What are the reference ranges for Chronic Kidney Disease (CKD) stage 2 and stage 3a based on the Glomerular Filtration Rate (GFR)?

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CKD Stage 2 and 3a Reference Ranges

CKD Stage 2 is defined as GFR 60-89 mL/min/1.73 m² with evidence of kidney damage, and Stage 3a is defined as GFR 45-59 mL/min/1.73 m². 1, 2, 3

GFR-Based Stage Definitions

Stage 2 CKD:

  • GFR range: 60-89 mL/min/1.73 m² 1, 3
  • Requires evidence of kidney damage (albuminuria ≥30 mg/g, proteinuria, or structural abnormalities) for diagnosis, as GFR alone is insufficient at this level 2, 3
  • Represents slightly decreased GFR with kidney damage 1

Stage 3a CKD:

  • GFR range: 45-59 mL/min/1.73 m² 1, 2, 3
  • Can be diagnosed based on GFR alone without requiring additional evidence of kidney damage 3
  • Represents mild to moderate decrease in kidney function 1

Critical Classification Requirements

Complete CKD staging requires both GFR category AND albuminuria measurement to fully assess risk and guide treatment decisions. 2, 3 The three albuminuria categories are:

  • A1: <30 mg/g creatinine (normal to mildly increased)
  • A2: 30-299 mg/g creatinine (moderately increased)
  • A3: ≥300 mg/g creatinine (severely increased) 2, 3

The subdivision of Stage 3 into 3a and 3b is endorsed by KDIGO and KDOQI because mortality and adverse outcome risks vary significantly between these subgroups, making this distinction clinically important. 2, 3

Diagnostic Considerations

All abnormalities must persist for at least 3 months to establish chronic kidney disease and distinguish it from acute kidney injury. 2, 3 A single GFR measurement does not establish CKD without confirmation over time. 2

GFR should be estimated using prediction equations (such as CKD-EPI) that account for serum creatinine, age, sex, and race, rather than relying on serum creatinine alone. 3, 4 The CKD-EPI equation demonstrates less bias than the MDRD equation, especially at GFR ≥60 mL/min/1.73 m². 3

Clinical Implications by Stage

Stage 2 CKD management:

  • Focus on early detection, CKD risk reduction, and treating comorbid conditions 3
  • Annual monitoring of both eGFR and UACR is the minimum recommended frequency 2

Stage 3a CKD management:

  • Medication dose adjustments are required at this GFR level, particularly for renally cleared drugs 2
  • Begin evaluation for complications as GFR falls below 60 mL/min/1.73 m² 3
  • ACE inhibitors or ARBs are preferred if the patient has diabetes with hypertension and any degree of albuminuria 1, 2
  • At Stage 3a with normal albuminuria (A1), the patient is classified as G3a/A1, representing moderate risk requiring annual monitoring 2
  • If albuminuria is elevated to A2 or A3 levels, risk increases substantially, requiring more frequent monitoring (twice to three times yearly) and consideration for nephrology referral 2

Common Pitfalls to Avoid

Avoid incomplete staging by using GFR alone. Always classify using the complete CGA system (Cause, GFR category, Albuminuria category) for proper risk stratification. 3 The combination of GFR and albuminuria provides better risk stratification for disease progression and outcomes than GFR alone. 3

Do not diagnose Stage 1 or 2 CKD based solely on GFR values. These stages require additional evidence of kidney damage such as albuminuria, proteinuria, or structural abnormalities on imaging. 2, 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

CKD Stage Classification for GFR 47

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Chronic Kidney Disease Staging and Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Glomerular filtration rate measurement and prediction equations.

Clinical chemistry and laboratory medicine, 2009

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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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