part i fea of metallic stents (f2514) documents/standards activities/international... · peru...
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Kenneth E. Perry, Ph.D.ECHOBIO LLC
Bainbridge Island, WA
PERU Workshop on Medical Device Regulation:Policy and Technical Aspects
Part I FEA of Metallic Stents (F2514)
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1.1 Purpose—This guide establishes general requirements and considerations for the development of finite element models used in the evaluation of the performance of a metallic vascular stent design under uniform radial loading. Suggested criteria are provided for evaluating the typical cases of metallic tents under uniform radially oriented and pulsatile loading.
Recommended procedures for checking and validating the finite element model(s) are provided as a means to assess the model and analysis results.
Finally, the recommended content of an engineering report covering the mechanical simulations is presented.
ASTM F2514
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ASTM publishes six different types of standards:
Test methodA definitive procedure that produces test result.
SpecificationAn explicit set of requirements to be satisfied by a material, product, system or service.
GuideA compendium of information or series of options that does not recommend a specific course of action.
TerminologyA document comprising definitions of terms; explanations of symbols, abbreviations, or acronyms.
PracticeA definitive set of instructions for performing one or more specific operation that does not include a test result.
Types of ASTM Standards
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1) Device geometry is subdivided into small elements2) Material properties are assigned to each element3) Boundary and loading conditions are applied4) System of equations are solved
• Results include detailed stress/strain for entire model• Peak values are compared to material limit properties
Finite Element Analysis
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Role of FEA in the Engineering of cardiovascular devices
• Proof of concept: materials and design• Evaluate new designs, gain insight• Identify and evaluate worst-case conditions• Demonstrate safety and efficacy
“The purpose of computing is insight, not numbers”R. W. Hamming
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FEA is central in the product development of an implantable medical device
FEA Is Fundamental To Gaining Regulatory Approval
Material Calibration
Performance Testing
Computer Modeling Design IterationsDevice Testing
Animal Studies Clinical Studies
Product Development and Regulatory Approval
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2 expansion steps:Strain > 12%Stent prototype BREAKS
4 expansion steps:Strain < 6%Stent prototype SUCCESS
Start-up loses time and money Start-up has more confidence, design improves more quickly
Optimize Prototype Fabrication
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Design changes are subtle
New design concepts can be evaluated and ranked
Performance properties can be compared to design requirements
Stent Diameter
Car
gaEvaluate Design Changes
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Sensitivity and Calibration Studies
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e[N
]
µ=0.0
µ=0.5
µ=0.2
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e[N
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t=0.01
t=0.25 t=0.05
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e[N
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σms=412σms=312
σms=212
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Displacement [mm]
Forc
e[N
]
Ε=100
Ε=10000 Ε=500
Plateau Stress Strap Thickness
Strap StiffnessFriction
Sensitivity studies can consider ideal behavior and hypothetical conditions and lead to insight and understanding. FEA can be used to relate loading conditions between animal and bench models directly in terms of the material’s strain capacity.
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Company identifies worst case size/loading conditions, confirms fractures consistent with bench/animal model data and gains regulatory approval.
Identify Worst Case Size/Loading
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0.11mm
0.085mm0.13mm
Specifications and dimensions may change during the product development process and differ from those on preliminary CAD drawings.
Confirm Input Geometry
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Use nominal dimensions for the base model analysis.
A sensitivity study can be performed on the worst-case combination of dimensional variances.
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Random inspection of the strut dimension for 32+ stents
Nominal strut dimension = 0.061Maximum strut dimension = 0.064Minimum strut dimension = 0.058
Consider Variance of Geometry Data
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Characterize Material Behavior
Test samples– Made from the same
source as the device: tubing, wire, etc
– Must experience the same manufacturing steps as the device
Measurements– Load– Displacement– Extensometer strain!
Tensile testing of nitinol tubing
Tensile testing of stainless steel wire
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The response of the model should be compared with experimental data
A single element model is generally used
The output from the model should match the experimental data over the range of anticipated loading
Confirm Material Behavior
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For example, repeated loading of a device can cause incremental changes in a material each cycle
Material properties may depend on temperature and/or environment (especially for bioabsorbale materials)
These scenarios require more sophisticated material models and generally more difficult to obtain calibration parameters.
The sophistication of the model should match the physics of the problem and the purpose of the analysis
Material Behavior may change over time
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• Material Behavior Properties describes the mechanical response of the material, the relationship between stress and strain.
• Material Limit Properties specify limitations of the material, critical values that if exceeded, result in damage or fracture of the structure.
• Material limit properties can sometimes be determined from handbooks or material specifications
• Other times, it is necessary to determine them experimentally
Material Limit Properties
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Fatigue and fracture of materials are inherently stochastic processes. There is random behavior associated with a fracture occurring, or not, for a given set of loading conditions.
A sufficient number of samples must be tested to achieve an estimate with confidence.
Material Limit Properties from Testing Equivalently Processed Samples
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`Coupon’ samples are clipped from the final device (like a `coupon’ from the newspaper).
`Surrogate’ samples are created to mimic the final device, but with a simpler geometry that facilitates fatigue testing.
In all cases, the samples should be subjected to the same manufacturing processes used on the device.
Material Limit Properties from Testing Equivalently Processed Samples
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Mesh Density Study and Solution
Mesh DOF CPU Strain Stress
2x2 405 1.5 1.0 480
3x2 972 4 2.0 620
4x3 2220 10 3.0 950
5x4 4410 22 3.2 962
6x5 7686 42 3.21 965
8x6 16065 112 3.22 970
A mesh density study is used to show that any further refinement of the element size yields a negligible effect on the output from the model.
Most computational models for cardiac devices involve solving non-linear equations which requires and numerical iteration.
The analyst must also demonstrate sufficient numerical stability and convergence criteria for the model.
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Expansion Recoil
Ideal ID Expansion [mm] 2.926 -
Maximum OD [mm] 3.34 3.19
Minimum ID [mm] 2.9 2.75
Expansion
Recoil
Minimum ID
Maximum OD
A simple way to validate a computational model for a stent is to compare measurements of the expanded or recoiled shape to that predicted by the model.
Simple Model Validation
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Radial force measurements from an iris-diaphram test compared to FEA results
Radial force measurements from a flat-plate test compared to FEA results
Validation is most effective when performed over the full range of physiologically relevant conditions and include multiple sizes for a scaling reference.
Validation of Model with Bench-Top Testing
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Can include manufacturing processes of raw materials• Wire, sheet and seamless drawn tubing
Can include device fabrication processes• Stent expansion and forming
Can include device handling, loading and packaging• Compression to catheter dimensions, sheathing
Can include clinical procedures• Deployment, balloon expansion, positioning or removal
Can include long term loading and environment conditions• Pulsatile loading from heart beat, tidal breathing
Can include other relevant anatomical loading• E.g. bending or focal compression
Complete Loading History of Device Must Be Considered!
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Loading History for a Balloon Expandable Stent (Before Fatigue)
Plastic Strain during balloon
expansion
Stresses during
Expansion and Recoil
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tic S
trai
n [%
]
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ectiv
e St
ress
[MPA
]
For laser-cut stents: No residual stressFor wire stents: Maybe residual stress
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810MPa
17%
520MPa
0%
% Cold Work Tensile Strength
Endurance Limit 1M+ cycles
0 520 MPa 260 MPa
17 810 MPa 405 MPa
Endurance limit is increased by the effect of plasticity
The ultimate strength is a function of the plastic strain, which is increased during balloon expansion
Se ~ 0.5 Sult
The endurance limit is assumed to be one half of the ultimate tensile strength of the material:
Handbook of Materials for Medical Devices, Editor J.R. Davis, 2004
Fatigue Analysis Using Material Limit Data from Handbook
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Fatigue Analyses relate the stress and strain output from FEA to the material failure criteria.
These criteria account for residual and mean stress conditions to determine a Safety Factor for the design.
More Fatigue Analysis
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Número de ciclos
ampl
itud
cícl
ica
Large amplitude pre-loads can influence the durability of implantable medical devices
Loading History Affects Fatigue
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Residual stress caused by balloon expansion of stents changes the material limit properties and may need to be considered when performing a fatigue analysis
Residual Stress Affects Fatigue
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X-Y Gong, T. Duerig, A. Mehta, V. Imbeni, B. Berg, Presented at Society for Experimental Mechanics 2004 Annual Meeting
Mean strain levels affect the durability of medical devices made from nitinol
Mean Strain Affects Fatigue
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• A combination of Testing and Modeling is essential for successful device development
• Testing provides:– Material behavior information– Device performance validation data– Material limit information
• Modeling provides:– Self-consistent approach utilizing all experimental data– Bounds on the impact of uncertain information– Safety factors for complex loading scenarios
Device Engineering Best Practice
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High Priorities at the FDA
Science Priority Areas
#1 Modernize Toxicology
#2 Stimulate Innovation in Clinical Evaluations and Personalized Medicine to Improve Product Development and Patient Outcomes
#4 Ensure FDA Readiness to Evaluate Innovative Emerging Technologies
#5 Harness Diverse Data through Information Sciences to Improve Health Outcomes
• (Q)SAR models to predict human risk• Computer models of cells, organs, and
systems to better predict product safety and efficacy
• Virtual physiologic patients for testing medical products
• Clinical trial simulations that reveal interactions between therapeutic effects, patient characteristics, and disease variables
• Knowledge building tools• Methods to verify, store, share
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http://www.fda.gov/downloads/ScienceResearch/SpecialTopics/RegulatoryScience/UCM268225.pdf
FDA has identified an important role for Computer Modeling and Simulation in its strategic priorities.
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M&S at the FDA• Guidance on documentation and reporting M&S results in
pre-market submissions;– FDA DRAFT Guidance on Reporting of Computational Modeling
Studies in Medical Device Submissions – published Jan 20141
• Systematic assessment and understanding of device-use conditions;– Critical Path Innitiative2
– FDA Library of Models and Simulation3
– Medical Device Innovation Consortium4
1, http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm371016.htm2, http://www.fda.gov/ScienceResearch/SpecialTopics/CriticalPathInitiative/default.htm3, http://www.fda.gov/MedicalDevices/NewsEvents/WorkshopsConferences/ucm346375.htm4, http://mdic.org/projects/computer-modeling/
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M&S at the FDA
• Methodologies to experimentally validate M&S; • Test methods and guidance document development
– CDRH at FDA is actively engaged with ASTM
• Sensitivity analyses and uncertainty quantification– ASME verification & validation standards committee V&V 40
• Better elicitation of the consequence of the M&S being incorrect.– CDRH is getting ready to launch a pilot program to expand the current
uses of M&S in regulatory submissions, and to implement the credibility strategy
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ASTM F04.30.06Medical and Surgical Materials and Devices: Interventional Cardiology Task Group
Acknowledgements
Tina Morrison
Andres SchulzPaul LabossiereKasondra Totura