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Published on: March 8, 2024
Hepatorenal syndrome: a proposal for kidney after liver transplantation (KALT)
Richard Ruiz1, Yousri M Barri, Linda W Jennings
1Baylor Regional Transplant Institute, Dallas, TX 75246, USA. richarru@baylorhealth.edu
Insights
Hepatorenal syndrome (HRS) complicates end-stage liver disease, impacting liver transplant survival. Kidney after liver transplantation (KALT) may improve outcomes for select HRS patients needing dialysis.
Area of Science:
- Nephrology
- Hepatology
- Transplantation
Background:
- Hepatorenal syndrome (HRS) is a serious complication of end-stage liver disease.
- Traditionally, HRS was considered reversible post-liver transplantation (LT), but it can necessitate long-term dialysis.
- The role of kidney transplantation in HRS patients is under debate.
Purpose of the Study:
- To evaluate the incidence and outcomes of HRS in patients undergoing LT.
- To assess the impact of HRS on post-transplant survival and kidney function.
- To explore the potential benefit of kidney after liver transplantation (KALT) for HRS patients.
Main Methods:
- Retrospective analysis of 130 patients undergoing LT over 10 years.
- Defined HRS using International Ascites Club guidelines (pretransplant serum creatinine >2.0 mg/dL).
- Compared survival and post-transplant kidney failure rates between HRS and non-HRS groups.
Main Results:
- The incidence of HRS among LT patients was 9%.
- HRS patients had significantly worse 1, 3, and 5-year survival rates compared to non-HRS patients (P=0.0001).
- Type 2 HRS patients showed a higher incidence of irreversible kidney failure post-LT (6% vs. 0.34%, P<0.0001).
Conclusions:
- Combined liver and kidney transplantation (CLKT) is not recommended for HRS patients.
- Kidney after liver transplantation (KALT) may be a viable option for select HRS patients.
- Addressing the need for dialysis >60 days post-transplant can improve outcomes in HRS patients.
Abstract:
Hepatorenal syndrome (HRS) is a well-recognized complication of end-stage liver disease. Once thought to be a reversible condition with liver transplantation (LT) alone, HRS may directly contribute to the requirement for long-term dialysis posttransplant. As a result, discussion has now focused on whether or when a kidney allograft should be considered for these patients. Using the International Ascites Club guidelines with a pretransplant serum creatinine (SCr) >2.0 mg/dL to define HRS, 130 patients undergoing LT over a 10-yr period were identified, for an overall incidence of 9%. Patient survival rates at 1, 3, and 5 yr were 74%, and 68%, and 62%, respectively. Survival was significantly worse when compared to non-HRS patients undergoing LT over the same study period (P = 0.0001). For patients presenting with type 2 HRS, 7 patients (6%) developed irreversible kidney failure posttransplant compared to 0.34% in the non-HRS population (P < 0.0001). Five of these patients died within 1 yr with a median survival time of 139 days. Combined liver and kidney transplantation (CLKT) for patients with HRS is not recommended. However, an improvement in outcome can be accomplished by addressing those patients who require dialysis greater than 60 days posttransplant. We propose a role for kidney after liver transplantation (KALT) in select HRS patients.
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