Personalized Bionic Cervical Disc Prosthesis Design

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Solution Overview

Problem

Existing artificial cervical disc prostheses fail to accurately match individual patient anatomical parameters, leading to abnormal instantaneous center of rotation (ICR) and inadequate restoration of physiological motion patterns, resulting in complications such as postoperative neck pain and prosthesis subsidence, particularly due to their design being based on European and American anatomical characteristics rather than Chinese patients.

Innovation Solution

A method for manufacturing a personalized bionic artificial cervical disc prosthesis involves creating a three-dimensional simulation model of the cervical spine, modifying morphological structures and material properties to mimic the patient's degenerated disc, and adjusting the prosthesis design to correct abnormal ICR and restore physiological motion patterns through finite element analysis and 3D printing technology.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If mass-produced artificial cervical disc prostheses with fixed specifications are used, then manufacturing efficiency is improved, but the match with individual patient anatomical parameters deteriorates

Engineering Contradiction:
Improvemanufacturing efficiencyVSAvoidmatch with patient anatomical parameters
Core Design Contradiction:
ProductivityVSManufacturing precision

Solution Approach 1:

The patent applies parameter changes by transitioning from fixed specification prostheses to customizable parameters. The manufacturing process allows adjustment of prosthesis parameters (size, shape, curvature) based on individual patient CT scan data, enabling each prosthesis to be optimized for the specific patient's anatomy while still using standardized manufacturing processes.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent implements preliminary action by performing patient-specific anatomical measurements and simulations before manufacturing. CT scans are acquired and processed to create patient-specific models, and the prosthesis design is optimized through finite element analysis prior to actual manufacturing, ensuring anatomical match before production begins.

Inventive Principle:
Principle #10Preliminary action

2Ease of manufacture

If prosthesis design is based on European and American anatomical characteristics, then standardized production is improved, but the suitability for Chinese patients deteriorates

Engineering Contradiction:
Improvestandardized productionVSAvoidsuitability for Chinese patients
Core Design Contradiction:
Ease of manufactureVSAdaptability or versatility

Solution Approach 1:

The patent applies local quality by tailoring the prosthesis design to match the specific patient's local anatomical characteristics. Rather than using a one-size-fits-all design based on Western anatomy, the system extracts patient-specific parameters from CT scans and customizes the prosthesis geometry to match that individual's cervical spine anatomy, including vertebral body dimensions and disc space characteristics.

Inventive Principle:
Principle #3Local quality

3Device complexity

If the prosthesis does not match patient-specific anatomical parameters, then manufacturing complexity is reduced, but the accuracy of instantaneous center of rotation deteriorates

Engineering Contradiction:
Improvemanufacturing complexityVSAvoidaccuracy of instantaneous center of rotation
Core Design Contradiction:
Device complexityVSMeasurement precision

Solution Approach 1:

The patent implements feedback through an iterative design and simulation process. Patient-specific anatomical data is used to create initial prosthesis designs, which are then tested through finite element analysis to evaluate ICR accuracy. The design is refined based on simulation feedback, and the process repeats until optimal ICR accuracy is achieved before manufacturing.

Inventive Principle:
Principle #23Feedback

4Device complexity

If prosthesis design fails to restore physiological motion patterns, then design simplicity is improved, but the risk of adjacent segment disease increases

Engineering Contradiction:
Improvedesign simplicityVSAvoidrisk of adjacent segment disease
Core Design Contradiction:
Device complexityVSReliability

Solution Approach 1:

The patent applies dynamics by designing the prosthesis to enable dynamic, physiological motion patterns rather than fixed mechanical movement. The patient-specific design allows the prosthesis to replicate the natural instantaneous center of rotation trajectory and couple motions of the native cervical disc, enabling adaptive movement that responds to physiological loading conditions.

Inventive Principle:
Principle #15Dynamics

Data Source

PatentUS20240277480A1Method for manufacturing personalized bionic artificial cervical disc prosthesis and prosthesis
Publication Date: 2024.08.22 BEIJING TIANTAN HOSPITAL AFFILIATED TO CAPITAL MEDICAL UNIV
  • US20240277480A1 patent drawing
  • US20240277480A1 patent drawing
  • US20240277480A1 patent drawing

AI summary

A method for manufacturing a personalized bionic artificial cervical disc prosthesis and a prosthesis can include establishing a three-dimensional simulation model of a cervical spine with a degenerated cervical disc; modifying morphological structures and material properties of the degenerated cervical disc to obtain a three-dimensional simulation model of the artificial cervical disc prosthesis; implanting the three-dimensional simulation model of the artificial cervical disc prosthesis into the three-dimensional simulation model of the cervical spine, applying a load to the three-dimensional simulation model of the cervical spine to mimic physiological motion of the cervical spine, and calculating kinematics and biomechanical indexes of an implanted segment and adjacent segments; adjusting the three-dimensional simulation model of the artificial cervical disc prosthesis until the abnormal ICR can be corrected and optimum biomechanical effects can be obtained after the prosthesis is implanted; and manufacturing the artificial cervical disc prosthesis.