PANCE Blueprint GI and Nutrition (8%)

Pancreatic Disorders (PEARLS)

The NCCPA™ Gastroenterology and Nutrition PANCE Content Blueprint covers acute and chronic pancreatitis under the category disorders of the pancreas

Acute and chronic pancreatitis
Patient will present as → a 37-year-old male complaining of rapid onset of severe mid-epigastric pain with radiation to the back after eating a large meal. The pain typically lessens when the patient leans forward or lies in the fetal position. Physical exam shows low-grade fever, epigastric tenderness, diminished bowel sounds, and bruising of the flanks. An abdominal CT scan shows localized dilation of the upper duodenum and a small collection of fluid in the left pleural cavity.

Describe Grey-Turner's sign
Flank ecchymosis often related to pancreatitis

Acute vs. Chronic Pancreatitis

Acute pancreatitis is most commonly caused by gallstones (most common overall) and alcohol (most common in men), diagnosed by 2 of 3 criteria: epigastric pain radiating to the back + lipase ≥3× ULN + characteristic CT findings; Ranson's criteria and BISAP score predict severity; hemorrhagic pancreatitis produces Grey Turner's sign (flank ecchymosis) and Cullen's sign (periumbilical ecchymosis); treatment is aggressive IV fluids, pain control, NPO, and early enteral nutrition for severe cases.

  • Gallstones (~40%) and alcohol (~30%)
  • Mnemonic: GET SMASHED (Gallstones, Ethanol, Trauma, Steroids, Mumps, Autoimmune, Scorpion sting, Hypercalcemia/Hypertriglyceridemia [TG >1000 mg/dL], ERCP, Drugs [furosemide, thiazides, azathioprine, tetracyclines, estrogen, valproic acid])
  • Key differentiator: pancreatitis pain is constant, severe, radiates to back, unlike biliary colic

DX: Diagnosis requires 2 of 3: (1) characteristic pain, (2) lipase ≥ 3× normal (most specific), (3) imaging findings; CT abdomen = best initial imaging if diagnosis unclear or severe

  • Labs: ↑ lipase (preferred over amylase); ALT >150 suggests gallstone pancreatitis; may see hypocalcemia in severe disease
  • DX:
    • Clinical + elevated lipase and amylase
    • CT is required to differentiate from necrotic pancreatitis
  • Signs: Grey Turner's sign (flank bruising), Cullen’s sign (bruising near the umbilicus) - think of "C" looks like an "O"

Hemorrhagic pancreatitis - Grey Turner's sign

This 40-year-old woman complained of worsening epigastric pain of five days duration. On examination, she had hypotension, a board-like abdomen, and extensive ecchymosis over her right loin (Grey Turner’s sign)

Cullen's sign

Acute pancreatitis with Cullen’s sign

Severity assessment: use BISAP or Ranson criteria

Ranson’s criteria for poor prognosis:

At admit:

  • Age > 55
  • Leukocyte: >16,000
  • Glucose: >200
  • LDH: >350
  • AST: >250

At 48 hrs:

  • Arterial PO2: <60
  • HCO3: <20
  • Calcium: <8.0
  • BUN: Increase by 1.8+
  • Hematocrit: decrease by >10%
  • Fluid sequestration >6L

TX: Aggressive IV fluids (lactated Ringer’s), NPO, and IV opioids for pain control; early fluids are the most important mortality-reducing step

  • Complication: pancreatic pseudocyst (a circumscribed collection of fluid rich in pancreatic enzymes, blood, and necrotic tissue)

Chronic Pancreatitis

Patient will present as → a 45-year-old man with a long history of alcohol use presenting with chronic epigastric pain radiating to the back, worse after meals, along with weight loss and bulky, foul-smelling stools (steatorrhea). Over time he develops diabetes mellitus. CT scan shows pancreatic calcifications. He is treated with pancreatic enzyme replacement (pancrelipase), alcohol cessation, pain control, and fat-soluble vitamin supplementation.

Chronic pancreatitis is progressive inflammatory fibrosis of the pancreas leading to irreversible exocrine and endocrine dysfunction (most commonly due to chronic alcohol use).

  • Chronic epigastric pain radiating to the back + steatorrhea + weight loss = classic triad; pain often worse after meals
  • Most common cause: chronic alcohol abuse (~70–80% in Western countries)
    • Other causes → cystic fibrosis, hereditary pancreatitis (PRSS1), hypercalcemia, hypertriglyceridemia
  • Pathophysiology: repeated inflammation → fibrosis, ductal obstruction, and pancreatic calcifications → loss of enzyme production
  • Exocrine insufficiency occurs firstfat malabsorption (steatorrhea) and fat-soluble vitamin (A, D, E, K) deficiency
  • Endocrine failure later → diabetes mellitus (type 3c, brittle DM)

DX: CT scan = best initial test showing pancreatic calcifications; fecal elastase ↓ confirms exocrine insufficiency (functional test)

  • Key differentiator: chronic pain + calcifications (vs acute pancreatitis = elevated lipase without calcifications)
  • Complications: pseudocysts, pancreatic cancer (increased risk), malnutrition

TX: Pancreatic enzyme replacement (pancrelipase) + alcohol and smoking cessation + pain control (stepwise, avoid opioids if possible)

  • Fat-soluble vitamin supplementation, low-fat diet, and insulin for diabetes; consider endoscopic or surgical decompression if refractory pain or obstruction

PEARLS:

  • Pancreatic calcifications on imaging = chronic pancreatitis (essentially pathognomonic)
Obesity and Metabolic Syndrome (ReelDx) (Prev Lesson)
(Next Lesson) Brian Wallace PA-C Podcast: Diseases of the Pancreas and Bowel Part 1
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