Management of Stage 3 Chronic Kidney Disease in a 74-Year-Old Male
This patient has Stage 3 chronic kidney disease (CKD) based on a GFR of 47 mL/min/1.73 m², requiring immediate evaluation for underlying causes, cardiovascular risk stratification, and initiation of nephroprotective strategies to slow progression. 1
Classification and Significance
GFR of 47 mL/min/1.73 m² places this patient in CKD Stage 3 (GFR 30-59 mL/min/1.73 m²), indicating moderate renal impairment that requires active management even though serum creatinine of 1.53 mg/dL may appear only mildly elevated. 1
The alkaline phosphatase of 39 U/L is within normal range and does not suggest significant bone disease at this stage, though monitoring for mineral-bone disorder becomes important as CKD progresses. 1
Serum creatinine alone is an inadequate marker of renal function, particularly in elderly patients where muscle mass is reduced; the estimated GFR provides a more accurate assessment of kidney function. 2, 3, 4
Essential Diagnostic Workup
Before implementing treatment, the following must be evaluated:
Urinalysis with albumin-to-creatinine ratio to assess for proteinuria, which predicts cardiovascular events and progression of kidney disease. Microalbuminuria (>30 mg/g creatinine) significantly increases risk even in non-diabetic patients. 1
Renal ultrasound to evaluate kidney size, rule out obstruction, and assess for structural abnormalities. 1
Assess for reversible causes: volume depletion, nephrotoxic medications (NSAIDs, aminoglycosides, contrast agents), hypercalcemia, hyperuricemia, and urinary obstruction. 1
Screen for underlying systemic diseases: diabetes (HbA1c, fasting glucose), hypertension (blood pressure monitoring), and autoimmune conditions if clinically indicated. 1
Blood Pressure Management
Target blood pressure <140/90 mmHg in the absence of proteinuria, or <130/80 mmHg if proteinuria is present (>1000 mg/day). 1
First-line agents: ACE inhibitors or angiotensin receptor blockers (ARBs) are preferred if proteinuria is present, as they provide nephroprotection by blocking the renin-angiotensin-aldosterone system. 1
Important caveat with ACE inhibitors/ARBs: Monitor serum creatinine and potassium within 1-2 weeks of initiation. A creatinine increase up to 20% is acceptable and does not indicate progressive renal deterioration. If creatinine increases >30% or exceeds 3 mg/dL, consider dose reduction or discontinuation. 1, 5
Hyperkalemia risk: At GFR 47 mL/min, this patient is at increased risk for hyperkalemia with ACE inhibitors/ARBs. Avoid potassium supplements, potassium-sparing diuretics, and potassium-containing salt substitutes. Monitor serum potassium regularly. 5
Alternative agents: Calcium channel blockers are reasonable alternatives, particularly if ACE inhibitors/ARBs are contraindicated or not tolerated. 1
Dietary and Lifestyle Modifications
Sodium restriction to <2 grams per day improves blood pressure control, reduces proteinuria, and enhances efficacy of RAAS inhibitors. 1
Protein intake: Avoid excessive protein (>1.3 g/kg/day). If GFR declines to <30 mL/min, consider reducing to 0.8 g/kg/day, though this must be balanced against malnutrition risk in elderly patients. 1
Bicarbonate supplementation if serum bicarbonate <22 mmol/L, as acidosis accelerates CKD progression. Balance this against sodium load and potential fluid retention. 1
Medication Management
Critical nephrotoxin avoidance:
Discontinue or avoid NSAIDs, which cause hemodynamic renal injury, particularly in patients on ACE inhibitors/ARBs. 1, 5
Avoid aminoglycosides and amphotericin B when possible; use alternative antibiotics. 1
Radiocontrast precautions: If contrast imaging is necessary, ensure adequate hydration, consider temporarily holding ACE inhibitors/ARBs, and use lowest possible contrast volume. 1
Dose adjustment required for renally-cleared medications based on GFR of 47 mL/min. 1
Monitoring and Follow-Up
Assess GFR and albuminuria at least annually, more frequently if proteinuria is present or GFR is declining. 1
Monitor for CKD complications: anemia (hemoglobin), mineral-bone disorder (calcium, phosphorus, PTH, vitamin D), and metabolic acidosis (serum bicarbonate). These typically manifest at GFR <45 mL/min. 1
Cardiovascular risk assessment: Impaired renal function is a strong independent predictor of cardiovascular mortality. Aggressive management of cardiovascular risk factors (lipids, diabetes, smoking cessation) is essential. 1
Nephrology Referral Criteria
Consider nephrology referral if:
- GFR declines to <30 mL/min (Stage 4 CKD). 1
- Proteinuria >1000 mg/day despite treatment. 1
- Rapid GFR decline (>5 mL/min/year). 1
- Unclear etiology of kidney disease requiring renal biopsy. 1
- Difficulty managing complications (anemia, mineral-bone disorder, refractory hypertension). 1
Common Pitfalls to Avoid
Do not rely on serum creatinine alone to assess renal function in elderly patients; always calculate eGFR. 2, 3, 6
Do not withhold ACE inhibitors/ARBs due to fear of creatinine elevation; modest increases (up to 20%) are expected and acceptable. 1
Do not overlook volume depletion as a reversible cause of worsening renal function, particularly with diuretic use or dehydration. 5
Do not assume normal alkaline phosphatase excludes bone disease; PTH and vitamin D levels are more sensitive markers of mineral-bone disorder in CKD. 1