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Nuclide imaging of vascular graft-platelet interactions: Comparison of indium excess and technetium subtraction techniques

dc.contributor.authorWakefield, Thomas W.en_US
dc.contributor.authorLindblad, Bengten_US
dc.contributor.authorGraham, Linda M.en_US
dc.contributor.authorWhitehouse, Walter M. Jr.en_US
dc.contributor.authorRipley, Shawn D.en_US
dc.contributor.authorPetry, Neil A.en_US
dc.contributor.authorSpaulding, Susan A.en_US
dc.contributor.authorBurkel, William E.en_US
dc.contributor.authorStanley, James C.en_US
dc.date.accessioned2006-04-07T19:32:47Z
dc.date.available2006-04-07T19:32:47Z
dc.date.issued1986-04en_US
dc.identifier.citationWakefield, Thomas W., Lindblad, Bengt, Graham, Linda M., Whitehouse, Jr., Walter M., Ripley, Shawn D., Petry, Neil A., Spaulding, Susan A., Burkel, William E., Stanley, James C. (1986/04)."Nuclide imaging of vascular graft-platelet interactions: Comparison of indium excess and technetium subtraction techniques." Journal of Surgical Research 40(4): 388-394. <http://hdl.handle.net/2027.42/26220>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WM6-4BNG1T4-74/2/d6b3aa6f28faec862dcf404005518c24en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/26220
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3517493&dopt=citationen_US
dc.description.abstractIndium-111-labeled platelet adherence to ePTFE thoracoabdominal vascular prostheses in a canine model (n = 10) was quantitated by (1) an indium-111 excess technique, contrasting graft radioactivity to that in a reference region, and (2) a technetium-99m subtraction technique, with radioactivity of circulating platelets eliminated by discounting background blood activity. Variation in graft thrombogenicity was provided by seeding six prostheses with enzymatically derived autologous endothelial cells, and implanting four prostheses without seeding. Grafts were imaged at 1, 4, and 6 weeks postimplantation, with platelet labeling using indium-111-oxine and red blood cell labeling using technetium-99m. At 7 weeks grafts were excised and gamma activity was measured in proximal, middle, and distal segments. Luminal generation of TxB2 and 6-keto-PGF1[alpha] from midportions of grafts was assayed. Indium-111 excess ratios at 6 weeks correlated with actual gamma activity of excised grafts (proximal r = 0.80, P r = 0.73, P r = 0.48, ns) but such a correlation did not exist for the technetium-99m subtraction technique (r = -0.05, -0.25, and 0.16, in the three segments, respectively, all ns). The ratio of graft to aortic TxB2 production revealed a positive correlation with graft gamma activity (r = 0.87, P 1[alpha] to TxB2 production also correlated with gamma counts (r = -0.64, P = 0.05). In this experimental setting technetium-99m subtraction analysis was an imprecise method of detecting graft platelet accumulation, whereas indium-111 excess ratios proved to be a more accurate method of quantitating vascular prosthetic thrombogenicity.en_US
dc.format.extent895175 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleNuclide imaging of vascular graft-platelet interactions: Comparison of indium excess and technetium subtraction techniquesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelSurgery and Anesthesiologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Surgery, Division of Peripheral Vascular Surgery, Ann Arbor, Michigan 48109, USA; Department of Medicine, Division of Nuclear Medicine, Ann Arbor, Michigan 48109, USA; Department of Anatomy and Cell Biology, Ann Arbor, Michigan 48109, USA; University of Michigan Medical School, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumDepartment of Surgery, Division of Peripheral Vascular Surgery, Ann Arbor, Michigan 48109, USA; Department of Medicine, Division of Nuclear Medicine, Ann Arbor, Michigan 48109, USA; Department of Anatomy and Cell Biology, Ann Arbor, Michigan 48109, USA; University of Michigan Medical School, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumDepartment of Surgery, Division of Peripheral Vascular Surgery, Ann Arbor, Michigan 48109, USA; Department of Medicine, Division of Nuclear Medicine, Ann Arbor, Michigan 48109, USA; Department of Anatomy and Cell Biology, Ann Arbor, Michigan 48109, USA; University of Michigan Medical School, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumDepartment of Surgery, Division of Peripheral Vascular Surgery, Ann Arbor, Michigan 48109, USA; Department of Medicine, Division of Nuclear Medicine, Ann Arbor, Michigan 48109, USA; Department of Anatomy and Cell Biology, Ann Arbor, Michigan 48109, USA; University of Michigan Medical School, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumDepartment of Surgery, Division of Peripheral Vascular Surgery, Ann Arbor, Michigan 48109, USA; Department of Medicine, Division of Nuclear Medicine, Ann Arbor, Michigan 48109, USA; Department of Anatomy and Cell Biology, Ann Arbor, Michigan 48109, USA; University of Michigan Medical School, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumDepartment of Surgery, Division of Peripheral Vascular Surgery, Ann Arbor, Michigan 48109, USA; Department of Medicine, Division of Nuclear Medicine, Ann Arbor, Michigan 48109, USA; Department of Anatomy and Cell Biology, Ann Arbor, Michigan 48109, USA; University of Michigan Medical School, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumDepartment of Surgery, Division of Peripheral Vascular Surgery, Ann Arbor, Michigan 48109, USA; Department of Medicine, Division of Nuclear Medicine, Ann Arbor, Michigan 48109, USA; Department of Anatomy and Cell Biology, Ann Arbor, Michigan 48109, USA; University of Michigan Medical School, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumDepartment of Surgery, Division of Peripheral Vascular Surgery, Ann Arbor, Michigan 48109, USA; Department of Medicine, Division of Nuclear Medicine, Ann Arbor, Michigan 48109, USA; Department of Anatomy and Cell Biology, Ann Arbor, Michigan 48109, USA; University of Michigan Medical School, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumDepartment of Surgery, Division of Peripheral Vascular Surgery, Ann Arbor, Michigan 48109, USA; Department of Medicine, Division of Nuclear Medicine, Ann Arbor, Michigan 48109, USA; Department of Anatomy and Cell Biology, Ann Arbor, Michigan 48109, USA; University of Michigan Medical School, Ann Arbor, Michigan 48109, USAen_US
dc.identifier.pmid3517493en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/26220/1/0000300.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0022-4804(86)90204-0en_US
dc.identifier.sourceJournal of Surgical Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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