Journal
JOURNAL OF PERIODONTAL AND IMPLANT SCIENCE
Volume 53, Issue 4, Pages 306-317Publisher
KOREAN ACAD PERIODONTOLOGY
DOI: 10.5051/jpis.2300640032
Keywords
Allografts; Bone regeneration; Bone substitutes; Dental implants; Randomized controlled trial
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This study compared the clinical and radiographic benefits of a newly developed BCP with DBBM for reconstructing peri-implant bone defects. The results showed that the newly developed BCP had similar outcomes to DBBM in terms of clinical, radiographic, postoperative discomfort, and early wound healing.
Purpose: Biphasic calcium phosphate (BCP), a widely used biomaterial for bone regeneration, contains synthetic hydroxyapatite (HA) and beta-tricalcium phosphate (beta-TCP), the ratio of which can be adjusted to modulate the rate of degradation. The aim of this study was to evaluate the clinical and radiographic benefits of reconstructing peri-implant bone defects with a newly developed BCP consisting of 60% beta-TCP and 40% HA compared to demineralized bovine bone mineral (DBBM). Methods: This prospective, multicenter, parallel, single-blind randomized controlled trial was conducted at the periodontology departments of 3 different dental hospitals. Changes in clinical (defect width and height) and radiographic (augmented horizontal bone thickness) parameters were measured between implant surgery with guided bone regeneration (GBR) and re-entry surgery. Postoperative discomfort (severity and duration of pain and swelling) and early soft-tissue wound healing (dehiscence and inflammation) were also assessed. Data were compared between the BCP (test) and DBBM (control) groups using the independent t-test and the chi 2 test. Results: Of the 53 cases included, 27 were in the test group and 26 were in the control group. After a healing period of 18 weeks, the full and mean resolution of buccal dehiscence defects were 59.3% (n=16) and 71.3% in the test group and 42.3% (n=11) and 57.9% in the control group, respectively. There were no significant differences between the groups in terms of the change in mean horizontal bone augmentation (test group: -0.50 +/- 0.66 mm vs. control groups: -0.66 +/- 0.83 mm, P=0.133), postoperative discomfort, or early wound healing. No adverse or fatal complications occurred in either group. Conclusions: The GBR procedure with the newly developed BCP showed favorable clinical, radiographic, postoperative discomfort-related, and early wound healing outcomes for periimplant dehiscence defects that were similar to those for DBBM.
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