Bone Augmentation With Alloplastic Graft Material in a Patient Under Bisphosphonate Therapy: A Case Report and Literature Review

Author:

Narahara Shun1,Ohba Seigo12,Ichinose Sosuke2,Yamanouch Yuya34,Kuroshima Shinichiro45,Shido Rena6,Sawase Takashi34,Yamada Tomohiro2

Affiliation:

1. 1 Department of Oral and Maxillofacial Surgery, Showa University School of Dentistry, Tokyo, Japan.

2. 2 Department of Oral and Maxillofacial Surgery, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.

3. 3 Dental Implant Center, Nagasaki University Hospital, Nagasaki, Japan.

4. 4 Department of Applied Prosthodontics, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.

5. 5 Department of Crown and Bridge Prosthodontics, Oral Functional Sciences, Graduate School of Dental Medicine, Hokkaido University, Hokkaido, Japan.

6. 6 Department of Oral and Maxillofacial Surgery, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

Abstract

Cases of relatively safe dental implant treatment in patients with low-volume bisphosphonate (BP) have been gradually reported. Although bone augmentation is commonly used when the bone volume is insufficient for implant placement, the studies and case reports regarding the safety of bone augmentation in patients treated with BP remain insufficient. Herein, we report a case wherein bone augmentation was performed after BP treatment with bone healing realized according to imaging, and we review the literature regarding BP and bone augmentation. A 67-year-old Japanese woman requested implant treatment for a hopeless lower right second molar. She had been taking minodronic acid hydrate (50 mg/4 wk) for 18 months to treat steroid-induced osteoporosis. After obtaining informed consent, tooth extraction and bone augmentation within the extraction socket were performed. The tooth was extracted atraumatically to preserve the surrounding alveolar bone, and the extraction socket was intensely curetted. Subsequently, the socket was filled with carbonate apatite granules and covered with a biodegradable membrane, and the wound was sutured without tension. Although protracted wound healing without any symptoms of infection was observed, the wound healed completely. No clinical symptoms were observed, the color of the mucosa at the site was healthy, and imaging findings at 6 months postoperation indicated that osteogenesis had progressed uneventfully.

Publisher

American Academy of Implant Dentistry

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