Small Diameter Fragmatome for Minimally Traumatic Lens Fragment Removal
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Solution Overview
Problem
Conventional methods for removing retained lens fragments during cataract surgery require large incisions and suturing, leading to increased patient trauma and prolonged healing time due to the use of large-diameter fragmatomes, which are not suitable for small-gauge instrumentation.
Innovation Solution
A small-diameter fragmatome with a tubular member of 23-gauge or less in diameter, capable of delivering emulsification energy and suction, is used through incisions no larger than 0.8 mm, allowing for minimally traumatic removal of lens fragments without the need for suturing.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Reliability
If conventional fragmatomes are used for lens fragment removal, then complete removal of lens fragments is achieved, but large incisions requiring suturing are required causing increased patient trauma and prolonged healing time
Solution Approach 1:
The patent changes the critical parameter of fragmatome diameter from conventional large sizes (20-gauge or larger, approximately 0.81 mm or more) to small sizes (23-gauge or smaller, approximately 0.57 mm or less). This parameter change enables the instrument to pass through small self-sealing incisions without requiring suturing, thereby reducing patient trauma and accelerating healing while maintaining the capability to effectively remove lens fragments
Solution Approach 2:
The patent replaces the conventional mechanical fragmatome system with a miniaturized version that uses ultrasonic or laser energy for emulsification. This substitution allows the instrument to achieve effective lens fragment removal through a smaller profile, eliminating the need for large incisions and suturing while maintaining therapeutic efficacy
2Productivity
If conventional combination fragmatome-aspirator is used, then lens fragments can be emulsified and removed simultaneously, but the larger operational profile requires even larger incisions
Solution Approach 1:
The patent miniaturizes the combination fragmatome-aspirator instrument, changing its operational profile from large conventional sizes to small 23-gauge or smaller dimensions. This parameter change enables the instrument to pass through small self-sealing incisions while maintaining the dual functionality of simultaneous emulsification and aspiration, thereby reducing patient trauma without sacrificing productivity
Solution Approach 2:
The patent integrates the aspirator function within the fragmatome instrument itself, creating a nested configuration where the aspiration lumen is incorporated into the fragmatome shaft. This nesting allows both emulsification and aspiration functions to be performed through a single small-profile instrument, eliminating the need for separate large instruments and reducing incision requirements
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
This approach reduces patient trauma and shortens recovery time by enabling the use of smaller incisions that do not require suturing, facilitating the removal of lens fragments with reduced trauma and faster healing.
Implementation Method 1
The tubular apparatus emulsifies the lens, typically with ultrasonic or laser energy provided at the tip, causing the natural lens, once lifted toward the front of the eye, to break apart.
Implementation Method 2
The tubular apparatus emulsifies the lens, typically with ultrasonic or laser energy provided at the tip, causing the natural lens, once lifted toward the front of the eye, to break apart.
Implementation Method 3
The tubular member may also be in suction communication with a suction source disposed to deliver suction at the distal end of the tubular member.
Data Source
AI summary
A medical instrument is disclosed, comprising a tubular member with proximal and distal ends. The distal end of the tubular member provides an elongated section having a substantially constant outside diameter of no more than 23-gauge (about 0.57 mm). The tubular member is in energy communication with an emulsification energy source disposed to deliver emulsification energy at the distal end of the tubular member. The tubular member may also be in suction communication with a suction source disposed to deliver suction at the distal end of the tubular member. The medical instrument may be used in a method to remove lens fragments from the eye, through incisions in the eye that are small enough not to require suturing after the operation.


