CKD Workup Investigations
A comprehensive CKD workup requires measurement of serum creatinine with eGFR calculation, urine albumin-to-creatinine ratio (ACR), urinalysis with microscopy, and a complete metabolic panel as core initial tests, with additional investigations guided by clinical presentation and disease severity. 1
Core Laboratory Tests (Required for All Patients)
Kidney Function Assessment
- Serum creatinine to calculate estimated glomerular filtration rate (eGFR) using the 2021 CKD-EPI equation—this is the primary measure of kidney function 2, 1
- Cystatin C should be measured in adults with eGFR 45-59 mL/min/1.73 m² who lack markers of kidney damage when confirmation of CKD is required; if eGFR based on cystatin C is also <60 mL/min/1.73 m², CKD diagnosis is confirmed 2
- Blood urea nitrogen (BUN) to assess kidney function severity 3
Kidney Damage Assessment
- Urine albumin-to-creatinine ratio (ACR) on an early morning spot urine sample—this is the preferred method for detecting proteinuria and quantifying kidney damage 2, 1
- Confirm ACR ≥30 mg/g on a random sample with a subsequent early morning urine sample 2
- Urinalysis with microscopy to evaluate for casts, cells, and crystals that indicate underlying causes of CKD 3, 1
Electrolyte and Metabolic Panel
- Complete metabolic panel including sodium, potassium, calcium, phosphorus, magnesium, bicarbonate to identify electrolyte imbalances and metabolic acidosis 3, 1
- Parathyroid hormone (PTH) and phosphorus levels to assess mineral metabolism disorders, especially in advanced CKD (stages 3-5) 3
Additional Laboratory Tests Based on Clinical Context
Hematologic Assessment
- Complete blood count (CBC) to evaluate for anemia associated with CKD 1
- Consider erythropoietin levels in patients with anemia 4
Etiologic Workup
- Hemoglobin A1c for patients with diabetes or suspected diabetes 1
- Fasting lipid panel to assess cardiovascular risk 1
- Serologic testing for autoimmune diseases (ANA, ANCA, anti-GBM antibodies) when glomerulonephritis is suspected 1
- Complement levels (C3, C4) for suspected immune-mediated kidney disease 1
- Hepatitis B, C, and HIV serology when clinically indicated 1
- Serum and urine protein electrophoresis if multiple myeloma or monoclonal gammopathy is suspected 2, 1
Imaging Studies
Primary Imaging
- Renal ultrasound to assess kidney size, echogenicity, cortical thickness, rule out obstruction, and evaluate for structural abnormalities such as polycystic kidney disease 3, 1
- Small echogenic kidneys indicate chronic parenchymal disease 3
Additional Imaging When Indicated
- Doppler examination of renal vessels to exclude renovascular disease in patients with risk factors for vascular disease or renal artery bruits on examination 3
- Renal artery stenosis is found in approximately 4.3% of CKD patients and is potentially treatable 5
Monitoring Frequency
Baseline CKD (Stages 1-3a)
- Assess eGFR and albuminuria at least annually in all people with CKD 2
- More frequent monitoring (every 3-6 months) for individuals at higher risk of progression or when measurements will impact therapeutic decisions 2
Advanced CKD (Stages 3b-5)
- Monitor eGFR, electrolytes, and relevant parameters more frequently (every 3 months or more often) based on disease severity and stability 2, 3
- Repeat measurements beyond 3 months are required to confirm chronicity and distinguish CKD from acute kidney injury 1
Confirmatory Testing for Diagnosis
- Persistence of abnormalities for >3 months is required to diagnose CKD—this can be established through review of past measurements, imaging findings, kidney biopsy, or repeat testing 1
- Following detection of elevated ACR, hematuria, or low eGFR, repeat tests to confirm presence of CKD 1
Specialized Testing
Novel Biomarkers (Specialized Settings)
- NGAL, KIM-1, and IL-18 may be considered to detect kidney damage before serum creatinine changes, particularly in acute-on-chronic kidney injury 3
Kidney Biopsy
- Consider when the cause is unclear and results would guide treatment decisions, particularly for rapidly progressive disease, nephrotic syndrome, or suspected glomerular disease 1
Common Pitfalls to Avoid
- Do not rely on serum creatinine concentration alone—always calculate eGFR using validated equations 2
- Do not use the term "microalbuminuria"—laboratories should report ACR values with appropriate categories 2
- Confirm positive reagent strip tests with quantitative laboratory measurements expressed as a ratio to creatinine 2
- Recognize that small fluctuations in eGFR are common and not necessarily indicative of progression 2
- Consider non-albumin proteinuria when indicated—use specific assays for α1-microglobulin or monoclonal proteins 2