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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.
Induction immunosuppression aims to prevent rejection after kidney transplantation but may increase infection risk. This study evaluated infectious and rejection outcomes with two Grafalon(Rabbit ATG) dosing regimens in high-immunological-risk patients.
In a prospective observational study over 18 months, 66 Immunological high-risk kidney transplant recipients (spousal, unrelated, cadaveric) received Grafalon induction—30 patients with 3 mg/kg body weight and 26 with 1 mg/kg body weight. Infectious and rejection episodes were recorded during the first 3 months. Fisher’s exact test, odds ratios (OR), and 95% confidence intervals (CI) were used.
The 3 mg/kg group had higher infection episodes per patient (1.33 vs 0.77; p=0.41) and a higher proportion of patients with infection (67%, 95% CI 50.0–83.5% vs 54%, 34.7–73.0%). Severe infections incidence was 26.7% (95% CI 10.8–42.5%) vs 7.7% (0–17.9%) (OR 4.36, 95% CI 0.83–22.81; p=0.09). Mortality was 6.7% (0–15.6%) vs 0% (OR 4.65, 95% CI 0.21–101.4; p=0.49). Rejection rates were comparable (3.3% vs 3.9%). All rejection episodes responded to treatment.The cost of the therapy also doubles or triples in higher dose regimens.
Higher-dose Grafalon (3 mg/kg) increases infection and mortality risk trends without improving rejection prevention compared to 1 mg/kg in high-risk kidney transplants. The lower dose may better balance immunosuppression safety and efficacy.The lower dose regimen gives an additional financial advantage too.