СКФ (скорость клубочковой фильтрации) eGFR, CKD-EPI
Code:7027
Analysis details
Methodology
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Expected Turnaround Time
1 day
Special Instructions
- Do not drink alcohol for 24 hours before testing.
- Fast for 12 hours before the blood draw.
- Withhold diuretics for 48 hours before starting urine collection if approved by the treating clinician.
- Avoid strenuous physical activity and emotional stress for 24 hours before specimen collection.
- Do not smoke for at least 30 minutes before the test.
How to use
Creatinine clearance (Rehberg test; creatinine clearance test) estimates glomerular filtration by comparing creatinine concentration in serum with that excreted in a timed urine collection. The test is used to assess overall kidney function, approximate the glomerular filtration rate (GFR), and assist with staging and monitoring chronic kidney disease. It supports clinical decision-making when nephrotoxic medications are prescribed and in settings where volume depletion may depress filtration, such as severe dehydration. Measured creatinine clearance is particularly useful when a direct clearance value is needed; however, in routine practice, estimated GFR derived from serum creatinine is often used for convenience.
Limitations
The kidneys filter circulating plasma through millions of glomeruli; most filtrate is reabsorbed, while solutes not reclaimed are eliminated in urine. Creatinine is generated at a relatively steady rate from creatine phosphate in muscle, is freely filtered, undergoes minimal tubular reabsorption, and a small fraction is secreted by the tubules. As filtration falls, serum creatinine rises. By measuring creatinine in a timed (often 24‑hour) urine collection together with a concurrent serum value, creatinine clearance can be calculated to approximate the glomerular filtration rate. In healthy young adults, clearance is roughly 125 mL/min, reflecting the aggregate filtration of all functioning nephrons. When kidney function is substantially reduced, the proportional contribution of tubular secretion increases, causing measured creatinine clearance to overestimate true GFR, particularly in advanced renal failure. Although clearance can be measured directly with urine collection, serum‑based equations that estimate GFR are frequently used in practice because they are simpler for patients and clinics. A reduced GFR warrants evaluation for underlying etiology. Chronic kidney disease is most commonly driven by hypertension and diabetes mellitus; if those are absent, additional diagnostic workup is indicated. Serial creatinine clearance (or serial eGFR) enables tracking of renal function over time and supports adjustment of drug therapy. Factors that suppress tubular creatinine secretion—such as cimetidine, trimethoprim, and ketoacids—can lower measured clearance and diminish the accuracy of GFR estimation, with the effect most evident in severe renal impairment.
| Reference interval |
| ||||
|---|---|---|---|---|---|
| Indications | Flank pain suggestive of renal pathology, Periorbital or ankle edema, Hypertension, including malignant hypertension, Oliguria or lower urinary tract symptoms (e.g., dysuria), Hematuria or dark (tea-colored) urine, Suspected or established chronic kidney disease, Alport syndrome, Amyloidosis with potential renal involvement, Cushing syndrome with possible renal effects, Dermatomyositis with possible renal involvement, Diabetes mellitus with possible nephropathy, Cardiac glycoside (digitalis) toxicity, Generalized tonic–clonic seizures, Goodpasture syndrome, Hemolytic uremic syndrome, Hepatorenal syndrome, Interstitial nephritis, Lupus nephritis, Membranoproliferative glomerulonephritis, Thrombotic thrombocytopenic purpura, Wilms tumor |
Specimen Requirements
| Specimen | Serum |
|---|---|
| Container | Gold/Tiger Top (SST, Gel Separator) |