Device and method for cardiac arrhythmia therapy with failure detection and backup

• US 5,571,141 A
• Filed: 09/30/1994
• Issued: 11/05/1996
• Est. Priority Date: 09/30/1994
• Status: Expired due to Term

• Current Assignee: Intermedics Incorporated
• Original Assignee: Intermedics Incorporated
• Inventors: Shankar, Balakrishnan, Cantrell, Lee A., McNeil, Ken R.
• Primary Examiner(s): Kamm, William E.
• Assistant Examiner(s): Getzow, Scott M.
• Application Number:
  US08/316,254
• Time in Patent Office: 767 Days
• Field of Search: 607/5, 607/27, 607/29, 607/63, 607/4
• US Class Current: 607/5
• CPC Class Codes: A61N 1/3706 Pacemaker parameters stimulation threshold A61N1/371
• CPC Class Codes: A61N 1/3931 Protecting, e.g. back-up systems

Abstract

An implantable automatic cardioverter/defibrillator device for a cardiac patient has a primary control mode for a defibrillation therapy delivery system. The primary control mode is responsive to detection of fibrillation of the patient'"'"'s heart for causing the delivery of a preselected electrical waveform therapy to the heart. The device also has a secondary control mode which is enabled by detecting a predetermined failure mechanism that causes malfunctioning of the primary mode. The enabled secondary control mode uses at least some of the functional part of the primary mode in responding to fibrillation of the patient'"'"'s heart to initiate generation of defibrillation therapy for application to the patient'"'"'s heart.

Claims

1. A cardioverter/defibrillator device structured to be implanted in a patient'"'"'s body for automatic response to sensing of electrical cardiac activity of the patient'"'"'s heart to detect and treat disorders thereof, comprising:

primary control mode means responsive to detection of fibrillation of the patient'"'"'s heart for causing the generation of a prescribed electrical waveform regimen as electrical defibrillation therapy for application to the heart, and

secondary control mode means responsive to a predetermined type of failure mechanism of the device that causes malfunction of the primary control mode means for thereupon assuming control of generation of the electrical defibrillation therapy from the primary control mode means, and further responsive to detection of fibrillation after assuming said control to cause the generation of the electrical fibrillation therapy as a backup system for defibrillation of the patient'"'"'s heart.

2. The device of claim 1, wherein:

the secondary control mode means includes fault detection means for detecting said predetermined type of failure mechanism.

3. The device of claim 2, including:

sensor means for detecting electrical cardiac activity of the patient'"'"'s heart, and

separate detection means for each of said primary and secondary control mode means responsive to said electrical cardiac activity of the patient'"'"'s heart for detecting fibrillation thereof.

4. The device of claim 3, wherein the sensor means includes:

electrode means for detecting electrical cardiac activity of the patient'"'"'s heart and transmitting an electrical signal indicative thereof,

sense amplifier means operatively coupled to the electrode means for processing the transmitted electrical signal, and operatively coupled to each of the primary control mode means and the secondary control mode means for applying the processed electrical signal thereto.

5. The device of claim 4, wherein the detection means for the primary control mode means includes microprocessor means responsive to the processed electrical signal to detect fibrillation of the patient'"'"'s heart and initiate said electrical defibrillation therapy.

6. The device of claim 5, wherein the microprocessor means includes means for applying fibrillation detection criteria to the processed electrical signal to detect fibrillation of the patient'"'"'s heart, wherein said fibrillation detection criteria are selected from a group including fibrillation rate, sustained fibrillation rate, sudden onset, rate stability, and combinations of criteria within said group.

7. The device of claim 4, wherein the detection means for the secondary control mode means includes:

first means responsive to the processed electrical signal for preliminarily detecting fibrillation of the patient'"'"'s heart after the assumption of control by the secondary control mode means, and

confirmation means operatively coupled to the first means and responsive to preliminary detection of fibrillation by said first means for applying preset criteria to the processed electrical signal to confirm ongoing fibrillation of the heart.

8. A method of delivering electrical defibrillation therapy to a patient'"'"'s heart from an implanted cardiac therapy device after malfunction of the device, comprising the device-implemented steps of:

detecting a predetermined failure mechanism causing malfunction in a primary control mode subsystem of a therapy delivery system of the device,

automatically enabling a secondary control mode subsystem of the therapy delivery system as a backup control mode upon detecting said failure mechanism,

sensing the patient'"'"'s cardiac activity to detect fibrillation, and

causing generation of a preselected therapy regimen by the enabled secondary control mode subsystem upon confirming sustained fibrillation.

9. The method of claim 8, wherein the steps of sensing and confirming are performed by applying predetermined fibrillation detection criteria to a signal representative of patient cardiac activity.

10. A defibrillator adapted to be implanted in a patient to monitor cardiac activity and to respond to fibrillation of the patient'"'"'s heart by generating defibrillation therapy, comprising:

means for generating defibrillation therapy,

a primary system to initiate said generation of defibrillation therapy for application to the heart,

a fault detector for sensing a defect of said primary system that prevents initiating said generation of defibrillation therapy by the primary system; and

a standby system responsive to sensing of a defect by said fault detector for replacing the defective primary system, and responsive to heart rate indicative of fibrillation for initiating said generation of defibrillation therapy to be applied to the heart.

11. The defibrillator of claim 10, wherein:

said standby system includes confirmation means responsive to preliminary indication of fibrillation from said heart rate for detecting sustained fibrillation before initiating said generation of defibrillation therapy.

12. The defibrillator of claim 11, wherein:

said fault detector comprises detection circuitry for detecting a fault selected from the group consisting of parity error, timing out of a watchdog timer, a failure in timing control of the primary system, and an inability of the primary system to write to a desired input/output location.