Management of CKD Stage 3 in Clinical Practice
All patients with CKD stage 3 should have their blood pressure controlled to <130/80 mmHg using ACE inhibitors or ARBs as first-line therapy, with additional agents added as needed to reach target. 1
Blood Pressure Management
Target Blood Pressure
- Maintain BP <130/80 mmHg in all CKD stage 3 patients, regardless of age or comorbidities 1, 2
- This lower target is supported by the SPRINT trial, where CKD patients (28% of study population) achieved the same cardiovascular and mortality benefits as the full cohort with intensive BP control 1
- Most CKD patients die from cardiovascular complications rather than progressing to ESRD, making cardiovascular protection the priority 1
First-Line Antihypertensive Therapy
- Start an ACE inhibitor (such as lisinopril 10 mg daily) as initial therapy 1, 2, 3
- ACE inhibitors are particularly indicated if albuminuria ≥300 mg/day or ≥300 mg/g albumin-to-creatinine ratio is present 1, 2
- If ACE inhibitor is not tolerated, substitute with an ARB (such as losartan 50 mg daily) 1, 2, 3
- For CKD stage 3 (eGFR 30-59 mL/min), standard dosing of lisinopril 10 mg daily is appropriate; dose adjustment to 5 mg daily is only needed if eGFR <30 mL/min 4
Additional Antihypertensive Agents
- Add a thiazide diuretic (hydrochlorothiazide 12.5 mg) as second-line therapy if BP target not achieved with ACE inhibitor/ARB alone 1, 2
- Consider calcium channel blockers or beta-blockers as third-line agents 2
- Never combine ACE inhibitor + ARB, as this increases adverse effects without additional benefit 1
Monitoring After ACE Inhibitor/ARB Initiation
Initial Monitoring Protocol
- Check serum creatinine, potassium, and BP within 2-4 weeks of starting or increasing ACE inhibitor/ARB dose 2, 3
- Continue therapy unless creatinine rises >30% within 4 weeks of initiation or dose increase 2, 3
- A 10-30% increase in serum creatinine is expected and acceptable due to hemodynamic effects on intraglomerular pressure 1
When to Discontinue ACE Inhibitor/ARB
- Creatinine increase >30% within 4 weeks 3
- Symptomatic hypotension that persists despite dose adjustment 3
- Uncontrolled hyperkalemia despite medical management 3
Important Caveat
- Do not discontinue ACE inhibitor/ARB even when eGFR falls below 30 mL/min per 1.73 m², unless one of the above discontinuation criteria is met 3
Management of Diabetic Kidney Disease (if applicable)
Glucose-Lowering Medications
- Metformin can be used if eGFR ≥45 mL/min/1.73 m²; use with caution and dose reduction if eGFR 30-45 mL/min/1.73 m² 2
- Add an SGLT2 inhibitor (such as empagliflozin or dapagliflozin) as it reduces CKD progression (RR 0.66) and heart failure hospitalizations (RR 0.64) 2
- Consider GLP-1 receptor agonist for cardiovascular protection and potential CKD progression benefit 2
Monitoring Schedule for CKD Stage 3
Regular Laboratory Monitoring (every 6-12 months)
- eGFR and albuminuria 2
- Electrolytes (particularly potassium) 2
- Hemoglobin and iron studies (for anemia screening) 2
- Calcium, phosphate, PTH, and vitamin D (for metabolic bone disease) 2
- Bicarbonate (for metabolic acidosis) 2
Clinical Monitoring
Special Considerations for Elderly or Frail Patients
- Do not withhold intensive BP control in elderly patients, even those ≥75 years with frailty 1
- SPRINT subgroup analysis showed frail elderly patients sustained benefit from BP <130/80 mmHg target 1
- Monitor carefully for orthostatic hypotension in elderly patients 5
- Consider incremental BP reduction with careful monitoring of physical and kidney function 1
Contrast Media Precautions (if imaging needed)
- Hydrate with normal saline before contrast administration 2
- Use low-osmolar or iso-osmolar contrast media 2
- Minimize contrast volume 2
Common Pitfalls to Avoid
- Never combine ACE inhibitor + ARB + direct renin inhibitor in any combination 1, 3
- Do not discontinue ACE inhibitor/ARB for modest creatinine increases (<30%) 3
- Do not use dihydropyridine calcium channel blockers as monotherapy in proteinuric patients; always combine with RAAS blocker 6
- Do not assume elderly or frail patients cannot tolerate intensive BP control 1