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KDIGO AKI staging (pediatric)

  • Category: Renal and metabolic
  • Version: v1.2.1
  • Reviewed: Reviewed 6 Sep 2026
  • Validation: Validation pending
Current serum creatinine Unit
Baseline serum creatinine Unit
How long that rate has been sustainedOptional
AnuriaOptional
Renal replacement therapy startedOptional

KDIGO stage is the maximum of two independently evaluated axes, never a sum.

SERUM-CREATININE AXIS
1.5–1.9× baseline, or a rise of ≥ 0.3 mg/dL, is Stage 1; 2.0–2.9× baseline is Stage 2; ≥ 3.0× baseline, renal replacement therapy initiated, an estimated GFR < 35 mL/min/1.73 m² (patients under 18 years only), or a creatinine ≥ 4.0 mg/dL is Stage 3. The ≥ 4.0 mg/dL route is not standalone: KDIGO requires the AKI definition (a rise of ≥ 0.3 mg/dL, or ≥ 1.5× baseline) to be met first, so a chronically elevated creatinine that never rose is not Stage 3 AKI. With no baseline entered, ≥ 4.0 mg/dL reports Stage 3 flagged as not settled.
URINE-OUTPUT AXIS
the four Table 2 rows are (rate, duration) pairs, not rate bands, and each is tested independently with the highest satisfied row governing. < 0.5 mL/kg/h for 6 to under 12 hours is Stage 1; < 0.5 mL/kg/h for 12 hours or more is Stage 2; < 0.3 mL/kg/h for 24 hours or more is Stage 3; anuria for 12 hours or more is Stage 3. Branching on the rate first is the classic defect: 0.25 mL/kg/h for 8 hours is Stage 1, not Stage 3. A rate < 0.5 mL/kg/h held for less than 6 hours meets no row. Anuria is a clinical flag, because KDIGO defines no millilitre figure and none is invented here, and it necessarily satisfies the < 0.5 mL/kg/h rows too, so anuria for 6 to under 12 hours is Stage 1.
UNRESOLVABLE AXIS
when the duration is missing, or “12 hours or more” is chosen with a rate < 0.3 mL/kg/h leaving the 24-hour row open, the stage shown is the highest certain stage with a “≥” flag, which is KDIGO’s own Table 10 notation. No duration is ever guessed, and the flag is set only where an open row could change the answer.

Other renal and metabolic scores

Important. For use by qualified health professionals as an informational and educational aid. It supports clinical judgment and does not replace it. Verify every result independently before making a clinical decision. This is not a medical device.