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Abnormal urinalysis

Differential Diagnosis Schema 🧠

Infective Causes

  • Urinary Tract Infection (UTI): Dysuria, frequency, urgency, and suprapubic pain.
  • Pyelonephritis: Flank pain, fever, and chills, with or without lower UTI symptoms.
  • Sexually Transmitted Infections (e.g., Chlamydia, Gonorrhoea): Dysuria, urethral discharge, or pelvic pain.

Glomerular Causes

  • Glomerulonephritis: Haematuria (often microscopic), proteinuria, hypertension, and possible oedema.
  • IgA Nephropathy: EpisodicΒ macroscopic haematuriaΒ often after an upper respiratory tract infection.
  • Post-Infectious Glomerulonephritis: Usually presents with haematuriaΒ and proteinuria after a streptococcal infection.
  • Rapidly Progressive Glomerulonephritis: Rapid decline in renal function with crescent formation on biopsy, haematuria, and proteinuria.

Tubular and Interstitial Causes

  • Acute Tubular Necrosis: Muddy brown casts in urine, often following ischaemia or nephrotoxin exposure.
  • Acute Interstitial Nephritis: Eosinophils in urine, fever, rash, and recent exposure to new medication (e.g., NSAIDs, antibiotics).
  • Chronic Interstitial Nephritis: Slow progression with mild proteinuria and decreased concentrating ability.

Vascular Causes

  • Renal Artery Stenosis: Hypertension that is resistant to treatment, possible abdominal bruit.
  • Atheroembolic Disease: Acute renal failureΒ following a vascular procedure, possible livedo reticularis.
  • Malignant Hypertension: Severe hypertension with haematuria, proteinuria, and end-organ damage.
  • Thrombotic Microangiopathy: Microangiopathic haemolytic anaemia, thrombocytopenia, and acute kidney injury.

Metabolic and Systemic Causes

  • Diabetes Mellitus: Glycosuria and possible ketonuria, polyuria, and polydipsia.
  • Multiple Myeloma: Proteinuria (Bence-Jones proteins), normocytic anaemia, and hypercalcemia.
  • Systemic Lupus Erythematosus: Proteinuria, haematuria, and systemic symptoms such as rash and arthralgia.
  • Rhabdomyolysis: Myoglobinuria, raised CK levels, and muscle pain/weakness.
  • Hypercalcaemia: Polyuria and nephrocalcinosis.
  • Sickle Cell Disease: Haematuria, proteinuria, and possible renal papillary necrosis.

Key Points in History πŸ₯Ό

Presenting Symptoms

  • Dysuria: Suggests UTI or sexually transmitted infections.
  • Frequency/Urgency: Common in UTIs, bladder irritants, or diabetes.
  • Haematuria: Can indicate glomerulonephritis, malignancy, or stones.
  • Oliguria/Anuria: Can suggest acute kidney injury or obstruction.
  • Polyuria/Nocturia: Common in diabetes, hypercalcemia, or diuretic use.
  • Frothy urine: Indicative of significant proteinuria, often seen in nephrotic syndrome.

Background

  • Past Medical History: History of diabetes, hypertension, or autoimmune diseases can suggest chronic kidney disease or nephropathy.
  • Drug History: Recent NSAID or antibiotic use may suggest acute interstitial nephritis.
  • Family History: Family history of polycystic kidney disease or hereditary nephritis (Alport syndrome).
  • Social History: Occupational exposure to nephrotoxins, recreational drug use (e.g., cocaine can cause rhabdomyolysis), and high-risk sexual behaviour (consider STIs).

Possible Investigations 🌑️

Urinalysis

  • Dipstick Analysis: Presence of leukocytes, nitrites, blood, protein, glucose, ketones, and pH. Useful for initial screening.
  • Microscopy: Identifies red blood cells, white blood cells, casts, crystals, and bacteria. Essential for diagnosing conditions such as glomerulonephritis or infection.
  • Culture and Sensitivity: Confirms infection and guides antibiotic treatment.

Blood Tests

  • Urea and Electrolytes (U&E): Assesses kidney function, electrolyte imbalance, and signs of acute or chronic kidney disease.
  • Full Blood Count (FBC): Detects anaemia, infection, and signs of systemic disease (e.g., eosinophilia in AIN).
  • C-Reactive Protein (CRP)/Erythrocyte Sedimentation Rate (ESR): Raised in infection, inflammation, or vasculitis.
  • Liver Function Tests (LFTs): May be altered in systemic conditions affecting multiple organs.
  • Autoantibody Screen: ANCA, ANA, Anti-GBM, and other specific antibodies for autoimmuneΒ causes.
  • Serum Calcium and Phosphate: To investigate hypercalcemia or hypophosphatemia related causes of renal disease.
  • Creatinine Kinase: Elevated in rhabdomyolysis.

Imaging

  • Ultrasound: First-line imaging for assessing kidney size, structure, and presence of obstruction or stones.
  • CT Scan: Useful for identifying renal stones, masses, and complications like abscesses.
  • MRI: Often used in more complex cases or where detailed anatomical information is needed (e.g., renal vein thrombosis).
  • Intravenous Urography: Occasionally used in structural abnormalities, though largely replaced by CT and MRI.

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