TY - JOUR
T1 - Alveolar bone augmentation with a newly designed microperforated pure titanium membrane
T2 - A clinical case series
AU - Akimoto, Tetsuo
AU - Hasegawa, Hiroshi
AU - Kudo, Kiyomi
AU - Ishida, Daichi
AU - Kaneko, Tetsuharu
AU - Kanno, Chihiro
AU - Endo, Manabu
AU - Yamazaki, Morio
AU - Kitabatake, Takehiro
AU - Yaginuma, Sadanoshin
AU - Honma, Hideaki
AU - Ishihata, Hiroshi
N1 - Funding Information:
We would like to thank Dr. Seiichiro Masui, Clinical Research Center, Fukushima Medical University Hospital for useful support to this study.
Publisher Copyright:
© 2022
PY - 2022/7
Y1 - 2022/7
N2 - Objective: This study aimed to evaluate the usefulness of a novel titanium membrane (Ti honeycomb membrane), which has ultrafine structures with dense microperforations, for the alveolar bone augmentation including guided bone regeneration (GBR). Patients and methods: Fifteen patients with 17 bone defects underwent alveolar bone augmentation surgery using the membranes with autologous bone grafting plus beta-tricalcium phosphate (β-TCP) (n = 9) or with β-TCP alone (n = 8). The membranes were removed at 6–8 months postoperatively, and the regenerated bone was evaluated clinically. In addition, the prognosis of the implants placed in the augmented bones was assessed. Results: Postoperative courses were uneventful in 14 sites without membrane exposures, in which CT analysis showed the bone volume required to place the implants and significantly higher bone density in the sites with autologous bone grafting plus β-TCP than in the sites with β-TCP alone (p = 0.019). In contrast, membrane exposures were found in three sites (17.6%) at< 4 weeks postoperatively (early membrane exposure) and the bone augmentations resulted in failure; however, implants could be placed in two of the three sites. Finally, the overall success rate of bone augmentation and implants placed in the augmented bone were 82.4% and 93.3%, respectively. Conclusions: This membrane was proved to be useful for alveolar bone augmentation, especially when using autologous bone grafting plus β-TCP; however, more efficient operative techniques are required to prevent early membrane exposure.
AB - Objective: This study aimed to evaluate the usefulness of a novel titanium membrane (Ti honeycomb membrane), which has ultrafine structures with dense microperforations, for the alveolar bone augmentation including guided bone regeneration (GBR). Patients and methods: Fifteen patients with 17 bone defects underwent alveolar bone augmentation surgery using the membranes with autologous bone grafting plus beta-tricalcium phosphate (β-TCP) (n = 9) or with β-TCP alone (n = 8). The membranes were removed at 6–8 months postoperatively, and the regenerated bone was evaluated clinically. In addition, the prognosis of the implants placed in the augmented bones was assessed. Results: Postoperative courses were uneventful in 14 sites without membrane exposures, in which CT analysis showed the bone volume required to place the implants and significantly higher bone density in the sites with autologous bone grafting plus β-TCP than in the sites with β-TCP alone (p = 0.019). In contrast, membrane exposures were found in three sites (17.6%) at< 4 weeks postoperatively (early membrane exposure) and the bone augmentations resulted in failure; however, implants could be placed in two of the three sites. Finally, the overall success rate of bone augmentation and implants placed in the augmented bone were 82.4% and 93.3%, respectively. Conclusions: This membrane was proved to be useful for alveolar bone augmentation, especially when using autologous bone grafting plus β-TCP; however, more efficient operative techniques are required to prevent early membrane exposure.
KW - Barrier membrane
KW - Bone augmentation
KW - Guided bone regeneration
KW - Titanium membrane
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U2 - 10.1016/j.ajoms.2022.01.002
DO - 10.1016/j.ajoms.2022.01.002
M3 - Article
AN - SCOPUS:85123267275
SN - 2212-5558
VL - 34
SP - 389
EP - 394
JO - Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology
JF - Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology
IS - 4
ER -