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Plasma Rich in Growth Factors (PRGF) in Intraoral Bone Grafting Procedures: A Systematic Review

While PRGF shows some promise in improving soft tissue healing and reducing post-operative pain and swelling, current evidence remains limited and inconsistent regarding its effectiveness in promoting new bone formation across intraoral grafting procedures.

woman staring directly at camera near pink wall

Dr. Theo Katsaros

Periodontist

PERIODONTAL SURGERY
MAXILLARY SINUS AUGMENTATION
DENTAL IMPLANTS
BONE GRAFTING
PERIODONTAL SURGERY
MAXILLARY SINUS AUGMENTATION
DENTAL IMPLANTS
BONE GRAFTING
PERIODONTAL SURGERY
MAXILLARY SINUS AUGMENTATION
DENTAL IMPLANTS
BONE GRAFTING

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Background & Clinical Context

Plasma Rich in Growth Factors (PRGF) is an autologous, leukocyte-free platelet concentrate prepared via a single centrifugation technique. It releases growth factors including TGF-β1, PDGF, VEGF, and IGF, with the aim of accelerating wound healing and promoting bone regeneration.

In vitro studies have shown PRGF stimulates fibroblast and osteoblast migration and proliferation. Pre-clinical work has demonstrated significant bone regeneration in peri-implant defects. Clinical applications have expanded to extraction socket management, sinus augmentation, ridge augmentation, chronic ulcer treatment, and orthopedic lesions — though the quality of controlled evidence supporting these uses has varied considerably.

Despite widespread clinical adoption, the evidence base for PRGF in formal bone augmentation procedures remained scattered and inconsistent.

Our systematic review was the first to rigorously evaluate PRGF across three clinically distinct procedures: ridge preservation, ridge augmentation, and maxillary sinus augmentation.

Key Findings by Procedure

Ridge Preservation

Two controlled trials compared PRGF-treated extraction sockets against natural blood clot healing, with conflicting results.

Study

Design

Primary outcome

PRGF effect on bone

Soft tissue / pain

Anitua et al., 2015

RCT

% regenerated bone volume at 10–12 weeks (CBCT + biopsy)

Significant benefit
96.7% vs. 45.5% sites with ≥75% RBV

Improved — lower pain & inflammation at days 3 & 7; thicker keratinized gingiva

Farina et al., 2013

CCT

Early bone deposition at 4–10 weeks (micro-CT + histomorphometry)

No significant benefit
No difference in BV, TMC, TMD, or vascularity

Not assessed

Interpreting the conflict

The differing results likely reflect timing of assessment: Farina evaluated early deposition (4–10 weeks), while Anitua assessed later-stage healing (10–12 weeks). PRGF's regenerative effect may manifest predominantly at later timepoints, consistent with its growth factor–driven mechanism of action.

Ridge augmentation

One RCT (Torres et al., 2010) examined PRGF membranes placed over titanium mesh (Ti-mesh) in 30 patients. No Ti-mesh exposures occurred in the PRGF group versus a 40% exposure rate in controls. Greater vertical and horizontal bone gain was recorded in PRGF-treated sites — attributed to maintained soft tissue closure rather than a direct osteogenic effect. No studies assessed post-operative symptomatology in this context.

Maxillary sinus augmentation

The most studied application, represented by five controlled trials with variable grafting materials (xenograft, β-TCP). Findings were predominantly mixed regarding new bone formation but more consistently positive for post-operative quality of life.

Outcome domain

Evidence direction

Notes

New bone formation (%)

Conflicting

One study (Torres 2009) showed SS benefit; two others (Taschieri 2015, Comert Kilic 2017) found no difference. Two of three had only 5 patients.

Vertical bone height gain

No benefit

Kilic & Gungormus 2016: no SS difference at 10 days or 6 months with β-TCP ± PRGF.

Post-operative pain

Reduced — days 2–3

Del Fabbro 2015: SS reduction in pain during 2nd and 3rd post-op days; no difference from day 4 onwards.

Swelling & function

Improved — week 1

Less hematoma, fewer limitations in chewing and speaking during the first post-operative week.

Implant survival

No difference

97.5% overall survival; no SS difference between PRGF and control groups across two studies.

Summary of evidence

Soft tissue healing

Consistent benefit seen across ridge preservation and augmentation

Post-op symptomatology

Early reduction in pain and swelling (first 3–7 days)

Bone regeneration

Conflicting results across procedures and timepoints

Clinical bottom line

PRGF offers reliable short-term benefits in soft tissue healing and post-operative comfort across extraction socket management, ridge augmentation with Ti-mesh, and sinus floor elevation; largely consistent with its leukocyte-free, growth factor–rich composition.

Its role as a substitute for bone grafting materials or barrier membranes is not supported by current evidence. Its benefit on new bone formation remains inconclusive and procedure-dependent. Given its autologous nature, favorable safety profile, and ease of preparation, PRGF is a clinically reasonable adjunct where reduced post-operative morbidity is a patient priority.

For the practitioner

PRGF offers reliable short-term benefits in soft tissue healing and post-operative comfort across extraction socket management, ridge augmentation with Ti-mesh, and sinus floor elevation — largely consistent with its leukocyte-free, growth factor–rich composition. Its role as a substitute for bone grafting materials or barrier membranes is not supported by current evidence. Its benefit on new bone formation remains inconclusive and procedure-dependent. Given its autologous nature, favorable safety profile, and ease of preparation, PRGF is a clinically reasonable adjunct where reduced post-operative morbidity is a patient priority.

Reference Article

Dragonas P, Schiavo JH, Avila-Ortiz G, Palaiologou A, Katsaros T. Plasma rich in growth factors (PRGF) in intraoral bone grafting procedures: a systematic review. J Cranio-Maxillofac Surg. 2019;47(3):443–453.

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