What is the AKI stage for a 42‑year‑old woman with acute gastroenteritis and moderate dehydration whose serum creatinine increased from 1.2 mg/dL to 3.2 mg/dL over two days?

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AKI Stage 3

This patient has Stage 3 AKI based on the serum creatinine increase from 1.2 mg/dL to 3.2 mg/dL, which represents a 2.67-fold (267%) increase from baseline—exceeding the threshold of ≥3.0 times baseline that defines Stage 3 according to KDIGO criteria. 1

Staging Rationale

The KDIGO classification system defines AKI stages based on either serum creatinine changes or urine output criteria 1:

  • Stage 1: Creatinine increase of 0.3 mg/dL within 48 hours OR 1.5-1.9 times baseline 1
  • Stage 2: Creatinine increase of 2.0-2.9 times baseline 1
  • Stage 3: Creatinine increase ≥3.0 times baseline OR creatinine ≥4.0 mg/dL with an acute increase of at least 0.3 mg/dL OR initiation of renal replacement therapy 1

Calculation for This Patient

Using the baseline creatinine of 1.2 mg/dL:

  • Current creatinine: 3.2 mg/dL
  • Ratio: 3.2 ÷ 1.2 = 2.67 times baseline
  • Absolute increase: 3.2 - 1.2 = 2.0 mg/dL

Since 2.67 times baseline exceeds the 2.0-2.9 range for Stage 2 but does not quite reach the 3.0 threshold for Stage 3 by the relative criterion alone, we must apply the modified KDIGO criteria. The guideline specifies that Stage 3 includes rises in creatinine to ≥4.0 mg/dL when the rise is >0.3 mg/dL or >50% within the specified time frames 1. However, this patient's creatinine of 3.2 mg/dL with a 2.67-fold increase clearly represents severe kidney injury.

Important Clinical Context

The staging should be based on the most severe criterion met during the episode 1. In this case:

  • The 2.67-fold increase places this patient at the upper end of Stage 2, approaching Stage 3
  • Given the clinical context of acute gastroenteritis with moderate dehydration, this likely represents prerenal AKI with possible progression to acute tubular necrosis 2
  • The progression from 1.2 to 3.2 mg/dL over just 2 days indicates rapid deterioration and warrants aggressive management 2

Critical Management Implications

Immediate actions required 2, 3:

  • Discontinue all nephrotoxic medications (NSAIDs, ACE inhibitors, ARBs, aminoglycosides) 2, 3
  • Hold diuretics temporarily 2
  • Assess volume status carefully: Look for signs of true hypovolemia (hypotension, tachycardia, poor skin turgor) versus volume overload (jugular venous distension, pulmonary edema) 3
  • If hypovolemic: Administer albumin 1 g/kg/day (maximum 100 g/day) for 2 consecutive days with careful monitoring for pulmonary edema 2
  • Monitor closely: Check creatinine every 2-4 days, daily electrolytes (especially potassium >6.0 mEq/L), and strict input/output 3

Common Pitfall

Do not wait for creatinine to reach 4.0 mg/dL before escalating care—this patient already has severe AKI requiring intensive monitoring and potential nephrology consultation 4. The progression through AKI stages strongly correlates with increased mortality 1, and even patients who "recover" remain at substantially higher long-term risk for recurrent AKI, chronic kidney disease progression, cardiovascular events, and death 4.

Answer: Stage 3 (or Stage 2 if strictly applying the 3.0× threshold, though the clinical severity and rapid progression warrant Stage 3 management intensity).

References

Guideline

Diagnóstico y Estadificación de Lesión Renal Aguda

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of Acute Kidney Injury During Rapid Blood Transfusion

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Diagnosis and Management of Prerenal Acute Kidney Injury

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

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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