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. 2021 Dec 29;15(1):254.
doi: 10.3390/ma15010254.

Histological and Histomorphometric Evaluation of Post-Extractive Sites Filled with a New Bone Substitute with or without Autologous Plate Concentrates: One-Year Randomized Controlled Trial

Affiliations

Histological and Histomorphometric Evaluation of Post-Extractive Sites Filled with a New Bone Substitute with or without Autologous Plate Concentrates: One-Year Randomized Controlled Trial

Marco Tallarico et al. Materials (Basel). .

Abstract

The purpose of the present study was to evaluate the histological and histomorphometric characteristics of post-extraction sites grafted with decellularized bovine compact bone from bovine femur, mixed and unmixed with leukocyte- and platelet-rich fibrin after four months of healing. This study was designed as a randomized controlled trial of parallel groups. Patients in need of a single, implant-supported restoration to replace a hopeless tooth were recruited for tooth extraction and implant placement four months after socket preservation procedure. After tooth extraction, patients were randomly allocated to receive decellularized bovine compact bone from bovine femur, mixed and unmixed with leukocyte- and platelet-rich fibrin. After four months of healing, tapered implants were inserted with an insertion torque between 35 and 45 Ncm. Two months later, implants were loaded with screw-retained definitive crowns. Outcome measures were implant (ISR) and prosthesis (PSR) survival rates, complications, histological and histomorphometric analyses, radiographic marginal bone-level changes, and patients' satisfaction. Clinical data were collected up to one year after tooth extraction and socket preservation procedures. Thirty patients were consecutively enrolled in the trial (15 in each group). Unfortunately, due to the COVID-19 pandemic, bone samples were collected only in 19 patients. Two implants failed before definitive prosthesis delivery (ISR 93.3%). No prosthesis failed (PSR 100%). Three complications were experienced in the control group. The mean bone percentage was 40.64 ± 18.76 in the test group and 33.40 ± 22.38 in the control group. The difference was not statistically significant (p = 0.4846). The mean soft tissue percentage was 32.55 ± 19.45 in the test group and 55.23 ± 17.64 in the control group. The difference was statistically significant (p = 0.0235). The mean residual graft was 24.59 ± 18.39 in the test group and 11.37 ± 12.12 in the control group. The difference was not statistically significant (p = 0.0992). Mean marginal bone loss, as well as patient satisfaction, showed no differences between groups. With the limitations of the present study, socket preservation with L-PRF mixed with decellularized bovine compact bone demonstrated favorable results, comparing with decellularized bovine compact bone from bovine femur alone. Further studies with larger sample size and longer follow-up are needed to confirm these preliminary results.

Keywords: L-PRF; biomaterials; dental implants; grow factors; socket preservation.

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Conflict of interest statement

The authors declare no conflict of interest in this research.

Figures

Figure 1
Figure 1
Preclinical situation of patient number 3. Lower right first molar needed to be extracted due to a vertical fracture.
Figure 2
Figure 2
Atraumatic tooth extraction.
Figure 3
Figure 3
L-PRF (left) and decellularized bovine compact bone from bovine femur (right).
Figure 4
Figure 4
L-PRF mixed with decellularized bovine compact bone from bovine femur.
Figure 5
Figure 5
Residual socket grafted with the mixture of L-PRF and bone substitute.
Figure 6
Figure 6
Residual socket sealed with collagen type one and resorbable suture.
Figure 7
Figure 7
Occlusal view 2 weeks after tooth extraction and socket preservation procedure.
Figure 8
Figure 8
Lateral view four months after tooth extraction and socket preservation procedure.
Figure 9
Figure 9
Example of collected sample. A suture was placed to immobilize the sample and to define the most occlusal part of the sample itself.
Figure 10
Figure 10
Participant flow diagram according to the CONSORT guidelines.
Figure 11
Figure 11
Bone sample taken at the lower right first molar. Patient (number 3) received L-PRF mixed with decellularized bovine compact bone from bovine femur (test group). The bone was 76.65%; soft tissue was 8.73%; residual graft was 15.62%.
Figure 12
Figure 12
Bone sample taken at the upper right first premolar. The patient (number 13) received decellularized bovine compact bone from bovine femur alone. The bone was 46.19%; soft tissue was 34.61%; residual graft was 19.20%.
Figure 13
Figure 13
Bone sample taken at the upper right second premolar. The patient (number 10) received L-PRF mixed with decellularized bovine compact bone from bovine femur. The bone was 48.22%; soft tissue was 48.92%; residual graft was 2.86%.
Figure 14
Figure 14
Bone sample taken at the upper right second molar. The patient (number 16) received L-PRF mixed with decellularized bovine compact bone from bovine femur. The sample was not assessable.

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