Can a healthcare provider be acting in a patient's best interest by diagnosing Chronic Kidney Disease (CKD) with a slightly elevated estimated Glomerular Filtration Rate (eGFR) of 64 mL/min/1.73 m², despite not meeting the technical criteria for stage 3a CKD?

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Diagnosing CKD with an eGFR of 64 mL/min/1.73 m²: The Provider Was Not Acting in the Patient's Best Interest

No, the provider was not acting in the patient's best interest by diagnosing CKD with an eGFR of 64 mL/min/1.73 m², as this value does not meet the technical criteria for CKD and such a diagnosis could lead to inappropriate labeling, unnecessary interventions, and potential harm. 1, 2

Why This Diagnosis Is Incorrect

The Diagnostic Criteria Are Clear and Specific

An eGFR of 64 mL/min/1.73 m² falls within Stage 2 CKD range (60-89 mL/min/1.73 m²), not Stage 3a (45-59 mL/min/1.73 m²). 1, 2 The cutoff of 60 mL/min/1.73 m² is not arbitrary in this context—it represents the threshold below which eGFR alone is sufficient to diagnose CKD. 1

For an eGFR between 60-89 mL/min/1.73 m², CKD diagnosis requires documented evidence of kidney damage (such as albuminuria, hematuria, pathological abnormalities on biopsy, or history of kidney transplantation) present for at least 3 months. 1, 2 Without these markers, a diagnosis of CKD cannot be made regardless of how "close" the eGFR is to 60. 2

The Temporal Component Is Essential

CKD diagnosis requires abnormalities present on at least two occasions over three months or longer. 2, 3 A single measurement of 64 mL/min/1.73 m² does not confirm CKD at any stage. 2 This temporal requirement exists precisely to avoid misdiagnosis based on transient changes in kidney function.

The Real Issue: Measurement Accuracy, Not Arbitrary Cutoffs

Creatinine-Based eGFR May Be Inaccurate

The provider's concern about cutoff points being "arbitrary" misses the actual clinical problem. The method used to estimate GFR matters significantly—creatinine-based equations may not accurately reflect true kidney function in individuals with variable muscle mass, malnutrition, or extreme body composition. 2

Research demonstrates that approximately 23% of patients with creatinine-based eGFR 45-59 mL/min/1.73 m² actually have normal kidney function (>60 mL/min/1.73 m²) when confirmed with measured GFR. 4

The Correct Approach: Confirmatory Testing

If there is genuine concern about kidney function in a patient with borderline eGFR values, KDIGO guidelines recommend measuring cystatin C in adults with eGFRcreat 45-59 mL/min/1.73 m² who lack other markers of kidney damage. 4, 1, 5

  • If eGFRcys or the combined eGFRcreat-cys is also <60 mL/min/1.73 m², the diagnosis of CKD is confirmed. 4
  • If eGFRcys or eGFRcreat-cys is ≥60 mL/min/1.73 m², the diagnosis of CKD is not confirmed. 4, 5

The combined creatinine-cystatin C equation provides 94.9% accuracy within 30% of measured GFR and should be the definitive value used for clinical decision-making when discordance exists. 1

Why "Close Enough" Is Harmful

Consequences of Inappropriate Diagnosis

Labeling a patient with CKD when they do not meet diagnostic criteria can lead to:

  • Psychological burden and anxiety from being diagnosed with a chronic, progressive disease 4
  • Inappropriate medication adjustments or withholding of beneficial therapies 5
  • Unnecessary specialist referrals and healthcare costs 4
  • Insurance and employment implications 4

The debate about CKD staging thresholds in the literature specifically addresses concerns about overdiagnosis, particularly in elderly individuals and women who may have age-appropriate reductions in GFR without true kidney disease. 4, 6

The Evidence Against Flexible Interpretation

Studies examining CKD diagnosis demonstrate that using a single screening test overestimates the proportion of people with CKD by approximately 25% compared to using two tests as recommended. 7 This underscores why adhering to diagnostic criteria—including the temporal component and the need for confirmatory evidence—is essential.

The Correct Clinical Algorithm

When encountering an eGFR of 64 mL/min/1.73 m² without evidence of kidney damage:

  1. Do not diagnose CKD, as the patient does not meet criteria 1, 2
  2. Assess for markers of kidney damage (albuminuria, hematuria, imaging abnormalities) 1, 2
  3. If no kidney damage is present, repeat eGFR in 3 months to assess stability 2, 7
  4. If there is clinical concern about the accuracy of creatinine-based eGFR (due to muscle mass, diet, or other factors), measure cystatin C and calculate eGFRcreat-cys 1, 5, 2
  5. Only diagnose CKD if persistent abnormalities are documented over ≥3 months 2, 3

Common Pitfalls to Avoid

Do not conflate "being cautious" with making a premature diagnosis. The appropriate cautious approach is close monitoring and confirmatory testing, not diagnostic labeling without meeting criteria. 2

Do not assume that cutoff values are arbitrary simply because they are numerical thresholds. The 60 mL/min/1.73 m² threshold is based on extensive epidemiological data linking values below this level with adverse outcomes. 4

Do not ignore the requirement for temporal persistence. A single abnormal value does not constitute CKD regardless of the eGFR level. 2, 7

References

Guideline

CKD Diagnosis Criteria

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Chronic Kidney Disease Diagnosis and Staging

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Estimating Glomerular Filtration Rate with Cystatin C

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

Screening for CKD with eGFR: doubts and dangers.

Clinical journal of the American Society of Nephrology : CJASN, 2008

Research

Impact of a single eGFR and eGFR-estimating equation on chronic kidney disease reclassification: a cohort study in primary care.

The British journal of general practice : the journal of the Royal College of General Practitioners, 2018

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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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