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Chronic Liver Disease/Cirrhosis

Chronic liver disease (CLD) is characterised by a diffuse, progressive fibrosis and structural abnormality of the liver. The end-stage of it is called Cirrhosis. The most common cause of it is Alcohol, Hepatitis B and C, and NAFLD. Other causes include:

  • Autoimmune

  • Drugs e.g. amiodarone, methotrexate

  • Genetics e.g. a1 anti-trypsin deficiency, haemochromatosis, wilson disease

Some of the stages of liver damage following steatosis - NIDDK

Compensated cirrhosis - Where sufficient liver function remains to keep the patient systemically well. Typically presents with:

  • Fatigue and poor appetite

  • Clubbing

  • Mild RUQ pain/discomfort

  • Spider naevi

  • Gynaecomastia

  • Caput medusa


Decompensated cirrhosis - Typically presents with:

  • Jaundice

  • Portal hypertension

    • Ascites

    • Encephalopathy (drowsiness, liver flap, hyperventilation)

    • Varices

  • Palmar erythema

  • Easy bruising

*References down below*

Complications:

  • Ascites - This is due to portal hypertension and hypoalbuminaemia

  • Portal hypertension - Leads to oesophageal varices and haemarrhoids

  • Spontaneous bacterial peritonitis (SBP) - This occurs in patients with ascites and often atypically presents with no abdominal tenderness/guarding. It should be suspected in any patient who deteriorates suddenly with no other obvious cause.

    • It's most common caustive organisms are E.coli and Klebsiella

    • Needs to be investigated with an ascitic tap, which will show neutrophils > 250mm³

  • Liver failure - Presents with hepatic encephalopathy and coagulopathy


Investigations:

  • Bloods - FBC, U&E, LFT, INR, Albumin, AFP (cancer marker)

  • Ascitic tap if appropriate (check for SBP)

  • FibroScan and USS

  • Liver biopsy


N.B. PT/INR is the best test to demonstrate the synthetic function of the liver.


Management:

The most important aspect when managing these patients is that they have total alcohol abstinence and good nutrition.


Management of complications:

  • Ascites - Fluid restriction +/- low-salt diet, or spironolactone (furosemide can be added if no improvement)

  • Encephalopathy - Prophylactic lactulose and rifaximin

  • SBP - Prophylactic Abx if high risk


Definitive treatment is with a liver transplant.


Important Links:

https://cks.nice.org.uk/topics/cirrhosis/

https://bestpractice.bmj.com/topics/en-gb/278

Palmar erythema © Jmarchn (Licensed under CC-BY 3.0) https://creativecommons.org/licenses/by/3.0/

"A person with massive ascites caused by portal hypertension due to cirrhosis" © James Heilman (Licensed under CC-BY 3.0) https://creativecommons.org/licenses/by/3.0/

“Clubbing fingers” © Wesalius (Licensed under CC-BY 4.0) https://creativecommons.org/licenses/by/4.0/

Gigantic cutaneous arterial spiders © Herbert L. Fred, MD and Hendrik A. van Dijk (Licensed under CC-BY 2.0) https://creativecommons.org/licenses/by/2.0/

"Torso of a male with very severe gynecomastia" © (Licensed under CC-BY 3.0) https://creativecommons.org/licenses/by/3.0/


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