Rationale and Objectives
To evaluate multidetector computed tomography (MDCT) for detecting the early changes and dynamic evolution of acute mesenteric ischemia (AMI) induced by the ligation of superior mesenteric vein (SMV) in an experimental porcine model.
Materials and Methods
Twelve pigs were randomly assigned to three experimental groups, and one control group with three pigs in each group. After laparotomy, the SMV was separated and ligated in nine pigs and separated without ligation in three controls. MDCT pre- and postcontrast with arterial, venous, and delayed phase scans, and CT angiography reconstructions of mesenteric vessels were carried out at preoperation, 6 hours, 12 hours, and 18 hours after ligation. The findings of mesenteric vessels, bowel, abdominal cavity at pre- and postoperation, and dynamic evolution were correlated with pathology.
Results
AMI-induced pathological changes were identified in all nine experimental pigs. MDCT angiography clearly delineated main trunk of the SMV, peripheral major and minor tributaries up to brushy vasa recta, and the location and shape of ligations. The early ischemic findings were bowel wall thickening, mesenteric edema, ascites, and pronounced bowel enhancement. Superior mesenteric artery and its major branches appeared spasm with poor filling and delayed and prolonged visualization. SMV and its tributaries were poorly delineated with delayed opacification. We also saw thinning of bowel wall, dilatating bowel with fluid, aggravating mesenteric edema and ascites, and poor enhanced bowel over time.
Conclusion
MDCT detects early changes of mesenteric ischemia and its evolution after ligation of porcine SMV, and may find application in early diagnosis of human venous occlusive AMI.
Mesenteric venous thrombosis (MVT) remains a lethal disease. It usually results in acute mesenteric ischemia (AMI) and even necrosis if not promptly treated. The 30-day mortality is 20%–27% . Because of variations in clinical manifestations, courses, and prognosis from different etiology of MVT, it is hard to diagnose acute MVT at an early stage. Improvements in noninvasive imaging techniques, especially multidetector computed tomography (MDCT), may lead to a more favorable outcome of acute MVT . Identifying patients earlier in their clinical courses can not only avoid intestinal necrosis and unnecessary surgery, but also prompt nonoperative management such as interventional therapy, and hence reduce mortality. According to Zhang et al , mortality rate reached up to 39% in patients with acute MVT who underwent surgical therapy, whereas nonoperative management or interventional therapy markedly reduced hospital mortality.
It was shown that sensitivity and specificity of MDCT for MVT were both higher than 90% when MVT occurs in main trunk of superior mesenteric vein (SMV) or portal vein, whereas characteristic changes of AMI usually appeared at a late stage. The value of MDCT remains uncertain in the identification of the early AMI, or in MVT involving predominantly the small mesenteric veins. A retrospective study by Kumar et al suggested that 44% of MVT predominantly involved the small mesenteric veins, which was more difficult to diagnose early, more likely to develop bowel necrosis, and more frequently required surgery.
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Materials and methods
Animal Preparation
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Imaging Protocols
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CT Data Analysis
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Pathological Analysis
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Statistical Analysis
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Results
CTA Manifestations of Normal SMV
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CTA Findings of Mesenteric Ischemia
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Abnormal CT Findings of Bowel and Abdominal Cavity
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Table 1
Abnormal Computed Tomography Findings of Bowel and Abdominal Cavity and Dynamic Evolution
Abnormal Computed Tomography Findings 6 Hours
( n = 9) 12 Hours
( n = 6) 18 Hours
( n = 3) Controls
( n = 3) Thickening of bowel wall 9 (100%) ∗ 5 (83%) ∗ 1 (33%) 0 Thinning of bowel wall 0 (0) 1 (17%) 2 (67%) 0 Bowel dilatation with fluid 1 (11%) 2 (33.3%) 3 (100%) 0 Mesenteric edema 9 (100%) ∗ 6 (100%) ∗ 3 (100%) 0 Ascites 8 (89%) ∗ 6 (100%) ∗ 3 (100%) 0 Increased enhancement of bowel wall 9 (100%) ∗ 0 (0) 0 (0) 0 Reduced enhancement of bowel wall 0 (0) 6 (100%) ∗ 3 (100%) 0
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Pathologic Findings
Gross observation
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Histological findings
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Discussion
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