Treatment for CKD Stage 3
Start an SGLT2 inhibitor (e.g., dapagliflozin 10 mg daily) immediately if eGFR ≥20 mL/min/1.73 m² and continue it even as kidney function declines, as this provides cardiovascular and renal protection independent of glucose-lowering effects. 1
Initial Risk Stratification
Measure urine albumin-to-creatinine ratio immediately, as albuminuria category fundamentally determines treatment intensity and prognosis 2:
- Albuminuria <30 mg/g: High risk—monitor closely 2
- Albuminuria 30-299 mg/g: Very high risk—intensify therapy 2
- Albuminuria ≥300 mg/g: Very high risk—maximal intervention required 2
Check baseline potassium, repeat creatinine to establish trajectory, and assess for diabetes and hypertension 2.
Blood Pressure Management
Target blood pressure ≤130/80 mmHg using ACE inhibitor or ARB as first-line therapy 2:
- For albuminuria ≥300 mg/g: ACE inhibitor or ARB is mandatory regardless of baseline blood pressure 3, 2
- For albuminuria 30-299 mg/g: ACE inhibitor or ARB if hypertensive 2
- Accept creatinine increases up to 30% as expected hemodynamic effect—do not discontinue unless volume depletion is present 2
- Target ≥30% reduction in albuminuria through ACE-I/ARB therapy, as this degree of reduction directly correlates with slower CKD progression 2
SGLT2 Inhibitor Therapy (Cornerstone of Treatment)
Initiate SGLT2 inhibitor when eGFR ≥20 mL/min/1.73 m² 1:
- Strong recommendation (Grade A) for patients with albuminuria ≥200 mg/g 1
- Moderate recommendation (Grade B) for patients with albuminuria <200 mg/g 1
- Continue therapy even when eGFR falls below 30 mL/min/1.73 m²—do not discontinue based on eGFR decline alone 1
- Discontinue only when dialysis begins 1
SGLT2 Inhibitor Mechanisms (Independent of Glucose Control)
These drugs provide renoprotection through 3, 1:
- Lowering intraglomerular pressure and systemic blood pressure 1
- Reducing albuminuria through hemodynamic actions 1
- Decreasing oxidative stress by over 50% 3, 1
- Inhibiting NLRP3 inflammasome activity 3, 1
- Blunting intrarenal angiotensinogen rise 1
Expected eGFR Changes
Anticipate an initial, reversible eGFR dip of 3-5 mL/min/1.73 m² within 1-3 months—this is hemodynamic, not pathological, and eGFR typically returns toward baseline by six months 1. Do not discontinue therapy for this expected change 1.
Diabetes-Specific Management (If Applicable)
- Metformin: Continue if eGFR ≥45 mL/min/1.73 m²; reduce maximum dose to 1,000 mg/day in stage 3b (eGFR 30-44); discontinue if eGFR <30 3
- Target HbA1c ~7% to slow progression 3
- Monitor HbA1c twice yearly, up to four times yearly if not at target 3
- DPP-4 inhibitors require dose adjustment: Sitagliptin 100 mg daily if eGFR >50, reduce to 50 mg if eGFR 30-50; saxagliptin 5 mg daily if eGFR ≥45, reduce to 2.5 mg if eGFR ≤45; linagliptin requires no adjustment 3
Medication Safety
Avoid NSAIDs completely in stage 3b (eGFR 30-44); use cautiously and briefly (≤5-7 days) in stage 3a (eGFR 45-59) only if absolutely necessary 4:
- NSAIDs significantly increase acute kidney injury risk and accelerate CKD progression 4, 5
- Never combine NSAIDs with ACE inhibitor/ARB plus diuretic ("triple whammy") as this dramatically raises AKI risk 4, 2
Safer Analgesic Alternatives
- First-line: Acetaminophen up to 3 g/day (no dose adjustment needed) 4
- Second-line: Topical NSAIDs (diclofenac or ibuprofen gel) with minimal systemic absorption 4
- Third-line: Tramadol 50 mg every 12 hours (max 200 mg/day) for severe pain 4
Dietary and Lifestyle Modifications
- Restrict dietary protein to ≤0.8 g/kg/day to lessen glomerular hyperfiltration 2, 5
- Limit sodium to <2 g/day to improve blood pressure control and reduce proteinuria 2
- Target BMI 20-25 kg/m² through weight management 2
- Exercise 30 minutes, 5 times weekly 2
- Smoking cessation if applicable 2
Monitoring for CKD Complications
Laboratory evaluations should occur 3:
- Every 6-12 months for stage 3a
- Every 3-5 months for stage 3b
Specific Monitoring Parameters
- Hemoglobin: At least once yearly in stage 3a, twice yearly in stage 3b to detect anemia 2
- Serum calcium, phosphate, PTH, alkaline phosphatase: At least once in stage 3b (eGFR <45) to establish baseline mineral-bone status 2
- Serum potassium and creatinine: Regularly, with closer surveillance when on ACE-I/ARB plus diuretics 3, 2
- Electrolyte abnormalities and metabolic acidosis: Evaluate with serum electrolytes 3
Cardiovascular Risk Reduction
Stage 3 CKD patients have markedly elevated cardiovascular mortality risk 2:
- Prescribe statin therapy for cardiovascular risk reduction 5
- Optimize blood pressure control as outlined above 2
Vaccination (Preventive Care)
- Annual inactivated influenza vaccine (Grade 1B recommendation) 2
- Polyvalent pneumococcal vaccine for stage 3b (eGFR <30) and high-risk stage 3a patients (nephrotic syndrome, diabetes, immunosuppression); revaccinate within 5 years 2
- Hepatitis B vaccine for high-risk patients with eGFR <30, especially those likely to progress to dialysis 2
Nephrology Referral Criteria
- eGFR falls below 30 mL/min/1.73 m² (transition to stage 4)
- Rapid GFR decline (>5 mL/min/1.73 m² per year or >25% drop in eGFR category)
- Albuminuria ≥300 mg per 24 hours
- Underlying kidney disease etiology is uncertain or management becomes complex
Common Pitfalls to Avoid
- Do not withhold ACE inhibitors/ARBs due to fear of creatinine elevation—small increases (≤30%) are expected and acceptable 2
- Do not delay SGLT2 inhibitor initiation—these provide proven kidney and cardiovascular protection 2
- Do not overlook albuminuria assessment—this is the single most important prognostic factor and treatment target 2
- Do not use combination ACE inhibitor + ARB therapy—insufficient evidence for benefit and increased harm risk 2
- Ensure adequate hydration before contrast procedures to prevent contrast-induced nephropathy 2
- Temporarily hold SGLT2 inhibitors during prolonged fasting, surgery, or critical illness due to ketosis risk 1
- Consider reducing concurrent loop or thiazide diuretics before starting SGLT2 inhibitor to minimize volume depletion and AKI risk 1