Shield for implantable cardioverter defibrillator

• US 5,749,910 A
• Filed: 06/07/1995
• Issued: 05/12/1998
• Est. Priority Date: 06/07/1995
• Status: Expired due to Fees

• Current Assignee: Angeion Corporation (Niterra Co., Ltd.)
• Original Assignee: Angeion Corporation (Niterra Co., Ltd.)
• Inventors: Nelson, Randall S., Kroll, Mark W., Brumwell, Dennis A., Perttu, Joseph S.
• Primary Examiner(s): Getzow, Scott M.
• Application Number:
  US08/486,759
• Time in Patent Office: 1,070 Days
• Field of Search: 607/36, 607/37, 607/38, 607/5, 357/68, 357/84
• US Class Current: 607/36
• CPC Class Codes: A61N 1/375 Constructional arrangements, e.g. casings
• CPC Class Codes: A61N 1/3758 Packaging of the components within the casing
• CPC Class Codes: A61N 1/3956 Implantable devices for applying electric shocks to the heart, e.g. for cardioversion

Abstract

An implantable cardioverter defibrillator capable of subcutaneous positioning within a patient delivers at least one electrical cardioversion/defibrillation countershocks to the heart of the patient. The implantable cardioverter defibrillator includes a housing, circuitry positioned within the housing to control delivery of the countershocks, and an energy source coupled with the circuitry to provide electrical energy to a capacitor in the circuitry that stores the electrical energy for delivery of the countershocks. Because the circuitry is susceptible to undesirable electromagnetic coupling effects of origin external to the circuitry, particularly the capacitive coupling effects between the circuitry and the housing of the device when at least a portion of the housing is utilized as an electrode, the implantable cardioverter defibrillator also includes a conductive shield, disposed between the housing and the circuitry, to shield the circuitry against such undesired coupling effects.

Claims

1. An implantable cardioverter defibrillator capable of subcutaneous positioning within a patient for delivering at least one electrical cardioversion/defibrillation countershocks of at least 0.5 Joules to at least two electrodes adapted to be positioned proximate the heart of the patient, the implantable cardioverter defibrillator comprising:

a housing comprising a biocompatible material;

circuitry positioned within the housing to control delivery of the countershocks, the circuitry being susceptible to undesirable coupling effects of origin external to the circuitry;

an energy source coupled with the circuitry to provide electrical energy to the circuitry;

a conductive shield disposed between the housing and the circuitry to shield the circuitry against the coupling effects; and

a reference point in the circuitry, the conductive shield being in electrical connection with the reference point to cause the conductive shield to shield the circuitry from the coupling effects.

2. The implantable cardioverter defibrillator of claim 1, wherein the housing includes at least a portion of the housing which is utilized as an electrode operatively coupled with the circuitry to deliver the cardioversion/defibrillation countershocks, and wherein the conductive shield shields the circuitry from undesirable capacitive coupling effects between the circuitry and the housing when the portion of the housing is utilized as an electrode.

3. The implantable cardioverter defibrillator of claim 1, wherein the circuitry comprises an interconnect conductor.

4. The implantable cardioverter defibrillator of claim 3, wherein the conductive shield shields the interconnect conductor against undesirable coupling effects between the interconnect conductor and external electromagnetic fields.

5. The implantable cardioverter defibrillator of claim 1, wherein the circuitry comprises an electronic circuit board.

6. The implantable cardioverter defibrillator of claim 1, wherein the reference point in electrical communication with the conductive shield comprises a ground.

7. The implantable cardioverter defibrillator of claim 1, wherein the energy source comprises a battery, further wherein the reference point in electrical connection with the conductive shield comprises a point on the battery.

8. The implantable cardioverter defibrillator of claim 1, wherein the circuitry comprises a flex tape assembly.

9. The implantable cardioverter defibrillator of claim 8, wherein the conductive shield is integrated to the flex tape assembly.

10. The implantable cardioverter defibrillator of claim 1, further comprising an internal housing liner in contact with the housing, the conductive shield being supported by the liner.

11. The implantable cardioverter defibrillator of claim 10, wherein the conductive shield is embedded in the liner.

12. The implantable cardioverter defibrillator of claim 10, wherein the liner comprises inner insulative material and outer insulative material, the conductive shield being disposed between the outer insulative material and the inter insulative material.

13. The implantable cardioverter defibrillator of claim 1 wherein the conductive shield comprises two layers of insulating material and the circuitry is operably disposed therebetween.

14. An implantable cardioverter defibrillator capable of subcutaneous positioning within a patient for delivering at least one electrical cardioversion/defibrillation countershocks of at least 0.5 J to at least two electrodes positioned proximate the heart of the patient, the implantable cardioverter defibrillator comprising:

capacitor means for storing electrical energy to generate the cardioversion/defibrillation countershocks;

circuit means for controlling delivery of the cardioversion/defibrillation countershocks to at least two electrodes;

battery means in electrical communication with the capacitor means and circuit means for providing electrical energy to the capacitor means and the circuit means;

housing means comprising a biocompatible material for housing the capacitor means, the circuit means and the battery means, the housing means including an electrode portion forming at least one of the at least two electrodes, the electrode portion of the housing means being in sufficiently close proximity to the circuit means to promote undesirable capacitive coupling effects between the housing means and circuit means; and

conductive shielding means disposed between the electrode portion of the housing means and the circuit means for shielding the circuit means against the capacitive coupling effects between the housing means and the circuit means, the conductive shielding means being in electrical communication with a reference point to cause the shielding means to shield the circuit means against the capacitive coupling effects.

15. The implantable cardioverter defibrillator of claim 14, wherein the circuit means comprises an interconnect conductor, further wherein the conductive shielding means shields the interconnect conductor against undesirable coupling effects between the interconnect conductor and an object external to the interconnect conductor.

16. The implantable cardioverter defibrillator of claim 14, wherein the reference point in electrical communication with the conductive shielding means comprises a ground.

17. The implantable cardioverter defibrillator of claim 14, wherein the reference point in electrical communication with the conductive shielding means comprises the battery means.

18. A method of delivering electrical cardioversion/defibrillation countershocks of at least 0.5 J from an implantable cardioverter defibrillator positioned subcutaneously within a patient to at least two electrodes positioned proximate the heart of the patient, the method comprising:

(a) storing electrical energy in at least one capacitor disposed within a housing of the implantable cardioverter defibrillation to generate the cardioversion/defibrillation countershocks;

(b) controlling delivery of the cardioversion/defibrillation countershocks to the at least two electrodes using circuitry disposed within the housing of the implantable cardioverter defibrillator; and

(c) using a conductive shield other than the housing to shield the circuitry from undesirable coupling effects between the circuitry and an electromagnetic field external to the circuitry.

19. The method of claim 18, wherein step (c) includes the step of connecting the conductive shield disposed between the circuitry and the housing to a ground.

20. The method of claim 18, wherein the step (c) includes the step of connecting the conductive shield disposed between the circuitry and the housing to the battery.

21. The method of claim 18, wherein the step (c) includes the step of shielding the circuitry from undesirable capacitive coupling effects between the circuitry and the housing when at least a portion of the housing is used as one of the at least two electrodes for delivery of countershocks to the patient.