» Articles » PMID: 9679823

Chronic Renal Failure Following Liver Transplantation: a Retrospective Analysis

Overview
Journal Transplantation
Specialty General Surgery
Date 1998 Jul 29
PMID 9679823
Citations 39
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Liver transplant recipients are at risk of chronic renal disease, principally as a result of nephrotoxicity of the commonly used immunosuppressive agents cyclosporine and tacrolimus. We have investigated the incidence of chronic renal failure and its risk factors in our transplant population, which was treated predominantly with cyclosporine.

Methods: A single-center retrospective study was done of 883 consecutive adult patients receiving a first liver transplant between 1982 and 1996. Potential risk factors for the development of chronic renal failure were recorded, including serial measurements of cyclosporine therapy and renal function.

Results: Severe chronic renal failure (serum creatinine level >250 microM/L for at least 6 months) developed in 25 patients, representing 4% of patients surviving 1 year or more. Twelve of these patients developed end-stage renal failure and mortality was 44%. The predominant cause of renal failure was cyclosporine nephrotoxicity. Serum creatinine as early as 3 months after surgery was strongly associated with the eventual development of severe chronic renal failure (P=0.001), and this group could be further subdivided into two groups with differing risk factors. The first group had early (<1 year) renal dysfunction, with older age (P=0.03), cytomegalovirus infection (P=0.03), need for perioperative renal replacement therapy (P=0.06), and regrafting (P=0.06) as risk factors for eventual renal failure; the second group had late-onset (>1 year) renal dysfunction, with cyclosporine levels at 1 month after surgery (P=0.007) and daily and cumulative cyclosporine dosage at 5 years (P=0.01 for both) as risk factors.

Conclusions: With improved survival of liver transplant recipients, chronic renal failure has become an important cause of morbidity and is associated with a high mortality. Many patients at risk of severe chronic renal failure may be identified at an early stage. Treatment regimens that avoid or prevent cyclosporine-induced nephrotoxicity are urgently required for this population.

Citing Articles

IPNA clinical practice recommendations for the diagnosis and management of children with IgA nephropathy and IgA vasculitis nephritis.

Vivarelli M, Samuel S, Coppo R, Barratt J, Bonilla-Felix M, Haffner D Pediatr Nephrol. 2024; 40(2):533-569.

PMID: 39331079 PMC: 11666671. DOI: 10.1007/s00467-024-06502-6.


An innocent bystander or a predisposing culprit? Kidney injury following pediatric liver transplantation.

Glass A, Goldberg O, Mozer-Glassberg Y, Waisbourd-Zinman O, Haskin O, Levi S Pediatr Nephrol. 2024; 40(3):849-857.

PMID: 39320550 DOI: 10.1007/s00467-024-06537-9.


Identification of genetic loci associated with renal dysfunction after lung transplantation using an ethnic-specific single-nucleotide polymorphism array.

Tomioka Y, Sugimoto S, Yamamoto H, Tomida S, Shiotani T, Tanaka S Sci Rep. 2023; 13(1):8912.

PMID: 37264212 PMC: 10235026. DOI: 10.1038/s41598-023-36143-y.


Tacrolimus 4-hour monitoring in liver transplant patients is non-inferior to trough monitoring: The randomized controlled FK04 trial.

Ruijter B, Tushuizen M, Moes D, Klerk B, van Hoek B Clin Transplant. 2022; 36(12):e14829.

PMID: 36193575 PMC: 10078353. DOI: 10.1111/ctr.14829.


Hepatocellular carcinoma in patients with renal dysfunction: Pathophysiology, prognosis, and treatment challenges.

Yeh H, Chiang C, Yen T World J Gastroenterol. 2021; 27(26):4104-4142.

PMID: 34326614 PMC: 8311541. DOI: 10.3748/wjg.v27.i26.4104.