Three-dimensional CT angiography of the canine hepatic vasculature
Eight Beagle dogs were anesthetized and were imaged using a single channel helical CT scanner. The contrast medium used in this study was iohexol (300 mg I/ml) and doses were 0.5 ml/kg for a cine scan, 3 ml/kg for an enhanced scan. The flow rate for contrast material administration was 2 ml/sec for...
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Published in | Journal of veterinary science (Suwŏn-si, Korea) Vol. 9; no. 4; pp. 407 - 413 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Korea (South)
대한수의학회
01.12.2008
The Korean Society of Veterinary Science |
Subjects | |
Online Access | Get full text |
ISSN | 1229-845X 1976-555X |
DOI | 10.4142/jvs.2008.9.4.407 |
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Abstract | Eight Beagle dogs were anesthetized and were imaged using a single channel helical CT scanner. The contrast medium used in this study was iohexol (300 mg I/ml) and doses were 0.5 ml/kg for a cine scan, 3 ml/kg for an enhanced scan. The flow rate for contrast material administration was 2 ml/sec for all scans. This study was divided into three steps, with unenhanced, cine and enhanced scans. The enhanced scan was subdivided into the arterial phase and the venous phase. All of the enhanced scans were reconstructed in 1 mm intervals and the scans were interpreted by the use of reformatted images, a cross sectional histogram, maximum intensity projection and shaded surface display. For the cine scans, optimal times were a 9-sec delay time post Ⅳ injection in the arterial phase, and an 18-see delay time post Ⅳ injection in the venous phase. A nine-sec delay time was acceptable for the imaging of the canine hepatic arteries by CT angiography. After completion of arterial phase scanning, venous structures of the liver were well visualized as seen on the venous phase. |
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AbstractList | Eight Beagle dogs were anesthetized and were imaged using a single channel helical CT scanner. The contrast medium used in this study was iohexol (300 mg I/ml) and doses were 0.5 ml/kg for a cine scan, 3 ml/kg for an enhanced scan. The flow rate for contrast material administration was 2 ml/sec for all scans. This study was divided into three steps, with unenhanced, cine and enhanced scans. The enhanced scan was subdivided into the arterial phase and the venous phase. All of the enhanced scans were reconstructed in 1 mm intervals and the scans were interpreted by the use of reformatted images, a cross sectional histogram, maximum intensity projection and shaded surface display. For the cine scans, optimal times were a 9-sec delay time post IV injection in the arterial phase, and an 18-sec delay time post IV injection in the venous phase. A nine-sec delay time was acceptable for the imaging of the canine hepatic arteries by CT angiography. After completion of arterial phase scanning, venous structures of the liver were well visualized as seen on the venous phase. Eight Beagle dogs were anesthetized and were imaged using a single channel helical CT scanner. The contrast medium used in this study was iohexol (300 mg I/ml) and doses were 0.5 ml/kg for a cine scan, 3 ml/kg for an enhanced scan. The flow rate for contrast material administration was 2 ml/sec for all scans. This study was divided into three steps, with unenhanced, cine and enhanced scans. The enhanced scan was subdivided into the arterial phase and the venous phase. All of the enhanced scans were reconstructed in 1 mm intervals and the scans were interpreted by the use of reformatted images, a cross sectional histogram, maximum intensity projection and shaded surface display. For the cine scans, optimal times were a 9-sec delay time post IV injection in the arterial phase, and an 18-sec delay time post IV injection in the venous phase. A nine-sec delay time was acceptable for the imaging of the canine hepatic arteries by CT angiography. After completion of arterial phase scanning, venous structures of the liver were well visualized as seen on the venous phase.Eight Beagle dogs were anesthetized and were imaged using a single channel helical CT scanner. The contrast medium used in this study was iohexol (300 mg I/ml) and doses were 0.5 ml/kg for a cine scan, 3 ml/kg for an enhanced scan. The flow rate for contrast material administration was 2 ml/sec for all scans. This study was divided into three steps, with unenhanced, cine and enhanced scans. The enhanced scan was subdivided into the arterial phase and the venous phase. All of the enhanced scans were reconstructed in 1 mm intervals and the scans were interpreted by the use of reformatted images, a cross sectional histogram, maximum intensity projection and shaded surface display. For the cine scans, optimal times were a 9-sec delay time post IV injection in the arterial phase, and an 18-sec delay time post IV injection in the venous phase. A nine-sec delay time was acceptable for the imaging of the canine hepatic arteries by CT angiography. After completion of arterial phase scanning, venous structures of the liver were well visualized as seen on the venous phase. Eight Beagle dogs were anesthetized and were imaged using a single channel helical CT scanner. The contrast medium used in this study was iohexol (300 mg I/ml) and doses were 0.5 ml/kg for a cine scan, 3 ml/kg for an enhanced scan. The flow rate for contrast material administration was 2 ml/sec for all scans. This study was divided into three steps, with unenhanced, cine and enhanced scans. The enhanced scan was subdivided into the arterial phase and the venous phase. All of the enhanced scans were reconstructed in 1 mm intervals and the scans were interpreted by the use of reformatted images, a cross sectional histogram, maximum intensity projection and shaded surface display. For the cine scans, optimal times were a 9-sec delay time post IV injection in the arterial phase, and an 18-sec delay time post IV injection in the venous phase. A nine-sec delay time was acceptable for the imaging of the canine hepatic arteries by CT angiography. After completion of arterial phase scanning, venous structures of the liver were well visualized as seen on the venous phase. KCI Citation Count: 9 Eight Beagle dogs were anesthetized and were imaged using a single channel helical CT scanner. The contrast medium used in this study was iohexol (300 mg I/ml) and doses were 0.5 ml/kg for a cine scan, 3 ml/kg for an enhanced scan. The flow rate for contrast material administration was 2 ml/sec for all scans. This study was divided into three steps, with unenhanced, cine and enhanced scans. The enhanced scan was subdivided into the arterial phase and the venous phase. All of the enhanced scans were reconstructed in 1 mm intervals and the scans were interpreted by the use of reformatted images, a cross sectional histogram, maximum intensity projection and shaded surface display. For the cine scans, optimal times were a 9-sec delay time post Ⅳ injection in the arterial phase, and an 18-see delay time post Ⅳ injection in the venous phase. A nine-sec delay time was acceptable for the imaging of the canine hepatic arteries by CT angiography. After completion of arterial phase scanning, venous structures of the liver were well visualized as seen on the venous phase. |
Author | Jeong, Y.C. (Seoul National University, Seoul, Republic of Korea) Jung, J.H. (Seoul National University, Seoul, Republic of Korea) Oh, S.K. (Seoul National University, Seoul, Republic of Korea) Choi, M.C. (Seoul National University, Seoul, Republic of Korea), E-mail: mcchoi@snu.ac.kr Yoon, J.H. (Seoul National University, Seoul, Republic of Korea) Lim, C.Y. (Seoul National University, Seoul, Republic of Korea) Chang, J.H. (Seoul National University, Seoul, Republic of Korea) |
AuthorAffiliation | Department of Radiology, College of Veterinary Medicine, Seoul National University, Seoul 151-742, Korea |
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CitedBy_id | crossref_primary_10_1111_j_1740_8261_2010_01770_x crossref_primary_10_1111_vru_12250 crossref_primary_10_1111_jvim_12272 crossref_primary_10_1111_jvim_15395 crossref_primary_10_1186_s40850_022_00151_8 crossref_primary_10_1111_ahe_12090 crossref_primary_10_1292_jvms_14_0469 crossref_primary_10_3892_etm_2018_6257 crossref_primary_10_1111_j_1476_4431_2011_00691_x crossref_primary_10_1111_vru_12902 crossref_primary_10_1111_vru_12957 crossref_primary_10_3390_ani14172609 crossref_primary_10_3390_vetsci6010010 crossref_primary_10_3390_ani13040621 crossref_primary_10_1111_jvim_14802 crossref_primary_10_1111_vru_12461 |
Cites_doi | 10.3348/kjr.2001.2.1.28 10.1097/00004728-199811000-00005 10.3348/kjr.2004.5.1.55 10.2214/ajr.175.6.1751735 10.1111/j.1740-8261.2004.04019.x 10.1148/radiol.2243011188 10.1111/j.1740-8261.1995.tb00251.x 10.1148/radiographics.21.2.g01mr19373 10.1148/radiographics.21.3.g01ma14691 10.1111/j.1740-8261.2003.tb00475.x |
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SubjectTerms | Angiography - methods Angiography - veterinary Animals computed tomography Contrast Media - pharmacology dogs Dogs - anatomy & histology dual phase hepatic artery Iohexol - pharmacology liver Liver - blood supply liver vasculature Original portal vein RADIOGRAFIA RADIOGRAPHIE RADIOGRAPHY three-dimensional image Tomography, X-Ray Computed - methods Tomography, X-Ray Computed - veterinary 수의학 |
Title | Three-dimensional CT angiography of the canine hepatic vasculature |
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