapy circuit includes one or more capacitors, with each capacitor including at least one foil that comprises;

first and second opposing sides each having one or more of cavities having an average depth less than one-half the foil thickness; and

three or more perforations through the foil, wherein the one or more perforations include at least three perforations and each of the perforations has an associated average maximum cross-sectional area between 500 square-microns and 32 square-millimeters, inclusive.

17. An implantable defibrillation or cardioversion device comprising:

an electrical circuit including one or more capacitors, with each capacitor including at least one foil that comprises;

first and second opposing sides each having one or more of cavities having an average depth less than one-half the foil thickness; and

two or more perforations through the foil, wherein the one or more perforations include at least three perforations and each of the perforations has an associated average maximum cross-sectional area between 500 square-microns and 32 square-millimeters, inclusive.

18. A method comprising:

providing at least a portion of defibrillation or cardioversion device; and

installing at least one capacitor in at least the portion of the defibrillator or cardioversion device, with the capacitor including one or more metal foils that comprise;

first and second opposing sides each having two or more of cavities having an average depth less than one-half the foil thickness; and

two or more perforations through the foil, wherein the two or more perforations include at least three perforations and each of the perforations has an associated average maximum cross-sectional area between 500 square-microns and 32 square-millimeters, inclusive.

19. An implantable cardiac rhythm management system comprising:

one or more leads for sensing electrical signals of a patient or for applying electrical energy to the patient;

a monitoring circuit for monitoring heart activity of the patient through one or more of the leads; and

a therapy circuit for delivering electrical energy through one or more of the leads to a heart of the patient, wherein the therapy circuit includes one or more capacitors, with each capacitor including;

one or more foil members comprising

first and second opposing sides each having one or more of cavities having an average depth less than one-half the foil thickness; and

means, including one or more perforations, for allowing flow of a liquid through the foil, with at least one of the perforations having no mounting member extending through it.

20. An implantable cardiac rhythm management system comprising:

one or more leads for sensing electrical signals of a patient or for applying electrical energy to the patient;

a monitoring circuit for monitoring heart activity of the patient through one or more of the leads; and

a therapy circuit for delivering electrical energy through one or more of the leads to a heart of the patient, wherein the therapy circuit includes one or more capacitors, with each capacitor including;

one or more foil members comprising

first and second opposing sides each having one or more of cavities having an average depth less than one-half the foil thickness; and

three or more perforations adapted for allowing flow of liquid through the foil.

21. An implantable cardiac rhythm management system comprising:

one or more leads for sensing electrical signals of a patient or for applying electrical energy to the patient;

a monitoring circuit for monitoring heart activity of the patient through one or more of the leads; and

a therapy circuit for delivering electrical energy through one or more of the leads to a heart of the patient, wherein the therapy circuit includes one or more capacitors, with each capacitor including;

one or more foil members comprising

first and second opposing sides each having one or more of cavities having an average depth less than one-half the foil thickness;

means, including three or more perforations, for allowing flow of a liquid through the foil, with at least one of the perforations having no mounting member extending through it; and

means between the first and second surfaces for enhancing durability.

22. An implantable cardiac rhythm management system comprising:

one or more leads for sensing electrical signals of a patient or for applying electrical energy to the patient;

a monitoring circuit for monitoring heart activity of the patient through one or more of the leads; and

a therapy circuit for delivering electrical energy through one or more of the leads to a heart of the patient, wherein the therapy circuit includes one or more capacitors, which include a foil that comprises;

first and second opposing surfaces which define a foil thickness, with the first opposing surface having one or more first cavities having a first average maximum depth less than the foil thickness and the second opposing surface having one or more second cavities having a second average maximum depth less than the foil thickness, with one or more of the first cavities intersecting one or more of the second cavities to define one or more perforations through the foil.