ReviewInternational journal of dentistry2026
Platelet-Rich Fibrin and Its Derivatives as Adjuncts to Dental Implant Osseointegration: A Scoping Review.
Review in International journal of dentistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
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Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Platelet-rich fibrin (PRF) is a family of autologous platelet concentrates whose solid and liquid formulations differ in cellular distribution, fibrin architecture, handling, and intended clinical use. Contemporary evidence suggests a possible influence on early peri-implant healing, but long-term osseointegration and implant-survival advantages are uncertain. Objective: To map human clinical evidence on leukocyte- and PRF (L-PRF), advanced PRF (A-PRF), injectable or liquid PRF (i-PRF/liquid PRF), and related PRF formulations used as adjuncts to dental implant osseointegration, with attention to preparation protocols, outcome methods, healing phase, and clinical limitations. Methods: A scoping review was conducted in accordance with JBI guidance and PRISMA-ScR. PubMed/MEDLINE, Web of Science Core Collection, and Embase were searched for English-language human clinical studies published from 2015 to 2025. Eligible studies assessed a PRF formulation during implant placement or site preparation and reported implant stability, radiographic bone outcomes, histological bone formation, or peri-implant clinical outcomes. Evidence was synthesized by PRF formulation, outcome modality, and early (within 3 months) versus later (6 months or longer) observation. Results: Nineteen human clinical studies met the eligibility criteria. RFA/ISQ was the most common outcome and frequently suggested a transient improvement in secondary stability during the first weeks of healing. Several radiographic studies reported favorable bone-density or marginal bone findings, whereas others found no between-group differences. Histological evidence was sparse and was not interchangeable with RFA or radiographic surrogate outcomes. Studies with follow-up of 6-12 months did not establish consistent superiority in marginal bone preservation, implant survival, or other long-term clinical endpoints. Preparation reporting was incomplete: rpm and time were often stated, but relative centrifugal force (RCF), rotor geometry, tube composition, and device specifications were commonly missing. Conclusions: PRF and its derivatives show promising potential as adjuncts that may accelerate early healing and secondary implant stability. The available evidence does not establish durable superiority for osseointegration or implant survival, nor does it identify one formulation as clinically superior. Standardized randomized trials with complete preparation reporting, validated outcome measures, long-term follow-up, patient-reported outcomes, and economic evaluation are required.
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