Medication Options for CKD with Hypertension
For patients with CKD and hypertension, initiate an ACE inhibitor or ARB as first-line therapy if albuminuria is present (≥30 mg/g), titrate to the maximum tolerated dose, target blood pressure <130/80 mmHg, and add SGLT2 inhibitors for patients with type 2 diabetes to reduce cardiovascular and renal risks. 1
Initial Assessment Required
- Measure urine albumin-to-creatinine ratio to stratify treatment—this single test determines whether RAS blockade is indicated and guides your entire medication strategy 2
- Check eGFR to determine medication dosing adjustments and contraindications 1
- Assess for diabetes status, as this fundamentally changes your medication algorithm 1
First-Line Antihypertensive Therapy
For Patients WITH Albuminuria (≥30 mg/g)
- Start ACE inhibitor or ARB immediately and titrate to the highest approved tolerated dose—this is the strongest recommendation (Grade 1B) for slowing CKD progression 1
- Target blood pressure <130/80 mmHg for all CKD patients with hypertension; consider <120-129 mmHg systolic for those with severely elevated albuminuria (≥300 mg/g) 1, 3
- Monitor serum creatinine and potassium within 2-4 weeks after initiation or dose changes 1, 3
- Continue RAS inhibitor even if creatinine increases up to 30% from baseline, unless symptomatic hypotension or uncontrolled hyperkalemia develops 1
For Patients WITHOUT Albuminuria (<30 mg/g)
- Do not use ACE inhibitor or ARB specifically for renal protection—other antihypertensive agents are equally effective for cardiovascular risk reduction in this population 1, 2
- Choose from calcium channel blockers, thiazide-like diuretics, or beta-blockers to achieve blood pressure target <130/80 mmHg 3, 4
Second-Line Antihypertensive Agents
- Add long-acting dihydropyridine calcium channel blocker (e.g., amlodipine) as second-line therapy 3, 4
- Add thiazide-like diuretic (chlorthalidone preferred over hydrochlorothiazide) as third-line, effective even in stage 4 CKD (eGFR 15-30 mL/min/1.73 m²) 4
- For treatment-resistant hypertension, add spironolactone 12.5-25 mg daily, but monitor potassium closely—risk of hyperkalemia increases significantly with eGFR <45 mL/min/1.73 m² 1, 4
Glucose-Lowering Medications (If Diabetic)
SGLT2 Inhibitors (Highest Priority)
- Initiate SGLT2 inhibitor for all patients with type 2 diabetes and CKD stage 3 or higher (eGFR <60 mL/min/1.73 m²), regardless of glycemic control—these agents slow CKD progression and reduce heart failure risk independent of glucose management 1
- Continue SGLT2 inhibitors even as eGFR declines, as renal and cardiovascular benefits persist 1
Metformin
- Do not initiate metformin if eGFR <45 mL/min/1.73 m² 1
- Contraindicated if eGFR <30 mL/min/1.73 m² 1
- Reassess risk-benefit when eGFR falls to <45 mL/min/1.73 m² in patients already taking metformin 1
- Temporarily discontinue before iodinated contrast procedures if eGFR 30-60 mL/min/1.73 m² 1
GLP-1 Receptor Agonists
- Consider GLP-1 RA for cardiovascular risk reduction in patients with type 2 diabetes and CKD, particularly if SGLT2 inhibitor is insufficient 1
Insulin
- Adjust insulin doses as eGFR declines—reduced renal clearance increases hypoglycemia risk 1
Lipid Management
- Initiate statin therapy for all CKD patients to reduce cardiovascular risk, which is the leading cause of death in this population 1, 5, 6
Antiplatelet Therapy
- Use aspirin for secondary prevention in patients with established cardiovascular disease 1
- Consider aspirin for primary prevention in high-risk individuals, but balance against increased bleeding risk, especially with low eGFR 1
Critical Medication Adjustments and Avoidance
- Avoid NSAIDs entirely—these are nephrotoxic and accelerate CKD progression 5, 7
- Adjust antibiotic dosing based on eGFR for renally cleared agents 5, 7
- Never combine ACE inhibitor + ARB—this increases risks of hyperkalemia and acute kidney injury without additional benefit 1, 2
- Avoid direct renin inhibitors (e.g., aliskiren) in combination with RAS blockade 2
Monitoring Protocol
- Check basic metabolic panel (creatinine, potassium) within 2-4 weeks after starting or titrating RAS inhibitors 1, 3
- Monitor hemoglobin A1c at least every 3 months if diabetic, targeting ≤7% in most patients (may be less intensive if life expectancy <10 years or severe comorbidities) 1
- Use home blood pressure monitoring to detect masked hypertension and avoid overtreatment 3, 4
- Recheck urine albumin-to-creatinine ratio annually to assess treatment response 5, 7
Common Pitfalls to Avoid
- Do not discontinue RAS inhibitor for creatinine increases <30%—this is an expected hemodynamic effect and does not indicate harm 1
- Do not target blood pressure <110/70 mmHg—excessive lowering increases risks of falls, acute kidney injury, and hospitalization 3
- Do not withhold SGLT2 inhibitors due to modest eGFR decline—the initial dip in eGFR is hemodynamic and protective long-term 1
- Do not use combination RAS blockade despite persistent albuminuria—harm outweighs benefit 1, 2
Lifestyle Modifications (Essential Adjuncts)
- Restrict sodium intake to <2 g/day (5 g salt)—this enhances effectiveness of RAS blockade 1, 2
- Limit protein intake to 0.8 g/kg/day for patients with eGFR <60 mL/min/1.73 m²; avoid high protein intake >1.3 g/kg/day 2
- Smoking cessation is mandatory—tobacco accelerates CKD progression 1
- Regular exercise improves blood pressure control and cardiovascular outcomes 1