Back
For best output, select "Paper Size" as "A4" and "Margin" as "0" or "None".
To save or print to PDF, please select Print Destination > Save as PDF, enable Background Graphics under "More Settings", then click "Save".
During the congress, E-Posters will be accessible to all participants on the congress website 24/7, as well as in the E-poster stations in the congress center.
Preparing your E-Poster
Please review the E-Poster format requirements carefully when preparing your E-Poster. Should your E-Poster not meet the mentioned requirements, it may not be displayed as described above.
E-Poster Submission Deadline
Please prepare and upload your E-Poster no later than March 14, 2026 11.59PM CET. After this date, you will no longer be able to prepare and upload your E-poster and it will not be displayed and accessible on the congress website.
Please follow the instructions below to input your abstract title.
Abstract titles should be brief and reflect the content of the abstract.
Achieving long-term graft survival with minimal patient morbidity are key goals in kidney transplantation (KT). However, clinical and biological factors differ significantly between pediatric and adult populations. Pediatric patients experience immune system maturation, affecting alloimmune responses and immunosuppression efficacy, and higher immune reactivity whereas adults are more prone to immune dysregulation and comorbidities. Despite these differences, pediatric treatment protocols are largely adapted from adult guidelines, with limited direct comparative studies. Therefore, we conducted a multicenter retrospective study comparing the outcomes of pediatric and adult kidney transplant recipients (KTR).
Subjects who received KT between Jan 1, 2017 and Dec 31, 2018, at four different Italian transplant centers, with an overall follow-up of 5 years, were included in the study. Patients were stratified into pediatric (≤18 years) and adult (>18 years) groups. We compared graft survival, rejection rates, peritransplant complications (surgical, delayed graft function - DGF), and native disease recurrence. Statistical analysis included Kaplan-Meier, log-rank test, and Chi-square test.
We enrolled 445 KTR (104 pediatric, 341 adult). Compared to adults, pediatric patients had a shorter dialysis duration prior to transplant, a different distribution of dialysis modalities, exclusively received standard criteria donor kidneys, and had a higher prevalence of genetic kidney disease. Data show a significantly higher use of thymoglobulin induction in adults. As for maintenance therapy, all pediatric patients received steroids, and they were more frequently treated with azathioprine (12.5% vs 0.3%, p < 0.001) and cyclosporine (6.7% vs 0.6%, p < 0.001), whereas mTOR inhibitors were used exclusively in adults (25.2% vs 0%, p < 0.001). Mycophenolate mofetil was slightly more common in pediatric patients (86.5% vs 76.2%, p = 0.025). Graft loss at 5 years occurred in 14.0% of adults and 8.2% of pediatric patients, with no significant difference (p = 0.129) (Fig.1A). The overall 5-year cumulative incidence of rejection was comparable between adults and pediatric patients (30.3% vs 37.8%, p = 0.166). However, pediatric patients had a significantly higher cumulative incidence of acute ABMR (25.4% vs 10.6%, p = 0.047) and acute TCMR (62.7% vs 39.4%, p = 0.012) (Fig.1B). Surgical and urological complications were comparable between groups, except for lymphocele, which was less frequent in pediatrics (8.5% vs. 1.9% vs. 8.5%; P = 0.025) (Fig.1C). Within the first month after transplantation, infection rates were comparable (11.1% vs. 16.5%, p=ns). Pediatric recipients showed a significantly higher rate of recurrence at 1 year compared with adults (22.7% vs. 5.5%; P = 0.023), whereas no significant differences were detected at 2 and at 5 years after KT (Fig.1D).
To the best of our knowledge, this is the first direct comparative study between pediatric and adult KT recipients, offering insights into the applicability of adult-based strategies in pediatric populations. Despite distinct immunological and clinical differences, graft survival, rejection rates, and disease recurrence were comparable between groups. Based on our results, future clinical trials should include pediatric cohorts to ensure equitable treatment across all age groups.