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The Fate of Porous Hydroxyapatite Granules Used in Facial Skeletal Augmentation
Authors:Bryan C. Mendelson  Steve R. Jacobson  Alain M. Lavoipierre  Richard J. Huggins
Affiliation:(1) Toorak Cosmetic Surgery Centre, 109 Mathoura Road, Toorak, VIC, 3142, Australia;(2) Division of Plastic Surgery, Mayo Clinic, 200 First St. SW, Rochester, MN 55905, USA;(3) MDI Radiology, 1155 Malvern Road, Malvern, VIC, 3144, Australia;(4) School of Dentistry, University of Queensland, Brisbane, QLD, Australia
Abstract:Facial appearance is largely determined by the morphology of the underlying skeleton. Hydroxyapatite is one of several materials available to enhance projection of the facial skeleton. This study evaluated the long-term maintenance of augmented bony projection when porous hydroxyapatite granules are used on the facial skeleton. Ten female patients aged 28–58 years were studied following aesthetic augmentation of the facial skeleton at 24 sites using porous hydroxyapatite granules. Postoperative CT scans at 3 months served as the baseline measurement and compared with scans taken at 1 and 2 years, with the thickness of the hydroxyapatite measured in axial and coronal planes. Thickness of original bone plus overlay of hydroxyapatite, thickness of the overlying soft tissue, and the overall projection (bone plus soft tissue) were recorded. It was found that 99.7% of the hydroxyapatite was maintained at 2 years, with no statistical difference (t test) from the baseline measurement. The overall projection (bony and soft tissue) was maintained as there was no evidence of native bone resorption or soft tissue atrophy. Radiographic results confirmed that the use of porous hydroxyapatite granules for enhancement of the facial skeleton is not only a predictable procedure, but maintains full bony projection at 2 years.
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