When to Diagnose Acute Kidney Injury
Diagnose acute kidney injury (AKI) when serum creatinine increases by ≥0.3 mg/dL within 48 hours, OR increases to ≥1.5 times baseline within 7 days, OR urine output falls below 0.5 mL/kg/hour for 6 hours. 1, 2
Diagnostic Criteria
The KDIGO criteria provide the standardized framework for AKI diagnosis and should be applied universally:
- Stage 1 AKI: Serum creatinine increase of 1.5-1.9× baseline OR ≥0.3 mg/dL increase OR urine output <0.5 mL/kg/h for 6-12 hours 3
- Stage 2 AKI: Serum creatinine increase of 2.0-2.9× baseline OR urine output <0.5 mL/kg/h for ≥12 hours 3
- Stage 3 AKI: Serum creatinine increase ≥3.0× baseline OR serum creatinine ≥4.0 mg/dL OR initiation of dialysis OR urine output <0.3 mL/kg/h for ≥24 hours 3
The diagnosis is made at the time any Stage 1 criterion is first met, not retrospectively. 1
Special Considerations for High-Risk Populations
Patients with Pre-existing Chronic Kidney Disease
Apply the same KDIGO criteria, but recognize that even small absolute creatinine rises represent significant AKI in CKD patients. 1 A rise to ≥4.0 mg/dL (≥354 mmol/l) when the increase is >0.3 mg/dL or >50% qualifies as Stage 3 AKI in CKD patients, whereas the same absolute rise in patients without CKD would be Stage 1. 1
- Obtain baseline eGFR before initiating nephrotoxic medications like metformin (contraindicated if eGFR <30 mL/min/1.73 m²) 4
- These patients require more intensive monitoring because they have higher risk of progression to acute kidney disease (AKD) and further CKD deterioration 1
Patients with Diabetes
Diabetic patients are at substantially higher risk for AKI and require lower thresholds for investigation. 5 When evaluating a diabetic patient:
- A rapid creatinine rise (e.g., from 60 to 160 μmol/L) with clear precipitants like vomiting/diarrhea confirms AKI 5
- Hold metformin immediately when AKI is suspected, as it increases lactic acidosis risk 4
- Discontinue ACE inhibitors/ARBs temporarily, as these alter intrarenal hemodynamics and can worsen pre-renal azotemia 5
Patients with Hypertension and Heart Disease
These patients have increased vulnerability to AKI, particularly from volume depletion and medication effects. 1
- Congestive heart failure is a key modifier requiring more frequent follow-up and kidney function assessment 1
- Antihypertensive medications (ACE inhibitors, ARBs, diuretics) can precipitate or exacerbate pre-renal AKI by reducing intravascular volume 5
- Cardiovascular collapse, acute myocardial infarction, and hypoxic states can cause prerenal azotemia and should trigger immediate AKI evaluation 4
Clinical Assessment for Diagnosis
Volume Status Evaluation
Assess for signs of volume depletion or overload:
- Volume depletion indicators: Orthostatic hypotension, dry mucous membranes, decreased skin turgor, recent severe vomiting/diarrhea 2
- Volume overload indicators: Dependent edema, elevated jugular venous pressure, hypertension from fluid retention 2
- Measure blood pressure both lying and standing 2
Medication Review
Immediately identify and hold nephrotoxic agents: ACE inhibitors, ARBs, diuretics, NSAIDs, and metformin 5, 4
Laboratory Evaluation
- Serum creatinine (compare to baseline from past 7 days and past 3 months) 1, 6
- Complete blood count 6
- Urinalysis 6
- Fractional excretion of sodium 6
Imaging
Perform renal ultrasonography in most patients, particularly older men, to exclude obstruction. 6, 7
Transition to Acute Kidney Disease (AKD)
If kidney function does not recover within 7 days, the patient transitions from AKI to AKD, which extends up to 3 months. 3, 8
AKD staging becomes relevant for patients with persistent dysfunction:
- Stage 0C: Creatinine <1.5× baseline but not returned to baseline 3
- Stage 0B: Creatinine returned to baseline but evidence of ongoing injury (new/worsened proteinuria, hypertension) 3
- Stages 1-3: Same creatinine criteria as AKI but persisting beyond 7 days 3
Follow-Up Requirements
All patients must be evaluated at 3 months post-AKI to determine if CKD has developed or worsened. 3
The intensity of surveillance should be proportionate to risk:
- Higher-risk patients (pre-existing CKD, diabetes, proteinuria, congestive heart failure, cirrhosis, malignancy) require earlier and more frequent monitoring 1
- More severe AKD (Stages 2-3) should prompt nephrology referral when feasible 3
- Check serum creatinine within 3 days (no later than 7 days) after cessation of acute RRT, followed by regular assessments 1
Common Pitfalls
- Failing to recognize AKI in CKD patients: The absolute creatinine value may still be "normal" but represents significant acute change 1
- Continuing nephrotoxic medications: This is a critical, often overlooked intervention that must occur immediately 5, 3
- Inadequate follow-up: Only 50-69% of patients have creatinine measured within 3 months of AKI, missing opportunities to prevent CKD progression 1
- Ignoring urine output criteria: Patients meeting oliguria criteria alone still have AKI and worse outcomes 9