MR-ProADM Risk Stratification for Polytrauma Complications

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Solution Overview

Problem

Current methods lack accurate and early identification of trauma-related complications in polytrauma patients, particularly sepsis and non-infection related issues like rhabdomyolysis, leading to prolonged intensive care and higher mortality rates.

Innovation Solution

Utilizing mid-regional proadrenomedullin (MR-proADM) levels in patient samples to diagnose, prognose, predict, and risk-stratify trauma-related complications by determining specific cut-off values for polytrauma patients, enabling early differentiation between high and low risk of complications.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If established biomarkers (CRP, PCT, IL-6) and clinical scores (SOFA, qSOFA) are used for complication identification, then routine clinical monitoring is maintained, but early and accurate prediction of trauma-related complications remains insufficient

Engineering Contradiction:
Improveprediction accuracyVSAvoidearly identification timing
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The patent introduces proADM as a new measurement parameter to complement existing biomarkers. By measuring proADM levels in addition to conventional markers, the system achieves earlier and more accurate prediction of complications without discarding established monitoring approaches.

Inventive Principle:
Principle #35Parameter changes

2Loss of time

If proADM is used for early identification of complications, then timely therapeutic decisions can be made, but differentiation between infection-related and non-infection related complications remains challenging

Engineering Contradiction:
Improvetherapeutic decision timingVSAvoidcomplication type differentiation
Core Design Contradiction:
Loss of timeVSLoss of information

Solution Approach 1:

The patent segments complication prediction into distinct categories by combining proADM with other biomarkers. Different biomarker patterns indicate different complication types: proADM alone for non-infection complications, and proADM combined with PCT for infection-related complications, enabling targeted therapeutic decisions.

Inventive Principle:
Principle #1Segmentation

3Measurement precision

If multiple biomarkers are combined for comprehensive complication assessment, then prediction accuracy improves, but system complexity increases

Engineering Contradiction:
Improvecomplication prediction accuracyVSAvoidbiomarker system complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent implements a tiered approach where proADM serves as the primary screening marker for all complications. Only when proADM indicates elevated risk does the system activate additional biomarker measurements, avoiding unnecessary complexity for low-risk patients while maintaining comprehensive monitoring for high-risk cases.

Inventive Principle:
Principle #16Partial or excessive action

Data Source

PatentUS20260056215A1Pro-ADM for Prognosis of Trauma-Related Complications in Polytrauma
Publication Date: 2026.02.26 BRAHMS GMBH

AI summary

The invention relates to a method for the diagnosis, prognosis, prediction, risk assessment and/or risk stratification of a subsequent trauma-related complication in a polytrauma patient, comprising providing a sample of said patient, wherein the sample is isolated from the patient after the polytrauma, determining a level of proADM or fragment(s) thereof in said sample, wherein said level of proADM or fragment(s) thereof correlates with the likelihood of a subsequent trauma-related complication.