Management of Stable CKD Stage 3 with Current Therapy
Continue the current regimen of losartan 50 mg, amlodipine 10 mg, and sodium bicarbonate 650 mg TID, while adding comprehensive monitoring for proteinuria and optimizing blood pressure control to slow disease progression. 1, 2
Confirm CKD Stage and Assess Disease Activity
Calculate eGFR using the MDRD or CKD-EPI equation rather than relying on creatinine alone, as a creatinine of 172.3 µmol/L (≈1.9 mg/dL) corresponds to approximately eGFR 35-45 mL/min/1.73 m², placing this patient in CKD Stage 3b (eGFR 30-44 mL/min/1.73 m²). 1, 2
Measure urinary albumin-to-creatinine ratio (UACR) from a spot urine sample immediately, as albuminuria is the most critical prognostic marker and treatment target in CKD. 1, 2
Obtain baseline proteinuria quantification with either protein-to-creatinine ratio or 24-hour urine collection if UACR is elevated, as proteinuria >500 mg/day indicates structural kidney injury requiring intensified therapy. 2, 3
Optimize Current Medications
Losartan Dosing
Increase losartan to 100 mg daily if proteinuria is present (UACR ≥30 mg/g or protein >0.5 g/day), as higher doses provide superior antiproteinuric effects independent of blood pressure reduction. 4, 5, 6
Losartan 50 mg reduces proteinuria by approximately 24-32% in CKD patients, while 100 mg provides maximal antiproteinuric benefit (up to 50% reduction after 20 weeks). 4, 6
Do not discontinue losartan if creatinine rises ≤30% from baseline, as this is an expected hemodynamic effect and does not indicate progressive kidney damage. 1
Blood Pressure Targets
Target blood pressure <130/80 mmHg (ideally <130/85 mmHg) to slow CKD progression and reduce cardiovascular risk. 1, 2, 3
The current combination of losartan 50 mg and amlodipine 10 mg is appropriate for blood pressure control; adjust doses based on actual BP measurements. 4, 7
Consider adding hydrochlorothiazide 12.5 mg daily to losartan if proteinuria is present and blood pressure remains >130/80 mmHg, as losartan/HCTZ provides greater proteinuria reduction than losartan alone through BP-independent mechanisms. 7
Sodium Bicarbonate Continuation
- Continue sodium bicarbonate 650 mg TID to maintain serum bicarbonate >22 mEq/L, as metabolic acidosis accelerates CKD progression. 2
Essential Monitoring Parameters
Immediate Laboratory Assessment
Check serum potassium and creatinine 2-4 weeks after any dose adjustment of losartan or addition of diuretics. 1, 3
Measure UACR every 6 months if albuminuria is present (≥30 mg/g), as a 30% reduction in proteinuria is the therapeutic target to slow progression. 1, 3
Monitor eGFR every 6-12 months depending on stability; increase frequency to every 3-6 months if eGFR is declining >5 mL/min/1.73 m² per year. 2, 3
Critical Safety Thresholds
Hold losartan immediately if serum potassium rises >5.6 mmol/L or if creatinine increases >30% from baseline without volume depletion. 1, 2
Do not stop losartan for minor creatinine increases (<30%) in the absence of hyperkalemia or volume depletion, as premature discontinuation eliminates renoprotective benefits. 1, 2
Dietary and Lifestyle Modifications
Restrict dietary sodium to <2 g/day (<100 mmol/day), as low sodium intake potentiates the antiproteinuric effects of losartan and improves blood pressure control. 3, 8
Moderate dietary potassium intake to avoid excessive levels (>200 mmol/day), as high potassium intake diminishes the antiproteinuric response to losartan by 50% during habitual sodium intake. 8
Limit dietary protein to 0.8 g/kg/day (the recommended daily allowance) for nondialysis-dependent CKD Stage 3, as protein restriction slows progression. 1
Strictly avoid NSAIDs (ibuprofen, naproxen, etc.), as they reduce renal blood flow and can precipitate acute kidney injury in CKD patients. 3
Nephrology Referral Criteria
Refer to nephrology promptly if any of the following are present: 1, 3
- UACR ≥300 mg/g (nephrotic-range proteinuria)
- Rapid eGFR decline >5 mL/min/1.73 m² per year
- eGFR approaching <30 mL/min/1.73 m² (Stage 4 CKD)
- Resistant hypertension despite 3+ antihypertensive agents
- Uncertainty about CKD etiology
- Active urinary sediment (hematuria with dysmorphic RBCs or casts)
Additional Cardiovascular Risk Management
Screen for diabetes mellitus if not already done, as diabetic kidney disease requires additional therapies including SGLT2 inhibitors. 1
Assess cardiovascular risk factors comprehensively, as CKD Stage 3 is a coronary heart disease risk equivalent with 10-30 times higher cardiovascular mortality. 1
Consider statin therapy for lipid management according to ATP III guidelines, as dyslipidemias accelerate both CKD progression and cardiovascular events. 1
Common Pitfalls to Avoid
Do not rely on serum creatinine alone without calculating eGFR, as creatinine underestimates kidney dysfunction, especially in elderly patients or those with reduced muscle mass. 1, 2, 3
Do not dismiss stable creatinine as "normal" without assessing albuminuria, as kidney damage can progress despite stable creatinine levels. 2, 3
Do not stop ACE inhibitors/ARBs prematurely for small creatinine rises (<30%), as this eliminates long-term renoprotection and worsens outcomes. 1, 2
Do not overlook medication dose adjustments for renally cleared drugs once eGFR falls below 60 mL/min/1.73 m², though most medications do not require adjustment until eGFR <45 mL/min/1.73 m². 1, 3