Pancreatic and Nutritional Pharmacology
Acute pancreatitis management · Enzyme replacement · Somatostatin analogues · Refeeding syndrome · Micronutrient deficiencies
Acute Pancreatitis: Key Pharmacological Decisions
Fluid Resuscitation
Lactated Ringer’s Preferred
  • 250–500 mL/hour for first 12–24 hours
  • Target: HR <120, MAP >65, urine output >0.5 mL/kg/hour
  • Lactated Ringer’s > normal saline (WATERFALL trial: lower SIRS rate)
  • Avoid over-resuscitation: abdominal compartment syndrome risk
Antibiotics
Do NOT Use Prophylactically
  • Prophylactic antibiotics: no mortality benefit in randomized controlled trials
  • Indicate only for: infected pancreatic necrosis or extrapancreatic infection
  • Infected necrosis: imipenem or meropenem (pancreatic tissue penetration)
  • Empiric use selects resistant organisms and promotes fungal superinfection
Nutrition
Early Enteral > Parenteral
  • Start enteral nutrition within 24–48 hours in severe pancreatitis
  • Preserves gut barrier; reduces infection complications
  • Nasojejunal preferred if nasogastric not tolerated
  • Parenteral only if enteral access cannot be established
Somatostatin Analogues and Functional Tumor Management
Tumor Hormone Drug Key Point
VIPoma Vasoactive intestinal peptide Octreotide or lanreotide Controls profuse secretory diarrhea; stabilizes before surgery
Glucagonoma Glucagon Octreotide or lanreotide Improves necrolytic migratory erythema and glucose intolerance
Carcinoid syndrome Serotonin Octreotide LAR or lanreotide autogel (monthly) Reduces flushing and diarrhea; antiproliferative activity
Insulinoma Insulin Diazoxide (ATP-K+ channel opener) Hyperpolarizes beta cells → suppresses insulin secretion; causes fluid retention (add diuretic)
Gastrinoma (ZES) Gastrin High-dose PPI (omeprazole 60–120 mg/day) Controls acid hypersecretion; doses far above standard peptic ulcer disease doses
Refeeding Syndrome and Nutritional Emergencies
Refeeding Syndrome
Hypophosphatemia on Restarting Nutrition
  • Mechanism: insulin surge drives PO4, K+, Mg2+ into cells → severe hypophosphatemia
  • Risk: BMI <16, >10% weight loss over 2 months, negligible intake >5 days, alcoholism, anorexia
  • Danger: respiratory failure (diaphragm weakness), arrhythmias, seizures
  • Prevention: correct electrolytes before starting; begin at 10 kcal/kg/day; increase slowly over 4–7 days
  • Give thiamine before any glucose in malnourished patients
Micronutrient Deficiencies
High-Yield Presentations
  • Thiamine (B1): Wernicke’s (ocular, ataxia, confusion) — give IV before glucose
  • Vitamin B12: megaloblastic anemia + subacute combined degeneration; IM hydroxocobalamin if no intrinsic factor
  • Folate: megaloblastic anemia, no neuro features; oral folate 5 mg daily
  • Iron: microcytic anemia; oral ferrous sulfate; IV iron if oral not absorbed
  • Vitamin D: low in exocrine pancreatic insufficiency; supplement to >30 ng/mL
Critical Rule — Thiamine Before Glucose

In any malnourished patient (alcoholism, anorexia, prolonged starvation), give thiamine 100–200 mg IV before any glucose-containing fluid or nutritional support. Glucose without thiamine in a deficient patient precipitates Wernicke’s encephalopathy, which can progress to irreversible Korsakoff syndrome.