Ascites - Medical Lecture Notes

 

Ascites - Medical Lecture Notes


Definition

Ascites is the pathological accumulation of fluid in the peritoneal cavity, most commonly due to portal hypertension caused by liver cirrhosis. It is a key sign of advanced liver disease, though other causes must be considered.

Pathophysiology

  • Portal Hypertension: Increased hydrostatic pressure due to cirrhosis causes fluid leakage into the peritoneal space.
  • Hypoalbuminemia: Reduced plasma oncotic pressure from impaired hepatic albumin synthesis allows fluid to leak out of capillaries.
  • Splanchnic Vasodilation: Nitric oxide release causes vasodilation, further reducing effective circulating volume.
  • RAAS Activation: Sodium and water retention worsens fluid accumulation.

Common Causes of Ascites

  • Cirrhosis (≈ 80% of cases)
  • Malignancy (Peritoneal carcinomatosis, lymphomas)
  • Infectious: Tuberculosis peritonitis
  • Nephrotic syndrome
  • Congestive heart failure
  • Pancreatitis
  • Chylous ascites (lymphatic obstruction)

Clinical Presentation

  • Progressive abdominal distension
  • Early satiety
  • Shortness of breath (due to diaphragmatic pressure)
  • Shifting dullness, fluid thrill
  • Peripheral edema (if hypoalbuminemia is present)

Diagnostic Work-up

  1. History & Physical Examination
  2. Ultrasound Abdomen: Most sensitive for small amounts of fluid (>100 ml)
  3. Diagnostic Paracentesis: Always performed in new-onset ascites, suspected infection or deterioration.

Ascitic Fluid Analysis

  • Appearance: Clear (transudate), cloudy/purulent (infection), bloody (malignancy/TB)
  • Serum Ascites Albumin Gradient (SAAG):
    • SAAG ≥1.1 g/dL → suggests portal hypertension (cirrhosis, CHF)
    • SAAG <1.1 g/dL → suggests non-portal hypertensive causes (TB, cancer, pancreatitis)
  • Cell count & differential: Neutrophils >250/mm³ suggest spontaneous bacterial peritonitis (SBP)
  • Culture, glucose, LDH, cytology, AFB if TB suspected

Types of Ascites

  1. Transudative Ascites – Low protein content (e.g., cirrhosis, nephrotic syndrome)
  2. Exudative Ascites – High protein content (e.g., TB, malignancy, pancreatitis)
  3. Hemorrhagic Ascites – Bloody ascitic fluid (e.g., trauma, malignancy)
  4. Chylous Ascites – Milky appearance due to lymph (e.g., lymphoma, TB, filariasis)

Complications

  • Spontaneous Bacterial Peritonitis (SBP): Life-threatening infection of ascitic fluid
  • Hepatorenal Syndrome (HRS)
  • Respiratory compromise
  • Malnutrition and sarcopenia

Management

  1. General Measures: Salt restriction (<2g/day), fluid restriction if hyponatremic
  2. Diuretics:
    • Spironolactone (first-line)
    • Furosemide added if needed (typical ratio 100:40 mg)
  3. Therapeutic Paracentesis: For tense ascites; replace albumin if large volume removed
  4. SBP Treatment: Empirical IV cefotaxime; prophylactic norfloxacin in high-risk cases
  5. Refractory Ascites: TIPS (Transjugular Intrahepatic Portosystemic Shunt)
  6. Definitive treatment: Liver transplant

Prognosis

Ascites indicates decompensated liver disease. Median survival is approximately 2 years without transplant, especially if refractory or complicated by SBP or hepatorenal syndrome.

Important Clinical Points

  • Always analyze ascitic fluid when new or worsening ascites appears.
  • Monitor renal function and electrolytes frequently during diuretic therapy.
  • SBP can be asymptomatic; always have a high index of suspicion.

References & Resources

  • Harrison's Principles of Internal Medicine
  • Davidson's Principles and Practice of Medicine
  • Oxford Handbook of Clinical Medicine
  • Uptodate: Evaluation of ascites in adults
  • American Association for the Study of Liver Diseases (AASLD) Guidelines

Created for medical education. For any personal health concerns, consult a licensed physician.

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