Independent Macrostrain Device With Flanges for Wound-Edge Force
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Solution Overview
Problem
Existing tissue treatment systems, particularly those utilizing negative-pressure therapy, lack effective mechanisms to enhance tissue growth and wound healing through macrostrain application and fluid management.
Innovation Solution
The introduction of a dressing interface that generates macrostrain at the tissue site via flanges or flaps under negative pressure, combined with a manifold for fluid distribution and a system for instillation therapy, which includes a macrostrain device and a sealing member to apply controlled negative pressure and fluid delivery.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Reliability
If negative-pressure therapy is applied to a tissue site, then tissue growth and wound healing are enhanced, but the existing systems lack effective mechanisms for macrostrain application and fluid management
Solution Approach 1:
The patent combines negative-pressure therapy with macrostrain application by integrating a bolster body with flanges that can be coupled to a dressing interface. This merging allows the system to simultaneously provide negative pressure for tissue growth enhancement and macrostrain through the flange mechanism, resolving the contradiction by unifying previously separate functions into a single integrated device.
Solution Approach 2:
The bolster body device is designed to perform multiple functions: it provides negative-pressure therapy, applies macrostrain through its flanges, and facilitates fluid management through integration with the dressing interface. This multi-functionality addresses the technical contradiction by making a single device capable of handling multiple therapeutic requirements without increasing overall system complexity.
2Productivity
If flanges or flaps are used to generate macrostrain under negative pressure, then tissue development is promoted, but the device structure becomes more complex
Solution Approach 1:
The bolster body is segmented into distinct functional components: a main body portion and detachable flanges. This segmentation allows the macrostrain-generating flanges to be separated from the negative-pressure delivery system, simplifying the overall structure while maintaining the ability to promote tissue development through macrostrain application.
Solution Approach 2:
The flanges are designed to be movable relative to the bolster body, allowing dynamic adjustment during use. This dynamic capability enables the flanges to generate macrostrain as needed while maintaining a relatively simple structure, as the complexity is introduced only when and where needed during the therapeutic process rather than being permanently integrated.
3Reliability
If a sealing member is added to apply controlled negative pressure and fluid delivery, then therapy effectiveness is improved, but the system complexity increases
Solution Approach 1:
The sealing member acts as an intermediary component between the bolster body and the dressing interface. It provides a controlled interface for negative pressure application and fluid delivery without requiring direct integration of complex mechanisms into the main device structure. This intermediary approach improves therapy effectiveness while minimizing the increase in overall system complexity.
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
Enhances tissue growth and wound healing by applying macrostrain and facilitating fluid management, thereby promoting tissue development and reducing healing times.
Implementation Method 1
a reduced pressure source configured to be fluidly coupled to the macrostrain device. The macrostrain device includes a base portion and one or more flanges. The one or more flanges are configured to be coupled to the sealing member and, in response to an application of negative pressure to the macrostrain device, the flanges are configured to generate a force at the tissue site
Implementation Method 2
New and useful systems, apparatuses, and methods for applying macrostrain to a wound edge in a negative-pressure therapy environment are set forth in the appended claims
Implementation Method 3
a manifold configured to be positioned adjacent the tissue site, a sealing member configured to be placed over the tissue site and the manifold
Data Source
AI summary
An apparatus for treating a tissue site may include a base having a first side and a second side, a first supply port coupled to the base, and a second supply port coupled to the base. The first supply port may be configured to be fluidly coupled to the tissue site and the second supply port may be configured to be fluidly coupled to the second side of the base. The apparatus may also include a plurality of flaps coupled to a portion of the base and configured to generate a force at the tissue site under a supply of negative pressure.


