Blood Pressure Management in Chronic Kidney Disease
Target Blood Pressure
For patients with CKD and albuminuria ≥30 mg/day (or albumin-to-creatinine ratio ≥30 mg/g), target blood pressure should be <130/80 mmHg. 1, 2 This represents the consensus across major guidelines and provides optimal cardiovascular and renal protection in albuminuric CKD.
If using standardized automated office BP measurement (5-minute rest, average of three readings), a more aggressive systolic target of <120 mmHg may be considered, though this is based on weaker evidence and applies specifically to the measurement technique used in SPRINT. 1, 2
For CKD patients without significant albuminuria (<30 mg/day), target BP <140/90 mmHg is appropriate, as lower targets have not demonstrated additional kidney or cardiovascular benefit in this population. 1, 2
Critical caveat: The <120 mmHg target is only valid when using standardized automated office BP measurement; applying this target to routine office measurements is potentially hazardous and may lead to overtreatment. 1, 2, 3
First-Line Pharmacologic Therapy
For CKD with Albuminuria
Start an ACE inhibitor as first-line therapy for all CKD patients with albuminuria ≥300 mg/day (severely increased albuminuria). 1, 2 This carries a strong (1B) recommendation from KDIGO guidelines.
For albuminuria 30-300 mg/day (moderately increased), ACE inhibitors or ARBs are suggested as first-line agents. 1, 2
If ACE inhibitor is not tolerated (typically due to dry cough), substitute an ARB. 1, 2, 3 ARBs are considered reasonable alternatives with similar renal and cardiovascular benefits.
Titrate ACE inhibitor or ARB to the maximum approved dose that is tolerated, as clinical trial benefits were achieved at these target doses. 1, 2, 3
For CKD without Albuminuria
When albuminuria is absent, initial therapy can include a dihydropyridine calcium channel blocker, thiazide-type diuretic, or ACE inhibitor/ARB—any of these classes is reasonable. 1, 2
Monitoring After Initiating RAS Inhibitors
Check serum creatinine and potassium 2-4 weeks after starting or increasing the dose of an ACE inhibitor or ARB. 1, 2, 3
Continue ACE inhibitor/ARB therapy unless serum creatinine rises by more than 30% within 4 weeks of initiation or dose increase. 1, 3 An initial creatinine increase up to 30% is expected due to reduced intraglomerular pressure and represents the intended hemodynamic effect.
Manage hyperkalemia through potassium-lowering measures (potassium-wasting diuretics, potassium binders, dietary restriction) rather than reducing or stopping the RAS inhibitor. 1, 2
Discontinue or reduce ACE inhibitor/ARB only if: uncontrolled hyperkalemia despite treatment, symptomatic hypotension, or creatinine rise >30% that persists. 1
Add-On Antihypertensive Medications
Most CKD patients require multiple agents (typically three or more) to achieve target BP. 2, 3
Second-Line Agent
Add either a thiazide-type diuretic or a dihydropyridine calcium channel blocker when BP remains uncontrolled on ACE inhibitor/ARB monotherapy. 1, 2, 3
For CKD stage 3b (eGFR 30-44 mL/min/1.73 m²), thiazide diuretics remain effective; chlorthalidone is preferred over hydrochlorothiazide at this level of kidney function. 3
For more advanced CKD (stage 4-5), loop diuretics are typically required for volume control. 1
Third-Line and Beyond
Add the other class not yet used (thiazide diuretic or calcium channel blocker). 1, 2
For resistant hypertension, add a mineralocorticoid receptor antagonist (spironolactone or eplerenone), though monitor closely for hyperkalemia. 1
Beta-blockers may be added, particularly in patients with coronary artery disease or heart failure. 1, 2
Critical Contraindications
Never combine ACE inhibitor + ARB (dual RAS blockade). 1, 3, 4 This combination increases risk of hyperkalemia, hypotension, and acute kidney injury without providing additional cardiovascular or renal benefit. The KDIGO guideline gives this a strong (1B) recommendation against combination therapy.
Lifestyle Modifications
These interventions are synergistic with pharmacologic therapy and should be implemented in all CKD patients:
Restrict dietary sodium to <2 g/day (approximately 5 g salt/day). 1, 2
Perform at least 150 minutes per week of moderate-intensity physical activity. 2
Limit protein intake to 0.8 g/kg/day for CKD stages 3-5; avoid high-protein diets >1.3 g/kg/day. 1, 2
Maintain healthy weight appropriate for age and comorbidities. 1, 2
Follow-Up and Monitoring Schedule
Schedule clinic visits every 6-8 weeks during medication titration until BP target is safely achieved. 2 Once stable, follow up every 3-6 months based on medication regimen and patient stability.
Implement home BP monitoring during titration to prevent excessive lowering (systolic <110 mmHg). 2
Repeat basic metabolic panel 2-4 weeks after adding or adjusting any agent affecting electrolytes or renal function. 1, 2, 3
Assess for symptoms of hypotension (fatigue, lightheadedness, dizziness) at each visit. 1, 2
Patient Education: Sick Day Management
Educate patients to hold or reduce antihypertensive doses during acute illnesses with vomiting, diarrhea, or reduced oral intake. 1, 2 This prevents volume depletion and acute kidney injury during intercurrent illness.
Special Populations
Elderly and Frail Patients
Less intensive BP targets may be appropriate for elderly patients with very limited life expectancy or symptomatic postural hypotension. 1 However, age alone should not preclude appropriate BP control.
Diabetic CKD
Patients with diabetes should follow the same BP targets and treatment principles as non-diabetic CKD, with ACE inhibitor or ARB as first-line for those with albuminuria ≥30 mg/day. 1, 2
Kidney Transplant Recipients
Target BP <130/80 mmHg using standardized office measurement. 1 Use dihydropyridine calcium channel blocker or ARB as first-line therapy, considering time post-transplant and calcineurin inhibitor use. 1
Common Pitfalls to Avoid
Do not apply the <120 mmHg target to routine office BP measurements—this target requires standardized automated measurement and may cause harm if misapplied. 1, 2, 3
Do not discontinue ACE inhibitor/ARB for creatinine increases <30%—this represents expected hemodynamic effect, not kidney injury. 1, 3
Do not automatically stop thiazide diuretics in CKD stage 3b—they remain effective at eGFR 30-44 mL/min/1.73 m². 3
Do not combine ACE inhibitor with ARB—this increases harm without benefit. 1, 3, 4