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Hydraulic sinus floor elevation using advanced platelet-rich fibrin: A randomized clinical trial with two-dimensional radiographic results. | LitMetric

AI Article Synopsis

  • A study was conducted to compare the effectiveness, complications, and survival rates of advanced platelet-rich fibrin versus xenografts in hydraulic sinus floor elevation in dental procedures.
  • The trial involved 40 patients and found that both methods led to 100% implant survival, though one patient in the xenograft group developed a sinus infection post-surgery.
  • Results showed no significant differences in bone regeneration between the two groups, indicating that advanced platelet-rich fibrin may be a good alternative to xenografts, but more long-term research is needed to fully assess its effectiveness.

Article Abstract

Purpose: To assess the radiographic outcomes, complications, and implant survival rates of advanced platelet-rich fibrin versus xenografts in hydraulic sinus floor elevation.

Methods: In this randomized trial, 40 patients with 46 implants were divided into two groups: a test group (advanced platelet-rich fibrin alone) and a control group (xenograft alone). The key outcome measures included bone regeneration, implant survival, and complications.

Results: Both groups achieved 100% implant survival. One case of maxillary sinus infection occurred in the control group after surgery. There was no significant difference in bone regeneration between the two groups at 6 months post-surgery and 12 months post-load (P > 0.05). The residual bone height and sinus width at the apex of the implant were significant negative predictors of bone regeneration (P < 0.05), whereas the presence of adjacent teeth was a significant positive predictor (P < 0.05).

Conclusions: Both advanced platelet-rich fibrin and xenografts effectively enhanced bone growth at sinus floor elevation, achieving high implant survival rates over one year. Advanced platelet-rich fibrin alone may be a viable xenograft alternative, necessitating further long-term studies to confirm its efficacy. The study was registered in the Chinese Clinical Trial Registry (http://www.chictr.org.cn/) with the registration number ChiCTR2100042060. This clinical trial was not registered before participant recruitment or randomization.

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Source
http://dx.doi.org/10.2186/jpr.JPR_D_24_00065DOI Listing

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