Pancreatic Disorders Flashcards

1
Q

In a patient with ARDS, what will the chest Xray look like?

A
  • bilateral diffuse fluffy infiltrates
  • normal cardiac size
  • Tracheostomy tub
  • Left subclavian central line going insdie the right atrium
  • ECG wires
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2
Q

Definition of Acute pancreatitis

A

Cellular injury from:

  • activation of protein kinases
  • inflammatory mediator
  • activation of digestive enzymes in pancreas
  • trypsinogen to trypsin results in autodigestion of pancreas and peri-pancreatic tissues
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3
Q

What 2 things were at the top of the Etiology list for pancreatitis?

A
  • gallstones <5mm

- Heavy alcohol use

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4
Q

What is needed to make the diagnosis of acute pancreatitis?

A

At least 2 of the 3 things:

  • Epigastric pain
  • Lipase (and amylase) 3x the ULN
  • CT changes consistent with pancreatitis
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5
Q

What was the one bolded lab finding for acute pancreatitis?

A

increased lipase 3x ULN

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6
Q

What is the thing with soap that happens during acute pancreatitis?

A

Saponification

-interaction of cations with FFAs released by the action of activated lipase on TGs in fat cells —> low blood calcium

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7
Q

What’s the deal with Amylase? Why are we more concerned with lipase than amylase?

A
  • Amylase may be elevated in other conditions

- Lipase is just more specific it looks like

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8
Q

Risk factors for acute pancreatitis?

A
  • smoking
  • high dietary glycemic load
  • abdominal adiposity
  • high age and obesity: increases changes of more severe course
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9
Q

Protective factors against acute pancreatitis?

A
  • veggies

- maybe the use of statins

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10
Q

What do we do to assess the severity of Pancreatitis?

A
  • Ranson criteria
  • APACHE II (>8= higher mortality)
  • greater the rise in BUN the greater the mortality
  • REvised Atlanta classification
  • CT Grade of severity index
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11
Q

What is the Ranson criteria for assessing the severity of acute pancreatitis?

A

3 or more or the following means severe course:

  • age >55
  • WBC>16
  • Blood glucose >200mg
  • LDH >350
  • AST >250

If these things happen, it just gets worse

  • HCT drop or more than 10%
  • BUN rise of >5
  • PO2 of <60
  • Serum Ca<8
  • Base deficit over 4
  • estimated fluid sequestration of > 6L
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12
Q

What’s the relationship between the number of Ranson criteria present and the mortality rate?

A

0-2 means mortality rate of 1%
3-4 is 16%
5-6 is 40%
7-8 is 100%

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13
Q

What is the goofy pneumonic that she gave us for the ranson criteria?

A

GA-LAW (at admission)
C and HOBBS (48 hrs after admission)
-bring this up if can’t remember, slide 26 of pancreas lecture

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14
Q

What is the revised ATLANTA criteria?

A
  • Mild: no organ failure, no local complications
  • Moderate: transient organ failure <48 hrs, local complications
  • Severe: persistent organ failure >48 hrs
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15
Q

What is Cullen’s sign?

A

ecchymosis of umbilicus from retroperitoneum fluid and bleeding

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16
Q

Grey turner sign

A

Ecchymosis of flank from fluid and blood in the retroperitoneum

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17
Q

Imaging of acute pancreatitis

A
  • sentinel loop
  • colon cutoff sign
  • rapid-bolud IV contrast enhanced CT
  • perfusion CT to figure out if an organ is failing or not
18
Q

Emphysematous pancreatitis

A

when there’s infected pancreatic necrosis with secondary gas formation
-from gas forming organisms: C perf, enterobacter aerogenes, enterococcus faecalis

19
Q

Tx of emphysematous pancreatitis

A

surgical debridement and abx

20
Q

What are some complications of severe acute pancreatitis?

A

Intravascualr volume depletion

  • walled-off necrosis
  • Pseudocysts (high amylase content)
  • ARDS
  • Pancreatic ascites
21
Q

How do you treat SAP (severe acute pancreatitis)?

A

just treat the cause

  • alcoholic: abstinence…
  • Gallstone: timely lap choecystectomy
  • etc…
22
Q

Tx. of mild acute pancreatitis?

A

80% resolve sponateously

23
Q

Tx of severe actue pancreatitis

A

within 48 hours of admission, start enteral feedings with nasogastric or nasojejunal tube- reduces risk of multiorgan failure and mortality

24
Q

Etiology

A

TIGAR-O

  • Toxic Metabolic (alcoholic)
  • Idiopathic
  • Genetic (CFTR, PSTI, SPINK1, PRSS1)
  • Autoimmune (IgG4)
  • Recurrent
  • Obstructive
25
What is SAPE?
Sentinel acute pancreatitis event - hypothesis of pathogenesis of chronic panreatitis - there's an initial (sentinel) acute pancreatitis event that initiates an inflammatory process that results in injury and later fibrosis ("necrosis-fibrosis")
26
What are some pancreatic funciton tests?
- Trypsinogen: level is low in insuficiency.... causes steatorrhea - Fecal elastase: low in insufficiency - stimulation tests: cholecystokinin/secretin
27
What will imaging show for chronic pancreatitis?
Calcifications | -tumefactive chronic pancreatitis= concern for pancreatic Cancer
28
What will EUS look like for chronic pancreatitis?
Autoimmune= diffuse enlargement of the pancreas, a peripheral rim of hypoattenuation, and irregular narrowing of the main PD
29
What does the exocrine pancreas secrete?
Amylase protease lipase
30
What does the endocrine pancreas secrete
insulin somatostatin glucagon
31
How is exocrine pancreatic insufficiency confirmed?
-by response to therapy with pancreatic enzyme supplements
32
What do most people with endocrine insufficiency develop?
Diabetes mellitus
33
What is absolutely forbidden in chronic pancreatitis?
alcohol
34
What is the main cause of death in chronic pancreatitis?
Pancreatic Cancer | -prognosis is better in patients with etiology from a remediable condition or autoimmune hepatitis
35
Which MEN syndrome is associated with hypoglycemia
MEN1 | -there's a hypersecretion of insulin
36
Where is a Gastrinoma most commonly found?
duodenum | -2nd most common spot is the pancreas
37
What does MEN1 have?
Pituitary adenoma Parathyroid hyperplasia Pancreatic tumors
38
what does MEN2A?
Parathyroid hyperplasia medullary thyroid carcinoma Pheochromocytoma
39
What does MEN2B have?
Mucosal neuromas Marfanoid body habitus Medullary thyroid carcinoma Pheochromocytoma
40
How do you dx MEN Type 1?
2 or more of the following: - Parathyroid: hypercalcemia, high intact PTH - Pancreas: Gastinoma (ZE), Insulinoma- hypoglycemia - Pituitary: cushing syndrome
41
MEN 2A
2 or three of the following: - Thyroid (Medullary Thyroid Ca): elevated calcitonin - Adrenal (Pheochromocytoma): elevated catcholamines - Parathyroid: Hypercalcemia, high intact PTH * 2-5% percent will develop Hirschsprung disease
42
MEN2B
- Marfanoid body habitus - Medullary thyroid cancer: elevated calcitonin - Pheochromocytomas: elevated catecholamines - Neuromas: occur on lips, tongue, mouth, eyelids, etx. - Frequently a new gene mutation: no family history