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Complications of Cirrhosis
Table 302 -1 Causes of Cirrhosis Alcoholism Cardiac cirrhosis Chronic viral hepatitis Inherited metabolic liver disease    Hepatitis B    Hemochromatosis    Hepatitis C    Wilson's disease  Autoimmune hepatitis           1  Antitrypsin deficiency    Nonalcoholic steatohepatitis    Cystic fibrosis Biliary cirrhosis Cryptogenic cirrhosis     Primary biliary cirrhosis      Primary sclerosing cholangitis       Autoimmune cholangiopathy  
Table 302-2  Complications of Cirrhosis Portal hypertension Coagulopathy    Gastroesophageal varices    Factor deficiency    Portal hypertensive gastropathy    Fibrinolysis    Splenomegaly, hypersplenism    Thrombocytopenia    Ascites Bone disease       Spontaneous bacterial peritonitis     Osteopenia Hepatorenal syndrome    Osteoporosis    Type 1    Osteomalacia    Type 2 Hematologic abnormalities Hepatic encephalopathy    Anemia Hepatopulmonary syndrome    Hemolysis Portopulmonary hypertension    Thrombocytopenia Malnutrition    Neutropenia
Portal hypertension ,[object Object],[object Object]
Table 302 -3 Classification of Portal Hypertension Pre-hepatic    Portal vein thrombosis    Splenic vein thrombosis    Massive splenomegaly (Banti's syndrome) Hepatic    Presinusoidal      Schistosomiasis      Congenital hepatic fibrosis    Sinusoidal      Cirrhosis—many causes      Alcoholic hepatitis    Postsinusoidal       Hepatic sinusoidal obstruction (venoocclusive syndrome) Posthepatic    Budd-Chiari syndrome    Inferior vena caval webs    Cardiac causes      Restrictive cardiomyopathy      Constrictive pericarditis      Severe congestive heart failure
Clinical features ,[object Object],[object Object],[object Object]
Gastroesophageal Varices ,[object Object],[object Object],[object Object],[object Object],[object Object]
Treatment ,[object Object],[object Object],[object Object],[object Object]
 
TIPS ,[object Object],[object Object],[object Object],[object Object]
Table 302-2 Complications of Cirrhosis Portal hypertension Coagulopathy    Gastroesophageal varices    Factor deficiency    Portal hypertensive gastropathy    Fibrinolysis    Splenomegaly, hypersplenism    Thrombocytopenia    Ascites Bone disease       Spontaneous bacterial peritonitis     Osteopenia Hepatorenal syndrome    Osteoporosis    Type 1    Osteomalacia    Type 2 Hematologic abnormalities Hepatic encephalopathy    Anemia Hepatopulmonary syndrome    Hemolysis Portopulmonary hypertension    Thrombocytopenia Malnutrition    Neutropenia
Ascites
Clinical History ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Physical Examination ,[object Object],[object Object],[object Object],[object Object],[object Object]
Ascites ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Etiologies ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
Table 44-1 Characteristics of Ascitic Fluid in Various Disease States  Condition Gross Appearance Protein, g/L Serum-Ascites Albumin Gradient, g/dL Cell Count Other Tests Red Blood Cells, >10,000/       L White Blood Cells, per       L Cirrhosis Straw-colored or bile-stained <25 (95%) >1.1 1% <250 (90%) a ; predominantly mesothelial     Neoplasm Straw-colored, hemorrhagic, mucinous, or chylous >25 (75%) <1.1 20% >1000 (50%); variable cell types Cytology, cell block, peritoneal biopsy Tuberculous peritonitis  Clear, turbid, hemorrhagic, chylous >25 (50%) <1.1 7% >1000 (70%); usually >70% lymphocytes Peritoneal biopsy, stain and culture for acid-fast bacilli Pyogenic peritonitis Turbid or purulent  If purulent, >25 <1.1 Unusual Predominantly polymorphonuclear leukocytes Positive Gram's stain, culture  Congestive heart failure  Straw-colored Variable, 15–53 >1.1 10% <1000 (90%); usually mesothelial, mononuclear   Nephrosis Straw-colored or chylous <25 (100%) <1.1 Unusual <250; mesothelial, mononuclear If chylous, ether extraction, Sudan staining Pancreatic ascites (pancreatitis, pseudocyst) Turbid, hemorrhagic, or chylous Variable, often >25 <1.1 Variable, may be blood-stained Variable Increased amylase in ascitic fluid and serum
Ascitic fluid analysis ,[object Object],[object Object]
Radiographic Exams  ,[object Object],[object Object]
Table 44-1 Characteristics of Ascitic Fluid in Various Disease States  Condition Gross Appearance Protein, g/L Serum-Ascites Albumin Gradient, g/dL Cell Count Other Tests Red Blood Cells, >10,000/       L White Blood Cells, per       L Cirrhosis Straw-colored or bile-stained <25 (95%) >1.1 1% <250 (90%) a ; predominantly mesothelial     Neoplasm Straw-colored, hemorrhagic, mucinous, or chylous >25 (75%) <1.1 20% >1000 (50%); variable cell types Cytology, cell block, peritoneal biopsy Tuberculous peritonitis  Clear, turbid, hemorrhagic, chylous >25 (50%) <1.1 7% >1000 (70%); usually >70% lymphocytes Peritoneal biopsy, stain and culture for acid-fast bacilli Pyogenic peritonitis Turbid or purulent  If purulent, >25 <1.1 Unusual Predominantly polymorphonuclear leukocytes Positive Gram's stain, culture  Congestive heart failure  Straw-colored Variable, 15–53 >1.1 10% <1000 (90%); usually mesothelial, mononuclear   Nephrosis Straw-colored or chylous <25 (100%) <1.1 Unusual <250; mesothelial, mononuclear If chylous, ether extraction, Sudan staining Pancreatic ascites (pancreatitis, pseudocyst) Turbid, hemorrhagic, or chylous Variable, often >25 <1.1 Variable, may be blood-stained Variable Increased amylase in ascitic fluid and serum
Treatment ,[object Object],[object Object],[object Object]
 
Spontaneous bacterial peritonitis ,[object Object],[object Object],[object Object],[object Object],[object Object]
Hepatorenal Syndrome ,[object Object],[object Object],[object Object],[object Object]
HRS ,[object Object],[object Object],[object Object]
Hepatic Encephalopathy ,[object Object],[object Object],[object Object],[object Object],[object Object]
Precipitating factors ,[object Object],[object Object],[object Object],[object Object],[object Object]
Treatment ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Malnutrition ,[object Object],[object Object],[object Object]
Coagulation abnormalities ,[object Object],[object Object],[object Object],[object Object]
Hematologic Abnormalities ,[object Object],[object Object],[object Object]

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Complications of cirrhosis

  • 2. Table 302 -1 Causes of Cirrhosis Alcoholism Cardiac cirrhosis Chronic viral hepatitis Inherited metabolic liver disease    Hepatitis B    Hemochromatosis    Hepatitis C    Wilson's disease Autoimmune hepatitis          1 Antitrypsin deficiency   Nonalcoholic steatohepatitis    Cystic fibrosis Biliary cirrhosis Cryptogenic cirrhosis    Primary biliary cirrhosis      Primary sclerosing cholangitis      Autoimmune cholangiopathy  
  • 3. Table 302-2 Complications of Cirrhosis Portal hypertension Coagulopathy    Gastroesophageal varices    Factor deficiency    Portal hypertensive gastropathy    Fibrinolysis    Splenomegaly, hypersplenism    Thrombocytopenia    Ascites Bone disease      Spontaneous bacterial peritonitis    Osteopenia Hepatorenal syndrome    Osteoporosis    Type 1    Osteomalacia    Type 2 Hematologic abnormalities Hepatic encephalopathy    Anemia Hepatopulmonary syndrome    Hemolysis Portopulmonary hypertension    Thrombocytopenia Malnutrition    Neutropenia
  • 4.
  • 5. Table 302 -3 Classification of Portal Hypertension Pre-hepatic    Portal vein thrombosis    Splenic vein thrombosis    Massive splenomegaly (Banti's syndrome) Hepatic    Presinusoidal      Schistosomiasis      Congenital hepatic fibrosis    Sinusoidal      Cirrhosis—many causes      Alcoholic hepatitis    Postsinusoidal      Hepatic sinusoidal obstruction (venoocclusive syndrome) Posthepatic    Budd-Chiari syndrome    Inferior vena caval webs    Cardiac causes      Restrictive cardiomyopathy      Constrictive pericarditis      Severe congestive heart failure
  • 6.
  • 7.
  • 8.
  • 9.  
  • 10.
  • 11. Table 302-2 Complications of Cirrhosis Portal hypertension Coagulopathy    Gastroesophageal varices    Factor deficiency    Portal hypertensive gastropathy    Fibrinolysis    Splenomegaly, hypersplenism    Thrombocytopenia    Ascites Bone disease      Spontaneous bacterial peritonitis    Osteopenia Hepatorenal syndrome    Osteoporosis    Type 1    Osteomalacia    Type 2 Hematologic abnormalities Hepatic encephalopathy    Anemia Hepatopulmonary syndrome    Hemolysis Portopulmonary hypertension    Thrombocytopenia Malnutrition    Neutropenia
  • 13.
  • 14.
  • 15.
  • 16.
  • 17.  
  • 18. Table 44-1 Characteristics of Ascitic Fluid in Various Disease States Condition Gross Appearance Protein, g/L Serum-Ascites Albumin Gradient, g/dL Cell Count Other Tests Red Blood Cells, >10,000/      L White Blood Cells, per      L Cirrhosis Straw-colored or bile-stained <25 (95%) >1.1 1% <250 (90%) a ; predominantly mesothelial     Neoplasm Straw-colored, hemorrhagic, mucinous, or chylous >25 (75%) <1.1 20% >1000 (50%); variable cell types Cytology, cell block, peritoneal biopsy Tuberculous peritonitis Clear, turbid, hemorrhagic, chylous >25 (50%) <1.1 7% >1000 (70%); usually >70% lymphocytes Peritoneal biopsy, stain and culture for acid-fast bacilli Pyogenic peritonitis Turbid or purulent If purulent, >25 <1.1 Unusual Predominantly polymorphonuclear leukocytes Positive Gram's stain, culture Congestive heart failure Straw-colored Variable, 15–53 >1.1 10% <1000 (90%); usually mesothelial, mononuclear   Nephrosis Straw-colored or chylous <25 (100%) <1.1 Unusual <250; mesothelial, mononuclear If chylous, ether extraction, Sudan staining Pancreatic ascites (pancreatitis, pseudocyst) Turbid, hemorrhagic, or chylous Variable, often >25 <1.1 Variable, may be blood-stained Variable Increased amylase in ascitic fluid and serum
  • 19.
  • 20.
  • 21. Table 44-1 Characteristics of Ascitic Fluid in Various Disease States Condition Gross Appearance Protein, g/L Serum-Ascites Albumin Gradient, g/dL Cell Count Other Tests Red Blood Cells, >10,000/      L White Blood Cells, per      L Cirrhosis Straw-colored or bile-stained <25 (95%) >1.1 1% <250 (90%) a ; predominantly mesothelial     Neoplasm Straw-colored, hemorrhagic, mucinous, or chylous >25 (75%) <1.1 20% >1000 (50%); variable cell types Cytology, cell block, peritoneal biopsy Tuberculous peritonitis Clear, turbid, hemorrhagic, chylous >25 (50%) <1.1 7% >1000 (70%); usually >70% lymphocytes Peritoneal biopsy, stain and culture for acid-fast bacilli Pyogenic peritonitis Turbid or purulent If purulent, >25 <1.1 Unusual Predominantly polymorphonuclear leukocytes Positive Gram's stain, culture Congestive heart failure Straw-colored Variable, 15–53 >1.1 10% <1000 (90%); usually mesothelial, mononuclear   Nephrosis Straw-colored or chylous <25 (100%) <1.1 Unusual <250; mesothelial, mononuclear If chylous, ether extraction, Sudan staining Pancreatic ascites (pancreatitis, pseudocyst) Turbid, hemorrhagic, or chylous Variable, often >25 <1.1 Variable, may be blood-stained Variable Increased amylase in ascitic fluid and serum
  • 22.
  • 23.  
  • 24.
  • 25.
  • 26.
  • 27.
  • 28.
  • 29.
  • 30.
  • 31.
  • 32.