Why is a patient with chronic kidney disease (CKD) prescribed Farxiga (dapagliflozin)?

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Why Farxiga (Dapagliflozin) is Prescribed for Chronic Kidney Disease

Farxiga (dapagliflozin) is prescribed for patients with chronic kidney disease because it significantly reduces the risk of kidney disease progression, end-stage kidney disease, cardiovascular death, and hospitalization for heart failure, with benefits seen regardless of whether patients have diabetes. 1

Evidence Supporting Dapagliflozin in CKD

Primary Benefits in CKD

  • Dapagliflozin is FDA-approved specifically "to reduce the risk of sustained eGFR decline, end-stage kidney disease, cardiovascular death, and hospitalization for heart failure in adults with chronic kidney disease at risk of progression" 1
  • In the landmark DAPA-CKD trial, dapagliflozin reduced the primary composite outcome (≥50% sustained decline in eGFR, end-stage kidney disease, or cardiovascular/renal death) by 39% compared to placebo (HR 0.61 [95% CI 0.51–0.72]; P < 0.001) 2
  • The kidney-specific composite outcome (sustained decline in eGFR of ≥50%, ESKD, or death from renal causes) was reduced by 44% (HR 0.56 [95% CI 0.45–0.68]; P < 0.001) 2

Cardiovascular Benefits

  • Dapagliflozin reduced the risk of cardiovascular death or hospitalization for heart failure by 29% (HR 0.71 [95% CI 0.55–0.92]; P = 0.009) 2
  • All-cause mortality was significantly decreased in patients taking dapagliflozin compared to placebo (P < 0.004) 2

Benefits Across Patient Populations

  • The benefits of dapagliflozin extend to both patients with and without type 2 diabetes 3
  • In DAPA-CKD, 67.5% of participants had type 2 diabetes, while the remaining one-third had CKD without diabetes 2
  • Efficacy was consistent regardless of the underlying cause of CKD (diabetic nephropathy, glomerulonephritides, ischemic/hypertensive CKD, or other causes) 3
  • Benefits were observed across all age groups, including older adults, and in both men and women 4

Dosing and Patient Selection

  • For CKD patients, the recommended dose is 10 mg orally once daily 1
  • Dapagliflozin can be used in patients with eGFR as low as 20 mL/min/1.73 m² 2
  • The DAPA-CKD trial included patients with eGFR 25-75 mL/min/1.73 m² and urinary albumin-to-creatinine ratio (UACR) 200-5,000 mg/g 2
  • Dapagliflozin is not recommended for CKD treatment in patients with polycystic kidney disease or those requiring or with recent history of immunosuppressive therapy for kidney disease 1

Long-Term Benefits

  • Treatment with dapagliflozin may delay time to kidney failure by approximately 6.6 years compared to standard therapy 5
  • The benefits are observed regardless of whether patients have established cardiovascular disease or not 6
  • Dapagliflozin's renoprotective effects appear to be independent of its glucose-lowering properties, making it effective even in non-diabetic CKD 3, 7

Potential Side Effects and Monitoring

  • Prior to initiating dapagliflozin, renal function and volume status should be assessed 1
  • Common side effects include increased urination and genitourinary infections 2
  • Volume depletion and ketoacidosis are potential risks but are generally outweighed by the significant renal and cardiovascular benefits 7

Clinical Implications

  • Dapagliflozin represents a paradigm shift in CKD management, offering protection beyond traditional renin-angiotensin system blockade 7
  • The medication should be considered for CKD patients regardless of diabetes status, as it provides significant mortality and morbidity benefits 2, 3
  • The robust evidence from DAPA-CKD and other trials has established SGLT2 inhibitors like dapagliflozin as a cornerstone of modern CKD treatment 7

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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