A CASE OF LIVER CIRRHOSIS & HEPATIC ENCEPHALOPATHY



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A CASE OF LIVER CIRRHOSIS & HEPATIC ENCEPHALOPATHY 2 1

Mr N.N. 56 yr old male. Admitted on 22/03/02. 1 month Hx of abdominal distention, confusion, inability to concentrate and dyspnoea Grade 111. Pmx: Diagnosed with alcohol- induced liver cirrhosis in Jan 2000 and defaulted Rx since August 2000. Social Hx: Excessive alcohol use for approx. 20 yrs. 2 2

On Examination Bp 130/70 Pulse 80 Apyrexial Jaundice, Clubbing,Foetor hepaticus present. No circulatory changes - palmer erythema, spider telangiectasia, cyanosis. No endocrine changes - gynecomastia, testicular atrophy. No bleeding tendency- bruises, purpura, epistaxis. 2 3

ABDOMEN: abdominal distention. marked ascites present. unable to detect visceromegaly. CVS: N S1 + S2 Not in CCF. CHEST: bibasal creps. NEURO: Apathetic, confused, disorientated, drowsy,slurred speech. Flapping tremor present. 2 4

INVESTIGATIONS FBC: Hb11.7L/Hct32.1L/MCV104.9H/MCH38.1 PLT263/WBC7.4/ I.N.R. 2.2 U&E: 125/4.8/97/20/8.8/257 GLUCOSE:3.9 LFT:ALP220/TBIL65/TP80/ALB25L/GGT137H/ALT21 Ascitic tap: results unavailable Ultrasound Abdomen: Margins are mildly nodular. Texture non-homogenous and coarse. No obvious focal lesions. Portal vein not dilated - 13.2mm. Features suggestive of cirrhosis. Ascites present. 2 5 Liver Bx not done.

DIAGNOSIS 1. Liver cirrhosis. COMPLICATIONS 1. Hepatic encephalopathy( grade 3). 2. Macrocytic anaemia. 3. Coagulation defect. 2 6

TREATMENT Furosemide 80mg tds ivi. Aldactone 100mg bd po. Thiamine 100mg dly po. Vit B12 1000µg dly imi. Pregamal 1 b.d po Vit K 10mg dly imi. Lactulose 30ml bd po. Flagyl 400mg tds po. Despite the above mentioned treatment the patient demised on the 25/03/02 2 7

ALCOHOLIC CIRRHOSIS Alcoholic cirrhosis is only one of many consequences resulting from chronic alcohol ingestion and often accompanies other forms of alcohol-induced liver injury,including alcoholic fatty liver and alcoholic hepatitis. Etiology Quantity and duration of alcohol intake are the most important risk factors involved in the development of alcoholic liver disease. Threshold for developing severe alcoholic liver disease in men is an intake of 60-80g/d of alcohol for 10 yrs; women by consuming 20-40g/day. 2 8

Concomitant chronic Hepatitis C virus infection accelerates development of alcoholic cirrhosis. Pathology This is usually, initially micronodular often with active inflammation in fibrous septae and marked peri-cellular fibrosis, and later becomes macronodular. Investigations Biochemical investigations are used to assess the severity and activity of the disease. Plasma transaminases reflect the activity of the disease which is usuallly low in established cirrhosis. 2 9

Plasma ALP reflects the severity of cholestasis and is highest in biliary forms of cirrhosis. Plasma bilirubin, albumin, the Vit K corrected prothrombin reflect the severity of liver damage. Imaging is required for assessing the structural effects of the disease. Liver biopsy establishes the diagnosis of cirrhosis. STAGING OF LIVER CIRRHOSIS A reliable staging system is the modified Child- Pugh classification with a scoring system of 5-15. Class A : 5-6 Class B : 7-9 2 10

Class C : 10-15 It is used to assess prognosis in cirrhosis and provides the standard criteria for liver transplantation (class B). 2 11

CHILD-PUGH CLASSIFICATION OF CIRRHOSIS FACTOR 1 2 3 Serum bilirubin (µmol/l) Serum albumin (g/l) <34 34-51 >51 >35 30-35 <30 Ascites Neurologic disorder none Easily controlled none minimal Poorly controlled Advanced coma Prothrombin 0-4 4-6 >6 time Or (INR) <1.7 1.7-2.3 >2.3 2 12

COMPLICATIONS Portal Hypertension Ascites Hepatic encephalopathy Renal failure Infection Hepatocellular carcinoma MANAGEMENT No treatment can reverse cirrhosis or prevent further progression. Medical therapy can promote improved general health and alleviate symptoms. 2 13

Specific treatment is directed at particular complications. Ascites : Restriction of Sodium intake. Spironolactone (100-400 mg/d) is the drug. of choice for long-term therapy because it is a.. powerful aldosterone antagonist. Paracentesis of 3-5L over 1-2 hrs. Nutrition - In the absence of hepatic encephalopathy or ascites, a high energy, protein-rich diet should be advised with strict avoidance of alcohol. 2 14

HEPATIC ENCEPHALOPATHY Hepatic encephalopathy is a complex neuropsychiatric syndrome characterized by disturbances in consciousness and behaviour, personality changes, fluctuating neurologic signs, asterixis and distinctive EEG changes. Encephalopathy may be acute and reversible or chronic and progressive. In severe cases, irreversible coma and death may occur. 2 15

Pathogenesis The most important factors in the pathogenesis are severe hepatocellular dysfunction and/or intrahepatic and extrahepatic shunting of blood into the systemic circulation so that the liver is largely bypassed. Various toxic substances absorbed by the intestine are not detoxified by the liver and lead to metabolic abnormalities in the CNS. Ammonia is the substance most often incriminated in the pathogenesis of encephalopathy.others include mercaptans, short- chain fatty acids and phenols. 2 16

Clinical Stages of Hepatic Encephalopathy Stages Mental Status Asterixis EEG i ii iii iv Euphoria or depression, mild confusion, slurred speech, disordered sleep Lethargy, moderate confusion Marked Confusion, incoherent speech, sleeping but arousable Coma, initially responsive to noxious stimuli, later unresponsive +/- Triphasic waves + Triphasic waves + Triphasic waves - Delta activity 2 17

Factors precipitating hepatic encephalopathy Uraemia Drugs- sedatives, anti-depressants, hypnotics Git bleeding Excess dietary protein Constipation Paracentesis (>3-5l) Hypokalemia Infection Trauma Portasystemic shunts 2 18

Treatment Dietary protein reduced <20g/d. Lactulose diminishes ammonia absorption and production. Intestinal ammonia production by bacteria can be decreased by by neomycin (0.5-1g 6hrly). Metronidazole can also be used. Levodopa,bromocriptine and I.V. amino-acid formulations are of unproven benefit. Haemoperfusion and extracorporeal liver assist devices are also of unproven value. 2 19

Initial Evaluation: - Exclude other causes of disordered mentation - Identify precipitants and correct - Determine electrolytes, Blood Urea Nitrogen, creatinine, NH3(optional), glucose Protein Restriction Laxative, e.g.. Lactulose 30-120 ml, 1 to 4 times daily until 4 stools/day Inadequate response? Broad-spectrum antibiotics (eg., neomycin 500-100 mg qid, or metronidazole 250 mg tid) Inadequate response? Consider liver 2transplantation 20

THE END 2 21