Custom-made titanium devices as membranes for bone augmentation in implant treatment: Clinical application and the comparison with conventional titanium mesh

被引:105
作者
Sumida, Tomoki [1 ]
Otawa, Naruto [1 ]
Yu, Kamata [1 ]
Kamakura, Satoshi [2 ]
Mtsushita, Tomiharu [3 ]
Kitagaki, Hisashi [4 ]
Mori, Shigeo [4 ]
Sasaki, Kiyoyuki [5 ]
Fujibayashi, Shunsuke [6 ]
Takemoto, Mitsuru [6 ]
Yamaguchi, Atsushi [7 ]
Sohmura, Taiji [7 ]
Nakamura, Takashi [6 ]
Mori, Yoshihide [1 ]
机构
[1] Kyushu Univ, Fac Dent Sci, Div Maxillofacial Diagnost & Surg Sci, Sect Oral & Maxillofacial Surg,Higashi Ku, Fukuoka 8128582, Japan
[2] Ehime Implant Clin, Masaki, Ehime 7913155, Japan
[3] Chubu Univ, Coll Life & Hlth Sci, Dept Biomed Sci, Kasugai, Aichi 4878501, Japan
[4] Osaka Yakin Kogyo Co Ltd, Yodogawa Ku, Osaka 5330005, Japan
[5] Sagawa Printing Co Ltd, Hyuga City, Kyoto 6178588, Japan
[6] Kyoto Univ, Grad Sch Med, Dept Orthoped Surg, Sakyo Ku, Kyoto 6068507, Japan
[7] Wada Precis Dent Labs Co Ltd, Higashiyodogawa Ku, Osaka 5330031, Japan
关键词
Clinical trial; Computer aided design; Custom-made device; Rapid prototyping; Selective laser melting; Guided bone regeneration; REGENERATION;
D O I
10.1016/j.jcms.2015.10.020
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: Development of new custom-made devices to reconstruct alveolar bone for implantation, and comparison with conventional methods were the goals of this study. Materials and methods: Using a computer-aided design technique, three-dimensional images were constructed. From these data, custom-made devices were produced by a selective laser melting method with pure titanium. Clinical trials also have been conducted with 26 participants who needed bone reconstruction before implantation; they were divided into 2 groups with 13 patients each. The first group uses custom-made devices; the other uses commercial titanium meshes that need to bend during operation. Some clinical aspects are evaluated after the trial. Results: The custom-made devices can be produced closely by following the data precisely. Devices are fit for bone defect site. Moreover, the operation time of the custom-made group (75.4 +/- 11.6 min) was significantly shorter than that of the conventional group (111.9 +/- 17.8 min) (p < 0.01). Mucosal rupture occurs, without significant difference (p = 0.27), in a patient in the custom-made without severe infection (7.7%), and 3 in conventional (23.1%), respectively. The retaining screw is significantly fewer in the custom-made group than commercial mesh group (p < 0.01). Conclusion: These results indicate that our novel protocol could be simple and safe for providing powerful support for guided bone regeneration. (C) 2015 European Association for Cranio-Maxillo-Facial Surgery. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2183 / 2188
页数:6
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