TY - JOUR
T1 - Sinus augmentation with simultaneous, non‐ submerged, implant placement using a minimally invasive hydraulic technique
AU - Chaushu, Liat
AU - Chaushu, Gavriel
AU - Better, Hadar
AU - Naishlos, Sarit
AU - Kolerman, Roni
AU - Aragoneses, Juan Manuel
AU - Calvo‐guirado, José Luis
AU - Nissan, Joseph
N1 - Publisher Copyright: © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/2
Y1 - 2020/2
N2 - Background and objectives: To evaluate whether sinus augmentation, using a minimally invasive implant device, via a non‐submerged surgical approach, might negatively influence the outcome. Materials and Methods: A retrospective cohort study was conducted by evaluating patients’ files, classifying them into two groups. Fifty patients (22 men 28 women) were included in the study, 25 in each group. The use of an implant device based on residual alveolar ridge height for sinus augmentation, radiographic evaluation, insertion torque, membrane perforation, post‐operative healing, and a minimum of 12 months follow‐up were evaluated. Results: The mean residual alveolar ridge height was 5.4 mm for the non‐submerged group and 4.2 mm for the submerged group. There were no intraoperative or postoperative complications (including membrane perforations). The mean insertion torque was 45 N/cm for the study group and 20 N/cm for the control group. Complete soft tissue healing was observed within three weeks. Mean bone gain height was 8 mm for the study and 9.3 mm for the control group. All implants osseointegrated after 6–9 months of healing time. Mean follow‐up was 17.5 months, range 12–36 months. Marginal bone loss at last follow‐up was not statistically significantly different: 1 mm in the non‐submerged vs. 1.2 mm in the submerged group. Conclusions: Submerged and non‐submerged healing following maxillary sinus augmentation was comparable provided residual alveolar ridge height >5 mm and insertion torque >25 N/cm.
AB - Background and objectives: To evaluate whether sinus augmentation, using a minimally invasive implant device, via a non‐submerged surgical approach, might negatively influence the outcome. Materials and Methods: A retrospective cohort study was conducted by evaluating patients’ files, classifying them into two groups. Fifty patients (22 men 28 women) were included in the study, 25 in each group. The use of an implant device based on residual alveolar ridge height for sinus augmentation, radiographic evaluation, insertion torque, membrane perforation, post‐operative healing, and a minimum of 12 months follow‐up were evaluated. Results: The mean residual alveolar ridge height was 5.4 mm for the non‐submerged group and 4.2 mm for the submerged group. There were no intraoperative or postoperative complications (including membrane perforations). The mean insertion torque was 45 N/cm for the study group and 20 N/cm for the control group. Complete soft tissue healing was observed within three weeks. Mean bone gain height was 8 mm for the study and 9.3 mm for the control group. All implants osseointegrated after 6–9 months of healing time. Mean follow‐up was 17.5 months, range 12–36 months. Marginal bone loss at last follow‐up was not statistically significantly different: 1 mm in the non‐submerged vs. 1.2 mm in the submerged group. Conclusions: Submerged and non‐submerged healing following maxillary sinus augmentation was comparable provided residual alveolar ridge height >5 mm and insertion torque >25 N/cm.
KW - Maxillent dental implant
KW - Membrane elevation
KW - Sinus elevation
KW - Sinus lift
UR - http://www.scopus.com/inward/record.url?scp=85079591046&partnerID=8YFLogxK
U2 - 10.3390/medicina56020075
DO - 10.3390/medicina56020075
M3 - مقالة
C2 - 32069970
SN - 1010-660X
VL - 56
JO - Medicina (Lithuania)
JF - Medicina (Lithuania)
IS - 2
M1 - 75
ER -