What are the treatment options for a patient with impaired renal function, indicated by a creatinine level of 1.81 and an estimated Glomerular Filtration Rate (eGFR) of 28, consistent with stage 4 Chronic Kidney Disease (CKD)?

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Last updated: December 6, 2025View editorial policy

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Management of Stage 4 Chronic Kidney Disease (Creatinine 1.81, eGFR 28)

You need immediate nephrology referral and must begin preparing for renal replacement therapy now, as your kidney function has reached Stage 4 CKD and is approaching kidney failure. 1

Immediate Nephrology Referral

  • Urgent nephrology consultation is required for any patient with eGFR <30 mL/min/1.73m², as recommended by the American Diabetes Association. 1
  • Referral should occur immediately to allow adequate time for dialysis access planning and transplant evaluation. 1
  • Do not delay nephrology referral hoping for spontaneous improvement—permanent kidney damage is likely present at this level of function. 1

Assessment for Emergency Dialysis Indications

Evaluate immediately for life-threatening complications that may require urgent dialysis: 1

  • Severe hyperkalemia (potassium >6.5 mEq/L or ECG changes) 2
  • Pulmonary edema unresponsive to diuretics 1, 2
  • Severe metabolic acidosis (pH <7.2) 1, 2
  • Uremic symptoms: pericarditis, encephalopathy, bleeding, intractable nausea/vomiting 1, 2
  • Volume overload refractory to medical management 1, 2

Preparation for Renal Replacement Therapy

Dialysis Access Planning

  • Arteriovenous fistula creation should be arranged now at eGFR 28 mL/min/1.73m². 1
  • Fistulas require 3-6 months to mature before use and are ideally created when GFR is 15-20 mL/min/1.73m². 1, 2
  • This timing is critical—you are at the optimal window for access creation before dialysis becomes necessary. 1

Transplant Evaluation

  • Kidney transplantation evaluation should begin immediately, as preemptive transplantation offers the best outcomes. 1
  • Transplantation is the optimal treatment and may be performed preemptively (before dialysis) or after dialysis initiation. 2

Medical Management

Medication Adjustments

  • All renally cleared medications must be dose-adjusted for eGFR 28 mL/min/1.73m². 1, 2
  • Continue ACE inhibitors or ARBs if already prescribed for proteinuria or hypertension, with careful monitoring of creatinine and potassium. 1
  • Monitor serum creatinine and potassium levels regularly when using ACE inhibitors, ARBs, or diuretics. 1
  • Avoid nephrotoxic agents: NSAIDs, aminoglycosides, and contrast dye (or use with extreme caution and adequate hydration). 2

Blood Pressure Management

  • Target systolic blood pressure <120 mm Hg based on the SPRINT trial data showing mortality benefit in non-diabetic CKD patients with eGFR 20-60 (death HR: 0.72,95% CI 0.53-0.99). 3
  • If diabetic, target blood pressure <130/80 mm Hg per ACCORD trial findings. 3

Management of Metabolic Complications

Anemia Management

  • Check hemoglobin, ferritin, transferrin saturation, vitamin B12, and folate. 1, 2
  • Evaluate and treat anemia as it commonly develops when eGFR <60 mL/min/1.73m². 1

Mineral Bone Disease

  • Monitor calcium, phosphorus, parathyroid hormone, and vitamin D levels. 1, 2
  • CKD-mineral bone disorder requires active management at this stage. 1

Metabolic Acidosis

  • Check serum bicarbonate and consider supplementation if <22 mEq/L. 2

Hyperkalemia Management

  • Implement dietary potassium restriction. 1, 2
  • Discontinue potassium-sparing medications. 1, 2

Volume Status

  • Careful fluid and sodium management to avoid both overload and depletion. 2

Dietary Modifications

  • Protein intake should be approximately 0.8 g/kg body weight per day for non-dialysis CKD patients to slow progression. 1
  • Implement sodium restriction to help control blood pressure and volume status. 1

Cardiovascular Risk Management

  • CKD Stage 4 markedly increases cardiovascular risk, requiring aggressive management of hypertension, diabetes, and dyslipidemia. 1
  • The cardiovascular pathways in CKD may differ from the general population, with medial arterial calcification playing a larger role than traditional plaque atherosclerosis. 3
  • Despite these differences, traditional cardiovascular risk factor management remains important and should be intensified. 3

Critical Monitoring

  • Do not rely on serum creatinine alone to assess kidney function in acute changes, as creatinine assumes steady-state conditions. 1
  • Regular monitoring of electrolytes, acid-base status, and volume status is essential at this stage. 1
  • Evaluate and manage all CKD complications when eGFR <60 mL/min/1.73m², including anemia, bone disease, acidosis, and electrolyte abnormalities. 1

Timeline for Dialysis Initiation

  • The recommended threshold for initiating kidney replacement therapy is GFR <10 mL/min/1.73m² in the absence of urgent indications. 2
  • Individual factors influencing timing include dialysis access availability, transplantation candidacy, peritoneal dialysis eligibility, age, declining nutritional status, fluid balance, and medication compliance. 2
  • At your current eGFR of 28, you have time to prepare properly, but action must begin now. 1

References

Guideline

Management of Stage 4 Chronic Kidney Disease

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Preparation for Renal Replacement Therapy in Advanced Kidney Disease

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 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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