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NUR2063 Essentials of Pathophysiology Final Exam Review Study Guide (Latest 2022)NUR2063 Essentials of Pathophysiology Final Exam Review Study Guide (Latest 2022)NUR2063 Essentials of Pathophysiology Final Exam Review Study Guide (Latest 2022)NUR2063 Essentials of Pathophysiology Final Exam Review Study Guide (Latest 2022)NUR2063 Essentials of Pathophysiology Final Exam Review Study Guide (Latest 2022)NUR2063 Essentials of Pathophysiology Final Exam Review Study Guide (Latest 2022)NUR2063 Essentials of Pathophysiology Final Exam Review Study Guide (Latest 2022)NUR2063 Essentials of Pathophysiology Final Exam Review Study Guide (Latest 2022)
Typology: Exams
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Liver pancreas and biliary system
DISCUSSION: Segments are the major subdivision of the right and left lobes of the liver. In either the classic lobar (American) or the segmental (French) system, the most variable aspect is the biliary system. Therefore the hepatic venous or portal system defines most segments. The French system depicts eight segments, with the caudate lobe as segment I and the other seven segments defined primarily by the hepatic venous system. Segments are not well-depicted by topography.
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DISCUSSION: All of these features are important. The angle of takeoff of the left hepatic duct may make operative visualization difficult with the patient in the supine position. Because there may be more than two major hepatic ducts, visualization of two large ducts does not ensure that the system is normal. Ducts from any of the right-side segments can join below the confluence. Dissecting one superior edge of the gallbladder before it joins the cystic duct is particularly important in preventing injury.
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DISCUSSION: The portal vein provides two thirds to three quarters of the total hepatic blood flow. The portal vein is incapable of direct autoregulation. The hepatic artery after transplantation classically infarcts portions of the biliary system, whereas hepatic metastases often arrive there via the portal vein. Most of their blood supply comes from the hepatic artery.
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DISCUSSION: Bile formation is an active process at both the canalicular and ductular sites. The paracellular pathway probably plays a minor physiologic role. Secretin and glucagon are likely physiologic regulators of biliary secretion. Bile salts are extremely important and are probably the most important agent in the changes that occur when enterohepatic circulation is interrupted.
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DISCUSSION: While other functions undoubtedly may be important postoperatively, the most common abnormalities occurring after a major hepatic resection are related to loss of protein synthesis and consequences of glucose metabolism. Therefore, it is usually advisable to administer supplemental amounts of protein and sugar postoperatively.
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DISCUSSION: Involvement of the right lobe with abscess formation approximates 70% of pyogenic abscesses. This is thought to be due to the streaming effect of superior mesenteric venous inflow to the right lobe. In addition, the greater volume of the right lobe predisposes more tissue to seeding by bacterial organisms. While appendicitis comprised 25% to 40% of cases in early series, early recognition and operative therapy for appendicitis have reduced its importance significantly. In current series, malignant or benign biliary obstruction is the underlying cause of 35% to 50% of cases. Recent studies have shown that the underlying disease or an immunocompromised host is more important prognostically than solitary versus multiple abscesses.
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DISCUSSION: The development of ultrasonography and computed tomography (CT) in the past two decades has enabled earlier diagnosis and advances in treatment of hepatic abscess. Formerly, open surgical drainage was considered necessary in essentially all cases of pyogenic abscess. Numerous recent series, however, have reported high success rates and low mortality from the percutaneous catheter drainage of abscesses under CT or ultrasonographic guidance. Optimal management of pyogenic abscess, however, involves not only treatment of the abscess, whether by percutaneous or surgical methods, but correction of the underlying source as well. All modes of therapy are more successful in treating solitary lesions than multiple ones.
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DISCUSSION: Mortality for uncomplicated amebic abscess should be less than 5%, in contrast to the 15% to 20% rate for pyogenic abscess. After the demonstration by radiologic examination of an abscess, appropriate serologic tests and resolution of symptoms after a course of treatment
with an antiamebic agent such as metronidazole constitute presumptive diagnosis of amebic abscess. Aspiration of abscess contents rarely yields amebic organisms. In contrast to pyogenic abscess, amebic abscess rarely requires surgical or percutaneous drainage, except in the case of an extremely large abscess or bacterial superinfection. Amebic abscess affects males in a 9:1 to 10:1 ratio and generally affects a younger population than pyogenic abscess. Additionally, in the United States the populations most affected are immigrants from endemic areas such as Mexico or Latin America and American tourists to those regions.
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DISCUSSION: Adenomas typically enlarge and cause symptoms, may rupture, and have a definite malignant potential. Therefore they should generally be resected when found. FNH is not a true neoplasm and generally has an uneventful course. Both are related to BCPs, although the relationship of adenoma is more firmly established. While small bile duct hamartomas are much more common, hemangiomas are the most common lesion to come to the attention of surgeons. They should not generally be biopsied because of possible hemorrhage. By definition, nodular regenerative hyperplasia occurs in the absence of cirrhosis.
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DISCUSSION: Although exact comparisons are impossible, hepatoma seems to be the most common cause of cancer death worldwide, despite its relative infrequency in the United States. Colorectal metastasis is a more common indication for surgical treatment in the United States. The fibrolamellar variant and possibly the very well-differentiated tumor probably have a better prognosis than hepatomas in general. Previous studies from Africa in which there was a high
incidence of rupture account for the poor prognosis that was generally attributed to hepatoma. Recent studies from Europe and the United States have shown that survival after presentation is usually measured in years.
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DISCUSSION: Most bile duct cancers are discovered after they are incurable, and only a tiny subset of resected proximal lesions are cured. The more distal the lesion, the more likely is resection to achieve cure (e.g., approximately 30% 5-year survival for periampullary lesions as compared with 0% to 10% for hilar lesions). The use of adjuvant or primary radiation remains controversial because of the heterogeneity of the patient populations on which this modality has been used. Because of the localized nature of this disease it would seem that transplantation would produce favorable results; however, this has not been the case.
DISCUSSION: The parasitic infection is fairly common in certain parts of Europe but very rare in the United States. Resection without peritoneal soilage is the treatment of choice. The E. multilocularis form, which is endemic to parts of the United States, is more likely to be fatal because it is rarely resectable. This form is more likely to resemble a malignancy than E. granulosus, although the natural course of the disease usually spans many years.
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DISCUSSION: By far the most common cause of hemobilia is trauma. Tumors also may cause the syndrome but are relatively uncommon causes. For severe hemobilia the best therapy is arteriographic embolization. Usually the site of bleeding or a false aneurysm can be identified. Operation should be reserved as a last resort or when the condition is recognized intraoperatively. Percutaneous cholangiography–associated intrabiliary hemorrhage is usually, but not always, minor and self-limiting. Ultrasonography is a very nonspecific diagnostic technique for hemobilia. Arteriography remains the best diagnostic method.
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DISCUSSION: Ligation of the right or left hepatic artery frequently causes enzyme elevation but is usually tolerated by the patient, particularly when this is a life-saving maneuver. Ligation of the hepatic artery distal to the gastroduodenal branch is more risky but is also usually tolerated. Ligation of the hepatic artery proximal to the gastroduodenal one does not normally cause enzyme abnormalities because of abundant collateral flow through that branch.
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DISCUSSION: Metabolic alkalosis and hypokalemia are common in patients with cirrhosis because they often have associated secondary hyperaldosteronism (especially those with ascites), diarrhea, and frequent emesis. Hyperaldosteronism enhances H+ and K+ exchange for Na+ in the distal tubule of the kidney. The cause of diarrhea in patients with cirrhosis is unknown, but malabsorption secondary to splanchnic venous hypertension may be a contributing factor. Emesis is common in alcoholic cirrhotics and patients with tense ascites. Deleterious effects of metabolic alkalosis include impaired tissue oxygen delivery secondary to shift of the oxyhemoglobin dissociation curve to the left and conversion of ammonium chloride to ammonia, which may contribute to encephalopathy.
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DISCUSSION: Pressure measured by wedging a catheter into a hepatic vein (hepatic venous wedge pressure) closely correlates with directly measured portal venous pressure in patients with portal hypertension when the site of elevated resistance is at the sinusoidal or postsinusoidal level. Such is the case in alcoholic cirrhosis and alcoholic hepatitis. When the site of increased resistance is at the presinusoidal level, either within (schistosomiasis) or outside (portal vein thrombosis) the liver, the hepatic venous wedge pressure is normal despite markedly elevated portal vein pressure. Although schistosomiasis is one of the more frequent causes of portal hypertension worldwide, in North America presinusoidal portal hypertension is considerably less common than alcoholic liver disease. A normal hepatic venous wedge pressure in a patient who has bled from varices should lead one to suspect a presinusoidal cause. A specific diagnosis can often be made by visceral angiography or liver biopsy.
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DISCUSSION: Shunt operations are the most effective means of preventing recurrent variceal hemorrhage. Rebleeding rates after endoscopic sclerotherapy range from 40% to 60%. Although extensive esophagogastric devascularization has effectively prevented recurrent bleeding in Japanese series, these operations have been followed by rebleeding rates in excess of 25% in most Western series. Although one controlled trial has shown more frequent recurrent hemorrhage following the distal splenorenal shunt than after the portacaval shunt, most series have reported rebleeding rates of less than 10% for both of these operations. Both the liver and the splanchnic viscera are important sites of ascites formation. Since the distal splenorenal shunt maintains sinusoidal and mesenteric venous hypertension and requires interruption of important retroperitoneal lymphatics, it tends to aggravate rather than relieve ascites. Hepatic sinusoidal pressure may be unchanged or even increased after an end-to-side portacaval shunt.
Only side-to-side portal-systemic shunts, such as the side-to-side portacaval shunt, reliably decompress both the liver and splanchnic viscera, thus preventing ascites formation.
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DISCUSSION: The conventional splenorenal shunt and side-to-side portacaval shunts completely divert portal flow away from the liver (nonselective shunts). The distal splenorenal shunt is a selective shunt that preserves hepatic portal perfusion in the majority of patients; however, the magnitude of portal flow is decreased because the gastrosplenic component is diverted into the renal vein. Additionally, many patients (especially alcoholic cirrhotics) develop collaterals between the mesenteric venous circulation and the shunt, resulting in gradual attrition of the remaining portal flow. Although there have been anecdotal reports of portal vein thrombosis after endoscopic sclerotherapy, two controlled trials have demonstrated better preservation of hepatic portal perfusion in sclerotherapy patients than in persons who receive the distal splenorenal shunt.
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DISCUSSION: The Sugiura procedure consists of devascularization of the esophagus to the inferior pulmonary vein and the proximal two thirds of the stomach, splenectomy, and distal esophageal transection. The devascularization component should be done as close to the esophagus and stomach as possible. The coronary vein and paraesophageal collaterals are preserved to maintain an effective portal-systemic collateral pathway and thereby discourage reformation of varices.
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A. Hypersplenism. B. Variceal hemorrhage. C. Ascites. D. Encephalopathy. Answer: B
DISCUSSION: While many patients with portal hypertension develop hypersplenism, it is rarely clinically significant. A splenectomy should not be performed unless platelet counts are persistently less than 20,000 per cu. mm. or white blood cell counts are less than 1200 per cu. mm. Unfortunately, splenectomy is sometimes done for clinically insignificant hypersplenism, thus obviating a distal splenorenal shunt if the patient should subsequently bleed from varices. The initial treatment for most patients with bleeding esophageal varices should be endoscopic sclerotherapy; however, operation is required for the approximately one third of patients who fail sclerotherapy and for noncompliant persons, those living in remote geographic locations, and patients bleeding from gastric varices. Ascites can be controlled by a medical regimen of dietary salt restriction and diuretic therapy in more than 95% of patients. When ascites is intractable to medical management, either intermittent large-volume paracenteses or a surgical peritoneovenous shunt should be done. With rare exceptions, encephalopathy should be treated medically. Most important is elimination of any precipitating factors that led to the neuropsychological disturbance. Lactulose, neomycin, and dietary protein restriction may also be components of the medical treatment regimen.
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DISCUSSION: Vasopressin acts through vasoconstriction of splanchnic arterioles. Both portal venous inflow and portal venous pressure are reduced, resulting in control of acute variceal bleeding in approximately 50% of patients. However, the adverse side effects of systemic hypertension, bradycardia, decreased cardiac output, and coronary vasoconstriction are quite common during vasopressin infusion. Simultaneous administration of nitroglycerin or nitroprusside eliminates these side effects—and in one controlled trial enhanced therapeutic effectiveness. Although the mechanism of action of this combined infusion is not clear, vasodilation of portal-systemic collaterals, resulting in a further reduction in portal pressure, may be responsible.
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DISCUSSION: The PVS is a palliative procedure that does not prolong life. In comparing the early risks of the procedure with those of repeated paracentesis, the shunt cannot be justified as a temporizing procedure to facilitate ascites control in the patient awaiting liver transplantation. Oliguria is common in the first 24 hours after shunt insertion. A correctly placed PVS (patency confirmed using an intraoperative “shuntogram”) expands the intravascular volume with a continuous reinfusion of ascites. Inspection should identify elevation of the jugular venous pressure, and a diuretic (usually furosemide) is needed. The mechanisms of action of the two shunts are very different. TIPSS reduces portal pressure and controls ascites by reducing the rate of ascites formation. PVS reinfuses the ascites fluid, thereby reducing the prerenal stimulus to sodium retention and making the patient more responsive to diuretic therapy.
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DISCUSSION: Because of the high complication rate and the long-term failure rate, the PVS is used only when other, more lasting options for therapy either are not available or are contraindicated. The chronic alcoholic patient may benefit from a peritoneovenous shunt because his ascites is the dominant problem related to his chronic liver disease, and persistent alcoholism is a contraindication to liver replacement in most centers. PVS may be quite effective for the temporary management of acute intractable postoperative ascites, such as in patient A; however, it is absolutely contraindicated in the presence of infection. Patient B has ascites as her dominant problem as well; however, with PBC as the underlying liver disease, she is an
excellent candidate for transplantation. Patient D also has ascites as the major problem; however, the side-to-side portosystemic shunt is a far better long-term treatment option than PVS. Ref – sabiston 20th^ ed. Pg-1418-
DISCUSSION: The ability to specifically identify persons infected with HCV has only recently become available. Therefore, data about epidemiology are less than complete. It is very likely not true that more blood donors carry HCV because of the large preponderance of HBV in the United States. It is true, however, that successful elimination of most of the HBV carriers occurs through routine testing. Although serologic tests are available for HCV, they are tests, not of antigen, but of antibody. Therefore, this test alone may not screen out persons who are infected but have not yet developed or may never develop antibody. Risk groups for the relatively newly defined HCV may well not be comprehensively established, and therefore this explanation may be a contributor. There are no differences in virulence between these classes of hepatitis virus.
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Answer: B
DISCUSSION: Although some types of hepatitis are more often asymptomatic than symptomatic, that is not the case for hepatitis B. Further, even if the HBV infection is asymptomatic, serious long-term side effects may occur. A prior infection with hepatitis B confers lifelong immunity even if the antibody titer wanes below the protective level of 10 mIU. HBIg is useful in reducing the incidence of postexposure HBV infection from around 30% with no intervention, to 15%
with standard immune globulin, to about 5% to 7% with HBIg. HBV infection is required for infection with HDV and is therefore an essential step toward, rather than preventive of, HBV infection.
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DISCUSSION: Most common duct stones originate in the gallbladder and migrate to the common duct, where they may become larger. These stones tend to consist predominantly of cholesterol (about 80% of gallbladder stones are predominantly cholesterol). Stones found in the bile ducts after cholecystectomy may have been overlooked, but de novo stone formation does occur. Arbitrarily, stones found 2 years after cholecystectomy are assumed to have formed within the duct system. Calcium bilirubinate stones are thought to result from precipitation of insoluble bilirubin monoglucuronide formed by deconjugation of bilirubin diglucuronide, a reaction promoted by the enzyme beta-glucuronidase, which is produced by bacteria in the biliary tract. Calcium bilirubinate stones are found almost exclusively in patients who have some form of biliary tract lesion that causes partial obstruction, and these patients tend to have bactibilia. Stones smaller than approximately 5 mm. often can be extracted through a dilated cystic duct or pushed into the duodenum. Larger stones are best left for postoperative endoscopic sphincterotomy and extraction. Patients with more than five stones or stones larger than 1.5 cm. should be treated by open choledocholithotomy or, when indicated, a biliary- enteric anastomosis. Not all patients with symptomatic common duct stones have elevated serum bilirubin, but when jaundice is present the bilirubin is only rarely greater than 15 mg. per dl.
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DISCUSSION: Even a minor obstructing lesion in the extrahepatic duct system can produce cirrhosis over time, and the development of portal hypertension, ascites, and esophageal varices. Therefore, all biliary strictures should be treated unless this is not possible or there is no chance for success. The presence or absence of jaundice is of no significance. Often, the only biochemical abnormality is mild elevation of alkaline phosphatase. The long -term results of percutaneous balloon dilatation are not yet known, but short-term results are good. Although some argue that balloon dilatation should be the initial treatment, its role is ill-defined, and it should not be viewed as standard therapy at this time. Biliary-enteric anastomoses are predisposed to stricture, for reasons that are ill-understood. A mucosa-to-mucosa anastomosis, large size of the anastomosis, a normal duct at the point of anastomosis, and stenting appear to be elements that work against stricture. About 70% of anastomoses are not complicated by strictures. Common duct strictures caused by chronic pancreatitis are located in the distal portion of the duct and are easily treated by side-to-side choledochoduodenostomy. A wide anastomosis is usually possible, and because of this stenting often is not necessary. Although a Roux-en-Y biliary-enteric reconstruction is acceptable treatment, no advantage over choledochoduodenostomy has been demonstrated.
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DISCUSSION: Cholangiography is essential for both diagnosis and evaluation of resectability. Brushings of the lesion for diagnosis and temporary stenting, done percutaneously or endoscopically, are often done at the time of cholangiography. Angiography and CT are helpful, but in the absence of hepatic artery or portal vein occlusion these tests are not accurate predictors of resectability. The primary obstacles to complete resection are invasion of the portal vein or the hepatic artery and proximal extension of the tumor into the liver. The long- range prognosis for patients who undergo treatment for extrahepatic bile duct cancer is poor, even when the lesion is surgically resectable and adjuvant therapy is given. Only about 10% of patients are alive without disease at 10 years. Nevertheless, bile duct cancer tends not to metastasize to distant sites, so resection and radiation therapy are useful in prolonging symptom-free life. Tumors in the proximal third of the extrahepatic bile duct system are treated by a Roux-en-Y biliary-enteric anastomosis. To ensure excision of the entire tumor this anastomosis usually must be made to the individual hepatic ducts, which must be stented individually. Tumors of the middle third usually require anastomosis to the proximal hepatic duct. In contrast, lesions of the distal third require Whipple's procedure with appropriate reconstruction. Thus, the treatment of extrahepatic bile duct cancer depends on the location of the tumor. Pain is not a prominent feature of bile duct cancer. Most cases become manifest by
the insidious development of jaundice.
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DISCUSSION: In the past, choledochal cyst was treated by Roux-en-Y cystojejunostomy, but long- term results were poor. Excision of the cyst is essential to prevent recurrent pancreatitis. In addition, the development of carcinoma in about 25% of patients mandates cyst excision. Accordingly, excision of the cyst with biliary reconstruction by Roux-en-Y hepaticojejunostomy and diversion of the flow of pancreatic juice through the ampulla of Vater is currently the standard treatment. Sclerosing cholangitis causes fibrosis of bile ducts both within and outside the liver. This process, which is poorly understood, causes strictures in the duct system, characteristically with normal or dilated segments between strictures. Unfortunately, this anatomic arrangement does not lend itself to biliary reconstructive procedures. Each case must be analyzed, however, because in some patients the anatomic situation may lend itself to balloon dilatation or reconstruction. When the gallbladder appears to be absent, a search should be made for an ectopically located organ in the retroduodenal area, within the falciform ligament, and within the substance of the right lobe of the liver. With true gallbladder agenesis the common duct may be dilated, and choledocholithiasis is present in about one fourth of those who undergo operation. Therefore, operative needle cholangiography should always be done. Dissection of a long, fused cystic duct is fraught with hazard because the cystic and common ducts may share a common wall and serious duct damage may occur. The cystic duct should be ligated and divided immediately proximal to the area of fusion.
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DISCUSSION: The presence of pain is the sine qua non of acute calculous cholecystitis. Chronic cholecystitis associated with cholelithiasis may develop in the absence of pain, and in critically ill patients pain may not be a prominent feature of acute acalculous cholecystitis. Only about 10% of patients with acute cholecystitis are jaundiced. Although an occasional patient may have concomitant bile duct obstruction, the jaundice associated with acute cholecystitis is probably due to absorption of bile pigments from the diseased gallbladder. The presence of jaundice in a patient with right-side upper quadrant pain should also suggest the possibility of acute cholangitis secondary to bile duct obstruction. Ultrasonography is very accurate in the detection of gallstones, but stones may be present in the absence of acute cholecystitis. Thickening of the gallbladder wall and a collection of fluid around the gallbladder are ultrasonographic findings in some patients with acute cholecystitis, but they are not always present and are not specific. Ultrasonography may be useful when the diagnosis is obscure because other conditions in the liver, pancreas, and kidney can be detected; however, it is not the definitive test for acute cholecystitis. Cholescintigraphy is specific for the diagnosis of acute calculous cholecystitis (accuracy over 95% in experienced hands). The rapidity, simplicity, and accuracy make cholescintigraphy the definitive diagnostic test in acute calculous cholecystitis; however, it must be interpreted cautiously in the context of another critical illness or recent surgery or trauma, because false-positives are not unusual in these situations.
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DISCUSSION: About half of the cases of acute acalculous cholecystitis are associated with other conditions, including sepsis, sarcoidosis, polyarteritis nodosa, and systemic lupus erythematosus. A majority of cases occur after trauma, burns, or major surgi cal procedures performed for other conditions. The precise pathogenesis has not been determined. The diagnosis of acute acalculous cholecystitis is often difficult because symptoms may be masked by another illness, injury, or the postoperative state. Unlike acute calculous cholecystitis, in which pain is always present, pain occurs in only about 70% of cases. In addition, cholescintigraphy is sometimes inaccurate. These factors make the diagnosis difficult, and a high index of suspicion is necessary, especially in patients who have had operations or trauma. Unexplained abdominal pain, sepsis, and ileus should prompt a thorough investigation. The mortality rate for acute acalculous cholecystitis is higher than that of the calculous type. The incidence of gangrene and perforation of the gallbladder is higher. The accompanying illnesses and conditions and the frequent delays in diagnosis undoubtedly contribute to the higher death rate. Percutaneous cholecystostomy has been used as a diagnostic and therapeutic maneuver in
patients who are thought to have acute acalculous cholecystitis. Aspiration and culture of bile assist in confirming the diagnosis, and continuous drainage successfully treats the acute condition. Surprisingly, persistent gangrene and subsequent complications have been infrequent. Immediate cholecystectomy should be done if significant improvement does not take place within 12 hours of percutaneous cholecystostomy. Long-term management of the tube and the need for elective cholecystectomy must be individualized. The experience with percutaneous cholecystostomy is too small to determine whether this technique reduces the mortality rate.
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DISCUSSION: Cholecystectomy should be done in an otherwise healthy patient as soon as the diagnosis is made and the patient is properly prepared for surgery. However, patients who have one or more significant risk factors such as a recent myocardial infarction, unstable angina, clinically significant coronary artery disease, or cirrhosis should not have immediate cholecystectomy unless they do not improve within 24 to 36 hours in response to antibiotic administration and supportive care. Antibiotic administration should commence as soon as the diagnosis is made and should be continued for 24 hours postoperatively—or for 7 days if significant peritonitis is present. This use of antibiotics has significantly reduced septic complications after cholecystectomy for acute cholecystitis. In most cases the gallbladder is tensely distended, making visualization and dissection of the cystic duct area difficult and perhaps dangerous. Decompression of the gallbladder by insertion of a needle facilitates retraction and dissection of the gallbladder. Although some advise that operative cholangiography be done only on a selective basis, its routine use helps to delineate anatomy and facilitates detection of an occasionally unsuspected bile duct stone. Accordingly, it is used routinely in elective cases. In acute cholecystitis, however, the biliary duct system may be very friable, and operative cholangiography should be done only when it is safe to do so.
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B. The presence of gallstones in an asymptomatic patient. C. The presence of symptomatic gallstones in a patient with angina pectoris. D. The presence of asymptomatic gallstones in a patient who has insulin-dependent diabetes. Answer: A
DISCUSSION: Cholecystectomy (and concomitant operative cholangiography) are indicated for symptomatic patients to relieve pain and to prevent the development of acute cholecystitis and its complications. Morbidity and expense are not as great for elective cholecystectomy as they are for cholecystectomy for acute cholelithiasis. The risk of the development of symptoms in patients who have asymptomatic stones is approximately 2% per year, a rate associated with mortality and morbidity that do not exceed those of elective cholecystectomy. Therefore, cholecystectomy is not indicated for asymptomatic patients. Patients who have angina pectoris should not have cholecystectomy until their coronary artery disease has been treated adequately, even if this requires a coronary artery bypass procedure. Heart disease is the most frequent cause of death after cholecystectomy. Prophylactic cholecystectomy, formerly recommended for insulin-dependent diabetics, is not indicated because several studies have shown that the mortality rate from acute cholecystitis is no higher for diabetics than for nondiabetics.
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DISCUSSION: Studies have clearly documented that postoperative pain following laparoscopic cholecystectomy is less than that experienced after open cholecystectomy and that patients can resume normal activity sooner. This appears to be related to the reduced trauma to the abdominal wall by virtue of the very small incisions used in laparoscopic procedures. The best evidence is that the bile duct injury rate (0.4%) is approximately double that for open cholecystectomy. The incidence of this serious complication will probably decrease with improved techniques, better training, and more advanced instrumentation. Only symptomatic patients should have cholecystectomy. Prophylactic removal of the gallbladder is not cost effective. All elective operations are contraindicated in the first trimester, so as to prevent fetal anomalies and spontaneous abortion. The laparoscopic technique is not contraindicated thereafter except in patients in whom peritoneal access cannot safely be established. This is rarely a problem. Premature labor is a risk in the third trimester. Thus, unless cholecystectomy can be avoided altogether during pregnancy, the second trimester is the most propitious time.
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A. Associated biliary tract disease is always present. B. Chills and fever are due to the presence of bacteria in the bile duct system. C. The most common cause of cholangitis is choledocholithiasis. D. All of the above Answer: D
DISCUSSION: Although Charcot's triad (pain, chills and fever, jaundice) is diagnostic of cholangitis, the complete triad occurs only in 50% to 70% of patients. Fever is the most common symptom; therefore, cholangitis should be considered in all patients who have unexplained fever. Episodes of pain, chills, and fever are often so brief as not to concern the patient. Cholangitis does not occur in the absence of partial or complete bile duct obstruction. All patients diagnosed as having cholangitis should have appropriate diagnostic studies to determine the cause. This usually involves cholangiography. The presence of bacteria in bile does not produce symptoms in the absence of partial or complete obstruction of the bile duct system. When obstruction is present, pressure within the system increases, giving rise to reflux of bacteria or their toxic products into the hepatic venous circulation. This cholangiovenous reflux produces chills, fever, and the hemodynamic changes of sepsis. Death may ensue if treatment is not instituted promptly. Choledocholithiasis, the most commonly associated problem, may produce partial or complete obstruction. When bacteria are not present in the bile duct system, choledocholithiasis may go undetected unless the degree of obstruction is sufficient to cause jaundice. Other causes of cholangitis are benign and malignant strictures, biliary-enteric anastomoses, invasive procedures, foreign bodies, and parasitic infestation of the bile ducts.
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DISCUSSION: Cholangitis does not occur in the presence of a normal bile duct system, and all patients with cholangitis have an abnormality. Thus, recurrent episodes of cholangitis signal the need for diagnostic studies. Cholangiography usually will be necessary. The presence of any foreign body in the biliary tract is frequently associated with bactibilia and recurrent episodes of cholangitis. Even a silk suture exposed to the lumen of a bile duct has been known to cause
cholangitis. Pigment stone and sludge formation may result from the bacterial deconjugation of bilirubin diglucuronide to bilirubin monoglucuronide, which precipitates as calcium bilirubinate. This material can occlude indwelling tubes and predispose to more frequent episodes of cholangitis. Long-term administration of an oral antibiotic may reduce the frequency and severity of attacks of cholangitis; however, this method of management should not be routine. Correction of the underlying problem is essential. Chronic obstruction and recurrent infection eventually lead to secondary biliary cirrhosis and its complications of portal hypertension, ascites, and bleeding esophageal varices. Once this stage of the disease is reached, correction of the underlying biliary tract problem does not reverse the changes in the liver. Once again, every effort should be made to eliminate the cause of the cholangitis early in the course of disease. The only effective treatment for end-stage liver disease is hepatic transplantation.
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DISCUSSION: Uncontrolled sepsis and the consequent multisystem organ failure are the life- threatening sequelae of acute toxic cholangitis. Thus, the initial goal of treatment is to decompress the biliary duct system to prevent reflux of bacteria and their toxic products into the circulation. This can be done by intubating the duct system through the percutaneous, transhepatic, or the endoscopic route or by insertion of a T tube in the common duct at operation. Removal of the stone causing the obstruction is not necessary to stabilize the patient. Only after the duct is decompressed should the cause of the obstruction be addressed. When transhepatic biliary drainage has been used, endoscopic or surgical removal of the stone can be carried out after the patient has recovered completely. When initial therapy is sphincterotomy, the stone should be removed as part of the procedure. Often the stone falls out without manipulation. If surgical placement of a T tube is the initial treatment, the stone should be removed only if it is convenient to do so. The long-range goal of treatment of patients with bile duct obstruction is to prevent cirrhosis, ascites, portal hypertension, and hemorrhage from esophageal varices; however, death from sepsis is the immediate th reat in acute toxic cholangitis. Gallstone pancreatitis may occur in patients who have an impacted stone in the distal duct, independent of the presence or absence of acute toxic cholangitis; however, gallstone pancreatitis is more often associated with the passage of a stone into the duodenum.
Ref – sabiston 20th^ ed. Pg-1482-
A. Air in the biliary tree. B. Small bowel obstruction. C. A stone at the site of obstruction. D. All of the above Answer: D
DISCUSSION: An antecedent biliary-enteric fistula is necessary to allow stone migration into the intestinal tract, and this results in air entering the biliary tree (pneumobilia). It also allows contamination of the bile ducts with intestinal bacteria, which in fact occurs in only a minority of such cases. The stone obstructs the narrower distal bowel, producing small bowel obstruction. Such a stone, if opaque, can be seen on plain radiography and, if not, can be appreciated by sonography. Stools are not acholic, since the cholecystoenteric fistula allows bile access to the intestinal lumen.
Ref – sabiston 20th^ ed. Pg-1482-
Answer: C
DISCUSSION: It is true that gallstone ileus occurs mostly in elderly women and should always be suspect when small bowel obstruction presents in this age group. The great majority of cases of gallstone ileus are preceded by a spontaneous fistula occurring between the gallbladder and duodenum, allowing gallstones to enter the intestinal tract, which can potentially block the terminal ileum. Finding air within the biliary tree should always arouse suspicion of the possibility of this diagnosis when it is associated with a radiographic pattern of small bowel obstruction. The initial part of the operative approach to this disease is to relieve the bowel obstruction by performing an enterotomy just proximal to the point of obstruction to remove the stone. Where possible, definitive repair of the fistula should be undertaken to avoid recurrent obstruction and to obviate the possible recurring complications of cholangitis. Percutaneous drainage of bile collections combined with endoscopic papillotomy may be sufficient treatment for external and internal biliary fistulas but is never an allowable approach in the presence of gallstone ileus with small bowel obstruction. Relief of the obstruction is mandated in this setting. Ref – sabiston 20th^ ed. Pg-1482-
carcinoma of the gallbladder? A. Cholecystoenteric fistula. B. A calcified gallbladder. C. Adenoma of the gallbladder. D. All of the above.
Answer: D
DISCUSSION: The prevalence of carcinoma of the gallbladder in patients who have or have had a cholecystoenteric fistula is believed to be 15%. The prevalence of carcinoma in a calcified, or “porcelain,” gallbladder is reported to range from 12.5% to 61%. It is generally accepted that adenoma of the gallbladder is a precancerous lesion that presents as a polypoid lesion. Xanthogranulomatous cholecystitis is a rare form of chronic cholecystitis believed to be associated with a higher incidence of cancer. This form of cholecystitis is also important because, grossly, it may mimic cancer of the gallbladder.
Ref – sabiston 20th^ ed. Pg-1482-1518
Answer: D
DISCUSSION: Radical resection, radiation therapy, and chemotherapy have been effective only anecdotally. Most believe that the dismal prognosis of carcinoma of the gallbladder does not justify anything more than palliative treatment. About 88% of patients are dead within a year of diagnosis, and only about 4% are alive after 5 years, regardless of the type of treatment. Those whose surgeon was unaware of the presence of the tumor at the time of cholecystectomy (approximately 12% of cases) are most likely to survive long term. There are insufficient data to support conclusively the proposition that the patient with unexpected carcinoma found on histologic examination should undergo reoperation with intent for radical excision. There also are indirect suggestions that the prognosis of gallbladder carcinoma may be improving, but it is not clear if this is spontaneous or due to either earlier diagnosis or surgical management.
Ref – sabiston 20th^ ed. Pg-1482-1518
B. Heterotopic pancreatic tissue predisposes to pancreatic adenocarcinoma. C. Annular pancreas does not cause gastrointestinal obstruction in children or in adults. D. Relative obstruction to the flow of pancreatic juice through the minor papilla appears to be the cause of pancreatitis in some patients with pancreas divisum. Answer: D
DISCUSSION: The clinically recognized embryonic malformations of the pancreas include heterotopic pancreas, pancreas divisum, and annular pancreas. Heterotopic pancreatic tissue most often takes the form of a firm nodule of variable size in the stomach, duodenum, small bowel, or Meckel's diverticulum. The typical complications of heterotopic pancreas include intestinal obstruction, ulceration, or hemorrhage. Pancreas divisum is an anatomic variant that results from failure of fusion of the two primordial pancreatic duct systems. In pancreas divisum the major portion of the pancreas is drained via the duct of Santorini through the minor duodenal papilla. Relative stenosis of the minor duodenal papilla can cause pancreatitis. Pancreas divisum is not associated with gastrointestinal bleeding. Annular pancreas results when histologically normal pancreatic tissue completely or partially encircles the second portion of the duodenum. Varying degrees of duodenal obstructive symptoms may be observed in both children and adults with this condition.
Ref – sabiston 20th^ ed. Pg-1520-1553
DISCUSSION: The pancreas occupies a retroperitoneal position in the upper abdomen, extending obliquely from the duodenal C loop to a more cephalad position where the pancreatic tail abuts the hilum of the spleen. The portion of the pancreas anterior to the confluence of the superior mesenteric vein, splenic vein, and portal vein is designated the neck of the gland. The uncinate process extends posterior to the superior mesenteric vein and approaches the superior mesenteric artery. The head of the pancreas is intimately associated with the second portion of the duodenum, and these two structures are jointly supplied by two arterial arcades known as the anterior and posterior pancreaticoduodenal arteries, which originate as branches of the celiac axis and superior mesenteric artery.
Ref – sabiston 20th^ ed. Pg-1520-1553
DISCUSSION: The endocrine portion of the pancreas is served by the islets of Langerhans, which number 1 million islets per gland. The islets of Langerhans drain their endocrine secretions into the bloodstream. Insulin-producing beta cells comprise the majority of the islet population. Alpha cells produce glucagon and constitute approximately 20% to 25% of the total islet cell number. Delta cells of the islets produce somatostatin. The acini and ductal systems constitute the exocrine portion of the pancreas. The acinar cells contain zymogen granules in their narrow, centrally located apical portion. The pancreatic duct system includes intercalated duct cells along the ductal pathway, terminating in the main excretory duct of the pancreas.
Ref – sabiston 20th^ ed. Pg-1520-1553
DISCUSSION: CCK is the most potent endogenous stimulant of pancreatic enzyme secretion. The pancreatic acinar cells respond to CCK with release of their zymogen granules into the ductal system. Peptidases are released in inactive form, later to be activated by contact with duodenal enterokinase and activated trypsin. Secretin is the most potent endogenous stimulant of pancreatic water and electrolyte secretion. The concentrations of the anions bicarbonate and chloride vary and are largely dependent on the secretory flow rate stimulated by secretin.
Ref – sabiston 20th^ ed. Pg-1520-1553
useful in the early evaluation of a patient with acute pancreatitis? A. Elevated blood glucose. B. Leukocytosis. C. Amylase value greater than 1000 U per dl. D. Serum lactic dehydrogenase (LDH) greater than 350 IU per dl. Answer: C
DISCUSSION: Several prognostic systems have been demonstrated to predict the severity of pancreatitis accurately. Two Ranson prognostic criteria have been developed: one each, for pancreatitis that is not due to gallstones and pancreatitis that is. The systems have minor differences. In both of the Ranson systems elevated blood glucose, leukocytosis, and elevations of serum LDH have proved to have prognostic importance. The degree of amylase elevation is not one of the parameters, nor is the degree of ALT elevation.
Ref – sabiston 20th^ ed. Pg-1520-1553
DISCUSSION: Standard therapy for all patients with mild acute pancreatitis should include intravenous fluid resuscitation, electrolyte replacement, and analgesics. Nasogastric decompression is typically reserved for patients with significant ileus who are at risk for emesis and aspiration. Subcutaneous therapy with octreotide, the octapeptide analog of somatostatin, has not been proven to influence the outcome in patients with mild pancreatitis. Prophylactic antibiotics are not used for mild pancreatitis. Antibiotics are reserved for patients with severe pancreatitis (defined as greater than three Ranson prognostic signs with associated CT evidence of pancreatic or peripancreatic necrosis).
Ref – sabiston 20th^ ed. Pg-1520-1553
DISCUSSION: Chronic pancreatitis is a clinical entity that includes recurrent or persistent abdominal pain with evidence of exocrine and endocrine pancreatic insufficiency. While chronic pancreatitis may result from repeated episodes of acute pancreatitis, not all patients with recurring acute pancreatitis progress to chronic pancreatitis. The most common causes of chronic pancreatitis include alcohol abuse, hyperparathyroidism, congenital anomalies of the pancreatic duct, pancreatic trauma, and cystic fibrosis. The most useful radiographic tests in patients with suspected chronic pancreatitis are CT and endoscopic retrograde cholangiopancreatography (ERCP). Mesenteric angiography has no role in the evaluation of most patients with chronic pancreatitis. Patients with disabling chronic pancreatitis who require operative intervention are candidates for a longitudinal pancreaticojejunostomy (Peustow procedure) if pancreatography demonstrates a dilated pancreatic duct. Total pancreatectomy is rarely performed because of the significant problems associated with labile insulin sensitivity, steatorrhea, and weight loss.
Ref – sabiston 20th^ ed. Pg-1520-1553
DISCUSSION: Pancreatic ascites typically occurs because of a pancreatic duct disruption, most commonly involving alcohol abuse and resultant acute pancreatitis. In pancreatic ascites, pancreatic exocrine secretions exit a pancreatic duct disruption and drain anteriorly into the peritoneal cavity. Patients typically present with painless massive ascites, as the pancreatic enzymes that extravasate into the peritoneal cavity are typically nonactivated. The diagnosis of pancreatic ascites is best made by paracentesis, in which the analysis of the ascites fluid reveals it to be high in amylase (more than 1000 U. per dl.) and high in albumin (more than 3 gm. per dl.). Nonoperative treatment is initially indicated in most patients with pancreatic ascites. Should nonoperative therapy fail, surgical therapy is directed to closure of the pancreatic duct disruption. Preoperative pancreatography is useful in directing surgical therapy. Distal pancreatic duct disruption may be treated with distal pancreatectomy or with Roux-en-Y pancreaticojejunostomy. Pancreatic leaks in the more proximal aspects of the gland are treated with Roux-en-Y pancreaticojejunostomy. Suture ligation of the pancreatic duct with omental patching is not considered appropriate therapy for pancreatic duct disruptions.