Using bone replacement grafts to repair intrabony defects
Periodontal disease in dogs and cats presents in many variations. Unfortunately, no one solution exists for all presentations. I reviewed suprabony (above the alveolar crestal bone) pocket care for stage 2 and 3 periodontal pockets in the January 2012 issue. In this article, I address defects below the alveolar crest.
What are intrabony pockets?
Your treatment options
A primary goal of periodontal surgery is pocket elimination. When faced with an intrabony defect, your treatment choices include performing an extraction, decreasing the size of the defect through flap exposure followed by apical flap reposition or filling the defect to decrease pocket depth.
Intrabony filling strategies include:
Keep in mind that curettage alone for removal of the pocket contents and gingivectomy to decrease the pocket depth often results in decreased pocket size but in most cases will allow periodontal disease to progress. After curettage, a clot is formed that initially occupies the cleaned intrabony defect. Soon the clot is replaced with granulation tissue and junctional epithelium. This tissue will decrease the pocket size but, unfortunately, there is no real new attachment of the tooth to the alveolus.
Bone replacement grafts
Bone grafts can be successfully used to preserve or restore the alveolar height in deep, narrow, three-walled intrabony pockets, such as palatal defects, that do not extend into the nasal cavity. With stringent postsurgical home care, the bone grafts help restore normal bony architecture, rebuild the periodontal ligament and soft tissue and prevent further periodontal pocket formation.
The grafts increase bone level, increase clinical attachment level and reduce probing pocket depths when compared with open flap débridement procedures alone. Bone replacement grafts should not be attempted on teeth with mobility stage 3 or furcation exposure or in patients that have significant comorbid factors that would affect healing such as poorly controlled diabetes mellitus and end-stage renal disease.
There are many options to select from when choosing bone graft material, including autografts (also called autologous, autoplastic, autogeneic or autogenous grafts), allografts (also called homografts or allologous, allogeneic, allogenous, homologous, homoplastic, homogeneic or homogenous grafts) and alloplasts.
In a 1999 study, freeze-dried demineralized canine cadaver bone graft was superior to bioactive glass granules in the treatment of intrabony defects in Beagles.1 Bone allograft contains bone morphogenetic proteins (BMPs) that stimulate osteoprogenitor cells in the patient's local periosteum to differentiate into osteoblasts. This process is known as osteoinduction. Inert alloplast synthetic material does not contain proteins helpful to promote bone growth. Synthetic materials commonly used by veterinarians do not contain BMPs. They do provide an inert scaffold for the host bone to slowly grow onto as long as the environment remains favorable. Within weeks to months, the inert alloplast material dissolves whereas the bone allograft integrates with the patient's own bone through the normal bone remodeling process.