Chronic pancreatitis Flashcards

1
Q

Define chronic pancreatitis.

A

Chronic inflammatory disease of the pancreas characterised by irreversible parenchymal atrophy and fibrosis leading to impaired endocrine and exocrine function and recurrent abdominal pain.

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2
Q

What is the epidemiology of chronic pancreatitis?

A
  • Annual incidence 1/100,000 in UK
  • Prevalence 3/100,000
  • Mean age 40-50 years in alcohol- associated disease
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3
Q

What are the risk factors for chronic pancreatitis?

A
  • Alcohol - (70-80% of all chronic pancreatitis)
  • Smoking
  • FH - mutations in PRSS1, SPINK1, CFTR
  • Coeliac disease –> IDIOPATHIC

Other: psoriasis, high-fat, high-protein diet

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4
Q

Which GI condition increases risk of developing any form of pancreatitis?

A

coeliac disease

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5
Q

What is the pathophysiology of chronic pancreatitis? Which cells are thought to be involved?

A

Chronic inflammation –> fibrosis and calcification, parenchymal atrophy, ductal dilatation, cyst and stone formation —> disruption of normal pancreatic glandular architecture

Pancreatic stellate cells - thought to play a role in pancreatitis by converting from quiescent fat storing cells to myofibroblast-like cells forming extracellular matrix, cytokines and GF in response to injury.

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6
Q

What is the pain in chronic pancreatitis thought to be associated with?

A

Pain is thought to be associated with raised intraductal pressure and inflammation.

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7
Q

What is the typical presentation of chronic pancreatitis?

A
  • Recurrent severe epigastric pain, radiating to back, relieved by sitting forward and exacerbated by eating or drinking alcohol
  • Weight loss
  • Bloating
  • Pale offensive stools (steatorrhoea)
  • Other: painful joints, SOB, skin nodules (pancreatic lipase leaks into circulation and causes fat necrosis at non-pancreatic sites).
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8
Q

What investigations would you do for chronic pancreatitis?

A

1st tests: CT/MRI +/- USS

Bedside:

  • Glucose - if high then endocrine dysfunction, GTT (glucose tolerance test)
  • Amylase/lipase - normal
  • Immunoglobulins - high esp IgG4 in autoimmune pancreatitis
  • Faecal elastase - reduced in severe disease

Imaging:

  • USS - percutaneous or endoscopic - hyperechoic foci with post-acoustic shadowing
  • ERCP/MRCP - see next
  • AXR - pancreatic calcification may be visible
  • CT scan - pancreatic cysts, calcification
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9
Q

What does ERCP/MRCP show in early and late stages of chronic pancreatitis?

A

Early - duct dilatation and stumping of branches

Late - duct strictures with alternating dilatation (“chain of lakes”/beading appearance)

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10
Q

How do you manage chronic pancreatitis?

A

Conservative - alcohol and cigarette cessation

Medical

  • Analgesics - if not sufficient → coeliac plexus block or transthoracic splanchnicectomy.
  • Lifestyle modification
  • Pancreatic enzymes (e.g. pancreatin/Creon) and PPI (e.g. omeprazole)
  • Dietary modification - low-fat

Endoscopic - pseudocyst decompression, sphincterotomy, stone extraction, dilatation, stenting or strictures. ESWL for pancreatic stone fragmentation prior to endoscopic removal.

Surgical -

  • drainage (modified Puestow procedure),
  • resection (pancreaticoduodenectomy/ Whipple’s),
  • limited resection (Beger procedure),
  • combined opening of pancreatic duct and excavation of pancreatic head (Frey procedure)
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11
Q

What are the local and systemic complications of chronic pancreatitis?

A

Local - pseudocysts, BD stricture, duodenal obstruction, calcifications, pancreatic ascites, pancreatic carcinoma

Systemic - exocrine insufficiency, diabetes, steatorrhoea, reduced QOL, chronic pain syndromes, opioid dependence

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12
Q

What is the prognosis in chronic pancreatitis?

A
  • Difficult to predict - may stabilise, worse, or improve
  • Surgery improves symptoms in 60-70% but results are not sustained
  • Life expectancy reduced by 10-20 years
  • Pain decreases or disappears over time
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