Sepsis Prediction Using Discriminating Features

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Solution Overview

Problem

Current methods for detecting sepsis in ICU patients are delayed due to the time required for standard blood cultures and antibiotic susceptibility testing, necessitating a reliable early prediction system using available lab data and vital signs.

Innovation Solution

A processor-implemented method that extracts discriminating features from physiological, laboratory, and demographic parameters using Minimum Redundancy Maximum Relevance (MRMR) ranking and classifiers like Random Forest and Adaptive Logistic Regression, normalizing data across sliding time windows to predict sepsis classification.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If standard blood cultures and antibiotic susceptibility testing are used to detect sepsis, then diagnostic accuracy is improved, but detection time is significantly delayed (6 hours to 5 days)

Engineering Contradiction:
Improvesepsis detection accuracyVSAvoiddetection time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The system performs preliminary analysis of laboratory parameters and vital signs to predict sepsis risk before definitive diagnosis is confirmed by slow-growing cultures. By continuously monitoring and analyzing trends in available data (lactate, white blood cell count, heart rate, etc.), the system generates early warnings that prompt earlier clinical intervention, effectively performing the diagnostic action in advance of traditional methods

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The patent introduces an intermediary prediction system that bridges the gap between rapid but non-specific vital sign monitoring and slow but definitive culture-based diagnosis. This intermediary layer uses machine learning classifiers to analyze patterns in routinely collected laboratory and vital sign data, providing a timely indicator of sepsis risk that neither traditional method can provide alone

Inventive Principle:
Principle #24Intermediary (Mediator)

2Measurement precision

If multiple laboratory parameters and vital signs are continuously monitored and analyzed, then early sepsis prediction accuracy is improved, but computational complexity and data processing requirements increase

Engineering Contradiction:
Improvesepsis prediction accuracyVSAvoidsystem complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The system extracts and focuses on a specific subset of the most discriminative features from the large volume of available laboratory and vital sign data. Using feature selection techniques, it identifies and extracts only the most relevant parameters (such as lactate trends, white blood cell count changes, heart rate variability) that contribute most to sepsis prediction, discarding redundant information and simplifying the input to the classification models

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent segments the complex prediction task into distinct processing stages: data preprocessing and normalization, feature extraction and selection, multiple parallel classifier implementations, and result aggregation. This segmentation allows each component to be optimized independently and facilitates implementation using distributed computing frameworks, reducing overall system complexity while maintaining predictive accuracy

Inventive Principle:
Principle #1Segmentation

Data Source

PatentUS11817217B2Discriminating features based sepsis prediction
Publication Date: 2023.11.14 TATA CONSULTANCY SERVICES LTD
  • US11817217B2 patent drawing
  • US11817217B2 patent drawing
  • US11817217B2 patent drawing

AI summary

Sepsis is one of the most prevalent causes of mortality in Intensive Care Units (ICUs) and delayed treatment is associated with increase in death and financial burden. There is no single laboratory test or clinical sign that by itself can be considered diagnostic of sepsis. The present disclosure provides discriminating domain specific continuous and categorical features that can reliably classify a subject being monitored into a sepsis class or a normal class. A combination of physiological parameters, laboratory parameters and demographic details are used to extract the discriminating features. Even though the parameters may be sporadic in nature, the systems and methods of the present disclosure make use of a sliding time window to generate continuous features that capture the trend in the sporadic data; and a binning approach to generate categorical features to discriminate deviation from the normal class and facilitate timely treatment.