How should chronic kidney disease be evaluated and managed, including staging, blood pressure targets, medication choices (ACE inhibitor/ARB, SGLT2 inhibitor, etc.), glycemic control, dietary measures, monitoring for complications, and referral criteria?

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Last updated: February 9, 2026View editorial policy

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Chronic Kidney Disease: Evaluation and Management

First-Line Foundational Therapy

Initiate SGLT2 inhibitors immediately as mandatory first-line therapy for all CKD patients with eGFR ≥20 mL/min/1.73 m², regardless of diabetes status, using dapagliflozin 10 mg daily or canagliflozin 100 mg daily. 1 Continue SGLT2 inhibitors even as eGFR declines below 20 mL/min/1.73 m² until dialysis initiation or transplantation. 1

CKD Staging and Surveillance

Initial Assessment

  • Measure both eGFR and urine albumin-to-creatinine ratio (UACR) to stage CKD and assess progression risk. 2
  • Stage CKD using the KDIGO classification system based on GFR categories (G1-G5) and albuminuria categories (A1-A3). 2

Monitoring Frequency

  • Stage G1-G2 (eGFR ≥60): Monitor annually 2
  • Stage G3a-G3b (eGFR 30-59): Monitor every 6-12 months 2
  • Stage G4 (eGFR 15-29): Monitor every 3-5 months 2
  • Stage G5 (eGFR <15): Monitor every 1-3 months 2
  • Higher albuminuria categories require more frequent monitoring regardless of GFR. 2

Defining Progression

  • CKD progression requires both a change in GFR category AND ≥25% decrease in eGFR to avoid misinterpreting small fluctuations. 2, 3

Blood Pressure Management

Target Blood Pressure

  • With albuminuria ≥30 mg/24 hours: Target BP ≤130/80 mmHg 2, 1
  • With albuminuria <30 mg/24 hours: Target BP ≤140/90 mmHg 2, 3
  • Optimal target is systolic BP <120 mmHg for most patients when tolerated. 2

Medication Selection

  • ACE inhibitors or ARBs: First-line for patients with albuminuria ≥30 mg/24 hours, titrated to maximum tolerated dose 2, 1, 4
  • Mandatory for albuminuria ≥300 mg/24 hours (macroalbuminuria) in both diabetic and non-diabetic patients 2, 4
  • Do NOT use ACE inhibitors or ARBs for primary prevention in patients with normal BP and normal albumin excretion (<30 mg/g). 4
  • Add dihydropyridine calcium channel blockers and/or diuretics if additional agents needed to reach BP target. 2

Monitoring on RAS Inhibitors

  • Monitor serum potassium periodically in patients with eGFR <60 mL/min/1.73 m² receiving ACE inhibitors, ARBs, or mineralocorticoid receptor antagonists. 2

Advanced Kidney Protection

Nonsteroidal Mineralocorticoid Receptor Antagonists

  • Add finerenone for patients with diabetic kidney disease already on RAS inhibition for additive kidney and cardiovascular protection. 2, 1, 3

Steroidal MRAs

  • Use steroidal mineralocorticoid receptor antagonists for resistant hypertension management. 2

Glycemic Control in Diabetic CKD

Target HbA1c

  • Maintain HbA1c at approximately 7% to reduce risk and slow CKD progression. 2, 4

Medication Selection

  • SGLT2 inhibitors: First-line for both glycemic control and kidney protection in diabetic CKD 1, 4
  • GLP-1 receptor agonists: Consider for additional cardiovascular risk reduction and albuminuria reduction 2, 4
  • Metformin: Acceptable if eGFR ≥30 mL/min/1.73 m², but AVOID when eGFR <30 mL/min/1.73 m² 1
  • AVOID sulfonylureas due to increased hypoglycemia risk 1

Therapeutic Target

  • Aim for ≥30% reduction in urinary albumin as a therapeutic target to slow CKD progression. 4

Cardiovascular Risk Reduction

Statin Therapy

  • Mandatory for all CKD patients ≥50 years: Use moderate-to-high intensity statin (atorvastatin 40-80 mg daily or rosuvastatin 20-40 mg daily) 2, 1, 3
  • Continue statins until dialysis or transplantation. 2
  • Consider ezetimibe or PCSK9 inhibitors based on ASCVD risk and lipid levels. 2

Antiplatelet Therapy

  • Aspirin 81 mg daily for lifelong secondary prevention in CKD patients with established cardiovascular disease 1

Dietary Management

Protein Intake

  • 0.8 g/kg body weight per day (the recommended daily allowance) for non-dialysis-dependent CKD 2, 1, 4
  • Do NOT reduce below 0.8 g/kg/day as it does not alter outcomes 2
  • AVOID high-protein intake (>20% of daily calories or >1.3 g/kg/day) as it accelerates kidney function loss 2
  • Do NOT restrict protein in patients who are cachexic, sarcopenic, or undernourished. 2

Sodium Restriction

  • <2 g per day (<2,300 mg/day) to control blood pressure and reduce cardiovascular risk 2, 1, 4

Weight Management

  • Target BMI 20-25 kg/m² 2, 1

Dietary Pattern

  • Encourage plant-based diets and Mediterranean-style diet to reduce cardiovascular risk. 2, 3

Lifestyle Modifications

  • Physical activity: 30 minutes of exercise 5 times per week compatible with cardiovascular health and frailty level 2
  • Smoking cessation: Mandatory for all CKD patients 2

Monitoring for CKD Complications

When eGFR Falls Below 60 mL/min/1.73 m²

Monitor for the following complications every 3-6 months: 2, 1

Anemia

  • Check hemoglobin regularly 2
  • Treat with iron supplementation before or with erythropoiesis-stimulating agents 1
  • Assess iron, iron saturation, and ferritin if indicated 2

Metabolic Bone Disease (CKD-MBD)

  • Monitor serum calcium, phosphate, parathyroid hormone, and vitamin 25(OH)D 2

Metabolic Acidosis

  • Check serum electrolytes and bicarbonate 2
  • Treat when bicarbonate <18 mmol/L to prevent anorexia, protein wasting, and bone disease 2

Electrolyte Abnormalities

  • Monitor serum potassium, especially in patients on diuretics, ACE inhibitors, ARBs, or MRAs 2
  • Individualize dietary potassium based on serum levels; avoid highly processed foods but do NOT restrict fruits and vegetables 2

Volume Overload

  • Assess at every clinical contact through history, physical examination, and weight 2

Hyperuricemia

  • Do NOT treat asymptomatic hyperuricemia; only treat if symptomatic (gout or tophi) 2

Medications to AVOID in CKD

  • NSAIDs: Increased risk of acute kidney injury 2, 1
  • Metformin when eGFR <30 mL/min/1.73 m²: Risk of lactic acidosis 1
  • Sulfonylureas: Increased hypoglycemia risk 1
  • Iodinated contrast: Minimize exposure, especially when eGFR <60 mL/min/1.73 m² 2

Medication Dosing Adjustments

  • Verify medication dosing for all patients with eGFR <60 mL/min/1.73 m², including antibiotics and oral hypoglycemic agents. 2, 5

Nephrology Referral Criteria

Immediate Referral Required When:

  • eGFR <30 mL/min/1.73 m² 1, 4, 5
  • Persistent electrolyte abnormalities despite treatment 1
  • Uncontrolled hypertension despite multiple agents 1, 3
  • Uncertainty about kidney disease etiology 3
  • Significant albuminuria increases despite good BP control 3
  • Rapid decline in eGFR 5
  • Albuminuria ≥300 mg per 24 hours 5

Regular Reassessment Schedule

Every 3-6 months, assess: 2, 1

  • eGFR and serum creatinine
  • Electrolytes (sodium, potassium, bicarbonate)
  • Urine albumin-to-creatinine ratio
  • Hemoglobin
  • Blood pressure
  • Lipid panel

Common Pitfalls to Avoid

  • Do NOT withhold ACE inhibitors/ARBs for small increases in serum creatinine or potassium unless clinically significant 2
  • Do NOT combine ACE inhibitors with ARBs; insufficient evidence for benefit and increased risk of adverse events 2
  • Do NOT delay SGLT2 inhibitor initiation; it is foundational therapy regardless of diabetes status 1
  • Do NOT restrict dietary protein below 0.8 g/kg/day 2
  • Do NOT interpret small GFR fluctuations as progression without meeting both criteria (category change AND ≥25% decrease) 2, 3

References

Guideline

Chronic Kidney Disease Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Nephrosclerosis Management Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Management of Proteinuria in Diabetes

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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