Management of Asymptomatic Patient with Creatinine 118 µmol/L
In an asymptomatic patient with a creatinine of 118 µmol/L (approximately 1.3 mg/dL), indicating CKD stage 3, dialysis is not indicated and management should focus on nephroprotective strategies including blood pressure control, ACE inhibitor therapy if proteinuria is present, and monitoring for progression. 1
Key Principle: Dialysis Timing
- There is no compelling evidence that initiation of dialysis based solely on kidney function measurements leads to improvement in clinical outcomes, including mortality 1
- The landmark IDEAL study demonstrated no benefit to early dialysis initiation (at creatinine clearance 12 mL/min) versus later initiation (at 9.8 mL/min), with no differences in death, cardiovascular events, or infectious complications 1
- In asymptomatic individuals, there is no reason to begin maintenance dialysis solely based on serum creatinine or eGFR values 1
- Dialysis should only be considered when patients develop uremic symptoms (such as altered mental status, uremic encephalopathy with BUN >100 mg/dL, or rapidly deteriorating neurological status) 2
Immediate Assessment Required
- Calculate estimated GFR using a validated equation (MDRD or CKD-EPI), not just serum creatinine alone, as creatinine can be misleading particularly in elderly patients or those with reduced muscle mass 1, 3
- A creatinine of 118 µmol/L (1.3 mg/dL) typically corresponds to CKD stage 3 (eGFR 30-59 mL/min/1.73 m²) 1
- Assess for proteinuria using albumin-to-creatinine ratio (ACR) or protein-to-creatinine ratio (PCR), as this determines both prognosis and treatment intensity 1
Nephroprotective Management Strategy
Blood Pressure Control
- Target blood pressure should be <125/75 mm Hg (MAP <92 mm Hg) if proteinuria exceeds 1 g/day (ACR ≥60 mg/mmol or PCR ≥100 mg/mmol) 4
- For proteinuria <1 g/day, target blood pressure should be approximately MAP 98 mm Hg (<130/80 mm Hg) 4
ACE Inhibitor Therapy
- ACE inhibitor therapy is recommended in preference to other antihypertensive classes for renoprotection, particularly in patients with proteinuria 4
- For patients with creatinine clearance >30 mL/min, standard dosing of ACE inhibitors can be used (e.g., lisinopril 5-40 mg daily) 5
- Tolerate initial increases in serum creatinine up to 30% after starting ACE inhibitor therapy, as this represents beneficial hemodynamic changes rather than kidney injury 6
- In the context of aggressive dual-goal therapy (targeting both blood pressure and proteinuria reduction), increases in creatinine >30% may be acceptable if the patient remains clinically stable, with favorable long-term outcomes demonstrated 6
Monitoring Strategy
- Monitor serum creatinine and potassium within 1-2 weeks after initiating or adjusting ACE inhibitor therapy 5
- Serum potassium should be monitored periodically as ACE inhibitors can cause hyperkalemia, particularly in patients with renal insufficiency 5
- Renal function should be reassessed when clinically indicated and at least annually 1
Nephrology Referral Criteria
- Referral to nephrology is indicated when eGFR falls below 30 mL/min/1.73 m² (CKD stage 4) 1
- Earlier referral should be considered for: persistent proteinuria >1 g/day (ACR ≥60 mg/mmol or PCR ≥100 mg/mmol), inability to meet blood pressure goals, rapid progression of CKD (sustained decrease in eGFR >20%), or unexplained kidney dysfunction 1
- Timely referral for planning renal replacement therapy should occur when the risk of kidney failure within 1 year is 10-20% or higher, as determined by validated risk prediction tools 1
Important Caveats
- Serum creatinine alone significantly underestimates CKD prevalence in older adults—80.6% of elderly patients with stage 3 CKD have creatinine ≤1.5 mg/dL 3
- Very low-protein diets (0.4 g/kg/day) should only be considered for patients with severe renal dysfunction (creatinine >350 µmol/L or >4.0 mg/dL), not for stage 3 CKD 4
- Avoid nephrotoxic medications including NSAIDs, and adjust doses of renally-cleared medications based on eGFR 1, 5
- The vast majority of patients with stage 3 CKD do not progress to end-stage renal disease but die mainly from cardiovascular causes—cardiovascular risk reduction should be strongly emphasized 1