1 / 35

Acute pancreatitis

Acute pancreatitis. The treatment of patients is dependent on the early assessment of disease severity. Potentially lethal attacks are known to occur in 2%–10% of patients with acute pancreatitis Early detect !. Classification. 1992 Atlanta, International Symposium on Acute Pancreatitis

annapowers
Download Presentation

Acute pancreatitis

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. Acute pancreatitis • The treatment of patients is dependent on the early assessment of disease severity. • Potentially lethal attacks are known to occur in 2%–10% of patients with acute pancreatitis • Early detect !

  2. Classification • 1992 Atlanta, International Symposium on Acute Pancreatitis • Mile pancreatitis: edematous or interstitial pancreatitis, most individuals • Severe pancreatitis: necrotizing pancreatitis, occurs in about 20%–30% of all patients

  3. Pancreatic necrosis • The importance of early detection of pancreatic necrosis in clinical practice cannot be overemphasized. • Interstitial pancreatitis: <1% mortality • Necrotizing pancreatitis: 10-23% mortality • Secondary bacterial infection: 40-70% necrotizing pancreatitis • Most patients with acute pancreatitis who develop multiorgan failure have necrotizing pancreatitis, and more than 80% of deaths occur in patients with pancreatic necrosis

  4. How to detect? • Clinical evaluation • Laboratory investigations • Imaging studies • Ideal system • have high sensitivity and positive predictive values • be able to depict necrosis early (48 hours) • be performed rapidly (4 hours) • be available in most hospitals • be relatively inexpensive, • be objective and not observer dependent

  5. Clinical Evaluation • Unreliable !!! • tachycardia, orthostatic hypotension, shock, respiratory distress, and signs of peritonitis: severe attack, but nonspecific, develop late • Old age, hyperlipidemia, and obesity: increased risk of death • However, these parameters are not reliable prognostic factors and cannot be used as indicators of disease severity.

  6. Cullen's sign Turner's sign

  7. Flank ecchymosis (Grey-Turner sign) • Periumbilical ecchymosis (Cullen sign) • More specific and have been associated with a 37% mortality rate • These signs are rarely present, however, and they often appear 48–72 hours after the onset of symptoms. • Clinical signs have only limited value for the assessment of the severity of acute pancreatitis.

  8. Laboratory Evaluation • Amylase/Lipase: no role in the assessment of disease severity • Serum trypsinogen • Urinary trypsinogen activated peptide levels • Methemalbumin: hemorrhagic pancreatitis • Pancreatic ribonuclease: necrotic tissue • TNF • IL-6 • Phospholipase A2 • Polymophonuclear cell elastase • CRP: 2-3 days after onset, low specific

  9. Multiple prognostic indexes

  10. Multiple prognostic indexes • Reflect systemic abnormalities • Not correlate well with severity and extent of local disease • Ranson scores: corresponding increase in the morbidity and mortality rates. • <3 : no mortality • >6 : mortality rate >50%, usually necrotizing pancreatitis • a total of 48 hours of observation for proper evaluation.

  11. Multiple prognostic indexes • Acute Physiology and Chronic Health Evaluation (APACHE II) • Corresponding increase in morbidity and mortality • >8: severe pancreatitis • Advantage: used throughout the patient’s hospital course in monitoring the patient’s response to therapy

  12. Imaging study • Conventional abdominal radiographs and barium studies: no role in the early evaluation of disease severity. • CXR ±renal function tests: useful for the prediction of severity • pulmonary findings (infiltrates, effusions) in acute pancreatitis is 15%–55%, seen mainly in patients with severe disease. • The predictive value is increased with left-sided or bilateral pleural effusions.

  13. Ultrasonographic Evaluation • Indicated early in an acute episode of pancreatitis • help evaluate gallbladder and/or common duct stones. • Interfered with bowel gas • Intraparenchymal and retroperitoneal fluid collections correlates poorly with pancreatic necrosis. • A diffusely enlarged and hypoechoic gland is consistent with interstitial edema, while extrapancreatic fluid collections (lesser sac, anterior pararenal space) are detected in patients with severe disease

  14. CT Evaluation • Contrast material–enhanced CT • quantify pancreatic parenchymal injury • mild pancreatitis have an intact capillary network

  15. The inability to reliably depict pancreatic necrosis

  16. Areas of diminished or no enhancement indicate decreased blood flow and relate to pancreatic zones of ischemia or necrosis • CT has shown an overall accuracy of 87%with a sensitivity of 100% for the detection of extended pancreatic necrosis and a sensitivity of 50% if only minor necrotic areas were present at surgery.

  17. Without necrosis: no mortality and a complication rate of only 6% • CT evidence of necrosis: mortality 23%, morbidity 82%.

  18. <30% necrosis: no mortality and a 48% morbidity rate, • >30%: mortality rate of 11–25%, morbidity 75%–100% • It should be emphasized, however, that systemic and local complications may occur during an episode of acute pancreatitis in patients without pancreatic necrosis.

  19. CT Severity Index

  20. CT Enhancement Values and Pitfalls • Fatty infiltration of the pancreas • Interstitial pancreatitis, due to parenchymal edema. • Small intrapancreatic fluid collections • The distinction is difficult and sometimes impossible to make unless previous or follow-up CT images are available for review.

  21. Pancreatic necrosis develops early, within the first 24–48 hours after the onset • zones of tissue liquefaction become better defined and more easily recognized 2–3 days after the initial onset • Thus CT scans obtained 3 days after clinical onset yield higher accuracy in the depiction of necrotizing pancreatitis

  22. Fat necrosis: occurs in patients with or without parenchymal necrosis • Favor secondary bacterial contamination. • 22% incidence of local complications in patients without pancreatic necrosis but with peripancreatic fluid collections • CT cannot be used to help reliably diagnose, nor can it help accurately quantify, retroperitoneal fat necrosis. • It has been suggested, therefore, that in clinical practice all heterogeneous peripancreatic collections should be considered areas of fat necrosis until proven otherwise

  23. CT Correlation with NumericSystems • There is a wide variation in the relationship of prognostic signs (Ranson, APACHE II) and early CT findings in acute pancreatitis. • CT evaluation results were found to be better prognostic indicators, owing to greater sensitivity and specificity.

  24. Magnetic Resonance Imaging • an excellent alternative noninvasive modality to help evaluate patients and stage acute pancreatitis • particularly useful in patients who cannot receive iodinated contrast material due to allergic reactions or renal insufficiency. • Gadolinium-enhanced T1-weighted: pancreatic necrosis as areas of nonenhanced parenchyma • Fat-suppression images: defining subtle, diffuse, or focal parenchymal abnormalities. • T2-weighted images: Fluid collections, pseudocysts, and areas of hemorrhage.

  25. CONCLUSIONS • Numeric systems (APACHE II, Ranson) are commonly used today to help detect organ failure, and the acquired data are used as indirect evidence of disease severity, with a sensitivity of about 70%. • Contrast-enhanced CT is the imaging modality of choice to help stage the severity of inflammatory processes, detect pancreatic necrosis, and depict local complications.

  26. Thanks for your attention

More Related