Hemostatic Anchorage Substrates for Implantable Medical Devices

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Solution Overview

Problem

Existing anchorage devices do not effectively stop or reduce blood flow at surgical sites and speed up the blood clotting process while securing implantable medical devices to tissue.

Innovation Solution

Anchorage devices incorporating a hemostatic agent, such as tranexamic acid, are integrated into the substrate, which can be woven, knitted, or braided from filaments or fibers, allowing for controlled elution to promote hemostasis.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If anchorage devices are used to secure implantable medical devices to tissue, then anchoring support is provided during healing, but blood flow at the surgical site is not effectively stopped or reduced

Engineering Contradiction:
Improveanchoring supportVSAvoidblood flow
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent combines two functions into a single device: the anchorage function (securing the implantable medical device) and the hemostatic function (stopping blood flow). The substrate that provides mechanical anchoring is integrated with a hemostatic agent, creating a unified device that simultaneously anchors tissue and controls bleeding, eliminating the need for separate hemostatic interventions.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The hemostatic agent acts as an intermediary substance that mediates between the surgical site and the blood flow. When incorporated into the substrate, this agent intercepts and neutralizes the harmful blood flow effect by promoting clotting, while allowing the substrate to maintain its anchoring function.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Reliability

If traditional anchorage devices are used, then tissue anchoring is achieved, but the blood clotting process is not accelerated

Engineering Contradiction:
Improvetissue anchoringVSAvoidblood clotting time
Core Design Contradiction:
ReliabilityVSLoss of time

Solution Approach 1:

The hemostatic agent is pre-incorporated into the substrate before implantation. This preliminary inclusion ensures that as soon as the device is implanted and contacts blood, the hemostatic action begins immediately without requiring additional steps or time for separate hemostatic interventions, thereby accelerating the overall clotting process.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The substrate with integrated hemostatic agent provides continuous hemostatic action throughout the healing process. The agent remains active within the substrate structure, continuously promoting clotting at the surgical site rather than providing a single-point intervention, which maintains reliable tissue anchoring while continuously managing blood flow.

Inventive Principle:
Principle #20Continuity of useful action

3Reliability

If hemostatic agents are added to anchorage devices, then blood clotting is enhanced, but device complexity increases

Engineering Contradiction:
Improvehemostatic effectivenessVSAvoiddevice structure
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

Rather than adding a separate hemostatic device or component, the patent merges the hemostatic agent directly into the substrate material itself. This integration approach maintains device simplicity by using a single unified structure that performs both anchoring and hemostatic functions, avoiding the complexity of multiple separate components or assembly steps.

Inventive Principle:
Principle #5Merging (Combining)

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 integration of a hemostatic agent like tranexamic acid enhances clotting by inhibiting fibrinolysis, effectively reducing bleeding and supporting implantable medical devices during the healing process.

Implementation Method 1

The integration of a hemostatic agent like tranexamic acid enhances clotting by inhibiting fibrinolysis, effectively reducing bleeding

Methodology Applied
Scientific EffectFibrinolysis inhibition: Coagulation

Implementation Method 2

anchorage devices incorporating a hemostatic agent, such as tranexamic acid, are integrated into the substrate, which can be woven, knitted, or braided from filaments or fibers, allowing for controlled elution to promote hemostasis

Methodology Applied
Scientific EffectElution: Diffusion

Data Source

PatentEP3452123B1Hemostatic devices and methods of use
Publication Date: 2025.09.24 MEDTRONIC INC
  • EP3452123B1 patent drawingFigure 1
  • EP3452123B1 patent drawingFigure 2~3
  • EP3452123B1 patent drawingFigure 4~5

AI summary

An anchorage device is provided that is configured to surround an implantable medical device. The anchorage device includes a substrate formed from a first material and a second material. At least one of the first and second materials includes a hemostatic agent. Kits, systems and methods are disclosed.