Pancreatitis Disease

DESCRIPTION
An inflammatory, auto-digestive process of the pancreas
  • Acute pancreatitis
    • Inflammatory episode with symptoms related to intrapancreatic activation of enzymes with pain, nausea and vomiting, and associated intestinal ileus
    • It varies widely in severity, complications, and prognosis
  • Chronic pancreatitis
    • Progressive functional destruction of the pancreas that may exist in the absence of an etiology
    • Results in both exocrine and endocrine deficiencies
    • Pain, maldigestion, and diabetes mellitus are the major features
  • System(s) affected: Gastrointestinal
  • Genetics: Hereditary pancreatitis is a very rare condition with an autosomally dominant inheritance pattern
  • Incidence/Prevalence in USA: Urban - 22/100,00; rural - 10/100,000
  • Predominant age:
    • Acute pancreatitis – none
    • Chronic pancreatitis – 35–45 years (usually related to alcohol)
  • Predominant sex: Male = Female
SIGNS AND SYMPTOMS
  • Abdominal pain – epigastric, may radiate straight through to back
  • Nausea and/or vomiting
  • Mild abdominal distention
  • Fever (100–101°F [37.7–38.3°C])
  • Hypotension/shock (40%)
  • Mild jaundice
  • Diminished or absent bowel sounds
  • Flank discoloration (Grey Turner's sign)
  • Umbilical discoloration (Cullen's sign)
  • Pleural effusion
CAUSES
  • Gallstones
  • Alcohol
  • Trauma/surgery
  • Post endoscopic retrograde cholangiopancreatography (ERCP)
  • Medications (eg, didanosine)
  • Metabolic
    • Hypertriglyceridemia
    • Hypercalcemia
    • Renal failure
  • Hereditary
  • Systemic lupus erythematosus
  • Infections
    • Mumps
    • Coxsackie B
    • Hepatitis A and B
    • Ascariasis
    • Salmonella
  • Penetrating peptic ulcer (rare)
  • Cystic fibrosis
  • Tumors (eg, ampullary)
  • Idiopathic
  • Pancreas divisum
  • Scorpion venom
  • Sphincter of Oddi dysfunction
RISK FACTORS

See Causes

LABORATORY
  • Acute pancreatitis
    • Elevated serum amylase
    • Elevated serum lipase
    • Elevated (mild) alanine aminotransferase (ALT) and/or aspartate aminotransferase (AST) – when associated with alcoholic hepatitis or choledocholithiasis
    • Elevated alkaline phosphatase (mild) – when associated with alcoholic hepatitis or choledocholithiasis
    • Hyperbilirubinemia – when associated with alcoholic hepatitis or choledocholithiasis
    • Glucose increased – in severe disease
    • Calcium decreased – in severe disease
    • WBC 10,000 – 25,000
  • Chronic pancreatitis
    • Sometimes none
    • Hyperglycemia
    • Steatorrhea
    • Flare-ups may mimic acute pancreatitis
    • Elevated alkaline phosphatase, bilirubin

Drugs that may alter lab results: Insulin and corticosteroids
Disorders that may alter lab results:

  • Biliary tract disease
  • Penetrating peptic ulcer
  • Intestinal obstruction
  • Intestinal ischemia/infarction
  • Ruptured ectopic pregnancy
  • Renal insufficiency
  • Burns
  • Macroamylasemia, macrolipasemia
PATHOLOGICAL FINDINGS
  • Acute pancreatitis: autodigestion of the pancreas, interstitial edema, hemorrhage, cell and fat necrosis
  • Chronic pancreatitis: calcification, fibrosis
SPECIAL TESTS
N/A
IMAGING
  • Acute pancreatitis
    • Plain film of abdomen – signs of ileus
    • Chest x-ray – pleural effusion
    • Ultrasound/CT scan of abdomen
    • Endoscopic retrograde cholangiopancreatography (ERCP)
    • Dynamic CT scan
  • Chronic pancreatitis
    • X-ray of abdomen – pancreatic calcification
    • Ultrasound and/or CT scan of abdomen – pseudocyst formation/calcification
    • Endoscopic retrograde cholangiopancreatography (ERCP) – ductal deformity, retained common bile duct (CBD) stone, pancreatic duct stones and strictures
    • Endoscopic sphincterotomy – early CBD stone removal improves outcome in severe cases
    • Endoscopic ultrasound
DIAGNOSTIC PROCEDURES
  • Acute pancreatitis
    • CT-guided aspiration of necrotic areas
    • ERCP for common duct stone removal
  • Chronic pancreatitis
    • Secretin stimulation test
    • Para-aminobenzoic acid test (bentiromide [Chymex] test)
    • Lunch test meal
APPROPRIATE HEALTH CARE
  • Acute pancreatitis – hospitalization, unless very mild and able to maintain oral intake
  • Chronic pancreatitis – outpatient except for complications
GENERAL MEASURES
  • Acute pancreatitis
    • P – pain control: meperidine
    • A – arrest shock: IV fluids
    • N – nasogastric tube for vomiting
    • C – calcium monitoring
    • R – renal evaluation
    • E – ensure pulmonary function
    • A – antibiotics
    • S – surgery or special procedures in selected cases
  • Chronic pancreatitis
    • Pain – alcohol abstinence, analgesia (avoid narcotics if possible), celiac ganglion block, surgery, pancreatic enzyme preparations
    • Maldigestion – pancreatic enzyme supplements, H2-blockers
    • Diabetes mellitus – insulin
SURGICAL MEASURES
  • Acute pancreatitis
    • Infected necrosis
    • Peritoneal lavage
  • Chronic pancreatitis
    • Pain
    • Pseudocyst drainage
ACTIVITY
  • Acute pancreatitis – usually bedrest although sitting in a chair may be more comfortable. Advance as able.
  • Chronic pancreatitis – not restricted
DIET
  • Acute pancreatitis: begin diet after pain, tenderness, and ileus have resolved; small amounts of high-carbohydrate, low-fat, and low-protein foods. Advance as tolerated. NPO or nasogastric tube if vomiting.
  • Chronic pancreatitis: small meals high in protein. Adjust if diabetes mellitus is present.
PATIENT EDUCATION

For patient education materials favorably reviewed on this topic, contact: National Digestive Diseases Information Clearinghouse, Box NDDIC, Bethesda, MD 20892, (301)468-6344

PREVENTION/AVOIDANCE
  • Avoid alcohol
  • Correct underlying causes, i.e., lipids, drug use, ARDS
POSSIBLE COMPLICATIONS
  • Acute pancreatitis – pseudocyst
  • Chronic pancreatitis – pseudocyst, abscess, biliary/duodenal obstruction, portal/splenic vein thrombosis, diabetes mellitus
EXPECTED COURSE AND PROGNOSIS
  • Acute pancreatitis: 85–90% resolve spontaneously, 3–5% mortality
    • Poor prognosis indicated by:
      • On admission: age > 55 years, WBC > 16,000/mm, blood glucose > 200 mg/dL (11.1 mmol/L), serum LDH > 2 × normal, serum SGOT > 6 × normal
      • Within 48 hours: hematocrit decrease > 10%, serum calcium < 8 mg/dL, BUN increase > 5 mg/dL, arterial pO2 < 60 mm Hg, base deficit > 4 mEq/L, fluid retention > 6 L
  • Chronic pancreatitis: may have recurrent episodes of “acute pancreatitis,” slow progression, may “burn out” with resolution of symptoms. Narcotic addiction is frequent.
ASSOCIATED CONDITIONS

N/A

AGE-RELATED FACTORS

Pediatric: Mumps, sometimes complicated by pancreatitis
Geriatric: Vascular disease
Others: N/A

PREGNANCY

Acute fatty liver of pregnancy

OTHER NOTES

N/A

ABBREVIATIONS

N/A

Clinical Investigations

ROLE OF HOMOEOPATHY

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