Abstract
A full-scale topology optimisation formulation has been developed to automate the design of cages used in instrumented transforaminal lumbar interbody fusion. The method incorporates the mechanical response of the adjacent bone structures in the optimisation process, yielding patient-specific spinal fusion cages that both anatomically and mechanically conform to the patient, effectively mitigating subsidence risk compared to generic, off-the-shelf cages and patient-specific devices. In this study, in silico medical device testing on a cohort of seven patients was performed to investigate the effectiveness of the anatomically and mechanically conforming devices using titanium and PEEK implant materials. A median reduction in the subsidence risk by 89% for titanium and 94% for PEEK implant materials was demonstrated compared to an off-the-shelf implant. A median reduction of 75% was achieved for a PEEK implant material compared to an anatomically conforming implant. A credibility assessment of the computational model used to predict the subsidence risk was provided according to the ASME V&V40–2018 standard.
Highlights
• A full-scale topology optimisation formulation to design anatomically and mechanically conforming patient-specific spinal fusion implants was tested, in silico, on a cohort of seven patients.
• The anatomically and mechanically conforming patient-specific spinal fusion cages reduced the median subsidence risk by 89% for titanium and 94% for PEEK implant materials compared to an off-the-shelf implant.
• The method was similarly effective for patients with low and high bone quality.
• The credibility of the in silico medical device testing procedure was evaluated according to the ASME V&V40–2018 standard.
1 Introduction
Recent advancements in patient-specific computational models enable in silico clinical trials to play an increasing role in the development of medical devices. The benefits of in silico clinical trials over conventional clinical trials include 1) cost and time efficiency; 2) collecting data before animals or humans are subjected to potential harm; 3) comparing multiple treatments per patient; and 4) a broader or more in-depth analysis of treatments (); ().
In recent years, there has been a surge in the use of in silico clinical trials, e.g., in the fields of pharmacology, cardiovascular stents, diabetes treatment, and orthopaedics (; ; ; ; ). Looking specifically at in silico clinical trials where finite element (FE) models were used, Kassab-Bachi et al. studied the effect of geometric variability in the spine on the biomechanical response, i.e., the intradiscal pressure and the facet joint contact pressure in a cohort of 152 patients (), and Aldieri et al. investigated the fracture risk of the proximal human femur () with a focus on proving the credibility of the computational models according to the ASME V&V40–2018 standard (). With further development, in silico clinical trials will potentially be accepted by regulatory agencies as supplementary material for market approval applications and may be used as a (partial) replacement of animal and human clinical trials () ().
The authors recently developed a topology optimisation (TO) strategy that automates the design of cages used in instrumented transforaminal lumbar interbody fusion (TLIF). The strategy incorporates the mechanical response of the adjacent bone structures in the optimisation process, with the goal to reduce subsidence risk. This results in anatomically and mechanically conforming devices (AMCDs) that successfully reduce the subsidence risk compared to off-the-shelf (OTS) cages and anatomically conforming devices (ACDs) () (). The optimisation and in silico testing process have been automated further to facilitate in silico medical device testing on multiple patients. Furthermore, the optimization and testing procedures were modified with the goal to increase the effectiveness of optimisation and improve the credibility of the in silico testing process. As Viceconti et al. suggested, the evaluation of the credibility of the computational model should be considered early in the development of new in silico methods using guidelines from regulatory agencies and examples e.g. .
Thus, the aim of this study was to perform in silico medical device testing of AMCDs on a cohort of seven patients and compare the AMCDs to OTS cages and ACDs, using titanium and PEEK implant materials. The credibility assessment of the computer model that was used in the subsidence risk prediction was carried out according to the ASME V&V40–2018 standard. We hypothesized that AMCDs reduce the subsidence risk over ACDs and OTS cages for patients with a broad range of bone quality. Furthermore, we hypothesised that PEEK cages have lower subsidence risk than titanium cages and that there is a negative correlation between the subsidence risk and bone quality.
2 Methods
2.1 Topology optimisation
Our newly developed TO strategy () () to optimise spinal fusion cages was, in this work, slightly modified to improve its effectiveness and to allow the optimisation of titanium and PEEK implant materials. The computational domain Ω comprised an implant domain (Ωimplant), a bone domain (Ωbone), and a rigid domain (Ωrigid), with Ω = Ωimplant ∪ Ωbone ∪ Ωrigid (Figure 1A). Ωbone contains the bone structures and patient-specific material properties. Ωimplant was the design domain that was subjected to optimisation in the TO process.
FIGURE 1
Domain Ω, with a size of 54 mm × 54 mm × 54 mm, was discretised using a structured grid of 1.728 million hexahedral elements with an isotropic element edge length of 0.45 mm. Resampling was performed using SimpleITK version 2.1.1.2 () to adjust the CT scan resolution to match the resolution of Ω and to position the Functional Spinal Unit (FSU) in the approximate centre of Ω. The vertebrae were partially embedded in Ωrigid.
Six load cases (axial compression, lateral shear, posterior–anterior shear, flexion, lateral bending, and axial rotation) were used in the TO process. The applied loads were based on the study by and the OrthoLoad dataset () (Figure 1C; Table 1). Loads were applied on nodes at the top of Ω. Nodes on the bottom of Ω were fixed in all directions. The load magnitude for all patients was scaled with respect to the patient’s body weight and the body weight of patient 1 (see Section 2.2), as was used in the subsidence risk assessment () (Zhang et al., 2017).
TABLE 1
| Description | Component | Patient 1 | Unit |
|---|---|---|---|
| Axial compression | −177 | N | |
| Posterior/anterior shear | 27 | N | |
| Lateral shear | 5 | N | |
| Flexion | 0.4 | Nm | |
| Lateral bending | 0.5 | Nm | |
| Axial rotation | 0.7 | Nm |
Spinal loads during daily living applied in the TO process, derived from the study by and the OrthoLoad dataset () from a patient with similar weight to patient 1 (see Section 2.2) [table from and ].
Similar to the TO formulation that was previously used () (), the compliance of the bone–implant system was minimised for all load cases (optimisation objective), but to avoid the overloading of the adjacent vertebrae, the maximum principal strains in Ωbone were constrained (optimisation constraints). Constraining the minimum principal strains was omitted because our previous work indicated that this constraint was inactive () () because the compression load from the implant is transferred to the shear, orthogonal to the endplate, along the periphery of the implant. In pure shear, the maximum and minimum principal strains have equal magnitudes but opposite signs, indicating that the tensile limit is reached first due to a lower threshold. Shearing is the dominant loading mode in the endplates, which was confirmed by several authors who identified shear failure of the vertebra endplates as the dominant failure mode in subsidence (); (). Furthermore, we use a local volume constraint on Ωimplant to create a porous implant structure. To promote manufacturability, the minimum strut diameter was controlled using robust TO formulation. No other manufacturing-specific constraints were added to make a comparison between titanium and PEEK fair because these materials have different manufacturability requirements.
The compliance minimisation problem with the maximum principal strain constraint and local volume constraint in discrete form is written as
where represents the six load cases with , is the objective function (Equation 1), is the constraint on the maximum principal strain response (Equation 2) for the compression load case in the Ωbone, and is the local volume constraint (Equation 3) on Ωimplant. The maximum principal strain constraint on the compression load case was used as this was the active constraint () () with a maximum principal strain limited to 0.73% based on the work by . The local volume constraint followed the implementation published by Wu et al. (2018). The local volume constraint was applied on the dilated design , with a local volume fraction of 0.35, a filter radius of 3.5, and p-mean penalty of 16. Finally, Poisson´s ratio for Ωimplant was set to 0.3 for titanium and 0.43 for PEEK. The E-modulus for the titanium implant was set to 110 GPa (), and for the PEEK implant, the E-modulus was set to 3 GPa (Zhao et al., 2018). The optimisation was run for 24 h on a computational cluster using 1,000 cores in parallel. The final design should at least exhibit a discreteness measure that is lower than 3%. This value is considered to be an acceptable convergence to a solid/void design (Wang et al., 2011).
The resulting cage designs from the optimisation process have a voxelised surface because of voxel-based discretisation. The final designs were achieved by applying the “Iso volume” filter to the optimised cage using a contour of 0.5 as the threshold and exporting to an .stl file using vtk 9.1.0 (). The resulting file was used in the subsidence risk assessment Section 2.3 and Section 2.4.
2.2 Study patient datasets
Anonymised pre-operative computed tomography (CT) scans with clinical resolution (voxel sizes of approximately 0.30 mm × 0.30 mm × 0.50 mm), from seven female patients, were provided by the Schulthess Klinik, Zürich (Table 2). The patients, who were diagnosed with degenerative spondylolisthesis or degenerative disk disease, were treated with a TLIF procedure. Patients with other spinal diseases such as trauma, infection, or tumour were excluded. The CT images from patients 1 and 2 were reused from a previous study () (), and all the patients provided informed consent for the use of their data for research purposes. The CT scans were calibrated using a phantom-less calibration procedure (). The vertebrae were segmented using open-source software MITK-GEM (). T-scores, based on DXA scans, were only available for the L4 level for three patients. Bone quantity was thus assessed by calculating the integral volumetric bone mineral density (vBMD) for each vertebra that was modelled, including the endplates and cortical bone in accordance with the work by (Table 2; Figure 2).
TABLE 2
| FSU ID | Age | Gender | BMI | Weight [kg] | Level | vBMD [g/cm3] | T-score |
|---|---|---|---|---|---|---|---|
| 1 | 66 | Female | 18.3 | 51 | L4 | 0.16 | −2.3 |
| L5 | 0.15 | NA | |||||
| 2 | 58 | Female | 25.6 | 75 | L4 | 0.40 | NA |
| L5 | 0.45 | NA | |||||
| 3 | 57 | Female | 24.2 | 70 | L4 | 0.16 | NA |
| L5 | 0.17 | NA | |||||
| 4 | 67 | Female | 41.6 | 100 | L4 | 0.52 | 1.5 |
| L5 | 0.54 | NA | |||||
| 5 | 76 | Female | 22.9 | 64 | L4 | 0.15 | NA |
| L5 | 0.21 | NA | |||||
| 6 | 76 | Female | 22.6 | 64 | L4 | 0.21 | NA |
| L5 | 0.27 | NA | |||||
| 7 | 52 | Female | 24.3 | 60 | L4 | 0.33 | 1.3 |
| L5 | 0.31 | NA |
Patient data overview. BMI, body mass index; vBMD, volumetric bone mineral density; T-scores based on DXA scans when available. NA, not available.
FIGURE 2
2.3 Finite element models
The model building process follows the workflow presented by () but is briefly described here for clarity and context. A commonly used, commercially available OTS cage, for a TLIF procedure with a height of 9 mm, was reengineered into a CAD model. The cages were placed anteriorly and across the mid-line in an optimal position, restoring spinal alignment as much as possible. The implant placement was checked by a spine surgeon according to standard surgical fusion techniques for the TLIF approach. The ACD and AMCD design domains were created by matching the top and bottom surfaces of the CAD model to the patient’s endplates. It was assumed that the intervertebral disc and cartilaginous endplates were removed during the surgery. The cages were placed according to standard surgical fusion procedures, and the implant position was checked by a spinal surgeon.
In the optimisation process (Section 2.1), daily living load cases were applied, which cause strains in the bone structures within the linear regime. The optimisation process was followed by the subsidence risk assessment (Section 2.4) that was performed in commercial FE analysis software where the cages were loaded with hyper-physiological loading that can potentially lead to non-linear material response, both in the implant and the bone structures.
In the subsidence risk assessment, 10-node tetrahedral elements (C3D10M) were used to mesh the bone and implant structures with an average edge length of 1.5 mm for the vertebrae and 0.5 mm for the cages. The apparent density-to-modulus relationship from the study by (Table 5) was used to assign material properties to the bone elements in the FE mesh based on an internal calibration of the CT grey levels to the apparent density. Poisson’s ratio was set to 0.3, and the minimum value for Young’s modulus was set to 25 MPa for the bone structures. The subsidence risk assessment was performed in an explicit non-linear FE solver (Abaqus 2021, Dassault Systèmes, Vélizy-Villacoublay, France), assuming non-linear geometry and a general contact formulation. The bone structures were modelled using a rate-independent elasto–plastic material model, which captures the asymmetric tension–compression post-yield behaviour of bone (Figure 3B) (). A compressive follower load (FL) of 310 N for patient 1 was assumed based on the study by and the OrthoLoad dataset (). The magnitude of FL for all patients was scaled with the patient’s body weight to the body weight of patient 1 and subsequently distributed on the superior endplate of the superior vertebra such that the direction of the load was as defined by (Figure 1B). The inferior endplate of the inferior vertebra was constrained in all translations. The models were solved on a computational cluster using 64 cores in parallel. Poisson’s ratio was set to 0.3 and 0.43 for titanium and PEEK, respectively. The material models for titanium and PEEK are shown in Figure 3A.
FIGURE 3
2.4 Subsidence risk assessment
The maximum factor of fracture risk (FFR) was used as a surrogate for subsidence risk. The maximum FFR is quantified as the degree of overloading of the vertebrae using a maximum principal strain limit of 1.5% and a minimum principal strain limit of −2.0% (
2.5 Computer model credibility assessment
Credibility assessments were performed following the ASME V&V40–2018 standard. Note that the following applies to the subsidence risk assessment of Section 2.3, 2.4. The process starts with the definition of the question of interest (QoI). The next step was to formulate the context of use (CoU) including the function and scope of the computer model that was used in answering the QoI (Table 3).
TABLE 3
| QoI | Do the new AMCDs reduce subsidence risk compared to ACDs and OTS implants? |
| CoU | A patient-specific FE model (Section 2.3) will be used to quantify the subsidence risk under a hyper-physiological loading condition. The patient-specific FE models are built using clinical CT scans including the FSU of interest. The subsidence risk assessment (Section 2.4) provides an estimate, for a given patient and implant, of the factor of fracture risk (FFR). The resulting maximum FFR is used as a surrogate for subsidence risk and as an outcome variable in a comparative study. Bench tests were performed to test the implant integrity and provide validation of the FE model ( |
Definition of the question of interest (QoI) and the context of use (CoU).
The model risk describes the possibility that the use of the computer model leads to a decision causing harm to the patient. The model risk is composed of the “model influence” and the “decision consequence.” The model influence describes how much influence the results of the computer model have on the decision maker.
The model influence is defined to be MEDIUM because the decision of the AMCD has lower subsidence risk than the ACD or OTS, for a specific patient, is informed by the results from the computer model, in combination with the observations and judgment of the spinal surgeon.
The decision consequence is the significance of harm to the patient in the case of an incorrect decision.
The decision consequence is defined to be LOW because a worst-case incorrect decision would lead to a patient being treated by an OTS cage, which is the current standard practise.
The selection of computer model credibility activities is based on the credibility requirements for the computational model that should correspond with the model risk that was defined (Table 4). Model credibility is defined as the trust in the predictive capability of the computer model for the CoU, according to the ASME V&V40–2018.
TABLE 4
| Context of use | Model influence | Decision consequence | Model risk |
|---|---|---|---|
| Patient-specific FE model used to assess the subsidence risk of an implant (Table 3) | MEDIUM | LOW | LOW |
Model risk summary for this study following example 6 in ASME V&V40–2018.
The ASME V&V40 standard suggests several credibility factors that should be evaluated to demonstrate that the overall credibility of the computational model agrees with that of the model risk (Table 8).
A mesh convergence study of the bone structures was performed by calculating changes in the maximum FFR for gradually decreasing element edge length. Mesh convergence of the implant structures was assessed by decreasing the element edge length of the implant mesh while maintaining an element edge length of 1.5 mm for the bone structures. The maximum FFRs were calculated, as well as the percentage difference in the maximum FFR between different meshes (). The simulations were run using patient 2 and the ACD in titanium. Furthermore, for the mesh convergence study, a homogeneous Young’s modulus of 350 MPa for the bone structures was used.
The sensitivity analysis of the maximum FFR with respect to the load magnitude was performed by calculating the variation in the maximum FFR while applying variations (2.5% and 25% change), positive or negative, to the applied load magnitude. The sensitivity analysis of the maximum FFR to different apparent density-to-modulus relationships was performed by calculating the maximum FFR using two alternative relationships, from the study by
TABLE 5
| Density-to-Young’s modulus relationships | |
|---|---|
Apparent density-to-Young’s modulus relationships used in sensitivity study with Ouyang et al. as baseline.
2.6 Statistical analysis
For statistical analysis, Spearman’s rank correlation coefficient analysis was used to calculate the correlation coefficient r with (−1 < r < 1) between two variables. A Mann–Whitney U test was used to compare two samples with statistical significance assumed when p < 0.05. The small sample size in this study does not allow for reliable normality testing (
3 Results
3.1 Optimised cages
The resulting AMCDs show a “box-like” design and are hollow in the inside with patient-specific internal strut structures, similar as found by
TABLE 6
| Titanium implant | PEEK implant | |
|---|---|---|
| Porosity | 58.47% ± 1.1% | 59.44% ± 1.5% |
| Mean pore diameter | 5.01 mm ± 0.54 mm | 4.88 mm ± 0.43 mm |
Mean +/− standard deviation of porosity and pore diameter for AMCDs.
3.2 Subsidence risk assessment
Figure 4 highlights elements with FFR larger than 1, which indicates mechanical overloading, for patient 1 for all three implant types. The red elements are associated with the titanium implant and the green elements with the PEEK implant. Figure 4 shows that the titanium implant leads to a higher volume of overloaded elements than the PEEK implant material by 15%, 5%, and 300%, for the OTS cage, ACD, and AMCD, respectively. Furthermore, the two separate concentrations in the superior vertebra compared to the evenly distributed overloaded elements in the lower vertebra are explained by the contact areas between the endplate and the OTS cage (Figure 4A). The ACD and AMCD were endplate conforming and show that the regions of overloaded elements were reduced (Figures 4B, C).
FIGURE 4

Elements with FFR >1 are highlighted with green for PEEK implant material and red for titanium implant material. (A) OTS model. (B) ACD model. (C) AMCD model. Data from patient 1.
The subsidence risk assessment provided the maximum FFR data for the three implant groups in PEEK and titanium implant materials for all patients (Figure 5A). In general, the subsidence risk for ACDs was reduced, compared to the OTS cages, and the subsidence risk for AMCDs was reduced, compared to the ACD, for all patients.
FIGURE 5

Results summarised: (A) Relationships between the maximum FFR and vBMD for the three implant groups. (B) Statistical significance of the reduction between different groups formed by the implant type and implant material.
Comparison of the maximum FFR results between PEEK and titanium implant materials, for the three implant types, showed that there was no statistical difference between the PEEK and titanium groups with p-values of 0.71, 0.95, and 0.53 for the OTS, ACD and AMCD implant types, respectively. The negative correlations between the maximum FFR and vBMD for the different implant types are given in Figure 5A. As an illustration, the linear correlations between the maximum FFR and vBMD indicate that, for a patient with a mean vBMD of 0.25 g/cm3, the maximum FFR values would be 14.8, 3.8, and 2.0 for the OTS cage, ACD, and AMCD, respectively.
A comparison of the implant type and implant materials is given in Figure 5B. This shows that the median maximum FFR reduction between the OTS PEEK to AMCD PEEK, OTS Ti to AMCD Ti, and ACD PEEK to AMCD PEEK is statistically significant with 94%, 89%, and 75%, respectively. The reduction in the maximum FFR for the OTS cage to the ACD, ACD to AMCD, and OTS cage to AMCD is not strongly significantly correlated with vBMD, with p-values of 0.18, 0.07, and 0.09 for the PEEK implant material and 0.12, 0.15, and 0.09 for titanium, respectively.
3.3 Computer model credibility assessment
An element edge length of 1.5 mm was chosen for the bone structures because subsequent decreases in element edge length produced percentage differences in the maximum FFR lower than the 5% threshold (Figure 6A). For the implant structures, an element edge length of 0.5 mm was chosen, and the mesh convergence study indicated that variations had little influence on the maximum FFR (Figure 6B).
FIGURE 6

Results from the mesh convergence study. The maximum FFR value is indicated by the blue line, the percentage difference is indicated by the green bars, and the 5% threshold is indicated by the black line. (A) Mesh convergence results for bone structures in the subsidence risk assessment. (B) Mesh convergence results of implant structures in the subsidence risk assessment.
Table 7 shows the results of the sensitivity studies. The sensitivity of the maximum FFR with respect to variations in load magnitude, different density-to-Young’s modulus relationships, and different constitutive models is illustrated by reporting the maximum percentage difference derivation from the base case. Patient 2 is loaded in the linear loading regime and shows little variation in the maximum FFR for the applied variations. On the other hand, patient 6 shows a larger variation in the maximum FFR because this patient is loaded in the non-linear loading regime.
TABLE 7
| Patient | 2 | 6 |
|---|---|---|
| Implant type | ACD | AMCD |
| Material | Titanium | PEEK |
| Variation load magnitude with 2.5% | 0.2% | 17.9% |
| Variation load magnitude with 25% | 1.5% | 76.5% |
| Density-to-Young’s modulus relationships | −0.8% | −0.1% |
| Constitutive models | 0.0% | 108% |
Overview of the sensitivity study. The maximum percentage difference deviation from the base case is reported. Variation load magnitude: sensitivity of the maximum FFR with respect to the variation in the load magnitude. Relationships: sensitivity of the maximum FFR regarding different density-to-Young’s modulus relationships. Constitutive model: sensitivity of the maximum FFR with respect to the constitutive model.
The credibility factors were assessed after the outputs of the verification and validation (V&V) activities were obtained. The robustness of the activities and level of rigour were evaluated according to the guidelines and examples from the ASME V&V40–2018 standard. This assessment is summarised in columns “Rigour selected” and “Achieved credibility” in Table 8.
TABLE 8
| Activity categories | Credibility factor | Rigour selected | Achieved credibility | |
|---|---|---|---|---|
| Verification | Code (5.1.1) | Referring to Dassault’s quality system | b | Medium |
| Calculation (5.1.2.1) | Mesh convergence of the bone domain | b | Medium | |
| Mesh convergence of the implant domain | b | Medium | ||
| Sensitivity of the maximum FFR to magnitude of load | b | Medium | ||
| Validation | Computational model (5.2.1.2.1) | Sensitivity of the maximum FFR of different density relationships | b | Medium |
| Sensitivity of the maximum FFR to constitutive model | b | Medium | ||
| Comparator (5.2.2.1 + 5.2.2.2) | Bench test validation was provided by | b-c-b-b-b-a-a-a-b | Medium | |
| Assessment (5.2.3) | Assessment of the rigour and achieved credibility | b-b-b-c-c | High | |
| Applicability | Relevance to the quantity of interest (5.3.1) | Section 3.3 | a | Low |
| Relevance to CoU (5.3.2) | Section 3.3 | b | Medium | |
Outcome of credibility assessment. Overview of the selected credibility activities according to
The quantities of interest considered in the verification and validation study were the maximum FFR and the force–displacement curve in the mechanical tests. Therefore, we consider the quantities of interest relevant but not identical since the maximum FFR cannot be calculated directly in mechanical testing of samples. In the validation study, the range of applied forces is physiological and, therefore, deemed relevant for the CoU. The mechanical tests did not include the bone structures; therefore, partial overlap between the validation and CoU is concluded.
4 Discussion
The aim of this study was to perform in silico medical device testing of AMCDs, which were designed and optimised by our recently developed full-scale TO strategy, and compare the subsidence risk to OTS cages and ACDs. We performed the study on seven patient datasets using titanium and PEEK implant materials. We hypothesised that AMCDs would reduce subsidence risk over OTS cages and ACDs. We found that AMCDs reduce the subsidence risk compared to OTS cages and ACDs and that the median reduction is statistically significant for OTS PEEK compared to AMCD PEEK, OTS Ti to AMCD Ti, and ACD PEEK to AMCD PEEK (Figure 5B). Similar results were published by Chatham et al., who compared a custom-shaped cage with a standard cage and found a significant reduction in stresses at the bone–implant interface (
Furthermore, we hypothesised that PEEK cages would have lower subsidence risk than titanium cages; however, our data did not show this to be the case. Other research studies confirm this observation and conclude that the implant geometry has a larger influence on subsidence risk than the implant material (
Lastly, we hypothesised that there is a negative correlation between subsidence risk, represented by the maximum FFR, and bone quality. We found that this negative correlation exists and is statistically significant for all three cage types (Figure 5A). This finding is in line with that of the previous literature (
We investigated how effective the optimisation method is in reducing the subsidence risk for patients with different bone densities; however, no significant correlation was found between the reduction for the maximum FFR and vBMD, suggesting that the effectiveness of the method is not strongly related to the bone quality of the patient. A possible explanation is the phenomena of sclerosis or thickening of the bony endplate in combination with degenerative disc disease (
Performing credibility activities enhances the understanding of the behaviour of the computer model to assess the subsidence risk. First, looking at the results for patient 2, the influence of the applied variations had only a minor influence on the maximum FFR (Table 7). This is important to know because the load that is applied per patient in the present study is indirectly selected through the weight of the patient and from a small dataset, and therefore, small variations are likely compared to the in vivo population-wide situation. The risk exists that the loads are underestimated and lead to a significantly different AMCD design, resulting in an underperforming implant. However, the risk of implant failure is low since titanium implants are strong compared to the loads they are subjected to in vivo. Looking at patient 6, we observe a larger variation in the maximum FFR. The reason is that this patient has relatively low bone quality. Therefore, patient 6 is loaded in the non-linear loading regime, explaining the variability. The constitutive model variation is shown to result in a small influence when the model is operated in the linear regime. When the model is operated in the non-linear regime, we see a large influence on the maximum FFR, as is the case for patient 6. This confirms the choice for a non-linear material model for the subsidence risk assessment. The variations in the maximum FFR by changing the density-to-Young’s modulus relationships are small for both patients 2 and 6, and the relationship that is used in this study is the worst case.
As in silico trials are increasingly used in research, the authors found it useful to include extensive V&V activities according to the ASME V&V40–2018 standard (
A limitation in this study was the use of continuum modelling and the surrogate measure, the maximum FFR, as a representation of subsidence risk. Using continuum models, in the worst case, could result in sub-optimal cage designs; however, several studies did show that continuum models can accurately represent the mechanical response of the trabecular structures (
5 Conclusion
In this in silico medical device testing study, we demonstrated that anatomically and mechanically conforming devices achieved a median reduction in subsidence risk by 89% for titanium and 94% for PEEK, compared to off-the-shelf implants. Comparing an anatomically and mechanically conforming cage to an anatomically conforming cage, a median reduction of 75% is achieved for PEEK implant material through additional mechanical optimisation. We could not show a significant dependency between the achieved reduction and bone quality. A credibility assessment of the in silico medical device testing procedure to assess subsidence risk was performed according to ASME V&V40–2018, and the subsidence risk assessment was deemed sufficiently credible for the context of use.
Statements
Data availability statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found at: https://github.com/thsmit/TopOpt_in_PETSc_wrapped_in_Python.
Ethics statement
Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.
Author contributions
TS: writing–original draft, visualisation, validation, methodology, investigation, and conceptualisation. NA: writing–review and editing and methodology. DH: writing–review and editing, resources, and conceptualisation. SF: writing–review and editing, supervision, and funding acquisition. BH: writing–review and editing, supervision, methodology, investigation, and conceptualisation.
Funding
The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This project received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie Grant Agreement No. 812765. Open access funding by ETH Zurich.
Acknowledgments
The authors thank Dave O’Riordan (Schulthess Klinik, Zürich) for his efforts to provide the CT data.
Conflict of interest
The authors declare that they have filed a patent application based on the topology optimization method that is used in this work.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors, and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
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Summary
Keywords
in silico, ASME V&V40, model credibility, medical device testing, topology optimisation, patient-specific, finite element analysis, lumbar spinal fusion implant
Citation
Smit T, Aage N, Haschtmann D, Ferguson SJ and Helgason B (2024) In silico medical device testing of anatomically and mechanically conforming patient-specific spinal fusion cages designed by full-scale topology optimisation. Front. Bioeng. Biotechnol. 12:1347961. doi: 10.3389/fbioe.2024.1347961
Received
01 December 2023
Accepted
07 August 2024
Published
10 September 2024
Volume
12 - 2024
Edited by
Wenxin Niu, Tongji University, China
Reviewed by
Alessandra Aldieri, Polytechnic University of Turin, Italy
Fulvio Tartara, University Hospital of Parma, Italy
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© 2024 Smit, Aage, Haschtmann, Ferguson and Helgason.
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*Correspondence: Thijs Smit, thsmit@ethz.ch
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