| Literature DB >> 33260793 |
Anna Machrowska1, Jakub Szabelski2, Robert Karpiński1, Przemysław Krakowski3, Józef Jonak1, Kamil Jonak4,5,6.
Abstract
The purpose of the study was to test the usefulness of deep learning artificial neural networks and statistical modeling in predicting the strength of bone cements with defects. The defects are related to the introduction of admixtures, such as blood or saline, as contaminants into the cement at the preparation stage. Due to the wide range of applications of deep learning, among others in speech recognition, bioinformation processing, and medication design, the extent was checked to which it is possible to obtain information related to the prediction of the compressive strength of bone cements. Development and improvement of deep learning network (DLN) algorithms and statistical modeling in the analysis of changes in the mechanical parameters of the tested materials will enable determining an acceptable margin of error during surgery or cement preparation in relation to the expected strength of the material used to fill bone cavities. The use of the abovementioned computer methods may, therefore, play a significant role in the initial qualitative assessment of the effects of procedures and, thus, mitigation of errors resulting in failure to maintain the required mechanical parameters and patient dissatisfaction.Entities:
Keywords: bone cement; deep learning networks (DLN); prediction, mechanical parameters, compressive strength; statistical modeling
Year: 2020 PMID: 33260793 PMCID: PMC7731130 DOI: 10.3390/ma13235419
Source DB: PubMed Journal: Materials (Basel) ISSN: 1996-1944 Impact factor: 3.623
Figure 1Strength characteristics (a) and error values (b) for 10% blood admixture.
Figure 2Strength characteristics (a) and error values (b) for 10% saline admixture.
Figure 3Strength characteristics (a) and error values (b) for 8% blood admixture.
Figure 4Strength characteristics (a) and error values (b) for 10% blood admixture.
Figure 5Strength characteristics (a) and error values (b) for 8% saline admixture.
Figure 6Strength characteristics (a) and error values (b) for 10% saline admixture.
Figure 7Comparison of the correlation between the admixture level and the compression strength of samples contaminated with saline up to approx. 8% by weight.
Parameters of selected polynomial models—α1x4 + α2x3 + α3x2 + a4x + ε—obtained from 0–8% data.
| Model Type | α1 | α2 | α3 | α4 | ε | R2 |
|---|---|---|---|---|---|---|
| blood 1° | - | - | - | −140.97 | 79.843 | 0.5552 |
| blood 2° | - | - | 3,047.6 | −388.31 | 82.203 | 0.6881 |
| blood 3° | - | −147,053 | 21,125 | −925.41 | 84.218 | 0.8431 |
| blood 4° | 2,662,604 | −572,121 | 41,532.17 | −1,210.6 | 84.524 | 0.8588 |
| saline 1° | - | - | - | −272.31 | 88.626 | 0.8428 |
| saline 2° | - | - | -23.8 | −270.27 | 88.606 | 0.8428 |
| saline 3° | - | 129,323 | -16,919 | 266.04 | 86.282 | 0.9019 |
| saline 4° | −4,944,022 | 965,912 | -59,549.84 | 906.92 | 85.216 | 0.9348 |
Parameters of exponential models—y = K0ekx—obtained from the 0–8% data.
| Model Type | K0 | k | R2 |
|---|---|---|---|
| blood exp. | 79.705 | −1.85 | 0.562 |
| saline exp. | 88.924 | −3.537 | 0.8684 |
Prediction accuracy of selected models for the case with 10% admixture from the 0–8% model.
| Model Type | Predicted Value 10% | Average Actual Value 10% | Average Absolute Difference | Average Relative Difference | RMSE | CV (RMSE) |
|---|---|---|---|---|---|---|
| blood 1° | 64.62 | 69.05 | 4.43 | 6% | 5.14 | 8% |
| blood 2° | 75.81 | 6.76 | 10% | 7.24 | 10% | |
| blood 3° | 45.43 | 23.62 | 34% | 23.76 | 52% | |
| blood 4° | 79.75 | 10.70 | 15% | 11.01 | 14% | |
| blood exp. | 65.65 | 3.78 | 5% | 4.59 | 7% | |
| saline 1° | 58.91 | 66.77 | 7.82 | 12% | 7.87 | 13% |
| saline 2° | 59.40 | 7.90 | 12% | 7.95 | 13% | |
| saline 3° | 80.47 | 14.98 | 22% | 15.00 | 18% | |
| saline 4° | 29.55 | 37.21 | 56% | 37.22 | 126% | |
| saline exp. | 60.44 | 6.29 | 9% | 6.34 | 10% |
Parameters of selected polynomial models—α1x3 + α2x2 + α3x + ε—obtained from the 0–6% data.
| Model Type | α1 | α2 | α3 | ε | R2 |
|---|---|---|---|---|---|
| blood 1° | - | - | −167.86 | 80.32 | 0.4968 |
| blood 2° | - | 7093.8 | −606.42 | 83.38 | 0.7647 |
| blood 3° | −264,373 | 31,084 | −1113.4 | 84.528 | 0.8634 |
| saline 1° | - | - | −299.3 | 89.107 | 0.7701 |
| saline 2° | - | −3,350.5 | −79.742 | 87.471 | 0.8016 |
| saline 3° | 299,365 | −32,258 | 577.4 | 85.571 | 0.8785 |
Parameters of exponential models—y = K0ekx—obtained from the 0–6% data.
| Model Type | K0 | k | R2 |
|---|---|---|---|
| blood exp. | 89.354 | −3.808 | 0.7963 |
| saline exp. | 80.144 | −2.16 | 0.4961 |
Prediction accuracy of selected models for (a) 8% and (b) 10% admixture from the 0–8% model.
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| blood | 66.56 | 69.45 | −2.89 | 4% | 2.72 | 4% |
| blood 2° | 81.35 | 11.90 | 17% | 12.83 | 16% | |
| blood 3° | 56.47 | −12.98 | 19% | 12.30 | 22% | |
| blood exp. | 65.39 | 4.06 | 6% | 3.69 | 6% | |
| saline 1° | 63.07 | 66.17 | −3.10 | 5% | 3.14 | 5% |
| saline 2° | 55.17 | −11.00 | 17% | 11.01 | 20% | |
| saline 3° | 88.78 | 22.61 | 21% | 22.61 | 25% | |
| saline exp. | 66.41 | 0.25 | 0% | 0.54 | 1% | |
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| blood 1° | 62.19 | 69.05 | 6.86 | 10% | 7.33 | 12% |
| blood 2° | 100.63 | 31.58 | 46% | 31.68 | 31% | |
| blood 3° | −6.19 * | 75.24 * | 109% * | 75.28 * | −1.216% * | |
| blood exp. | 59.22 | 9.83 | 11% | 10.16 | 17% | |
| saline 1° | 56.78 | 66.77 | 9.99 | 8% | 10.02 | 18% |
| saline 2° | 39.78 | 26.99 | 42% | 27.00 | 68% | |
| saline 3° | 148.79 | 82.02 | 115% | 82.02 | 55% | |
| saline exp. | 63.33 | 3.44 | 5% | 3.53 | 6% | |
* Negative value of predicted compression strength.
Figure 8A comparison of R2 of the model and the absolute value of the degree of inaccuracy of the modeled compressive strength for different variants of contamination and different ranges of the teaching data for the model: (a) 8% contamination from the model taught in the range of 0–6%, (b) 10% contamination from the model taught in the range of 0–6%, (c) 10% contamination from the model taught in the range of 0–8%, and (d) an overall comparison.
Compressive strength prediction accuracy for DLN taught in the range of 0–6%: (a) 8% contamination and (b) 10% contamination.
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| blood—averaged | 63.05 | 69.45 | 6.40 | 9.2% |
| blood—random series | 64.66 | 4.79 | 6.9% | |
| saline—averaged | 62.70 | 66.17 | 3.47 | 5.2% |
| saline—random series | 64.88 | 1.29 | 1.9% | |
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| blood—averaged | 51.34 | 69.05 | 17.71 | 25.6% |
| blood—random series | 55.98 | 13.07 | 18.9% | |
| saline—averaged | 58.78 | 66.77 | 7.99 | 12.0% |
| saline—random series | 61.65 | 5.12 | 7.7% | |
Compressive strength prediction accuracy for DLN taught in the range of 0–8% of contamination.
| Contamination Dataset | Predicted Value 10% | Average Actual Value 10% | Absolute Difference | Relative Difference |
|---|---|---|---|---|
| blood—averaged | 51.30 | 69.05 | 17.75 | 25.7% |
| blood—random series | 52.49 | 16.56 | 24.0% | |
| saline—averaged | 56.98 | 66.77 | 9.79 | 14.7% |
| saline—random series | 58.33 | 8.44 | 12.6% |
Figure 9Uncertainty of prediction of strength at 8% contamination based on data from the 0–6% range.
Figure 10Uncertainty of strength predictions at 10% contamination based on the results obtained by different methods and from different ranges.
Comparison of deep learning networks and statistical analysis advantages and drawbacks.
| DLN | Statistical Analysis |
|---|---|
| Requires special tools | Can be conducted using dedicated software or simple spreadsheets (Microsoft Excel or similar) |
| Often requires expensive software | Freeware/open software can be used |
| Requires knowledge in the area of general DLN theory and the ability to work in a specific program | Requires medium statistical knowledge |
| The results are satisfactory | The results depend heavily |
| Possibility of generalization | Limited possibilities of problem generalization (possibility of reliable forecasting in the analyzed range) |