TY - JOUR
T1 - Diagnosis of persistent intestinal ischemia in the rabbit using proton magnetic resonance imaging
AU - Park, Adrian
AU - Towner, Rheal A.
AU - Langer, Jacob C.
N1 - Funding Information:
Received 22 June 1993, accepted 20 January 1994. This study was funded in part by the University of Guelph MRI Facility, the McMaster Uni- versity Department of Surgery Resident Research Fund, and Medical Research Council of Canada Grant #MA-I0878. This article was originally presented as a poster to thc American Academy of Pediatrics, Surgical Section, San Francisco, California, October 9-1 1, 1992. Address correspondence to Jacob C. Langer, MD, Department of Surgery, Washington University School of Medicine, Rm 5W12, St. Louis Children’s Hospital, One Children’s Place, St. Louis, MO 63 1 10.
Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 1994
Y1 - 1994
N2 - Noninvasive diagnosis of persistent intestinal ischemia remains an elusive goal. Magnetic resonance imaging (MRI) recognizes changes in tissue water content, and several authors have demonstrated increased intensity within 6 hours of intestinal ischemia. To simulate the clinical situation more closely, we studied the efficacy of MRI in drfferentiating ischemic from viable segments of bowel 24 hours after injury in a rabbit model. A segment of distal ileum was rendered ischemic by vascular isolation and ligation. Controls underwent sham operation without vascular ligation. After 24 hours, multislice transverse scans were done using both T1 and T2 weighting. Image intensity was calculated from the isolated loop (absolute intensity), and paraspinal muscle intensity was used as an internal standard to calculate relative intensity (isolated bowel/paraspinal muscle). Animals were killed and bowel necrosis was confirmed histologically. Both absolute and relative intensity were significantly higher in animals undergoing persistent intestinal ischemia. This was true using both T1 and T2 weighting. In a further group of rabbits using the same model, intensity was calculated both before and after intravenous gadolinium. No significant difference was seen between sham and ischemic animals. Our data show that (1) MRI can differentiate ischemic from viable bowel 24 hours after ischemic injury, and (2) the use of intravenous contrast does not improve accuracy. We conclude that MRI may represent a useful noninvasive technique for the diagnosis of persistent intestinal ischemia and that clinical studies should be initiated.
AB - Noninvasive diagnosis of persistent intestinal ischemia remains an elusive goal. Magnetic resonance imaging (MRI) recognizes changes in tissue water content, and several authors have demonstrated increased intensity within 6 hours of intestinal ischemia. To simulate the clinical situation more closely, we studied the efficacy of MRI in drfferentiating ischemic from viable segments of bowel 24 hours after injury in a rabbit model. A segment of distal ileum was rendered ischemic by vascular isolation and ligation. Controls underwent sham operation without vascular ligation. After 24 hours, multislice transverse scans were done using both T1 and T2 weighting. Image intensity was calculated from the isolated loop (absolute intensity), and paraspinal muscle intensity was used as an internal standard to calculate relative intensity (isolated bowel/paraspinal muscle). Animals were killed and bowel necrosis was confirmed histologically. Both absolute and relative intensity were significantly higher in animals undergoing persistent intestinal ischemia. This was true using both T1 and T2 weighting. In a further group of rabbits using the same model, intensity was calculated both before and after intravenous gadolinium. No significant difference was seen between sham and ischemic animals. Our data show that (1) MRI can differentiate ischemic from viable bowel 24 hours after ischemic injury, and (2) the use of intravenous contrast does not improve accuracy. We conclude that MRI may represent a useful noninvasive technique for the diagnosis of persistent intestinal ischemia and that clinical studies should be initiated.
UR - http://www.scopus.com/inward/record.url?scp=0028568557&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0028568557&partnerID=8YFLogxK
U2 - 10.3109/08941939409015365
DO - 10.3109/08941939409015365
M3 - Article
C2 - 7893635
AN - SCOPUS:0028568557
SN - 0894-1939
VL - 7
SP - 485
EP - 492
JO - Journal of Investigative Surgery
JF - Journal of Investigative Surgery
IS - 6
ER -