# The Safety and Efficacy of Platelet-Rich Plasma in Enhancing Outcomes Following Circumcision in Children

**Authors:** Tahsin Onat Kamci, Mustafa Azizoglu, Sergey Klyuev, Mehmet Hanifi Okur, Hakkari Aydogdu, Maria Escolino, Asli Pinar Zorba Yildiz, Ciro Esposito, Sameh Shehata

PMC · DOI: 10.3390/jcm14217620 · Journal of Clinical Medicine · 2025-10-27

## TL;DR

This study shows that using platelet-rich plasma during circumcision in children may reduce swelling and bleeding, and is generally safe.

## Contribution

The study provides new evidence on the safety and potential benefits of PRP in pediatric circumcision.

## Key findings

- PRP application reduced penile edema and postoperative bleeding in children undergoing circumcision.
- PRP was associated with lower pain scores at all time points compared to standard circumcision.
- PRP complications were minor and resolved without intervention.

## Abstract

Background: The primary objectives of platelet-rich plasma (PRP) therapy are to enhance the wound-healing process, reduce pain, and minimize the loss of productivity due to recovery time. Localized application of PRP, which is enriched with growth factors such as PDGF, TGF-β1, IGF-1, VEGF, and FGF-2, as well as interleukins (IL-1, IL-4, IL-6, IL-10, and IL-13), has been documented to accelerate the healing process by approximately 30–40%. This study aimed to assess the safety and efficacy of platelet-rich plasma (PRP) in enhancing outcomes following circumcision in male children. Methods: The patients were divided into two groups: one undergoing standard circumcision and the other receiving PRP application during circumcision. Pain scores, edema level, bleeding, local infection, and safety of PRP were evaluated. Results: This study evaluated 80 male children undergoing circumcision, divided into two groups: Group CS (n = 44) underwent classical circumcision, and Group PRP (n = 36) received PRP application. Median ages were comparable (p = 0.101). Penile edema occurred less frequently in the PRP group (5.6%) compared to the CS group (18.2%) (p = 0.089), with no severe edema observed in the PRP group. Postoperative bleeding was present in 6.8% of the CS group but absent in the PRP group (p = 0.110). Other complications, such as nausea (CS: 6.8%, PRP: 5.6%, p = 0.816), vomiting (CS: 4.5%, PRP: 2.8%, p = 0.679), local infection (CS: 2.3%, PRP: 0%, p = 0.363), wound dehiscence (CS: 2.3%, PRP: 0%, p = 0.363), and skin tunnel formation (CS: 6.8%, PRP: 2.8%, p = 0.409), showed no significant differences. No cases of necrosis, chordee, rotational anomaly, or secondary phimosis were observed. Safety analysis of PRP revealed minor complications during blood draw: hypotension in one patient (2.8%) and local ecchymosis in two patients (5.6%), resolving without intervention. During PRP application, one allergic reaction (2.8%) occurred, presenting as a transient rash that resolved spontaneously. Group PRP consistently reported lower pain scores than Group CS at all time points. Conclusions: PRP application during circumcision is safe. The findings provide preliminary but important evidence regarding the potential benefits of PRP in pediatric circumcision.

## Linked entities

- **Proteins:** pdgfa.S (platelet derived growth factor subunit A S homeolog), TGFB1 (transforming growth factor beta 1), IGF1 (insulin like growth factor 1), VEGFA (vascular endothelial growth factor A), FGF2 (fibroblast growth factor 2), IL1A (interleukin 1 alpha), IL4 (interleukin 4), IL6 (interleukin 6), IL10 (interleukin 10), IL13 (interleukin 13)

## Full-text entities

- **Genes:** FGF2 (fibroblast growth factor 2) [NCBI Gene 2247] {aka BFGF, FGF-2, FGFB, HBGF-2}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}
- **Diseases:** hypotension (MESH:D007022), bleeding (MESH:D006470), Pain (MESH:D010146), CS (MESH:D006223), vomiting (MESH:D014839), infection (MESH:D007239), necrosis (MESH:D009336), nausea (MESH:D009325), edema (MESH:D004487), wound dehiscence (MESH:D013529), Penile (MESH:D010409), allergic reaction (MESH:D004342), rash (MESH:D005076), ecchymosis (MESH:D004438), rotational anomaly (MESH:D009759), phimosis (MESH:D010688)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12608403/full.md

## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12608403/full.md

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Source: https://tomesphere.com/paper/PMC12608403