How do you classify Chronic Kidney Disease (CKD) stages?

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Classification of Chronic Kidney Disease Stages

CKD is classified using a comprehensive system that combines GFR categories (G1-G5) with albuminuria categories (A1-A3), creating a matrix that stratifies risk for disease progression, cardiovascular events, and mortality. 1

GFR Categories (G Stages)

The five GFR stages are defined by estimated glomerular filtration rate (eGFR) in mL/min/1.73 m²: 1

  • G1 (Normal or high): eGFR ≥90 mL/min/1.73 m² - requires evidence of kidney damage (albuminuria, imaging abnormalities, or biopsy findings) to diagnose CKD 1
  • G2 (Mildly decreased): eGFR 60-89 mL/min/1.73 m² - also requires evidence of kidney damage to diagnose CKD 1
  • G3a (Mildly to moderately decreased): eGFR 45-59 mL/min/1.73 m² 1
  • G3b (Moderately to severely decreased): eGFR 30-44 mL/min/1.73 m² 1
  • G4 (Severely decreased): eGFR 15-29 mL/min/1.73 m² 1
  • G5 (Kidney failure): eGFR <15 mL/min/1.73 m² 1

Albuminuria Categories (A Stages)

Albuminuria is measured using urine albumin-to-creatinine ratio (UACR) from a spot urine sample: 1

  • A1 (Normal to mildly increased): UACR <30 mg/g creatinine (or <3 mg/mmol) 1
  • A2 (Moderately increased): UACR 30-299 mg/g creatinine (or 3-29 mg/mmol) 1
  • A3 (Severely increased): UACR ≥300 mg/g creatinine (or ≥30 mg/mmol) 1

Complete CKD Classification

The complete classification requires specifying cause (C), GFR category (G), and albuminuria category (A). For example: "CKD G3a, A2 due to diabetes" or "CKD G4, A3 due to hypertension." 1, 2

Risk Stratification Using the CGA Matrix

The combination of GFR and albuminuria categories creates a color-coded risk matrix for CKD progression and adverse outcomes: 1, 2

  • Green (Low risk): G1A1, G2A1 - annual monitoring 1, 2
  • Yellow (Moderately high risk): G1A2, G2A2, G3aA1 - monitoring at least once yearly 1
  • Orange (High risk): G1A3, G2A3, G3aA2, G3bA1 - monitoring twice yearly 1
  • Red (Very high risk): G3aA3, G3bA2, G3bA3, G4A1, G4A2, G4A3 - monitoring three times yearly 1
  • Dark red (Highest risk): G5A1, G5A2, G5A3 - monitoring four times yearly 1

Critical Diagnostic Requirements

For stages G1 and G2, CKD cannot be diagnosed by eGFR alone - there must be evidence of kidney damage (albuminuria, imaging abnormalities, or biopsy findings) present for >3 months. 1, 3

For stages G3-G5, an eGFR <60 mL/min/1.73 m² persisting for >3 months is sufficient to diagnose CKD, even without albuminuria. 1, 3

Confirmation of Albuminuria

Two of three UACR specimens collected within a 3-6 month period should be abnormal before confirming high albuminuria, due to biological variability exceeding 20% between measurements. 1, 2

Nephrology Referral Thresholds

Refer to nephrology when: 1

  • eGFR <30 mL/min/1.73 m² (stages G4-G5) regardless of albuminuria 1
  • Any stage with A3 albuminuria (≥300 mg/g) 1, 2
  • Rapidly declining eGFR or rapidly increasing albuminuria 1
  • Active urinary sediment, nephrotic syndrome, or absence of retinopathy in type 1 diabetes 1

Common Pitfalls

The eGFR must be calculated using validated equations - the CKD-EPI equation is preferred over the older MDRD equation as it provides better accuracy, especially at higher GFR levels. 1, 4, 5

Avoid diagnosing CKD based on a single measurement - both eGFR <60 mL/min/1.73 m² and albuminuria must persist for >3 months to meet diagnostic criteria. 1, 3

Do not use descriptive terms like "mild," "moderate," or "severe" CKD - always specify the complete CGA classification (cause, GFR category, albuminuria category) for accurate risk stratification and treatment planning. 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Diabetic Nephropathy Classification and Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Kidney Disease: Chronic Kidney Disease.

FP essentials, 2021

Research

Glomerular filtration rate measurement and prediction equations.

Clinical chemistry and laboratory medicine, 2009

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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