Is Jardiance (empagliflozin) safe to use in an adult patient with type 2 diabetes and impaired renal function, specifically a glomerular filtration rate (GFR) of 24?

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Jardiance Use with GFR 24

Jardiance (empagliflozin) should NOT be initiated in a patient with a GFR of 24 mL/min/1.73 m², but if the patient is already taking it, continuation may be reasonable for cardiovascular and renal protection until dialysis is required. 1

Guideline-Based Initiation Threshold

The most recent KDIGO 2024 guidelines provide the clearest direction on this clinical scenario:

  • SGLT2 inhibitors are recommended for initiation only when eGFR ≥20 mL/min/1.73 m² for patients with type 2 diabetes and CKD (Recommendation 3.7.1, Grade 1A). 1
  • At a GFR of 24 mL/min/1.73 m², this patient falls just above the minimum threshold of 20 mL/min/1.73 m², making initiation technically permissible but requiring careful consideration. 1
  • Once initiated, SGLT2 inhibitors should be continued even if eGFR falls below 20 mL/min/1.73 m² unless not tolerated or kidney replacement therapy is initiated (Practice Point 3.7.1). 1

Critical Distinction: Glycemic Control vs. Cardiorenal Protection

This is the most important clinical nuance at this level of renal function:

  • Do NOT use Jardiance for glycemic control at GFR 24 mL/min/1.73 m² - the glucose-lowering efficacy is minimal to absent due to the drug's mechanism requiring adequate renal filtration. 2, 3
  • The FDA label explicitly states that glucose-lowering efficacy decreases significantly when eGFR <45 mL/min/1.73 m², with least square mean HbA1c reductions of only -0.2% at eGFR 30-45 mL/min/1.73 m². 2
  • However, cardiovascular and renal protective benefits are preserved at lower eGFR levels, independent of glycemic effects. 1, 4

Evidence Supporting Use at Low eGFR

The EMPA-KIDNEY trial provides the strongest recent evidence:

  • Empagliflozin reduced progression of kidney disease and cardiovascular death by 28% (HR 0.72,95% CI 0.64-0.82) in patients with eGFR as low as 20 mL/min/1.73 m². 1
  • Approximately half of the 6,609 participants had diabetes, demonstrating benefit regardless of diabetes status. 1
  • The trial specifically enrolled patients with eGFR ≥20 but <45 mL/min/1.73 m² or those with eGFR 45-90 mL/min/1.73 m² with significant albuminuria. 1

Clinical Decision Algorithm for GFR 24

If considering NEW initiation:

  1. Assess the primary indication - Is this for glycemic control or cardiorenal protection? 1
  2. If for glycemic control alone: Do NOT initiate Jardiance; use alternative agents (insulin, GLP-1 RA with dose adjustment). 1, 2
  3. If for cardiorenal protection (heart failure, CKD with albuminuria ≥200 mg/g, or established cardiovascular disease):
    • Check that eGFR is ≥20 mL/min/1.73 m² (at 24, this criterion is met). 1
    • Assess volume status and correct any volume depletion before initiation. 1
    • Consider reducing concurrent diuretic doses to prevent excessive volume depletion. 1
    • Initiate at 10 mg once daily (no dose adjustment needed; this is the standard dose for cardiorenal protection). 1, 2

If patient is ALREADY on Jardiance:

  • Continue 10 mg daily for cardiorenal protection even though glycemic efficacy is lost. 1
  • Monitor closely for adverse effects (volume depletion, genital infections, ketoacidosis risk if on insulin). 1, 2
  • Continue until dialysis is initiated or drug is not tolerated. 1

Monitoring and Safety Considerations at GFR 24

  • Expect a transient eGFR dip of 3-5 mL/min/1.73 m² within the first 2-4 weeks - this is hemodynamic, reversible, and does NOT indicate harm. 1
  • Check eGFR and serum creatinine within 2-4 weeks of initiation. 1
  • Withhold Jardiance during acute illness, prolonged fasting, or major surgery to prevent ketoacidosis and volume depletion. 1
  • Monitor for genital mycotic infections (occurs in ~6% of patients) and urinary tract infections. 2, 5
  • Risk of euglycemic diabetic ketoacidosis exists, particularly in insulin-requiring patients - educate patients to check ketones if experiencing malaise, nausea, or vomiting even with normal glucose. 1, 2

Common Pitfalls to Avoid

  • Do NOT discontinue Jardiance solely because eGFR is <45 mL/min/1.73 m² - the cardiorenal benefits persist even when glycemic efficacy is lost. 1
  • Do NOT use Jardiance as a glucose-lowering agent at this eGFR - it will be ineffective and may lead to inadequate diabetes management. 2
  • Do NOT forget to adjust other medications - metformin should be discontinued if eGFR <30 mL/min/1.73 m²; DPP-4 inhibitors require dose reduction. 1
  • Do NOT initiate in patients with type 1 diabetes at this eGFR - significantly elevated ketoacidosis risk without proven benefit. 6

Alternative Agents for Glycemic Control at GFR 24

If additional glucose lowering is needed:

  • Insulin remains the most reliable option at this level of renal function (no dose adjustment based on eGFR, though clearance is reduced). 1
  • GLP-1 receptor agonists may be used for cardiovascular protection and can provide some glycemic benefit, though some require dose adjustment at eGFR <30 mL/min/1.73 m². 1
  • DPP-4 inhibitors can be used with appropriate dose reductions (e.g., sitagliptin 25 mg daily, linagliptin 5 mg daily without adjustment). 1

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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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