Eligible patients
From January 1 to April 1, 2019, patients who required to have their impacted third molars extracted at the Peking University School of Stomatology's Department of Oral and Maxillofacial Surgery were recruited for this study. The Human Ethics Committee at our hospital granted ethical approval for this study, which was carried out in accordance with the Helsinki Declaration (No. PKUSSIRB-201415068), and it was recorded in the Chinese Clinical Trial Registry (ChiCTR2000040767).
The following inclusion criteria were applied: (1) Between the ages of 18 and 40. (2) Good general and local health. (3) Radiographic evidence of an impacted third molar in the jaw. The exclusion criteria were as follows: (1) The presence of periodontitis, odontogenic cysts or tumors, trauma, or any signs of infection around the IM3M. (2) Postoperative cases with suppurative infections. (3) Not all follow-up was completed.
Study design
It was a self-control study. 46 volunteers were enrolled in total; 16 individuals were excluded from the trial due to loss of follow-up or suppurative infections. These 30 participants' bilateral sides were split into two groups: the surgery sides group and the non-surgical sides group. The non-surgical sides group was utilized to confirm the accuracy and repeatability of the 3dMD imaging method, while the surgical sides group was used to access the consecutive trend of face swelling following surgery.
Operation
Before surgery, informed consent was signed by each participant patient. The same surgeons carried out each procedure. Under local anesthetic, the third molar on the mandible was surgically removed. The procedure involved raising a full-thickness, three-cornered mucoperiosteal flap and performing bone removal and tooth sectioning. The surgical incision was stitched shut with a 4-0 silk suture after the mucoperiosteal flap was repositioned.
Scanning procedure
In this investigation, photographs of the samples were taken using the 3dMDface system (3dMD Ltd, Atlanta, Ga), a structured light system based on stereo photogrammetry and the structured light technique, with a natural head position, a relaxed facial expression, and eyes directed straight ahead. With three cameras on each side, the 3dMD system uses synchronized digital multicamera technology to produce photos of photorealistic quality. The device can take a 180-degree image of a person's entire face, including the area under the chin, in approximately 1.5 milliseconds at high resolution, with a theoretical accuracy of 0.2 millimeters. The follow-up is extended by 5 to 10 minutes with the 3dMD system[9,10].
A 3D facial image was taken six times of each patient. A preoperative 3dMD image was taken right before surgery (T0) for comparison with the postoperative image in order to assess the con changes. At five different times after surgery—24 hours (T1), 48 hours (T2), 72 hours (T3), the fourth day (T4), and the fifth day (T5)—3dMD pictures were taken.
Data processing and measurement method
The same researcher used the same tool to capture each 3dMD image. All images were saved as. TSB files and edited with 3D software (3dMD patients Version 4.0). The 3D models of each patient were imported into the software to calculate the changes in shape brought on by the swelling. The forehead and bridge of the nose were used to align and record the two related 3D models (the model before and one day after surgery), as those regions did not differ regardless of the level of swelling (Figure.1A). After completing the superimpositions of two models, we applied the root mean square (RMS) value until it reached the smallest value. The RMS value, which is specified in the software manually and determines how consistent the registration process is, was recorded for individual, and the superimpositions with the RMS value below 1 were re-evaluated.
Four linear references on the facial images have been selected to help reduce error: line A, the first cervical stripe line, line B, the ala-tragus line, from the tragus to the base of the nasal wing, line C, the facial midline, and line D, the contour of the auricle to the hairline (Figure 1B-E). Following that, we deleted the excess data,and the region of interest (ROI) was chosen for the calculation. After we aligned the two 3D models(before and one day after surgery) and delineated the ROI,the thickness of swelling(TOS) and volume of swelling(VOS)were calculated by subtracting the two models (Figure 1F). The volume in milliliters and the thickness in millimeters of the swelling were measured.
Statistical analysis
The statistical analysis was conducted using the IBM SPSS statistics 22.0 program. The Shapiro-Wilcoxon test was used to determine whether the data were consistent with a normal distribution. To assess swelling changes between all-time points within patients, descriptive statistics and repeated measures analysis of variance were computed for TOS and VOS in the two groups, and the Bonferroni test was utilized for the post hoc analyses. P < 0.05 was considered statistically significant.