GI Liver.Pancreas Flashcards

1
Q

What are the 6 functions of the liver?

A
  1. Carbohydrate metabolism 2. Protein synthesis 3. Lipid metabolism 4. Drug metabolism 5. Hormone metabolism 6. Bile production
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2
Q

Where does bilirubin come from?

A

Breakdown of RBCs and hemoglobin.

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3
Q

What is unconjugated bilirubin?

A

Bilirubin prior to liver processing, without albumin. AKA indirect bilirubin.

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4
Q

What happens to bile salts once they are released into the intestine via the liver?

A

90% are reasborbed in the ileum as urobilinogen. 10% lost in feces as stercobilinogen.

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5
Q

What is hemolytic anemia?

A

excessive destruction of RBCs.

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6
Q

Newborns are commonly born jaundiced. What is the cause of this?

A

Either reduced uptake of circulating bilirubin, OR reduced glucuronyl transferase. **This typically resolves as liver fully develops over the next few weeks.

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7
Q

If transaminases are elevated and AST > ALT, what disease is most likely?

A

Alcoholic liver disease.

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8
Q

If transaminases are elevated and ALT > AST, what disease is most likely?

A

Viral hepatitis.

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9
Q

What lab tests demonstrate the health and wellbeing of the hepatocytes specifically?

A

Transaminases: ALT and AST.

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10
Q

What lab tests demonstrate biliary tree disease or abnormalities?

A

Alkaline phosphatase and GGT.

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11
Q

What lab tests can be used to test the severity of liver disease?

A

Serum albumin and PT. **These are the actual liver FUNCTION tests. This tells you how well the liver is doing its job.

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12
Q

What is cholestasis?

A

Decrease in bile flow through the intrahepatic canaliculi.

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13
Q

What abnormalities occur with cholestasis?

A

Increase in cholesterol, bilirubin, and bile acids in the blood.

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14
Q

What are the 2 types of cholestasis can occur? Which bilirubin abnormalities occur with each?

A

Extrahepatic/obstructive (elevated conjugated bilirubin) and intrahepatic/hepatocellular (elevated unconjugated bilirubin) cholestasis.

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15
Q

What is the cause of jaundice? What other symptom is commonly associated with this?

A

Excess bilirubin in the blood that then builds up in the skin. Itching!

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16
Q

This type of jaundice is R/T blood transfusin, hereditary, and in newborn?

A
  1. Hemolytic (prehepatic)
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17
Q

Mr. Bil has itcterus, Labs show Elevated liver damage related to drugs, which Jaundice is suspected?

A

HEpatocellular- DED in bilirubin uptake, thus DEC conjugated bilirbin. UNGONJUGATED dominant

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18
Q

If Conjugated bilirubin is INC in labs, what is suspected?

A

Obstrutive POSThepatic- MC cholelithiasis, congential artresia, Tumors (Cholangiocarcinoma)

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19
Q

What are s/s of cholestatis?

A

Pruritis-plasma bile salts, healed with fluid 2. Jaundice INC conjugated bilirubin 3. Skin Xanthome-hypercholersterolemia 4. INC Alk PHos 5. ADEK definicines, bile obstuctied can’t breakdown fat

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20
Q

What are non-viral causes of hepatitis?

A
  • Malaria - Staphylococcal bacteremia - Salmonellosis - Candidiasis - Amebiasis - Miliary TB
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21
Q

What viruses can cause hepatitis which will enlarge liver or spleen?

A
  • Hep A, B, C, D, E - Cytolmegalovirus - Epstein-Barr virus - Herpes virus - Yellow fever - Rubella, adenovirus, and enterovirus.
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22
Q

What is fulminant hepatitis?

A

Massive hepatic necrosis.

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23
Q

What is the difference between acute and chronic hepatitis?

A

Acute is self limited and resolves. Chronic is lasting longer than 6 months.

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24
Q

Which hepatitis viruses are transmitted via fecal-oral route?

A

Hep A and E

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25
Which hepatitis viruses are transmitted via blood?
B, C, and D.
26
What type of viruses are the hepatitis viruses?
All are RNA except B —> DNA.
27
Who commonly gets Hep A infections?
80% due to travelers. 35% seen with homosexual activity.
28
With what viruses is it most common to develop fulminant hepatitis?
Hep B + D coinfection, and Hep E infection in pregnant women.
29
Which HEP is MC carrier state w/ no clinical dz, but + serum markers?
HEP B
30
Pt is ASY anicteric, but later HBsAB is determined?
Subclinical Infection
31
Which HEP is VC in 50% of us by 50y?
HEP A -INC 2-6 wks. Vacc or not will be seek when gets back
32
What is the only DNA HEP w/ long incubation upt 7mo?
HEP B- most stable/thus long incub. CP- polyarthritis, vasculity, nephritis, urticaria. Uncooked meats
33
Describe HEP C?
MIlder than HEP B. 2. RNA 3. 6-12wk INCub 4. MC in alcoholic liver 5 Repeated bouts of damage with episodic LFTs. 6. Chronic 7. MC Baby boomers
34
Which is poor prognois for pregnant women?
HEP E-rare
35
Which HEP are chroinic hep infx?
HEB B and MC HEP C. Both risk for Liver CA
36
What is requried for HEP A DX?
ANTI HAV IGM-active, ANTI HAV-IGG inactive
37
What is used for HEP C DX?
ELISA and PCER ANTI HCV, prev infectin
38
The Pt ahs the following: POS-HBsAG, HBeAG/HBV DNA, ANTI HBc IgM
Acut HBV infection. IGM and HBsAG first to show
39
What if ONLY ANTI HBc IGm is POS?
Recoving from infection
40
What if ONLY ANTI HBc IGG and ANTI-HBs POS?
Had prev. infx not infectious
41
What means PT is vaccinated?
ANTI HBs POS
42
What is health active carrier?
POS HBSAG and POS ANTI HBc IGM
43
Which serum markers indicate chronic HEP?
HBsAG, ANitBc, ANtiHBE, HBeAG
44
When will jaundice, ALT, and Sx show in HEP B?
Jaundice late-12-28wk, ALT-10-24wks, SX- upt 28wks
45
Pt present with fatigue, malaise, bouts of jaundice, loss of appetite. What is on DDX?
1. Chronic viral hep B 2. Alcholism, 3. TB drugs or RA drugs
46
What would indicate chronic HEP?
1. INC PT 2. Hyperbilli 3. MIld AP 4. INC ALT/AST
47
This conditions is extrahepatic stasis in bile ducts, obstructive jaundice, thus Conjugated Bil is high w/ AP high labs?
Secondary Biliary
48
This autoimmune dz has HIGH conjugaed bilirubin, IGm, where dens lympohcytes block the part tract?
Primary Bilary Cirrosis
49
THis condition has HIHG conjugated bilirubin, AP. IGM and HIHG GAMMA globulins, where periportal tract fibroisis is affected?
Primary sclerosing cholangitis
50
IF a pt has fattly changes in liver, jaundice, TTP, AN, asites and fever, what is suspsected?
Alchoolic induced liver dz
51
These conditions from alcoholism, HEP B,C, Hemochromastosis, and wilson dz cause what?
Cirrhosis- End stage liver dz
52
WHat are some secondary result of cirrhois?
1. Esophageal varices 2. Caput Medusa 3. Hemorroids 4. Arteriovenous shuntin-back of fluid in gut, 5. HSM-anemia, neutropenia, thrompcytopenia 6. Marked ascites-albumin
53
Which sign of liver failure is related to colloid osmotic pressure?
Ascites- less protein made, INC H20 resorbtio in other vessels
54
If a Pt is confused w/ h/o of liver dz. What is the mech?
INC toxins b/c liver not working
55
Duing liver failure, this reduces plasma oncotic pressure, which inc acitis and pitting edema?
HYPOalbuminemia
56
How are hormones affect in Liver failure?
Inability to degrade estrogen-Men gynecomastia, skin changes, testicular atrophy, female hair
57
What can be seen in teh kidney with LIVER failure?
Secondary Hyperaldosterims- INC NA+H2O, cant metabolise aldosterone
58
Which gland make bicarbonate and secretes enzyme to break down all macronutrients?
Pancrease- Acni, langherans- Alpha- Gucoga, Beta Insulin
59
when will pancrease release amylase, lipase, proteas?
Active only when entering small intsting. IF BLOCKED, enzymes can degrade panrease
60
What are CP of pancreatisis?
Alcohol, BAck pain, stabbing epigastric pain. RX, trauma or viral causes
61
What is stimulant of the pancreas the released from duodenum?
CHolecystokinin- stimulated by peptone and FA in chyme
62
What Hormone realease from small intested d/t acid in the chyme is triggers the pacrease to release bicarbonate?
Secretin
63
What phase are the pancreatis secretions?
Intestinal phase- activated by ACH in PNS
64
What is important about Pancreatitis labs?
DX is only if 3x the normal amylase and lipase
65
Which marker is most important in pancreatitis?
LIPASE- 4-8hr early and last longer. Amylase- later, shorter. Also will not rise as high w/ alcoholic and TGs