Background & Aims: Current pancreatic function tests are cumbersome and unavailable to the clinical gastroenterologist. We have developed a function test that can be modified to a purely endoscopic collection method (ePFT). The aim of this study was to compare the endoscopic and traditional Dreiling tube collection methods. Methods: Two separate groups of healthy subjects and patients with chronic pancreatitis underwent pancreatic function testing. One group underwent the endoscopic collection method (ePFT). Intravenous cholecystokinin (CCK 40 ng · kg-1 · h -1) was started in preprocedure area. Duodenal fluid was collected with upper endoscope during endoscopy at 30, 40, 50, and 60 minutes during infusion. Another group underwent the traditional Dreiling collection method. Intravenous CCK was started in postprocedure area after endoscopic tube placement. Duodenal fluid was collected at 0, 20, 40, 60, and 80 minutes during infusion. Lipase concentration was determined (IU/L) on laboratory autoanalyzer. Results: Seventy-three patients were studied. Thirty-four underwent endoscopic collection and 39 underwent Dreiling collection. The mean peak lipase concentrations (± standard deviation) for healthy subjects and patients with chronic pancreatitis in the endoscopic collection method group were 1,612,500 ± 556,152 IU/L and 369,594 ± 281,624 IU/L, respectively (P < 0.001). The mean peak lipase concentrations (± standard deviation) for healthy subjects and patients with chronic pancreatitis in the Dreiling tube collection method group were 1,670,324 ± 786,731 IU/L and 478,956 ± 406,061 IU/L, respectively (P < 0.001). There was no statistical difference between collection methods at distinguishing healthy subjects and patients with chronic pancreatitis. Receiver operating characteristic curves (ROC) for the endoscopic and Dreiling collection methods were 0.993 (standard error of mean, 0.009) and 0.921 (standard error of mean, 0.041). A lipase concentration cut point of 810,600 IU/L distinguishes healthy subjects from patients with chronic pancreatitis with a sensitivity and specificity of 92% and 95%, respectively. The ePFT was safe, short in duration, minimized costs ($1890 vs. $2659), required small amounts of fluid for analysis (1-3 mL), and eliminated radiation exposure. Conclusions: Analysis of timed endoscopic aspirations of pancreatic juice after hormonal stimulation can distinguish healthy subjects from patients with chronic pancreatitis. This new endoscopic collection method (ePFT) is less cumbersome and more time efficient, when compared to traditional collection methods. The ePFT broadens the availability of function testing to the practicing clinical gastroenterologist.
|Number of pages||6|
|Journal||Clinical Gastroenterology and Hepatology|
|State||Published - May 1 2003|
Bibliographical noteFunding Information:
Support for this research was provided by educational grants from Solvay Pharmaceuticals and Astra-Zeneca.
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