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Published on: August 9, 2013
The evolving concept of acute kidney injury in patients with cirrhosis
1Department of Medicine, Division of Gastroenterology, Toronto General Hospital, University Health Network, University of Toronto, 200 Elizabeth Street, Toronto, ON M5G2C4, Canada.
Insights
New criteria define acute kidney injury (AKI) in cirrhosis patients, renaming hepatorenal syndrome (HRS) to HRS-AKI. Even early-stage AKI indicates a worse prognosis, highlighting the need for better diagnostics.
Area of Science:
- Nephrology
- Hepatology
- Internal Medicine
Background:
- Renal dysfunction is common in advanced cirrhosis.
- Traditional Type 1 hepatorenal syndrome (HRS) criteria are too stringent, leading to underdiagnosis.
- Acute kidney injury (AKI) is proposed to better characterize renal dysfunction in cirrhosis.
Purpose of the Study:
- To introduce and define the new criteria for AKI in cirrhosis.
- To rename Type 1 HRS to HRS-AKI.
- To highlight the prognostic implications of AKI stages in cirrhosis.
Main Methods:
- Defined AKI as a serum creatinine increase of 0.3 mg/dl in <48h or 50% from baseline within 3 months.
- Established AKI stages based on serum creatinine level increases (Stage 1: 0.3 mg/dl or 50% increase; Stage 2: two-fold increase; Stage 3: three-fold increase).
Main Results:
- The new AKI criteria, including Stage 1, are associated with a worse prognosis in cirrhosis patients.
- Progression of AKI stages correlates with substantially worse outcomes.
Conclusions:
- The proposed AKI definition and staging system offer a more applicable framework for renal dysfunction in cirrhosis.
- Early identification of AKI (Stage 1) is crucial for prognosis.
- Future research aims to incorporate biomarkers to enhance AKI diagnosis and determine etiology.
Abstract:
Renal dysfunction is prevalent in patients with advanced cirrhosis and decompensation. The presence of type 1 hepatorenal syndrome (HRS) has traditionally been defined by a set of stringent criteria based on serum creatinine levels. These diagnostic criteria have been found to be too stringent to be widely applicable to patients with cirrhosis, leading to underdiagnosis of renal failure in this population. Acute kidney injury (AKI) has now been proposed to characterize renal dysfunction in patients with cirrhosis and is defined as an increase in serum creatinine by 0.3 mg/dl in <48 h or an increase in serum creatinine by 50% from a stable baseline reading within 3 months. Type 1 HRS is renamed HRS-AKI. Stage 1 AKI is defined by 0.3 mg/dl serum creatinine or a 50% increase, stages 2 and 3 AKI are defined by a two-fold and three-fold increase in serum creatinine levels, respectively. Data collected so far suggests that even stage 1 AKI is associated with worse prognosis in patients with cirrhosis. The progression of AKI usually indicates substantially worse outcomes. A panel of biomarkers, including inflammatory markers, are envisaged to complement and enhance our current diagnostic criteria in the future and provide aetiology of the AKI.
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