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. 2025 Feb 1;31(2):140-150.
doi: 10.1097/LVT.0000000000000463. Epub 2024 Aug 26.

Hospital readmission for acute kidney injury is independently associated with de novo end-stage renal disease after liver transplantation

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Hospital readmission for acute kidney injury is independently associated with de novo end-stage renal disease after liver transplantation

Therese Bittermann et al. Liver Transpl. .

Abstract

End-stage renal disease (ESRD) after liver transplantation (LT) is associated with high morbidity and mortality. The consequences of hospitalizations for post-LT acute kidney injury (AKI) are poorly understood. Using linked Medicare claims and transplant registry data, we analyzed adult liver alone recipients not receiving pretransplant dialysis between January 1, 2007, and December 31, 2016. Covariate-adjusted Cox proportional hazards models stratified by center evaluated factors associated with AKI readmission during the first post-LT year, and whether AKI readmission was associated with de novo early (<1 y) or late (≥1 y) ESRD post-LT. The cohort included 10,559 patients and was 64.5% male, 72.5% White, 8.1% Black, and 14.0% Hispanic with median age 62 years. Overall, 2875 (27.2%) patients had ≥1 AKI hospitalization during the first year. Estimated glomerular filtration rate at LT was associated with AKI readmission (adjusted HR: 1.16 per 10 mL/min/1.73m 2 decrease; p <0.001). The adjusted HR for early ESRD in patients with ≥1 AKI readmission <90 days post-LT was 1.90 ( p <0.001). The adjusted HRs for late ESRD with 1 and ≥2 prior AKI readmissions were 1.57 and 2.80, respectively ( p <0.001). AKI readmissions in the first post-LT year impact over one-quarter of recipients. These increase the risk of subsequent ESRD, but may represent an opportunity to intervene and mitigate further renal dysfunction.

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Conflict of interest statement

Disclosure

The authors of this manuscript have no conflicts of interest to disclose as described by the American Journal of Transplantation. This study was funded by a K08 Career Development Award from the National Institute of Diabetes and Digestive and Kidney Diseases (PI: Bittermann; DK117013). Dr. Bittermann also receives research support from the National Institute on Aging (R01-AG079911) and from the National Institute on Alcohol Abuse and Alcoholism (R01-AA030963). Dr. Schaubel receives funding from the National Institute of Diabetes, Digestive, and Kidney Diseases (R01-DK070869). Dr. Lewis receives funding from the National Institute of Diabetes, Digestive, and Kidney Diseases (P30-DK050306).

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