Is an estimated Glomerular Filtration Rate (eGFR) of 58 considered alarming?

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Last updated: December 9, 2025View editorial policy

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Is an eGFR of 58 Alarming?

An eGFR of 58 mL/min/1.73 m² is not immediately alarming but requires prompt evaluation and management, as it indicates Stage 3a chronic kidney disease (CKD) with moderately decreased kidney function that carries increased cardiovascular and mortality risk. 1, 2

Understanding the Clinical Significance

  • An eGFR of 58 mL/min/1.73 m² falls just below the critical threshold of 60 mL/min/1.73 m², which defines CKD regardless of other markers of kidney damage 1
  • This level represents Stage 3a CKD (eGFR 45-59 mL/min/1.73 m²), classified as "moderately decreased" kidney function with moderately increased risk for cardiovascular complications 1, 2
  • The cardiovascular disease risk at this level is approximately 16% higher than in individuals with normal kidney function, though this risk is heavily modified by the presence or absence of albuminuria 3
  • Research demonstrates that individuals with eGFR 60-69 mL/min/1.73 m² experience 40% higher cardiovascular disease incidence over long-term follow-up, suggesting eGFR of 58 carries similar or greater risk 4

Immediate Actions Required

You must obtain a repeat eGFR measurement within 3 months to confirm chronicity, as CKD requires abnormalities present for ≥3 months. 1

  • Measure urine albumin-to-creatinine ratio (UACR) immediately, as albuminuria dramatically amplifies cardiovascular and kidney disease progression risk even with preserved eGFR 2, 3
  • Review all current medications and adjust doses for reduced kidney function, as many drugs require modification when eGFR <60 mL/min/1.73 m² 2
  • Immediately discontinue NSAIDs if being used, as they reduce renal blood flow and can precipitate acute kidney injury 2

Mandatory Screening for CKD Complications

When eGFR is <60 mL/min/1.73 m², you must screen for the following every 6-12 months: 2

  • Blood pressure monitoring (target <130/80 mmHg if albuminuria present)
  • Volume status assessment
  • Electrolyte abnormalities (particularly potassium)
  • Metabolic acidosis
  • Anemia
  • Mineral bone disease

Risk Stratification Based on Albuminuria

The presence or absence of albuminuria fundamentally changes the risk profile: 3

  • If UACR <30 mg/g (normal): The eGFR of 58 may represent age-related decline rather than progressive kidney disease, particularly in older adults
  • If UACR 30-300 mg/g (microalbuminuria): Significantly increased cardiovascular and CKD progression risk requiring aggressive intervention
  • If UACR >300 mg/g (macroalbuminuria): Substantially elevated risk requiring immediate nephrology referral 2

Blood Pressure and Cardiovascular Management

  • If albuminuria is present, initiate ACE inhibitor or ARB as first-line antihypertensive therapy, monitoring serum creatinine and potassium after starting 2
  • Target blood pressure <130/80 mmHg to slow CKD progression 2
  • Uncontrolled systolic blood pressure accelerates GFR deterioration and must be addressed aggressively 3
  • The European Heart Journal guidelines emphasize that renal impairment at this level requires particularly vigorous cardiovascular risk factor control 1

Dietary and Lifestyle Modifications

  • Limit dietary protein to approximately 0.8 g/kg body weight per day 2
  • Restrict sodium to <2 g/day to reduce blood pressure and maximize diuretic effectiveness if needed 2
  • These interventions can slow progression and reduce cardiovascular complications 2

Nephrology Referral Criteria

Refer promptly to nephrology if any of the following are present: 2

  • Uncertainty about the etiology of kidney disease
  • Difficult management issues
  • Rapidly progressing kidney disease (eGFR decline >4-8 mL/min per year)
  • Persistent albuminuria despite optimal management

Monitoring Strategy Going Forward

  • Measure eGFR and UACR at least annually 2
  • Serial eGFR measurements over time are more informative than a single value for determining if this represents stable age-related decline versus progressive disease 3
  • If eGFR is declining >4-8 mL/min per year, this indicates accelerated kidney disease requiring intervention 3

Critical Context: Not All eGFR <60 Represents Disease

A crucial caveat is that GFR declines physiologically with age at approximately 1-2 mL/min per year beginning in the third or fourth decade of life 3. In older adults, an eGFR of 58 may represent normal aging rather than pathologic kidney disease, particularly if:

  • No albuminuria is present
  • eGFR has been stable over time
  • No other markers of kidney damage exist
  • The patient is elderly (>65 years)

However, this distinction can only be made after proper evaluation including UACR measurement and serial eGFR monitoring 1, 3.

Special Considerations for Medication Safety

  • Drug accumulation due to reduced renal excretion is a major cause of adverse drug reactions when eGFR <60 mL/min/1.73 m² 3
  • Use the Cockroft-Gault formula for medication dose adjustments, as most drug labeling is based on this calculation rather than MDRD or CKD-EPI equations 1
  • Contrast-induced nephropathy risk is elevated at this eGFR level; use isosmolar contrast agents if angiography is required 1

Vaccination Considerations

Hepatitis B vaccination should be administered early in patients likely to progress to end-stage kidney disease, as immune response diminishes with worsening kidney function 2.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Management of eGFR 40 mL/min/1.73 m²

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Chronic Kidney Disease Assessment and Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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