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Anatomic Distribution
Prerenal disease Post renal disease Intrinsic renal disease : : : poor renal perfusion obstractive urinary tract - Glomerular - Tubular - Interstitial - Vascular - Ischemic
Acute Tubular Necrosis (Olliguric/Polyuric) Acute Glomerulonephritis : poststreptococcal infection collagen-vascular disease Acute Interstitial Nephritis : allergic reaction, drug reaction
Diuresis :
Polyuri Oliguri Anuri : : : urine formation increase urine less than 400 cc/day urine less than 100 cc/day
Anaemi
Low in erythropoetin production rare in initial ARF Small kidneys in CRF Normal - large kidneys in CRF and ARF
Laboratory Examination :
I. II. Urinalysis : - must be examined within 1 hour - midstream Proteinuri : - greater than 150-160 mg / 24 hours - underlying diseases - usually glomerular in origin if greater than 1 gr / day 4 primary reasons : 1.Functional Proteinuri 2.Overload : Bence Jones
multiple myeloma myoglobulinuria (rhabdomyolysis) hemoglobinuria acute tubular necrosis toxic injury (Pb, aminoglycoside) drug induced hereditary metabolic diseases (Wilson diseases, Fanconi syndrome)
albuminuri nephrotic
Examination
1. 2. 3. 4. 5. 6. USG IVP CT Scan MRI Scan Arteriography / Venography Renal Biopsy
1. Ischemic 2. Nephrotoxin
Ischemic :
- Tubular damage - Prerenal azotemia - Renal blood flow decrease - Major surgery : i. prolonged hypoperfusion ii. vasodelating effect of anesthetic agent
Indication HD :
- encephalopaty - pericarditis uremic complication - seizures - hyperkalemi - volume overload - worsening acidosis
Intrarenal Vascular disease - Arterial, arteriolar, venous Glomerular disease - Acute glomerulonephritis (immune complex, vasculitis, anti-GBM) - Thrombotic microangiopathy (TTP/HUS) - Monoclonal immunoglobulin deposition disease