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review of literature on clinical pancreatology - The Pancreapedia

review of literature on clinical pancreatology - The Pancreapedia

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c<strong>on</strong>centrati<strong>on</strong>s, treatment with low-level intravenous unfracti<strong>on</strong>ated heparin led to promptreducti<strong>on</strong> in plasma triglyceride c<strong>on</strong>centrati<strong>on</strong> and may have prevented the development <str<strong>on</strong>g>of</str<strong>on</strong>g>hypertriglyceridemia-associated acute pancreatitis. One article <str<strong>on</strong>g>review</str<strong>on</strong>g>ed the rati<strong>on</strong>ale for thistreatment and surveys prior publicati<strong>on</strong>s using heparin in this and similar settings [183].d-DimerStudies <strong>on</strong> the <strong>clinical</strong> value <str<strong>on</strong>g>of</str<strong>on</strong>g> parameters <str<strong>on</strong>g>of</str<strong>on</strong>g> hemostasis in predicting pancreatitisassociatedcomplicati<strong>on</strong>s are still scarce. <strong>The</strong> aim <str<strong>on</strong>g>of</str<strong>on</strong>g> <strong>on</strong>e prospective study was to identifythe useful hemostatic markers for accurate determinati<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> the subsequent development <str<strong>on</strong>g>of</str<strong>on</strong>g>organ failure during the very early course <str<strong>on</strong>g>of</str<strong>on</strong>g> acute pancreatitis. In 91 c<strong>on</strong>secutive primarilyadmitted patients with acute pancreatitis, prothrombin time, activated partial thromboplastintime, fibrinogen, antithrombin III, protein C, plasminogen activator inhibitor 1, d-dimer, andplasminogen were measured in plasma within the first 24 hours <str<strong>on</strong>g>of</str<strong>on</strong>g> admissi<strong>on</strong> and 24 hoursthereafter. Two study groups comprising 24 patients with organ failure and 67 patientswithout organ failure were compared. Levels <str<strong>on</strong>g>of</str<strong>on</strong>g> prothrombin time, fibrinogen, and d-dimer <strong>on</strong>admissi<strong>on</strong> were significantly different between the organ failure and n<strong>on</strong>-organ failuregroups, and all these parameters plus antithrombin III were significantly different 24 hourslater. d-Dimer in predicting the development <str<strong>on</strong>g>of</str<strong>on</strong>g> organ failure had a sensitivity, specificity, andpositive and negative predictive values <str<strong>on</strong>g>of</str<strong>on</strong>g> 90, 89, 75, and 96 percent, respectively [184].CTA prospective study aimed at evaluating dynamic computed tomography (CT) as aprognostic indicator <str<strong>on</strong>g>of</str<strong>on</strong>g> local complicati<strong>on</strong>s in patients with pancreatic necrosis. It wasanalyzed the relati<strong>on</strong>ship between the anatomic pattern <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreatic necrosis at dynamicCT (pancreatic necrosis, peripancreatic necrosis, and transparenchymal necrosis) and thedevelopment <str<strong>on</strong>g>of</str<strong>on</strong>g> local complicati<strong>on</strong>s (infected pancreatic necrosis and pseudocyst). Onehundred thirty-eight patients were included in the study. Nine patients were excluded, and 86required surgery. Average time from the <strong>on</strong>set <str<strong>on</strong>g>of</str<strong>on</strong>g> symptoms to dynamic CT was 8.3 days.Multivariate analysis identified prognostic factors for local complicati<strong>on</strong>s:- extent <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreatic necrosis (odds ratio, 7)- presence <str<strong>on</strong>g>of</str<strong>on</strong>g> peripancreatic necrosis (odds ratio 37)- transparenchymal necrosis with upstream viable (enhancing) pancreas (odds ratio36)- no peripancreatic necrosis (odds ratio 0.016)It was c<strong>on</strong>cluded that dynamic CT prognostic factors useful to predict local complicati<strong>on</strong>s inpatients with pancreatic necrosis were the extent <str<strong>on</strong>g>of</str<strong>on</strong>g> pancreatic necrosis, presence <str<strong>on</strong>g>of</str<strong>on</strong>g>peripancreatic necrosis, and the finding <str<strong>on</strong>g>of</str<strong>on</strong>g> transparenchymal necrosis with upstream viable(enhancing) pancreas [185].MRDiffusi<strong>on</strong>-weighted imaging (DWI) is a new magnetic res<strong>on</strong>ance imaging (MRI) techniquethat evaluates the random moti<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> water molecules in biological tissues. <strong>The</strong> <strong>clinical</strong> utility<str<strong>on</strong>g>of</str<strong>on</strong>g> DWI has been established for acute stroke and brain tumors. Recent technicaladvancements in MRI have enabled DWI for the body and several studies have revealed theefficacy <str<strong>on</strong>g>of</str<strong>on</strong>g> DWI for detecting various diseases. One study documented the efficacy <str<strong>on</strong>g>of</str<strong>on</strong>g> DWIfor the evaluati<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> acute pancreatitis. MRI was performed with sequences including T1-weighted, T2-weighted, diffusi<strong>on</strong>-weighted imaging, MR cholangiopancreatography (MRCP)and computed tomography (CT) examinati<strong>on</strong>s <strong>on</strong> 11 patients with mild acute pancreatitis.MRI examinati<strong>on</strong>s were performed using 1.5-T imager. Two experienced radiologists

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