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[Delayed graft function after DCD kidney transplantation: risk factors for and impact on transplantation]
Mingjie Shao1, Qifa Ye, Yingzi Ming
1Central South University, Changsha, China.
Insights
Delayed graft function (DGF) in kidney transplants from donation after cardiac death (DCD) donors is influenced by the cause of brain death, donor creatinine, and recipient dialysis time. DGF did not impact patient or graft survival in this study.
Area of Science:
- Nephrology
- Transplantation immunology
- Critical care medicine
Background:
- Donation after cardiac death (DCD) kidney transplantation is a growing source of organs.
- Delayed graft function (DGF) is a common complication in DCD kidney transplants.
- Understanding DGF risk factors is crucial for optimizing outcomes.
Purpose of the Study:
- To identify risk factors associated with DGF in DCD kidney transplantation.
- To assess the impact of DGF on patient and graft survival after DCD kidney transplantation.
Main Methods:
- Retrospective study of 48 DCD kidney transplantations.
- Classification of recipients into immediate graft function (IGF) and DGF groups.
- Analysis of pre-transplant, donor, and ischemia time variables.
Main Results:
- DGF occurred in 37.5% of DCD kidney transplants.
- DGF did not significantly affect patient or graft survival (P=0.098 and P=0.447, respectively).
- Independent risk factors for DGF included cerebral hemorrhage as cause of brain death (OR=39.652), donor creatinine ≥177 μmol/L (OR=57.148), and recipient dialysis time ≥12 months (OR=15.060).
Conclusions:
- Cerebral hemorrhage, high donor creatinine, and prolonged recipient dialysis are independent risk factors for DGF in DCD kidney transplantation.
- DGF occurrence did not adversely impact long-term transplant outcomes in this cohort.
- Targeting these risk factors may help mitigate DGF incidence and improve DCD kidney transplant success.
Objective:
To evaluate the risk factors of delayed graft function (DGF) and its impact on renal transplantation from donation after cardiac death (DCD).
Methods:
We conducted a retrospective study consisting of 48 subjects who underwent a DCD kidney transplantation from February 2010 to March 2012. We classified the recipients into two groups: an IGF (immediate graft function) group (n=30) and a DGF group (n=18), and analyzed the risk factors of DGF and its impact on transplantation.
Results:
DGF occurred in 18 of the 48 (37.5%) kidneys from DCD donors, and the occurrence of DGF did not adversely influence the survival of patients (P=0.098) and graft (P=0.447). In the univariate analysis, the preoperative dialysis time of recipients (P<0.001), HLA mismatch site (P<0.001), the cause of brain death (P=0.011), BMI (P<0.001), preoperative serum creatinine of donors (P=0.0001), norepinephrine used in donors (P<0.001), warm ischema time (WIT) (P<0.001), cold ischema time (CIT) (P<0.001) showed significant differences. In the multivariate analysis, cerebral hemorrhage as the cause of brain death (P=0.022, OR=39.652), preoperative serum creatinine of donors≥177 μmol/L (P=0.008, OR=57.148) and the preoperative dialysis time of recipients≥12 months (P=0.060, OR=15.060) were independent risk factors for DGF development.
Conclusion:
The independent risk factors for DGF are the cause of brain death, the terminal creatinine level, and the preoperative dialysis time.
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