1. Deceased donor renal transplant outcome in a south Indian tertiary care hospital with zonal allocation model - An observational study
- Author
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Kandasamy Sadayandi, Devdas Madhavan, Prabu Murugesan, Balamurugan Mathavan, Kuppurajan Narayanasamy, Pollachi Balasundaraj Baranikumar, Anandan Murugesan, Sengoda G Balasundaram, Vengetesh Kilvani Sengottayan, R Vasanthan, and S Jeevithan
- Subjects
basiliximab ,deceased donor renal transplant ,donor-specific antibody ,mycophenolate mofetil ,tacrolimus ,Surgery ,RD1-811 - Abstract
Background: With the rising incidence of diabetes and hypertension, the prevalence of end-stage renal disease has increased greatly so as the need for renal replacement therapy. Availability of suitable living-related donors is a major problem which increases the demand for deceased donor renal transplantation (DDRT), making it a lifeline for the patients on dialysis without any living donors. Methodology: This is a retrospective analysis of 118 DDRT done between 2012 and 2020, in a private quaternary care hospital in a south Indian state. All patients received basiliximab induction, with maintenance immunosuppression using steroids, mycophenolate mofetil (MMF) or mycophenolate sodium, and tacrolimus. Results: In our study, we report unadjusted graft survival of 93.2% and 81.3%, patient survival of 94.9% and 83.1% at the end of 1 and 5 years, respectively. The recipients with age < 60 years had 5 years graft survival of 87%. The study group consisted of 15.25% of the patients with panel reactive antibody (PRA) positive and 10.16% of them with donor-specific antibody (DSA) during renal transplantation, and there was only one allograft loss in this subset of the patients. Conclusion: This study confirms that human leukocyte antigen matching is not very important with the current immunosuppressive protocol using tacrolimus and MMF. Early initiations of tacrolimus do not increase the incidence of delayed graft function. We report 91.6% graft survival in the DSA-positive group, with basiliximab induction and desensitization protocol.
- Published
- 2022
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