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Anuria and Oliguria

Signs and Symptoms

  • Clinicians need to search for specific signs of underlying renal disease.
    • Severe anemia due to hemolytic-uremic syndrome
    • Butterfly rash on face/musculoskeletal involvement in systemic lupus erythematosus
    • Purpuric rash over buttocks and extensor surface of lower extremity in Henoch-Schönlein purpura.
    • Palpable kidney may be due to:
      • Renal vein thrombosis
      • Polycystic kidney disease
      • Multicystic dysplastic kidney
      • Hydronephrosis
  • Palpable bladder with weak urine stream or dribbling suggests obstruction.
  • Sacral tuft of hair or myelomeningocele may be seen with neurogenic bladder (can cause obstructive uropathy/postrenal oliguria or anuria).
  • Symptoms of prerenal cause
    • Vomiting
    • Diarrhea
    • Hemorrhage
    • Sepsis
    • Decreased oral intake
    • Increased thirst
    • Palpitations
    • Fatigue
    • Clinical signs of dehydration
    • Weight loss
  • Symptoms of hypovolemia (ie, prerenal pathology)
    • Tachycardia
    • Dry mucous membranes
    • Sunken eyes
    • Orthostatic blood pressure changes
    • Decreased skin turgor
    • Hypotension
  • Symptoms of intrinsic renal disease
    • Gross hematuria
      • Pharyngitis or impetigo a few weeks before the onset of gross hematuria
    • Hypertension
    • Edema
    • Bloody diarrhea
      • Often precedes hemolytic-uremic syndrome
    • Younger children, particularly infants: signs of congestive heart failure
      • Hepatomegaly
      • Gallop rhythm
      • Pulmonary edema
  • Symptoms of systemic vasculitis (eg, systemic lupus erythematosus)
    • May see history of fever, joint pains, and skin rash
  • Recurrent sinusitis or lower respiratory tract infections may suggest Wegener granulomatosis.
  • Hemoptysis may indicate pulmonary-renal syndrome, due to either:
    • Goodpasture syndrome
    • Microscopic polyangiitis

Diagnostic Approach

  • Thorough history and physical examination are important in identifying the cause of oliguria or anuria.
    • Comprehensive physical examination is key to assessing severity of the disease process and possible cause.
    • In prerenal and postrenal ARF, early diagnosis and prompt treatment often result in quick recovery.
  • Detailed history of recent or ongoing long-term medication use is important for excluding possible interstitial nephritis.
  • In neonates, history of umbilical artery catheterization implies renal artery thrombosis.
  • Family history is helpful in diagnosing such conditions as diabetes insipidus and polycystic kidney disease.

Laboratory Findings

  • Risk factors, history, and results of physical examination will help in the selection of appropriate laboratory tests.
  • Urinalysis is the most important noninvasive diagnostic test.
    • Thorough examination of a freshly voided or bladder-catheterized urine sample helps distinguish prerenal from renal causes.
      • Normal or near-normal urinalysis, with few cells, few or no casts, or little or no proteinuria, is seen in prerenal disease, obstruction, and some cases of acute tubular necrosis.
      • A sample showing muddy-brown granular casts and epithelial cell casts strongly suggests acute tubular necrosis.
      • Erythrocyte casts are diagnostic of glomerulonephritis.
      • Proteinuria indicates glomerular disease.
  • Urinary indices important for diagnosis of oliguria
    • Urinary sodium
      • < 10 mEq/L in oliguria resulting from intravascular volume depletion
      • Neonates: prerenal disease is associated with urine sodium concentration < 20–30 mEq/L.
    • Specific gravity
      • > 1020 in prerenal oliguria
    • Creatinine
      • Urine/plasma creatinine ratio > 40 in prerenal oliguria
      • Urine/plasma creatinine ratio < 20 if renal cause
    • Osmolality
      • Urine/plasma osmolality > 1.5 in prerenal oliguria
      • Urine/plasma osmolality < 1.5 if renal cause
  • Fractional excretion of sodium
    • < 1% suggests reabsorption of almost all filtered sodium in response to decreased renal perfusion (prerenal).
    • In acute tubular necrosis: > 2%
  • Blood urea nitrogen (BUN) and serum creatinine
    • In prerenal oliguria, increased BUN level is marked and the BUN/serum creatinine ratio is > 20.
    • BUN/creatinine ration of 10–15 suggests intrinsic renal damage.

Imaging

  • Renal ultrasonography
    • Generally not indicated in children with prerenal failure from dehydration who respond promptly to fluid resuscitation
    • Provides important information regarding
      • Kidney size and echogenicity
      • Renal blood flow
      • Collecting system
      • Urinary bladder
    • Children with intrinsic causes
      • Echogenic and slightly enlarged kidneys
    • Bilateral hydronephrosis or hydroureteronephrosis and bladder wall thickening indicate obstruction of bladder outlet causing postrenal oliguria/anuria.
    • Ultrasonography can detect congenital disorders, such as polycystic kidney disease and multicystic dysplastic kidney.
  • Doppler examination of renal blood flow is helpful in diagnosing renal vascular thrombosis.

Classification

  • Prerenal: dehydration is the most common cause of oliguria/anuria in children.
  • Renal: intrinsic renal disorders, such as acute tubular necrosis and glomerulonephropathies
  • Postrenal: obstruction to urinary flow in posterior urethral valves in boys

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