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Published on: May 2, 2013
Infection Risks With Thymoglobulin Use for Delayed Graft Function in Deceased Donor Kidney Transplantation: Research
Mathew Kunthara1, Greg A Knoll2, David Massicotte-Azarniouch2
1Division of Nephrology, Department of Medicine, University of Ottawa, ON, Canada.
Anti-thymocyte globulin (ATG) use for delayed graft function in low-risk kidney transplant recipients did not increase infection risk or improve outcomes. Further research is needed to balance risks and benefits.
Area of Science:
- Nephrology
- Immunology
- Transplantation
Background:
- Delayed graft function (DGF) is a common complication after kidney transplantation.
- Anti-thymocyte globulin (ATG) is used for DGF but its safety in low-immunological risk recipients is unclear.
- ATG may increase infection risk while potentially reducing rejection.
Purpose of the Study:
- To evaluate the safety and efficacy of using ATG for DGF in low-immunological risk kidney transplant recipients.
- To compare infection rates, rejection, and graft outcomes between recipients who received ATG for DGF and those who did not.
Main Methods:
- Retrospective cohort study of 139 deceased donor kidney transplant recipients (June 2019-June 2023).
- Compared 68 recipients who received ATG for DGF with 71 controls receiving basiliximab induction only.
- Outcomes included BK virus, CMV, serious infections, acute rejection, graft loss, and death.
Main Results:
- ATG recipients were older and received more high-risk donor kidneys.
- No significant differences in BK, CMV, or serious infection rates between groups.
- Similar rates of acute rejection, graft loss, and death were observed.
Conclusions:
- Using ATG for DGF in low-immunological risk kidney transplant recipients did not significantly increase infection risk.
- ATG did not improve graft outcomes in this population.
- The risk-benefit profile of ATG for DGF in low-risk recipients requires further investigation.
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