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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.
Post-transplant diabetes mellitus (PTDM) is a frequent metabolic complication following kidney transplantation, contributing to higher cardiovascular risk, infection rates, and potential graft dysfunction. Understanding its determinants is essential for optimizing patient outcomes. This study aimed to evaluate the clinical profile, risk factors, and outcomes of PTDM among renal transplant recipients over a ten-year period at a tertiary-care center.
This retrospective observational study analyzed 184 renal transplant recipients who underwent transplantation between January 2013 and December 2023 at Kasturba Medical College, Manipal. PTDM was diagnosed in accordance with the 2014 International Consensus Guidelines. Demographic, clinical, and biochemical parameters were extracted from hospital records. Post-transplant infections, cytomegalovirus (CMV) status, graft function, and mortality were compared between patients with and without PTDM. Univariate and multivariate logistic regression analyses identified independent predictors of PTDM.
PTDM occurred in 32.6 % of recipients (n = 60). Mean age was similar between PTDM and non-PTDM groups (31.5 ± 9.25 years vs. 36.6 ± 10.08 years; p = 0.39), with male predominance in both (81.7 % vs. 81 %). Post-transplant infections were significantly higher in PTDM patients (48.3 % vs. 31.4 %; p = 0.01), as was CMV infection (13.3 % vs. 6.45 %; p = 0.03). On multivariate analysis, CMV infection remained an independent predictor of PTDM (Odds Ratio 4.52, 95 % CI 1.32–15.49; p = 0.01). Graft outcomes, including serum creatinine (p = 0.82) and eGFR (p = 0.16) at one year, did not differ significantly. Mortality rates were comparable between groups (p = 0.51).
PTDM developed in approximately one-third of kidney transplant recipients. CMV infection emerged as a significant independent risk factor, and PTDM was associated with higher post-transplant infection rates. Despite these complications, short-term graft function and mortality were unaffected. Early detection and management of modifiable risks, particularly CMV infection, are crucial to improving metabolic and transplant outcomes in this population