Académique Documents
Professionnel Documents
Culture Documents
Cirrhosis
Chronic generalized liver disease A condition that is defined histopathologically and has a
variety of clinical manifestations and complications, some of which can be life threatening.
Pathologic features : development of fibrosis to the point
that there is architectural distortion with formation of regenerative nodules ( micronodular / macronodular )
This results in decrease in hepatocellular mass, thus
function .
Epidemiology
40% cases asymptomatic It is the 12th leading cause of death in United
States.
Approximately 30,000 to 50,000 deaths per year
Additional 10,000 deaths due to liver cancer
secondary to cirrhosis
Etiology of Cirrhosis
Alcoholic liver disease Viral hepatitis Billiary disease Primary hemochromatosis Cryptogrnis cirrhosis Wilsons alfa 1AT def
Pathogenesis
Ethyal alcohol is a common cause of acute/chronic liver disease Patterns of alcoholic liver disease : 1. fatty change 2. Acute hepatitis 3. Chronic hepatitis with fibrosis 4. Cirrhosis, chronic liver failure All reversible except cirrhosis stage
Lab
Imaging
Ultrasonogram examination
- Liver may show coarse ecotexture - Dilated portal veins - Splenomegaly - Ascites CT SCAN may show hepatosplenomegaly and dilated collaterals are seen in chronic liver disease Upper GI Endoscopy : oesophageal varices may seen LIVER BIOPSY IS CONFIRMATORY
Complications
Portal hypertension and esophageal varices
Peripheral edema and ascites Hepatic encephalopathy Fetor hepaticus
complications
Ascites - Treatment
Small amounts of ascites dietary sodium
restriction ( <2g/day ) Moderate : diuretic is essential Spiranolactone 100-200 mg/day OD Furosemide 40-80 mg/day - if peripheral edema + Pt is compliant but ascitic fluid + , then Spiranolactone 400 -600 mg/day Furosemide 120-160 mg/day If ascites still + , then it is REFRACTORY ASCITES
Ascites - treatment
Refractory ascites Large volume paracentesis
TIPS Liver Transplantation Prognosis pts of cirrhosis with ascites- poor <50 % of pts survive 2 yrs after the onset of ascites.
abdominal pain/discomfort Treatment : cephalosporins In pts with an episode(s) of SBP and recovered , once weekly- administration of antibiotic as prophylactic measure
Hepatorenal Syndrome
Functional renal failure without renal pathology 10% of pts with cirrhosis / advanced liver failure Diagnosis : presence of large amount of ascites
progressive rise in creatinine urinary sodium <10 mEq Type 1 HRS : progressive impairment of renal function & significant reduction in creatinine clearance within 1- 2 wks . BAD PROGNOSIS Type 2 HRS : reduction in GFR, with rise in S.Creat BETTER PROGNOSIS
Hepatorenal Syndrome
Seen in refractory ascites
HEPATIC ENCEPHALOPATHY
TreatmentCORRECT/ AVOID PRECIPITATING
FACTORS
Dietary protein restriction-30 - 40 gm protein / day Non absorbable disaccharide LACTULOSE 15 to 45
ml BID / QID
Lactulose enema
HEPATOPULMONARY SYNDROME
Clubbing, cyanosis, spider nevi, orthodeoxia Hypoxia in standing position-ORTHODEOXIA Hypoxia is due to intrapulmonary shunting through direct arteriovenous communications Intra Pulmonary Vascular dilatation in the absence of intrinsic cardio pulmonary disease Resistant hypoxaemia (PaO2 < 9.3 kPa or 70 mmHg), intrapulmonary vascular dilatation and chronic liver disease with portal hypertension Treatment : liver transplantation
Classification Points
2 3
Encephalopathy
Ascites Bilirubin (mg/dl)
None
Absent <2 (4) >3.5 1-4
Grade I & II
Slight-moderate 2-3 (4-10) 2.8-3.5 4-6
Albumin (g/dl)
Prothrombin Time
Grade A
5-6
Grade B
Grade C
7-9
10-15
THANK YOU