Cirrhosis: Difference between revisions
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− | == |
+ | == Background == |
* End-stage hepatic fibrosis with hepatic dysfunction |
* End-stage hepatic fibrosis with hepatic dysfunction |
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− | == Epidemiology == |
+ | === Epidemiology === |
* 25% of Canadians have NAFLD |
* 25% of Canadians have NAFLD |
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− | == Etiology == |
+ | === Etiology === |
* Infectious |
* Infectious |
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− | ** Chronic |
+ | ** Chronic [[hepatitis B]] |
− | ** '''Chronic |
+ | ** '''Chronic [[hepatitis C]]''' |
+ | **[[Brucellosis]], [[echinococcosis]], [[syphilis]] |
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− | * Toxin |
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+ | * Toxins and drugs |
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** '''Alcohol''' |
** '''Alcohol''' |
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+ | **Medications: [[isoniazid]], [[methotrexate]] |
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* Autoimmune/inflammatory |
* Autoimmune/inflammatory |
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− | ** Autoimmune hepatitis (AIH) |
+ | ** [[Autoimmune hepatitis]] (AIH) |
− | ** Primary biliary cirrhosis (PBC) |
+ | ** [[Primary biliary cirrhosis]] (PBC) |
+ | **[[Primary sclerosing cholangitis]] |
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+ | **[[Celiac disease]] |
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* Metabolic |
* Metabolic |
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− | ** '''NASH''' |
+ | ** '''[[NASH]]''' |
− | ** Wilson |
+ | ** [[Wilson disease]] |
+ | ** [[Hereditary hemochromatosis]] |
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− | ** Hemochromatosis |
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− | ** |
+ | ** [[α-1 antitrypsin deficiency]] |
+ | *Other |
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+ | **Right-sided [[heart failure]] |
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+ | **[[Veno-occlusive disease]] |
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+ | **[[Hereditary hemorrhagic telangiectasia]] |
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+ | **[[Polycystic liver disease]] |
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+ | **[[Granulomatous liver disease]] |
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== JAMA Rational Clinical Exam == |
== JAMA Rational Clinical Exam == |
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* Lab abnormalities in liver failure, in order: |
* Lab abnormalities in liver failure, in order: |
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− | * Decrease in platelets |
+ | ** Decrease in platelets |
− | * Increase in bilirubin |
+ | ** Increase in bilirubin |
− | * Decrease in albumin |
+ | ** Decrease in albumin |
− | * Increase in INR |
+ | ** Increase in INR |
+ | *Investigations for possible causes of cirrhosis include: |
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+ | **Liver ultrasound |
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+ | **Hepatitis B and C serologies |
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+ | **Ferritin and transferrin saturation, for [[hereditary hemochromatosis]] |
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+ | **Autoimmune serologies |
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+ | ***ANA and anti-smooth muscle antibodies, for [[PSC]] and [[AIH]] |
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+ | ***Anti-mitochondrial antibodies and anti-parietal cell antibodies, for [[PBC]] |
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+ | ***Consider anti-LKM-1, for [[PSC]] |
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+ | **Quantitative immunoglobulins, for elevated IgM in [[PBC]] or [[hypergammaglobulinemia]] in [[AIH]] |
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+ | **Consider serum ceruloplasmin, for [[Wilson disease]] |
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+ | **Consider α-1 antitripsyin levels, for deficiency |
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== Management == |
== Management == |
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* Decompensated |
* Decompensated |
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− | ** Rule out [[ |
+ | ** Rule out [[spontaneous bacterial peritonitis]] with every episode |
* Ascites |
* Ascites |
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** Furosemide 40 and spironolactone 100 (max 160/400) |
** Furosemide 40 and spironolactone 100 (max 160/400) |
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=== Preventative Care === |
=== Preventative Care === |
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− | * Avoid raw oysters (high risk of |
+ | * Avoid raw oysters (high risk of [[Vibrio vulnificus]] infection in cirrhosis) |
== Prognosis == |
== Prognosis == |
Latest revision as of 22:23, 26 November 2021
Background
- End-stage hepatic fibrosis with hepatic dysfunction
Epidemiology
- 25% of Canadians have NAFLD
Etiology
- Infectious
- Chronic hepatitis B
- Chronic hepatitis C
- Brucellosis, echinococcosis, syphilis
- Toxins and drugs
- Alcohol
- Medications: isoniazid, methotrexate
- Autoimmune/inflammatory
- Metabolic
- Other
JAMA Rational Clinical Exam
- Ascites (LR+ 7.2)
- Platelet count <160 (LR+ 6.3; LR- 0.29 if ≥160)
- Spider nevi (LR+ 4.3)
- Bonacini cirrhosis discriminant score >7 (LR+ 9.4)
- Lok index <0.2 (LR- 0.09)
- Absence of hepatomegaly (LR- 0.37)
Investigations
- Lab abnormalities in liver failure, in order:
- Decrease in platelets
- Increase in bilirubin
- Decrease in albumin
- Increase in INR
- Investigations for possible causes of cirrhosis include:
- Liver ultrasound
- Hepatitis B and C serologies
- Ferritin and transferrin saturation, for hereditary hemochromatosis
- Autoimmune serologies
- Quantitative immunoglobulins, for elevated IgM in PBC or hypergammaglobulinemia in AIH
- Consider serum ceruloplasmin, for Wilson disease
- Consider α-1 antitripsyin levels, for deficiency
Management
- Decompensated
- Rule out spontaneous bacterial peritonitis with every episode
- Ascites
- Furosemide 40 and spironolactone 100 (max 160/400)
- Serial therapeutic paracentesis
- Small-volume (<4-5L) does not need albumin
- Large-volume needs 6-8 g of 25% albumin per litre removed
- Avoid indwelling drain
- TIPS can be considered but precipitates encephalopathy
- Prophylaxis/chronic
- SBP: maybe?
- Encephalopathy: no role for primary prophylaxis
- Surveillance with upper endoscopy
- Ultrasound q6mo for HCC
Preventative Care
- Avoid raw oysters (high risk of Vibrio vulnificus infection in cirrhosis)
Prognosis
- Median survival 1.6 years after admission for decompensated cirrhosis