Serial contrast-enhanced MRI of the pancreas: Correlation with secretin-stimulated endoscopic pancreatic function test

被引:16
作者
Balci, N. Cem [1 ]
Alkaade, Samer
Akduman, Isin E.
Bilgin, Mehmet
Murdock, Christopher P.
Burton, Frank R.
机构
[1] St Louis Univ, Dept Radiol, St Louis, MO 63103 USA
[2] St Louis Univ, Dept Gastroenterol, St Louis, MO 63103 USA
[3] Univ Giessen, D-35390 Giessen, Germany
关键词
MRI; contrast agent; secretin pancreas; function; pancreatitis;
D O I
10.1016/j.acra.2006.08.008
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Rationale and Objectives. The purpose of this study was to determine the relationship between the pancreatic enhancement on serial contrast-enhanced MRI (CEMRI) and pancreatic exocrine function using the secretin-stimulated endoscopic pancreatic function test (ePFT). Materials and Methods. A total of 30 patients with clinical symptoms consistent with chronic pancreatitis underwent CEMRI of the abdomen and ePFT within a 1- to 4-week interval. CEMRI was performed in arterial, early venous, and late venous phases. Secretin ePFT was pet-formed with the measurement of HCO3 concentration from the duodenal aspirates after secretin stimulation. Contrast enhancement ratio of the arterial phase to early venous phase was measured on CEMRI (SIRa/SIRv). A three-point evaluation system was used for grading the HCO3 concentration and the enhancement ratio on MRI. For the significance of correlation, kappa statistics was used. Sensitivity and specificity of CEMRI was determined for the diagnosis of early chronic pancreatitis accepting ePFT as a reference. Results. Twenty patients had identical scores on both secretin ePFT and CEMRI. Ten patients revealed discrepancy in scores. Kappa statistics revealed moderate agreement between MRI and ePFT (kappa = 0.44). Sensitivity and specificity values for the diagnosis of pancreatitis were 82% and 57%, respectively. Positive predictive value was 56%, and negative predictive value was 86%. Conclusion. The results of our data indicate that serial CEMRI is an appropriate imaging technique to rule out early chronic pancreatitis. However, secretin-stimulated imaging or ePFT may still be needed for the definite diagnosis of pancreatic exocrine dysfunction.
引用
收藏
页码:1367 / 1372
页数:6
相关论文
共 25 条
[1]   Chronic Pancreatitis: Recent Advances and Ongoing Challenges - In brief [J].
Ahmad, SA ;
Wray, CJ ;
Rilo, HR ;
Choe, KA ;
Gelrud, A ;
Howington, J ;
Lowy, AM ;
Matthews, JB .
CURRENT PROBLEMS IN SURGERY, 2006, 43 (03) :127-238
[2]  
AXON ATR, 1989, RADIOL CLIN N AM, V27, P39
[3]   Feasibility of an endoscopic secretin test: Preliminary results [J].
Ceryak, S ;
Steinberg, WM ;
Marks, ZH ;
Ruiz, A .
PANCREAS, 2001, 23 (02) :216-218
[4]   Dynamic contrast-enhanced MRI of the pancreas: Initial results in healthy volunteers and patients with chronic pancreatitis [J].
Coenegrachts, K ;
Van Steenbergen, W ;
De Keyzer, F ;
Vanbeckevoort, D ;
Bielen, D ;
Chen, F ;
Dockx, S ;
Maes, F ;
Bosmans, H .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2004, 20 (06) :990-997
[5]   An endoscopic pancreatic function test with synthetic porcine secretin for the evaluation of chronic abdominal pain and suspected chronic pancreatitis [J].
Conwell, DL ;
Zuccaro, G ;
Vargo, JJ ;
Trolli, PA ;
VanLente, F ;
Obuchowski, N ;
Dumot, JA ;
O'Laughlin, C .
GASTROINTESTINAL ENDOSCOPY, 2003, 57 (01) :37-40
[6]   Is a 15-minute collection of duodenal secretions after secretin stimulation sufficient to diagnose chronic pancreatitis? [J].
Draganov, P ;
George, S ;
Toskes, PP ;
Forsmark, CE .
PANCREAS, 2004, 28 (01) :89-92
[7]   Diffusion-weighted MR imaging in the evaluation of pancreatic exocrine function before and after secretin stimulation [J].
Erturk, SM ;
Ichikawa, T ;
Motosugi, U ;
Sou, H ;
Araki, T .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2006, 101 (01) :133-136
[8]  
Gohde SC, 1997, AM J ROENTGENOL, V168, P689
[9]  
HAYAKAWA T, 1992, AM J GASTROENTEROL, V87, P1170
[10]   RELATIONSHIP BETWEEN FUNCTIONAL AND HISTOLOGICAL-CHANGES IN CHRONIC-PANCREATITIS [J].
HEIJ, HA ;
OBERTOP, H ;
VANBLANKENSTEIN, M ;
TENKATE, FW ;
WESTBROEK, DL .
DIGESTIVE DISEASES AND SCIENCES, 1986, 31 (10) :1009-1013