1 / 43

Pancreas and hepatobiliary disorders

Pancreas and hepatobiliary disorders. Feb 12 2004 Andrea Wilson. Case 1 (emedhome.com). 28 yo male “ulcer pain acting up”. Has a known peptic ulcer. Epigastric tenderness intermittent x 2 days not relieved with antacids No rebound or guarding. Normal rectal. Busy shift

hea
Download Presentation

Pancreas and hepatobiliary disorders

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Pancreas and hepatobiliary disorders Feb 12 2004 Andrea Wilson

  2. Case 1 (emedhome.com) • 28 yo male • “ulcer pain acting up”. Has a known peptic ulcer. • Epigastric tenderness intermittent x 2 days not relieved with antacids • No rebound or guarding. Normal rectal. • Busy shift • Pt felt better after demerol and wanted to go home.

  3. Grey-Turner’s sign • associated with hemorrhagic pancreatitis. • However, this sign develops in <3% of patients with acute pancreatitis • retroperitoneal hemorrhage, splenic rupture, ruptured aortic aneurysm, and ectopic pregnancy. • blood along fascial planes and cause ecchymoses over the flanks. (lateral edge of the quadratus lumbrum muscle)

  4. Acute Pancreatitis • Up to 80% of pts will have uneventful recovery • Ranson’s criteria correlate with risk of major complications and death • Overall mortality ranges from 7-20%

  5. At admission or diagnosis Age > 55 years WBC > 16,000/mm3 Blood glucose > 200mg/dl Serum LDH > 350 IU/ml SGOT > 250 Sigma-Frankel units/dl During initial 48 hours Hematocrit fall > 10% BUN rise > 5 mg/dl Serum calcium level < 8.0 Arterial oxygen pressure < 60 mm Hg Base deficit > 4 mEq/L Estimated fluid sequestration > 6,000 ml Ranson’s criteria

  6. So… • Hypotension, • tachycardia >130, • PO2 <60, • oliguria, • increasing BUN/Cr • and hypocalcemia • = BAD

  7. Pancreatitis • Obstruction of ampulla with reflux of bile into pancreatic duct then activation of digestive enzymes and autodigestion of the pancreas • Gallstones + Etoh = >70%

  8. Other causes • GET SMASHED • Gallstones, ethanol, tumors, scorpion bite?, microbiology (bacteria, virus, parasites), autoimmune (SLE, PAN, Crohn’s), surgery/trauma, hyperlipidemia/ hypercalcemia, emboli/ischemia, drugs • Also: pregnancy, liver disease, DKA

  9. Symptoms Sharp epigastric pain Radiates to back Improves leaning frwd N&V Pain referred to RUQ or LUQ Aggravated by eating Signs Jaundice Tachycardia (pain or volume depletion) Fever Grey Turner’s -flank Cullen’s – umbil (neither specific) Acute pancreatitis

  10. Amylase – If 3x N then 80-90%sens , 75% spec may return to normal within 24 hrs of pain onset Fallopian tubes, ovaries, testes, adipose tissue, small bowel, lung, thyroid, sk muscle, neoplasms Lipase 90% sens and specific Remain elevated for several days after pain onset (7-14 ) Diagnostic evaluation

  11. What else would you order? • AXR – calcification of the pancreas or gallstones if calcified, free air, ileus, colon “cut-off” if transverse colon involved • CXR – atelectasis, effusion • U/S and CT if further evaluation needed – diffusely enlarged pancreas, dilated CBD • CT negative in 30% of mild pancreatitis

  12. Complications • Phlegmon 18% - • Pancreatic abscess 3% • Pancreatic pseudocyst 10% • Ascites • Thrombosis of the central portal system • Shock, ARDS and MSOF • Profound metabolic disturbances including hyperglycemia and hypocalcemia

  13. Management • 1) hemodyanmic stabilization • 2) allevation of pain • 3) stop progression of damage • 4) tx of local and systemic complications • Admit • NPO, IV analgesics, NG if emesis/ileus • Aminoglycoside or cephalosporin if deterioration suggests abscess

  14. Chronic Pancreatitis • Fibrosis, ductal abnormality, calcification and cellular atrophy • Leads to chronic pancreatic insufficiency and chronic pain. • Autodigestion from pancreatic digestive enzymes + other vasoactive substances causing chemical irritation ->edema – hemorrhage/necrosis

  15. Chronic pancreatitis • ALCOHOL • DM, protein-calorie malnutrition, hereditary pancreatitis, cystic fibrosis, hyperparathyroidism, pancreas divisum • Pseudocyst, ascites, CBD stricture • If>90% exocrine function lost then trouble! • Steatorrhea (fat), azotorrhea (protein), progressive weight loss.

  16. Case 2 • 56 yo male • new onset diabetes • Dull epigastric pain worse at hs • 10 lb weight loss in past 6 months • Mildly jaundiced • ?palpable gallbladder • No Murphy’s

  17. Pancreatic cancer • Males: females 2:1 • 6 month survival • Usually ductal cell adenocarcinoma and usually in the head of the pancreas • Smoking, high fat/protein diet, DM, DDT exposure • Courvoisier’s law

  18. 4 main gallstone problems • Symptomatic cholelithiasis (biliary colic) • Cholecystitis • Cholangitis • Pancreatitis

  19. Back to med school… • Bile needed for absorption of fats and fat soluble nutrients from small intestine • Imbalance of chol + solubilizing agents • 70% of gallstones are >70% cholesterol (radiolucent) • 20% are pigment stones bc of abnormal solubility of unconjugated bilirubin with the precipitation of calcium salts • 10% mixed

  20. Gallstone risk factors • Cholesterol – female, 20-40, pregnant/OCP, parity, obsesity/ profound weight loss, TPN, fam hx, C.F., Crohn’s, clofibrate, ceftriaxone, Pima indians • (fat, female, forty, fertile, ethnic, estrogen, diet, drugs) • Pigment stones – Asian, chronic biliary tract infection, chronic liver disease, intravasc hemolysis (sickle cell or spherocytosis)

  21. Protective factors • ascorbic acid (?increased cholesterol catabolism) • coffee (3-4 cups/day 40% less likely to develop gallstones) Yeah!

  22. Biliary colic • Stone lodged in cystic or CBD -> inc in intraluminal pressure/ distention -> N&V& pain (15%) • Usually constant (not colic) but <6 hrs • Epig or RUQ dull/visceral pain with radiation to R post shoulder + N&V • Eating after fasting or fatty meal • May have post-attack soreness for 1-2 days

  23. Cholecystitis • If obstruction persists – inflammation +/- infection of gallbladder wall • May develop gangrene +/- perf -> more localized pain/ peritonitis • More parietal pain • Murphy’s sign (97% sens, only 48% in elderly) • May have fever/chills

  24. Acalculous cholecystitis • 5-10% of cholecystitis • Elderly + DM + immunosuppressed ( trauma, burn, labor, surgery, vasculitis, gallbladder torsion, parasitic or bacterial infections of the biliary tract.) • Do worse

  25. Investigations • CBC (but WBC may be Normal) ? Low Hb • Lipase +/- liver function tests (may be normal) • U/S sensitivity >95% for stones > 2mm, spec 78% • False neg and pos rates 2-4% may miss cholecystitis • Emergency physician U/S • HIDA/DISIDA best for cholecystitis sensitivity almost 100%, spec 90% but start with U/S • 12 lead ECG, U/A, preg test, AXR, CXR

  26. DDx • Gastritis, PUD, hepatitis, hepatic abscess, intraabd abscess, ischemic gut, Fitz-Hugh-Curtis syndrome (GC or Chlamydial perihepatitis), pancreatitis, GERD, Appendicitis • Renal colic, pyelonephritis • Pneumonia, acute MI, • PID +/- TOA, ectopic pregnancy

  27. Bactobilia • 35-65% of pts with cholecystitis • E. coli or Klebsiella in 70% • Also Enterococcus, Bacteroides, Clostridium, GDS, Staph • For non-septic: third generation cephalosporin • Septic: amp, gent and clinda

  28. Cholangitis • Complete obstruction + bacteria = cholangitis • Backup into lymphatic vessels and hepatic veins • High mortality rate • Stone, stricture, Ca • Increased ALP, GGT, bili (late) +/- AST, ALT • E. coli, Klebsiella, Pseudomonas

  29. Triads and pentads • 25% Charcot’s triad • Fever jaundice, RUQ pain • Reynold’s pentad • Altered LOC, distributive shock

  30. Cholangitis management EMR Aug 12 , 2002 • Volume resuscitation +/- vasopressors • Broad-spectrum antibiotics • Surgery or endoscopic decompression

  31. Weird and wonderful • Gallbladder empyema • Emphysematous (gangrenous) cholecystitis (1% of cholecystitis) • Hydrops= mucous accumulation in gallbladder due to cystic duct obstruction • Gangrene perforation • Cholecystoenteric fistula (repeated attacks) • Gallstone ileus – cholecystoenteric connection with impacted stone at ileocecal valve, pneumobilia

  32. Management • Urgent biliary decompression for pts in extremis or with clinical deterioration • Consider operating if porcelain gallbladder (15-20% assoc Ca) , DM, hx of biliary pancreatitis • Demerol vs morphine, antiemetics • Admit, hydrate, antibiotics (even though questionable in cholecystitis)

  33. What about ERCP? • Severe pancreatitis, continuing biliary colic, cholangitis, obstructive jaundice, stones in CBD or CBD dilation • Ultimately endoscopic sphincterotomy and stone extraction followed by laparoscopic cholecystectomy is preferred tx for choledocholithiasis.

  34. Cholecystectomy • Best management for • Frequent or severe attacks • Hx of gallstone complications • Stones over 2 cm • Congenitally abnormal hepatobiliary system, • +/- DM

  35. Discharge home if: • Resolution of symptoms (4-6 hrs) • Correction of intravascular volume deficits • Restored ability to drink • Give them analgesics • Keep if high risk with CBD stones or if pregnant

  36. Then what? • Asymptomatic gallstones develop complications • 10% at 5 yrs • 15% at 10 yrs • 18% at 15-20 yrs • Close observation even for most diabetic patients

  37. Primary biliary cirrhosis • Autoimmune associations • Antimitochondrial antibody in >90% • Not fully understood. Necrotizing inflammation leading to bile duct fibrosis • Often detected by elevated ALP on routine screening • Women, age 35-60, pruritus, fatigue, jaundice, hyperpigmentation, eventual cirrhosis • Biopsy, colchicine, methotrexate/cyclosporine, ursodiol, transplant

  38. Secondary biliary cirrhosis • Postop strictures/ gallstones • Usually with superimposed infectious cholangitis • Congenital biliary atresia, CF, choledochal cysts • Signs and symptoms like PBC but also intermittent bouts of colic/cholangitis • AMA negative • Suspect if bile flow obstruction, especially postop

  39. Sclerosing cholangitis • Affects extrahepatic +/- intrahepatic • On ERCP see thickened ducts with narrow, beaded lumina • Often associated with IBD, fibrosing conditions, AIDS • Cholestyramine for pruritus, transplant • Age, bili, histologic stage and splenomegaly predict survival

  40. What should I remember • Pancreatitis – get smashed • Biliary colic - <6 hrs • Cholecystitis – usually antibiotics, consider acaculous cholecystitis • Weird and wonderful complications • When to discharge colic

  41. References • Cholangiography and Pancreatography, by M. Ohta, et al., Eds. Igaku-Shoin Ltd., Tokyo, University Park Press, Baltimore, 1978 • Emergency Medicine. Tintinalli, Kelen, Stapczynski. • Emergency Medicine Reports – Presentation and mangement of Acute biliary Tract Disorders in the Emergency Department – optimizing Assessment and Treatment of Cholelithiasis and cholecystitis Aug 12 2002 • Harrison’s principles of Internal Medicine 14th edition 1984 • http://www.bupa.co.uk/health_information/html/organ/liver.html • Presentation by Rob Hall 2002 • Thomson, A.B.R., Shaffer E.A First Principles of Gastroenterology. 1997 • www.emedhome.com

More Related