Abstract
Purpose Evaluation of donor co-morbidities is critical in order to risk-stratify and optimize post-transplant survival among simultaneous heart and kidney transplant (HKT) patients. We aimed to characterize the effect of donor glomerular filtration rates (GFR) on HKT recipient survival at 60 months post-transplantation. Methods All patients registered in the UNOS database who received HKT from 1/1/2010 - 6/1/2021 were analyzed. HKT recipients with donors of GFR >30 mL/min/1.73 m2 (n =1934) and donors with GFR <=30 mL/min/1.73 m2 (n = 59) were compared. HKT recipients with donors of GFR >60 mL/min/1.73 m2 (n=1611) and <=60mL/min/1.73 m2 (n=382) were also compared. Baseline characteristics were compared using Mann-Whitney U and Chi-square analyses. Mean age among all recipients was 55.8 years (SE 10.8). Comorbidities including diabetes, smoking, pre transplant dialysis requirements, donor age, use of ventricular assist devices, life support ventilators, intra-aortic balloon pumps, and ischemic time were similar among groups. Kaplan-Meier survival analysis was performed at 60 months post-transplantation. Results At 60 months post-transplant, there were no significant differences in survival among HKT patients with donor GFR <=60mL/min/1.73 m2 and donor GFR>60mL/min/1.73 m2 groups, respectively (p=0.858). At 60 months post transplant, there was no significant survival change among those with donor GFR <=30 mL/min/1.73 m2 and >30 mL/min/1.73 m2 (p=0.400). After adjusting for variables listed above, HKT recipients with donors of GFR <=60 compared to >60 had similar survival rates (adjusted HR 1.016, 95% CI 0.776-1.332, p=0.904). A similar trend was seen for patients with donors of GFR <= 30 mL/min/1.73 m2 compared to those of GFR >30 mL/min/1.73 m2 (adjusted HR 0.650, 95% CI 0.290-1.457, p=0.295). Conclusion Donor GFR in isolation had no significant impact on survival among simultaneous heart kidney transplant recipients at 60 months post transplantation after controlling for comorbidities. Donor kidney function In isolation should also not prohibit consideration for dual organ transplantation. Evaluation of donor co-morbidities is critical in order to risk-stratify and optimize post-transplant survival among simultaneous heart and kidney transplant (HKT) patients. We aimed to characterize the effect of donor glomerular filtration rates (GFR) on HKT recipient survival at 60 months post-transplantation. All patients registered in the UNOS database who received HKT from 1/1/2010 - 6/1/2021 were analyzed. HKT recipients with donors of GFR >30 mL/min/1.73 m2 (n =1934) and donors with GFR <=30 mL/min/1.73 m2 (n = 59) were compared. HKT recipients with donors of GFR >60 mL/min/1.73 m2 (n=1611) and <=60mL/min/1.73 m2 (n=382) were also compared. Baseline characteristics were compared using Mann-Whitney U and Chi-square analyses. Mean age among all recipients was 55.8 years (SE 10.8). Comorbidities including diabetes, smoking, pre transplant dialysis requirements, donor age, use of ventricular assist devices, life support ventilators, intra-aortic balloon pumps, and ischemic time were similar among groups. Kaplan-Meier survival analysis was performed at 60 months post-transplantation. At 60 months post-transplant, there were no significant differences in survival among HKT patients with donor GFR <=60mL/min/1.73 m2 and donor GFR>60mL/min/1.73 m2 groups, respectively (p=0.858). At 60 months post transplant, there was no significant survival change among those with donor GFR <=30 mL/min/1.73 m2 and >30 mL/min/1.73 m2 (p=0.400). After adjusting for variables listed above, HKT recipients with donors of GFR <=60 compared to >60 had similar survival rates (adjusted HR 1.016, 95% CI 0.776-1.332, p=0.904). A similar trend was seen for patients with donors of GFR <= 30 mL/min/1.73 m2 compared to those of GFR >30 mL/min/1.73 m2 (adjusted HR 0.650, 95% CI 0.290-1.457, p=0.295). Donor GFR in isolation had no significant impact on survival among simultaneous heart kidney transplant recipients at 60 months post transplantation after controlling for comorbidities. Donor kidney function In isolation should also not prohibit consideration for dual organ transplantation.
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