Although acute renal failure (ARF) immediately following orthotopic liver transplantation (OLT) occurs commonly, the incidence of chronic kidney disease (CKD) and end-stage renal disease increases with time. Data from the Scientific Registry of Transplant Recipients reveal that the cumulative incide
Transplantation: Impact of pretransplant renal insufficiency
β Scribed by Ranjeeta Bahirwani; Mical S. Campbell; Tim Siropaides; James Markmann; Kim Olthoff; Abraham Shaked; Roy D. Bloom; K. Rajender Reddy
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 107 KB
- Volume
- 14
- Category
- Article
- ISSN
- 1527-6465
- DOI
- 10.1002/lt.21367
No coin nor oath required. For personal study only.
β¦ Synopsis
Pre-liver transplant renal dysfunction is associated with decreased survival following transplantation and is also a prognostic indicator of posttransplant chronic kidney disease. Selection of patients for combined liver/kidney transplantation versus orthotopic liver transplantation alone (OLTa) is often difficult given the lack of a reliable method to predict which patients will have ongoing severe renal dysfunction in the absence of concomitant kidney transplantation. We hypothesized that most patients with pretransplant renal dysfunction (serum creatinine Υ 1.5 mg/dL for at least 2 weeks prior to and at time of transplant) will not experience a rapid decline in estimated glomerular filtration rates (eGF) post-OLTa to the point of necessitating consideration for kidney transplantation, even in the setting of calcineurin inhibitor-based immunosuppression. We performed a single-center retrospective study of 60 OLTa patients with pretransplant renal dysfunction transplanted between 2000 and 2005. Kaplan-Meier analysis was performed of the time interval to develop eGFR Ο½ 20 mL/minute post-OLTa. At OLTa, the mean patient age was 59 years, and median serum creatinine was 1.8 mg/dL; 42% patients were hepatitis C-positive, 32% were diabetic, 38% had kidney dysfunction ΟΎ 12 weeks, and 5% were receiving hemodialysis. After 36 months median follow-up post-OLTa, only 8 patients (13%) with significant renal dysfunction pre-OLTa achieved eGFR Ο½ 20 mL/minute. Patients with pretransplant kidney dysfunction ΟΎ 12 weeks were at increased risk for eGFR Ο½ 20 mL/minute (hazard ratio Ο 5.3, P Ο 0.04), a risk that escalated after adjustment for age and serum creatinine at transplant (hazard ratio Ο 8.9, P Ο 0.01). Significant predictors of eGFR Ο½ 20 mL/minute post-OLTa in this patient cohort were the presence of diabetes and the serum creatinine level at transplant. In conclusion, few patients with preexisting renal dysfunction, especially if Ο½12 weeks duration, experience a significant drop in eGFR post-OLTa.
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