Management of Acute Kidney Injury with Severe Electrolyte Disturbances in a 5-Year-Old
This child requires immediate hospitalization with urgent nephrology consultation and aggressive supportive care for acute kidney injury with severe hyponatremia, hypovolemic shock, and likely nephrotic syndrome. 1, 2
Immediate eGFR Calculation and Interpretation
Using the Schwartz formula for pediatric eGFR: eGFR = (k × height in cm) / serum creatinine (mg/dL), where k = 0.413 for children aged 1-12 years 3
- Converting creatinine: 401.45 μmol/L = 4.54 mg/dL
- Assuming average height for 5-year-old female (~110 cm): eGFR ≈ 10 mL/min/1.73m² 3
- This represents severe kidney dysfunction (KDIGO stage G5) 1
- The BUN/Cr ratio of 74 mmol/L ÷ 4.54 mg/dL = 16.3, which is within normal range, suggesting intrinsic renal disease rather than prerenal azotemia 4, 5
Critical Initial Assessment and Stabilization
The combination of hypotension (93/33 mmHg), tachycardia (168/min), tachypnea (45/min), and severe hyponatremia (121.8 mmol/L) indicates hypovolemic shock requiring immediate intervention 1, 2
Volume Status Assessment
- Clinical indicators of hypovolemia are present: hypotension, tachycardia, and likely oliguria given the severe AKI 1, 2
- The 3+ proteinuria with specific gravity 1.010 suggests nephrotic-range proteinuria with loss of concentrating ability 1, 6
- Administer 20% albumin infusion (0.5-1 g/kg over 2-4 hours) followed by furosemide (1-2 mg/kg IV) at the end of infusion to enhance diuresis and restore intravascular volume 1, 2
Severe Hyponatremia Management
- The sodium of 121.8 mmol/L with neurological risk (tachypnea may indicate compensatory response) requires cautious correction 1
- Correct sodium at maximum 10-12 mmol/L per 24 hours to avoid osmotic demyelination syndrome 1
- Use 3% hypertonic saline only if symptomatic (seizures, altered mental status), otherwise correct with albumin infusion and fluid restriction 1
Diagnostic Workup
The urinalysis showing turbid, dark urine with 3+ protein strongly suggests nephrotic syndrome, though the presentation includes nephritic features 1, 2, 6
Essential Laboratory Studies
- Spot urine protein-to-creatinine ratio to quantify proteinuria (likely >2 g/g given 3+ dipstick) 1, 2
- Serum albumin, total protein, lipid panel to confirm nephrotic syndrome 1, 2
- Complete blood count with differential, inflammatory markers (ESR, CRP) 1
- Complement levels (C3, C4), ANA, anti-dsDNA, ANCA panel to evaluate for secondary causes 6
- Hepatitis B, C, HIV screening given the proteinuria 1
- Urine microscopy for RBC casts (suggests nephritic component) 6
Imaging
- Renal ultrasound with Doppler to assess kidney size, echogenicity, rule out obstruction, and evaluate for renal vein thrombosis (complication of nephrotic syndrome) 1
Ongoing Management Strategy
Fluid and Electrolyte Management
- Strict fluid restriction to insensible losses plus urine output (approximately 400-600 mL/m²/day) 1, 2
- Avoid intravenous saline; concentrate oral fluids 1
- Monitor serum electrolytes every 6-12 hours initially, then daily once stable 1
- Potassium is currently normal (3.67 mmol/L) but requires close monitoring as it may rise with worsening AKI 1
Diuretic Therapy
- After volume resuscitation with albumin, initiate furosemide 1-2 mg/kg IV every 6-12 hours 1
- If inadequate response, consider sequential nephron blockade with addition of metolazone 0.1-0.2 mg/kg/dose once daily 1
- Monitor for hypokalemia with aggressive diuresis, though current potassium is acceptable 1
Blood Pressure Management
- Current BP (93/33 mmHg) is hypotensive for age; once euvolemia achieved, reassess for hypertension typical of nephritic syndrome 6
- If hypertension develops after volume restoration, initiate ACE inhibitor (enalapril 0.08 mg/kg/day) for both BP control and antiproteinuric effect 1
Renal Replacement Therapy Considerations
- With eGFR ~10 mL/min/1.73m² and clinical instability, prepare for potential dialysis if: 1
- Severe hyperkalemia develops (>6.5 mmol/L)
- Refractory fluid overload with pulmonary edema
- Symptomatic uremia (pericarditis, encephalopathy)
- Inability to correct severe hyponatremia safely
- Severe metabolic acidosis (pH <7.1)
Nephrology Consultation and Definitive Diagnosis
Urgent pediatric nephrology consultation is mandatory given the severity of presentation and need for potential kidney biopsy 1, 2
Biopsy Considerations
- Kidney biopsy should be strongly considered once hemodynamically stable and coagulation parameters acceptable to determine underlying etiology 1, 2
- The combination of severe proteinuria, AKI, and young age raises concern for congenital nephrotic syndrome, focal segmental glomerulosclerosis, or minimal change disease with acute tubular necrosis 1, 2
- Biopsy is particularly important given the severity and to guide immunosuppressive therapy decisions 2
Genetic Testing
- Send genetic panel for congenital nephrotic syndrome genes (NPHS1, NPHS2, WT1, LAMB2) given age and severity 1
Infection Prophylaxis and Complications
Children with nephrotic syndrome and severe hypoalbuminemia are at high risk for bacterial infections, particularly spontaneous bacterial peritonitis and sepsis 1
- Consider prophylactic antibiotics if albumin <2 g/dL and peritoneal signs develop 1
- Avoid central venous lines if possible due to thrombosis risk; if required, provide prophylactic anticoagulation 1
- Monitor for signs of infection at every clinical contact 1
Monitoring Parameters
Given KDIGO stage G5 CKD, laboratory monitoring should occur every 1-3 months once stabilized 1
- Serum electrolytes, BUN, creatinine 1
- Acid-base status (venous blood gas or total CO₂) 1
- Calcium, phosphate, PTH, 25-OH vitamin D 1
- Hemoglobin and iron studies 1
- Spot urine protein-to-creatinine ratio 1, 2
Critical Pitfalls to Avoid
- Do not rely on serum creatinine alone in children; always calculate eGFR using age-appropriate formulas 3, 4
- Do not administer albumin based solely on low levels; only give for clinical hypovolemia 1, 2
- Do not correct severe hyponatremia too rapidly (>10-12 mmol/L per 24 hours) 1
- Do not assume nephrotic syndrome alone; the severe AKI and mixed picture require biopsy for definitive diagnosis 1, 2, 6
- Do not delay nephrology referral; this child requires subspecialty management immediately 1, 2