Lecture 11 2/10/25 Flashcards

1
Q

What are the early, non-specific signs of liver disease?

A

-hyporexia
-vomiting
-lethargy
-weight loss
-diarrhea
-PU/PD

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2
Q

What are the late stage, more specific signs of liver disease?

A

-icterus
-hepatic encephalopathy
-hypoglycemia
-ascites
-bleeding tendencies

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3
Q

How does the development time of liver disease impact the clinical signs seen?

A

-chronic/slowly developing dz gives the liver time to adapt, which can reduce clinical sign severity
-acute/acute on chronic damage leaves no time for adaptation and can result in more severe clinical signs

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4
Q

What are the clinical signs of acute hepatopathy in dogs and cats?

A

-anorexia
-hepatic encephalopathy
-vomiting
-polydipsia
-dehydration
-jaundice
-fever
-cranial abdominal pain
-coagulopathy/petechiae/melena/hematemesis
-ascites
-splenomegaly
-acute kidney injury

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5
Q

What are the clinical signs of chronic hepatopathy in dogs and cats?

A

-vomiting and/or diarrhea
-hematemesis/melena
-inappetence
-weight loss
-PU/PD
-ascites
-jaundice
-hepatic encephalopathy
-bleeding tendencies

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6
Q

What is icterus?

A

yellow discoloration of tissues and body fluids secondary to hyperbilirubinemia and bile pigment deposition

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7
Q

Where are the most sensitive places to identify icterus?

A

-sclera
-conjunctiva
-soft palate
-below the tongue

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8
Q

What are the clin path findings in a patient with prehepatic/hemolytic icterus?

A

-moderate or marked decrease in hematocrit
-possible spherocytes
-possible auto-agglutination
-possible positive Coombs test
-possible hemoglobinemia and/or hemoglobinuria

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9
Q

What are the clin path findings in a patient with hepatic icterus?

A

-normal hematocrit or mildly decreased hematocrit
-high increases in ALT and AST
-increases in ALP and GGT
-decreases in albumin, cholesterol, glucose, and urea

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10
Q

What are the clin path findings in a patient with posthepatic icterus?

A

-normal hematocrit or mildly decreased hematocrit
-increases in ALT, AST, and cholesterol
-high increases in ALP and GGT
-WNL albumin, glucose, and urea

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11
Q

What is ascites?

A

accumulation of free fluid within the abdominal cavity

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12
Q

How is ascites detected?

A

-abdominal distention (severe)
-positive ballottement (severe)
-radiography
-abdominal ultrasound

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13
Q

What are the causes of ascites that are related to the hepatobiliary system?

A

-portal hypertension
-hypoalbuminemia
-gallbladder rupture

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14
Q

What causes portal hypertension?

A

increased resistance and/or blood flow in portal circulation

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15
Q

What is hepatic encephalopathy?

A

neurologic dysfunction in patients with liver dz

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16
Q

What is the general etiology of hepatic encephalopathy?

A

dysmetabolism of toxins due to liver dysfunction and/or portsystemic bypass

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17
Q

What are the most common causes of hepatic encephalopathy in dogs?

A

-congenital portosystemic shunts
-acquired portosystemic shunts due to portal hypertension
-acute liver failure without shunting

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18
Q

What are the most common causes of hepatic encephalopathy in cats?

A

-congenital portosystemic shunts
-arginine deficiency secondary to hepatic lipidosis
-acute liver failure without shunting

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19
Q

What is the pathogenesis of portosystemic shunt/liver dysfunction?

A

ammonia-rich blood from portal circulation “bypasses” the liver and flows directly into systemic circulation

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20
Q

What percent of dogs and cats with congenital portosystemic shunt develop hepatic encephalopathy?

A

around 70%

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21
Q

Which brain neurotoxins/neuroinhibitors are implicated in hepatic encephalopathy pathogenesis?

A

-ammonia***
-glutamine
-gamma-aminobutyric acid
-benzos/benzo-like substances
-tryptophan/serotonin
-aromatic amino acids
-manganese
-opioids

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22
Q

What are the early clinical signs of hepatic encephalopathy?

A

-mild confusion
-inappetance
-dullness
-irritability

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23
Q

What are the advanced clinical signs of hepatic encephalopathy?

A

-ataxia
-circling
-head pressing
-salivation
-seizures
-stupor
-coma

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24
Q

How is hepatic encephalopathy diagnosed?

A

-evidence of liver dysfunction in patient with neurological signs
-exclusion of other known brain diseases
-episodic signs of encephalopathy that may worsen after eating
-hyperammonemia

25
Q

What are precipitating factors for hepatic encephalopathy?

A

-GI hemorrhage
-excessive protein intake
-infection
-medications
-hyponatremia
-hypokalemia
-metabolic alkalosis
-renal failure
-dehydration
-constipation
-overzealous diuretic use
-diarrhea

26
Q

What are the screening tests that should be done in patients with suspected hepatopathy?

A

-CBC
-serum chem
-UA
-fecal
-abdominal radiographs
-abdominal ultrasound

27
Q

What should be done if the screening tests indicate hepatopathy?

A

-rule out secondary hepatopathy
-confirm with more specific tests such as tissue sampling

28
Q

What are the common causes of secondary hepatopathy?

A

-right sided CHF
-hypoxia
-glucocorticoids
-diabetes mellitus
-hyperlipidemia
-hyperthyroidism
-hypothyroidism
-non-hepatic inflammatory dz
-drug-induced
-metastatic neoplasia

29
Q

What interpretations may be made regarding hepatopathy once history, PE, screening tests, and specific tests are completed?

A

-primary vs secondary disorder
-pattern of disease
-estimate of degree of hepatobiliary dysfunction

30
Q

What is the most important test for determining the type and severity of hepatobiliary dz?

A

liver biopsy

31
Q

Which hepatobiliary conditions DO NOT require a liver biopsy for definitive diagnosis?

A

-gall bladder mucocele
-congenital vascular anomalies
-biliary tract infections

32
Q

Which biochemical tests help to determine primary vs secondary hepatobiliary dz?

A

-hepatocellular liver enzymes; ALT and AST
-hepatobiliary/cholestatic liver enzymes; ALP and GGT
-bilirubin

33
Q

Which nonspecific biochemical tests can provide indications of liver function?

A

-total protein and albumin
-coagulation tests
-urea
-glucose
-cholesterol (if no evidence of cholestasis)

34
Q

Which biochemical tests can provide more specific indications of liver function and or/portosystemic shunting?

A

-pre- and post-meal bile acids testing (if no evidence of cholestasis)
-ammonia

35
Q

Which biochemical tests can provide more specific indications of liver function only?

A

bilirubin (if no evidence of cholestasis)

36
Q

Which liver diseases can present with normal liver enzymes?

A

-portosystemic shunt
-microvascular dysplasia
-metastatic hepatic neoplasia
-end-stage cirrhosis

37
Q

Which diseases will often present with increased liver enzymes and normal functional indices?

A

secondary hepatopathies

38
Q

What are the general characteristics of liver enzymes?

A

-degree of increase is related to degree of damage, not liver function
-degree of enzyme increase is NOT prognostic
-increase is more common in primary liver dz
-reactive hepatopathy can occur when organs with portal venous drainage are damaged

39
Q

What are the characteristics of ALT?

A

-more sensitive for liver injury than AST; higher increase
-most specific to liver injury

40
Q

What are the characteristics of AST?

A

-less sensitive than ALT
-less specific than ALT due to presence in liver, muscle, and RBCs
-increased AST w/ normal ALT indicates extrahepatic source
-AST > ALT with elevated CK indicates muscle origin; normal CK indicates RBC origin

41
Q

What are the characteristics of ALP?

A

most common change on biochem panel in dogs
-lowest specificity for hepatobiliary dz in dogs
-increases with cholestatic dz, hepatocellular carcinoma, steroids, and feline hepatic lipidosis

42
Q

What are the characteristics of GGT?

A

-production stimulated by steroids in dogs
-increases in feline cholangitis

43
Q

What is delta bilirubin?

A

conjugated bilirubin in plasma bound irreversibly to albumin via covalent bonds

44
Q

What are the characteristics of bile acids?

A

-increase in portosystemic shunt, parenchymal hepatic dz, and cholestasis
-sensitive and specific for hepatobiliary dz and/or portosystemic shunt IF there is no cholestasis
-severity of increase does not relate to disease category

45
Q

What are the characteristics of hyperammonemia?

A

-portosystemic shunt and acute hepatocellular inability to detoxify ammonia into urea can lead to hepatic encephalopathy
-must see >70% reduction in urea cycle function to see hyperammonemia
-arginine is essential AA for urea cycle in cats; anorexia can reduce urea cycle

46
Q

What are the characteristics of coagulation proteins and hepatopathy?

A

-abnormal coagulation is common but spontaneous bleeding is rare
-marked coagulopathy correlates with functional failure as a prognostic value
-PT increase is the most common coagulopathy in cats

47
Q

What are the characteristics of protein C?

A

-anticoagulant protein synthesized in the liver
-biomarker of hepatoportal perfusion
-can be used to distinguish between macroscopic shunting and microvascular dysplasia

48
Q

How is protein C activity level interpreted in the face of abnormal bile acids and no evidence of severe liver injury or cholestasis?

A

-protein C activity level <70% is consistent with PSS
-protein C activity level >100% is consistent with microvascular dysplasia

49
Q

What can be identified on abdominal radiography with regards to the liver?

A

-liver size
-normal gastric axis
-hepatomegaly
-microhepatica
-ascites
-free gas in region of liver

50
Q

What are the characteristics of abdominal ultrasound for liver evaluation?

A

-low sensitivity; liver can appear unremarkable despite severe dz
-normal appearance does not rule out hepatic dz
-allows for visualization of internal structure/echogenicity and lesions within parenchyma

51
Q

Which conditions is abdominal ultrasound most useful for assessment?

A

-extrahepatic bile duct obstruction
-cholecystitis
-choleliths
-gallbladder mucocele**
-ascites**
-portal hypertension**
-PSS

52
Q

What are the characteristics of CT evaluation of the liver?

A

-used to evaluate liver size, hepatic mass lesions, and PSS
-CT angiography has good sensitivity and specificity for CPSS
-less operator-dependent than ultrasound

53
Q

What are the characteristics of trans-splenic portal scintigraphy?

A

-used when evaluating CPSS
-used to determine shunt termination
-provides quantitative analysis of shunt fraction

54
Q

What are the pros of liver FNA compared to biopsy?

A

-less invasive
-fewer risks
-faster results
-less expensive

55
Q

What are the cons of liver FNA compared to biopsy?

A

-low cellularity
-chance for artifacts
-no assessment of tissue architecture

56
Q

What is the overall agreement between liver FNA and histology?

A

between 30 and 61%

57
Q

Which diseases can liver FNA help detect?

A

-vacuolar hepatopathy
-hepatic lipidosis
-round-cell neoplasia
-infection

58
Q

What are the most common techniques for hepatic biopsy?

A

-core needle biopsy
-laparoscopic biopsy
-surgical biopsy