Blood Sequestration Device with Air-Permeable Barrier

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Solution Overview

Problem

Blood culture contamination leads to false positive results and increased healthcare costs due to improper skin antisepsis, vein collapse, and mechanical manipulation during blood collection, with existing methods failing to effectively reduce contamination rates.

Innovation Solution

A blood sequestration device with an air permeable blood barrier that passively collects the initial aliquot of blood using the patient's own pressure, eliminating the need for additional user steps and reducing vein collapse, while ensuring contaminant-free samples by diverting the initial aliquot away from the main blood sample pathway.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If conventional blood collection methods are used with manual manipulation, then blood samples can be collected, but contamination rates increase due to improper skin antisepsis, vein collapse, and mechanical manipulation

Engineering Contradiction:
Improveblood culture accuracyVSAvoidcollection process complexity
Core Design Contradiction:
ReliabilityVSEase of operation

Solution Approach 1:

The blood collection system is segmented into multiple chambers: a first chamber that receives and isolates the initial contaminated blood aliquot, and a second chamber that receives the clean blood sample. This segmentation physically separates contaminants from the diagnostic sample, resolving the contradiction between reliability and ease of operation by automating the contamination removal process.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

A valve mechanism acts as an intermediary between the blood collection needle and the culture bottle. The valve automatically directs the initial contaminated aliquot to a waste chamber while allowing subsequent clean blood to flow to the culture bottle. This intermediary device eliminates manual manipulation errors and improves reliability without increasing operational complexity.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Productivity

If forceful aspiration or small hypodermic needles are used to increase blood flow, then blood can be drawn faster, but red blood cells lyse and potassium is released, rendering samples abnormal

Engineering Contradiction:
Improveblood collection speedVSAvoidsample integrity
Core Design Contradiction:
ProductivityVSReliability

Solution Approach 1:

The system performs preliminary action by collecting and isolating the initial blood aliquot in a first chamber before it can cause harm. This preliminary collection of potentially contaminated or lysed blood prevents it from reaching the diagnostic sample, allowing faster blood flow rates without compromising sample integrity.

Inventive Principle:
Principle #10Preliminary action

3Ease of operation

If vacuum pressure is applied to facilitate blood draw, then collection is easier, but vein collapse occurs in patients with delicate veins

Engineering Contradiction:
Improveblood draw facilitationVSAvoidvein collapse
Core Design Contradiction:
Ease of operationVSObject-affected harmful factors

Solution Approach 1:

A flow control valve serves as an intermediary between the vacuum source and the patient's vein. The valve regulates and limits the vacuum pressure applied during blood collection, preventing excessive negative pressure that would cause vein collapse in delicate patients while still facilitating adequate blood flow for collection.

Inventive Principle:
Principle #24Intermediary (Mediator)

4Reliability

If initial blood aliquot is discarded to remove contaminants, then false positives are reduced, but additional user steps are required and time is lost

Engineering Contradiction:
Improveculture result accuracyVSAvoidcollection procedure duration
Core Design Contradiction:
ReliabilityVSLoss of time

Solution Approach 1:

The system performs preliminary action by automatically collecting and isolating the initial contaminated blood aliquot in a first chamber during the blood draw process itself. This preliminary separation occurs without requiring additional user steps or time beyond the standard collection procedure, thereby improving reliability without increasing time loss.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The device performs self-service by automatically directing and separating the initial contaminated blood from the clean blood sample through its internal chamber design and valve mechanism. This automated self-service eliminates the need for manual discarding steps performed by healthcare workers, reducing time loss while maintaining high culture result accuracy.

Inventive Principle:
Principle #25Self-service

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

The solution significantly reduces blood culture contamination and vein collapse, providing accurate samples by isolating contaminants in the initial aliquot and ensuring subsequent samples are uncontaminated, thereby minimizing false positives and healthcare costs.

Implementation Method 1

The blood sequestration device includes a vent comprising an air permeable blood barrier

Methodology Applied
Scientific EffectAir permeable barrier: Semipermeable Membrane

Implementation Method 2

The blood sequestration device includes a one-way air valve

Methodology Applied
Scientific EffectOne-way valve: Valve

Data Source

PatentUS12257051B2Blood contaminant sequestration device with one-way air valve and air-permeable blood barrier with closure mechanism
Publication Date: 2025.03.25 KURIN INC
  • US12257051B2 patent drawing
  • US12257051B2 patent drawing
  • US12257051B2 patent drawing

AI summary

Blood sample optimization systems and methods are described that reduce or eliminate contaminates in collected blood samples, which in turn reduces or eliminates false positive readings in blood cultures or other testing of collected blood samples. A blood sample optimization system can include a blood sequestration device located between a patient needle and a sample needle. The blood sequestration device can include a sequestration chamber for sequestering an initial, potentially contaminated aliquot of blood, and may further include a sampling channel that bypasses the sequestration chamber to convey likely uncontaminated blood between the patient needle and the sample needle after the initial aliquot of blood is sequestered in the sequestration chamber.