Liver Disease Flashcards

(31 cards)

1
Q

What occurs with sinusoid obstruction and why?

A

Blood flow decreases so pressure builds and fluid leaves into the peritoneal cavity (ascites)

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2
Q

What is ascites?

A

4-8 extra liters of fluid in the peritoneal cavity

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3
Q

Where is bile reabsorbed?

A

Ileum, along with bile salts

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4
Q

How is cholestyramine r/t enterohepatic circulation?

A

Instead of reabsorbed bile going from the ileum back to the liver, this drug captures the bile so the liver has to regenerate new bile from cholesterol.

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5
Q

What is jaundice?

A

Symptom
Lots of bilirubin in ECF
Yellow skin when >2.4-3.0mg/dL
B/c rapid destruction of RBC, decreased liver uptake of bilirubin, blocked bile ducts so bilirubin not released

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6
Q

What do Kupffer cells do?

A

In the liver, they are macrophages
Filter bacteria and proteins
Break and get rid of old RBC

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7
Q

What are LFTs and what do the screen for?

A
Liver disfunction 
Bilirubin
Alkaline phosphatase
ALT/AST
Albumin 
PTT
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8
Q

Key lab: what happens to blood ammonia when liver function decreases?

A

It goes up because the liver is not turning it into urea for excretion

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9
Q

What can cause hepatitis?

A
Hep B (tools and body fluids) 
Hep C (needles and sex and BB virus) 
Anorexia, fatigue, high bilirubin, AP, AST
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10
Q

MNT with hepatitis?

A

Decrease protein
30-35 kcal/kg (>3000kcals)
1.1-1.2 g/kg
Water sol vits and maybe MCT

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11
Q

Alcoholism common deficiencies

A
Protein 
Folic acid 
Thiamin (ADH cofactor) 
Vitamin A 
Zinc (needed and ADH cofactor)
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12
Q

If alcohol to ADH ratio is too high, or NAD is low, what pathway breaks alcohol?

A

MEOS

Microsomal ethanol oxidizing system and it uses energy without making any

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13
Q

How do you find kcals in EtOH?

A

%alcohol of beverage x 2=proof

Then .8 kcal per proof

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14
Q

carbohydrate functions of liver

A
Glucogenesis
Gluconeogenesis
Glycogenesis 
Glycolysis
Glycogenolysis
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15
Q

Protein functions of liver

A

Ammonia to urea
Aa turned to glucose
Make albumin, transferrin, PA, prothrombin and fibrinogen

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16
Q

Lipid functions of liver

A

FA to energy (B oxidation)
Make ketones
Make TG, lipids and cholesterol
Make VLDL and HDL

17
Q

Vitamin functions of liver

A
Store fat soluble 
Activate Vit D 
Folate into active 5-THF 
B carotene to Vit A 
Store minerals: Fe, Mg, B12, Zn, Cu
18
Q

2 levels of NAFLD?

A

Steatosis- fat accumulates in interstitial space of liver

Steatohepatitis- inflammation and fat accumulation in liver

19
Q

What 3 conditions is NAFLD associated with?

A

DM2
Metabolic syndrome
Obesity

20
Q

What is NASH?

A

Non alcoholic steatohepatitis
Fibrous tissue formed in liver
Could be insulin resistance caused
Manage with DM2 drugs and wt loss

21
Q

3 stages of liver disease?

A

Fatty liver (steatosis)- reversible
Alcoholic hepatitis- toxic liver injury, high labs
Cirrhosis- portal HTN, GI bleeding, Ascites, hepatic encephalopathy

22
Q

What is cirrhosis specifically caused by EtOH?

A

Laennec’s Cirrhosis

23
Q

What is esophageal varices?

A

Thin lining of esophagus tends to bleed with portal HTN

24
Q

Difference between ascites and Anasarca?

A

Ascites- edema in peritoneal

Anasarca- extreme edema everywhere

25
MNT goal with Ascites
``` Remove fluid Prevent electrolyte imbalance Prevent loss of LBM/anorexia Sodium 500-1000mg FR- 1000-1500mL/day 1.25-1.75 protein IBW No glutamine ```
26
What is hepatic encephalopathy?
Can't eliminate toxic products so toxic to brain Delirious Usually high ammonia levels
27
MNT with advanced liver disease
Low protein Restrict fluids Antibiotic (neomycin to kill fluid retaining Bact)
28
2 drugs used to manage encephalopathy?
Lactulose- laxative Makes colon acidic so Ammonia is not absorbed Neomycin- antibiotic Destroys colonic bacteria that make ammonia
29
MNT references for liver disease
``` BEE x 1.2-1.75 25-35 kcals encephalopathy 20-40% fat, MCT if needed Up to 1.6 g/kg protein 40g/d protein- encephalopathy BCAA for encephalopathy ```
30
How does high NH4 affect BCAA in blood
High ammonia stimulates glucagon which causes hyperglycemia and high insulin. Muscles uptake BCAA and BCAA in blood are low.
31
What is Wilson's disease?
Autosomal recessive disorder Less biliary copper excretion Copper accumulates Might supplement with zinc to decrease CU absorption.