Shape Memory Cavity Creation Device for Vertebral Fracture
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Solution Overview
Problem
Current treatments for vertebral compression fractures and related spinal deformities are limited in their ability to effectively create or enlarge cavities in bone tissue, particularly in a minimally invasive manner, which hinders the restoration of vertebral body height and correction of spinal curvature.
Innovation Solution
A system comprising a cannula and a cavity creation device with a friction reduction covering and a cavity creation member that can move from a retracted to a deployed position, allowing for the creation or enlargement of a cavity in the vertebral body, utilizing a guidewire and cannula to facilitate minimally invasive procedures.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Ease of operation
If a cannula or bone needle is used to insert bone cement into the vertebral body, then the procedure can be performed minimally invasively, but the ability to create or enlarge cavities in the bone tissue is limited
Solution Approach 1:
The cavity creation device is divided into separate functional components: a cavity creation member for generating the cavity, a friction reduction covering to facilitate movement, and a retention mechanism to hold the components together. This segmentation allows each part to perform its specific function effectively while maintaining overall minimally invasive capability.
Solution Approach 2:
The cavity creation member is designed to be movable between a retracted position (for insertion through the cannula) and a deployed position (for cavity creation). This dynamic transformation enables the device to transition from a simple minimally invasive instrument to an effective cavity creation tool at the target site.
2Reliability
If a mechanical device or balloon expansion is used to create space in the compressed vertebral body, then cavity creation is improved, but the device complexity increases
Solution Approach 1:
The friction reduction covering is extracted as a separate component that can be easily attached to and removed from the cavity creation member. This extraction simplifies the overall device structure by allowing the cavity creation member to be the primary functional element, with the covering serving as an optional additive component only when needed.
Solution Approach 2:
The cavity creation member is designed to nest within the friction reduction covering when not in use, and the entire assembly nests within the cannula during insertion. This nested configuration reduces device complexity by allowing multiple components to occupy the same space when not actively functioning, simplifying storage and handling.
3Reliability
If the cavity creation member is moved from retracted to deployed position, then cavity creation effectiveness is improved, but friction resistance increases
Solution Approach 1:
The friction reduction covering acts as an intermediary element between the cavity creation member and the surrounding tissue/cannula. By introducing this intermediate layer with reduced friction properties, the device can move more smoothly from the retracted to deployed position, overcoming the friction resistance that would otherwise hinder cavity creation effectiveness.
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
Enables the creation or enlargement of cavities in bone tissue with reduced friction, allowing for effective vertebral body height restoration and spinal curvature correction, thereby improving treatment outcomes for vertebral compression fractures.
Implementation Method 1
a friction reduction covering that includes a covering body sized to be received in a cannula opening
Implementation Method 2
The cavity creation member can include a portion that is biased to move from a first shape when in the retracted position to a second shape when in the deployed position
Data Source
AI summary
A system is configured to create or enlarge a cavity in a tissue body and generally includes a cannula, a friction reduction covering, and a cavity creation member. The cavity creation member includes an end portion that is configured to transition between a first shape and a second shape that is different from the first shape. In operation, retracting the friction reduction covering relative to end portion causes the end portion to change shape from the first shape to the second shape such that the cavity creation member is configured to create or enlarge a cavity in the tissue body as the second end portion exits the friction reduction member.


