Perforated Sponge for Customizable Endoluminal Vacuum Therapy

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Solution Overview

Problem

Current medical devices for treating gastrointestinal tract wounds, such as post-surgical leaks or perforations, are limited by the need for frequent foam replacement and risk of infection, with existing endoluminal vacuum therapy (EVT) devices lacking customization and stability.

Innovation Solution

A medical device comprising a sponge with perforated tear surfaces that can be customized in size and shape by removing detachable layers, attached to a vacuum tube for use in EVAC procedures, allowing for precise sizing and shape adjustment for wound treatment.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Adaptability or versatility

If a fixed-size foam is used in endoluminal vacuum therapy, then the device structure is simple, but the device cannot be customized to fit different wound sizes and shapes, requiring frequent replacement

Engineering Contradiction:
Improvecustomization capabilityVSAvoiddevice structure
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The foam is divided into multiple detachable layers that can be selectively removed to customize the foam size and shape. Each layer can be independently detached to achieve the desired configuration for different wound sizes and anatomical locations.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The foam transitions from a fixed static structure to a dynamic customizable structure. The detachable layers allow the foam to be adapted in real-time during the procedure to match various wound geometries and sizes.

Inventive Principle:
Principle #15Dynamics

2Duration of action of moving object

If a standard foam size is used, then manufacturing is simple, but the foam must be replaced frequently to achieve proper fit, increasing treatment time and infection risk

Engineering Contradiction:
Improvefoam retention timeVSAvoidreplacement frequency
Core Design Contradiction:
Duration of action of moving objectVSLoss of time

Solution Approach 1:

The foam's detachable layers enable precise sizing customization, allowing the foam to be perfectly fitted to the wound dimensions. This eliminates the need for frequent replacements and extends the foam's effective retention time at the treatment site.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The foam size and shape parameters can be adjusted by removing specific layers, allowing optimization of the foam-wound interface. This customization ensures proper fit and contact pressure, extending the duration the foam can remain in place effectively.

Inventive Principle:
Principle #35Parameter changes

3Reliability

If frequent foam replacement is required, then a simple fixed foam design suffices, but infection risk increases due to repeated insertions and manipulations

Engineering Contradiction:
Improveinfection riskVSAvoidfoam design complexity
Core Design Contradiction:
ReliabilityVSEase of manufacture

Solution Approach 1:

The detachable layer structure allows the foam to be customized in-office without requiring complete replacement. This reduces the number of times the foam needs to be removed and reinserted, thereby reducing infection risk from repeated manipulations.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The foam is pre-configured with detachable layers that allow for easy customization. This preliminary design enables the foam to be adapted to different wound sizes without requiring complete replacement, reducing the frequency of insertions and associated infection risks.

Inventive Principle:
Principle #10Preliminary action

Data Source

PatentUS20250090385A1Endoluminal treatment devices and related methods
Publication Date: 2025.03.20 BOSTON SCIENTIFIC SCIMED INC
  • US20250090385A1 patent drawing
  • US20250090385A1 patent drawing
  • US20250090385A1 patent drawing

AI summary

Medical devices and related methods useful for EVAC procedures are described. The medical device may include a sponge. The sponge may include a plurality of perforations that form one or more tear surfaces. The one or more tear surfaces may define a predefined location for removing a first portion of the sponge from a second portion of the sponge. The one or more tear surfaces may form a boundary between a radially inner surface of the first portion and a radially outer surface of the second portion. The medical device may further include a tube coupled to a proximal portion of the sponge.