Studies on split-thickness skin grafts
The 2026 meta-analysis included 7 randomized and 3 observational studies. Certainty of evidence was nevertheless rated low to very low.
Platelet-rich plasma (PRP) is being investigated in plastic and reconstructive surgery for rhinoplasty, cartilage grafts, skin grafts, wound healing, scars and postoperative recovery. The evidence is not uniform: some questions have controlled clinical data, while others remain clearly experimental.
The biological rationale is plausible: platelets contain mediators involved in coagulation, cell signalling and tissue repair. Biological plausibility, however, is not proof of clinical benefit. Controlled human studies must show whether relevant outcomes such as wound closure, graft take, scar quality or postoperative symptoms actually improve.
The 2026 meta-analysis included 7 randomized and 3 observational studies. Certainty of evidence was nevertheless rated low to very low.
The 2026 semi-dried PRP-stabilized diced cartilage technique is a feasibility series without a control group.
PRP and PRF data must not be conflated. Preparation, fibrin architecture and biological properties differ.
The matrix separates clinical signals from low or inconsistent evidence and early experimental concepts. It is not a ranking of treatment options.
Controlled studies report possible benefits for selected early healing parameters such as crusting. Results for pain, bleeding, synechiae and overall postoperative recovery are not consistent.
Not supported: a general claim that PRP improves rhinoplasty outcomes.
A 2026 technique was described in two primary rhinoplasties and one revision rhinoplasty. At six months, no clinically visible migration, infection or contour irregularity was reported.
Only 3 patients; no control group, objective volume measurement or histological validation.
A 2026 meta-analysis found higher mean graft take and fewer hematomas with adjunctive PRP. Findings for graft loss were not stable in sensitivity analyses.
GRADE: low to very low certainty.
Some studies report better scar scores. Pooled analyses do not show a consistently superior effect across relevant time points and scar types.
Patient-reported improvement at 6 months was reported, but heterogeneity was high.
Split-face and pilot studies provide isolated signals for less edema or bruising, but sample sizes are too small for robust general conclusions.
The term combines very different outcomes. An improvement in crusting or hematoma does not equal faster overall recovery.
Controlled studies and systematic analyses are now available in nasal surgery, but they combine different operations, PRP preparations and endpoints. Some studies report less crusting or favorable early mucosal findings, while others show no significant difference for several postoperative outcomes.
The 2024 randomized study with 40 patients found differences in dryness and crusting, but this does not establish a global improvement in rhinoplasty outcome. Current evidence supports cautious wording: PRP is being investigated for selected aspects of early nasal healing and clinical signals exist; reliable improvement of aesthetic, functional or overall recovery outcomes has not been established.
Autologous cartilage grafting is an established surgical tool in rhinoplasty. In diced-cartilage techniques, cartilage is cut into small fragments for contouring or augmentation, and different carrier or stabilization methods are being investigated.
In August 2026, a small technical series described liquid PRP combined with diced cartilage and processed under controlled warm air to create a moldable graft. The technique was used in three patients. At one and six months, the authors reported maintained contour without clinically visible migration, infection or relevant surface irregularity.
A separate 2026 comparison of diced cartilage with fibrin glue, PRP or warm blood likewise did not establish a general superiority of PRP. PRP stabilization of cartilage grafts should therefore still be regarded as a research approach.
The clinical evidence is comparatively broader for split-thickness skin grafts. A 2026 systematic review and meta-analysis included ten comparative studies, seven of them randomized controlled trials. Pooled data showed higher graft take and fewer hematomas with adjunctive PRP.
The authors nevertheless rated the certainty of evidence as low to very low. Reasons included heterogeneity in wound causes, PRP protocols, study design and assessment of graft take. For graft loss, the effect was no longer statistically stable in a sensitivity analysis.
This illustrates why a statistically positive pooled result should not be equated with established clinical efficacy.
A meta-analysis of 11 randomized trials with 539 participants found no statistically significant advantage in observer-based scar scores at three months. At six months, however, a significant patient-reported PSAS difference favored PRP.
Because scar type, location, PRP preparation, application and follow-up varied considerably and heterogeneity was high, it remains inappropriate to claim that PRP generally prevents or visibly reduces postoperative scars.
Small studies in facial plastic surgery have examined whether platelet concentrates affect swelling or bruising. Some report trends favoring the treated side, but the samples are too small and the methods too heterogeneous for a reliable general statement.
The term ‘postoperative recovery’ should also be used carefully. Studies actually measure concrete endpoints such as epithelialization, pain, crusting, edema, hematoma, scar scores, graft take or patient satisfaction. A benefit in one parameter does not prove faster overall recovery.
Select a factor. The graphic shows why even a single technical variable can limit transferability of a study result to another system.
Type and amount of anticoagulant can influence activation, calcium balance and subsequent processing. Studies should report this parameter transparently.
The more key protocol parameters differ between two studies, the more cautiously their results should be transferred.
Clinical signals exist for split-thickness skin grafts and selected parameters of nasal healing, justifying further controlled research.
For scars, swelling and broadly defined postoperative recovery, results are not sufficiently consistent.
PRP as a biological scaffold for diced cartilage is technically interesting, but a clinically established additional benefit has not been demonstrated.
PRP in plastic and reconstructive surgery is not one uniformly validated procedure; it is a research field with markedly different levels of evidence by indication. Clinical signals exist for skin grafts and selected aspects of nasal healing. Scar evidence remains inconsistent, while PRP-stabilized cartilage grafts are still in an early clinical phase.
Assessment of each study requires knowing what PRP was actually produced. Findings should only be transferred to a specific system when preparation, composition, protocol and application are sufficiently comparable.
Because a biological mechanism does not prove clinical efficacy. Controlled human trials with suitable comparators and patient-relevant endpoints are needed.
No. Transferability depends on anticoagulant, centrifugation, cellular composition, activation, volume and application. Relevant differences preclude scientific equivalence.
No. Both are autologous blood preparations, but their processing and structure differ. In particular, positive PRF findings for cartilage grafts must not be presented as PRP evidence.
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