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CIRRHOSIS
AND ITS
COMPLICATIONS
Ujala Abdul Rashid
House Officer, MU-2
Presentation
Outline
What is
Cirrhosis
Causes of
Cirrhosis
Reaching a
Diagnosis
Staging the
Disease
Complications
Management
What is
Cirrhosis
• Defined histopathologically
• Development of fibrosis leading
to architectural distortion with
the formation of regenerative
nodules.
• This results in:
Decrease in cell mass, and
thus function
An alteration of blood flow
Causes of Cirrhosis
90%
40%
40-45%
40-45%
Alcoholic Cirrhosis
(Western Statistics)
Cirrhosis due to
Chronic hepatitis B or
C infection
Cirrhosis due to
Autoimmune hepatitis
and Non Alcoholic
Steatohepatitis
Others:
Biliary Cirrhosis
Cardiac Cirrhosis
Cryptogenic Cirrhosis
Cirrhosis due to
metabolic disorders
Reaching a
Diagnosis
Staging
History
Investigations
Physical
Examinati
on
History
Physical
Examination
Investigations
CBC:
Anemia.
Thrombocytopenia
LFTs:
Serum total bilirubin elevated with advanced disease
ALT, AST are elevated, A/G ratio is usually 2:1 ratio in severe heapatocellular damage
Elevated GGT and ALP (in cholestasis)
Albumin levels are decreased
Prothrombin times are prolonged
S/E:
Serum sodium levels are decreased if patient has ascites largely due to ingestion of excess free water.
Viral studies:
Auto immune markers:
Anti ANA, anti ASMA antibodies (AIH)
Anti mitochondrial antibodies (PBC)
P-ANCA (PSC)
Imaging Studies
Endoscopy
Iron studies and copper studies
Liver Biopsy: (most specific)
Micronodular cirrhosis: Alcoholic cirrhosis
Macronodular cirrhosis
Mixed pattern: Hepatitis C
Non invasive markers
Staging the
Disease
• Compensated cirrhosis
• Decompensated cirrhosis
•Portal hypertension leading to
ascities and bleeding from varices
•Portosystemic encephalopathy
Child Turcotte Pugh Classification:
Complications
• Complications due to
architectural damage
• Complications due to hepatic
dysfunction
Portal hypertension
• Gastroesophageal varices
• Portal hypertensive
gastropathy
• Splenomegaly, hypersplenism
• Ascities
• Spontaneous bacterial
peritonitis
Complications due
to hepatic
dysfunction:
• Hepatic encephalopathy
• Hepatorenal syndrome
• Hepatopulmonary
syndrome
• Malnutrition
• Coagulopathy
• Bone disease
• Hematologic abnormalities
Portopulmonary
hypertension
Complications due to
architectural damage:
Ascities:
 Clinical features:
Abdominal distension
 On Examination:
• Increase in abdominal girth
• Umbilicus everted/protruding
• Fluid thrill/ Shifting dullness
 Chemical Analysis:
• Clear, straw colored or light green
• Transudative and contains relatively less cells
• SAAG> 1.1 g/dl
• Low amylase and triglycerides
• Glucose: normal
• Abcence of malignant cells
 Management:
• Sodium restriction (100 mmol/24 hr) and water
restriction (1-1.5 L/24 hrs)
• Diuretics (spironolactone 100-400 mg/day or amiloride
5-10 mg)
• Paracentesis
• TIPSS
 Complications:
• Renal failure
• Hepatorenal syndrome
• Spontaneous bacterial peritonitis
Hepatic Encephalopathy:
 Clinical features:
• Changes of intellect, personality, emotions and consciousness with or without neurological signs
 On Examination:
• Flapping tremors
• Constructional apraxia
• Hyperreflexia with up going planters
• Fetor hepaticus
 Precipitating factors:
• Drugs
• Dehydration
• Infection
• Hypokalemia
• Constipation
• Portosystemic shunting
 Management:
• Treat and remove the precipitating cause
• Lactulose (15-30 ml TDS)
• Rifaximin (400 mg TDS)
• Liver transplant
Management:
Cause Management
Alcoholic cirrhosis Abstinence, glucocorticoids, pentoxyfylline
Cirrhosis due to viral hepatitis Anti viral agents (adefovir, lamivudine, interferon,
ribavirin)
Cirrhosis due to AIH and non alcoholic
steatohepatitis
Glucorticoids, immunosuppressive therapy, liver
transplant
Biliary cholangitis Ursodeoxycholic acid, obeticholic acid,
immunosuppressive agents
For pruritus: Antihistamines, naltrexone, rifampin or
cholestyramine, plasmaphoresis
For osteopenia: bisphosphonates
Endoscopic dilatation of strictures
Liver transplant
Cardiac cirrhosis Treatment of cardiac failure
Metabolic causes Regular therapeutic phlebotomy
Copper-chelating medications
Liver transplant
Cause Directed Management:
Thank You

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Cirrhosis and its complications

  • 1. CIRRHOSIS AND ITS COMPLICATIONS Ujala Abdul Rashid House Officer, MU-2
  • 2. Presentation Outline What is Cirrhosis Causes of Cirrhosis Reaching a Diagnosis Staging the Disease Complications Management
  • 3. What is Cirrhosis • Defined histopathologically • Development of fibrosis leading to architectural distortion with the formation of regenerative nodules. • This results in: Decrease in cell mass, and thus function An alteration of blood flow
  • 4. Causes of Cirrhosis 90% 40% 40-45% 40-45% Alcoholic Cirrhosis (Western Statistics) Cirrhosis due to Chronic hepatitis B or C infection Cirrhosis due to Autoimmune hepatitis and Non Alcoholic Steatohepatitis Others: Biliary Cirrhosis Cardiac Cirrhosis Cryptogenic Cirrhosis Cirrhosis due to metabolic disorders
  • 8. Investigations CBC: Anemia. Thrombocytopenia LFTs: Serum total bilirubin elevated with advanced disease ALT, AST are elevated, A/G ratio is usually 2:1 ratio in severe heapatocellular damage Elevated GGT and ALP (in cholestasis) Albumin levels are decreased Prothrombin times are prolonged S/E: Serum sodium levels are decreased if patient has ascites largely due to ingestion of excess free water. Viral studies: Auto immune markers: Anti ANA, anti ASMA antibodies (AIH) Anti mitochondrial antibodies (PBC) P-ANCA (PSC) Imaging Studies Endoscopy Iron studies and copper studies Liver Biopsy: (most specific) Micronodular cirrhosis: Alcoholic cirrhosis Macronodular cirrhosis Mixed pattern: Hepatitis C Non invasive markers
  • 9. Staging the Disease • Compensated cirrhosis • Decompensated cirrhosis •Portal hypertension leading to ascities and bleeding from varices •Portosystemic encephalopathy
  • 10. Child Turcotte Pugh Classification:
  • 11. Complications • Complications due to architectural damage • Complications due to hepatic dysfunction
  • 12. Portal hypertension • Gastroesophageal varices • Portal hypertensive gastropathy • Splenomegaly, hypersplenism • Ascities • Spontaneous bacterial peritonitis Complications due to hepatic dysfunction: • Hepatic encephalopathy • Hepatorenal syndrome • Hepatopulmonary syndrome • Malnutrition • Coagulopathy • Bone disease • Hematologic abnormalities Portopulmonary hypertension Complications due to architectural damage:
  • 13. Ascities:  Clinical features: Abdominal distension  On Examination: • Increase in abdominal girth • Umbilicus everted/protruding • Fluid thrill/ Shifting dullness  Chemical Analysis: • Clear, straw colored or light green • Transudative and contains relatively less cells • SAAG> 1.1 g/dl • Low amylase and triglycerides • Glucose: normal • Abcence of malignant cells  Management: • Sodium restriction (100 mmol/24 hr) and water restriction (1-1.5 L/24 hrs) • Diuretics (spironolactone 100-400 mg/day or amiloride 5-10 mg) • Paracentesis • TIPSS  Complications: • Renal failure • Hepatorenal syndrome • Spontaneous bacterial peritonitis
  • 14. Hepatic Encephalopathy:  Clinical features: • Changes of intellect, personality, emotions and consciousness with or without neurological signs  On Examination: • Flapping tremors • Constructional apraxia • Hyperreflexia with up going planters • Fetor hepaticus  Precipitating factors: • Drugs • Dehydration • Infection • Hypokalemia • Constipation • Portosystemic shunting  Management: • Treat and remove the precipitating cause • Lactulose (15-30 ml TDS) • Rifaximin (400 mg TDS) • Liver transplant
  • 16. Cause Management Alcoholic cirrhosis Abstinence, glucocorticoids, pentoxyfylline Cirrhosis due to viral hepatitis Anti viral agents (adefovir, lamivudine, interferon, ribavirin) Cirrhosis due to AIH and non alcoholic steatohepatitis Glucorticoids, immunosuppressive therapy, liver transplant Biliary cholangitis Ursodeoxycholic acid, obeticholic acid, immunosuppressive agents For pruritus: Antihistamines, naltrexone, rifampin or cholestyramine, plasmaphoresis For osteopenia: bisphosphonates Endoscopic dilatation of strictures Liver transplant Cardiac cirrhosis Treatment of cardiac failure Metabolic causes Regular therapeutic phlebotomy Copper-chelating medications Liver transplant Cause Directed Management:

Editor's Notes

  1. Anemia due to blood loss, nutritional deficiencies, or hypersplenism related to portal hypertension, or as a direct suppressive effect of alcohol on the bone marrow Hypersplenism Iaging: usg, cholangiography, mrcp, ercp, Alpha macroglobin, hepatoglobin