Chronic Liver Disease and Cirrhosis

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Introduction

Chronic liver disease is very common aorund the world and has many causes, including inflammatory, toxic, metabolic, and congestive liver problems. Cirrhosis is often the irreversible end result of chronic liver disease.

Cirrhosis may be asymptomatic, with incidental diagnosis following laboratory testing. In other patients, signs and symptoms that can bring it to attention include ascites, jaundice, and gastrointestinal bleeding.

 

 

 

The Case of Thomas R.

Thomas is a 68 year old man who recently retired as a truck driver. You know some of his lifestyle choices have been potentially dangerous, with unsafe sex, as well as alcohol and drug use. He comes to you because he has recently noticed his skin turning yellow, though he feels fine otherwise. Physical exam reveals, amongst other findings, a hard, nodular liver. You are of course concerned about the possibility of liver disease.

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Causes and Risk Factors

Chronic liver disease (occurring over 6 months) can be caused by many things, and it can be difficult to find the cause.

Chronic hepatitis follows acute hepatitis B in 5-10% of the time, and acute on chronic cases can occur.

Chronic hepatitis C occurs in up to 75% of people with infection.

Autoimmune liver disease most often occurs in young women and is characterized by many plasma cells, hypergammaglobulinemia, as well as anti-nuclear or anti-smooth muscle antibodies.

Nonalcoholic fatty liver disease most commonly occurs in people who are overweight, and have diabetes and hyperlipidemia.

drugs

  • alcohol
  • toxins
  • vitamin A
  • methotrexate

infections

  • hepatitis B
  • hepatitis C
  • schistosomiasis

 

 

fatty liver disease

  • obesity
  • T2DM
  • hyperlipidemia
  • total parental nutrition

 

other conditions

  • congestive heart failure
  • hemochromatosis
  • Wilson's disease
  • autoimmune diseases
  • sarcoidosis
  • Bud-Chiari syndrome
  • a1-AT deficiency
  • idiopathic

 

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Pathophysiology

Acute injury can lead to chronic inflammation and hepatocyte death, associated with lymphocyte infiltration and the development of fibrosis. Normal hepatocyte function is disturbed by resulting inadequacy of blood flow and ongoing inflammatory, toxic, and metabolic damage. Decreased cell numbers lead to reduced metabolic action on bilirubin and loss of synthetic function of proteins such as clotting factors and albumin. Decreased production of transaminases can result in normal or low values.

 

Disruption of normal architecture through fibrosis distorts the vasculature. Pressure increases and subsequent portal system hypertension leads to blood backup into veins in the esophagus, abdominal wall, and elsewhere. Spleen enlargement leads to platelet sequestration and thrombocytopenia.

 

Cirrhosis is characterized by deposition of interconnective bands of fibrous tissue which surround nodules of regenerating hepatocytes. The grade of injury is determined by the numbers and location of inflammatory cells, while the stage of disease depends on degree, location, and distortion caused by fibrosis. Small nodules <3mm are typical of alcoholic cirrhosis, while larger nodules follow chronic active hepatitis.

Hepatic encephalopathy is believed to result from substances produced by gut bacteria that are toxic to the brain. These include ammonia, mercaptans, phenols, and short-chain fatty acids. Normally these are metabolized by the liver following transport from the gut via the portal system, after which they are excreted. However, with advanced liver disease, both portal transport to the liver and hepatocyte metabolism may be compromised, resulting in entry into the circulation by these substances.

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Signs and Symptoms

Liver damage is most often silent until 75% of the liver function is lost. Cirrhosis too can be asymptomatic initially.

 

Decompensation results in ascites, jaundice, and encephalopathy.

 

Cirrhosis: fibrosis encircled with regenerative nodules.

Stages I-IV can be diagnosed histologically

Fatty liver disease can cause macrocytosis.

 

  • history
  • physical exam

History

anorexia

nausea

abdominal discomfort

itchiness

Autoimmune hepatitis can lead to amenorrhea, rashes, acne, vasculitis, thyroiditis, and Sjogren's syndrome.

Physical Exam

Findings of chronic liver disease include:

  • jaundice
  • splenomegaly
  • ascites (due to portal hypertension and transudation, hypoalbuminemia (low oncotic pressure)
  • dilated abdominal wall veins (Kaput medusa)
  • hemorrhoids
  • gynecomastia in men
  • spider nevi
  • palmar erythema, clubbing, leukonicia, Dupetreuyn's contractures
  • peripheral edema
  • asterixis: a problem with attention span: people lose focus on their hands, which then fall with gravity; people draw their hands back quickly.
  • scant body hair
  • hepatic encephalopathy: liver problems can affect neurotransmitters

Encephalopathy may be graded in a number of ways, one being the West Haven Criteria (Ferenci et al, 2002).

  • trivial lack of awareness; euphoria or anxiety; shortened attention span; impaired performance on basic math
  • lethargy, apathy; some disorientation; some personality change; innapropriate behaviour
  • somnolence, but responsive to verbal stimuli; confusion; significant disorientation
  • coma

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Investigations

  • lab investigations
  • diagnostic imaging
  • biopsy

Lab Investigations

Serum transaminases (ALT, AST) are typcially elevated over 10x, while serum alkaline phosphatase is less than 3x normal. However, if liver disease is significant, these markers may be normal.

Decreased synthetic function can lead to prolonged prothrombin time (INR), hypoalbuminemia, and unconjugated hyperbilirubinemia.

Thrombocytopenia and leucopenia can follow portal hypertension and splenic sequestration.

New-onset ascites may be evaluated by paracentesis, with cell count, protein count, albumin, and C&S. Paracentesis should also be performed in cases of encephalopathy.

Hepatocellular carcinoma screening using alpha-fetoprotein may be considered.

Diagnostic Imaging

Imaging

abnormal ECG

Liver ultrasound - can be used to detect gallbladder and bile duct disease, including stones.(Stones move; polyps do not)

Imaging such as ultrasound, CT, and MRI can be used to support the clinical diagnosis of cirrhosis.

Hepatocellular carcinoma should be considered for patients with cirrhosis. CT, ultrasound, and MRI may all be used.

Biopsy

Liver biopsy can be very important for diagnosis and is good for diffuse disease, but not as much for patchy conditions.

The diagnosis of chronic hepatitis requires the presence of inflammatory cells, which can be accompanied by significant fibrous deposition, disruption of hepatic lobular architecture, and possible progression towards cirrhosis.

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Differential Diagnosis

The differential for encephalopathy includes:

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Treatments

Management guidelines suggest that the best care is provided by a team approach of primary care provider and specialist(s).

Abstinence from alcohol is critical, especially if transplant is being considered.

Immunizations against hepatitis A and B should be offered as appropriate.

Ascites may be treated with salt restriction and dieuretics, including combination furosemide and spironolactone.

Spontaneous bacterial peritonitis should receive prompt antibiotics with cefotaxime or ciprofloxacin. Prophylaxis should be considered after resolution.

Encephalopathy should be treated first at the level of reversible causes. If this does not change the patient's status, dissarcharides such as lactulose may be used. These are believed to cause absorption of nitrogen by gut bacteria, reducing ammonia production. Antibiotics that remain in the gut such as rifaximin may also be used to reduce the gut load of bacteria.

Patients with encephalopathy should not drive.

Esophageal varices may be treated if identified via screening through beta blockade or endoscopic ligation. Frank bleeding should be treated with fluid recuscitation, somatostatin analogue, and endoscopy for ligation when stable. Surgical repair using the transjugular intrahepatic portsystemic shunt (TIPS) may be explored as a last resort.

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Consequences and Course

Compensated cirrhosis can lead to uncompensated cirrhosis, hepatocellular carcinoma, or death.

Fulminant liver failure is a serious result of acute liver damage.

Complications of cirrhosis include portal hypertension, hepatocellular dysfunction, and hepatocellular carcinoma.

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Resources and References

Canadian Liver Foundation

American Liver Foundation

Medline Plus resources on liver diseases

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Topic Development

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