Acute Kidney Injury Management Protocol
Immediately discontinue all nephrotoxic medications (NSAIDs, ACE inhibitors, ARBs, aminoglycosides), hold diuretics and beta-blockers, search rigorously for infection, and initiate volume resuscitation with isotonic crystalloids targeting euvolemia. 1, 2
Initial Assessment and Diagnosis
- Define AKI presence using any of: serum creatinine increase ≥0.3 mg/dL within 48 hours, creatinine ≥1.5× baseline within 7 days, or urine output <0.5 mL/kg/h for 6 hours 1
- Stage severity according to creatinine and urine output changes, as higher stages predict worse outcomes 1
- Monitor biochemistry with serum urea, creatinine, and electrolytes at least every 48 hours (more frequently in high-risk patients) 1
- Perform diagnostic paracentesis in cirrhotic patients to exclude spontaneous bacterial peritonitis 1
Immediate Interventions
Medication Management
- Stop all nephrotoxic drugs unless absolutely essential, including NSAIDs, ACE inhibitors, ARBs, and aminoglycosides 1, 2
- Hold diuretics and nonselective beta-blockers when AKI is diagnosed 1
- Avoid dopamine, diuretics, N-acetylcysteine, or recombinant human insulin-like growth factor 1 for AKI treatment—these lack efficacy 1
Fluid and Hemodynamic Management
- Use isotonic crystalloids (not colloids or starch-containing fluids) for initial volume expansion 1, 2
- Target euvolemia through daily clinical examination and fluid balance monitoring 1
- Maintain mean arterial pressure >65 mmHg using vasopressors in conjunction with fluids if vasomotor shock is present 2
- Monitor fluid status daily by clinical examination and strict intake/output records 1
Nutritional Support
- Provide 20-30 kcal/kg/day total energy intake, preferably via enteral route 2
- Administer 0.8-1.0 g/kg/day protein in noncatabolic AKI patients without dialysis 2
- Increase to 1.0-1.5 g/kg/day protein in patients requiring renal replacement therapy 2
Renal Replacement Therapy (RRT) Indications
Emergent Indications (Initiate Immediately)
- Severe hyperkalemia with ECG changes (peaked T waves, widened QRS, bradycardia) 3
- Severe metabolic acidosis with impaired respiratory compensation 3
- Pulmonary edema unresponsive to diuretics 3
- Uremic complications (encephalopathy, pericarditis, bleeding) 3
- Severe symptomatic dysnatremia resistant to medical management 3
RRT Modality Selection
- Use continuous RRT (CRRT) in hemodynamically unstable patients requiring vasopressors, those with acute brain injury, or when intracranial pressure is a concern 4, 1, 3
- Use intermittent hemodialysis in hemodynamically stable patients for faster correction of severe hyperkalemia 3
- Both modalities have equivalent outcomes in randomized trials, so choose based on hemodynamic stability and local expertise 4
CRRT Parameters (When Selected)
- Modality: CVVHDF preferred 3
- Effluent dose: 20-25 mL/kg/hour 3
- Replacement fluid: Bicarbonate-based 3
- Anticoagulation: Regional citrate if no contraindications 3
Intermittent Hemodialysis Parameters (When Selected)
- Blood flow rate: 300-400 mL/min 3
- Dialysate flow rate: 500-800 mL/min 3
- Target Kt/V: 1.2-1.4 per session for 3 sessions weekly 3
- Dialysate: Bicarbonate-based 3
- Potassium bath: 0-1 mEq/L if severe hyperkalemia; 2 mEq/L for maintenance 3
- Calcium bath: 2.5 mEq/L 3
- Ultrafiltration rate: Limit to <13 mL/kg/hour to avoid intradialytic hypotension and further renal injury 3
Vascular Access
- Use uncuffed non-tunneled dialysis catheter of appropriate length and gauge 4, 3
- Preferred insertion sites (in order): right internal jugular vein, femoral vein, left internal jugular vein, subclavian vein (last choice due to stenosis risk) 3
- Always use ultrasound guidance for insertion 3
Special Considerations
Hepatorenal Syndrome
- When creatinine remains >2× baseline despite initial measures, treat with albumin plus vasoactive agents for HRS-AKI 1
Contrast-Induced AKI Prevention
- Do not withhold IV contrast in life-threatening conditions where imaging has important therapeutic implications 4
- Modern contrast agents carry far fewer risks than previously thought, and significant injury is unusual with normal or mildly reduced baseline kidney function 4
- Volume expansion with sodium bicarbonate and oral N-acetylcysteine lack efficacy based on PRESERVE and POSEIDON trials 4
Transition from CRRT to Intermittent Hemodialysis
- Consider transition when vasopressor support has stopped, intracranial hypertension has resolved, and positive fluid balance can be controlled by intermittent hemodialysis 4
Monitoring During RRT
- Vital signs: Hourly with assessment for hypotension 3
- Electrolytes and acid-base status: Every 2-4 hours initially 3
- Pre- and post-dialysis weights: Each session 3
- Urine output: Monitor if any residual function present 3
Assessment of Renal Recovery
- If dialysis continues beyond 14 days, assess renal recovery weekly with pre-dialysis creatinine and residual kidney function measurements 3
- Proteinuria is associated with worse long-term outcomes and serves as a valuable risk-stratification tool in the post-AKI period 4
- RRT modality choice does not impact recovery, so base selection on shared decision-making, local expertise, and patient characteristics 4
Follow-Up After AKI
- Monitor for development or progression of chronic kidney disease after AKI 1
- Prioritize follow-up evaluation for patients with risk factors for CKD progression, particularly those who suffered severe AKI requiring temporary RRT 1
- Assess patient-centered outcomes including quality of life and functional recovery 4
Critical Pitfalls to Avoid
- Never continue nephrotoxic medications during AKI recovery phase 2
- Do not use dopamine, diuretics, or N-acetylcysteine as AKI treatments—they are ineffective 1
- Avoid excessive ultrafiltration rates (>13 mL/kg/hour) that can cause intradialytic hypotension and worsen kidney injury 3
- Do not delay RRT when emergent indications are present—life-threatening complications require immediate intervention 3