Cardiac event categorization system

• US 8,483,812 B2
• Filed: 03/31/2008
• Issued: 07/09/2013
• Est. Priority Date: 02/04/2002
• Status: Expired due to Fees

• Current Assignee: Angel Medical Systems, Inc.
• Original Assignee: Angel Medical Systems, Inc.
• Inventors: Fischell, Robert E., Fischell, David R., Fischell, Tim A., Fischell, Scott J. S.
• Primary Examiner(s): Holmes, Rex R
• Application Number:
  US12/059,146
• Publication Number:
  US 20080183091A1
• Time in Patent Office: 1,926 Days
• Field of Search: 607 2- 7, 607/17, 600508-509, 600515-519
• US Class Current: 600/515
• CPC Class Codes: A61L 2300/236 Glycosaminoglycans, e.g. heparin, hyaluronic acid, chondroitin
• CPC Class Codes: A61L 2300/254 Enzymes, proenzymes
• CPC Class Codes: A61L 2300/42 Anti-thrombotic agents, anticoagulants, anti-platelet agents
• CPC Class Codes: A61L 27/54 Biologically active materials, e.g. therapeutic substances A61L27/227 takes precedence

Abstract

Disclosed are methods for detecting an acute myocardial infarction (i.e., a heart attack) at the earliest possible time and promptly warning the patient that he should immediately seek medical care. The present invention includes an implantable electronic system that can sense a change in the patient'"'"'s electrogram that is indicative of a heart attack. If a heart attack is sensed, the device would then cause an implantable and/or externally located alarm to be actuated to warn the patient of his condition and a medical practitioner at a remote diagnostic center would receive the patient'"'"'s electrogram for analysis. The patient or a caretaker would then be informed to self-inject medication through a subcutaneous, pass-through drug port that can be a separate device or integrated into the implanted device that is designed for the early detection of a heart attack. The methods of the present invention include determining if a human patient is likely to have a heart attack and, if he is, then implanting within that patient a device that can sense when a heart attack occurs and alarm the patient to take appropriate actions if a heart attack does occur.

Claims

1. A system for detecting a cardiac event in a human patient, the system including:

at least two electrodes adapted for implantation in a patient for obtaining an electrical signal from the patient'"'"'s heart;

an implantable device including a radio transceiver, a memory and a processor configured to;

process the electrical signal to obtain R-R interval values and values of a heart signal parameter defining an ST deviation therefrom;

categorize detected cardiac events into a low severity level and a high severity level based upon a combined function of said R-R interval values and said ST deviation values for comparison with a predetermined threshold for a selected R-R interval value;

operative upon categorizing a cardiac event as a high severity level event, cause the transceiver to transmit a high severity event signal that includes both electrical signal waveform data associated with the high severity level event and an indication of the high severity level of the cardiac event;

operative upon categorizing a cardiac event as a low severity level event, perform at least one of the following actions;

(i) cause the transceiver to transmit a low severity event signal that includes both electrical signal waveform data associated with the low severity level event and an indication of the low severity level of the cardiac event;

(ii) store electrical signal waveform data associated with the low severity level event.

2. The system of claim 1 wherein the high severity level event pertains to an acute myocardial infarction.

3. The system of claim 1 wherein the low severity level event pertains to chronic ischemia.

4. The system of claim 1 further comprising an alarm operatively coupled to the implantable device, and wherein the implantable device is configured to cause the alarm to issue different types of alarms associated with corresponding types of cardiac events.

5. The system of claim 1 further comprising an external device that includes a transceiver, and wherein the external device is configured to extract the severity level indication from the signal transmitted from the implantable device.

6. The system of claim 5 further comprising an external device that includes a transceiver and an alarm generator, and wherein the external device is configured to generate an emergency alarm upon receiving the high severity level event signal.

7. The system of claim 5 further comprising an external device that includes a transceiver, and wherein the external device is configured to cause the transceiver to transmit a signal to a remote location upon receiving the high severity level event signal.