GI: Liver

 

Acute liver failure
Causes
·
Drugs
(Acetaminophen)
·
Viruses
·
Ischemia (Shock)
·
Autoimmune
·
Infiltrative
S/S
·
Acute onset of
liver sx
·
Kidney injury
Dx
Requirements:
1.
Sky high AST/ALT
(>1000)
2.
Encephalopathy
(confusion)
3.
Liver Synthetic
failure (INR
🆎)
Tx
Only definitive therapy is transplant
Cirrhosis
Cirrhosis
?
Irreversible liver damage resulting in fibrosis
S/S
·
Fatigue, Hepatic
Encephalopathy
·
Cirrhosis
Stigmata
Dx
Clx → LFT
Tx

 

·
Serial US every 6
months
Tx
Ascites
⤵️
Spironolactone
and other diuretics.
Serial paracenteses for large-
volume ascites.
Coagulopathy
⤵️ PLT
FFP and/platelets only
if bleeding occurs
Encephalopathy
Lactulose and rifaximin
Varices
Propranolol
and banding via endoscopy
Hepatorenal
syndrome
Somatostatin
(octreotide), midodrine
Ascites
Dx
·
Imaging:
US or CT
·
Most important: Paracentesis.
Indications:
·
New onset ascites
·
Ascites → fever,
tenderness (SBP)
·
AMS
·
vitally unstable
(
⤵️
HR,
⤵️
BP..)
Ascites fluid characteristics
Color
·
Bloody: Trauma, malignancy, TB (rarely)
·
Milky: Chylous, pancreatic
·
Turbid: Possible infection
·
Straw color: Likely more benign causes
·
<250: No peritonitis
·
≥250: Peritonitis (secondary or
spontaneous bacterial)
Total Protein
2.5 g/dL (high-protein ascites)
·
CHF, constrictive pericarditis, TB,
Budd-Chiari, fungal (coccidioidomycosis)
<2.5 g/dL (low-protein ascites)
·
Cirrhosis, nephrotic syndrome
SAAG
≥1.1 (indicates portal HTN)
·
Cardiac ascites, cirrhosis, Budd-Chiari
syndrome
<1.1 (no portal HTN)
·
TB, peritoneal cancer, pancreatic ascites,
nephrotic
Common causes of Ascites
Extraperitoneal
• Cirrhosis
• Acute liver failure
• Alcoholic hepatitis
• Budd-Chiari syndrome
• Heart failure
• Hypoalbuminemia
• Malnutrition
• Nephrotic syndrome
Peritoneal
• Malignancy (ovarian, pancreatic)
• Infection (tuberculosis, fungal)
Hepatic Encephalopathy
Make it worse
·
Drugs
·
Hypovolemia (eg,
diarrhea)
·
Electrolyte
(Hypokalemia)
·
⤴️ Nitrogen load
(Gl bleeding)
·
Infection (eg,
pneumonia, UTI, SBP)
·
Portosystemic
shunting (TIPS)
Clx
(AMS / Ataxia / Asterixis)
Tx
·
Correct U/C
(Fluids, antibiotics, electrolytes)
·
⤵️  Blood ammonia concentration (Lactulose,
rifaximin)
SBP
S/S
·
T: ≥37.8
·
Abdominal
pain/tenderness
·
AMS (abnormal
connect-the-numbers test)
·
Hypotension,
hypothermia,
·
paralytic ileus
with severe infection (seen on X-ray as air)
Dx
by
TAP
·
PMNs >250
·
culture, often
gram e organisms
·
Protein <1
·
SAAG ≥1.1
(Indicate Portal HTN)
Tx
Empiric Abx – 30 generation cephalosporins (eg,
cefotaxime)
Fluoroquinolones for SBP prophylaxis
How to ddx from 2˚ Peritonitis (caused by infxn
from a treatable surgical cause — perforation)? TAP.
Solid liver masses
Focal nodular hyperplasia
·
Associated with
anomalous arteries
·
Arterial flow
& central scar on imaging
Hepatic adenoma
·
👩🏻
+ OCPs
·
Possible
hemorrhage or malignant transformation
Regenerative nodules
Acute or chronic liver injury (eg, cirrhosis)
Hepatocellular carcinoma
·
Systemic Sx
·
Chronic hepatitis
or cirrhosis
·
⤴️
alpha-fetoprotein
Liver metastasis
·
Single/multiple
lesions
·
Known
extrahepatic malignancy
Hepatic Adenoma
Features
·
Benign epithelial
liver tumor
·
Primarily young
women
👩🏻
on OCPs
S/S
·
Often Asx
(incidentally found)
·
Episodic RUQ pain
Imaging
·
Solitary,
solid lesion in right lobe of liver
·
Multiple lesions
occasionally occur
Tx
·
Asx & <5
cm – stop oral contraception
·
Sx or >5 cm –
surgical resection
Comp
·
Malignant
transformation (10%)
·
Rupture &
hemorrhage shock
Ascites fluid characteristics
Color
·
Bloody:
Trauma, malignancy, TB (rarely)
·
Milky:
Chylous, pancreatic
·
Turbid:
Possible infection
·
Straw
color
: Likely more benign causes
·
<250:
No peritonitis
·
≥250:
Peritonitis (secondary or spontaneous bacterial)
Total Protein
2.5 g/dL (high-protein ascites)
·
CHF, constrictive
pericarditis, TB, Budd-Chiari, fungal (coccidioidomycosis)
<2.5 g/dL (low-protein ascites)
·
Cirrhosis,
nephrotic syndrome
SAAG
≥1.1 (indicates portal HTN)
·
Cardiac ascites,
cirrhosis, Budd-Chiari syndrome
<1.1 (no portal HTN)
·
TB, peritoneal
cancer, pancreatic ascites, nephrotic
Hereditary Hemochromatosis
Skin
Bronze (bronze diabetes)
MSK
Joint / Chondrocalcinosis
GI

LFT / Cirrhosis (Late)
HCC
Endo
DM, 2˚ hypogonadism & hypothyroidism
Cardio
Restrictive or dilated cardiomyopathy
Infections
·
Listeria,
·
Vibrio vulnificus
&
·
Yersinia
enterocolitica
Hepatorenal Syndrome
RF
Advanced cirrhosis with portal hypertension
& edema
Precepitators
·
⤵️ Renal perfusion
·
Gl bleed,
vomiting, sepsis, excessive diuretic use, SBP
·
⤵️ Glomerular
pressure & GFR NSAID
(constricts afferent arterioles)
Dx
·
Renal
hypoperfusion
·
FeNa <1% (or
urine Na <1)
·
Absence of
tubular injury
·
No RBC, protein,
or granular casts in urine
·
No improvement in
renal function with fluids
Tx
·
Address
precipitating factors (Hypovolemia, anemia, infection)
·
Splanchnic vasoconstrictors
(midodrine, octreotide, norepinephrine)
·
Liver
transplantation
Acute Liver Failure
Causes
·
Viral hepatitis
·
Drugs
(Acetaminophen overdose)
·
Ischemia (Shhock
liver, Budd-Chiari)
·
Autoimmune
·
Wilson disease
·
Malignant
infiltration
Clx
·
Generalized Sx
(fatigue, lethargy, anorexia, nausea)
·
RUQ abdominal
pain
·
Pruritus &
jaundice due to hyperbilirubinemia
·
Renal
insufficiency
·
⤵️ PLTs
·
⤵️ Glu
Dx Req
·
Severe acute
liver injury (ALT & AST <1000)
·
Signs of hepatic encephalopathy
(Confusion, asterixis)
·
Synthetic liver
dysfunction (INR ≥1.5)
Carcinoid Syndrome
Clx
·
Skin:
flushing, telangiectasias, cyanosis
·
GI: diarrhea,
cramping
·
Cardiac: valvular
lesions (right > left side)
·
Pulmonary:
bronchospasm
·
Miscellaneous:
Niacin deficiency (dermatitis, diarrhea & dementia)
Dx
·
⤴️ 24-hour urinary
excretion of 5-HIAA
·
CT/MRI of abdomen
& pelvis to localize tumor
·
OctreoScan to
detect metastases
·
Echo (if sx of
carcinoid heart disease are
)
Tx
·
Octreotide for sx
pts
·
Surgery for liver
metastases
Alcoholic Hepatitis
Clx
·
Jaundice,
anorexia, fever
·
RUQ pain
·
Abdominal
distension
·
Proximal muscle
weakness from muscle wasting (if malnourished)
·
Hepatic
encephalopathy
Dx
·
Elevated AST
& ALT, usually <300
·
AST:ALT ≥2
·
⤴️ GGT  bilirubin, INR
·
⤴️ WBCs (mainly
neutrophils)
·
⤵️ albumin if
malnourished
·
Abdominal imaging
may show fatty liver
Nonalcoholic fatty liver disease
?
·
Hepatic steatosis
on imaging or biopsy
·
Exclusion of
significant alcohol use
·
Exclusion of
other causes of fatty liver
S/S
·
Mostly Asx
·
Metabolic
syndrome
·
± Steatohepatitis
(AST/ALT ratio <1)
·
Hyperechoic
texture on US
Tx
·
Diet &
exercise
·
Consider
bariatric surgery if BMI ≥35
Wilson disease
Path
·
AR
·
ATP7B
·
Hepatic copper
accumulation → leak from damaged hepatocytes → deposits in tissues (basal
ganglia, cornea)
Clx
·
Hepatic (acute
liver failure, chronic hepatitis, cirrhosis)
·
Neurologic
(parkinsonism, gait disturbance, dysarthria)
·
Psychiatric
(depression, personality changes, psychosis)
Dx
·
⤵️ Ceruloplasmin
&
⤴️
urinary copper excretion
·
Kayser-FIeischer
rings
·
⤴️
Copper content on liver bx
Tx
·
Chelators
(D-penicillamine, trientine)
·
Zinc (interferes
with copper absorption)
Budd-Chiari Syndrome
Features
Hepatic venous outflow obstruction
Usually due to:
·
Myeloproliferative
disorder (PV)
·
Malignancy (HCC)
·
Oral
contraception use/pregnancy
S/S
Acute
·
Jaundice, hepatic
encephalopathy, variceal bleeding
·
Prolonged
INR/PTT;
⤴️
transaminases
Subacute/chronic
·
Vague,
progressive abdominal pain
·
Hepatomegaly,
splenomegaly,
ascites
·
Mild/moderate ⤴️
in bilirubin, transaminases
Dx
·
Abdominal Doppler
US –
⤵️  hepatic vein flow
·
Investigation for
underlying disorders (JAK2 testing for PV)

 

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