Should a non-diabetic patient with impaired renal function be started on Farxiga (Dapagliflozin)?

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Should This Patient Be Started on Farxiga (Dapagliflozin)?

Yes, this non-diabetic 35-year-old African American male with hypertension, GFR 54 mL/min/1.73 m², and creatinine 1.67 mg/dL should be started on Farxiga (dapagliflozin) 10 mg daily to reduce the risk of progressive kidney disease, cardiovascular death, and hospitalization for heart failure.

Rationale Based on Renal Function

Dapagliflozin is specifically indicated for chronic kidney disease with GFR ≥25 mL/min/1.73 m², regardless of diabetes status. 1 This patient's GFR of 54 mL/min/1.73 m² falls well within the approved range for initiation.

  • The landmark DAPA-CKD trial demonstrated that dapagliflozin reduced the composite outcome of sustained ≥50% decline in eGFR, end-stage kidney disease, or renal/cardiovascular death by 39% (HR 0.61,95% CI 0.51-0.72, NNT=19) in patients with chronic kidney disease 1
  • The benefit was identical in patients without diabetes (HR 0.61) compared to those with diabetes, making diabetes status irrelevant to the decision 2
  • Dapagliflozin slowed the rate of eGFR decline from -2.85 to -1.09 mL/min/1.73 m² per year, providing long-term kidney protection 3

Safety Considerations at This GFR Level

The patient's GFR of 54 mL/min/1.73 m² is above the threshold where dapagliflozin requires caution or dose adjustment. 4

  • Dapagliflozin should be used with caution in patients with moderate renal insufficiency (GFR 30-50 mL/min), but this patient is above that threshold 5
  • A mild, transient drop in eGFR may occur after initiation, but this is followed by long-term kidney protection 5
  • The FDA label confirms safety and efficacy in patients with eGFR 45 to <60 mL/min/1.73 m² 4

Cardiovascular and Mortality Benefits

Beyond kidney protection, dapagliflozin reduces cardiovascular death and all-cause mortality in patients with chronic kidney disease. 2

  • The composite of cardiovascular death or heart failure hospitalization was reduced by 29% (HR 0.71,95% CI 0.55-0.92) 1
  • All-cause mortality was reduced by 31% (HR 0.69,95% CI 0.53-0.88) 1
  • These benefits occurred regardless of cardiovascular disease history at baseline 2

Practical Implementation

Start dapagliflozin 10 mg once daily without dose titration required. 5

  • Unlike other heart failure medications, SGLT2 inhibitors do not affect blood pressure, heart rate, or potassium levels significantly 5
  • No dose adjustment or up-titration is needed 5
  • Benefits occur within weeks of initiation 5
  • Monitor for genital mycotic infections (more common) and assess for volume depletion, particularly since the patient is on losartan 4

Monitoring After Initiation

Check renal function 2-4 weeks after starting dapagliflozin to document the expected transient eGFR dip. 5

  • A small initial decline in eGFR is expected and does not indicate harm 5
  • Continue therapy unless eGFR drops below 25 mL/min/1.73 m² 1
  • Monitor for signs of volume depletion, especially in combination with losartan and if diuretics are added 4

Key Contraindications to Rule Out

Ensure the patient does not have active bladder cancer or diabetic ketoacidosis risk factors before initiating. 4, 6

  • Dapagliflozin should not be used in patients with bladder cancer 6
  • While primarily a concern in type 1 diabetes, assess for ketoacidosis risk factors 4

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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