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CaP Coating and Low-Level Laser Therapy to Stimulate Early Bone Formation and Improve Fixation of Rough Threaded Implants

DOI:10.1097/ID.0000000000000824 期刊:Implant Dentistry 出版年份:2018 更新时间:2025-09-23 15:23:52
摘要: Purpose: This study aimed to compare in vivo osteogenesis on rough threaded dental implants with and without calcium phosphate (CaP) coating deposition, alone or in association with low-level laser therapy (LLLT) by gallium aluminum arsenide. Material and Methods: Four groups were studied: G1: implant; G2: implant + CaP coating; G3: implant + LLLT; and G4: implant + CaP coating + LLLT. LLLT was applied for 7 days at the surgical site before and after placing the implant. Topographic characterization was performed before surgery using scanning electron microscopy and energy dispersion spectrophotometry. Bone-implant contact (BIC) was measured after 1, 2, and 6 weeks and reverse torque after 6 weeks. In short periods, G2, G3, and G4 showed significantly greater BIC than G1 (P < 0.05), but no difference in BIC was observed at 6 weeks. However, the values for the removal torque test at 6 weeks were higher in G2 and G4 (P < 0.05). Conclusion: Both CaP coating alone and using LLLT induce cellular stimulation and improve BIC in short-term healing, resulting in higher implant fixation, and should be considered in clinical practice due to their low cost and high effectiveness.
作者: Renata Falchete do Prado,Milagros del Valle El Abras Ankha,Daiane Acácia Griti Bueno,Evelyn Luzia de Souza Santos,ítalo Rigotti Pereira Tini,Carolina Judica Ramos,Marianne Spalding,Luis Gustavo Oliveira de Vasconcellos,Luana Marotta Reis de Vasconcellos
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To compare in vivo osteogenesis on rough threaded dental implants with and without calcium phosphate (CaP) coating deposition, alone or in association with low-level laser therapy (LLLT) by gallium aluminum arsenide.

Both calcium phosphate coating and low-level laser therapy, individually or combined, enhance early bone formation and implant fixation in short-term healing. They are effective, low-cost methods that should be considered in clinical practice to improve osseointegration, particularly in cases requiring accelerated healing.

The study is limited to an animal model (rabbits), which may not fully translate to human clinical scenarios. The short evaluation periods (up to 6 weeks) may not capture long-term effects. The sample size (n=5 per group per time point) might be small for broader generalizations. Potential variations in individual animal responses were not accounted for.

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