Antitachycardia pacing pulse from a subcutaneous defibrillator
Devices and methods for single therapy pulse (STP) therapy for tacharrythmia are disclosed. The STP therapy can be delivered from a far-field position to allow a “global” capture approach to pacing. Due to the global capture in STP, a series of pulses, which is indicative of conventional anti-tachycardia pacing (ATP) delivered by transvenous systems, becomes unnecessary. One to four pulses at most are needed for STP, and after delivery of the one to four pulses, therapy delivery can be interrupted to determine whether the previously delivered therapy has been successful.
1. A method of treating a patient in an implantable cardiac rhythm management device (CRMD) comprising a canister housing circuitry for performing data analysis and therapy delivery, coupled to a lead electrode having electrodes for body implantation suitable for sensing electrical signals, the method comprising:
receiving cardiac signals from the patient using one or more of the electrodes on the lead;
identifying that a tachycardia is occurring based on the received cardiac signals showing a cardiac rate in excess of a rate threshold;
determining that the tachycardia is not supraventricular in nature and declaring a treatable episode of tachycardia;
determining that the tachycardia is monomorphic;
delivering synchronized pacing pulses to the patient using far-field electrodes in response to the monomorphic tachycardia;
calculating the cardiac rate of the patient following the delivery of the synchronized pacing pulses;
determining that the cardiac rate dropped in response to the synchronized pacing pulses; and
terminating the episode and storing data related to the episode.
2. The method of claim 1 wherein the CRMD is a subcutaneous-only CRMD and the far-field electrodes used for therapy delivery are subcutaneously placed electrodes.
3. The method of claim 1 wherein the CRMD is a transvenous CRMD having at least one transvenous lead, and the far-field electrodes used for therapy delivery include a transvenous coil electrode and an electrode disposed on the canister.
4. The method of claim 1 wherein the rate threshold is in the range of 120-220 beats per minute.
5. The method of claim 1 wherein the CRMD determines that the tachycardia is not supraventricular in nature by determining that the detected cardiac signals comprise a wide morphology.
6. The method of claim 1 wherein the CRMD determines that the tachycardia is not supraventricular in nature by determining that the detected cardiac signals do not match a template of normal sinus rhythm.
7. The method of claim 1 wherein the CRMD determines that the tachycardia is not supraventricular in nature by comparing atrial and ventricular detections.
8. The method of claim 1 wherein the CRMD determines that the tachycardia is monomorphic by comparing the shape of one detected cardiac beat to one or more previous detected cardiac beats.
9. The method of claim 1 wherein the CRMD determines that the tachycardia is monomorphic by comparing the width of one detected cardiac beat to one or more previous detected cardiac beats.
10. An implantable cardiac rhythm management device (CRMD) comprising a canister housing operational circuitry for performing data analysis and therapy delivery, coupled to a lead electrode assembly having electrodes for body implantation suitable for sensing electrical signals, wherein the operational circuitry is configured to perform a method comprising:
the operational circuitry receiving cardiac signals from the patient using one or more of the electrodes on the lead;
the operational circuitry identifying that a tachycardia is occurring based on the received cardiac signals showing a cardiac rate in excess of a rate threshold;
the operational circuitry determining that the tachycardia is not supraventricular in nature and declaring a treatable episode of tachycardia;
the operational circuitry determining that the tachycardia is monomorphic;
the operational circuitry delivering synchronized pacing pulses to the patient using far-field electrodes on the lead electrode assembly and/or canister in response to the monomorphic tachycardia;
the operational circuitry calculating the cardiac rate of the patient following the delivery of the synchronized pacing pulses;
the operational circuitry determining whether the cardiac rate dropped in response to the synchronized pacing pulses; and
in response to determining that the cardiac rate dropped in response to the synchronized pacing pulses, the operational circuitry terminating the episode and storing data related to the episode in memory.
11. The CRMD of claim 10 wherein the CRMD is a subcutaneous-only CRMD and the lead electrode assembly is designed for subcutaneous placement, such that the far-field electrodes are designed for subcutaneous placement.
12. The CRMD of claim 10 wherein the CRMD is a transvenous CRMD and the lead electrode assembly is configured for transvenous placement and includes a coil electrode such that far-field electrodes used for therapy delivery include the coil electrode and an electrode disposed on the canister.
13. The CRMD of claim 10 wherein the operational circuitry is configured such that the rate threshold is in the range of 120-220 beats per minute.
14. The CRMD of claim 10 wherein the method that the operational circuitry is configured to perform further comprises, in response to determining that the cardiac rate did not drop in response to the synchronized pacing pulses, the operational circuitry preparing for and delivering defibrillation therapy to the patient using the far field electrodes.
15. The CRMD of claim 10 wherein the operational circuitry is configured to determine that the tachycardia is not supraventricular in nature by determining that the detected cardiac signals comprise a wide morphology.
16. The CRMD of claim 10 wherein the operational circuitry is configured to determine that the tachycardia is not supraventricular in nature by determining that the detected cardiac signals do not match a template of normal sinus rhythm.
17. The CRMD of claim 10 wherein the operational circuitry is configured to determine that the tachycardia is not supraventricular in nature by comparing atrial and ventricular detections.
18. The CRMD of claim 10 wherein the operational circuitry is configured to determine that the tachycardia is monomorphic by comparing the shape of one detected cardiac beat to one or more previous detected cardiac beats.
19. The CRMD of claim 10 wherein the operational circuitry is configured to determine that the tachycardia is monomorphic by comparing the width of one detected cardiac beat to one or more previous detected cardiac beats.
20. A method of treating a patient in an implantable cardiac rhythm management device (CRMD) comprising a canister housing circuitry for performing data analysis and therapy delivery, coupled to a lead electrode having electrodes for body implantation suitable for sensing electrical signals, the method comprising:
receiving cardiac signals from the patient using one or more of the electrodes on the lead;
identifying that a tachycardia is occurring based on the received cardiac signals showing a cardiac rate in excess of a rate threshold;
determining that the tachycardia is not supraventricular in nature and declaring a treatable episode of tachycardia;
determining that the tachycardia is monomorphic;
(a) delivering synchronized pacing pulses to the patient using far-field electrodes in response to the monomorphic tachycardia;
(b) calculating the cardiac rate of the patient following (a);
(c) determining that the cardiac rate calculated at (b) did not drop;
(d) in response to (c), determining whether the tachycardia remains monomorphic following (a), and:
if the tachycardia remains monomorphic, returning to (a) up to a predetermined quantity of iterations, or
if the tachycardia is no longer monomorphic or the predetermined quantity of iterations has already taken place, preparing for and delivering defibrillation therapy.