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. 2024 Jul 25;12(8):1661.
doi: 10.3390/biomedicines12081661.

Sinus Floor Augmentation with Synthetic Hydroxyapatite (NanoBone®) in Combination with Platelet-Rich Fibrin: A Case Series

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Sinus Floor Augmentation with Synthetic Hydroxyapatite (NanoBone®) in Combination with Platelet-Rich Fibrin: A Case Series

Luís Francisco et al. Biomedicines. .

Abstract

Several techniques have been described for maxillary sinus graft augmentation, including the lateral window technique and crestal approach with osteotomes or osseodensification. Platelet-rich fibrin has been used in maxillary sinus lift procedures due to its ability to accelerate soft and hard tissue healing. The aim of this study was to evaluate the potential of PRF in combination with the synthetic hydroxyapatite NanoBone® to enhance bone regeneration in sinus floor elevation with the lateral window technique. Out of the 50 individuals screened in a preoperative assessment visit from the CESPU-Famalicão clinical unit and intervened upon between January 2023 and December 2023, only 6 patients who met the study's inclusion criteria consented to participate. In a split-mouth study, twelve sinus graft surgeries were carried out. Our observations reveal that for the test group (NanoBone®/PRF), there is a 27.5 ± 4.9% increase new vital bone, 23.0 ± 3.7% increase in inert bone particles, and 49.4 ± 2.8% increase in connective tissue. Meanwhile, for the control group (NanoBone®), there is a 19.5 ± 3.0% increase in new vital bone, 23.4 ± 5.7% increase in inert bone particles, and 57.0 ± 3.5% increase in connective tissue. The results strongly indicate that mixing liquid PRF with NanoBone® does not have a negative influence on the amount of viable bone formation, and it seems to slightly increase the amount of new bone formation and revascularization in sinus bone graft procedures with the lateral window technique compared to the single use of NanoBone®.

Keywords: biomaterials; maxillary sinus augmentation; platelet-rich fibrin; sinus floor augmentation.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
A visual representation of the surgery. (a) Bony window with Acteon Satelec® piezoelectric device; (b) Schneiderian membrane elevated; (c) Aggregation of NanoBone® with liquid fibrin; (d) Biomaterial insertion in the sinus cavity; (e) Straumann® Fex collagen membrane over the bony window.
Figure 2
Figure 2
Harvesting of the bone specimen with a 2.5 mm diameter trephine bur. (a) Surgical site; (b) Trephine drill with collected bone; (c) Trephine drill with bone specimen in a 10% formaldehyde sterile vial.
Figure 3
Figure 3
CONSORT flowchart.
Figure 4
Figure 4
Newly formed bone, residual bone graft material, and connective tissue for both control (NanoBone® alone) and test groups (NanoBone®/liquid fibrin). Bars represent the mean and standard deviation of individuals results. (A) New vital bone, (B) particles, (C) new vital bone + particles, and (D) connective tissue. (*** p < 0.0005).
Figure 5
Figure 5
Histologic results in both groups: (a) test group; (b) control group. 10 × 0.5 magnification and toluidine blue staining.
Figure 6
Figure 6
Histologic results in both groups: (a) test group; (b) control group. 10 × 0.5 magnification and toluidine blue staining.
Figure 7
Figure 7
Histologic results in both groups: (a) test group; (b) control group. 10 × 0.5 magnification and toluidine blue staining.
Figure 8
Figure 8
Histologic results in both groups: (a) test group; (b) control group. 10 × 0.5 magnification and toluidine blue staining.
Figure 9
Figure 9
Histologic results in the test group. 10 × 0.5 magnification and toluidine blue staining.
Figure 10
Figure 10
Histologic results in both groups: (a,b) test group; (c) control group. 10 × 0.5 magnification and toluidine blue staining.
Figure 11
Figure 11
Histologic results in the control group. 10 × 0.5 magnification and toluidine blue staining.

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