Atrial Fibrillation Warning Sampling for Target Molecule Research

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Solution Overview

Problem

Current methods lack effective early warning and research tools for predicting the onset of atrial fibrillation, making it difficult to collect clinical samples before and after the condition for in-depth study of targeted treatments.

Innovation Solution

An experimental method involving continuous monitoring with an atrial fibrillation warning system, alarm-triggered sampling, control sampling, data analysis, and targeted treatment research to identify and validate targeting molecules for atrial fibrillation treatment.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If continuous monitoring and alarm-triggered sampling are implemented, then measurement precision and research capability are improved, but device complexity and operational difficulty increase

Engineering Contradiction:
Improvetiming precision of sample collectionVSAvoidcomplexity of monitoring system
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The monitoring system is pre-configured with alarm thresholds and sampling protocols before clinical use. The system proactively detects atrial fibrillation onset and automatically triggers sampling at predetermined time points (immediate, 10min, 30min, 60min, 120min), eliminating the need for complex real-time decision-making during sampling operations.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The system implements continuous feedback loops where monitoring data is constantly analyzed against predefined criteria. When alarm conditions are met, the system provides feedback signals to trigger automated sampling sequences, ensuring precise timing while maintaining operational simplicity through rule-based automation.

Inventive Principle:
Principle #23Feedback

2Loss of information

If multiple sampling time points are collected, then data completeness and research value are improved, but loss of time and operational burden increase

Engineering Contradiction:
Improvecompleteness of clinical dataVSAvoidtime required for sampling operations
Core Design Contradiction:
Loss of informationVSLoss of time

Solution Approach 1:

Sampling time points and protocols are predetermined and prepared in advance. The system has pre-established sampling schedules (immediate, 10min, 30min, 60min, 120min post-alarm) that are automatically executed, eliminating the need for complex real-time scheduling and reducing operational time burden.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The monitoring system automatically manages the entire sampling process without requiring continuous human intervention. It self-monitors for alarm conditions, self-triggers sampling sequences, and self-manages the timing of multiple sample collections, significantly reducing operational burden while maintaining complete data collection.

Inventive Principle:
Principle #25Self-service

3Productivity

If automated alarm-triggered sampling is implemented, then productivity and data quality are improved, but device complexity increases

Engineering Contradiction:
Improveefficiency of sample collectionVSAvoidcomplexity of automated system
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

All sampling parameters, alarm thresholds, and timing protocols are pre-configured before system deployment. The automated system executes predetermined sampling sequences triggered by alarm events, achieving high productivity through simple rule-based automation rather than complex adaptive algorithms.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The system uses straightforward feedback mechanisms where monitoring data is compared against predefined thresholds. When conditions are met, automated sampling is triggered through simple signal transmission to collection devices, achieving efficient automation without requiring complex control systems or artificial intelligence.

Inventive Principle:
Principle #23Feedback

Data Source

PatentUS20260007351A1Experimental method for clinical research of targeting molecules based on atrial fibrillation warning system
Publication Date: 2026.01.08 GENERAL HOSPITAL OF THE NORTHERN WAR ZONE OF THE CHINESE PEOPLES LIBERATION ARMY
  • US20260007351A1 patent drawing

AI summary

This application relates to the technical field of medical research and clinical experiments, and provides an experimental method for clinical research of targeting molecules based on an atrial fibrillation warning system. The method includes: continuously monitoring dynamic electrocardiograms of a patient using an atrial fibrillation warning system; when the atrial fibrillation warning system issues an alert indicating imminent atrial fibrillation, immediately collecting blood or other clinical information of the patient; collecting blood or other clinical information of the patient when the patient has not experienced atrial fibrillation and the atrial fibrillation warning system has not issued an alert, to serve as control data; comparing biological indicators during atrial fibrillation occurrence and non-occurrence, and analyzing potential triggering factors and targeting molecules; and based on the identified targeting molecules, conducting targeted treatment research to validate effectiveness of the targeting molecules.