Use of three points to determine the accuracy of guided implantation
Authors:
Ye Liang aff001; ShanShan Yuan aff002; JingJing Huan aff001; HuiXin Wang aff001; YiYi Zhang aff001; ChangYun Fang aff001; Jia-Da Li aff003
Authors place of work:
Department of Stomatology, Xiangya Hospital of Central South University, Changsha, Hunan Province, China
aff001; Affiliated Stomatology Hospital of Guangzhou Medical University, Guangzhou, Guangdong, China
aff002; School of Life Sciences, Central South University, Changsha, Hunan Province, China
aff003
Published in the journal:
PLoS ONE 14(12)
Category:
Research Article
doi:
https://doi.org/10.1371/journal.pone.0225823
Summary
Aim
'This study aims to establish an open-source algorithm using Python to analyze the accuracy of guided implantation, which simplifies interstudy comparisons.
Methods
Given ≥3 landmark pairs, this Tri-Point (TriP) method can register images. With ≥4 landmark pairs, TriP can calculate system errors for image registration. We selected 8 indicators from the literature. Considering development errors in new bone on cone beam computed tomography (CBCT), we added the indicators of apical rectified deviation (ARD) and coronal rectified deviation (CRD), providing accurate references but neglecting depth deviations. Our program can calculate and output these indicators. To evaluate the TriP method’s feasibility, an implantation group assisted by a Visual Direction-INdicating Guide (VDING) was analyzed. Accuracy was measured with the traditional and proposed TriP methods. Factors affecting the system error of the method were then analyzed.
Results
Comparisons with paired-sample t-tests showed that our TriP method was similar to the traditional method in evaluating implantation accuracy, with no significant difference (P>0.05). The average system error was 0.30±0.10 mm when the TriP method evaluated the VDING template. The results showed that increasing the provided landmarks from 4 to 5 pairs decreased the between-group differences significantly (P<0.05). With ≥6 pairs of landmarks, the system error tended to be stable, and the groups showed no statistically significant differences (P>0.05). Large distances between landmarks are helpful in reducing system error, as demonstrated with a geometric method.
Conclusions
This study established an open-source algorithm to analyze the accuracy of guided implantation with system errors reported.
Keywords:
Teeth – Imaging techniques – Medical devices and equipment – Medical implants – Surgical and invasive medical procedures – Computed axial tomography – Computer software – Open source software
Introduction
As a bridge between virtual and real systems, digital technology-based guide templates can make implantation more precise than manual implantation. Nevertheless, to thoroughly analyze the template or further increase the accuracy, we need to further analyze the accuracy of guided implantation.
At present, some commercial software programs provide methods for analyzing accuracy with the original data in DICOM or STL files [1,2,3]. However, most of the algorithms are not public and provide no system error. Additionally, because most commercial software is expensive, most studies have used only one software package to calculate the accuracy [1,4], making it difficult to evaluate the measurement accuracy of the analysis itself.
Additionally, analyses of implantation accuracy must include calculations of related indicators. Some commonly used indicators include coronal global deviation (CGD), apical global deviation (AGD), and angular deviation (AD). However, implantation descriptions involving just these 3 indicators have shortcomings. Therefore, some studies have added depth and horizontal deviation [5]. Furthermore, some studies have used nontraditional indicators [6,7]. Moreover, few indicators describe the implanted cover screw and healing abutment, which are ignored. Therefore, better indicators are needed.
Differences between methods and indicators render it difficult to compare different research results. To solve this problem, we attempt to establish an open-source method for analyzing implantation accuracy that can compute system errors. Simultaneously, we screened some relatively mature evaluation indicators of implant accuracy by referring to previous studies and added some indicators based on our research. We hope that our open-source software will enable direct calculation of the results of these indicators.
In this study, we applied this open-source software to a guide template called Visual Direction-INdicating Guide (VDING) and compared our software with the traditional commercial software Mimics. The guide template was modified to address the lack of angular restriction provided by the short guide sleeves used when the occlusal distances at implant sites are slightly insufficient for normal height templates. Because the VDING template adds a visual direction-indicating device, the operator can more easily and objectively observe the angle of the drill needle in real time without relying entirely on the mechanical structure of the guide sleeve.
We hope that our open-source program can better promote digital technology and help further improve the accuracy of implant surgery.
Materials and methods
Ethics statement
The study itself excluded the involvement of human beings, nor did it cause harm to human beings. However, clinical examination data were partly used in the study, and the use of these data was approved by Ethics Commitee of Xiangya Hospital of Central South University, approval number: 201512515. All Patients provided written informed consent to the use of CBCT data in this research.
Tri-Point (TriP) image registration method
The data for the planned and real implants are in preoperative and postoperative cone bean computed tomography (CBCT) images, respectively, so the positions of the planned and real implants cannot be directly compared.
To compare the differences, we need to align the two images via features in the images to geometrically transform the two image spaces. Our Tri-Point (TriP) method is established for researchers who TRY to test the IMPLANT PLAN accuracy. This method defines a new coordinate system by using relatively unchanged anatomical sites before and after surgery, allowing comparison of the positions of the planned and real implants.
Space vector-based relative coordinate system
The coordinate system Σ has 3 noncollinear points with coordinates A(X1,Y1,Z1), B(X2,Y2,Z2), and C(X3,Y3,Z3) (Fig 1A).
To establish a relative coordinate system, we define A as the origin and the vector AB→ as the positive direction of the X-axis. Therefore, the X-axis unit vector x→ can be obtained as:
The noncollinear points A, B, and C can define a plane (Fig 1B). Points Cx and Cy are the projections of point C on the X-axis and the Y-axis, respectively. θ is the value of ∠CAB.
We set the Y-axis in the ABC plane, so point C exists in the XAY plane and satisfies:
Therefore, we can obtain the unit vector y→ of the Y-axis as:
We set n→ as the normal vector of plane ABC, so this vector satisfies:
The unit vector of the Z-axis is obtained as:
The obtained unit vectors, x→,y→,z→, of the three coordinate axes can be used to establish a three-dimensional rectangular coordinate system, Φ (Fig 1C).
Conversion from the original coordinate system to a relative coordinate system
Point G is the point targeted for conversion, and its coordinates are G(X4,Y4,Z4) in coordinate system Σ and G’(X4′,Y4′,Z4′) in coordinate system Φ. The spatial relationship between point G’ and points ABC remains the same as the relationship for point G (Fig 1D and 1E).
G’(X4′,Y4′,Z4′) is solved with Eqs (2-1) to (2-5). These equations indicate that point G’ satisfies:
The coordinates of 4 points in coordinate system Σ are A(X1,Y1,Z1), B(X2,Y2,Z2), C(X3,Y3,Z3), and G(X4,Y4,Z4). The 3 coordinate axes of the coordinate system obtained above are x→=(XX,XY,XZ),y→=(YX,YY,YZ), and z→=(ZX,ZY,ZZ). By substituting these known values into Eq (2-6), the value of X4′,Y4′andZ4′ are obtained. The solution of G’(X4′,Y4′,Z4′) is the coordinates of the original point G in coordinate system Φ.
The points in the planned image are in coordinate system P, and the points in the real implant image are in coordinate system R. In each coordinate system, the corresponding anatomical landmarks L1, L2, and L3 are selected as the basic points A, B and C described above. These three pairs of basic points are anatomically congruent. Thus, coordinate systems P and R are converted to the same coordinate system, N. The detailed process is described in Appendix 1.
Error evaluation and option of landmark points
Errors occur when selecting each landmark point in images. Thus, using different landmarks as basic points in steps 2.1.3 will lead to different system errors. To determine whether to select or reject a landmark point, we use the following method to evaluate the system error.
From congruent triangle rules (side-side-side), we hypothesize that if the triangles formed by three identical pairs of points selected from 2 images are congruent, the error in these three pairs of points is the smallest and is recorded as zero.
Then, we define the triangle error Et that satisfies:
‖L1L2‖ is the percentage of the length difference of the line segment L1L2 in 2 images:
t reflects the similarity of 2 triangles:
The above formulas indicate that, when the three edges of the corresponding triangles are equal in length in the two coordinate systems, Et = 0. Conversely, when the lengths of the three edges are unequal, Et>0. The greater the length difference is, the greater Et. Considering the parameter t, Et is smaller when the edges vary proportionally.
Then, the error of each landmark is judged. The error Ei of a point i satisfies:
In this formula: M = {1,2,…,m }; m is the sum of pairs of landmarks; i,u,v∈M; u≠v≠i.
In the error evaluation system, the pairs of points with large errors will affect the pairs with small errors. However, the maximum error of points is always Emax = max(Ei). Step-by-step sorting of Emax can provide the error value of each pair of points. Finally, the three pairs of points with the least error are obtained and used as points L1,L2, and L3 for the geometric transformation in the TriP method.
When given ≥4 pairs of landmarks, our program will choose the 3 best pairs with the least error to build the coordinate system N and will calculate system error with the 4th pair. The details of the algorithm are in Appendix 1.
Analysis of factors affecting the system error of the TriP method
The effects of the number of landmarks provided and the distance between the selected points on system errors were analyzed.
The first factor was analyzed experimentally. We selected 4–16 pairs of points in turn for system error calculations and drew the variation curve for the average system error. Then, the paired-sample t-test was performed for the system errors of two adjacent groups with different numbers of landmarks to determine whether the system error differed. Subsequently, the distance between the selected points was analyzed with geometric calculation methods.
Accuracy indicators: Selection and calculation
The first indicator selected in this study was the height of the cover screw, which helps to integrate different implants into the same system. The calculation and the method of correcting the height of the cover screw are provided in Appendix 1.
One study [2] indicated that the parameters describing position deviations between the planned implant (blue) and the real implant (red) are AD, CGD, coronal vertical deviation (CVD), coronal lateral deviation (CLD), AGD, apical vertical deviation (AVD), and apical lateral deviation (ALD) (Fig 1G).
Because of the underestimation of new bone by CBCT and the incomplete bone calcification, there is a discrepancy between the height of the bone surface from the CBCT data and the actual findings during the operation. During the manual insertion stage, the surgeon often adjusts the implant depth subjectively by observation, causing implant deviation via a nontemplate cause. Therefore, we proposed new indicators—coronal and apical rectified deviations (CRD and ARD, respectively)—to provide corrections for the subjective depth adjustments performed during manual implant insertion to simply analyze the accuracy of the implant template (Fig 1H). The details of the algorithm are in Appendix 1.
Traditional image registration method
Traditional image registration was performed with Mimics software, version 10.01 (Materialise n.v., Belgium), and the same indicators were calculated. The detailed steps are shown in Appendix 1.
Application and accuracy analysis of the Visual Direction-INdicating Guide (VDING)
This study aimed to verify the precision of the VDING template. The guide template is a depth-control template combined with a visual direction-indicating device (Fig 2A). This template was developed to accommodate the low angle restriction of a short guide sleeve when the interarch distance in the implantation area is slightly insufficient for a normal height template [8]. The design idea and fabrication method are shown in Appendix 1.
After the ethics examination and approval, we applied VDING. After obtaining informed consent, 13 patients with 15 missing teeth who planned to receive implantation at the Stomatology Center of Xiangya Hospital participated in the clinical study of the VDING template (cases and inclusion criteria appear in Appendix 1).
After jaw data collection with a CBCT machine (KaVo Dental GmbH, Germany; 0.25 mm slice interval), VDING templates were fabricated and tried in patients before operation. Before surgery, the guide template was sterilized under the conditions of normal temperature and atmospheric pressure by plasma sterilization (Sterrad 100S, Johnson and Johnson, USA). The operation was performed according to the guidelines for implant surgery (Fig 2B).
The patients in the study underwent CBCT examinations immediately after the operations in the examination conditions.
Comparison and statistical analysis of the TriP and traditional methods
The individuals who analyzed the accuracy of the TriP method received training in selecting image registration landmarks. The accuracy analysts also passed a consistency evaluation before selecting landmarks. The landmark selection process was performed by one researcher with supervision by another researcher.
Sixteen pairs of landmarks were selected. The coordinates of the coronal endpoint RIC and the apical endpoint RIA of the real implant were recorded. The coordinates of the planned implant endpoints PIC and PIA were output from the design software. The coordinates of these points were recorded and saved. Then, a program (https://github.com/coolleafly/VDING) written with the Python 3.6 platform was used for the calculations. The program outputs all the implantation accuracy indicators described in 2.1 and the system errors for each implant.
The traditional method was executed by the steps described in 2.2. The mean value of the measured implant position determined by two trained inspectors was taken.
To compare the two accuracy analysis methods, a normality test and a paired-sample t-test were performed to compare the implantation accuracy results by SPSS 21.0 statistical analysis software. The test level was set at α = 0.05.
Results
Analysis of factors affecting system error
Influence of number of provided landmark points on system error
In the same cases, 4 to 16 landmarks were provided, and the system errors of the TriP image registration method with different numbers of landmarks are shown in Fig 3A.
A paired-sample t-test was performed to evaluate the system errors with two adjacent number of points. The results are as follows (Table 1):
Influence of distance between the 3 selected pairs of landmark points on system error
A geometric method was used to deduce that because the error in point selection is small and similar, increasing the distance between landmarks decreases the angle error in the geometric transformation (Fig 1F). The specific deduction process is shown in Appendix 1. The results indicate that selecting dispersed landmarks helps reduce the system error of the TriP method.
Comparison of implantation accuracy calculation by the two methods
Normality test
The Shapiro-Wilk test was used to assess the normality of each implant accuracy indicator. All the indicators used in the two methods were normally distributed (P>0.05). Therefore, the mean value±standard deviation is used to describe each indicator.
Comparison of the results for cover screw heights
Using the calculation methods above, the results for each indicator with the TriP method and the traditional method were obtained and are shown in Fig 3B. The results of paired-sample t-tests comparing the 2 methods are shown in Table 2. For each indicator, the two methods showed no significant difference (P>0.05). The two image registration methods are considered consistent.
System error of the TriP method
The image registration error of each implant was evaluated by the method in 2.1.5, as shown in Fig 3C. The overall system error for all the samples was 0.30±0.10 mm.
Discussion
System error and its optimization in accuracy calculation
Operator proficiency affects the accuracy of image registration, and the accuracy is not easy to judge. Without a system error value provided by analysis software, comparisons of accuracy between different studies can be questioned, and the registration process is hard to optimize.
To evaluate the registration system error objectively, the system error was calculated in our study. This calculation not only increases the reliability of calculating implant accuracy but also facilitates comparisons of implant accuracy statistics between different studies. Moreover, this evaluation allows researchers to identify landmarks that have low error and improve registration efficiency.
Ways to reduce the system error in image registration
As indicated in 3.1.1, increasing the number of selected points does not improve the results. As the number of selected points increases, the system error approaches convergence. Selecting too many points causes problems: 1. The number of clear and sharp landmarks is insufficient; 2. Useless work increases; and 3. The distance between landmarks becomes too small. Our results indicate that the number of recommended landmarks is 5 to 7. According to the deduction in 3.1.2, a sufficient distance between landmarks is conducive to reducing system error.
Additionally, after many training processes, we recommend selecting the following landmarks to improve accuracy: 1. the enlarged dot-like pit in the crown of posterior teeth; 2. the spiculate pulp angle; and 3. the sharp tip of tooth roots (Fig 2C and 2D). After comparison, the following locations were eliminated: 1. a crown with a filling or restoration or a root with root canal treatment; 2. a fissure or triangular crack in the enlarged view; and 3. a pulp angle with an irregular shape (Fig 2E–2I). To improve the visualization of boundary lines, brightness and contrast can be changed, and a scaling function should be used (Fig 2J).
Possible sources of errors in the guided implantation process
Although the implant guide template provides a method to improve precision, the follow errors remain:
The following data collection errors remain that affect the guide template design. The limited spatial resolution of CBCT cause errors in selecting landmarks (Fig 2K and 2L). Slight patient motion leads to bias in CBCT sampling. CT images reflect new bone surfaces with bias [9]. Materials shrink during the plaster casting performed to take impressions [10].
When producing the guide template, the accuracy of 3D printing is limited, and the subsequent process produces further errors [11].
The bur-cylinder gap between the implant drill needle and the guide sleeve may cause mechanical errors during guided implantation [12].
Because of inhomogeneities in bone density, the implant tends to squeeze the low-density bone wall, leading to deviations. Manual implant insertion may lead to deviations [13].
Errors can be introduced during measurement. Existing cover screws, healing abutments and image registration can all lead to errors.
Implantation accuracy analysis indicator and its function
Different analysis indicators have been proposed in different studies. In this study, the indicators AD, CGD, CVD, CLD, CRD, AGD, AVD, ALD, and ARD are considered to reflect the overall implant accuracy.
AD reflects the axial deviation and is the core indicator when analyzing the precision of the guide template. This indicator is related to the accuracy of the guide template position, the length of the guide sleeve, the tightness of the guide sleeve, and the existence of other auxiliary directional devices.
CGD, CVD, CLD and CRD reflect the deviation during implant entry. CGD is the most intuitive and recognized overall position deviation indicator. When CLD and CRD are both large, the implant entry deviation is too large, most likely due to poor placement of guide templates. If CVD is large, and CRD is small, the unsatisfactory development of new bone on CBCT likely results in inaccurate implant depth in the surgical plan. If AD is small in this case, the guide template may still have good accuracy.
The indicators reflecting apical deviation are AGD, AVD, ALD and ARD. If AD and AGD are both small, the guide template is excellent. If there is some deviation but CRD and ARD are both small, the implant still moves along the predetermined axis and entry path, but the depth of the manual implant insertion differs from the planned depth. In this case, the guide template is still excellent and generally does not affect the important surrounding anatomical structures. AVD reflects the implant apical vertical deviation, which can result in injury of the inferior alveolar nerve or maxillary sinus. Therefore, the use of a guide template with a large AVD should maintain a sufficient safe distance. In contrast, if AVD is small, the safe distance can be reduced appropriately to decrease the operation complexity. ALD reflects the horizontal apical deviation, which can lead to damage to adjacent teeth and accidental penetration of cortical bone. Therefore, if ALD is large, the guide should be used cautiously in a narrow implantation area.
Supporting information
S1 File [hs]
Registration of the planned image and the real implant image.
Zdroje
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