* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download QUESTION
Survey
Document related concepts
Transcript
Question • Injury to the common bile duct during laparoscopic cholecystectomy is most likely to occur as a result of – – – – – A. use of a 30 degree scope B. lateral retraction of the infundibulum Dissection of the cystic duct-gallbladder junction Dissection of the triangle of Calot Intraoperative cholangiography Question • Injury to the common bile duct during laparoscopic cholecystectomy is most likely to occur as a result of – – – – – A. use of a 30 degree scope B. lateral retraction of the infundibulum Dissection of the cystic duct-gallbladder junction Dissection of the triangle of Calot Intraoperative cholangiography Question • Injury to the common bile duct during laparoscopic cholecystectomy is most likely to occur as a result of – – – – – A. use of a 30 degree scope B. lateral retraction of the infundibulum C. Dissection of the cystic duct-gallbladder junction D. Dissection of the triangle of Calot E. Intraoperative cholangiography ANATOMY • Triangle of Calot – Common Hepatic duct – Cystic duct – Inferior surface of the Liver – Cystic Artery is within – Anatomic variants • Cystic Duct may be absent, short, posterior, low or anterior to CBD, or directly from the RHD • Cystic artery may arise from gastroduodenal artery ANATOMY • Injuries (Causes) – – – – – Failure to occlude duct Too deep a dissection plane Thermal Injury Tenting injury Misidentification • CBD thought to be cystic duct • Injury of aberrant duct ANATOMY • Injuries (Bismuth classification) – – – – Type A Cystic duct leaks/Liver bed duct injury Type B/C Aberrant Right hepatic ducts Type D Lateral injury to major duct Type E Transection/Ligation – Immediate referral is preferred – 1-6 weeks – Drain/stent & operate in 3months ANATOMY • Portahepatis (Hepatoduodenal lig) – Portal vein posterior – Common hepatic artery to left anterior – CBD to the right anterior PHYSIOLOGY • Bile – Lecithin – Bile Salt – Cholesterol • Gallbladder Contraction – Cholecystokinin • Fatty acid • Amino acid CHOLELITHIASIS • • • • • 10-20% of population Female age obesity family hx Crystallization-contraction of bile salt pool 1-2% develop symptoms Types – Cholesterol – Pigmented • Brown/Black Asymptomatic Stones • Prophylactic cholecystectomy not indicated • Exceptions – Transplant • Renal- NO • Cardiac -YES – Chronic TPN -Probably YES • 35 develop stones • Develop symptoms more than expected – Bariatrics-NO – Hemoglobinopathy -YES • 50 develop complication • Crisis mimics biliary colic Asymptomatic Stones • Incidental cholecystectomy – During laparotomy stones are discovered – Over 70 -higher incidence of sepsis/MSOF when CCY NOT done ACUTE CHOLECYSTITIS • Signs and Symptoms • Labs – Leukocytosis – Bilirubin • Choledocholithiasis • Mirizzi syndrome – Amylase • Radiographic – Ultrasound – CT – HIDA ACUTE CHOLECYSTITIS • Treatment – Antibiotics-broad spectrum • Ecoli, Klebsiella, Clostridium, Proteus, Enterobacter – CBD stones • Preop -ERCP • Intraop – CBDE – Postop ERCP • Surgery – Expose Calot triangle • Fundus superior • Infundibulum lateral/inferior • Critical view of safety • Avoid electrocautery ACUTE CHOLECYSTITIS – Cholangiogram • Anatomy • LFT elevation • H/O pancreatitis/jaundice • Injury • Timing – Early is better • Complications of AC – Gangrene.empyema.perforation – Male, older, T>38,WBC>18 – Mortality 20% ACUTE CHOLECYSTITIS • Complications of LC – Bile duct injury - 0.3% • Manage w/ERCP/stent • T-tube • Hepaticojejunostomy – Stone spillage 10% • Abscess ACUTE CHOLECYSTITIS • Acute acalculous cholecystitis – 4-8% of AC cases – M>F/Critically ill – Trauma/surgery/burns – Childbirth – Mult transfusions – Shock/sepsis – TPN/narcotics – SLE/Sarcoidosis/Polyart nodosa Acute acalculous cholecystitis • • • • Dx usually delayed HIDA, US., CT High risk of gangrene Treatment – Percutaneous cholecystostomy – Cholecystectomy Critically Ill • Cholecystostomy 95-100% successful • Facilitates delayed LC • No change in mortality vs conservative therapy. • Higher conversion, complication rate during subsequent lap chole PREGNANCY • • • • 0.04% develop AC Conservative Rx if poss 7% develop preterm labory Positioning – L side down ( take pressure off IVC)/ Rev Trend – SCD’s – Low pneumoperitoneum – Supraumbilical trocar w/ Hasson technique – US for CBDE/Lead shielding for cholangiogram – Monitor fetus pre/post-op Pregnancy • If possible (and necessary) surgery should be done in 2nd trimester – 1st trimester – open and lap assoc w/ spontaneous abortion – 3rd trimester – injury to uterus and premature labor – Control symptoms – wait for 2nd trimester or delivery. Recurrence 50-75% – If pain intractable or course worsens – cholesystostomy is reasonable until 2nd trimester/ delivery is reached. Question • A 27 yo woman who is 16 weeks pregnantpresents with 12 hours of RUQ abdominal pain and vomiting. She is afebrile and stable hemodynamically. She has a WBC of 13,200 and normal LFT’s. Ultrasound reveals cholelithiasis and distention, but no pericholecystic fluid or thickening. • Antibiotics and IV fluids are started, but after 12 hours her symptoms and exam worsen and her T=100.5 • The best management would be: – – – – – A. Magnesium sulfate B. percutaneous cholecystostomy C. Laparoscopic cholecystectomy D. ERCP E. Broaden antibiotic coverage Question • A 27 yo woman who is 16 weeks pregnantpresents with 12 hours of RUQ abdominal pain and vomiting. She is afebrile and stable hemodynamically. She has a WBC of 13,200 and normal LFT’s. Ultrasound reveals cholelithiasis and distention, but no pericholecystic fluid or thickening. • Antibiotics and IV fluids are started, but after 12 hours her symptoms and exam worsen and her T=100.5 • The best management would be: – – – – – A. Magnesium sulfate B. percutaneous cholecystostomy C. Laparoscopic cholecystectomy D. ERCP E. Broaden antibiotic coverage Acute Cholangitis • ETIOLOGY – Bile Stasis – Growth of bacteria • Stones • Papillary stenosis • Mirizzi syndrome • Choledochal cyst • Sclerosing cholangitis • Parasites/viral • Iatrogenic Acute Cholangitis • Charcot Triad – Abdominal pain – Fever – Jaundice • Reynolds Pentad - ADD: – Shock – Altered mental status Common Duct Stones • PRE-OP – ERCP • 70-90% effective • 40-60% no stones • Morbidity 5-19% • Mortality 1.9% • Longer LOS – Lap CBDE – 70-90% effective Common Duct Stones Intraop – Small stones • Glucagon to relax Oddi • Flush – LCBDE – OCBDE • Unable to do LCBDE • ERCP not possible • Impacted stone • Longer LOS/higher morbidity – ERCP/ES • Postop – ERC/ES Open CBDE • Contraindication – Small duct w/ small stones– risk of stricture – Portal HTN – Severe inflammation – Cholangitis w/shock Open CBDE • Steps – Flush/milk – Fogarty balloons – Choledochoscope – Baskets • If unsuccessful: • Transduodenal sphincterotomy – Anterior 10-11 oclock • avoid PD – Close if >10mm • Choledochoduodenostomy Question – The most effective long term treatmentfor extrahepatic choledochal cysts is • • • • • Antibiotics and Urodeoxycholic acid Placements of self expanding stents Resection Laser ablation Endoscopy/ES – The most common form of choledochal cyst is • • • • • Extrahepatic diffuse Extrahepatic saccular Intraduodenal (choledochocele) Intra- and Extrahepatic Intrahepatic only (Caroli’s) Choledochal Cysts – – – – – Type I Extrahepatic and fusiform (MOST COMMON) Type II Extrahepatic and saccular Type III Intraduodenal (choledochocele) Type IV Extrahepatic and Intrahepatic (Next M.C.) Type V Intrahepatic only (Caroli’s disease) – – – – Uncommon in West, but incidence increasing Triad of Symptoms: RUQ mass, pain, jaundice is RARELY EVIDENT Adults usually present w pancreatitis or cholecystitis Dx: Imaging U/s, MRCP/CT/ERCP Choledochal Cysts – Complications • Stone formation • Recurrent sepsis • MALIGNANT DEGENERATION (10%) – Treatment • Cyst excision w/ hepaticojejunostomy • Jejunal interposition may be better for surveillance Question – A 33 yo woman presents w 4 weeks of anorexia, weight loss, fatigue and jaundice. Evaluation including ERCP reveals primary scleerosisng cholangitis (PSC) • PSC – – – – – Occurs mostly in women Has a known etiology Is associated with retroperitoneal fibrosis More oftern assoiated with Crohn’s disease than Ulcerative colitis Lacks pathogomatic signs Question – A 33 yo woman presents w 4 weeks of anorexia, weight loss, fatigue and jaundice. Evaluation including ERCP reveals primary scleerosisng cholangitis (PSC) • PSC – – – – – Occurs mostly in women Has a known etiology Is associated with retroperitoneal fibrosis More oftern assoiated with Crohn’s disease than Ulcerative colitis Lacks pathogomatic signs Question – A 33 yo woman presents w 4 weeks of anorexia, weight loss, fatigue and jaundice. Evaluation including ERCP reveals primary scleerosisng cholangitis (PSC) – The most definitive treatments would be • • • • • Long term antibiotics Urodeoxycholic acid Long term steroids Roux-en-Y choledochoduodenotomy Hepatic transplantation