Abstract
Introduction. Platelet-rich plasma (PRP) is a regenerative therapy that delivers concentrated platelets and growth factors to promote angiogenesis, modulate inflammation, and support tissue repair. While its use is well established in adults, evidence on PRP for neonatal and pediatric wound management remains scarce and heterogeneous. This scoping review aimed to map the existing literature on PRP for cutaneous wound healing in patients aged 0-18 years and to assess the presence of standardized preparation or application protocols.
Methods. The review followed Arksey and O’Malley’s methodological framework, enhanced by Levac et al., and was reported according to PRISMA-ScR guidelines. Searches were conducted in PubMed, Scopus, and Google Scholar (January 2014-April 2025), complemented by backward/forward reference screening and gray literature searches. Eligible studies included neonates, children, or adolescents receiving PRP for any cutaneous wound etiology. Data were extracted on study design, population characteristics, wound type, PRP preparation/application, and clinical outcomes.
Results. A total of 1,812 records were identified, with 8 sources meeting inclusion criteria: 4 clinical pediatric wound-care studies, 3 randomized surgical trials, and 1 congress-level protocol. Reported outcomes included rapid healing of neonatal and pediatric surgical dehiscence (mean ~12 days), complete resolution of a chronic neuropathic ulcer within 2 weeks, and >50% ulcer reduction in pediatric chronic graft-versus-host disease. Surgical trials showed reduced fistula formation, postoperative edema, and complications. One transient citrate-related reaction was the only adverse event recorded. Across studies, substantial heterogeneity in PRP preparation techniques and absence of validated pediatric protocols were observed.
Discussion and conclusions. Findings suggest that PRP is safe and potentially effective for complex wounds and postoperative recovery in neonates and children, especially when conventional treatments are insufficient. However, methodological variability, small sample sizes, and the lack of standardized pediatric protocols limit comparability and clinical implementation. Pediatric-specific challenges – such as limited blood volume, venipuncture difficulty, and risks of iatrogenic anemia – further underline the need for tailored approaches. High-quality, prospective pediatric studies and validated clinical protocols are required to support evidence-based adoption.
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