What are the clinical criteria for staging Acute Kidney Injury (AKI) according to the KDIGO (Kidney Disease: Improving Global Outcomes) classification system?

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Last updated: December 15, 2025View editorial policy

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KDIGO Clinical Criteria for AKI Staging

The KDIGO classification uses three clinical criteria to stage AKI: (1) serum creatinine changes, (2) urine output measurements, and (3) need for renal replacement therapy. 1

The Three Core Clinical Criteria

1. Serum Creatinine (SCr) Changes

The KDIGO system defines AKI stages based on the magnitude of creatinine elevation from baseline 1:

  • Stage 1: SCr increase of 1.5-1.9 times baseline OR absolute increase ≥0.3 mg/dL (≥26.5 μmol/L) 1
  • Stage 2: SCr increase of 2.0-2.9 times baseline 1
  • Stage 3: SCr increase ≥3.0 times baseline OR SCr ≥4.0 mg/dL (≥353.6 μmol/L) with an acute increase of ≥0.3 mg/dL OR initiation of renal replacement therapy 1

The creatinine criteria use differential timing: a 48-hour window for the 0.3 mg/dL absolute increase and a 7-day window for relative increases from baseline 1, 2.

2. Urine Output (UO) Measurements

Urine output criteria provide parallel staging independent of creatinine 1:

  • Stage 1: UO <0.5 mL/kg/h for 6-12 hours 1
  • Stage 2: UO <0.5 mL/kg/h for ≥12 hours 1
  • Stage 3: UO <0.3 mL/kg/h for ≥24 hours OR anuria for ≥12 hours 1

Important caveat: Urine output criteria are generally applicable only in intensive care settings where accurate monitoring is feasible, and should not be relied upon in patients receiving diuretics or those with cirrhosis and ascites 2, 3.

3. Renal Replacement Therapy (RRT)

Initiation of RRT automatically classifies the patient as Stage 3 AKI, regardless of creatinine or urine output values 1. In patients <18 years, a decrease in eGFR to <35 mL/min/1.73 m² also defines Stage 3 1.

Staging Algorithm

Patients are staged according to the highest severity criterion met, whether by creatinine, urine output, or RRT need 1. The staging is performed retrospectively when the episode is complete, though early detection should occur in real-time based on initial marker changes 2, 3.

Clinical Significance and Validation

The KDIGO criteria have been independently validated in multiple studies and demonstrate strong correlation between stage progression and mortality 1, 2. Even Stage 1 AKI (particularly the 0.3 mg/dL creatinine increase) is independently associated with approximately four-fold increased hospital mortality 1. Research shows that when patients meet both creatinine and urine output criteria simultaneously, outcomes are significantly worse than when meeting only one criterion 4.

Common Pitfalls to Avoid

Do not wait for creatinine to reach 1.5 mg/dL before diagnosing AKI, as this outdated threshold often indicates GFR has already fallen to approximately 30 mL/min 3. Monitor temporal changes at 48-hour intervals to detect the 0.3 mg/dL threshold early 3.

In patients with cirrhosis and ascites, focus exclusively on serum creatinine changes rather than urine output, as these patients are frequently oliguric with avid sodium retention despite maintaining relatively normal GFR 3. A creatinine threshold of ≥1.5 mg/dL predicts AKI progression and worse prognosis in this population 3.


Note: You did not provide specific patient data (baseline creatinine, current creatinine, urine output measurements, or clinical context), so I cannot determine what stage this patient is at. To stage the patient, apply the criteria above to their specific laboratory values and clinical parameters.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Acute Kidney Injury Diagnosis and Staging

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Diagnóstico y Estadificación de Lesión Renal Aguda

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Classifying AKI by Urine Output versus Serum Creatinine Level.

Journal of the American Society of Nephrology : JASN, 2015

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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