IMD Atrioventricular Synchrony Assessment via Far-Field Ventricular Signals

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Solution Overview

Problem

Existing medical devices face challenges in determining atrioventricular (AV) synchrony, particularly in patients with conduction abnormalities, where ventricular pacing without an atrial lead makes it difficult to sense and track atrial events, affecting the maintenance of AV synchrony.

Innovation Solution

An implantable medical device (IMD) is configured to sense cardiac signals, including far-field ventricular event signals, to determine a ventricular activity metric and calculate an AV synchrony metric, which indicates the performance of a ventricular pacemaker in maintaining AV synchrony, allowing for adjustments in atrial pacing parameters or transmission of signals indicating AV asynchrony.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of manufacture

If a ventricular intracardiac pacemaker is implanted without an atrial lead, then the device can provide ventricular rate support, but sensing and tracking of atrial events to maintain AV synchrony becomes challenging

Engineering Contradiction:
Improveimplantation simplicityVSAvoidatrial event sensing capability
Core Design Contradiction:
Ease of manufactureVSMeasurement precision

Solution Approach 1:

The patent uses far-field ventricular event signals as an intermediary to indirectly assess AV synchrony. Instead of directly sensing atrial events, the device detects ventricular events and uses them as a proxy to determine whether atrial contraction is properly synchronized with ventricular contraction, thereby resolving the contradiction between simplified implantation and maintained sensing capability

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The patent replaces the electrical sensing system (atrial lead) with a mechanical/motion-based approach using accelerometer signals to detect atrial contraction. This substitution allows the device to maintain AV synchrony monitoring without requiring an atrial lead, achieving both implantation simplicity and measurement capability

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

2Adaptability or versatility

If far-field ventricular event signals are used to determine AV synchrony, then atrial event tracking is enabled without an atrial lead, but signal discrimination becomes more difficult

Engineering Contradiction:
Improvesensing capabilityVSAvoidsignal discrimination
Core Design Contradiction:
Adaptability or versatilityVSDifficulty of detecting and measuring

Solution Approach 1:

The patent applies preliminary filtering and signal processing to the accelerometer signal to isolate the QRS complex before using it for AV synchrony determination. By pre-processing the signal to enhance the ventricular event detection, the device reduces the difficulty of discriminating far-field signals from other mechanical artifacts

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The patent transitions from electrical signal detection (traditional ECG approach) to mechanical signal detection (accelerometer approach). This dimensional change from electrical to mechanical sensing space allows the device to detect ventricular events without electrical leads, though it introduces new signal discrimination challenges that are addressed through signal processing

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

Data Source

PatentUS20240082583A1Medical device and method for determining atrioventricular synchrony
Publication Date: 2024.03.14 MEDTRONIC INC
  • US20240082583A1 patent drawing
  • US20240082583A1 patent drawing
  • US20240082583A1 patent drawing

AI summary

A medical device is configured to sense a cardiac signal that includes far field ventricular event signals and determine a ventricular activity metric from the sensed cardiac signal. The ventricular activity metric may be representative of a ventricular rate or an atrioventricular time interval. The medical device is configured to determine an atrioventricular synchrony metric based on the ventricular activity metric and generate an output based on the atrioventricular synchrony metric. The device may include a memory configured to store data corresponding to the atrioventricular synchrony metric.